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Targeting the anaphase promoting complex: common pathways for viral infection and cancer therapy

期刊

EXPERT OPINION ON THERAPEUTIC TARGETS
卷 15, 期 6, 页码 767-780

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1517/14728222.2011.558008

关键词

anaphase promoting complex/cyclosome (APC/C); anti-mitotic therapy; apoptosis; Cdc20; Cdh1; mitotic slippage; viral proteins

资金

  1. Canadian Institute of Health Research (CIHR) [MOP-179122]
  2. Natural Science and Engineering Research Council (NSERC) of Canada
  3. McGill University Cancer Consortium

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Introduction: The anaphase promoting complex/cyclosome (APC/C) is a ubiquitin ligase involved in regulation of the cell cycle through ubiquitination-dependent substrate proteolysis. Many viral proteins have been shown to interact with the APC/C, derailing cell cycle progression in order to facilitate their own replication. Induction of G(2)/M arrest by viral APC/C inhibition can lead to apoptotic cell death. Some viral proteins cause cytotoxicity specifically in tumour cells, providing evidence that targeting the APC/C could be exploited to selectively eliminate cancer cells. Areas covered: In this review, we provide a summary of studies from viral APC/C interactions over the last decade, as well as recent discoveries identifying the APC/C as a promising target in the context of cancer therapy. Expert opinion: Current therapeutic strategies inducing mitotic arrest rely on activation of the spindle assembly checkpoint (SAC) for their function. Many cancer cells have a weakened SAC and escape apoptosis through mitotic slippage. Recent evidence has demonstrated that targeting the APC/C, particularly the co-activator Cdc20, might be a better alternative. Tumour cells display greater dependency on APC/C function than normal cells and oncogenic transformation can lead to increased mitotic stress, rendering cancer cells more vulnerable to APC/C inhibition.

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