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CDK4-CDK6 inhibitors induce autophagy-mediated degradation of DNMT1 and facilitate the senescence antitumor response
Véronique Bourdeau, Gerardo Ferbeyre
Autophagy · 2016 · ▲ 28 citations
Epigenetic alterations
Cellular senescence
Altered intercellular communication
Disabled macroautophagy
Abstract
Senescence(definition) is a natural anticancer defense program disabled in tumor cells. We discovered that deregulated CDK4 (cyclin dependant kinase 4) and CDK6 activities contribute to senescence bypass during tumorigenesis and that their inhibition restores the senescence response in tumor cells. CDK4 and CDK6 phosphorylate RB1/RB, preventing its inhibitory interaction with the E2Fs, the cell cycle transcription factors. However, we also found that CDK4 interacts and phosphorylates the DNMT1 (DNA methyltransferase 1) protein protecting it from macroautophagy/autophagy(definition)-mediated protein degradation. This discovery highlights a new epigenetic component of CDK4-CDK6 signaling that could be exploited in cancer treatment.
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- 10.1080/15548627.2016.1214779
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- 2026-08-07 MST
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APA
Bourdeau, V., & Ferbeyre, G. (2016). CDK4-CDK6 inhibitors induce autophagy-mediated degradation of DNMT1 and facilitate the senescence antitumor response. <em>Autophagy</em>. https://doi.org/10.1080/15548627.2016.1214779
Vancouver
Bourdeau V, Ferbeyre G. CDK4-CDK6 inhibitors induce autophagy-mediated degradation of DNMT1 and facilitate the senescence antitumor response. Autophagy. 2016. doi:10.1080/15548627.2016.1214779.
BibTeX
@article{vronique2016CDKCDK,
title = {CDK4-CDK6 inhibitors induce autophagy-mediated degradation of DNMT1 and facilitate the senescence antitumor response},
author = {Véronique Bourdeau and Gerardo Ferbeyre},
journal = {Autophagy},
year = {2016},
doi = {10.1080/15548627.2016.1214779},
}
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