首页> 美国卫生研究院文献>Journal of Cancer >Proteasome Inhibitor YSY01A Enhances Cisplatin Cytotoxicity in Cisplatin-Resistant Human Ovarian Cancer Cells
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Proteasome Inhibitor YSY01A Enhances Cisplatin Cytotoxicity in Cisplatin-Resistant Human Ovarian Cancer Cells

机译:蛋白酶体抑制剂YSY01A增强顺铂耐药的人卵巢癌细胞的顺铂细胞毒性。

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摘要

Cisplatin is one of the most common drugs used for treatment of solid tumors such as ovarian cancer. Unfortunately, the development of resistance against this cytotoxic agent limits its clinical use. Here we report that YSY01A, a novel proteasome inhibitor, is capable of suppressing survival of cisplatin-resistant ovarian cancer cells by inducing apoptosis. And YSY01A treatment enhances the cytotoxicity of cisplatin in drug-resistant ovarian cancer cells. Specifically, YSY01A abrogates regulatory proteins important for cell proliferation and anti-apoptosis including NF-κB p65 and STAT3, resulting in down-regulation of Bcl-2. A dramatic increase in cisplatin uptake was also observed by inductively coupled plasma-mass spectrometry following exposure to YSY01A. Taken together, YSY01A serves as a potential candidate for further development as anticancer therapeutics targeting the proteasome.
机译:顺铂是用于治疗实体瘤(例如卵巢癌)的最常见药物之一。不幸的是,对这种细胞毒剂的抗药性的发展限制了其临床用途。在这里我们报告YSY01A,一种新型的蛋白酶体抑制剂,能够通过诱导细胞凋亡来抑制顺铂耐药的卵巢癌细胞的存活。 YSY01A处理可增强顺铂在耐药性卵巢癌细胞中的细胞毒性。具体来说,YSY01A消除了对细胞增殖和抗凋亡重要的调节蛋白,包括NF-κBp65和STAT3,导致Bcl-2的下调。暴露于YSY01A后,电感耦合等离子体质谱法也观察到了顺铂吸收的显着增加。综上所述,YSY01A作为靶向蛋白酶体的抗癌治疗剂,可作为进一步开发的潜在候选者。

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