p202 prevents apoptosis in murine AKR-2B fibroblasts

被引:28
作者
Koul, D [1 ]
Lapushin, R [1 ]
Xu, HJ [1 ]
Mills, GB [1 ]
Gutterman, JU [1 ]
Choubey, D [1 ]
机构
[1] Univ Texas, Md Anderson Canc Ctr, Dept Mol Oncol, Houston, TX 77030 USA
关键词
D O I
10.1006/bbrc.1998.8804
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
p202 is an interferon (IFN)-inducible, primarily nuclear, phosphoprotein (52-kDa) whose overexpression in transfected cells inhibits colony formation. p202 binds to the retinoblastoma tumor suppressor protein and two other members of the pocket family proteins (p107 and p130). Moreover, overexpression of p202 in transfected cells inhibits the transcriptional activity of E2Fs (E2F-1/DP-1 and E2F-4/DP-1), p53, AP-1 c-Fos and c-Jun, NF-kappa B p50 and p65. Here we demonstrate that inhibition of endogenous p202 production in murine AKR-2B fibroblasts did not result in an increase in cell proliferation. Instead, these cells exhibited increased susceptibility to apoptosis in response to decrease in serum concentrations in the growth medium. These observations are consistent with the notion that normal levels of p202 may be needed for the regulation of cell proliferation. (C) 1998 Academic Press.
引用
收藏
页码:379 / 382
页数:4
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