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Target gene-independent functions of MYC oncoproteins
Open accessAbstract
Oncoproteins of the MYC family are major drivers of human tumorigenesis. Since a large body of evidence indicates that MYC proteins are transcription factors, studying their function has focused on the biology of their target genes. Detailed studies of MYC-dependent changes in RNA levels have provided contrasting models of the oncogenic activity of MYC proteins through either enhancing or repressing the expression of specific target genes, or as global amplifiers of transcription. In this Review, we first summarize the biochemistry of MYC proteins and what is known (or is unclear) about the MYC target genes. We then discuss recent progress in defining the interactomes of MYC and MYCN and how this information affects central concepts of MYC biology, focusing on mechanisms by which MYC proteins modulate transcription. MYC proteins promote transcription termination upon stalling of RNA polymerase II, and we propose that this mechanism enhances the stress resilience of basal transcription. Furthermore, MYC proteins coordinate transcription elongation with DNA replication and cell cycle progression. Finally, we argue that the mechanism by which MYC proteins regulate the transcription machinery is likely to promote tumorigenesis independently of global or relative changes in the expression of their target genes.
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“Myc proteins, synthesized after transcription and translation of Myc gene, plays a critical role in pathways related to tumor development, including proliferation, apoptosis, differentiation, metabolism, and adaptive cancer resistance.412–414”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [413]
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Cites
Dang, C. V. (2012) · Cell · doi:10.1016/j.cell.2012.03.003 · Cited by 3,390
Oncogene-induced senescence is part of the tumorigenesis barrier imposed by DNA damage checkpoints
Bartkova, J., Rezaei, N., Liontos, M., Karakaidos, P., Kletsas, D., Issaeva, N., Vassiliou, L.-V. F., Kolettas, E., Niforou, K., Zoumpourlis, V. C., et al. (2006) · Nature · doi:10.1038/nature05268 · Cited by 1,986
A Phase Separation Model for Transcriptional Control
Hnisz, D., Shrinivas, K., Young, R. A., Chakraborty, A. K., & Sharp, P. A. (2017) · Cell · doi:10.1016/j.cell.2017.02.007 · Cited by 1,753
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 1,543
Stine, Z. E., Walton, Z. E., Altman, B. J., Hsieh, A. L., & Dang, C. V. (2015) · Cancer Discovery · doi:10.1158/2159-8290.cd-15-0507 · Cited by 1,435
MYC regulates the antitumor immune response through CD47 and PD-L1
Casey, S. C., Tong, L., Li, Y., Do, R., Walz, S., Fitzgerald, K. N., Gouw, A. M., Baylot, V., Gütgemann, I., Eilers, M., et al. (2016) · Science · doi:10.1126/science.aac9935 · Cited by 1,403
Self-citationc-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
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 1,106
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
Welcker, M., Orian, A., Jin, J., Grim, J. A., Harper, J. W., Eisenman, R. N., & Clurman, B. E. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402770101 · Cited by 942
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Liu, M., Wang, Y., Zhang, Y.-B., Hu, D., Tang, L., Zhou, B., & Yang, L. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-02112-8 · Cited by 189
Wang, L., Chen, C., Song, Z., Wang, H., Ye, M., Wang, D., Kang, W., Liu, H., & Qing, G. (2022) · Nature Communications · doi:10.1038/s41467-021-27609-6 · Cited by 151
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Yang, L., Jia, R., Ge, T., Ge, S., Zhuang, A., Chai, P., & Fan, X. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01176-8 · Cited by 136
Beaulieu, M.-È., Castillo, F., & Soucek, L. (2020) · Cells · doi:10.3390/cells9041038 · Cited by 110
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Das, S., Kuzin, V., Cameron, D. P., Sanford, S., Jha, R. K., Nie, Z., Rosello, M. T., Holewinski, R. J., Andrésson, Þ., Wiśniewski, J., et al. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.11.016 · Cited by 112
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Liu, H., Liu, K., & Dong, Z. (2020) · Cancer Research · doi:10.1158/0008-5472.can-20-2245 · Cited by 101
Deubiquitination of MYC by OTUB1 contributes to HK2 mediated glycolysis and breast tumorigenesis
Han, X., Ren, C., Lü, C., Qiao, P., Yang, T., & Yu, Z. (2022) · Cell Death and Differentiation · doi:10.1038/s41418-022-00971-8 · Cited by 103
Röschert, I., Poon, E., Henssen, A. G., García, H. D., Gatti, M., Giansanti, C., Jamin, Y., Ade, C. P., Gallant, P., Schülein‐Völk, C., et al. (2021) · Nature Cancer · doi:10.1038/s43018-020-00171-8 · Cited by 103
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Liu, Z., Chen, S. S., Clarke, S., Veschi, V., & Thiele, C. J. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2020.623679 · Cited by 95
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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
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Li, M., & Ma, S. (2024) · Food Research International · doi:10.1016/j.foodres.2024.114682 · Cited by 105
Popay, T. M., Wang, J., Adams, C. M., Howard, G. C., Codreanu, S. G., Sherrod, S. D., MCLEAN, J. A. J., Thomas, L. R., Lorey, S. L., Machida, Y., et al. (2021) · eLife · doi:10.7554/elife.60191 · Cited by 93
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Čermáková, K., & Hodges, H. C. (2023) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2023.01.004 · Cited by 96
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Liu, J.-Y., Chen, Y., Feng, H.-H., Chen, Z., Wang, Y., Yang, J., & Zhuang, S. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-04238-x · Cited by 75
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Yang, K., Zhang, W., Zhong, L., Xiao, Y., Sahoo, S., Fassan, M., Zeng, K., Magee, P., Garofalo, M., & Shi, L. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01160-x · Cited by 72
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Xu, Y., Fan, X., & Hu, Y. (2021) · Cell & Bioscience · doi:10.1186/s13578-021-00542-3 · Cited by 64
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Yang, J., Chung, C.-I., Koach, J., Liu, H., Navalkar, A., He, H., Ma, Z., Zhao, Q. C., Yang, X., He, L., et al. (2024) · Nature Structural & Molecular Biology · doi:10.1038/s41594-024-01322-6 · Cited by 67
Endres, T., Solvie, D., Heidelberger, J. B., Andrioletti, V., Baluapuri, A., Ade, C. P., Muhar, M., Eilers, U., Vos, S. M., Cramer, P., et al. (2021) · Molecular Cell · doi:10.1016/j.molcel.2020.12.035 · Cited by 57
Self-citationTargeting Myc-driven stress addiction in colorectal cancer
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Shi, W., Wang, Y., Xu, C., Li, Y., Ge, S., Bai, B., Zhang, K., Wang, Y., Zheng, N., Wang, J., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-35797-6 · Cited by 50
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He, J., Huo, X., Pei, G., Jia, Z., Yan, Y., Yu, J., Qu, H., Xie, Y., Yuan, J., Zheng, Y., et al. (2024) · Cell · doi:10.1016/j.cell.2024.03.023 · Cited by 46
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Ma, J., Li, L., Ma, B., Liu, T., Wang, Z., Ye, Q., Peng, Y., Wang, B., Chen, Y., Xu, S., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-45796-w · Cited by 48
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Wu, G., Suo, C., Yang, Y., Shen, S., Sun, L., Li, S., Zhou, Y., Yang, D., Wang, Y., Cai, Y., et al. (2021) · EMBO Reports · doi:10.15252/embr.202051519 · Cited by 44
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Pellanda, P., Dalsass, M., Filipuzzi, M., Loffreda, A., Verrecchia, A., Cano, V. C., Thabussot, H., Doni, M., Morelli, M. J., Soucek, L., et al. (2021) · The EMBO Journal · doi:10.15252/embj.2020105464 · Cited by 44
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Radaeva, M., Ton, A., Hsing, M., Ban, F., & Cherkasov, A. R. (2021) · Drug Discovery Today · doi:10.1016/j.drudis.2021.07.018 · Cited by 46
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Mathsyaraja, H., Catchpole, J., Freie, B. W., Eastwood, E., Babaeva, E., Geuenich, M., Cheng, P. F., Ayers, J., Yu, M., Wu, N., et al. (2021) · eLife · doi:10.7554/elife.64212 · Cited by 40
eIF4E S209 phosphorylation licenses myc- and stress-driven oncogenesis
Ruan, H., Li, X., Xu, X. M., Leibowitz, B. J., Tong, J., Chen, L., Ao, L., Xing, W., Luo, J., Yu, Y., et al. (2020) · eLife · doi:10.7554/elife.60151 · Cited by 41
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Weber, L. I., & Hartl, M. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1142111 · Cited by 43
Gao, M., Yang, J., Gong, H., Lin, Y., & Liu, J. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.760055 · Cited by 37
Perri, P., Ponzoni, M., Corrias, M. V., Ceccherini, I., Candiani, S., & Bachetti, T. (2021) · Cancers · doi:10.3390/cancers13215528 · Cited by 40
Krenz, B., Gebhardt-Wolf, A., Ade, C. P., Gaballa, A., Roehrig, F., Vendelova, E., Baluapuri, A., Eilers, U., Gallant, P., D’Artista, L., et al. (2021) · Cancer Research · doi:10.1158/0008-5472.can-21-1677 · Cited by 41
Self-citationRole of c-Myc in lung cancer: Progress, challenges, and prospects
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Mark, K. G., & Rapé, M. (2021) · EMBO Reports · doi:10.15252/embr.202051078 · Cited by 39
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Wang, D., Tian, J., Yan, Z., Yuan, Q., Wu, D., Liu, X., Yang, S., Guo, S., Wang, J., Yang, Y., et al. (2022) · Molecular Therapy · doi:10.1016/j.ymthe.2022.01.032 · Cited by 34
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Self-citationTargeting MYC: From understanding its biology to drug discovery
Ross, J., Miron, C. E., Plescia, J., LaPlante, P., McBride, K. M., Moitessier, N., & Möröy, T. (2020) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2020.113137 · Cited by 35
Bai, L., Ma, Y., Wang, X., Feng, Q., Zhang, Z., Wang, S., Zhang, H., Lu, X., Xu, Y., Zhao, E., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.587218 · Cited by 34
Guan, X., Yang, J., Wang, W., Zhao, B., Hu, S., Yu, D., Yuan, L., Shi, Y., Xu, J., Dong, J., et al. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106703 · Cited by 33
Sahoo, S. S., Ramanand, S. G., Gao, Y., Abbas, A., Kumar, A., Cuevas, I., Li, H., Aguilar, M., Xing, C., Mani, R. S., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci157574 · Cited by 32
Anatskaya, O. V., & Vinogradov, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23179691 · Cited by 27
Wyn, J. D., Zimmerman, M. W., Weichert‐Leahey, N., Nunes, C., Cheung, B. B., Abraham, B. J., Beckers, A., Volders, P., Decaesteker, B., Carter, D. R., et al. (2021) · Cancers · doi:10.3390/cancers13194783 · Cited by 30
Targeting Myc Interacting Proteins as a Winding Path in Cancer Therapy
Zhou, Y., Gao, X., Meng, Y. G., Yang, B., He, Q., & Cao, J. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.748852 · Cited by 29
Schukur, L., Zimmermann, T., Niewoehner, O., Kerr, G., Gleim, S., Bauer-Probst, B., Knapp, B., Galli, G. G., Liang, X., Mendiola, A., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-76960-z · Cited by 28
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Asami, M., Lam, B., Hoffmann, M., Suzuki, T., Lu, X., Yoshida, N., Ma, M. K. L., Rainbow, K., Gužvić, M., VerMilyea, M. D., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112023 · Cited by 26
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Luo, C., Yu, T., Young, K. H., & Yu, L. (2022) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b2200016 · Cited by 24
Cencioni, C., Scagnoli, F., Spallotta, F., Nasi, S., & Illi, B. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24044217 · Cited by 28
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Wang, M., Hu, S., Yang, J., Liang, Y., Han, L., Liang, F., Zhang, F., Zhao, H., Liu, Y., & Gao, N. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155391 · Cited by 23
Shibasaki, H., Kinoh, H., Cabral, H., Quader, S., Mochida, Y., Liu, X., Toh, K., Miyano, K., Matsumoto, Y., Yamasoba, T., et al. (2021) · ACS Nano · doi:10.1021/acsnano.1c00364 · Cited by 24
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Cui, Z., Zou, F., Wang, R., Wang, L., Cheng, F., Wang, L., Pan, R., Guan, X., Zheng, N., & Wang, W. (2023) · World Journal of Surgical Oncology · doi:10.1186/s12957-023-03187-3 · Cited by 22
Ai, M., Ma, H., He, J., Xu, F., Ming, Y., Ye, Z., Zheng, Q., Luo, D., Yang, K., Li, J., et al. (2024) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2024.116978 · Cited by 23
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Metadata
- Authors
- Baluapuri, A., Wolf, E., & Eilers, M.
- Affiliations
- University of Würzburg (DE)
- Corresponding author
- Eilers, Martin
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2020-02-18
- Volume
- 21
- Issue
- 5
- Pages
- 255-267
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- PMC
- PMC7611238
- OpenAlex
- W3007097494
- Cited by
- 310
- References
- 130
- Citations by year
- 2026: 29 · 2025: 48 · 2024: 63 · 2023: 60 · 2022: 50 · 2021: 51 · 2020: 9
- FWCI
- 4.09
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Reviews Molecular Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- 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 › Chromatin Remodeling and Cancer
- Keywords
- Myc oncoprotein, MYCN, transcription factors, target genes, RNA polymerase II stalling, transcription termination, transcription elongation, DNA replication, cell cycle progression, stress resilience, basal transcription, carcinogenesis, protein-protein interaction network, transcriptional regulation
- MeSH terms
- N-Myc Proto-Oncogene Protein, Cell Cycle, DNA Replication, Humans, Neoplasms, Transcription Factors, Transcription, Genetic, Oncogene Proteins, Proto-Oncogene Proteins c-myc, Cell Proliferation, Carcinogenesis
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