Metformin potentiates the effects of paclitaxel in endometrial cancer cells through inhibition of cell proliferation and modulation of the mTOR pathway |
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Authors: | Hanna Rabbie K Zhou Chunxiao Malloy Kimberly M Sun Li Zhong Yan Gehrig Paola A Bae-Jump Victoria L |
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Institution: | a University of North Carolina, Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Chapel Hill, NC, USAb Department of Gynecologic Oncology, Shandong Cancer Hospital, Shandong, Chinac Department of Gynecologic Oncology, Linyi Tumor Hospital, Shandong, China |
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Abstract: | ObjectivesTo examine the effects of combination therapy with metformin and paclitaxel in endometrial cancer cell lines.MethodsECC-1 and Ishikawa endometrial cancer cell lines were used. Cell proliferation was assessed after exposure to paclitaxel and metformin. Cell cycle progression was assessed by flow cytometry. hTERT expression was determined by real-time RT-PCR. Western immunoblotting was performed to determine the effect of metformin/paclitaxel on the mTOR pathway.ResultsPaclitaxel inhibited proliferation in a dose-dependent manner in both cell lines with IC50 values of 1-5 nM and 5-10 nM for Ishikawa and ECC-1 cells, respectively. Simultaneous exposure of cells to various doses of paclitaxel in combination with metformin (0.5 mM) resulted in a significant synergistic anti-proliferative effect in both cell lines (Combination Index < 1). Metformin induced G1 arrest in both cell lines. Paclitaxel alone or in combination with metformin resulted in predominantly G2 arrest. Metformin decreased hTERT mRNA expression while paclitaxel alone had no effect on telomerase activity. Metformin stimulated AMPK phosphorylation and decreased phosphorylation of the S6 protein. In contrast, paclitaxel inhibited AMPK phosphorylation in the ECC-1 cell line and induced phosphorylation of S6 in both cell lines. Treatment with metformin and paclitaxel resulted in decreased phosphorylation of S6 in both cell lines but only had an additive effect on AMPK phosphorylation in the ECC-1 cell line.ConclusionsMetformin potentiates the effects of paclitaxel in endometrial cancer cells through inhibition of cell proliferation and modulation of the mTOR pathway. This combination may be a promising targeted therapy for endometrial cancer. |
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Keywords: | Endometrial cancer Metformin Paclitaxel mTOR pathway |
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