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含羞草碱通过一条不依赖p53的途径使p21WAF1/CIP1/SDI1升高。

p21WAF1/CIP1/SDI1 is elevated through a p53-independent pathway by mimosine.

作者信息

Alpan R S, Pardee A B

机构信息

Division of Cell Growth and Regulation, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA.

出版信息

Cell Growth Differ. 1996 Jul;7(7):893-901.

PMID:8809407
Abstract

Tumor suppressor p53 is a nuclear protein that is induced by DNA damage and is involved in G1 and G2 phase control of the cell cycle. p21WAF1/CIP1/SDI1 (p21), a cyclin-dependent kinase inhibitor, is a downstream target and effector of p53 to induce G1 arrest. Mimosine is a potent reversible late G1 phase blocker of the cell cycle. In this study, we showed that mimosine can increase both p21 mRNA and protein levels, indirectly inhibit cyclin E-associated kinase activity without affecting the cyclin E protein level, block human breast cancer cells (21PT) in the late G1 phase of the cell cycle, and induce a p53-independent p21 pathway in these cells. These results support the possibility of restoring a G1 checkpoint by use of mimosine. They also suggest that the mechanism of the effect of mimosine is complex and may have more than one target in the cell.

摘要

肿瘤抑制蛋白p53是一种核蛋白,可由DNA损伤诱导产生,并参与细胞周期的G1期和G2期调控。p21WAF1/CIP1/SDI1(p21),一种细胞周期蛋白依赖性激酶抑制剂,是p53诱导G1期阻滞的下游靶点和效应分子。含羞草碱是一种有效的、可逆的细胞周期G1期晚期阻滞剂。在本研究中,我们发现含羞草碱可增加p21的mRNA和蛋白水平,间接抑制细胞周期蛋白E相关激酶活性而不影响细胞周期蛋白E的蛋白水平,将人乳腺癌细胞(21PT)阻滞在细胞周期的G1期晚期,并在这些细胞中诱导一条不依赖p53的p21通路。这些结果支持了使用含羞草碱恢复G1期检查点的可能性。它们还表明,含羞草碱的作用机制复杂,可能在细胞中有多个靶点。

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