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2000
Volume 6, Issue 7
  • ISSN: 1566-5240
  • E-ISSN: 1875-5666

Abstract

The retinoblastoma tumor suppressor (RB) is functionally inactivated at high frequency in human cancers. Based on the role of RB as a negative regulator of cell cycle this event would be expected to contribute to deregulated proliferation. However, evidence suggests that loss of RB not only mediates aberrant proliferation, but compromises the fidelity of cell cycle transitions leading to a breakdown in genome integrity. This review is focused on the mechanisms underlying this facet of RB function and the contibution of this process to tumorigenesis.

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/content/journals/cmm/10.2174/156652406778773420
2006-11-01
2025-06-26
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/content/journals/cmm/10.2174/156652406778773420
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  • Article Type:
    Research Article
Keyword(s): Cell Cycle; Centrosome Duplication Cycle; DNA replication; E2F pathway; RB interaction
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