维生素D3联合二甲双胍对人乳腺癌MDA-MB-231细胞的协同抗肿瘤活性涉及m-TOR相关信号通路。

Li-Shu Guo, Hong-xia Li, Chun-Yang Li, Shengyan Zhang, Jia Chen, Qi-long Wang, Jing-Miao Gao, Jia-Qi Liang, M. Gao, Yong-jie Wu
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引用次数: 26

摘要

二甲双胍通常用于治疗2型糖尿病。近年来,许多研究表明,二甲双胍和维生素D具有广谱抗肿瘤活性。我们的研究目的是研究维生素D3联合二甲双胍对人乳腺癌细胞株MDA-MB-231细胞凋亡的诱导作用及其机制。采用甲基噻唑四氮唑(MTT)法检测细胞增殖。Hoechst 33342染色观察细胞凋亡形态。本研究表明,维生素D3 280 μg/ml、维生素D3 300 μg/ml或维生素D3 320 μg/ml单独与二甲双胍15000 μg/ml联合使用对细胞增殖和凋亡具有协同作用。潜在的抗肿瘤机制可能涉及m-TOR相关通路,这些通路与激活cleaved caspase-3、Bax和p-AMPK的表达以及抑制p-Bcl-2、c-Myc、p-IGF-IR、p-mTOR、p-P70S6K、p-S6的表达有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synergistic antitumor activity of vitamin D3 combined with metformin in human breast carcinoma MDA-MB-231 cells involves m-TOR related signaling pathways.
Metformin is usually used for the treatment of type 2 diabetes. Recently, many studies suggest that metformin and vitamin D have broad-spectrum antitumor activities. Our aim in this research was to study the effects of vitamin D3 combined with metformin on the apoptosis induction and its mechanisms in the human breast cancer cell line MDA-MB-231. Cell proliferation was measured by methylthiazol tetrazolium (MTT) assay. The morphology of cell apoptosis was observed after Hoechst 33342 staining. Here we show that vitamin D3 280 μg/ml or vitamin D3 300 μg/ml or vitamin D3 320 μg/ml seperately combined with metformin 15000 μg/ml exhibited synergistic effects on cell proliferation and apoptosis. The underlying anti-tumor mechanisms may involve m-TOR related pathways, which are related to activating expression of cleaved caspase-3, Bax and p-AMPK, as well as inhibiting expressions of p-Bcl-2, c-Myc, p-IGF-IR, p-mTOR, p-P70S6K, p-S6.
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