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格尔德霉素可诱导K562红白血病细胞发生细胞周期阻滞。

Geldanamycin induces cell cycle arrest in K562 erythroleukemic cells.

作者信息

Kim H R, Lee C H, Choi Y H, Kang H S, Kim H D

机构信息

Department of Molecular Biology, College of Natural Sciences, Pusan National University, Korea.

出版信息

IUBMB Life. 1999 Oct;48(4):425-8. doi: 10.1080/713803539.

Abstract

Geldanamycin (GA), a benzoquinone ansamycin, is one of the specific inhibitors of 90-kDa heat shock protein and induces growth inhibition and apoptosis in certain cancer cell lines. We have investigated the mechanism of GA-induced growth inhibition in K562 erythroleukemic cells. DNA flow-cytometric analysis indicated that GA-induced growth arrest was associated with G2/M phase arrest of the cell cycle. GA treatment down-regulated the expression of cyclin B1 and inhibited phosphorylation of Cdc2 protein, both key regulatory proteins at the G2/M boundary. GA also markedly inhibited the Cdc2 kinase activity, which may be in part a result of up-regulation of p27KIP1 by GA. The present results suggest a novel mechanism that p27KIP1 could be involved in the regulation of G2 to M phase transition.

摘要

格尔德霉素(GA)是一种苯醌安莎霉素,是90 kDa热休克蛋白的特异性抑制剂之一,可诱导某些癌细胞系的生长抑制和凋亡。我们研究了GA诱导K562红白血病细胞生长抑制的机制。DNA流式细胞术分析表明,GA诱导的生长停滞与细胞周期的G2/M期停滞有关。GA处理下调了细胞周期蛋白B1的表达,并抑制了Cdc2蛋白的磷酸化,这两种蛋白都是G2/M边界的关键调节蛋白。GA还显著抑制了Cdc2激酶活性,这可能部分是由于GA上调了p27KIP1所致。目前的结果提示了一种新的机制,即p27KIP1可能参与了G2到M期转换的调控。

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