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Metformin Inhibits Castration-Induced EMT in Prostate Cancer by Repressing COX2/PGE2/STAT3 Axis
Cancer Letters
  • Dali Tong
  • Qiuli Liu
  • Gaolei Liu
  • Jing Xu
  • Weihua Lan
  • Yao Jiang
  • Hualiang Xiao
  • Dianzheng Zhang, Philadelphia College of Osteopathic Medicine
  • Jun Jiang
Document Type
Article
Publication Date
12-30-2016
Abstract
Castration is the standard therapeutic treatment for advanced prostate cancer but with limited benefit due to the profound relapse and metastasis. Activation of inflammatory signaling pathway and initiation of epithelial-mesenchymal transition (EMT) are closely related to drug resistance, tumor relapseas well as metastasis. In this study, we demonstrated that metformin is capable of inhibiting prostate cancer cell migration and invasion by repressing EMT evidenced by downregulating the mesenchymal markers N-cadherin, Vimentin, and Twist and upregulating the epithelium E-cadherin. These effects have also been observed in our animal model as well as prostate cancer patients. In addition, we showed the effects of metformin on the expression of genes involved in EMT through repressing the levels of COX2, PGE2 and phosphorylated STAT3. Furthermore, inactivating COX2 abolishes metformin's regulatory effects and exogenously administered PGE2 is capable of enhancing STAT3 phosphorylation and expression of EMT biomarker. We propose that metformin represses prostate cancer EMT and metastasis through targeting the COX2/PGE2/STAT3 axis. These findings suggest that metformin by itself or in combination with other anticancer drugs could be used as an anti-metastasis therapy.
PubMed ID
28043910
Comments

This article was published in Cancer Letters, Volume 389, Pages 23-32.

The published version is available at http://dx.doi.org/S0304-3835(16)30801-1.

Copyright © 2016.

Citation Information
Dali Tong, Qiuli Liu, Gaolei Liu, Jing Xu, et al.. "Metformin Inhibits Castration-Induced EMT in Prostate Cancer by Repressing COX2/PGE2/STAT3 Axis" Cancer Letters Vol. 389 (2016) p. 23 - 32
Available at: http://works.bepress.com/dianzheng_zhang/49/