Drug repurposing: Metformin's effect against liver tissue damage in diabetes and prostate cancer model

Pınar Koroglu Aydın1, Ismet Burcu Turkyılmaz2, Ilknur Bugan Gul3

  • 1Faculty of Medicine, Department of Histology and Embryology, Halic University, Istanbul, Turkey.

Abstract

Insights

Metformin, an antidiabetic drug, significantly reduced liver damage in rats with prostate cancer and diabetes. This suggests metformin

Area of Science:

  • Oncology
  • Endocrinology
  • Hepatology

Background:

  • Diabetes mellitus is linked to the pathogenesis and progression of various cancers.
  • Metformin, a common antidiabetic medication, lowers circulating glucose and insulin levels, particularly in patients with insulin resistance and hyperinsulinemia.

Purpose of the Study:

  • To investigate the therapeutic potential of metformin in mitigating liver damage.
  • To evaluate the effects of metformin on liver tissue in rats with co-existing diabetes and prostate cancer.

Main Methods:

  • Male Copenhagen rats were assigned to six groups: control, diabetic, cancer, diabetic + cancer, and metformin-treated groups (diabetic + cancer + metformin, cancer + metformin).
  • Diabetes was induced using streptozotocin; prostate cancer was induced by inoculating Mat-LyLu cells.
  • Metformin was administered daily via gavage. Liver damage was assessed using histopathological scoring and biochemical analyses, including serum prostate-specific antigen (PSA) levels and hepatic enzyme activities.

Main Results:

  • Significant reductions in histopathological and biochemical markers of liver damage were observed in metformin-treated rats with cancer and diabetes.
  • Metformin treatment ameliorated liver injury in both cancer-induced and diabetes-induced conditions.

Conclusions:

  • The findings suggest that metformin possesses protective effects against liver tissue damage.
  • Metformin may be a viable therapeutic option for attenuating liver damage associated with prostate cancer and diabetes, highlighting its potential for drug repositioning.