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Metformin Elicits Antitumor Effects and Downregulates the Histone Methyltransferase Multiple Myeloma SET Domain (MMSET) in Prostate Cancer Cells
Author(s) -
WhiteAl Habeeb Nicole M. A.,
Garcia Julia,
Fleshner Neil,
Bapat Bharati
Publication year - 2016
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/pros.23235
Subject(s) - du145 , metformin , gene knockdown , prostate cancer , cancer research , pi3k/akt/mtor pathway , biology , medicine , lncap , endocrinology , cancer , cell culture , signal transduction , microbiology and biotechnology , genetics , diabetes mellitus
BACKGROUND This study explored the biological effects of metformin on prostate cancer (PCa) cells and determined molecular pathways and epigenetic regulators implicated in its mechanism of action. METHODS We performed mRNA expression profiling in 22Rv1 cells following 2.5 mM and 5 mM metformin treatment. Genes significantly modified by metformin treatment were ranked based on altered expression, involvement with cancer‐related processes, and reported dysregulation in PCa. The effects of the top ranked gene, MMSET, on the proliferative and invasive capabilities of PCa cells were investigated via siRNA knockdown alone and also combined with metformin treatment. RESULTS Metformin treatment decreased cell growth of PCa cell line 22Rv1 and stalled cells at the G1/S checkpoint in a time‐ and dose‐dependent manner, resulting in increased cells in G1 ( P < 0.05) and decreased cells in S ( P < 0.05) phase. Metformin activated the AMPK/mTOR signaling pathway as shown by increased p‐AMPK and decreased p‐p70S6K. mRNA expression profiling following metformin treatment identified significant changes in 136 chromatin‐modifying genes. The top ranked gene, multiple myeloma SET domain (MMSET) showed increased expression in PCa cell lines (22Rv1 and DU145) when compared to the benign prostate epithelium‐derived cell‐line RWPE‐1, and its expression was decreased upon metformin treatment. siRNA‐mediated knockdown of MMSET showed decreased cellular migration and invasion in DU‐145 cells. MMSET knockdown in combination with metformin treatment resulted in further reduction in the capacity of PCa cells to migrate and invade. CONCLUSIONS These data suggest MMSET may play a role in the inhibitory effect of metformin on PCa and could serve as a potential novel therapeutic target for PCa. Prostate 76:1507–1518, 2016 . © 2016 Wiley Periodicals, Inc.