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9-羟基玫瑰树碱通过突变型p53介导诱导细胞周期在G1期停滞并凋亡。

Mutant p53 mediated induction of cell cycle arrest and apoptosis at G1 phase by 9-hydroxyellipticine.

作者信息

Sugikawa E, Hosoi T, Yazaki N, Gamanuma M, Nakanishi N, Ohashi M

机构信息

Drug Discovery Research Laboratory, Tanabe Seiyaku, Co., Ltd., Saitama, Japan.

出版信息

Anticancer Res. 1999 Jul-Aug;19(4B):3099-108.

Abstract

Wild-type p53 causes cell-cycle arrest at late G1 phase and induction of apoptosis by up- regulation of waf1 and bax, respectively. Although in many cancer cells p53 is frequently mutated and loses its functions, we have proposed that mutant p53 may be involved in the anticancer mechanism of 9-hydroxy ellipticine (9HE). It was shown using flow cytometry that 9HE (10 microM) caused induction of apoptosis in G1 phase of the cell cycle in mutant p53 (p53ala143, p53his175, orp53his273) transfected Saos-2 cells, but not in p53-deficient parental Saos-2 cells. Similar induction of apoptosis was observed 24-48 h after treatment with 9HE in mutant p53-containing SW480, SK-BR-3 and MKN-1, but not in p53-deficient KATO m cells. Using G1 phase cells isolated by centrifugal elutriation, it was confirmed that 9HE caused cell cycle arrest at G1 phase and subsequently induced G1 phase-restricted apoptosis. In accordance with the induction of arrest and apoptosis in G1 phase, 9HE caused up-regulation of waf1 and bax mRNA in mutant p53-containing cells, but not in p53-deficient parental Saos-2 cells. In control experiments, adriamycin (ADR) showed neither G1-restricted apoptosis nor elevation of bax mRNA. It is suggested that 9HE may cause G1 arrest and induction of G1 phase-restricted apoptosis by restoring the wild-type function of mutant p53 protein.

摘要

野生型p53分别通过上调waf1和bax,导致细胞周期在G1期晚期停滞并诱导细胞凋亡。尽管在许多癌细胞中p53经常发生突变并丧失其功能,但我们提出突变型p53可能参与9-羟基玫瑰树碱(9HE)的抗癌机制。流式细胞术结果显示,9HE(10微摩尔)可诱导转染了突变型p53(p53ala143、p53his175或p53his273)的Saos-2细胞在细胞周期的G1期发生凋亡,但对p53缺陷的亲本Saos-2细胞无此作用。在用9HE处理24 - 48小时后,在含有突变型p53的SW480、SK - BR - 3和MKN - 1细胞中观察到类似的凋亡诱导现象,但在p53缺陷的KATOⅢ细胞中未观察到。使用通过离心淘析分离的G1期细胞,证实9HE导致细胞周期在G1期停滞,随后诱导G1期特异性凋亡。与G1期停滞和凋亡的诱导一致,9HE导致含有突变型p53的细胞中waf1和bax mRNA上调,但在p53缺陷的亲本Saos-2细胞中未上调。在对照实验中,阿霉素(ADR)既未显示G1期特异性凋亡,也未使bax mRNA升高。提示9HE可能通过恢复突变型p53蛋白的野生型功能,导致G1期停滞并诱导G1期特异性凋亡。

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