Literature DB >> 12553003

P2P-R deficiency modifies nocodazole-induced mitotic arrest and UV-induced apoptosis.

R E Scott1, S Gao.   

Abstract

BACKGROUND: Cell cycle progression from G1 through S to mitosis can be influenced by microtubule-dependent mechanisms that involve AP1 factors and c-Jun N-terminal kinase (JNK) activity. UV irradiation-induced apoptosis also involves AP1 factors and JNK activity. The current studies evaluated the outcome of P2P-R deficiency on these mechanisms because P2P-R expression is repressed in association with a decrease in AP1 inducibility and cell cycle progression during differentiation, and P2P-R overexpression promotes apoptosis.
MATERIALS AND METHODS: The ability of the microtubule disruption drug nocodazole to induce mitotic arrest and the ability of UV irradiation to induce apoptosis was evaluated in native versus cells made P2P-R deficient by P2P-R antisense treatment.
RESULTS: P2P-R deficiency restricts cell cycle progression from G1 through S to mitosis in a microtubule-dependent manner and P2P-R deficiency represses UV irradiation-induced apoptosis.
CONCLUSION: P2P-R may influence AP1 and/or JNK signaling pathways.

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Year:  2002        PMID: 12553003

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  5 in total

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Journal:  Genetics       Date:  2006-03-17       Impact factor: 4.562

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  5 in total

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