TGFβ-induced growth inhibition involves cell cycle inhibitor p21 and pRb independent from p15 expression

被引:0
|
作者
Voss, M
Wolff, B
Savitskaia, N
Ungefroren, H
Deppert, W
Schmiegel, W
Kalthoff, H
Naumann, M
机构
[1] Max Planck Inst Infekt Biol, Mol Biol Abt, D-10117 Berlin, Germany
[2] Univ Kiel Klinikum, Abt Thoraxchirurg & Allgemiene Chirurg, D-24105 Kiel, Germany
[3] Ruhr Univ Bochum, Med Klin, D-44892 Bochum, Germany
[4] Heinrich Pette Inst Expt Virol & Immunol, D-20251 Hamburg, Germany
关键词
cell cycle inhibitors; TGF beta; pRb; p15; p16; p21;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It is generally assumed that TGF beta induces cell cycle arrest through the cooperative action of cell cycle inhibitors p15, p27 and p21. Here, we found that several pancreatic carcinoma cell lines exert TGF beta-induced negative growth control in spite of the loss of p15 and p16 expression. In these cell lines, TGF beta-induced growth control correlates with the upregulation of the p21 protein and active pRb expression. Conversely, cells without p21 and/or pRb expression are resistant to TGF beta-induced growth inhibition. Moreover, overexpression of p21 in the p21-deficient cell line Pane Tu1 leads to growth arrest. Thus, TGF beta-induced growth control correlates with p21 expression and pRb status independent of p15 and/or p16 expression.
引用
收藏
页码:93 / 101
页数:9
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