1. Academic Validation
  2. Metformin suppresses the growth of colorectal cancer by targeting INHBA to inhibit TGF-β/PI3K/AKT signaling transduction

Metformin suppresses the growth of colorectal cancer by targeting INHBA to inhibit TGF-β/PI3K/AKT signaling transduction

  • Cell Death Dis. 2022 Mar 2;13(3):202. doi: 10.1038/s41419-022-04649-4.
Qing Xiao 1 Jiani Xiao 1 Jiaqi Liu 1 Jiaxin Liu 1 Guang Shu 2 3 Gang Yin 4 5
Affiliations

Affiliations

  • 1 Department of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, 410013, China.
  • 2 Department of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, 410013, China. [email protected].
  • 3 Department of Histology and Embryology, School of Basic Medical Sciences, Central South University, Changsha, 410013, China. [email protected].
  • 4 Department of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, 410013, China. [email protected].
  • 5 China-Africa Research Center of Infectious Diseases, School of Basic Medical Sciences, Central South University, Changsha, 410013, China. [email protected].
Abstract

Multiple evidence shows that metformin serves as a potential agent for Colorectal Cancer (CRC) treatment, while its molecular mechanisms still require detailed investigation. Here, we revealed that metformin specifically suppressed the proliferation of CRC cells by causing G1/S arrest, and INHBA is a potential target for metformin to play an anti-proliferation effect in CRC. We verified the oncogene role of INHBA by knocking down and overexpressing INHBA in CRC cells. Silencing INHBA abrogated the cell growth, while overexpression INHBA promotes the proliferation of CRC cells. As an oncogene, INHBA was aberrant overexpression in CRC tissues and closely related to the poor prognosis of CRC patients. In mechanism, INHBA is an important ligand of TGF-β signaling and metformin blocked the activation of TGF-β signaling by targeting INHBA, and then down-regulated the activity of PI3K/Akt pathway, leading to the reduction of cyclinD1 and cell cycle arrest. Together, these findings indicate that metformin down-regulates the expression of INHBA, then attenuating TGF-β/PI3K/Akt signaling transduction, thus inhibiting the proliferation of CRC. Our study elucidated a novel molecular mechanism for the anti-proliferation effect of metformin, providing a theoretical basis for the application of metformin in CRC therapy.

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