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首页> 外文期刊>Journal of biochemical and molecular toxicology >Triggering p53 activation is essential in ziyuglycoside I‐induced human retinoblastoma WERI‐Rb‐1 cell apoptosis
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Triggering p53 activation is essential in ziyuglycoside I‐induced human retinoblastoma WERI‐Rb‐1 cell apoptosis

机译:触发P53活化是Ziyuglycoside I诱导的人视网膜母细胞瘤Weri-RB-1细胞凋亡的必需病

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摘要

Abstract Ziyuglycoside I (Ziyu I), one of the major components isolated from the root of Sanguisorba officinalis L., has been proved for the antitumor properties on oral cancer, prostate cancer, and colorectal cancer. However, the effect of Ziyu I on retinoblastoma (RB) is not well understood. In this study, we investigated the inhibitory effect and underlying molecular mechanism of Ziyu I on human RB WERI‐Rb‐1 cells. Our results indicated that Ziyu I could suppress cell viability and induce mitochondrial‐dependent cell apoptosis in WERI‐Rb‐1 cells. Furthermore, Ziyu I treatment increased p53 expression as well as improved p53 stabilization through downregulation of pS166‐Mdm2 and upregulation of phosphorylated‐ and acetylated‐p53. Blockade of p53 significantly attenuated Ziyu I‐induced mitochondrial dysfunction. Our findings demonstrate that Ziyu I exhibits excellent anticancer effect on human RB WERI‐Rb‐1 cells by triggering p53 activation, and imply Ziyu I as a potential compound for chemotherapy of human RB.
机译:摘要齐杨苷I(Ziyu I),已证明从患儿癌症,前列腺癌和结肠直肠癌的抗肿瘤特性证明了从Sanguisorba Officinalis L中分离的主要成分之一。然而,枣宇I对视网膜母细胞瘤(RB)的影响尚不清楚。在这项研究中,我们研究了在人RB WERI-RB-1细胞上的Ziyu I的抑制作用和潜在的分子机制。我们的研究结果表明,紫玉抑制细胞活力并诱导WERI-RB-1细胞中的线粒体依赖性细胞凋亡。此外,紫牛I治疗增加P53表达,并通过下调PS166-MDM2的下调和磷酸化 - 和乙酰化-P53的上调改善P53稳定化。封锁P53显着减弱了紫云I诱导的线粒体功能障碍。我们的研究结果表明,通过触发P53活化对人RB WERI-RB-1细胞表现出优异的抗癌影响,并意味着Ziyu I作为人RB化疗的潜在化合物。

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