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Tumor suppression by Ink4a-Arf:: progress and puzzles

Journal

CURRENT OPINION IN GENETICS & DEVELOPMENT
Volume 13, Issue 1, Pages 77-83

Publisher

CURRENT BIOLOGY LTD
DOI: 10.1016/S0959-437X(02)00013-8

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Funding

  1. NCI NIH HHS [P30 CA008748] Funding Source: Medline

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The two products of the Ink4a-Arf locus, p16(Ink4a) and p19(Arf) (p14(ARF) in humans), are potent tumor suppressors that regulate the activities of the retinoblastoma protein and the p53 transcription factor. These proteins form part of a signaling network that is disrupted in most, if not all, cancer cells. The Ink4a-Arf locus responds to stress signals, limiting cell proliferation and modulating oncogene-induced apoptosis. Recent evidence emerging from mouse tumor models distinguishes the activities of p16(Ink4a) and p19(Arf) in regulating tumor onset and identifies differences in their responsiveness to drugs.

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