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Abstract Title:

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

Abstract Source:

Pharmazie. 2015 Feb ;70(2):123-8. PMID: 25997253

Abstract Author(s):

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

Article Affiliation:

Li-Shu Guo

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 320μg/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 ofBax 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.

Study Type : In Vitro Study

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Sayer Ji
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