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Growth inhibiting effects of terazosin on androgen-independent prostate cancer cell lines

机译:特拉唑嗪对雄激素非依赖性前列腺癌细胞系的生长抑制作用

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摘要

Objective To study the effects of an α_1-adrenoceptor antagonist, terazosin on the androgen-independent prostate cancer cell lines PC-3 and DU145. Methods Two androgen independent cell lines, PC-3 and DU145, were used to determine cell viability, colony-forming ability, as well as cell cycle distribution, after exposure to terazosin. Western blot analysis was used to determine the expression of p21WAF1 and p27KIP1. Results This study shows that terazosin inhibits not only prostate cancer cell growth but also its colony forming ability, both of which are main targets of clinical treatment. In addition, terazosin is shown to inhibit cell growth through G1 phase cell cycle arrest and the up-regulation of p27~(KIP1). Conclusion This study provides evidence that the α_1-adrenoceptor antagonist terazosin may have therapeutic potential in the treatment of advanced hormone refractory prostate cancer.
机译:目的研究α_1肾上腺素能受体拮抗剂特拉唑嗪对非雄激素依赖性前列腺癌细胞系PC-3和DU145的作用。方法使用两种不依赖雄激素的细胞系PC-3和DU145来测定暴露于特拉唑嗪后的细胞活力,集落形成能力以及细胞周期分布。使用蛋白质印迹分析确定p21WAF1和p27KIP1的表达。结果该研究表明,特拉唑嗪不仅抑制前列腺癌细胞的生长,而且抑制其集落形成能力,这两者都是临床治疗的主要目标。此外,还显示特拉唑嗪通过G1期细胞周期停滞和p27〜(KIP1)上调抑制细胞生长。结论这项研究提供了证据,证明α_1-肾上腺素能受体拮抗剂特拉唑嗪可能具有治疗晚期激素难治性前列腺癌的潜力。

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