MYC: Connecting selective transcriptional control to global RNA production
Abstract
Two opposing models have been proposed to describe the function of the MYC oncoprotein in shaping cellular transcriptomes: one posits that MYC amplifies transcription at all active loci; the other that MYC differentially controls discrete sets of genes, the products of which affect global transcript levels. Here, we argue that differential gene regulation by MYC is the sole unifying model that is consistent with all available data. Among other effects, MYC endows cells with physiological and metabolic changes that have the potential to feed back on global RNA production, processing and turnover. The field is progressing steadily towards a full characterization of the MYC-regulated genes and pathways that mediate these biological effects and - by the same token - endow MYC with its pervasive oncogenic potential.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Endurance-oriented stimuli may bias translational machinery toward oxidative metabolism and mitochondrial adaptation, whereas resistance exercise may favor ribosomal configurations more suitable for myofibrillar accretion, offering one explanation for the interference effect.
“This could offer one explanation for the interference effect observed during concurrent training: rather than entirely suppressing ribosome biogenesis, endurance-oriented stimuli may bias translational machinery toward proteins involved in oxidative metabolism and mitochondrial adaptation, whereas resistance exercise may favor ribosomal configurations more suitable for myofibrillar accretion [188,”
From Ribosome Biogenesis as a Putative Bottleneck to Skeletal Muscle Hypertrophy: Mechanisms, Human Evidence, and Practical Modulators (2026) · cites this paper as [193]
Cites
1 retracted
Csibi, A., Lee, G., Yoon, S.-O., Tong, H., Ilter, D., Elia, I., Fendt, S., Roberts, T. M., & Blenis, J. (2014) · Current Biology · doi:10.1016/j.cub.2014.08.007 · Cited by 253 · see citing works
RetractedLodish, H. F. (1986) · Cited by 5,640 · see citing works
Identification of c- <i>MYC</i> as a Target of the APC Pathway
He, T.-C., Sparks, A. B., Rago, C., Hermeking, H., Zawel, L., da Costa, L. T., Morin, P. J., Vogelstein, B., & Kinzler, K. W. (1998) · Science · doi:10.1126/science.281.5382.1509 · Cited by 4,566 · see citing works
Dang, C. V. (2012) · Cell · doi:10.1016/j.cell.2012.03.003 · Cited by 3,390 · see citing works
CpG islands and the regulation of transcription
Deaton, A. M., & Bird, A. (2011) · Genes & Development · doi:10.1101/gad.2037511 · Cited by 3,187 · see citing works
Tumorigenic conversion of primary embryo fibroblasts requires at least two cooperating oncogenes
Land, H., Parada, L. F., & Weinberg, R. A. (1983) · Nature · doi:10.1038/304596a0 · Cited by 2,804 · see citing works
Bromberg, J. F., Wrzeszczynska, M. H., Devgan, G., Zhao, Y., Pestell, R. G., Albanese, C., & Darnell, J. E. (1999) · Cell · doi:10.1016/s0092-8674(00)81959-5 · Cited by 2,790 · see citing works
The transcription factor Myc controls metabolic reprogramming upon T lymphocyte activation
Wang, R., Dillon, C. P., Shi, L. Z., Milasta, S., Carter, R., Finkelstein, D., McCormick, L. L., Fitzgerald, P., Chi, H., Munger, J., et al. (2011) · Immunity · doi:10.1016/j.immuni.2011.09.021 · Cited by 2,140 · see citing works
Gao, P., Tchernyshyov, I., Chang, T.-C., Lee, Y.-S., Kita, K., Ochi, T., Zeller, K. I., De Marzo, A. M., Van Eyk, J. E., Mendell, J. T., et al. (2009) · Nature · doi:10.1038/nature07823 · Cited by 2,124 · see citing works
Wise, D. R., DeBerardinis, R. J., Mancuso, A., Sayed, N., Zhang, X.-Y., Pfeiffer, H. K., Nissim, I., Daikhin, E., Yudkoff, M., McMahon, S. B., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810199105 · Cited by 2,001 · see citing works
Max: A Helix-Loop-Helix Zipper Protein That Forms a Sequence-Specific DNA-Binding Complex with Myc
Blackwood, E. M., & Eisenman, R. N. (1991) · Science · doi:10.1126/science.2006410 · Cited by 1,681 · see citing works
Reflecting on 25 years with MYC
Meyer, N., & Penn, L. Z. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2231 · Cited by 1,575 · see citing works
Activation of a cellular onc gene by promoter insertion in ALV-induced lymphoid leukosis
Hayward, W. S., Neel, B. G., & Astrin, S. M. (1981) · Nature · doi:10.1038/290475a0 · Cited by 1,569 · see citing works
Transcriptional Amplification in Tumor Cells with Elevated c-Myc
Lin, C. Y., Lovén, J., Rahl, P. B., Paranal, R. M., Burge, C. B., Bradner, J. E., Lee, T. I., & Young, R. A. (2012) · Cell · doi:10.1016/j.cell.2012.08.026 · Cited by 1,498 · see citing works
Emerging landscape of oncogenic signatures across human cancers
Ciriello, G., Miller, M. L., Aksoy, B. A., Şenbabaoğlu, Y., Schultz, N. D., & Sander, C. (2013) · Nature Genetics · doi:10.1038/ng.2762 · Cited by 1,382 · see citing works
Multiple Ras-dependent phosphorylation pathways regulate Myc protein stabilityPreprint
Sears, R. C., Nuckolls, F., Haura, E. B., Taya, Y., Tamai, K., & Nevins, J. R. (2000) · Genes & Development · doi:10.1101/gad.836800 · Cited by 1,379 · see citing works
Widespread microRNA repression by Myc contributes to tumorigenesis
Chang, T.-C., Yu, D., Lee, Y., Wentzel, E. A., Arking, D. E., West, K. M., Dang, C. V., Thomas‐Tikhonenko, A., & Mendell, J. T. (2007) · Nature Genetics · doi:10.1038/ng.2007.30 · Cited by 1,326 · see citing works
An Extended Transcriptional Network for Pluripotency of Embryonic Stem Cells
Kim, J., Chu, J., Shen, X., Wang, J., & Orkin, S. H. (2008) · Cell · doi:10.1016/j.cell.2008.02.039 · Cited by 1,321 · see citing works
c-Myc Regulates Transcriptional Pause Release
Rahl, P. B., Lin, C. Y., Seila, A. C., Flynn, R. A., McCuine, S., Burge, C. B., Sharp, P. A., & Young, R. A. (2010) · Cell · doi:10.1016/j.cell.2010.03.030 · Cited by 1,279 · see citing works
The Many Pathways of RNA Degradation
Houseley, J. M., & Tollervey, D. W. (2009) · Cell · doi:10.1016/j.cell.2009.01.019 · Cited by 1,220 · see citing works
Promoter-proximal pausing of RNA polymerase II: emerging roles in metazoans
Adelman, K., & Lis, J. T. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3293 · Cited by 1,186 · see citing works
HnRNP proteins controlled by c-Myc deregulate pyruvate kinase mRNA splicing in cancer
David, C. J., Chen, M., Assanah, M., Canoll, P., & Manley, J. L. (2010) · Nature · doi:10.1038/nature08697 · Cited by 1,179 · see citing works
(1987) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(87)90455-5 · Cited by 1,130 · see citing works
Transcriptional regulation and transformation by Myc proteins
Adhikary, S., & Eilers, M. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1703 · Cited by 1,122 · see citing works
c-Myc transactivation of <i>LDH-A</i> : Implications for tumor metabolism and growth
Shim, H., Dolde, C., Lewis, B. C., Wu, C.-S., Dang, G., Jungmann, R. A., Dalla-Favera, R., & Dang, C. V. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.13.6658 · Cited by 1,092 · see citing works
c-Myc Is a Universal Amplifier of Expressed Genes in Lymphocytes and Embryonic Stem Cells
Nie, Z., Hu, G., Wei, G., Cui, K., Yamane, A., Resch, W., Wang, R., Green, D. R., Tessarollo, L., Casellas, R. C., et al. (2012) · Cell · doi:10.1016/j.cell.2012.08.033 · Cited by 1,075 · see citing works
Context-dependent control of alternative splicing by RNA-binding proteins
Fu, X.-D., & Ares, M. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3778 · Cited by 1,044 · see citing works
Genomic targets of the human c-Myc proteinPreprint
Fernandez, P. C., Frank, S. R., Wang, L., Schroeder, M., Liu, S., Greene, J. R., Cocito, A., & Amati, B. B. (2003) · Genes & Development · doi:10.1101/gad.1067003 · Cited by 963 · see citing works
MYC as a regulator of ribosome biogenesis and protein synthesis
van Riggelen, J., Yetil, A., & Felsher, D. W. (2010) · Nature Reviews Cancer · doi:10.1038/nrc2819 · Cited by 956 · see citing works
Eilers, M., & Eisenman, R. N. (2008) · Genes & Development · doi:10.1101/gad.1712408 · Cited by 927 · see citing works
Reversible tumorigenesis by MYC in hematopoietic lineages.
Felsher, D., & Bishop, J. (1999) · Molecules and Cells · doi:10.1016/s1097-2765(00)80367-6 · Cited by 917 · see citing works
Soufi, A., Donahue, G., & Zaret, K. S. (2012) · Cell · doi:10.1016/j.cell.2012.09.045 · Cited by 887 · see citing works
Zhang, H., Gao, P., Fukuda, R., Kumar, G., Krishnamachary, B., Zeller, K. I., Dang, C. V., & Semenza, G. L. (2007) · Cancer Cell · doi:10.1016/j.ccr.2007.04.001 · Cited by 885 · see citing works
Getting up to speed with transcription elongation by RNA polymerase II
Jonkers, I., & Lis, J. T. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3953 · Cited by 876 · see citing works
MYC inactivation uncovers pluripotent differentiation and tumour dormancy in hepatocellular cancer
Shachaf, C. M., Kopelman, A. M., Arvanitis, C., Karlsson, Å., Beer, S., Mandl, S., Bachmann, M. H., Borowsky, A. D., Ruebner, B., Cardiff, R. D., et al. (2004) · Nature · doi:10.1038/nature03043 · Cited by 874 · see citing works
c-Myc is an important direct target of Notch1 in T-cell acute lymphoblastic leukemia/lymphomaPreprint
Weng, A. P., Millholland, J. M., Yashiro–Ohtani, Y., Arcangeli, M.-L., Lau, A. N., Wai, C., Bianco, C. D., Rodríguez, C. G., Sai, H., Tobias, J. W., et al. (2006) · Genes & Development · doi:10.1101/gad.1450406 · Cited by 863 · see citing works
c-Myc controls the balance between hematopoietic stem cell self-renewal and differentiation
Wilson, A., Murphy, M. J., Oskarsson, T., Kaloulis, K., Bettess, M. D., Oser, G. M., Pasche, A.-C., Knabenhans, C., MacDonald, H. R., & Trumpp, A. (2004) · Genes & Development · doi:10.1101/gad.313104 · Cited by 823 · see citing works
Modelling Myc inhibition as a cancer therapy
Soucek, L., Whitfield, J. R., Martins, C. P., Finch, A. J., Murphy, D. J., Sodir, N. M., Karnezis, A. N., Swigart, L. B., Nasi, S., & Evan, G. I. (2008) · Nature · doi:10.1038/nature07260 · Cited by 822 · see citing works
Palomero, T., Lim, W. K., Odom, D. T., Sulis, M. L., Real, P. J., Margolin, A. A., Barnes, K., O’Neil, J., Neuberg, D. S., Weng, A. P., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606108103 · Cited by 821 · see citing works
Wang, J., Zhuang, J., Iyer, S., Lin, X.-Y., Whitfield, T. W., Greven, M. C., Pierce, B. G., Dong, X., Kundaje, A. B., Cheng, Y., et al. (2012) · Genome Research · doi:10.1101/gr.139105.112 · Cited by 820 · see citing works
MYC Activation Is a Hallmark of Cancer Initiation and MaintenancePreprint
Gabay, M., Li, Y., & Felsher, D. W. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a014241 · Cited by 808 · see citing works
Medulloblastoma Growth Inhibition by Hedgehog Pathway Blockade
Berman, D. M., Karhadkar, S. S., Hallahan, A. R., Pritchard, J. I., Eberhart, C. G., Watkins, D. N., Chen, J., Cooper, M. K., Taipale, J., Olson, J. M., et al. (2002) · Science · doi:10.1126/science.1073733 · Cited by 802 · see citing works
Marcu, K. B., Bossone, S., & Patel, A. J. (1992) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.61.070192.004113 · Cited by 799 · see citing works
Pioneer Transcription Factors Target Partial DNA Motifs on Nucleosomes to Initiate Reprogramming
Soufi, A., Garcia, M. F., Jaroszewicz, A., Osman, N., Pellegrini, M., & Zaret, K. S. (2015) · Cell · doi:10.1016/j.cell.2015.03.017 · Cited by 780 · see citing works
RNA polymerase stalling at developmental control genes in the Drosophila melanogaster embryo
Zeitlinger, J., Stark, A., Kellis, M., Hong, J., Nechaev, S., Adelman, K., Levine, M., & Young, R. A. (2007) · Nature Genetics · doi:10.1038/ng.2007.26 · Cited by 766 · see citing works
An expansive human regulatory lexicon encoded in transcription factor footprints
Neph, S. J., Vierstra, J. D., Stergachis, A. B., Reynolds, A. P., Haugen, E., Vernot, B., Thurman, R. E., John, S., Sandstrom, R. S., Johnson, A., et al. (2012) · Nature · doi:10.1038/nature11212 · Cited by 746 · see citing works
Cai, L., Sutter, B. M., Li, B., & Tu, B. P. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.05.004 · Cited by 701 · see citing works
Metabolic Regulation of Epigenetics
Lu, C., & Thompson, C. B. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.06.001 · Cited by 699 · see citing works
c-Myc binds to human ribosomal DNA and stimulates transcription of rRNA genes by RNA polymerase I
Grandori, C., Gomez-Roman, N., Felton-Edkins, Z. A., Ngouenet, C., Galloway, D. A., Eisenman, R. N., & White, R. J. (2005) · Nature Cell Biology · doi:10.1038/ncb1224 · Cited by 659 · see citing works
Kim, J.-W., Gao, P., Liu, Y.-C., Semenza, G. L., & Dang, C. V. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00440-07 · Cited by 658 · see citing works
Non-transcriptional control of DNA replication by c-Myc
Dominguez-Sola, D., Ying, C. Y., Grandori, C., Ruggiero, L., Chen, B., Li, M., Galloway, D. A., Gu, W. J., Gautier, J., & Dalla‐Favera, R. (2007) · Nature · doi:10.1038/nature05953 · Cited by 652 · see citing works
Drosophila myc Regulates Cellular Growth during Development
Johnston, L. A., Prober, D. A., Edgar, B. A., Eisenman, R. N., & Gallant, P. (1999) · Cell · doi:10.1016/s0092-8674(00)81512-3 · Cited by 648 · see citing works
Sustained Loss of a Neoplastic Phenotype by Brief Inactivation of MYC
Jain, M., Arvanitis, C., Chu, K., Dewey, W. C., Leonhardt, E. A., Trinh, M., Sundberg, C. D., Bishop, J. M., & Felsher, D. W. (2002) · Science · doi:10.1126/science.1071489 · Cited by 647 · see citing works
CDK7 Inhibition Suppresses Super-Enhancer-Linked Oncogenic Transcription in MYCN-Driven Cancer
Chipumuro, E., Marco, E., Christensen, C. L., Kwiatkowski, N. P., Zhang, T., Hatheway, C. M., Abraham, B. J., Sharma, B., Yeung, C. M., Altabef, A. B., et al. (2014) · Cell · doi:10.1016/j.cell.2014.10.024 · Cited by 631 · see citing works
Pelengaris, S., Khan, M., & Evan, G. I. (2002) · Cell · doi:10.1016/s0092-8674(02)00738-9 · Cited by 623 · see citing works
Revisiting Global Gene Expression Analysis
Lovén, J., Orlando, D. A., Sigova, A. A., Lin, C. Y., Rahl, P. B., Burge, C. B., Levens, D. L., Lee, T. I., & Young, R. A. (2012) · Cell · doi:10.1016/j.cell.2012.10.012 · Cited by 616 · see citing works
Myc Stimulates Nuclearly Encoded Mitochondrial Genes and Mitochondrial Biogenesis
Li, F., Wang, Y., Zeller, K. I., Potter, J. J., Wonsey, D. R., O’Donnell, K. A., Kim, J., Yustein, J. T., Lee, L. A., & Dang, C. V. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.14.6225-6234.2005 · Cited by 615 · see citing works
Myc deletion rescues Apc deficiency in the small intestine
Sansom, O. J., Méniel, V. S., Muncan, V., Phesse, T. J., Wilkins, J. A., Reed, K. R., Vass, J. K., Athineos, D., Clevers, H. C., & Clarke, A. R. (2007) · Nature · doi:10.1038/nature05674 · Cited by 614 · see citing works
MYC, Metabolism, Cell Growth, and TumorigenesisPreprint
Dang, C. V. (2013) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a014217 · Cited by 600 · see citing works
Repression of p15INK4b expression by Myc through association with Miz-1
Staller, P., Peukert, K., Kiermaier, A. C., Seoane, J., Lukas, J., Karsunky, H., Möröy, T., Bártek, J., Massagué, J., Hänel, F., et al. (2001) · Nature Cell Biology · doi:10.1038/35070076 · Cited by 574 · see citing works
The Myc oncoprotein as a therapeutic target for human cancer
Vita, M. F., & Arsenian‐Henriksson, M. (2006) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2006.07.015 · Cited by 554 · see citing works
X-Ray Structures of Myc-Max and Mad-Max Recognizing DNA
Nair, S. K., & Burley, S. K. (2003) · Cell · doi:10.1016/s0092-8674(02)01284-9 · Cited by 551 · see citing works
Global mapping of c-Myc binding sites and target gene networks in human B cells
Zeller, K. I., Zhao, X., Lee, C. W. H., Chiu, K. P., Yao, F., Yustein, J. T., Ooi, H., Orlov, Y. L., Shahab, A., Yong, H. C., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604129103 · Cited by 518 · see citing works
Activation and repression by oncogenic MYC shape tumour-specific gene expression profiles
Walz, S., Lorenzin, F., Morton, J. P., Wiese, K. E., von Eyß, B., Herold, S., Rycak, L., Dumay‐Odelot, H., Karim, S. A., Bartkuhn, M., et al. (2014) · Nature · doi:10.1038/nature13473 · Cited by 502 · see citing works
The spliceosome is a therapeutic vulnerability in MYC-driven cancer
Hsu, T. Y. T., Simon, L. M., Neill, N. J., Marcotte, R., Sayad, A., Bland, C. S., Echeverria, G. V., Sun, T., Kurley, S. J., Tyagi, S., et al. (2015) · Nature · doi:10.1038/nature14985 · Cited by 493 · see citing works
TGFβ influences Myc, Miz-1 and Smad to control the CDK inhibitor p15INK4b
Seoane, J., Pouponnot, C., Staller, P., Schader, M. B., Eilers, M., & Massagué, J. (2001) · Nature Cell Biology · doi:10.1038/35070086 · Cited by 489 · see citing works
Zeller, K. I., Jegga, A. G., Aronow, B. J., O’Donnell, K. A., & Dang, C. V. (2003) · Genome biology · doi:10.1186/gb-2003-4-10-r69 · Cited by 483 · see citing works
Bim is a suppressor of Myc-induced mouse B cell leukemia
Egle, A., Harris, A. W., Bouillet, P., & Cory, S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401471101 · Cited by 482 · see citing works
E2F4/5 and p107 as Smad Cofactors Linking the TGFβ Receptor to c-myc Repression
Chen, C.-R., Kang, Y., Siegel, P. M., & Massagué, J. (2002) · Cell · doi:10.1016/s0092-8674(02)00801-2 · Cited by 482 · see citing works
Selective transcriptional regulation by Myc in cellular growth control and lymphomagenesis
Sabò, A., Kress, T. R., Pelizzola, M., de Pretis, S., Gorski, M. M., Tesi, A., Morelli, M. J., Bora, P., Doni, M., Verrecchia, A., et al. (2014) · Nature · doi:10.1038/nature13537 · Cited by 478 · see citing works
c-Myc associates with ribosomal DNA and activates RNA polymerase I transcription
Arabi, A., Wu, S., Ridderstråle, K., Bierhoff, H., Shiue, C.-N., Fátyol, K., Fahlén, S., Hydbring, P., Söderberg, O., Grummt, I., et al. (2005) · Nature Cell Biology · doi:10.1038/ncb1225 · Cited by 471 · see citing works
Chromatin connectivity maps reveal dynamic promoter–enhancer long-range associations
Zhang, Y., Wong, C., Birnbaum, R. Y., Li, G., Favaro, R., Ngan, C. Y., Lim, J., Tai, E., Poh, H. M., Wong, E., et al. (2013) · Nature · doi:10.1038/nature12716 · Cited by 470 · see citing works
Tilgner, H., Knowles, D. G., Johnson, R., Davis, C., Chakrabortty, S. K., Djebali, S., Curado, J., Snyder, M. P., Gingeras, T., & Guigó, R. (2012) · Genome Research · doi:10.1101/gr.134445.111 · Cited by 463 · see citing works
The pluripotent regulatory circuitry connecting promoters to their long-range interacting elements
Schoenfelder, S., Furlan-Magaril, M., Mifsud, B., Tavares-Cadete, F., Sugar, R., Javierre, B.-M., Nagano, T., Katsman, Y., Sakthidevi, M., Wingett, S. W., et al. (2015) · Genome Research · doi:10.1101/gr.185272.114 · Cited by 460 · see citing works
Ras Enhances Myc Protein Stability
Sears, R. C., Leone, G. W., DeGregori, J. V., & Nevins, J. R. (1999) · Molecular Cell · doi:10.1016/s1097-2765(00)80308-1 · Cited by 454 · see citing works
Evasion of the p53 tumour surveillance network by tumour-derived MYC mutants
Hemann, M. T., Bric, A., Teruya‐Feldstein, J., Herbst, A., Nilsson, J. A., Cordon‐Cardo, C., Cleveland, J. L., Tansey, W. P., & Lowe, S. W. (2005) · Nature · doi:10.1038/nature03845 · Cited by 452 · see citing works
Myc represses transcription through recruitment of DNA methyltransferase corepressor
Brenner, C., Deplus, R., Mirjolet, C., Loriot, A. E., Viré, E. A., Smet, C. D., Gutiérrez, A., Danovi, D., Bernard, D., Boon, T., et al. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600509 · Cited by 443 · see citing works
Anczuków, O., Rosenberg, A. Z., Akerman, M., Das, S., Zhan, L., Karni, R., Muthuswamy, S. K., & Krainer, A. R. (2012) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2207 · Cited by 441 · see citing works
Suppression of Myc oncogenic activity by ribosomal protein haploinsufficiency
Barna, M., Pusic, A., Zollo, O., Costa, M. J., Kondrashov, N., Rego, E., Rao, P., & Ruggero, D. (2008) · Nature · doi:10.1038/nature07449 · Cited by 434 · see citing works
Direct activation of RNA polymerase III transcription by c-Myc
Gomez-Roman, N., Grandori, C., Eisenman, R. N., & White, R. J. (2003) · Nature · doi:10.1038/nature01327 · Cited by 434 · see citing works
Padovan-Merhar, O. M., Nair, G. P., Biaesch, A. G., Mayer, A., Scarfone, S., Foley, S. W., Wu, A. R., Churchman, L. S., Singh, A., & Raj, A. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.03.005 · Cited by 434 · see citing works
The c-myc oncogene perturbs B lymphocyte development in Eμ-myc transgenic mice
Langdon, W. Y., Harris, A. W., Cory, S., & Adams, J. M. (1986) · Cell · doi:10.1016/0092-8674(86)90361-2 · Cited by 433 · see citing works
Koromilas, A. E., Lazaris-Karatzas, A., & Sonenberg, N. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05508.x · Cited by 422 · see citing works
Myc represses the p21 (WAF1/CIP1) promoter and interacts with Sp1/Sp3
Gartel, A. L., Ye, X., Goufman, E., Shiyanov, P. A., Hay, N., Najmabadi, F., & Tyner, A. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081074898 · Cited by 416 · see citing works
Control of Transcriptional Elongation
Kwak, H., & Lis, J. T. (2013) · Annual Review of Genetics · doi:10.1146/annurev-genet-110711-155440 · Cited by 412 · see citing works
MYC recruits the TIP60 histone acetyltransferase complex to chromatin
Frank, S. R., Parisi, T., Taubert, S., Fernandez, P. C., Fuchs, M., Chan, H., Livingston, D. M., & Amati, B. B. (2003) · EMBO Reports · doi:10.1038/sj.embor.embor861 · Cited by 402 · see citing works
STAT3 Is Required for the gp130-mediated Full Activation of the c-myc Gene
Kiuchi, N., Nakajima, K., Ichiba, M., Fukada, T., Narimatsu, M., Mizuno, K., Hibi, M., & Hirano, T. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.189.1.63 · Cited by 396 · see citing works
Myc-dependent regulation of ribosomal RNA synthesis during Drosophila development
Grewal, S., Li, L., Orian, A., Eisenman, R. N., & Edgar, B. A. (2005) · Nature Cell Biology · doi:10.1038/ncb1223 · Cited by 387 · see citing works
Genomic binding by the Drosophila Myc, Max, Mad/Mnt transcription factor networkPreprint
Orian, A., van Steensel, B., Delrow, J. J., Bussemaker, H. J., Li, L., Sawado, T., Williams, E., Loo, L. W. M., Cowley, S. M., Yost, C., et al. (2003) · Genes & Development · doi:10.1101/gad.1066903 · Cited by 385 · see citing works
Myc influences global chromatin structure
Knoepfler, P. S., Zhang, X.-Y., Cheng, P. F., Gafken, P. R., McMahon, S. B., & Eisenman, R. N. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601152 · Cited by 385 · see citing works
MYC regulates the core pre-mRNA splicing machinery as an essential step in lymphomagenesis
Koh, C. M., Bezzi, M., Low, D. H. P., Ang, W. X., Teo, S. X., Gay, F. P. H., Al‐Haddawi, M., Tan, S., Osato, M., Sabò, A., et al. (2015) · Nature · doi:10.1038/nature14351 · Cited by 379 · see citing works
Myc-binding-site recognition in the human genome is determined by chromatin context
Guccione, E., Martinato, F., Finocchiaro, G., Luzi, L., Tizzoni, L., Olio, V. D., Zardo, G., Nervi, C., Bernard, L., & Amati, B. B. (2006) · Nature Cell Biology · doi:10.1038/ncb1434 · Cited by 365 · see citing works
c-Myc enhances protein synthesis and cell size during B lymphocyte development
Iritani, B. M., & Eisenman, R. N. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.23.13180 · Cited by 364 · see citing works
Schweingruber, C., Rufener, S. C., Zünd, D., Yamashita, A., & Mühlemann, O. (2013) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2013.02.005 · Cited by 356 · see citing works
Cyclins D1 and D2 mediate Myc‐induced proliferation via sequestration of p27Kip1 and p21Cip1
Pérez‐Roger, I., Kim, S., Griffiths, B. L., Sewing, A., & Land, H. (1999) · The EMBO Journal · doi:10.1093/emboj/18.19.5310 · Cited by 327 · see citing works
Global Regulation of Nucleotide Biosynthetic Genes by c-Myc
Liu, Y.-C., Li, F., Handler, J., Huang, C. R. L., Xiang, Y., Neretti, N., Sedivy, J. M., Zeller, K. I., & Dang, C. V. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002722 · Cited by 317 · see citing works
New cell cycle compartments identified by multiparameter flow cytometry
Darżynkiewicz, Z., Traganos, F., & Melamed, M. R. (1980) · Cytometry · doi:10.1002/cyto.990010203 · Cited by 314 · see citing works
Interaction with WDR5 Promotes Target Gene Recognition and Tumorigenesis by MYC
Thomas, L. R., Wang, Q., Grieb, B. C., Phan, J., Foshage, A. M., Sun, Q., Olejniczak, E. T., Clark, T., Dey, S., Lorey, S., et al. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.02.028 · Cited by 310 · see citing works
Vennström, B., Sheiness, D. K., Zabielski, J., & Bishop, J. M. (1982) · Journal of Virology · doi:10.1128/jvi.42.3.773-779.1982 · Cited by 307 · see citing works
Negative Regulation of the Mammalian UV Response by Myc through Association with Miz-1
Herold, S., Wanzel, M., Beuger, V., Frohme, C., Beul, D., Hillukkala, T., Syväoja, J. E., Saluz, H., Haenel, F., & Eilers, M. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00633-0 · Cited by 305 · see citing works
Control of cell growth by c-Myc in the absence of cell division
Schuhmacher, M., Staege, M. S., Pajic, A., Polack, A., Weidle, U. H., Bornkamm, G. W., Eick, D., & Kohlhuber, F. (1999) · Current Biology · doi:10.1016/s0960-9822(99)80507-7 · Cited by 288 · see citing works
Repression of transcription of the p27Kip1 cyclin-dependent kinase inhibitor gene by c-Myc
Yang, W. E., Shen, J., Wu, M., Arsura, M., Fitzgerald, M. J., Suldan, Z., Kim, D. W., Hofmann, C. S., Pianetti, S., Romieu, R., et al. (2001) · Oncogene · doi:10.1038/sj.onc.1204245 · Cited by 277 · see citing works
Inhibition of Transcriptional Regulator Yin-Yang-1 by Association with c-Myc
Shrivastava, A., Saleque, S., Kalpana, G. V., Artandi, S. E., Goff, S. P., & Calame, K. L. (1993) · Science · doi:10.1126/science.8266081 · Cited by 272 · see citing works
Dysregulation of the Hedgehog pathway in human hepatocarcinogenesis
Sicklick, J. K., Li, Y.-X., Jayaraman, A., Kannangai, R., Qi, Y. P., Vivekanandan, P., Ludlow, J. W., Owzar, K., Chen, W., Torbenson, M. S., et al. (2005) · Carcinogenesis · doi:10.1093/carcin/bgi292 · Cited by 270 · see citing works
Notch1 Contributes to Mouse T-Cell Leukemia by Directly Inducing the Expression of c-myc
Sharma, V. M., Calvo, J. A., Draheim, K., Cunningham, L. A., Hermance, N. M., Beverly, L. J., Krishnamoorthy, V., Bhasin, M., Capobianco, A. J., & Kelliher, M. A. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.01091-06 · Cited by 265 · see citing works
Myc Requires Distinct E2F Activities to Induce S Phase and Apoptosis
Leone, G. W., Sears, R. C., Huang, E. S., Rempel, R. E., Nuckolls, F., Park, C., Giangrande, P. H., Wu, L., Saavedra, H. I., Field, S. J., et al. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00275-1 · Cited by 265 · see citing works
Cunningham, J. T., Moreno, M. V., Lodi, A., Ronen, S. M., & Ruggero, D. (2014) · Cell · doi:10.1016/j.cell.2014.03.052 · Cited by 260 · see citing works
Myc Recruits P-TEFb to Mediate the Final Step in the Transcriptional Activation of the cad Promoter
Eberhardy, S. R., & Farnham, P. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m207441200 · Cited by 259 · see citing works
Rosenwald, I. B., Rhoads, D. B., Callanan, L., Isselbacher, K. J., & Schmidt, E. V. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.13.6175 · Cited by 256 · see citing works
Jones, R. M., Branda, J. A., Johnston, K. A., Polymenis, M., Gadd, M. A., Rustgi, A. K., Callanan, L., & Schmidt, E. V. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.9.4754 · Cited by 237 · see citing works
Eukaryotic Initiation Factor 6 is rate-limiting in translation, growth and transformation
Gandin, V., Miluzio, A., Barbieri, A., Beugnet, A., Kiyokawa, H., Marchisio, P., & Biffo, S. (2008) · Nature · doi:10.1038/nature07267 · Cited by 235 · see citing works
Feng, X., Liang, Y.-Y., Liang, M., Zhai, W., & Lin, X. (2002) · Molecular Cell · doi:10.1016/s1097-2765(01)00430-0 · Cited by 232 · see citing works
Warner, B. J., Blain, S. W., Seoane, J., & Massagué, J. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.9.5913 · Cited by 230 · see citing works
Pérez‐Roger, I., Solomon, D. L., Sewing, A., & Land, H. (1997) · Oncogene · doi:10.1038/sj.onc.1201197 · Cited by 230 · see citing works
Frederick, J. P., Liberati, N. T., Waddell, D. S., Shi, Y., & Wang, X. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.6.2546-2559.2004 · Cited by 221 · see citing works
Eischen, C. M., Woo, D. D. L., Roussel, M. F., & Cleveland, J. L. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.15.5063-5070.2001 · Cited by 213 · see citing works
The c‐myc Promoter: Still MysterY and Challenge
(2008) · Advances in Cancer Research · doi:10.1016/s0065-230x(07)99004-1 · Cited by 211 · see citing works
Myc‐induced proliferation and transformation require Akt‐mediated phosphorylation of FoxO proteins
Bouchard, C., Marquardt, J., Brás, A., Medema, R. H., & Eilers, M. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600279 · Cited by 211 · see citing works
Coordinating genome expression with cell size
Marguerat, S., & Bähler, J. (2012) · Trends in Genetics · doi:10.1016/j.tig.2012.07.003 · Cited by 203 · see citing works
Deregulated Myc Requires MondoA/Mlx for Metabolic Reprogramming and Tumorigenesis
Carroll, P. A., Diolaiti, D., McFerrin, L. G., Gu, H., Djukovic, D., Du, J., Cheng, P. F., Anderson, S., Ulrich, M. L., Hurley, J. B., et al. (2015) · Cancer Cell · doi:10.1016/j.ccell.2014.11.024 · Cited by 202 · see citing works
Oncogenic Splicing Factor SRSF1 Is a Critical Transcriptional Target of MYC
Das, S., Anczuków, O., Akerman, M., & Krainer, A. R. (2012) · Cell Reports · doi:10.1016/j.celrep.2011.12.001 · Cited by 202 · see citing works
A MAPK/HNRPK pathway controls BCR/ABL oncogenic potential by regulating MYC mRNA translation
Notari, M., Neviani, P., Santhanam, R., Blaser, B. W., Chang, J.-S., Galietta, A., Willis, A. E., Roy, D., Caligiuri, M. A., Marcucci, G., et al. (2005) · Blood · doi:10.1182/blood-2005-09-3732 · Cited by 202 · see citing works
CDK9-mediated transcription elongation is required for MYC addiction in hepatocellular carcinomaPreprint
Huang, C., Lujambio, A., Zuber, J. A., Tschaharganeh, D. F., Doran, M. G., Evans, M. J., Kitzing, T. M., Zhu, N., de Stanchina, E., Sawyers, C. L., et al. (2014) · Genes & Development · doi:10.1101/gad.244368.114 · Cited by 201 · see citing works
Nikiforov, M. A., Chandriani, S. J., O’Connell, B. C., Petrenko, O., Kotenko, I., Beavis, A. J., Sedivy, J. M., & Cole, M. D. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.16.5793-5800.2002 · Cited by 201 · see citing works
Januszyk, K., & Lima, C. D. (2014) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2014.01.011 · Cited by 199 · see citing works
MAD1 and c‐MYC regulate UBF and rDNA transcription during granulocyte differentiation
Poortinga, G., Hannan, K., Snelling, H., Walkley, C. R., Jenkins, A., Sharkey, K., Wall, M., Brandenburger, Y., Palatsides, M., Pearson, R., et al. (2004) · EMBO Journal · doi:10.1038/sj.emboj.7600335 · Cited by 198 · see citing works
Kim, S., Li, Q., Dang, C. V., & Lee, L. A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.200372597 · Cited by 187 · see citing works
Mao, D. Y. L., Watson, J. D., Yan, P. S., Baršytė-Lovejoy, D., Khosravi, F., Wong, W. W.-L., Farnham, P., Huang, T. H. ‐., & Penn, L. Z. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00297-5 · Cited by 183 · see citing works
c-Myc recruits P-TEFb for transcription, cellular proliferation and apoptosis
Kanazawa, S., Soucek, L., Evan, G. I., Okamoto, T., & Peterlin, B. M. (2003) · Oncogene · doi:10.1038/sj.onc.1206800 · Cited by 181 · see citing works
Endogenous Myc maintains the tumor microenvironmentPreprint
Sodir, N. M., Swigart, L. B., Karnezis, A. N., Hanahan, D., Evan, G. I., & Soucek, L. (2011) · Genes & Development · doi:10.1101/gad.2038411 · Cited by 179 · see citing works
Cheng, A. S. L., Jin, V. X., Fan, M., Smith, L. T., Liyanarachchi, S., Yan, P. S., Leu, Y., Chan, M. W. Y., Plass, C., Nephew, K. P., et al. (2006) · Molecular Cell · doi:10.1016/j.molcel.2005.12.016 · Cited by 177 · see citing works
Tumor cell-selective regulation of NOXA by c-MYC in response to proteasome inhibition
Nikiforov, M. A., Riblett, M., Tang, W. H. W., Grachtchouk, V., Zhuang, D., Fernández, Y., Verhaegen, M. E., Varambally, S., Chinnaiyan, A. M., Jakubowiak, A. J., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708380104 · Cited by 174 · see citing works
Miltenberger, R. J., Sukow, K. A., & Farnham, P. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.5.2527 · Cited by 172 · see citing works
AREsite: a database for the comprehensive investigation of AU-rich elements
Gruber, A. R., Fallmann, J., Kratochvill, F., Kovarik, P., & Hofacker, I. L. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq990 · Cited by 162 · see citing works
Large-Scale Identification of c-MYC-Associated Proteins Using a Combined TAP/MudPIT Approach
Koch, H., Zhang, R., Verdoodt, B., Bailey, A. O., Zhang, C.-D., Yates, J. R., Menssen, A., & Hermeking, H. (2007) · Cell Cycle · doi:10.4161/cc.6.2.3742 · Cited by 162 · see citing works
Ji, H., Wu, G. Y., Zhan, X., Nolan, A., Koh, C. M., Marzo, A. D., Doan, H. M., Fan, J., Cheadle, C., Fallahi, M., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026057 · Cited by 162 · see citing works
Bax is a transcriptional target and mediator of c-myc-induced apoptosis.
Mitchell, K. O., Ricci, M. S., Miyashita, T., Dicker, D. T., Jin, Z., Reed, J. C., & El‐Deiry, W. S. (2000) · PubMed · Cited by 161 · see citing works
c-myc protein expression in untransformed fibroblasts.
Waters, C. M., Littlewood, T. D., Hancock, D. C., Moore, J. P., & Evan, G. I. (1991) · PubMed · Cited by 160 · see citing works
Global target mRNA specification and regulation by the RNA-binding protein ZFP36
Mukherjee, N., Jacobs, N. C., Hafner, M., Kennington, E. A., Nusbaum, J. D., Tuschl, T., Blackshear, P. J., & Ohler, U. (2014) · Genome biology · doi:10.1186/gb-2014-15-1-r12 · Cited by 155 · see citing works
Mammalian MYC Proteins and Cancer
Tansey, W. P. (2014) · New Journal of Science · doi:10.1155/2014/757534 · Cited by 153 · see citing works
Morrish, F. M., Noonan, J., Olsen, C. P., Gafken, P. R., Fitzgibbon, M., Kelleher, J. K., VanGilst, M., & Hockenbery, D. M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.141606 · Cited by 152 · see citing works
Cowling, V. H., & Cole, M. D. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.01828-06 · Cited by 150 · see citing works
Conditional transgenic models define how MYC initiates and maintains tumorigenesis
Arvanitis, C., & Felsher, D. W. (2006) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2006.07.012 · Cited by 146 · see citing works
Kress, T. R., Cannell, I. G., Brenkman, A. B., Samans, B., Gaestel, M., Roepman, P., Burgering, B. M. T., Bushell, M., Rosenwald, A., & Eilers, M. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.01.023 · Cited by 146 · see citing works
Lee, B.-K., Bhinge, A., Battenhouse, A., McDaniell, R. M., Liu, Z., Song, L., 倪, 运., Birney, E., Lieb, J. D., Furey, T. S., et al. (2011) · Genome Research · doi:10.1101/gr.127597.111 · Cited by 138 · see citing works
Taming of the beast: shaping Myc-dependent amplification
Wolf, E., Lin, C. Y., Eilers, M., & Levens, D. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.10.006 · Cited by 135 · see citing works
Connecting Variability in Global Transcription Rate to Mitochondrial Variability
das Neves, R. P., Jones, N. S., Andreu, L. F., Gupta, R., Enver, T., & Iborra, F. J. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000560 · Cited by 133 · see citing works
Hubert, C. G., Bradley, R. K., Ding, Y., Toledo, C. M., Herman, J., Skutt-Kakaria, K., Girard, E. J., Davison, J., Berndt, J. D., Corrin, P. D., et al. (2013) · Genes & Development · doi:10.1101/gad.212548.112 · Cited by 133 · see citing works
Transcriptional Repression: The Dark Side of Myc
Herkert, B., & Eilers, M. (2010) · Genes & Cancer · doi:10.1177/1947601910379012 · Cited by 130 · see citing works
A positive role for Myc in TGFβ-induced Snail transcription and epithelial-to-mesenchymal transition
Smith, A. P., Verrecchia, A., Fagà, G., Doni, M., Perna, D., Martinato, F., Guccione, E., & Amati, B. B. (2008) · Oncogene · doi:10.1038/onc.2008.395 · Cited by 128 · see citing works
c-Myc Augments Gamma Irradiation-Induced Apoptosis by Suppressing Bcl-X L
Maclean, K. H., Keller, U. B., Galindo, C. R., Nilsson, J. A., & Cleveland, J. L. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.20.7256-7270.2003 · Cited by 128 · see citing works
Myc and its interactors take shape
Tu, W. B., Helander, S., Pilstål, R., Hickman, K. A., Lourenco, C., Jurišica, I., Raught, B., Wallner, B., Sunnerhagen, M., & Penn, L. Z. (2014) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2014.06.002 · Cited by 125 · see citing works
c-MYC-Induced Genomic InstabilityPreprint
Kuzyk, A. C., & Mai, S. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a014373 · Cited by 124 · see citing works
Tristetraprolin Impairs Myc-Induced Lymphoma and Abolishes the Malignant State
Rounbehler, R. J., Fallahi, M., Yang, C., Steeves, M. A., Li, W., Doherty, J. R., Schaub, F. X., Sanduja, S., Dixon, D. A., Blackshear, P. J., et al. (2012) · Cell · doi:10.1016/j.cell.2012.06.033 · Cited by 119 · see citing works
Myc regulates keratinocyte adhesion and differentiation via complex formation with Miz1
Gebhardt, A., Frye, M., Herold, S., Benitah, S. A., Braun, K., Samans, B., Watt, F. M., Elsässer, H.-P., & Eilers, M. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200506057 · Cited by 118 · see citing works
Beier, R., Bürgin, A., Kiermaier, A. C., Fero, M. L., Karsunky, H., Saffrich, R., Möröy, T., Ansorge, W. J., Roberts, J., & Eilers, M. (2000) · The EMBO Journal · doi:10.1093/emboj/19.21.5813 · Cited by 114 · see citing works
MicroRNAs as regulators and mediators of c-MYC function
Jackstadt, R., & Hermeking, H. (2014) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2014.04.003 · Cited by 113 · see citing works
Genome Recognition by MYCPreprint
Sabò, A., & Amati, B. B. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a014191 · Cited by 109 · see citing works
Deep Sequencing of MYC DNA-Binding Sites in Burkitt Lymphoma
Seitz, V., Butzhammer, P., Hirsch, B., Hecht, J., Gütgemann, I., Ehlers, A., Lenze, D., Oker, E., Sommerfeld, A., von der Wall, E., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026837 · Cited by 109 · see citing works
Genome-wide mapping of Myc binding and gene regulation in serum-stimulated fibroblasts
Perna, D., Fagà, G., Verrecchia, A., Gorski, M. M., Barozzi, I., Narang, V., Khng, J., Lim, K., Sung, W.-K., Sanges, R., et al. (2011) · Oncogene · doi:10.1038/onc.2011.359 · Cited by 107 · see citing works
van Riggelen, J., Müller, J., Otto, T., Beuger, V., Yetil, A., Choi, P. S., Kosan, C., Möröy, T., Felsher, D. W., & Eilers, M. (2010) · Genes & Development · doi:10.1101/gad.585710 · Cited by 105 · see citing works
Translational control of c-MYC by rapamycin promotes terminal myeloid differentiation.
Wall, M., Poortinga, G., Hannan, K., Pearson, R., Hannan, R., & McArthur, G. (2008) · Blood · doi:10.1182/blood-2007-09-111856 · Cited by 103 · see citing works
Mechanism for the transcriptional repression by c-Myc on PDGF β-receptor
Izumi, H., Molander, C., Penn, L. Z., Ishisaki, A., Kohno, K., & Funa, K. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.8.1533 · Cited by 102 · see citing works
Regulation of Cyclin D1 RNA Stability by SNIP1
Bracken, C. P., Wall, S. J., Barré, B., Panov, K. I., Ajuh, P., & Perkins, N. D. (2008) · Cancer Research · doi:10.1158/0008-5472.can-08-1217 · Cited by 97 · see citing works
c-Myc-induced transcription factor AP4 is required for host protection mediated by CD8+ T cells
Chou, C., Pinto, A. K., Curtis, J. D., Persaud, S. P., Cella, M., Lin, C., Edelson, B. T., Allen, P. M., Colonna, M., Pearce, E. L., et al. (2014) · Nature Immunology · doi:10.1038/ni.2943 · Cited by 95 · see citing works
Neri, F., Zippo, A., Křepelová, A., Cherubini, A., Rocchigiani, M., & Oliviero, S. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.06148-11 · Cited by 91 · see citing works
P-TEFb is a Crucial Co-Factor for Myc Transactivation
Gargano, B., Amente, S., Majello, B., & Lania, L. (2007) · Cell Cycle · doi:10.4161/cc.6.16.4554 · Cited by 86 · see citing works
Myc and SAGA rewire an alternative splicing network during early somatic cell reprogrammingPreprint
Hirsch, C. L., Coban‐Akdemir, Z., Wang, L., Jayakumaran, G., Trcka, D., Weiss, A., Hernández, J. J., Pan, Q., Han, H. R., Xu, X., et al. (2015) · Genes & Development · doi:10.1101/gad.255109.114 · Cited by 85 · see citing works
Sequence specificity incompletely defines the genome-wide occupancy of Myc
Guo, J., Li, T., Schipper, J. L., Nilson, K. A., Fordjour, F. K., Cooper, J. J., Gordân, R., & Price, D. H. (2014) · Genome biology · doi:10.1186/s13059-014-0482-3 · Cited by 84 · see citing works
Kaur, M., & Cole, M. D. (2012) · Cancer Research · doi:10.1158/0008-5472.can-12-2522 · Cited by 84 · see citing works
MYC regulates the non-coding transcriptome
Hart, J. R., Roberts, T. C., Weinberg, M. S., Morris, K. V., & Vogt, P. K. (2014) · Oncotarget · doi:10.18632/oncotarget.3033 · Cited by 83 · see citing works
Gene Regulation and Epigenetic Remodeling in Murine Embryonic Stem Cells by c-Myc
Lin, C.-H., Lin, C. W., Tanaka, H., Fero, M. L., & Eisenman, R. N. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007839 · Cited by 79 · see citing works
Specific regulation of mRNA cap methylation by the c-Myc and E2F1 transcription factors
Cole, M. D., & Cowling, V. H. (2009) · Oncogene · doi:10.1038/onc.2008.463 · Cited by 75 · see citing works
Myc Function in DrosophilaPreprint
Gallant, P. (2013) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a014324 · Cited by 74 · see citing works
Ras and Myc can drive oncogenic cell proliferation through individual D-cyclins
Yu, Q., Ciemerych, M. A., & Siciński, P. (2005) · Oncogene · doi:10.1038/sj.onc.1208853 · Cited by 73 · see citing works
Kwan, K. Y., Shen, J., & Corey, D. P. (2014) · Stem Cell Reports · doi:10.1016/j.stemcr.2014.11.001 · Cited by 73 · see citing works
Lawlor, E. R., Soucek, L., Swigart, L. B., Shchors, K., Bialucha, C. U., & Evan, G. I. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-3826 · Cited by 73 · see citing works
Inhibition of cell differentiation: A critical mechanism for MYC-mediated carcinogenesis?
León, J., Ferrándiz, N., Acosta, J. C., & Delgado, M. D. (2009) · Cell Cycle · doi:10.4161/cc.8.8.8126 · Cited by 69 · see citing works
Feedback Regulation of c-Myc by Ribosomal Protein L11
Dai, M., Sears, R. C., & Lu, H. (2007) · Cell Cycle · doi:10.4161/cc.6.22.4895 · Cited by 67 · see citing works
Premetazoan Ancestry of the Myc–Max Network
Young, S. L., Diolaiti, D., Conacci‐Sorrell, M., Ruiz‐Trillo, I., Eisenman, R. N., & King, N. (2011) · Molecular Biology and Evolution · doi:10.1093/molbev/msr132 · Cited by 65 · see citing works
Fujii, M., Lyakh, L. A., Bracken, C. P., Fukuoka, J., Hayakawa, M., Tsukiyama, T., Soll, S. J., Harris, M. D., Rocha, S., Roche, K. C., et al. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.11.006 · Cited by 63 · see citing works
Fernández-Sánchez, M. E., Gonatopoulos-Pournatzis, T., Preston, G., Lawlor, M. A., & Cowling, V. H. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.00973-09 · Cited by 62 · see citing works
Cellular MYCro Economics: Balancing MYC Function with MYC ExpressionPreprint
Levens, D. (2013) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a014233 · Cited by 60 · see citing works
Schneider, A., Peukert, K., Eilers, M., & Hänel, F. (1997) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-60801-8_14 · Cited by 57 · see citing works
Tao, J., Zhao, X., & Tao, J. (2014) · Cell Cycle · doi:10.4161/cc.27646 · Cited by 56 · see citing works
Miz1 is required to maintain autophagic flux
Wolf, E., Gebhardt, A., Kawauchi, D., Walz, S., von Eyß, B., Wagner, N., Renninger, C., Krohne, G., Asan, E., Roussel, M. F., et al. (2013) · Nature Communications · doi:10.1038/ncomms3535 · Cited by 56 · see citing works
Kim, T., Cui, R., Jeon, Y.-J., Fadda, P., Alder, H., & Croce, C. M. (2015) · Oncotarget · doi:10.18632/oncotarget.3909 · Cited by 55 · see citing works
Overexpression of the c-myc Oncogene Inhibits Nonsense-mediated RNA Decay in B Lymphocytes
Wang, D., Wengrod, J., & Gardner, L. B. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.266361 · Cited by 53 · see citing works
Determination of Copy Number of c-Myc Protein per Cell by Quantitative Western Blotting
Rudolph, C., Adam, G., & Simm, A. (1999) · Analytical Biochemistry · doi:10.1006/abio.1999.3095 · Cited by 53 · see citing works
Drosophila Myc: A master regulator of cellular performance
Grifoni, D., & Bellosta, P. (2014) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2014.06.021 · Cited by 46 · see citing works
Cellular MYCro Economics: Balancing MYC Function with MYC ExpressionPreprint
Levens, D. (2013) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a022483 · Cited by 46 · see citing works
Mitochondrial p32 is upregulated in Myc expressing brain cancers and mediates glutamine addiction
Fogal, V., Babić, I., Chao, Y. S., Pastorino, S., Mukthavaram, R., Jiang, P., Cho, Y., Pingle, S. C., Crawford, J. R., Piccioni, D. E., et al. (2014) · Oncotarget · doi:10.18632/oncotarget.2708 · Cited by 45 · see citing works
Transcriptional control of DNA replication licensing by Myc
Valovka, T., Schönfeld, M., Raffeiner, P., Breuker, K., Dunzendorfer-Matt, T., Hartl, M., & Bister, K. (2013) · Scientific Reports · doi:10.1038/srep03444 · Cited by 43 · see citing works
Kinetic profiling of the c-Myc transcriptome and bioinformatic analysis of repressed gene promoters
Yap, C.-S., Peterson, A. L., Castellani, G., Sedivy, J. M., & Neretti, N. (2011) · Cell Cycle · doi:10.4161/cc.10.13.16249 · Cited by 41 · see citing works
Sauvé, S., Naud, J., & Lavigne, P. (2006) · Journal of Molecular Biology · doi:10.1016/j.jmb.2006.10.044 · Cited by 40 · see citing works
Repression of SRF target genes is critical for Myc‐dependent apoptosis of epithelial cells
Wiese, K. E., Haikala, H. M., von Eyß, B., Wolf, E., Esnault, C., Rosenwald, A., Treisman, R., Klefström, J. T., & Eilers, M. (2015) · The EMBO Journal · doi:10.15252/embj.201490467 · Cited by 32 · see citing works
Kim, C.-H., Kim, J.-W., Jang, S., An, J., Seo, S., & Choi, K. (2015) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2014.993914 · Cited by 26 · see citing works
Vaux, D. L., Adams, J. M., Alexander, W. S., & Pike, B. L. (1987) · The Journal of Immunology · doi:10.4049/jimmunol.139.11.3854 · Cited by 21 · see citing works
Davis‐Turak, J., Allison, K. A., Shokhirev, M. N., Ponomarenko, P. M., Tsimring, L. S., Glass, C. K., Johnson, T., & Hoffmann, A. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1338 · Cited by 19 · see citing works
Miz-1 Activates Gene Expression via a Novel Consensus DNA Binding Motif
Barrilleaux, B. L., Burow, D. A., Lockwood, S. H., Yu, A. S., Segal, D. J., & Knoepfler, P. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101151 · Cited by 18 · see citing works
Flagged first, then by citations
1 of the 201 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
A Cancer Cell Program Promotes T Cell Exclusion and Resistance to Checkpoint Blockade
Jerby-Arnon, L., Shah, P., Cuoco, M. S., Rodman, C., Su, M.-J., Melms, J. C., Leeson, R., Kanodia, A., Mei, S., Lin, J.-R., et al. (2018) · Cell · doi:10.1016/j.cell.2018.09.006 · Cited by 1,429 · see citing works
The MYC oncogene — the grand orchestrator of cancer growth and immune evasion
Dhanasekaran, R., Deutzmann, A., Mahauad‐Fernandez, W. D., Hansen, A. S., Gouw, A. M., & Felsher, D. W. (2021) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-021-00549-2 · Cited by 1,010 · see citing works
Lu, H., Zhou, Q., He, J., Jiang, Z., Peng, C., Tong, R., & Shi, J. (2020) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-00315-3 · Cited by 891 · see citing works
Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma
Robertson, A. G., Shih, J., Yau, C. S. F., Gibb, E. A., Oba, J., Mungall, K. L., Hess, J. M., Uzunangelov, V., Walter, V., Danilova, L., et al. (2017) · Cancer Cell · doi:10.1016/j.ccell.2017.07.003 · Cited by 894 · see citing works
The role of ubiquitination in tumorigenesis and targeted drug discovery
Deng, L., Meng, T., Chen, L., Wei, W., & Wang, P. (2020) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-0107-0 · Cited by 744 · see citing works
Stem cell programs in cancer initiation, progression, and therapy resistance
Huang, T., Song, X., Xu, D., Tiek, D., Goenka, A., Wu, B., Sastry, N., Hu, B., & Cheng, S.-Y. (2020) · Theranostics · doi:10.7150/thno.41648 · Cited by 524 · see citing works
RAF-MEK-ERK pathway in cancer evolution and treatment
Ullah, R., Yin, Q., Snell, A. H., & Wan, L. (2022) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2021.05.010 · Cited by 553 · see citing works
FBXW7: a critical tumor suppressor of human cancers
Yeh, C., Bellon, M., & Nicot, C. (2018) · Molecular Cancer · doi:10.1186/s12943-018-0857-2 · Cited by 513 · see citing works
Wang, Z., Yang, B., Zhang, M., Guo, W., Wu, Z., Wang, Y., Jia, L., Li, S., Johnson, R., Demchok, J. A., et al. (2018) · Cancer Cell · doi:10.1016/j.ccell.2018.03.006 · Cited by 467 · see citing works
Small-Molecule MYC Inhibitors Suppress Tumor Growth and Enhance Immunotherapy
Han, H., Jain, A. D., Truica, M. I., Izquierdo-Ferrer, J., Anker, J. F., Lysy, B., Sagar, V., Luan, Y., Chalmers, Z. R., Unno, K., et al. (2019) · Cancer Cell · doi:10.1016/j.ccell.2019.10.001 · Cited by 466 · see citing works
Promoter of lncRNA Gene PVT1 Is a Tumor-Suppressor DNA Boundary Element
Cho, S. W., Xu, J., Sun, R., Mumbach, M. R., Carter, A. C., Chen, Y. G., Yost, K. E., Kim, J., He, J., Nevins, S. A., et al. (2018) · Cell · doi:10.1016/j.cell.2018.03.068 · Cited by 459 · see citing works
Pan-cancer Alterations of the MYC Oncogene and Its Proximal Network across the Cancer Genome Atlas
Schaub, F. X., Dhankani, V., Berger, A. C., Trivedi, M., Richardson, A. B., Shaw, R., Zhao, W., Zhang, X., Ventura, A., Liu, Y., et al. (2018) · Cell Systems · doi:10.1016/j.cels.2018.03.003 · Cited by 431 · see citing works
“Pan-cancer Canonical and Non-canonical MYC-Specific Gene Set Enrichment Alteration of MYC expression leads to broad transcriptional changes through both direct and indirect effects, as observed in many experimental systems (as reviewed in Kress et al., 2015).”
Lipid metabolism in cancer progression and therapeutic strategies
Fu, Y., Zou, T., Shen, X., Nelson, P. J., Li, J., Wu, C., Yang, J., Zheng, Y., Bruns, C. J., Zhao, Y., et al. (2020) · MedComm · doi:10.1002/mco2.27 · Cited by 406 · see citing works
The role of enhancers in cancer
Sur, I., & Taipale, J. (2016) · Nature reviews. Cancer · doi:10.1038/nrc.2016.62 · Cited by 382 · see citing works
SLAM-seq defines direct gene-regulatory functions of the BRD4-MYC axis
Muhar, M., Ebert, A., Neumann, T., Umkehrer, C., Jude, J., Wieshofer, C., Rescheneder, P., Lipp, J., Herzog, V. A., Reichholf, B., et al. (2018) · Science · doi:10.1126/science.aao2793 · Cited by 364 · see citing works
Target gene-independent functions of MYC oncoproteins
Baluapuri, A., Wolf, E., & Eilers, M. (2020) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-0215-2 · Cited by 310 · see citing works
The MYC transcription factor network: balancing metabolism, proliferation and oncogenesis
Carroll, P. A., Freie, B. W., Mathsyaraja, H., & Eisenman, R. N. (2018) · Frontiers of Medicine · doi:10.1007/s11684-018-0650-z · Cited by 289 · see citing works
Hua, Q., Jin, M., Mi, B., Xu, F., Li, T. X., Zhao, L., Liu, J., & Huang, G. (2019) · Journal of Hematology & Oncology · doi:10.1186/s13045-019-0773-y · Cited by 262 · see citing works
Kühl, I., Miranda, M., Atanassov, I., Kuznetsova, I., Hinze, Y., Mourier, A., Filipovska, A., & Larsson, N. (2017) · eLife · doi:10.7554/elife.30952 · Cited by 251 · see citing works
The Expanding World of N-MYC–Driven Tumors
Rickman, D. S., Schulte, J. H., & Eilers, M. (2018) · Cancer Discovery · doi:10.1158/2159-8290.cd-17-0273 · Cited by 237 · see citing works
MYC and tumor metabolism: chicken and egg
Dejure, F. R., & Eilers, M. (2017) · The EMBO Journal · doi:10.15252/embj.201796438 · Cited by 240 · see citing works
Lemos, D. R., McMurdo, M., Karaca, G., Wilflingseder, J., Leaf, I. A., Gupta, N. R., Miyoshi, T., Susa, K., Johnson, B. G., Soliman, K., et al. (2018) · Journal of the American Society of Nephrology · doi:10.1681/asn.2017121283 · Cited by 220 · see citing works
Opposing macrophage polarization programs show extensive epigenomic and transcriptional cross-talk
Piccolo, V., Curina, A., Genua, M., Ghisletti, S., Simonatto, M., Sabò, A., Amati, B. B., Ostuni, R., & Natoli, G. (2017) · Nature Immunology · doi:10.1038/ni.3710 · Cited by 209 · see citing works
Intrinsic cell-penetrating activity propels Omomyc from proof of concept to viable anti-MYC therapy
Beaulieu, M.-È., Jauset, T., Massó-Vallés, D., Martínez-Martín, S., Rahl, P. B., Maltais, L., Fluck, M. F. Z., Casacuberta‐Serra, S., del Pozo, E. S., Fiore, C., et al. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aar5012 · Cited by 211 · see citing works
Yue, M., Jiang, J., Gao, P., Liu, H., & Qing, G. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.12.002 · Cited by 201 · see citing works
Structural basis of N-Myc binding by Aurora-A and its destabilization by kinase inhibitors
Richards, M. W., Burgess, S. G., Poon, E., Carstensen, A., Eilers, M., Chesler, L., & Bayliss, R. W. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1610626113 · Cited by 184 · see citing works
MYC—Master Regulator of the Cancer Epigenome and Transcriptome
Poole, C. J., & van Riggelen, J. (2017) · Genes · doi:10.3390/genes8050142 · Cited by 177 · see citing works
c-MYC mediates the crosstalk between breast cancer cells and tumor microenvironment
Gao, F., Li, X.-T., Xu, K., Wang, R., & Guan, X. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-023-01043-1 · Cited by 175 · see citing works
Expression profiles, biological functions and clinical significance of circRNAs in bladder cancer
Yang, X., Ye, T., Liu, H., Lv, P., Duan, C., Wu, X., Jiang, K., Lu, H., Ding, X., Peng, E., et al. (2021) · Molecular Cancer · doi:10.1186/s12943-020-01300-8 · Cited by 168 · see citing works
Functionally diverse human T cells recognize non-microbial antigens presented by MR1
Lepore, M., Kalinichenko, A., Calogero, S., Kumar, P., Paleja, B. S., Schmaler, M., Narang, V., Zolezzi, F., Poidinger, M., Mori, L., et al. (2017) · eLife · doi:10.7554/elife.24476 · Cited by 164 · see citing works
Biophysical properties of AKAP95 protein condensates regulate splicing and tumorigenesis
Li, W., Hu, J., Shi, B., Palomba, F., Digman, M. A., Gratton, E., & Jiang, H. (2020) · Nature Cell Biology · doi:10.1038/s41556-020-0550-8 · Cited by 163 · see citing works
Different promoter affinities account for specificity in MYC-dependent gene regulation
Lorenzin, F., Benary, U., Baluapuri, A., Walz, S., Jung, L. A., von Eyß, B., Kisker, C., Wolf, J., Eilers, M., & Wolf, E. (2016) · eLife · doi:10.7554/elife.15161 · Cited by 162 · see citing works
Discovery of a Functional Covalent Ligand Targeting an Intrinsically Disordered Cysteine within MYC
Boike, L., Cioffi, A. G., Majewski, F. C., Co, J., Henning, N. J., Jones, M. D., Liu, G., McKenna, J. M., Tallarico, J. A., Schirle, M., et al. (2021) · Cell Chemical Biology · doi:10.1016/j.chembiol.2020.09.001 · Cited by 154 · see citing works
BPTF is required for c-MYC transcriptional activity and in vivo tumorigenesis
Richart, L., Pau, E. C. D. S., Río-Machín, A., de Andrés, M. P., Cigudosa, J., Lobo, V. J. S.-A., & Real, F. (2016) · Nature Communications · doi:10.1038/ncomms10153 · Cited by 118 · see citing works
Pluripotency and the origin of animal multicellularity
(2019) · doi:10.1038/s41586-019-1290-4 · Cited by 146 · see citing works
Mission Possible: Advances in MYC Therapeutic Targeting in Cancer
Allen-Petersen, B. L., & Sears, R. C. (2019) · BioDrugs · doi:10.1007/s40259-019-00370-5 · Cited by 143 · see citing works
Zimmerli, D., Brambillasca, C. S., Talens, F., Bhin, J., Linstra, R., Romanens, L., Bhattacharya, A., Joosten, S. E. P., Silva, A. M. D., Padrão, N., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34000-6 · Cited by 153 · see citing works
Lacerda, R., Menezes, J., & Romão, L. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2428-2 · Cited by 144 · see citing works
The MYC Enhancer-ome: Long-Range Transcriptional Regulation of MYC in Cancer
Lancho, O., & Herranz, D. (2018) · Trends in cancer · doi:10.1016/j.trecan.2018.10.003 · Cited by 137 · see citing works
Regulation and signaling pathways in cancer stem cells: implications for targeted therapy for cancer
Zeng, Z., Fu, M., Hu, Y., Wei, Y., Wei, X., & Luo, M. (2023) · Molecular Cancer · doi:10.1186/s12943-023-01877-w · Cited by 143 · see citing works
Stabilization of the Max Homodimer with a Small Molecule Attenuates Myc-Driven Transcription
Struntz, N. B., Chen, A., Deutzmann, A., Wilson, R. M., Stefan, E., Evans, H. L., Ramirez, M. A., Liang, T., Caballero, F., Wildschut, M. H. E., et al. (2019) · Cell Chemical Biology · doi:10.1016/j.chembiol.2019.02.009 · Cited by 130 · see citing works
MYC Recruits SPT5 to RNA Polymerase II to Promote Processive Transcription Elongation
Baluapuri, A., Hofstetter, J., Dudvarski Stankovic, N., Endres, T., Bhandare, P., Vos, S. M., Adhikari, B., Schwarz, J. D., Narain, A., Vogt, M., et al. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.02.031 · Cited by 138 · see citing works
Concise Review: Control of Cell Fate Through Cell Cycle and Pluripotency Networks
Boward, B., Wu, T., & Dalton, S. (2016) · Stem Cells · doi:10.1002/stem.2345 · Cited by 132 · see citing works
Advances in targeted therapy for malignant lymphoma
Wang, L., Qin, W. D., Huo, Y., Li, X., Shi, Q., Rasko, J. E. J., Janin, A., & Zhao, W. (2020) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-0113-2 · Cited by 140 · see citing works
Proteomic profiling of VCP substrates links VCP to K6‐linked ubiquitylation and c‐Myc function
Heidelberger, J. B., Voigt, A., Borisova, M. E., Petrosino, G., Ruf, S., Wagner, S. A., & Beli, P. (2018) · EMBO Reports · doi:10.15252/embr.201744754 · Cited by 116 · see citing works
Wang, J., Yang, Y., Shao, F., Meng, Y., Guo, D. S., He, J., & Lu, Z. (2024) · Nature Metabolism · doi:10.1038/s42255-024-01037-4 · Cited by 137 · see citing works
Chen, D., Zhao, Z., Huang, Z., Chen, D.-C., Zhu, X., Wang, Y., Yan, Y., Tang, S., Madhavan, S., Ni, W., et al. (2018) · Bone Research · doi:10.1038/s41413-018-0009-8 · Cited by 135 · see citing works
Abbas, H. A., Hao, D., Tomczak, K. J., Barrodia, P., Im, J. S., Reville, P. K., Alaniz, Z., Wang, W., Wang, R., Wang, F., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-26282-z · Cited by 130 · see citing works
Targeting MYC in multiple myeloma
Jovanović, K., Roche‐Lestienne, C., Ghobrial, I. M., Facon, T. T. F., Quesnel, B., & Manier, S. (2018) · Leukemia · doi:10.1038/s41375-018-0036-x · Cited by 128 · see citing works
Castell, A., Yan, Q., Fawkner, K., Hydbring, P., Zhang, F., Verschut, V., Franco, M., Zakaria, S. M., Bazzar, W., Goodwin, J., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-28107-4 · Cited by 126 · see citing works
DAXX in cancer: phenomena, processes, mechanisms and regulation
Mahmud, I., & Liao, D. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz634 · Cited by 121 · see citing works
Tu, W. B., Shiah, Y.-J., Lourenco, C., Mullen, P. J., Dingar, D. D., Redel, C., Tamachi, A., Ba-Alawi, W., Aman, A. M., Al‐awar, R., et al. (2018) · Cancer Cell · doi:10.1016/j.ccell.2018.09.001 · Cited by 119 · see citing works
Andrews, F. H., Singh, A. R., Joshi, S., Smith, C. A., Morales, G. A., Garlich, J. R., Durden, D. L., & Kutateladze, T. G. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1613091114 · Cited by 119 · see citing works
The Hippo Pathway Prevents YAP/TAZ-Driven Hypertranscription and Controls Neural Progenitor Number
Lavado, A., Park, J. Y., Paré, J., Finkelstein, D., Pan, H., Xu, B., Fan, Y., Kumar, R. P., Neale, G. A. M., Kwak, Y. D., et al. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.09.021 · Cited by 114 · see citing works
Kawasaki, Y., Komiya, M., Matsumura, K., Negishi, L., Suda, S., Okuno, M., Yokota, N., Osada, T., Nagashima, T., Hiyoshi, M., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.08.015 · Cited by 113 · see citing works
Jaenicke, L. A., von Eyß, B., Carstensen, A., Wolf, E., Xu, W., Greifenberg, A. K., Geyer, M., Eilers, M., & Popov, N. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.11.007 · Cited by 110 · see citing works
MYC Targeted Long Noncoding RNA DANCR Promotes Cancer in Part by Reducing p21 Levels
Lu, Y., Hu, Z., Mangala, L. S., Stine, Z. E., Hu, Z., Jiang, D., Xiang, Y., Zhang, Y., Pradeep, S., Rodriguez‐Aguayo, C., et al. (2017) · Cancer Research · doi:10.1158/0008-5472.can-17-0815 · Cited by 111 · see citing works
Li, W., Gupta, S. K., Han, W., Kundson, R. A., Nelson, S., Knutson, D. L., Greipp, P. T., Elsawa, S. F., Sotomayor, E. M., & Gupta, M. (2019) · Journal of Hematology & Oncology · doi:10.1186/s13045-019-0761-2 · Cited by 106 · see citing works
Single-molecule footprinting identifies context-dependent regulation of enhancers by DNA methylation
Kreibich, E., Kleinendorst, R., Barzaghi, G., Kaspar, S., & Krebs, A. R. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.01.017 · Cited by 97 · see citing works
Jung, L. A., Gebhardt, A., Koelmel, W., Ade, C. P., Walz, S., Kuper, J., von Eyss, B., Letschert, S., Redel, C., d'Artista, L., et al. (2017) · Oncogene · doi:10.1038/onc.2016.354 · Cited by 101 · see citing works
MYC and therapy resistance in cancer: risks and opportunities
Donati, G., & Amati, B. B. (2022) · Molecular Oncology · doi:10.1002/1878-0261.13319 · Cited by 99 · see citing works
Iwai, K., Yaguchi, M., Nishimura, K., Yamamoto, Y., Tamura, T., Nakata, D., Dairiki, R., Kawakita, Y., Mizojiri, R., Ito, Y., et al. (2018) · EMBO Molecular Medicine · doi:10.15252/emmm.201708289 · Cited by 101 · see citing works
Mahé, M., Dufour, F., Neyret‐Kahn, H., Moreno-Vega, A. I., Béraud, C., Shi, M., Hamaidi, I., Sánchez‐Quiles, V., Krucker, C., Dorland‐Galliot, M., et al. (2018) · EMBO Molecular Medicine · doi:10.15252/emmm.201708163 · Cited by 97 · see citing works
MAX is an epigenetic sensor of 5-carboxylcytosine and is altered in multiple myeloma
Wang, D., Hashimoto, H., Zhang, X., Barwick, B. G., Lonial, S., Boise, L., Vertino, P. M., & Cheng, X. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw1184 · Cited by 91 · see citing works
Targeting MYCN in Pediatric and Adult Cancers
Liu, Z., Chen, S. S., Clarke, S., Veschi, V., & Thiele, C. J. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2020.623679 · Cited by 94 · see citing works
Shared Oncogenic Pathways Implicated in Both Virus-Positive and UV-Induced Merkel Cell Carcinomas
González-Vela, M. D. C., Curiel‐Olmo, S., Derdak, S. V., Beltrán, S., Santibáñez, M., Martı́nez, N., Trujillo, O. A. C., Gut, M., Sánchez-Pacheco, R. E., Almaráz, C., et al. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.08.015 · Cited by 95 · see citing works
MYC multimers shield stalled replication forks from RNA polymerase
Solvie, D., Baluapuri, A., Uhl, L., Fleischhauer, D., Endres, T., Papadopoulos, D., Aziba, A., Gaballa, A., Mikičić, I., Isaakova, E. A., et al. (2022) · Nature · doi:10.1038/s41586-022-05469-4 · Cited by 95 · see citing works
Downregulation of ribosome biogenesis during early forebrain development
Chau, K. F., Shannon, M. L., Fame, R. M., Fonseca, E., Mullan, H., Johnson, M. B., Sendamarai, A. K., Springel, M. W., Laurent, B., & Lehtinen, M. K. (2018) · eLife · doi:10.7554/elife.36998 · Cited by 94 · see citing works
Pulikkan, J. A., Hegde, M. B., Ahmad, H. M., Belaghzal, H., Illendula, A., Yu, J., O’Hagan, K., Ou, J., Müller‐Tidow, C., Wolfe, S. A., et al. (2018) · Cell · doi:10.1016/j.cell.2018.05.048 · Cited by 91 · see citing works
Regulatory mechanisms of PD-L1 expression in cancer cells
Shi, Y. (2018) · Cancer Immunology, Immunotherapy · doi:10.1007/s00262-018-2226-9 · Cited by 92 · see citing works
SUMO protease SENP1 deSUMOylates and stabilizes c-Myc
Sun, X., Chen, Y., Su, Y., Wang, X., Chauhan, K. M., Liang, J., Daniel, C. J., Sears, R. C., & Dai, M. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1802932115 · Cited by 92 · see citing works
MYC Modulation around the CDK2/p27/SKP2 Axis
Hydbring, P., Castell, A., & Larsson, L. (2017) · Genes · doi:10.3390/genes8070174 · Cited by 90 · see citing works
Cao, L., Zhang, P., Li, J., & Wu, M. (2017) · eLife · doi:10.7554/elife.30433 · Cited by 90 · see citing works
Molecular Crosstalk Between MYC and HIF in Cancer
Li, Y., Sun, X., Qian, D. Z., & Dai, M. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.590576 · Cited by 90 · see citing works
Transcriptional integration of mitogenic and mechanical signals by Myc and YAPPreprint
Croci, O., Fazio, S., Biagioni, F., Donato, E., Cagánová, M., Curti, L., Doni, M., Sberna, S., Aldeghi, D., Biancotto, C., et al. (2017) · Genes & Development · doi:10.1101/gad.301184.117 · Cited by 86 · see citing works
Drugging “undruggable” genes for cancer treatment: Are we making progress?
Duffy, M. J., & Crown, J. P. (2020) · International Journal of Cancer · doi:10.1002/ijc.33197 · Cited by 85 · see citing works
MYC amplifies gene expression through global changes in transcription factor dynamics
Patange, S., Ball, D. A., Wan, Y., Karpova, T., Girvan, M., Levens, D., & Larson, D. R. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110292 · Cited by 86 · see citing works
Induction of LEF1 by MYC activates the WNT pathway and maintains cell proliferation
Hao, Y.-H., Lafita‐Navarro, M. C., Zacharias, L. G., Borenstein‐Auerbach, N., Kim, M., Barnes, S. D., Kim, J., Shay, J. W., DeBerardinis, R. J., & Conacci‐Sorrell, M. (2019) · Cell Communication and Signaling · doi:10.1186/s12964-019-0444-1 · Cited by 85 · see citing works
MYC and HIF in shaping immune response and immune metabolism
Gnanaprakasam, J. R., Sherman, J. W., & Wang, R. (2017) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2017.03.004 · Cited by 84 · see citing works
Concepts to Target MYC in Pancreatic Cancer
Wirth, M., Mahboobi, S., Krämer, O. H., & Schneider, G. (2016) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-16-0050 · Cited by 79 · see citing works
MYC and the unfolded protein response in cancer: synthetic lethal partners in crime?
Zhang, T., Li, N., Sun, C., Jin, Y., & Sheng, X. (2020) · EMBO Molecular Medicine · doi:10.15252/emmm.201911845 · Cited by 82 · see citing works
Targeting MYC in cancer therapy: RNA processing offers new opportunities
Koh, C. M., Sabò, A., & Guccione, E. (2016) · BioEssays · doi:10.1002/bies.201500134 · Cited by 79 · see citing works
A Time for MYC: Metabolism and TherapyPreprint
Dang, C. V. (2016) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2016.81.031153 · Cited by 78 · see citing works
Human MYC G-quadruplex: From discovery to a cancer therapeutic target
Wang, W., Hu, S., Gu, Y., Yan, Y., Stovall, D. B., Li, D., & Sui, G. (2020) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2020.188410 · Cited by 77 · see citing works
MYC and KRAS cooperation: from historical challenges to therapeutic opportunities in cancer
Casacuberta‐Serra, S., González-Larreategui, Í., Capitán-Leo, D., & Soucek, L. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01907-z · Cited by 80 · see citing works
Novel therapeutic approaches targeting L-type amino acid transporters for cancer treatment
Hayashi, K., & Anzai, N. (2017) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v9.i1.21 · Cited by 76 · see citing works
Pancreatic Neuroendocrine Tumors: Molecular Mechanisms and Therapeutic Targets
Maharjan, C. K., Ear, P. H., Tran, C. G., Howe, J. R., Chandrasekharan, C., & Quelle, D. E. (2021) · Cancers · doi:10.3390/cancers13205117 · Cited by 75 · see citing works
The role of circadian clock genes in tumors
Li, H.-X. (2019) · OncoTargets and Therapy · doi:10.2147/ott.s203144 · Cited by 77 · see citing works
Annunziato, S., de Ruiter, J. R., Henneman, L., Brambillasca, C. S., Lutz, C., Vaillant, F., Ferrante, F., Drenth, A. P., van der Burg, E., Siteur, B., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08301-2 · Cited by 69 · see citing works
An early Myc‐dependent transcriptional program orchestrates cell growth during B‐cell activation
Tesi, A., de Pretis, S., Furlan, M., Filipuzzi, M., Morelli, M. J., Andronache, A., Doni, M., Verrecchia, A., Pelizzola, M., Amati, B. B., et al. (2019) · EMBO Reports · doi:10.15252/embr.201947987 · Cited by 71 · see citing works
The MYC mRNA 3′‐UTR couples RNA polymerase II function to glutamine and ribonucleotide levels
Dejure, F. R., Royla, N., Herold, S., Kalb, J., Walz, S., Ade, C. P., Mastrobuoni, G., Vanselow, J. T., Schlösser, A., Wolf, E., et al. (2017) · The EMBO Journal · doi:10.15252/embj.201796662 · Cited by 69 · see citing works
Manier, S., Huynh, D., Shen, Y. J., Zhou, J., Yusufzai, T. M., Salem, K. Z., Ebright, R. Y., Shi, J., Park, J., Glavey, S. V., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aal2668 · Cited by 71 · see citing works
c-Src Promotes Tumorigenesis and Tumor Progression by Activating PFKFB3
Ma, H., Zhang, J., Zhou, L., Wen, S., Tang, H.-Y., Jiang, B., Zhang, F., Suleman, M., Sun, D., Chen, A., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.03.005 · Cited by 68 · see citing works
Berberine Inhibits Growth of Liver Cancer Cells by Suppressing Glutamine Uptake
Zhang, P., Wang, Q., Lin, Z., Yang, P., Dou, K., & Zhang, R. (2020) · OncoTargets and Therapy · doi:10.2147/ott.s235667 · Cited by 68 · see citing works
Dissecting transcriptional amplification by MYC
Nie, Z., Guo, C., Das, S., Chow, C. C., Batchelor, E., Simons, S. S., & Levens, D. (2020) · eLife · doi:10.7554/elife.52483 · Cited by 68 · see citing works
Poon, E., Liang, T., Jamin, Y., Walz, S., Kwok, C., Hakkert, A., Barker, K. T., Urban‐Wójciuk, Z., Thway, K., Zeid, R., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci134132 · Cited by 69 · see citing works
Oncogene-regulated release of extracellular vesicles
Kilinc, S., Paisner, R., Camarda, R., Gupta, S., Momčilović, O., Kohnz, R. A., Avşaroğlu, B., L’Étoile, N. D., Perera, R. M., Nomura, D. K., et al. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.05.014 · Cited by 68 · see citing works
See, Y. X., Chen, K., & Fullwood, M. J. (2022) · Genome Research · doi:10.1101/gr.276313.121 · Cited by 62 · see citing works
The mitochondrial translation machinery as a therapeutic target in Myc-driven lymphomas
D’Andrea, A., Gritti, I., Nicoli, P., Giorgio, M., Doni, M., Conti, A., Bianchi, V., Casoli, L., Sabò, A., Mironov, A., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.11719 · Cited by 63 · see citing works
Su, Y., Pelz, C., Huang, T., Torkenczy, K. A., Wang, X., Cherry, A. E., Daniel, C. J., Liang, J. B., Nan, X., Dai, M., et al. (2018) · Genes & Development · doi:10.1101/gad.314377.118 · Cited by 65 · see citing works
- Authors
- Kress, T. R., Sabò, A., & Amati, B.
- Affiliations
- Italian Institute of Technology (IT)
- Corresponding author
- Amati, Bruno
- Venue
- Nature reviews. Cancer
- Published
- 2015-09-18
- Volume
- 15
- Issue
- 10
- Pages
- 593-607
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- OpenAlex
- W1878169898
- Cited by
- 521
- References
- 201
- Citations by year
- 2026: 27 · 2025: 41 · 2024: 52 · 2023: 52 · 2022: 47 · 2021: 57 · 2020: 48 · 2019: 42 · 2018: 58 · 2017: 52 · 2016: 40 · 2015: 5
- FWCI
- 5.01
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Cancer (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Associazione Italiana per la Ricerca sul Cancro
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Keywords
- c-Myc, transcriptional regulation, RNA biogenesis, global transcriptome, differential gene regulation, cell proliferation, carcinogenesis, cellular metabolism, RNA processing, RNA turnover
- MeSH terms
- Humans, RNA, Messenger, Gene Expression Regulation, Neoplastic, Proto-Oncogene Proteins c-myc
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review