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积雪草苷诱导的胶质母细胞瘤细胞死亡

Glioblastoma cell death induced by asiatic acid.

作者信息

Cho C W, Choi D S, Cardone M H, Kim C W, Sinskey A J, Rha C

机构信息

Biomaterials Science and Engineering Laboratory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.

出版信息

Cell Biol Toxicol. 2006 Nov;22(6):393-408. doi: 10.1007/s10565-006-0104-2. Epub 2006 Aug 1.

Abstract

Asiatic acid (AA), a triterpene, is known to be cytotoxic to several tumor cell lines. AA induces dose- and time-dependent cell death in U-87 MG human glioblastoma. This cell death occurs via both apoptosis and necrosis. The effect of AA may be cell type-specific as AA-induced cell death was mainly apoptotic in colon cancer RKO cells. AA-induced glioblastoma cell death is associated with decreased mitochondrial membrane potential, activation of caspase-9 and -3, and increased intracellular free Ca2+. Although treatment of glioblastoma cells with the caspase inhibitor zVAD-fmk completely abolished AA-induced caspase activation, it did not significantly block AA-induced cell death. AA-induced cell death was significantly prevented by an intracellular Ca2+ inhibitor, BAPTA/AM. Taken together, these results indicate that AA induces cell death by both apoptosis and necrosis, with Ca2+-mediated necrotic cell death predominating.

摘要

齐墩果酸(AA)是一种三萜类化合物,已知对多种肿瘤细胞系具有细胞毒性。AA在U-87 MG人胶质母细胞瘤中诱导剂量和时间依赖性细胞死亡。这种细胞死亡通过凋亡和坏死两种方式发生。AA的作用可能具有细胞类型特异性,因为AA诱导的细胞死亡在结肠癌RKO细胞中主要是凋亡性的。AA诱导的胶质母细胞瘤细胞死亡与线粒体膜电位降低、半胱天冬酶-9和-3的激活以及细胞内游离Ca2+增加有关。尽管用半胱天冬酶抑制剂zVAD-fmk处理胶质母细胞瘤细胞完全消除了AA诱导的半胱天冬酶激活,但它并没有显著阻断AA诱导的细胞死亡。细胞内Ca2+抑制剂BAPTA/AM可显著预防AA诱导的细胞死亡。综上所述,这些结果表明AA通过凋亡和坏死两种方式诱导细胞死亡,其中Ca2+介导的坏死性细胞死亡占主导。

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