CDK6—a review of the past and a glimpse into the future: from cell-cycle control to transcriptional regulation
Abstract
The G1 cell-cycle kinase CDK6 has long been thought of as a redundant homolog of CDK4. Although the two kinases have very similar roles in cell-cycle progression, it has recently become apparent that they differ in tissue-specific functions and contribute differently to tumor development. CDK6 is directly involved in transcription in tumor cells and in hematopoietic stem cells. These functions point to a role of CDK6 in tissue homeostasis and differentiation that is partially independent of CDK6's kinase activity and is not shared with CDK4. We review the literature on the contribution of CDK6 to transcription in an attempt to link the new findings on CDK6's transcriptional activity to cell-cycle progression. Finally, we note that anticancer therapies based on the inhibition of CDK6 kinase activity fail to take into account its kinase-independent role in tumor development.
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ATP-competitive inhibitors cannot disrupt scaffolding functions of CDK6.
“Moreover, ATP-competitive inhibitors cannot disrupt the scaffolding functions of CDK6, which is important for the transcription function of CDK6 [124, 125].”
From Proteolysis targeting chimeras (PROTACs) are emerging therapeutics for hematologic malignancies (2020) · cites this paper as [125]
Cyclin D1 and the CDK4-related kinase CDK6 can associate with target genes and function as transcriptional regulators.
“Previous studies revealed that Cyclin D140,41 as well as the CDK4-related kinase CDK642 can associate with target genes and function as transcriptional regulators.”
From CDK4 inhibition diminishes p53 activation by MDM2 antagonists (2018) · cites this paper as [42]
Cites
CDK inhibitors: positive and negative regulators of G1-phase progression
Sherr, C. J., & Roberts, J. M. (1999) · Genes & Development · doi:10.1101/gad.13.12.1501 · Cited by 6,115 · see citing works
An Integrated Genomic Analysis of Human Glioblastoma Multiforme
Parsons, D. W., Jones, S., Zhang, X., Lin, J. C.-H., Leary, R. J., Angenendt, P., Mankoo, P., Carter, H., Siu, I.-M., Gallia, G. L., et al. (2008) · Science · doi:10.1126/science.1164382 · Cited by 5,857 · see citing works
Oncogenic ras provokes premature cell senescence associated with accumulation of p53 and p16INK4a
Serrano, M., Lin, A. W., McCurrach, M. E., Beach, D., & Lowe, S. W. (1997) · Cell · doi:10.1016/s0092-8674(00)81902-9 · Cited by 5,178 · see citing works
The landscape of somatic copy-number alteration across human cancers
Beroukhim, R., Mermel, C. H., Porter, D., Wei, G., Raychaudhuri, S., Donovan, J., Barretina, J., Boehm, J. S., Dobson, J., Urashima, M., et al. (2010) · Nature · doi:10.1038/nature08822 · Cited by 4,017 · see citing works
Core Signaling Pathways in Human Pancreatic Cancers Revealed by Global Genomic Analyses
Jones, S., Zhang, X., Parsons, D. W., Lin, J. C.-H., Leary, R. J., Angenendt, P., Mankoo, P., Carter, H., Kamiyama, H., Jimeno, A., et al. (2008) · Science · doi:10.1126/science.1164368 · Cited by 3,969 · see citing works
Cell cycle, CDKs and cancer: a changing paradigm
Malumbres, M., & Barbacid, M. (2009) · Nature Reviews Cancer · doi:10.1038/nrc2602 · Cited by 3,957 · see citing works
p21 is a universal inhibitor of cyclin kinases
Xiong, Y., Hannon, G., Zhang, H., Casso, D., Kobayashi, R., & Beach, D. (1993) · Nature · doi:10.1038/366701a0 · Cited by 3,691 · see citing works
A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4.
Serrano, M., Hannon, G. J., & Beach, D. (1993) · Nature · doi:10.1038/366704a0 · Cited by 3,650 · see citing works
A cell cycle regulator potentially involved in genesis of many tumor types
Kamb, A., Gruis, N. A., Weaver-Feldhaus, J., Liu, Q., Harshman, K., Tavtigian, S. V., Stockert, E., Day, R. S., Johnson, B. E., & Skolnick, M. H. (1994) · Science · doi:10.1126/science.8153634 · Cited by 2,751 · see citing works
Whole genomes redefine the mutational landscape of pancreatic cancer
Initiative, A. P. C. G., Waddell, N., Pajic, M., Patch, A.-M., Chang, D. K., Kassahn, K. S., Bailey, P., Johns, A. L., Miller, D., Nones, K., et al. (2015) · Nature · doi:10.1038/nature14169 · Cited by 2,642 · see citing works
The regulation of E2F by pRB-family proteins.
Dyson, N. (1998) · Genes & Development · doi:10.1101/gad.12.15.2245 · Cited by 2,317 · see citing works
CYCLIN-DEPENDENT KINASES: Engines, Clocks, and Microprocessors
Morgan, D. O. (1997) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.13.1.261 · Cited by 2,248 · see citing works
p27, a novel inhibitor of G1 cyclin-Cdk protein kinase activity, is related to p21.
Toyoshima, H., & Hunter, T. (1994) · Cell · doi:10.1016/0092-8674(94)90573-8 · Cited by 2,208 · see citing works
Polyák, K., Lee, M.-H., Erdjument‐Bromage, H., Koff, A., Roberts, J. M., Tempst, P., & Massagué, J. (1994) · Cell · doi:10.1016/0092-8674(94)90572-x · Cited by 2,118 · see citing works
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 · see citing works
pl5INK4B is a potentia| effector of TGF-β-induced cell cycle arrest
Hannon, G. J., & Beach, D. (1994) · Nature · doi:10.1038/371257a0 · Cited by 1,950 · see citing works
Polyak, K., Kato, J., Solomon, M., Sherr, C., Massagué, J., Roberts, J., & Koff, A. (1994) · Genes & Development · doi:10.1101/gad.8.1.9 · Cited by 1,949 · see citing works
Wilson, A., Laurenti, E., Oser, G., van der Wath, R. C., Blanco-Bose, W., Jaworski, M., Offner, S., Dunant, C. F., Eshkind, L., Bockamp, E., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.048 · Cited by 1,908 · see citing works
Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers
Nobori, T., Miura, K., Wu, D. J., Lois, A., Takabayashi, K., & Carson, D. A. (1994) · Nature · doi:10.1038/368753a0 · Cited by 1,742 · see citing works
NF‐κB and the link between inflammation and cancer
DiDonato, J. A., Mercurio, F., & Karin, M. (2012) · Immunological Reviews · doi:10.1111/j.1600-065x.2012.01099.x · Cited by 1,490 · see citing works
Cdks, cyclins and CKIs: roles beyond cell cycle regulation
Lim, S., & Kaldis, P. (2013) · Development · doi:10.1242/dev.091744 · Cited by 1,483 · see citing works
To cycle or not to cycle: a critical decision in cancer
Malumbres, M., & Barbacid, M. (2001) · Nature reviews. Cancer · doi:10.1038/35106065 · Cited by 1,475 · see citing works
New functional activities for the p21 family of CDK inhibitors.
LaBaer, J., Garrett, M. D., Stevenson, L. F., Slingerland, J. M., Sandhu, C., Chou, H. S., Fattaey, A., & Harlow, E. (1997) · Genes & Development · doi:10.1101/gad.11.7.847 · Cited by 1,402 · see citing works
Inflammation meets cancer, with NF-κB as the matchmaker
Ben‐Neriah, Y., & Karin, M. (2011) · Nature Immunology · doi:10.1038/ni.2060 · Cited by 1,378 · see citing works
Mammalian cyclin-dependent kinases
Malumbres, M., & Barbacid, M. (2005) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2005.09.005 · Cited by 1,294 · see citing works
(1993) · Genes & Development · doi:10.1101/gad.7.3.331 · Cited by 1,264 · see citing works
Retinoblastoma protein recruits histone deacetylase to repress transcription
Brehm, A., Miska, E. A., McCance, D. J., Reid, J. L., Bannister, A. J., & Kouzarides, T. (1998) · Nature · doi:10.1038/35404 · Cited by 1,231 · see citing works
A p16 INK4a -Insensitive CDK4 Mutant Targeted by Cytolytic T Lymphocytes in a Human Melanoma
Wölfel, T., Hauer, M., Schneider, J., Serrano, M., Wölfel, C., Klehmann, E., Plaen, E. D., Hankeln, T., Büschenfelde, K. M. Z., & Beach, D. (1995) · Science · doi:10.1126/science.7652577 · Cited by 1,153 · see citing works
Cheng, M., Olivier, P., Diehl, J. A., Fero, M., Roussel, M. F., Roberts, J. M., & Sherr, C. J. (1999) · The EMBO Journal · doi:10.1093/emboj/18.6.1571 · Cited by 1,142 · see citing works
Living with or without cyclins and cyclin-dependent kinases
Sherr, C. J., & Roberts, J. M. (2004) · Genes & Development · doi:10.1101/gad.1256504 · Cited by 1,089 · see citing works
Lundberg, A. S., & Weinberg, R. A. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.2.753 · Cited by 1,077 · see citing works
D-Type Cyclin-Dependent Kinase Activity in Mammalian Cells
Matsushime, H., Quelle, D. E., Shurtleff, S. A., Shibuya, M., Sherr, C. J., & Kato, J. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.3.2066 · Cited by 1,067 · see citing works
Harbour, J. W., Luo, R. X., Santi, A. D., Postigo, A. A., & Dean, D. C. (1999) · Cell · doi:10.1016/s0092-8674(00)81519-6 · Cited by 1,057 · see citing works
Inhibition of cyclin-dependent kinases by p21.
Harper, J. W., Elledge, S. J., Keyomarsi, K., Dynlacht, B. D., Tsai, L., Zhang, P., Dobrowolski, S. F., Bai, C., Connell‐Crowley, L., & Swindell, E. C. (1995) · Molecular Biology of the Cell · doi:10.1091/mbc.6.4.387 · Cited by 1,025 · see citing works
Sherr, C. J. (1995) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(00)89005-2 · Cited by 980 · see citing works
Minireview: Cyclin D1: Normal and Abnormal Functions
Fu, M., Wang, C., Li, Z., Sakamaki, T., & Pestell, R. G. (2004) · Endocrinology · doi:10.1210/en.2004-0959 · Cited by 961 · see citing works
Rb Interacts with Histone Deacetylase to Repress Transcription
Luo, R. X., Postigo, A. A., & Dean, D. C. (1998) · Cell · doi:10.1016/s0092-8674(00)80940-x · Cited by 957 · see citing works
A family of human cdc2‐related protein kinases.
Meyerson, M. M., Enders, G. H., Wu, C. L., Su, L., Gorka, C., Nelson, C. E., Harlow, E., & Tsai, L. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05360.x · Cited by 925 · see citing works
Burkitt lymphoma pathogenesis and therapeutic targets from structural and functional genomics
Schmitz, R., Young, R. M., Ceribelli, M., Jhavar, S. G., Xiao, W., Zhang, M., Wright, G. W., Shaffer, A. L., Hodson, D. J., Buras, E. D., et al. (2012) · Nature · doi:10.1038/nature11378 · Cited by 920 · see citing works
The p16INK4a/CDKN2A tumor suppressor and its relatives
Ruas, M., & Peters, G. (1998) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/s0304-419x(98)00017-1 · Cited by 911 · see citing works
Crystal structure of the p27Kip1 cyclin-dependent-kinase inibitor bound to the cyclin A–Cdk2 complex
Russo, A. A., Jeffrey, P. D., Patten, A. K., Massagué, J., & Pavletich, N. P. (1996) · Nature · doi:10.1038/382325a0 · Cited by 907 · see citing works
Cell cycle kinases as therapeutic targets for cancer
Lapenna, S., & Giordano, A. (2009) · Nature Reviews Drug Discovery · doi:10.1038/nrd2907 · Cited by 906 · see citing works
Rb targets histone H3 methylation and HP1 to promoters
Nielsen, S. J., Schneider, R., Bauer, U., Bannister, A. J., Morrison, A. J., O’Carroll, D., Firestein, R., Cleary, M. L., Jenuwein, T., Herrera, R. E., et al. (2001) · Nature · doi:10.1038/35087620 · Cited by 901 · see citing works
Matsushime, H., Ewen, M. E., Strom, D. K., Kato, J.-Y., Hanks, S. K., Roussel, M. F., & Sherr, C. J. (1992) · Cell · doi:10.1016/0092-8674(92)90360-o · Cited by 897 · see citing works
Lee, M., Reynisdóttir, I., & Massagué, J. (1995) · Genes & Development · doi:10.1101/gad.9.6.639 · Cited by 889 · see citing works
The diverse and complex roles of NF-κB subunits in cancer
Perkins, N. D. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3204 · Cited by 845 · see citing works
Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma
Zuo, L., Weger, J., Yang, Q., Goldstein, A. M., Tucker, M. A., Walker, G. J., Hayward, N., & Dracopoli, N. C. (1996) · Nature Genetics · doi:10.1038/ng0196-97 · Cited by 818 · see citing works
Identification of G1 kinase activity for cdk6, a novel cyclin D partner.
Meyerson, M. M., & Harlow, E. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.3.2077 · Cited by 799 · see citing works
Mammalian cells cycle without the D-type cyclin-dependent kinases Cdk4 and Cdk6
Malumbres, M., Sotillo, R., Santamarı́a, D., Galán, J., Cerezo, A., Ortega, S., Dubus, P., & Barbacid, M. (2004) · Cell · doi:10.1016/j.cell.2004.08.002 · Cited by 793 · see citing works
Physical interaction of the retinoblastoma protein with human D cyclins
Dowdy, S. F., Hinds, P. W., Louie, K., Reed, S. I., Arnold, A., & Weinberg, R. A. (1993) · Cell · doi:10.1016/0092-8674(93)90137-f · Cited by 746 · see citing works
Signatures of mutation and selection in the cancer genome
Bignell, G. R., Greenman, C. D., Davies, H., Butler, A. P., Edkins, S., Andrews, J. M., Buck, G., Chen, L., Beare, D., Latimer, C., et al. (2010) · Nature · doi:10.1038/nature08768 · Cited by 707 · see citing works
Rane, S. G., Dubus, P., Mettus, R. V., Galbreath, E. J., Boden, G., Reddy, E. P., & Barbacid, M. (1999) · Nature Genetics · doi:10.1038/8751 · Cited by 700 · see citing works
Zhang, H. S., Gavin, M., Dahiya, A., Postigo, A. A., Ma, D., Luo, R. X., Harbour, J. W., & Dean, D. C. (2000) · Cell · doi:10.1016/s0092-8674(00)80625-x · Cited by 658 · see citing works
Regulation of G1 cyclin-dependent kinases in the mammalian cell cycle
Ekholm, S. V., & Reed, S. I. (2000) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(00)00151-4 · Cited by 587 · see citing works
p16 <sup>INK4A</sup> is a robust <i>in vivo</i> biomarker of cellular aging in human skin
Ressler, S., Bartkova, J., Niederegger, H., Bartek, J., Scharffetter‐Kochanek, K., Jansen‐Dürr, P., & Wlaschek, M. (2006) · Aging Cell · doi:10.1111/j.1474-9726.2006.00231.x · Cited by 557 · see citing works
Anders, L., Ke, N., Hydbring, P., Choi, Y. J., Widlund, H. R., Chick, J. M., Zhai, H., Vidal, M., Gygi, S. P., Braun, P., et al. (2011) · Cancer Cell · doi:10.1016/j.ccr.2011.10.001 · Cited by 543 · see citing works
Subunit rearrangement of the cyclin-dependent kinases is associated with cellular transformation.Preprint
Xiong, Y., Zhang, H., & Beach, D. (1993) · Genes & Development · doi:10.1101/gad.7.8.1572 · Cited by 507 · see citing works
Cyclin-dependent kinases regulate the antiproliferative function of Smads
Matsuura, I., Denissova, N. G., Wang, G., He, D., Long, J., & Liu, F. (2004) · Nature · doi:10.1038/nature02650 · Cited by 506 · see citing works
Cyclin-dependent kinases: a family portrait
Malumbres, M., Harlow, E. E., Hunt, T., Hunter, T. R., Lahti, J. M., Manning, G., Morgan, D. O., Tsai, L., & Wolgemuth, D. J. (2009) · Nature Cell Biology · doi:10.1038/ncb1109-1275 · Cited by 499 · see citing works
Cheng, M., Sexl, V., Sherr, C. J., & Roussel, M. F. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.3.1091 · Cited by 496 · see citing works
Self-citationJares, P., Colomer, D., & Campo, E. (2007) · Nature Reviews Cancer · doi:10.1038/nrc2230 · Cited by 466 · see citing works
Moonlighting proteins: An intriguing mode of multitasking
Huberts, D. H. E. W., & van der Klei, I. J. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2010.01.022 · Cited by 456 · see citing works
Function of a human cyclin gene as an oncogene.
Hinds, P. W., Dowdy, S. F., Eaton, E. N., Arnold, A., & Weinberg, R. A. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.2.709 · Cited by 451 · see citing works
CDKN2 (p16/MTS1) gene deletion or CDK4 amplification occurs in the majority of glioblastomas.
Schmidt, E., Ichimura, K., Reifenberger, G., & Collins, V. P. (1994) · PubMed · Cited by 436 · see citing works
Requirement for CDK4 kinase function in breast cancer
Yu, Q., Sicinska, E., Geng, Y., Ahnström, M., Zagozdzon, A., Kong, Y., Gardner, H., Kiyokawa, H., Harris, L. N., Stål, O., et al. (2006) · Cancer Cell · doi:10.1016/j.ccr.2005.12.012 · Cited by 429 · see citing works
Puyol, M., Martín, A., Dubus, P., Mulero, F., Pizcueta, P., Khan, G., Guerra, C., Santamaría, D., & Barbacid, M. (2010) · Cancer Cell · doi:10.1016/j.ccr.2010.05.025 · Cited by 415 · see citing works
A Mechanism of Cyclin D1 Action Encoded in the Patterns of Gene Expression in Human Cancer
Lamb, J., Ramaswamy, S., Ford, H. L., Contreras, B., Martinez, R. V. P., Kittrell, F. S., Zahnow, C. A., Patterson, N. J., Golub, T. R., & Ewen, M. E. (2003) · Cell · doi:10.1016/s0092-8674(03)00570-1 · Cited by 410 · see citing works
Endogenous Purification Reveals GREB1 as a Key Estrogen Receptor Regulatory Factor
Mohammed, H., D’Santos, C., Serandour, A. A., Ali, H. R., Brown, G. D., Atkins, A., Rueda, O. M., Holmes, K. A., Theodorou, V., Robinson, J. L. L., et al. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.01.010 · Cited by 400 · see citing works
Targeted Disruption of CDK4 Delays Cell Cycle Entry with Enhanced p27 <sup>Kip1</sup> Activity
Tsutsui, T., Hesabi, B., Moons, D. S., Pandolfi, P. P., Hansel, K. S., Koff, A., & Kiyokawa, H. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.10.7011 · Cited by 395 · see citing works
Therapeutic CDK4/6 inhibition in breast cancer: key mechanisms of response and failure
Dean, J. L., Thangavel, C., McClendon, A. K., Reed, C. A., & Knudsen, E. S. (2010) · Oncogene · doi:10.1038/onc.2010.154 · Cited by 393 · see citing works
Cyclin D1 Stimulation of Estrogen Receptor Transcriptional Activity Independent of cdk4†
Neuman, E., Ladha, M. H., Lin, N., Upton, T. M., Miller, S. J., DiRenzo, J., Pestell, R. G., Hinds, P. W., Dowdy, S. F., Brown, M. A., et al. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.9.5338 · Cited by 393 · see citing works
Tailoring to RB: tumour suppressor status and therapeutic response
Knudsen, E. S., & Knudsen, K. E. (2008) · Nature reviews. Cancer · doi:10.1038/nrc2401 · Cited by 345 · see citing works
The Requirement for Cyclin D Function in Tumor Maintenance
Choi, Y. J., Li, X., Hydbring, P., Sanda, T., Stefano, J., Christie, A. L., Signoretti, S., Look, A. T., Kung, A. L., von Boehmer, H., et al. (2012) · Cancer Cell · doi:10.1016/j.ccr.2012.09.015 · Cited by 342 · see citing works
CDK6 Levels Regulate Quiescence Exit in Human Hematopoietic Stem Cells
Laurenti, E., Frelin, C., Xie, S. Z.-J., Ferrari, R., Dunant, C. F., Zandi, S., Neumann, A. L., Plumb, I., Doulatov, S. R., Chen, J., et al. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.01.017 · Cited by 340 · see citing works
A function for cyclin D1 in DNA repair uncovered by protein interactome analyses in human cancers
Jirawatnotai, S., Hu, Y., Michowski, W., Elias, J. E., Becks, L., Bienvenu, F., Zagozdzon, A., Goswami, T., Wang, Y. E., Clark, A. B., et al. (2011) · Nature · doi:10.1038/nature10155 · Cited by 333 · see citing works
Cyclin D1-dependent kinase activity in murine development and mammary tumorigenesis
Landis, M. W., Pawlyk, B. S., Li, T., Sicinski, P., & Hinds, P. W. (2006) · Cancer Cell · doi:10.1016/j.ccr.2005.12.019 · Cited by 329 · see citing works
Min, I. M., Pietramaggiori, G., Kim, F. S., Passegue, E. A., Stevenson, K. E., & Wagers, A. J. (2008) · Cell stem cell · doi:10.1016/j.stem.2008.01.015 · Cited by 327 · see citing works
Michaud, K., Solomon, D. A., Oermann, E. K., Kim, J.-S., Zhong, W.-Z., Prados, M. D., Ozawa, T., James, C. D., & Waldman, T. A. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-4559 · Cited by 321 · see citing works
FOXM1, a typical proliferation-associated transcription factor
Wierstra, I., & Alves, J. (2007) · Biological Chemistry · doi:10.1515/bc.2007.159 · Cited by 313 · see citing works
A Kinase-Independent Function of CDK6 Links the Cell Cycle to Tumor Angiogenesis
Kollmann, K., Heller, G., Schneckenleithner, C., Warsch, W., Scheicher, R., Ott, R. G., Schäfer, M., Fajmann, S., Schlederer, M., Schiefer, A.-I., et al. (2013) · Cancer Cell · doi:10.1016/j.ccr.2013.07.012 · Cited by 313 · see citing works
Self-citationExpression of p16 and Retinoblastoma Determines Response to CDK4/6 Inhibition in Ovarian Cancer
Konecny, G. E., Winterhoff, B. J. N., Kolarova, T. R., Qi, J., Manivong, K., Dering, J., Yang, G., Chalukya, M., Wang, H.-J., Anderson, L. A., et al. (2011) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-10-2307 · Cited by 303 · see citing works
Witkiewicz, A. K., Knudsen, K. E., Dicker, A. P., & Knudsen, E. S. (2011) · Cell Cycle · doi:10.4161/cc.10.15.16776 · Cited by 286 · see citing works
Signaling through cyclin D-dependent kinases
Choi, Y., & Anders, L. (2013) · Oncogene · doi:10.1038/onc.2013.137 · Cited by 279 · see citing works
Blain, S. W., Montalvo, E., & Massagué, J. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.41.25863 · Cited by 279 · see citing works
Transcriptional role of cyclin D1 in development revealed by a genetic-proteomic screen
Bienvenu, F., Jirawatnotai, S., Elias, J. E., Meyer, C. A., Mizeracka, K., Marson, A., Frampton, G. M., Cole, M. F., Odom, D. T., Odajima, J., et al. (2010) · Nature · doi:10.1038/nature08684 · Cited by 276 · see citing works
Fu, M., Rao, M., Bouras, T., Wang, C., Wu, K., Zhang, X., Li, Z., Yao, T., & Pestell, R. G. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m500403200 · Cited by 274 · see citing works
CDK6 as a key regulator of hematopoietic and leukemic stem cell activation
Scheicher, R., Hoelbl‐Kovacic, A., Bellutti, F., Tigan, A.-S., Prchal‐Murphy, M., Heller, G., Schneckenleithner, C., Salazar‐Roa, M., Zöchbauer‐Müller, S., Zuber, J. A., et al. (2014) · Blood · doi:10.1182/blood-2014-06-584417 · Cited by 263 · see citing works
Self-citationBates, S., Bonetta, L. P., MacAllan, D., Parry, D., Holder, A. A., Dickson, C., & Peters, G. (1994) · PubMed · Cited by 260 · see citing works
Rubin, S. M., Gall, A.-L., Zheng, N., & Pavletich, N. P. (2005) · Cell · doi:10.1016/j.cell.2005.09.044 · Cited by 253 · see citing works
Aggarwal, P., Vaites, L. P., Kim, J. K., Mellert, H. S., Gurung, B., Nakagawa, H., Herlyn, M., Hua, X., Rustgi, A. K., McMahon, S. B., et al. (2010) · Cancer Cell · doi:10.1016/j.ccr.2010.08.012 · Cited by 243 · see citing works
Structural basis of inhibition of CDK–cyclin complexes by INK4 inhibitorsPreprint
Jeffrey, P. D., Tong, L., & Pavletich, N. P. (2000) · Genes & Development · doi:10.1101/gad.851100 · Cited by 239 · see citing works
Crosstalk between chromatin state and DNA damage response in cellular senescence and cancer.
Sulli, G., Di Micco, R., & di Fagagna, F. D. (2012) · Nature Reviews Cancer · doi:10.1038/nrc3344 · Cited by 238 · see citing works
Cyclin dependent kinase (CDK) inhibitors as anticancer drugs
Sánchez-Martínez, C., Gelbert, L. M., Lallena, M. J., & de Dios, A. (2015) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2015.05.100 · Cited by 236 · see citing works
Cyclin D1-Cdk4 controls glucose metabolism independently of cell cycle progression
Lee, Y., Dominy, J. E., Choi, Y. J., Jurczak, M., Tolliday, N., Camporez, J. P., Chim, H., Lim, J.-H., Ruan, H.-B., Yang, X., et al. (2014) · Nature · doi:10.1038/nature13267 · Cited by 234 · see citing works
Pattern of retinoblastoma pathway inactivation dictates response to CDK4/6 inhibition in GBM
Wiedemeyer, W. R., Dunn, I. F., Quayle, S. N., Zhang, J., Chheda, M. G., Dunn, G. P., Zhuang, L., Rosenbluh, J., Chen, S., Xiao, Y., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1001613107 · Cited by 223 · see citing works
Tam, S. W., Shay, J. W., & Pagano, M. (1994) · PubMed · Cited by 222 · see citing works
Vandel, L., Nicolas, E., Vaute, O., Ferreira, R., Ait‐Si‐Ali, S., & Trouche, D. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.19.6484-6494.2001 · Cited by 214 · see citing works
Pestell, R. G. (2013) · The American Journal of Pathology · doi:10.1016/j.ajpath.2013.03.001 · Cited by 197 · see citing works
Cyclin D1 Repression of Peroxisome Proliferator-Activated Receptor γ Expression and Transactivation
Wang, C., Pattabiraman, N., Zhou, J., Fu, M., Sakamaki, T., Albanese, C., Li, Z., Wu, K., Hulit, J., Neumeister, P., et al. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.17.6159-6173.2003 · Cited by 195 · see citing works
Knudsen, K. E., Cavenee, W. K., & Arden, K. C. (1999) · PubMed · Cited by 185 · see citing works
Therapeutic Targeting of the Cyclin D3:CDK4/6 Complex in T Cell Leukemia
Sawai, C. M., Freund, J., Oh, P., Ndiaye-Lobry, D., Bretz, J. C., Strikoudis, A., Genesca, L., Trimarchi, T., Kelliher, M. A., Clark, M., et al. (2012) · Cancer Cell · doi:10.1016/j.ccr.2012.09.016 · Cited by 183 · see citing works
The Transcription Factor FOXM1 (Forkhead box M1)
Wierstra, I. (2013) · Advances in cancer research · doi:10.1016/b978-0-12-407173-5.00004-2 · Cited by 174 · see citing works
Parry, D., Mahony, D., Wills, K., & Lees, E. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.3.1775 · Cited by 174 · see citing works
Requirement for CDK6 in MLL-rearranged acute myeloid leukemia
Placke, T., Faber, K., Nonami, A., Putwain, S. L., Salih, H. R., Heidel, F. H., Krämer, A., Root, D. E., Barbie, D. A., Krivtsov, A. V., et al. (2014) · Blood · doi:10.1182/blood-2014-02-558114 · Cited by 170 · see citing works
Inoue, K., & Sherr, C. J. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.3.1590 · Cited by 168 · see citing works
Modification of the DNA Damage Response by Therapeutic CDK4/6 Inhibition
Dean, J. L., McClendon, A. K., & Knudsen, E. S. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.365494 · Cited by 156 · see citing works
Burke, J. R., Deshong, A. J., Pelton, J. G., & Rubin, S. M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.108167 · Cited by 148 · see citing works
Promoter hypermethylation: a common cause of reduced p16(INK4a) expression in uveal melanoma.
van der Velden, P. A., Metzelaar-Blok, J. A. W., Bergman, W., Monique, H., Hurks, H. M. H., Frants, R. R., Gruis, N. A., & Jager, M. J. (2001) · PubMed · Cited by 147 · see citing works
Schwartz, R., Engel, I., Fallahi‐Sichani, M., Petrie, H. T., & Murre, C. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0603728103 · Cited by 144 · see citing works
Inoue, K., Roussel, M. F., & Sherr, C. J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.7.3993 · Cited by 144 · see citing works
Zou, X., Ray, D., Aziyu, A., Christov, K. T., Boiko, A. D., Gudkov, A. V., & Kiyokawa, H. (2002) · Genes & Development · doi:10.1101/gad.1033002 · Cited by 143 · see citing works
PRMT5 is required for lymphomagenesis triggered by multiple oncogenic drivers
Li, Y., Chitnis, N., Nakagawa, H., Kita, Y., Natsugoe, S., Yang, Y., Li, Z., Wasik, M., Klein-Szanto, A. J. P., Rustgi, A. K., et al. (2015) · Cancer Discovery · doi:10.1158/2159-8290.cd-14-0625 · Cited by 143 · see citing works
Cyclin-Dependent Kinase 6 Is a Chromatin-Bound Cofactor for NF-κB-Dependent Gene Expression
Handschick, K., Beuerlein, K., Jurida, L., Bartkuhn, M., Müller, H., Soelch, J., Weber, A., Dittrich-Breiholz, O., Schneider, H., Scharfe, M., et al. (2014) · Molecular Cell · doi:10.1016/j.molcel.2013.12.002 · Cited by 141 · see citing works
Identification of mutations that disrupt phosphorylation-dependent nuclear export of cyclin D1
Benzeno, S., Lu, F., Guo, M., Barbash, O., Zhang, F., Herman, J. G., Klein, P. S., Rustgi, A. K., & Diehl, J. A. (2006) · Oncogene · doi:10.1038/sj.onc.1209644 · Cited by 141 · see citing works
Ogasawara, T., Kawaguchi, H., Jinno, S., Hoshi, K., Itaka, K., Takato, T., Nakamura, K., & Okayama, H. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.15.6560-6568.2004 · Cited by 140 · see citing works
Singh, A. M., Chappell, J., Trost, R., Lin, L., Wang, T., Tang, J., Wu, H., Zhao, S., Jin, P., & Dalton, S. (2013) · Stem Cell Reports · doi:10.1016/j.stemcr.2013.10.009 · Cited by 136 · see citing works
Pauls, E., Ruiz, A., Badía, R., Permanyer, M., Gubern, A., Riveira‐Muñoz, E., Torres‐Torronteras, J., Álvarez, M., Mothe, B., Brander, C., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1400873 · Cited by 127 · see citing works
Singh, A. M., Chappell, J., Trost, R., Lin, L., Wang, T., Tang, J., Matlock, B. K., Weller, K. P., Wu, H., Zhao, S., et al. (2014) · Stem Cell Reports · doi:10.1016/j.stemcr.2014.02.009 · Cited by 126 · see citing works
Hussain, M. S., Baig, S. M., Neumann, S., Peche, V. S., Szczepanski, S., Nürnberg, G., Tariq, M., Jameel, M., Khan, T. N., Fatima, A., et al. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt374 · Cited by 126 · see citing works
Alternative Cyclin D1 Splice Forms Differentially Regulate the DNA Damage Response
Li, Z., Jiao, X., Wang, C., Shirley, L. A., Elsaleh, H., Dahl, O., Wang, M., Soutoglou, E., Knudsen, E. S., & Pestell, R. G. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-0312 · Cited by 124 · see citing works
Targeting cell cycle regulators in hematologic malignancies
Aleem, E. A., & Arceci, R. J. (2015) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2015.00016 · Cited by 122 · see citing works
Cyclin D1-Cdk4 Induce Runx2 Ubiquitination and Degradation
Shen, R., Wang, X., Drissi, H., Liu, F., O’Keefe, R. J., & Chen, D. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m603439200 · Cited by 117 · see citing works
A Requirement for Cyclin-Dependent Kinase 6 in Thymocyte Development and Tumorigenesis
Hu, M. G., Deshpande, A., Enos, M., Mao, D., Hinds, E. A., Hu, G., Chang, R., Guo, Z., Dose, M., Mao, C., et al. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-2473 · Cited by 116 · see citing works
ChIP sequencing of cyclin D1 reveals a transcriptional role in chromosomal instability in mice
Casimiro, M. C., Crosariol, M., Loro, E., Ertel, A., Yu, Z., Dampier, W., Saria, E. A., Papanikolaou, A., Stanek, T. J., Li, Z., et al. (2012) · Journal of Clinical Investigation · doi:10.1172/jci60256 · Cited by 115 · see citing works
Fujimoto, T., Anderson, K., Jacobsen, S. E. W., Nishikawa, S.-I., & Nerlov, C. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601675 · Cited by 110 · see citing works
Cyclin-Dependent Kinase 4 Expression Is Essential for Neu-Induced Breast Tumorigenesis
Reddy, H. K. D. L., Mettus, R. V., Rane, S. G., Graña, X., Litvin, J., & Reddy, E. P. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-2639 · Cited by 105 · see citing works
Proteomic Identification of a Direct Role for Cyclin D1 in DNA Damage Repair
Jirawatnotai, S., Hu, Y., Livingston, D. M., & Siciński, P. (2012) · Cancer Research · doi:10.1158/0008-5472.can-11-3549 · Cited by 105 · see citing works
Aagaard, L., Lukas, J., Bártková, J., Kjerulff, A. A., Strauss, M., & Bártek, J. (1995) · International Journal of Cancer · doi:10.1002/ijc.2910610120 · Cited by 102 · see citing works
Lazaro, J., Bailey, P. J., & Lassar, A. B. (2002) · Genes & Development · doi:10.1101/gad.u-9988r · Cited by 100 · see citing works
Opposing roles of NF-κB in anti-cancer treatment outcome unveiled by cross-species investigationsPreprint
Hua, J., Kase, J., Dörr, J. R., Milanovic, M., Lenze, D., Grau, M., Beuster, G., Ji, S., Reimann, M., Lenz, P., et al. (2011) · Genes & Development · doi:10.1101/gad.17620611 · Cited by 99 · see citing works
Chilosi, M., Doglioni, C., Yan, Z., Lestani, M., Menestrina, F., Sorio, C., Benedetti, A., Vinante, F., Pizzolo, G., & Inghirami, G. (1998) · Europe PMC (PubMed Central) · Cited by 96 · see citing works
Buss, H., Handschick, K., Jurrmann, N., Pekkonen, P., Beuerlein, K., Müller, H., Wait, R., Saklatvala, J., Ojala, P. M., Schmitz, M. L., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051847 · Cited by 92 · see citing works
Cyclin D1 Represses p300 Transactivation through a Cyclin-dependent Kinase-independent Mechanism
Fu, M., Wang, C., Rao, M., Wu, X., Bouras, T., Zhang, X., Li, Z., Jiao, X., Yang, J., Li, A., et al. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503188200 · Cited by 91 · see citing works
Regulation of transcription and chromatin structure by pRB: Here, there and everywhere
Talluri, S., & Dick, F. A. (2012) · Cell Cycle · doi:10.4161/cc.21263 · Cited by 88 · see citing works
CDK6 kinase activity is required for thymocyte development
Hu, M. G., Deshpande, A., Schlichting, N., Hinds, E. A., Mao, C., Dose, M., Hu, G., Etten, R. A. V., Gounari, F., & Hinds, P. W. (2011) · Blood · doi:10.1182/blood-2010-08-300517 · Cited by 84 · see citing works
Gallagher, S. J., Kefford, R. F., & Rizos, H. (2006) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2006.02.008 · Cited by 81 · see citing works
Multiple Functions of D-Type Cyclins Can Antagonize pRb-Mediated Suppression of Proliferation
Baker, G. L., Landis, M. W., & Hinds, P. W. (2004) · Cell Cycle · doi:10.4161/cc.4.2.1485 · Cited by 79 · see citing works
Amplification at 7q22 targets cyclin-dependent kinase 6 in T-cell lymphoma
Nagel, S., Leich, E., Quentmeier, H., Meyer, C., Kaufmann, M., Drexler, H. G., Zettl, A., Rosenwald, A., & MacLeod, R. (2007) · Leukemia · doi:10.1038/sj.leu.2405028 · Cited by 77 · see citing works
Matushansky, I., Radparvar, F., & Skoultchi, A. I. (2003) · Oncogene · doi:10.1038/sj.onc.1206484 · Cited by 77 · see citing works
Activation of cyclin D1-kinase in murine fibroblasts lacking both p21Cip1 and p27Kip1
Sugimoto, M., Martin, N., Wilks, D. P., Tamai, K., Huot, T. J. G., Pantoja, C., Okumura, K., Serrano, M., & Hara, E. (2002) · Oncogene · doi:10.1038/sj.onc.1206019 · Cited by 77 · see citing works
Negative Regulation of TSC1-TSC2 by Mammalian D-Type Cyclins
Zacharek, S. J., Xiong, Y., & Shumway, S. D. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-2236 · Cited by 72 · see citing works
Zhang, L., Fried, F. B., Guo, H. W., & Friedman, A. D. (2007) · Blood · doi:10.1182/blood-2007-08-109702 · Cited by 68 · see citing works
Inoue, K., Mallakin, A., & Frazier, D. P. (2007) · Oncogene · doi:10.1038/sj.onc.1210226 · Cited by 67 · see citing works
Ogasawara, T., Katagiri, M., Yamamoto, A., Hoshi, K., Takato, T., Nakamura, K., Tanaka, S., Okayama, H., & Kawaguchi, H. (2004) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.2004.19.7.1128 · Cited by 62 · see citing works
The Stat3 paradox: A killer and an oncogene
Resemann, H. K., Watson, C. J., & Lloyd‐Lewis, B. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.06.029 · Cited by 58 · see citing works
In B-cell chronic lymphocytic leukemias, 7q21 translocations lead to overexpression of the CDK6 gene
Hayette, S., Tigaud, I., Callet‐Bauchu, E., Ffrench, M., Gazzo, S., Wahbi, K., Callanan, M. B., Felman, P., Dumontet, C., Magaud, J., et al. (2003) · Blood · doi:10.1182/blood-2003-04-1220 · Cited by 56 · see citing works
Nakajima, K., Inagawa, M., Uchida, C., Okada, K., Tane, S., Kojima, M., Kubota, M., Noda, M., Ogawa, S., Shirato, H., et al. (2011) · Development · doi:10.1242/dev.059295 · Cited by 54 · see citing works
MLL fusion-driven activation ofCDK6potentiates proliferation inMLL-rearranged infant ALL
der Linden, M. V., Willekes, M., Roon, E. H. J. V., Seslija, L., Schneider, P., Pieters, R., & Stam, R. W. (2014) · Cell Cycle · doi:10.4161/cc.27757 · Cited by 51 · see citing works
Therapeutic Targets in the ARF Tumor Suppressor Pathway
Saporita, A. J., Maggi, L. B., Apicelli, A. J., & Weber, J. D. (2007) · Current Medicinal Chemistry · doi:10.2174/092986707781058869 · Cited by 49 · see citing works
The dark and the bright side of Stat3: proto-oncogene and tumor-suppressor
Ecker, A. (2009) · Frontiers in bioscience · doi:10.2741/3425 · Cited by 48 · see citing works
Brito‐Babapulle, V., Gruszka, A., Platt, G., Andersen, C. L., Elnenaei, M. O., Matutes, E., Wotherspoon, A. C., Weston-Smith, S., & Catovsky, D. (2002) · PubMed · Cited by 47 · see citing works
Transcriptional Regulation by a DNA-associated Form of Cyclin D1
Bienvenu, F., Barré, B., Giraud, S., Avril, S., & Coqueret, O. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-08-0654 · Cited by 47 · see citing works
Lucas, J. J., Szepesi, Á., Modiano, J. F., Domenico, J. M., & Gelfand, E. W. (1995) · The Journal of Immunology · doi:10.4049/jimmunol.154.12.6275 · Cited by 47 · see citing works
Cerqueira, A., Martín, A. L., Symonds, C. E., Odajima, J., Dubus, P. R., Barbacid, M., & Santamarı́a, D. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.01163-13 · Cited by 47 · see citing works
Kinase-independent role of cyclin D1 in chromosomal instability and mammary tumorigenesis
Casimiro, M. C., Sante, G. D., Crosariol, M., Loro, E., Dampier, W., Ertel, A., Yu, Z., Saria, E. A., Παπανικολάου, Α., Li, Z., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.3267 · Cited by 46 · see citing works
Burke, J. R., Liban, T. J., Restrepo, T., Lee, H., & Rubin, S. M. (2013) · Journal of Molecular Biology · doi:10.1016/j.jmb.2013.09.031 · Cited by 45 · see citing works
Cyclin-dependent kinase inhibitors for cancer therapy: a patent review (2009 – 2014)
Malínková, V., Vylíčil, J., & Kryštof, V. (2015) · Expert Opinion on Therapeutic Patents · doi:10.1517/13543776.2015.1045414 · Cited by 44 · see citing works
Bourgo, R. J., Thangavel, C., Ertel, A., Bergseid, J., McClendon, A. K., Wilkens, L., Witkiewicz, A. K., Wang, J. Y. J., & Knudsen, E. S. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.06.029 · Cited by 42 · see citing works
Conserved RB functions in development and tumor suppression
Gordon, G. M., & Du, W. (2011) · Protein & Cell · doi:10.1007/s13238-011-1117-z · Cited by 42 · see citing works
Cyclin D3-dependent control of the dNTP pool and HIV-1 replication in human macrophages
Ruiz, A., Pauls, E., Badía, R., Torres‐Torronteras, J., Riveira‐Muñoz, E., Clotet, B., Martí, R., Ballana, E., & Esté, J. A. (2015) · Cell Cycle · doi:10.1080/15384101.2015.1030558 · Cited by 38 · see citing works
Lien, H., Lin, C.-W., Huang, P., Chang, M., & Hsu, S.-M. (2000) · Laboratory Investigation · doi:10.1038/labinvest.3780093 · Cited by 34 · see citing works
Cyclin D3-associated Kinase Activity Is Regulated by p27kip1in BALB/c 3T3 Cells
Dong, F., Agrawal, D., Bagui, T. K., & Pledger, W. J. (1998) · Molecular Biology of the Cell · doi:10.1091/mbc.9.8.2081 · Cited by 34 · see citing works
Cyclin D1 Induces Chromosomal Instability
Casimiro, M. C., & Pestell, R. G. (2012) · Oncotarget · doi:10.18632/oncotarget.476 · Cited by 33 · see citing works
Cdk4 and Cdk6 cooperate in counteracting the INK4 family of inhibitors during murine leukemogenesis
Rodríguez, E., Quereda, V., Bellutti, F., Prchal‐Murphy, M., Partida, D., Eguren, M., Kollmann, K., de Cedrón, M. G., Dubus, P. R., Cañamero, M., et al. (2014) · Blood · doi:10.1182/blood-2014-02-555292 · Cited by 33 · see citing works
Self-citationCDK-Mediated Regulation of Cell Functions via c-Jun Phosphorylation and AP-1 Activation
Bush, T. J. V., & Bishop, G. A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019468 · Cited by 32 · see citing works
CDK6 and p16INK4A in lymphoid malignancies
Kollmann, K., & Sexl, V. (2013) · Oncotarget · doi:10.18632/oncotarget.1541 · Cited by 32 · see citing works
Self-citationChoe, K., Ujhelly, O., Wontakal, S. N., & Skoultchi, A. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.077727 · Cited by 31 · see citing works
Clinicopathologic Features of CDK6 Translocation-associated B-cell Lymphoproliferative Disorders
Chen, D., Law, M. E., Theis, J. D., Gamez, J. D., Caron, L. B., Vrana, J. A., & Doǧan, A. (2009) · The American Journal of Surgical Pathology · doi:10.1097/pas.0b013e3181934244 · Cited by 27 · see citing works
Kinase independent oncogenic cyclin D1
Casimiro, M. C., Arnold, A., & Pestell, R. G. (2015) · Aging · doi:10.18632/aging.100773 · Cited by 19 · see citing works
Cyclin D1 is a NF-κB corepressor
Rubio, M. F., Fernandez, P., Alvarado, C. V., Panelo, L. C., Grecco, M. R., Coló, G. P., Martínez-Noël, G. M. A., Micenmacher, S., & Costas, M. A. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.01.009 · Cited by 17 · see citing works
CDK6 binds and promotes the degradation of the EYA2 protein
Kohrt, D., Crary, J. I., Zimmer, M., Patrick, A. N., Ford, H. L., Hinds, P. W., & Grossel, M. J. (2013) · Cell Cycle · doi:10.4161/cc.26755 · Cited by 16 · see citing works
Cell Cycle Inhibitors Make Progress
Brower, V. (2014) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/dju221 · Cited by 12 · see citing works
CDK6, a new target in MLL-driven leukemia
Antony‐Debré, I., & Steidl, U. G. (2014) · Blood · doi:10.1182/blood-2014-05-572917 · Cited by 10 · see citing works
Unexpected Outcomes of CDK4/6 Inhibition
Choi, Y. J., & Siciński, P. (2013) · Oncotarget · doi:10.18632/oncotarget.912 · Cited by 7 · see citing works
CDK6 is a regulator of stem cells “Egr” to wake up
Guzmán, M. L. (2015) · Blood · doi:10.1182/blood-2014-11-609230 · Cited by 7 · see citing works
Emerging Roles of Cell Cycle Regulators in Adipocyte Metabolism
Carine Chavey, A., Lagarrigue, S., Annicotte, J., & Lluis Fajas, A. (2012) · Springer eBooks · doi:10.1007/978-2-8178-0343-2_2 · Cited by 6 · see citing works
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Northcott, P. A., Robinson, G. W., Kratz, C. P., Mabbott, D., Pomeroy, S. L., Clifford, S. C., Rutkowski, S., Ellison, D. W., Malkin, D. M., Taylor, M. D., et al. (2019) · Nature Reviews Disease Primers · doi:10.1038/s41572-019-0063-6 · Cited by 673 · see citing works
Yang, C., Li, Z., Bhatt, T., Dickler, M. N., Giri, D. D., Scaltriti, M., Baselga, J. M., Rosen, N. X., & Chandarlapaty, S. (2016) · Oncogene · doi:10.1038/onc.2016.379 · Cited by 413 · see citing works
Mechanisms of Sensitivity and Resistance to CDK4/6 Inhibition
Álvarez‐Fernández, M., & Malumbres, M. (2020) · Cancer Cell · doi:10.1016/j.ccell.2020.03.010 · Cited by 395 · see citing works
Molecular mechanisms of resistance to CDK4/6 inhibitors in breast cancer: A review
Pandey, K., An, H. J., Kim, S., Lee, S. A., Kim, S., Lim, S. M., Kim, G. M., Sohn, J., & Moon, Y. W. (2018) · International Journal of Cancer · doi:10.1002/ijc.32020 · Cited by 366 · see citing works
Cell-Cycle Proteins Control Production of Neutrophil Extracellular Traps
Amulic, B., Knackstedt, S. L., Abed, U. A., Deigendesch, N., Harbort, C. J., Caffrey, B. E., Brinkmann, V., Heppner, F. L., Hinds, P. W., & Zychlinsky, A. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.10.013 · Cited by 269 · see citing works
Structural insights into the functional diversity of the CDK–cyclin family
Wood, D. J., & Endicott, J. (2018) · Open Biology · doi:10.1098/rsob.180112 · Cited by 264 · see citing works
Homolog-Selective Degradation as a Strategy to Probe the Function of CDK6 in AML
Brand, M., Jiang, B., Bauer, S., Donovan, K. A., Liang, Y., Wang, E. S., Nowak, R. P., Yuan, J. C., Zhang, T., Kwiatkowski, N., et al. (2019) · Cell Chemical Biology · doi:10.1016/j.chembiol.2018.11.006 · Cited by 258 · see citing works
Cyclin dependent kinase (CDK) inhibitors as anticancer drugs: Recent advances (2015–2019)
Sánchez-Martínez, C., Lallena, M. J., Sanfeliciano, S. G., & de Dios, A. (2019) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2019.126637 · Cited by 200 · see citing works
Nebenfuehr, S., Kollmann, K., & Sexl, V. (2020) · International Journal of Cancer · doi:10.1002/ijc.33054 · Cited by 185 · see citing works
Self-citationRugo, H. S., Huober, J., García-Sáenz, J. Á., Masuda, N., Sohn, J., Andre, V. A. M., Barriga, S., Cox, J., & Goetz, M. P. (2020) · The Oncologist · doi:10.1002/onco.13531 · Cited by 185 · see citing works
New and Emerging Targeted Therapies for Advanced Breast Cancer
Lau, K., Tan, A. M., & Shi, Y. H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042288 · Cited by 171 · see citing works
Targeted protein degradation: current and future challenges
Hanzl, A., & Winter, G. E. (2020) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2019.11.012 · Cited by 157 · see citing works
Steinebach, C., Ng, Y. L. D., Sosič, I., Lee, C.-S., Chen, S., Lindner, S., Vu, L. P., Bricelj, A., Haschemi, R., Monschke, M., et al. (2020) · Chemical Science · doi:10.1039/d0sc00167h · Cited by 148 · see citing works
CDK4/6 inhibitor resistance mechanisms and treatment strategies (Review)
Huang, J., Zheng, L., Sun, Z., & Li, J. (2022) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2022.5184 · Cited by 141 · see citing works
Proteolysis targeting chimeras (PROTACs) are emerging therapeutics for hematologic malignancies
He, Y., Khan, S., Huo, Z., Lv, D., Zhang, X., Liu, X., Yuan, Y., Hromas, R., Xu, M., Zheng, G., et al. (2020) · Journal of Hematology & Oncology · doi:10.1186/s13045-020-00924-z · Cited by 126 · see citing works
Poratti, M., & Marzaro, G. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.03.064 · Cited by 115 · see citing works
Moorefield, E., Andres, S. F., Blue, R. E., Landeghem, L. V., Mah, A. T., Santoro, M. A., & Ding, S. (2017) · Aging · doi:10.18632/aging.101279 · Cited by 110 · see citing works
Niu, Y., Xu, J., & Sun, T. (2019) · Journal of Cancer · doi:10.7150/jca.32628 · Cited by 98 · see citing works
Casà, V., Gines, M. M., Gusmao, E. G., Slotman, J. A., Zirkel, A., Josipović, N., Oole, E., van IJcken, W. F. J., Houtsmuller, A. B., Papantonis, A., et al. (2020) · Genome Research · doi:10.1101/gr.253211.119 · Cited by 91 · see citing works
Cdk2 strengthens the intra-S checkpoint and counteracts cell cycle exit induced by DNA damage
Bačević, K., Lossaint, G., Achour, T. N., Georget, V., Fisher, D., & Dulić, V. (2017) · Scientific Reports · doi:10.1038/s41598-017-12868-5 · Cited by 84 · see citing works
CDK6 protects epithelial ovarian cancer from platinum‐induced death via FOXO3 regulation
Dall’Acqua, A., Sonego, M., Pellizzari, I., Pellarin, I., Canzonieri, V., D’Andrea, S., Benevol, S., Sorio, R., Giorda, G., Califano, D., et al. (2017) · EMBO Molecular Medicine · doi:10.15252/emmm.201607012 · Cited by 79 · see citing works
Yang, G., Zhang, Y., & Yang, J. (2019) · Medical Science Monitor · doi:10.12659/msm.916902 · Cited by 77 · see citing works
CDK6 Antagonizes p53-Induced Responses during Tumorigenesis
Bellutti, F., Tigan, A.-S., Nebenfuehr, S., Dolezal, M., Zojer, M., Grausenburger, R., Hartenberger, S., Kollmann, S., Doma, E., Prchal‐Murphy, M., et al. (2018) · Cancer Discovery · doi:10.1158/2159-8290.cd-17-0912 · Cited by 76 · see citing works
Self-citationLessons Learned from Past Cyclin-Dependent Kinase Drug Discovery Efforts
Xie, Z., Hou, S., Yang, X., Duan, Y., Han, J., Wang, Q., & Liao, C. (2022) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.1c02190 · Cited by 73 · see citing works
Zhang, L., Li, Y., Hu, C., Chen, Y., Chen, Z., Chen, Z., Zhang, J., & Fang, S. (2022) · Molecular Cancer · doi:10.1186/s12943-022-01524-w · Cited by 68 · see citing works
Wu, Z., Guo, W., Yang, L., He, Q., & Zhou, S. (2018) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2018.09.002 · Cited by 68 · see citing works
Cheng, C., Chen, X., Wang, Y., Cheng, W., Zuo, X., Tang, W., & Huang, W. (2021) · Molecular Medicine · doi:10.1186/s10020-021-00324-0 · Cited by 69 · see citing works
miR-1299 suppresses cell proliferation of hepatocellular carcinoma (HCC) by targeting CDK6
Zhu, H., Wang, G., Zhou, X., Song, X., Gao, H., Ma, C., Chang, H., Li, H., Liu, F., Lu, J., et al. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.07.037 · Cited by 66 · see citing works
Wang, Z., Sun, H., Provazník, J., Hackert, T., & Zöller, M. (2019) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-019-1129-8 · Cited by 63 · see citing works
RetractedCBX3 promotes colon cancer cell proliferation by CDK6 kinase-independent function during cell cycle
Fan, Y., Li, H., Liang, X., & Xiang, Z. (2017) · Oncotarget · doi:10.18632/oncotarget.15253 · Cited by 62 · see citing works
Exosomal miR-21-5p contributes to ovarian cancer progression by regulating CDK6
Cao, J., Zhang, Y., Mu, J., Yang, D., Gu, X., & Zhang, J. (2021) · Human Cell · doi:10.1007/s13577-021-00522-2 · Cited by 61 · see citing works
Regulatory Mechanisms of Cell Polyploidy in Insects
Ren, D., Song, J., Ni, M., Kang, L., & Guo, W. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00361 · Cited by 59 · see citing works
The interplay of CDK4 and CDK6 in melanoma
Kollmann, K., Briand, C., Bellutti, F., Schicher, N., Blunder, S., Zojer, M., & Höeller, C. (2019) · Oncotarget · doi:10.18632/oncotarget.26515 · Cited by 55 · see citing works
Self-citationHaines, E., Chen, T., Kommajosyula, N., Chen, Z., Herter-Sprie, G. S., Cornell, L., Wong, K., & Shapiro, G. I. (2018) · Oncotarget · doi:10.18632/oncotarget.25803 · Cited by 53 · see citing works
Zhang, J., Liu, X., Zhou, W., Cheng, G., Wu, J., Guo, S., Jia, S., Liu, Y., Li, B., Zhang, X., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-68224-7 · Cited by 50 · see citing works
CDK4/6 and MAPK—Crosstalk as Opportunity for Cancer Treatment
Scheiblecker, L., Kollmann, K., & Sexl, V. (2020) · Pharmaceuticals · doi:10.3390/ph13120418 · Cited by 47 · see citing works
Self-citationSTAT3-Induced lncRNA SNHG17 Exerts Oncogenic Effects on Ovarian Cancer through Regulating CDK6
Pan, X., Guo, Z., Chen, Y., Zheng, S., Peng, M., Yang, Y., & Wang, Z. (2020) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2020.08.006 · Cited by 47 · see citing works
Targeting CDK4/6 for Anticancer Therapy
Qi, J., & Ouyang, Z. (2022) · Biomedicines · doi:10.3390/biomedicines10030685 · Cited by 47 · see citing works
Identification of Targetable Lesions in Anaplastic Thyroid Cancer by Genome Profiling
Ravi, N., Yang, M., Gretarsson, S., Jansson, C., Mylona, N., Sydow, S., Woodward, E. L., Ekblad, L., Wennerberg, J., & Paulsson, K. M. (2019) · Cancers · doi:10.3390/cancers11030402 · Cited by 46 · see citing works
The RNA-binding protein LRPPRC promotes resistance to CDK4/6 inhibition in lung cancer
Zhou, W., Wang, W., Liang, Y., Jiang, R., Qiu, F.-S., Shao, X., Liu, Y., Fang, L., Ni, M., Yu, C.-H., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39854-y · Cited by 45 · see citing works
CDK4 inhibition diminishes p53 activation by MDM2 antagonists
Sriraman, A., Dickmanns, A., Najafova, Z., Johnsen, S. A., & Dobbelstein, M. (2018) · Cell Death & Disease · doi:10.1038/s41419-018-0968-0 · Cited by 40 · see citing works
Zangouei, A. S., Zangoue, M., Taghehchian, N., Zangooie, A., Rahimi, H. R., Saburi, E., Alavi, M. S., & Moghbeli, M. (2023) · Biological Research · doi:10.1186/s40659-022-00411-4 · Cited by 39 · see citing works
Golmohammadi, M., Zamanian, M., Jalal, S., Noraldeen, S. A. M., Ramírez-Coronel, A., Oudaha, K. H., Obaid, R., Almulla, A. F., Bazmandegan, G., & Kamiab, Z. (2023) · Food Science & Nutrition · doi:10.1002/fsn3.3699 · Cited by 30 · see citing works
Reduction of Movement in Neurological Diseases: Effects on Neural Stem Cells Characteristics
Adami, R., Pagano, J., Colombo, M., Platonova, N., Recchia, D., Chiaramonte, R., Bottinelli, R., Canepari, M., & Bottai, D. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00336 · Cited by 36 · see citing works
miR-9 induces cell arrest and apoptosis of oral squamous cell carcinoma via CDK 4/6 pathway
Shang, A., Lu, W., Yang, M. G., Zhou, C., Zhang, H., Cai, Z., Wang, W., Wang, W., & Wu, G. (2017) · Artificial Cells Nanomedicine and Biotechnology · doi:10.1080/21691401.2017.1391825 · Cited by 36 · see citing works
Swadi, R., Sampat, K., Herrmann, A., Losty, P. D., Sée, V., & Moss, D. (2019) · Scientific Reports · doi:10.1038/s41598-019-45571-8 · Cited by 34 · see citing works
Cyclin-dependent kinases and rare developmental disorders
Colas, P. (2020) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-020-01472-y · Cited by 31 · see citing works
Zhang, Y., Duan, S., Jang, A., Mao, L., Liu, X., & Huang, G. (2020) · Experimental Eye Research · doi:10.1016/j.exer.2020.108304 · Cited by 28 · see citing works
SUMOylated MAFB promotes colorectal cancer tumorigenesis
Yang, L., Zhang, X., Xie, Y., Sun, X., Zhao, R., & Huang, Q. (2016) · Oncotarget · doi:10.18632/oncotarget.13129 · Cited by 28 · see citing works
Liu, X., Tan, N., Liao, H., Pan, G., Xu, Q. R., Zhu, R., Zou, L., He, S., & Zhu, H. (2017) · Oncotarget · doi:10.18632/oncotarget.23420 · Cited by 28 · see citing works
High-content analysis screening for cell cycle regulators using arrayed synthetic crRNA libraries
Strezoska, Ž., Perkett, M. R., Chou, E. T., Maksimova, E. M., Anderson, E. M., McClelland, S., Kelley, M. L., Vermeulen, A., & Smith, A. V. B. (2017) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2017.04.017 · Cited by 24 · see citing works
Zhang, L., Zhao, G., Ji, S., Yuan, Q., & Zhou, H. (2020) · Medical Science Monitor · doi:10.12659/msm.921594 · Cited by 27 · see citing works
Giovanni, C. D., Novellino, E., Chilin, A., Lavecchia, A., & Marzaro, G. (2016) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2016.1234603 · Cited by 25 · see citing works
Piersanti, A., Juganson, K., Mozzicafreddo, M., Wei, W., Zhang, J., Zhao, K., Ballarini, P., Mortimer, M., Pucciarelli, S., Miao, W., et al. (2020) · Environmental Pollution · doi:10.1016/j.envpol.2020.115965 · Cited by 24 · see citing works
Wang, Y., Tan, X., Wu, Y., Cao, S., Lou, Y., Zhang, L., & Hu, F. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.673229 · Cited by 24 · see citing works
lncRNA SNHG15 Promotes Ovarian Cancer Progression through Regulated CDK6 via Sponging miR‐370‐3p
Wang, Y., Ding, M., Yuan, X., Ruibao, J., Zhu, D., Huang, W., Deng, W., & Liu, Y. (2021) · BioMed Research International · doi:10.1155/2021/9394563 · Cited by 24 · see citing works
AC002454.1 and CDK6 synergistically promote endometrial cell migration and invasion in endometriosis
Liu, J., Wang, Y., Chen, P., Ma, Y., Wang, S., Tian, Y., Wang, A., & Wang, D. (2019) · Reproduction · doi:10.1530/rep-19-0005 · Cited by 24 · see citing works
Katayama, M., Kiyono, T., Ohmaki, H., Eitsuka, T., Endoh, D., Inoue‐Murayama, M., Nakajima, N., Onuma, M., & Fukuda, T. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27417 · Cited by 23 · see citing works
Zhang, C., Liu, X., Gu, C., Su, Y., Lv, J., Liu, Y., Gao, Y., Chen, H., Xu, N., Xiao, J., et al. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.07.029 · Cited by 22 · see citing works
Pathways Controlling Formation and Maintenance of the Osteocyte Dendrite Network
Wang, J. S., & Wein, M. N. (2022) · Current Osteoporosis Reports · doi:10.1007/s11914-022-00753-8 · Cited by 24 · see citing works
Shu, Y., Wang, L., Ding, Y., & Zhang, Q. (2023) · Drug Safety · doi:10.1007/s40264-023-01334-z · Cited by 23 · see citing works
Zou, D., Li, K., Su, L., Liu, J., Lu, Y., Huang, R., Li, M., Mang, X., Geng, Q., Li, P., et al. (2024) · Developmental Cell · doi:10.1016/j.devcel.2024.04.002 · Cited by 22 · see citing works
Ullah, R., Naz, A., Akram, H. S., Ullah, Z., Tariq, M. S., Mithani, A., & Faisal, A. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-01848-8 · Cited by 22 · see citing works
CDK6 Is a Therapeutic Target in Myelofibrosis
Dutta, A., Nath, D., Yang, Y., Le, B. T., & Mohi, G. (2021) · Cancer Research · doi:10.1158/0008-5472.can-21-0590 · Cited by 21 · see citing works
Mun, D., Kang, M., Shin, M., Choi, H., Kang, A., Ryu, S., Unno, T., Maburutse, B. E., Oh, S., & Kim, Y. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.00121-23 · Cited by 21 · see citing works
A New Way to Treat Brain Tumors: Targeting Proteins Coded by Microcephaly Genes?
Lang, P. Y., & Gershon, T. R. (2018) · BioEssays · doi:10.1002/bies.201700243 · Cited by 20 · see citing works
Chen, B., Ji, F., Wen, X., & Jin, Z. (2020) · PubMed Central · Cited by 20 · see citing works
LncRNA ROR modulates myocardial ischemia-reperfusion injury mediated by the miR-185-5p/CDK6 axis
Sun, J., Zhu, Y., Liu, Q., Hu, Y.-H., Li, C., Jie, H., Xu, G., Xiao, R., Xing, X., Yu, S., et al. (2022) · Laboratory Investigation · doi:10.1038/s41374-021-00722-2 · Cited by 20 · see citing works
Wang, X., Zhang, L., Dai, Q., Si, H., Zhang, L., Eltom, S. E., & Si, H. (2021) · Cancers · doi:10.3390/cancers13092116 · Cited by 20 · see citing works
Progress in understanding the relationship between long noncoding RNA and endometriosis
Yan, W., Hu, H., & Tang, B. (2019) · European Journal of Obstetrics & Gynecology and Reproductive Biology X · doi:10.1016/j.eurox.2019.100067 · Cited by 20 · see citing works
Zhao, L., Wang, J., Yang, W., Zhang, C., Zhang, W., & Chen, J. (2025) · Physical Chemistry Chemical Physics · doi:10.1039/d4cp04579c · Cited by 19 · see citing works
Ho, C. N. Q., Tran, M. T., Chung, Đ. C., Sơn, H. N., Tran, D. H., & Long, L. T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094550 · Cited by 19 · see citing works
Role of NF-kappaB2-p100 in regulatory T cell homeostasis and activation
Dhar, A., Chawla, M., Chattopadhyay, S., Oswal, N., Umar, D., Gupta, S., Bal, V., Rath, S., George, A., Arimbasseri, G. A., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-50454-z · Cited by 19 · see citing works
Foffano, L., Cucciniello, L., Nicolò, E., Migliaccio, I., Noto, C., Reduzzi, C., Malorni, L., Cristofanilli, M., Gerratana, L., & Puglisi, F. (2024) · The Breast · doi:10.1016/j.breast.2024.103863 · Cited by 18 · see citing works
T Cell-Intrinsic CDK6 Is Dispensable for Anti-Viral and Anti-Tumor Responses In Vivo
Klein, K., Witalisz‐Siepracka, A., Gotthardt, D., Agerer, B., Sternberg, F., Grausenburger, R., Knab, V. M., Bergthaler, A., & Sexl, V. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.650977 · Cited by 18 · see citing works
Self-citationSalgado, M. T. S. F., Silva, E. F. E., Matsumoto, A. M., Mattozo, F. H., de Amarante, M. C. A., Kalil, S. J., & Votto, A. P. D. S. (2022) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2022.105757 · Cited by 18 · see citing works
Ataei-Nazari, S., Amoushahi, M., Madsen, J., Jensen, J., Heuck, A., Mohammadi‐Sangcheshmeh, A., & Lykke‐Hartmann, K. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1036917 · Cited by 18 · see citing works
Strategy of combining CDK4/6 inhibitors with other therapies and mechanisms of resistance
Xue, Y. (2024) · International Journal of Clinical and Experimental Pathology · doi:10.62347/hgni4903 · Cited by 18 · see citing works
Luo, C., Hou, M., Huang, C., Wu, C., Ou‐Yang, F., Li, Q.-L., Wu, C.-C., & Pan, M. (2020) · PubMed Central · Cited by 18 · see citing works
Chen, Q., Fu, L., Hu, J., Guo, G., & Xie, A. (2021) · Cancer Cell International · doi:10.1186/s12935-021-01934-8 · Cited by 17 · see citing works
CASC21, a FOXP1 induced long non-coding RNA, promotes colorectal cancer growth by regulating CDK6
Gong, T., Yu, L., Feng, L., Fang, M., Dai, G., Huang, X. Y., Yang, Y., & Liu, S. (2020) · Aging · doi:10.18632/aging.103376 · Cited by 17 · see citing works
miR‑449a‑5p suppresses CDK6 expression to inhibit cardiomyocyte proliferation
Li, B., Zhi, W., Yang, F., Huang, J., Hu, X., Deng, S., Tian, M., & Si, X. (2020) · Molecular Medicine Reports · doi:10.3892/mmr.2020.11652 · Cited by 17 · see citing works
Zhu, D., Gu, X., Lin, Z., Yu, D., & Wang, J. (2021) · Oncogenesis · doi:10.1038/s41389-021-00330-1 · Cited by 16 · see citing works
Huang, S., Li, J., Wu, S., Zheng, Z., Wang, C., Li, H., Zhao, L., Zhang, X., Huang, H., Huang, C., et al. (2023) · Oncogene · doi:10.1038/s41388-023-02656-z · Cited by 16 · see citing works
Fluorescent Peptide Biosensor for Probing CDK6 Kinase Activity in Lung Cancer Cell Extracts
Soamalala, J., Diot, S., Pellerano, M., Blanquart, C., Galibert, M., Jullian, M., Puget, K., & Morris, M. C. (2020) · ChemBioChem · doi:10.1002/cbic.202000677 · Cited by 16 · see citing works
Identification of Functional lncRNAs Associated With Ovarian Endometriosis Based on a ceRNA Network
Bai, J., Wang, B., Wang, T., & Ren, W. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.534054 · Cited by 16 · see citing works
Chen, X., Wu, Y., Wang, X., Xu, C., Wang, L., Jian, J., Wu, D., & Wu, G. (2022) · European journal of medical research · doi:10.1186/s40001-022-00730-y · Cited by 16 · see citing works
PROteolysis‐Targeting Chimeras (PROTACs) in leukemia: overview and future perspectives
Vicente, A. T. S., & Salvador, J. A. R. (2024) · MedComm · doi:10.1002/mco2.575 · Cited by 14 · see citing works
Knockdown of ALPK2 blocks development and progression of renal cell carcinoma
Jiang, J., Han, P., Qian, J., Zhang, S., Wang, S., Cao, Q., & Shao, P. (2020) · Experimental Cell Research · doi:10.1016/j.yexcr.2020.112029 · Cited by 14 · see citing works
Feng, Q., Xu, D., Zhou, M., Wu, Z., Wu, Z., Wang, Z., Bi, J., & Pei, W. (2021) · Cancer Cell International · doi:10.1186/s12935-021-01845-8 · Cited by 14 · see citing works
Identification of Upstream Kinases by Fluorescence Complementation Mass Spectrometry
Zeng, L., Wang, W., Arrington, J. V., Shao, G., Geahlen, R. L., Hu, C., & Tao, W. A. (2017) · ACS Central Science · doi:10.1021/acscentsci.7b00261 · Cited by 13 · see citing works
Unraveling the role of miRNAs in the diagnosis, progression, and drug resistance of oral cancer
Doghish, A. S., Elshaer, S. S., Fathi, D., Rizk, N. I., Elrebehy, M. A., AL‐Noshokaty, T. M., Elballal, M. S., Abdelmaksoud, N. M., Abdel‐Reheim, M. A., Mageed, S. S. A., et al. (2023) · Pathology - Research and Practice · doi:10.1016/j.prp.2023.155027 · Cited by 13 · see citing works
Chen, H., Cheng, C., & Gao, S. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.07.092 · Cited by 13 · see citing works
Chi, H., SON, H., Chung, Đ. C., HUAN, L., DIEM, T., & Long, L. T. (2020) · Physiological Research · doi:10.33549/physiolres.934472 · Cited by 13 · see citing works
Gong, W., Wang, L., Zheng, Z., Chen, W., Du, P., & Zhao, H. (2020) · Translational Cancer Research · doi:10.21037/tcr.2019.11.21 · Cited by 12 · see citing works
Baig, M. H., Yousuf, M., Khan, M. I., Khan, I., Ahmad, I. S., Alshahrani, M. Y., Hassan, M. I., & Dong, J.-J. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.865454 · Cited by 12 · see citing works
Zhao, L., Wang, J., Yang, W., Zhao, K., Sun, Q., & Chen, J. (2024) · Molecules · doi:10.3390/molecules29112681 · Cited by 11 · see citing works
Redundant and specific roles of cohesin STAG subunits in chromatin looping and transcription controlPreprint
Casà, V., Gines, M. M., Gusmao, E. G., Slotman, J. A., Zirkel, A., Josipović, N., Oole, E., van IJcken, W. F. J., Houtsmuller, A. B., Papantonis, A., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/642959 · Cited by 11 · see citing works
Protein Phosphorylation Alterations in Myotonic Dystrophy Type 1: A Systematic Review
Costa, A., Cruz, A. C., Martins, F., & Rebelo, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043091 · Cited by 10 · see citing works
CXCL14 Maintains hESC Self-Renewal through Binding to IGF-1R and Activation of the IGF-1R Pathway
Cheng, C., Yang, S.-C., Lai, C.-Y., Wang, C.-K., Chang, C., Lin, C.-Y., Chen, W., Lin, P.-Y., Wu, H., Ma, N. J.-L., et al. (2020) · Cells · doi:10.3390/cells9071706 · Cited by 10 · see citing works
- Authors
- Tigan, A.-S., Bellutti, F., Kollmann, K., Tebb, G., & Sexl, V
- Affiliations
- University of Veterinary Medicine Vienna (AT)
- Corresponding author
- Sexl, V
- Venue
- Oncogene
- Published
- 2015-10-26
- Volume
- 35
- Issue
- 24
- Pages
- 3083-3091
- ISSN
- 0950-9232 (ISSN-L)
- 1476-5594
- OpenAlex
- W1874582198
- Cited by
- 204
- References
- 177
- Citations by year
- 2026: 15 · 2025: 16 · 2024: 22 · 2023: 20 · 2022: 35 · 2021: 17 · 2020: 38 · 2019: 17 · 2018: 11 · 2017: 9 · 2016: 4
- FWCI
- 0.86
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Oncogene (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Keywords
- CDK6, CDK4, cell cycle progression, transcriptional regulation, kinase-independent function, hematopoietic stem cells, carcinogenesis, tissue homeostasis, cell differentiation, CDK6 inhibitors, cancer therapy
- MeSH terms
- Transcriptional Activation, Cyclin-Dependent Kinase 6, Cell Cycle Checkpoints
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