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维生素D3增强二甲双胍对人膀胱癌细胞SW-780的抗肿瘤活性。

Vitamin D3 enhances antitumor activity of metformin in human bladder carcinoma SW-780 cells.

作者信息

Guo Li-Shu, Li Hong-Xia, Li Chun-Yang, Zhang Sheng-Yan, Chen Jia, Wang Qi-Long, Gao Jing-Miao, Liang Jia-Qi, Gao Ming-Tang, Wu Yong-Jie

出版信息

Pharmazie. 2015 Feb;70(2):123-8.

Abstract

OBJECTIVE

To study the effects of vitamin D3 combined with metformin on the proliferation and apoptosis in human bladder cancer cell line SW-780 and its possible mechanism.

METHODS

MTT assay and fluorescence microscope observations were used to study the effects of vitamin D3 combined with metformin on the proliferation and apoptosis of SW-780 cells in vitro. Western blot was used to detect the expression of apoptosis-related proteins p-Bcl-2, Bax, Cyclin D1, c-Myc and related signaling pathways activated proteins p-IGF-IR, p-mTOR, p-P70S6K, p-S6.

RESULTS

MTT results showed that 320 μg/ml vitamin D3 combined with 620 μg/ml metformin acting on cells for 48h had a significant synergistic effect on proliferation. Fluorescence microscope observations showed that compared with negative control group and monotherapy treatment group, the apoptosis features of combination treatment group were obvious and the apoptosis rate increased greatly. Western blot showed that compared with the negative control group and monotherapy treatment group, the expression levels of p-Bcl-2, Cyclin D1 and c-Myc in combination treatment group significantly decreased, whereas the expression level of Bax significantly increased, and the expression levels of p-IGF-IR, p-mTOR, p-P70S6K and p-S6 in combination treatment group significantly decreased.

CONCLUSION

Vitamin D3 combined with metformin exhibited obvious inhibitory effects on the cell proliferation and apoptosis induction in SW-780 cells. The underlying anti-tumor mechanism might be related to inhibiting the expressions of p-Bcl-2, Cyclin D1, c-Myc, p-IGF-IR, p-mTOR, p-P70S6K, p-S6 and activating the expression of Bax.

摘要

目的

研究维生素D3联合二甲双胍对人膀胱癌细胞系SW - 780增殖和凋亡的影响及其可能机制。

方法

采用MTT法和荧光显微镜观察研究维生素D3联合二甲双胍对SW - 780细胞体外增殖和凋亡的影响。采用蛋白质免疫印迹法检测凋亡相关蛋白p - Bcl - 2、Bax、细胞周期蛋白D1、c - Myc的表达以及相关信号通路激活蛋白p - IGF - IR、p - mTOR、p - P70S6K、p - S6的表达。

结果

MTT结果显示,320μg/ml维生素D3联合620μg/ml二甲双胍作用于细胞48小时,对增殖有显著协同作用。荧光显微镜观察显示,与阴性对照组和单药治疗组相比,联合治疗组凋亡特征明显,凋亡率大幅增加。蛋白质免疫印迹法显示,与阴性对照组和单药治疗组相比,联合治疗组p - Bcl - 2、细胞周期蛋白D1和c - Myc的表达水平显著降低,而Bax的表达水平显著升高,联合治疗组p - IGF - IR、p - mTOR、p - P70S6K和p - S6的表达水平显著降低。

结论

维生素D3联合二甲双胍对SW - 780细胞的增殖和凋亡诱导具有明显抑制作用。潜在的抗肿瘤机制可能与抑制p - Bcl - 2、细胞周期蛋白D1、c - Myc、p - IGF - IR、p - mTOR、p - P70S6K、p - S6的表达以及激活Bax的表达有关。

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