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首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Human beta-galactoside alpha-2,3-sialyltransferase (ST3Gal III) attenuated Taxol-induced apoptosis in ovarian cancer cells by downregulating caspase-8 activity.
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Human beta-galactoside alpha-2,3-sialyltransferase (ST3Gal III) attenuated Taxol-induced apoptosis in ovarian cancer cells by downregulating caspase-8 activity.

机译:人β-半乳糖苷α-2,3-唾液酸转移酶(ST3Gal III)通过下调caspase-8活性来减轻紫杉醇诱导的卵巢癌细胞凋亡。

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摘要

Taxol triggers apoptosis in a variety of cancer cells, but it also upregulates cytoprotective proteins and/or pathways that compromise its therapeutic efficacy. In this report, we found that Taxol treatment resulted in caspase-8-dependent apoptosis in SKOV3 human ovarian cancer cells. Moreover, Taxol-induced apoptosis was associated with caspase-3 activation. Interestingly, Taxol treatment upregulated alpha-2,3-sialyltransferase (ST3Gal III) expression and forced expression of ST3Gal III attenuated Taxol-induced apoptosis. Furthermore, ST3Gal III overexpression inhibited Taxol-triggered caspase-8 activation, indicating that ST3Gal III upregulation produces cellular resistance to Taxol and hence reduces the efficacy of Taxol therapy.
机译:紫杉酚在多种癌细胞中触发凋亡,但它也上调了细胞保护蛋白和/或损害其治疗功效的途径。在此报告中,我们发现紫杉醇治疗可导致SKOV3人卵巢癌细胞中caspase-8依赖性凋亡。此外,紫杉醇诱导的凋亡与caspase-3激活有关。有趣的是,紫杉醇治疗上调了α-2,3-唾液酸转移酶(ST3Gal III)的表达,而ST3Gal III的强制表达减弱了紫杉醇诱导的细胞凋亡。此外,ST3Gal III的过表达抑制了紫杉醇触发的caspase-8激活,表明ST3Gal III的上调产生了对紫杉醇的细胞抗性,因此降低了紫杉醇治疗的疗效。

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