Li Yu, Mi Can
Department of Pathology, Chongqing Medical University, Chongqing, PR China.
Ai Zheng. 2003 Jun;22(6):586-91.
BACKGROUND & OBJECTIVE: It was reported that Genistein possess inhibitory effects on various carcinomas. But the report on the effects of Genistein on human ovarian carcinoma was rare. This study was aimed to investigate the proliferation inhibition and apoptosis onset in human ovarian carcinoma cell lines SKOV(3) induced by Genistein and to discuss its antitumor mechanism.
Inhibitory effect of Genistein on SKOV(3) proliferation was tested by MTT method. Apoptotic cell and apoptotic bodies were observed by acridine orange/ethidium bromide(AO/EB) staining and electron microscope (EM). Cell apoptosis percentage and cell cycle phase distribution were measured by flow cytometric assay (FCM). The characteristic DNA ladders of apoptosis were determined by agarose gel electrophoresis (AGE). The expression of proliferation and apoptosis associated proteins and their mRNA were determined using immunocytochemistry and RT-PCR.
A time- dependent and dose-dependent proliferation inhibition of Genistein was demonstrated in SKOV(3); the prominent inhibitory concentrations were 20 micromol/L and 40 micromol/L (P< 0.01) and the 72(nd) hour was the most apparent phase (P< 0.01). The growth inhibition rates of the cancer cells reached 72.07% and 74.93%. A G(2)/M cell cycle arrest was induced in SKOV(3) exposed to 20 micromol/L Genistein. The characteristic morphological changes of apoptosis were observed by AO/EB staining and EM in SKOV(3) exposed to Genistein. The apoptosis rate was highest at 20 micromol/L concentration, reached 23.7%. DNA ladder appeared by AGE. The expression of bcl-2 mRNA was decreased, p21(WAF1/CIP1) and bax mRNA was increased (P< 0.05), the expression of PCNA, Bcl-2,and cyclin B1 protein were decreased, Bax and p21(WAF1/CIP1) protein were increased in SKOV(3) exposed to 20 micromol/L Genistein for 48 hours (P< 0.01).
Genistein could inhibit proliferation and induce apoptosis in ovarian carcinoma cell lines SKOV(3). Its inhibitory effect appears to be due to the up-regulation of p21(WAF1/CIP1) mRNA and protein expression, down-regulation of PCNA and cyclin B1 protein. The onset of apoptosis in ovarian carcinoma cell is related to the up-regulation of bax and down-regulation of bcl-2 in mRNA and protein level induced by Genistein.
据报道,染料木黄酮对多种癌具有抑制作用。但关于染料木黄酮对人卵巢癌作用的报道较少。本研究旨在探讨染料木黄酮对人卵巢癌细胞系SKOV(3)增殖的抑制作用及诱导凋亡的作用,并探讨其抗肿瘤机制。
采用MTT法检测染料木黄酮对SKOV(3)增殖的抑制作用。通过吖啶橙/溴化乙锭(AO/EB)染色和电子显微镜(EM)观察凋亡细胞和凋亡小体。采用流式细胞术(FCM)检测细胞凋亡率和细胞周期阶段分布。用琼脂糖凝胶电泳(AGE)检测凋亡特征性DNA梯带。采用免疫细胞化学和RT-PCR检测增殖和凋亡相关蛋白及其mRNA的表达。
染料木黄酮对SKOV(3)的增殖抑制呈时间和剂量依赖性;显著抑制浓度为20 μmol/L和40 μmol/L(P<0.01),72小时最为明显(P<0.01)。癌细胞的生长抑制率分别达到72.07%和74.93%。20 μmol/L染料木黄酮可诱导SKOV(3)细胞出现G(2)/M期阻滞。通过AO/EB染色和EM观察到染料木黄酮处理的SKOV(3)细胞出现凋亡特征性形态学改变。20 μmol/L浓度时凋亡率最高,达23.7%。AGE显示出现DNA梯带。20 μmol/L染料木黄酮处理48小时的SKOV(3)细胞中,bcl-2 mRNA表达降低,p21(WAF1/CIP1)和bax mRNA表达增加(P<0.05),PCNA、Bcl-2和细胞周期蛋白B1蛋白表达降低,Bax和p21(WAF1/CIP1)蛋白表达增加(P<0.01)。
染料木黄酮可抑制卵巢癌细胞系SKOV(3)的增殖并诱导其凋亡。其抑制作用似乎是由于p21(WAF1/CIP1) mRNA和蛋白表达上调,PCNA和细胞周期蛋白B1蛋白表达下调。卵巢癌细胞凋亡的发生与染料木黄酮诱导的bax上调和bcl-2在mRNA和蛋白水平下调有关。