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Diversity within the pRb pathway: is there a code of conduct?

期刊

ONCOGENE
卷 31, 期 40, 页码 4343-4352

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/onc.2011.603

关键词

pRb; E2F-1; phosphorylation; acetylation; methylation

资金

  1. CRUK
  2. MRC
  3. LRF
  4. EU
  5. AICR
  6. MRC [G1000807] Funding Source: UKRI
  7. Medical Research Council [G1000807] Funding Source: researchfish

向作者/读者索取更多资源

The failure of cell proliferation to be properly regulated is a hallmark of tumourigenesis. The retinoblastoma protein (pRb) pathway represents a key component in the regulation of the cell cycle and tumour suppression. Recent findings have revealed new levels of complexity reflecting a repertoire of post-translational modifications that occur on pRb together with its key effector E2F-1. Here we provide an overview of the modifications and consider the possibility of a 'code' that endows pRb with the ability to function in diverse physiological settings. Oncogene (2012) 31, 4343-4352; doi: 10.1038/onc.2011.603; published online 16 January 2012

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