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TGX-221 抑制人神经胶质瘤细胞的增殖并诱导其凋亡。

TGX-221 inhibits proliferation and induces apoptosis in human glioblastoma cells.

机构信息

Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuchang, Wuhan, Hubei 430060, P.R. China.

出版信息

Oncol Rep. 2017 Nov;38(5):2836-2842. doi: 10.3892/or.2017.5991. Epub 2017 Sep 22.

Abstract

Glioblastoma is the most common type of primary brain tumor in adults, with high mortality and morbidity rates. More effective therapeutic strategies are imperative. Previous studies have shown that the known p110-β-selective inhibitor TGX-221 blocks the activation of PKB/Akt in PTEN-deficient cells. We treated U87 and U251 glioblastoma cells with TGX-221 to determine the effect of TGX-221. We performed a Cell Counting Kit-8 (CCK-8) test, EDU staining and cell cycle distribution analysis and found that TGX-221 inhibited glioblastoma cell proliferation. Next, the effect of TGX-221 on cell apoptosis was investigated using flow cytometry. These results demonstrated that TGX-221 induced apoptosis in glioblastoma cells. Moreover, migration and invasion assays revealed that TGX-221 inhibited human glioblastoma cell migration and invasion. Collectively, our study revealed that TGX-221 could inhibit proliferation and induce apoptosis in glioblastoma cells.

摘要

胶质母细胞瘤是成人中最常见的原发性脑肿瘤,死亡率和发病率都很高。更有效的治疗策略势在必行。先前的研究表明,已知的 p110-β 选择性抑制剂 TGX-221 可阻断 PTEN 缺陷细胞中 PKB/Akt 的激活。我们用 TGX-221 处理 U87 和 U251 胶质母细胞瘤细胞,以确定 TGX-221 的作用。我们进行了细胞计数试剂盒-8 (CCK-8) 测试、EDU 染色和细胞周期分布分析,发现 TGX-221 抑制胶质母细胞瘤细胞增殖。接下来,我们使用流式细胞术研究了 TGX-221 对细胞凋亡的影响。这些结果表明 TGX-221 诱导胶质母细胞瘤细胞凋亡。此外,迁移和侵袭实验表明 TGX-221 抑制人胶质母细胞瘤细胞的迁移和侵袭。总之,我们的研究表明 TGX-221 可抑制胶质母细胞瘤细胞的增殖并诱导其凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f95d/5780035/bdfe57f090d3/OR-38-05-2836-g00.jpg

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