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氯喹增强雷帕霉素诱导的MG63细胞凋亡。

Chloroquine Enhances Rapamycin-induced Apoptosis in MG63 Cells.

作者信息

Ishibashi Yoichi, Nakamura Osamu, Yamagami Yoshiki, Nishimura Hideki, Fukuoka Natsuko, Yamamoto Tetsuji

机构信息

Department of Orthopaedic Surgery, Kagawa University Faculty of Medicine, Kagawa, Japan.

Department of Orthopaedic Surgery, Kagawa University Faculty of Medicine, Kagawa, Japan

出版信息

Anticancer Res. 2019 Feb;39(2):649-654. doi: 10.21873/anticanres.13159.

Abstract

BACKGROUND/AIM: We previously showed that the use of autophagy inhibitors in combination with chemotherapy can enhance anticancer effects in sarcoma cell lines. In this study, we investigated the combined effect of the autophagy inhibitor chloroquine and the mTOR inhibitor rapamycin on MG63 osteosarcoma cells.

MATERIALS AND METHODS

Effects of chloroquine and/or rapamycin on cell proliferation were assessed by WST-1 assays. Effects of chloroquine and/or rapamycin on the mTOR pathway components, autophagy, and apoptosis were investigated by western blot, flow cytometry, and fluorescence microscopy using immunocytochemical staining of LC3 and Annexin V-FITC/propidium iodide.

RESULTS

Rapamycin suppressed cell growth and inhibited the mTOR pathway. Rapamycin promoted autophagy by blocking the mTOR pathway, and chloroquine enhanced apoptosis by blocking autophagy.

CONCLUSION

Chloroquine enhances the effects of rapamycin in inducing apoptosis via autophagy inhibition in MG63 cells. Thus, the combined therapy of chloroquine and rapamycin may be a potent treatment for osteosarcoma.

摘要

背景/目的:我们之前表明,自噬抑制剂与化疗联合使用可增强肉瘤细胞系的抗癌效果。在本研究中,我们研究了自噬抑制剂氯喹和mTOR抑制剂雷帕霉素对MG63骨肉瘤细胞的联合作用。

材料与方法

通过WST-1分析评估氯喹和/或雷帕霉素对细胞增殖的影响。使用LC3免疫细胞化学染色和膜联蛋白V-异硫氰酸荧光素/碘化丙啶,通过蛋白质印迹、流式细胞术和荧光显微镜研究氯喹和/或雷帕霉素对mTOR信号通路成分、自噬和凋亡的影响。

结果

雷帕霉素抑制细胞生长并抑制mTOR信号通路。雷帕霉素通过阻断mTOR信号通路促进自噬,氯喹通过阻断自噬增强凋亡。

结论

氯喹通过抑制MG63细胞自噬增强雷帕霉素诱导凋亡的作用。因此,氯喹和雷帕霉素联合治疗可能是骨肉瘤的有效治疗方法。

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