4.8 Review

The emerging role of APC/CCdh1 in controlling differentiation, genomic stability and tumor suppression

Journal

ONCOGENE
Volume 29, Issue 1, Pages 1-10

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/onc.2009.325

Keywords

anaphase-promoting complex; ubiquitin; proteasome; differentiation; genomic instability; tumor suppression

Funding

  1. NIGMS NIH HHS [R01 GM047238-06, R01 GM047238-14, R01 GM047238-11, R01 GM047238-09, R01 GM047238-12, R01 GM047238-07, R01 GM047238-16, R01 GM047238, R01 GM047238-08, R01 GM047238-10, T32 GM007739, R01 GM047238-15, R01 GM047238-13, R01 GM047238-05A2] Funding Source: Medline

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Deregulation of the G1/G0 phase of the cell cycle can lead to cancer. During G1, most cells commit alternatively to DNA replication and division, or to cell-cycle exit and differentiation. The anaphase-promoting complex or cyclosome (APC/C) activated by Cdh1 coordinately eliminates positive cell-cycle regulators as well as inhibitors of differentiation, thereby coupling cell-cycle exit and differentiation. Misregulation of Cdh1 thus has the potential to promote both cell-cycle re-entry and either perturbed differentiation or dedifferentiation. In addition, APC/C-Cdh1 is required to maintain genomic stability. As a result, loss of Cdh1 can contribute to tumorigenesis in the form of proliferation of poorly differentiated and genetically unstable cells.

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