Cell growth arrest and induction of cyclin-dependent kinase inhibitor p21WAF1/CIP1 Mediated by STAT1

Yue E. Chin, Motoo Kitagawa, Wu Chou S. Su, Zhi Hao You, Yoshiki Iwamoto, Xin Yuan Fu

研究成果: Article同行評審

704 引文 斯高帕斯(Scopus)

摘要

Signal transducers and activators of transcription (STAT) proteins can be conditionally activated in response to epidermal growth factor (EGF) and interferon (IFN)-γ. STAT activation was correlated with cell growth inhibition in response to EGF and IFN-γ. Activated STAT proteins specifically recognized the conserved STAT-responsive elements in the promoter of the gene encoding the cyclin-dependent kinase (CDK) inhibitor p21WAF1/CIP1 and regulated the induction of p21 messenger RNA. IFN-γ did not inhibit the growth of U3A cells, which are deficient in STAT1, but did inhibit the growth of U3A cells into which STAT1α was reintroduced. Thus, STAT1 protein is essential for cell growth suppression in response to IFN-γ. The STAT signaling pathway appears to negatively regulate the cell cycle by inducing CDK inhibitors in response to cytokines.

原文English
頁(從 - 到)719-722
頁數4
期刊Science
272
發行號5262
DOIs
出版狀態Published - 1996 五月 3

All Science Journal Classification (ASJC) codes

  • 多學科

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