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Abrogation of heat-shock protein (HSP)70 expression induced cell growth inhibition and apoptosis in human androgen-independent prostate cancer cell line PC-3m

机译:休克热休克蛋白(HSP)70表达诱导人非雄激素依赖性前列腺癌细胞系PC-3m的细胞生长抑制和凋亡

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Aim: To investigate the effect of abrogating heat shock protein (HSP) 70 expression by antisense HSP70 oligonucleotides treatment on human androgen-independent prostate cancer cell line PC-3m growth. Methods: PC3m cells were treated with 0-16μmol/L antisense HSP70 oligomers for 0-100 hr. Cell growth inhibition was analyzed using a trypan blue dye exclusion test. Apoptotic cells were detected and confirmed by flow cytometric analysis and DNA fragmentation analysis. The protein expression of HSP70 and bcl-2 affected by antisense HSP70 oligomers were determined using Western blot. Results: Antisense HSP70 oligomer induced apoptosis and then inhibited proliferation of PC-3m cells in a dose- and time-dependent manner. Ladder-like patterns of DNA fragments were observed in PC-3m cells treated with 10μmol/L antisense HSP70 oligomer for 48 hr or 8μtmol/L for 72 hr on agarose gel electrophoresis. Antisense HSP70 oligomer pretreatment enhanced the subsequent induction of apoptosis by heat shock in PC-3m cells. In addition, undetectable HSP70 expression was observed at a concentration of 10μtmol/L antisense HSP70 oligomer treatment for 48 hr or 8μtmol/L for 72 hr in Western blot, which was paralleled by decreased expression levels of anti-apoptotic protein bcl-2. Conclusion: HSP70 antisense oligomer treatment abro-gates the expression of HSP70, which may disrupt HSP70-bcl-2-interactions and further down-regulate bcl-2 expression,in turn inducing apoptosis and inhibiting cell growth in PC-3m cells. (Asian JAndro12004 Dec;6:319-324)
机译:目的:研究通过反义HSP70寡核苷酸治疗消除热休克蛋白(HSP)70表达对人雄激素非依赖性前列腺癌细胞株PC-3m生长的影响。方法:将PC3m细胞用0-16μmol/ L反义HSP70低聚物处理0-100小时。使用锥虫蓝染料排除测试分析细胞生长抑制。通过流式细胞术分析和DNA片段化分析检测并确认凋亡细胞。使用蛋白质印迹法测定反义HSP70寡聚体影响的HSP70和bcl-2的蛋白表达。结果:反义HSP70寡聚物诱导细胞凋亡,然后以剂量和时间依赖性方式抑制PC-3m细胞的增殖。在琼脂糖凝胶电泳中,在用10μmol/ L反义HSP70低聚物处理48小时或8μtmol/ L处理72小时的PC-3m细胞中观察到了阶梯状的DNA片段模式。反义HSP70低聚物预处理可增强PC-3m细胞通过热休克诱导的凋亡。此外,在Western blot中,在浓度为10μtmol/ L的反义HSP70低聚物处理48小时或8μtmol/ L的浓度为72小时时,未观察到HSP70表达,这与抗凋亡蛋白bcl-2的表达水平降低相平行。结论:HSP70反义寡聚物处理可废除HSP70的表达,这可能破坏HSP70-bcl-2的相互作用并进一步下调bcl-2的表达,进而诱导PC-3m细胞凋亡并抑制细胞生长。 (亚洲JAndro12004年12月; 6:319-324)

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