MiR-513a-3p promotes radiation-induced apoptosis of human lung cells by inhibiting glutathione S-transferase P1

Pharmazie. 2022 Apr 10;77(3):121-124. doi: 10.1691/ph.2022.1872.

Abstract

Radiotherapy is a common treatment for lung cancer. However, radiation pneumonitis caused by radiotherapy can affect the quality of life and prognosis of lung cancer patients. miR-513a-3p has been found to sensitize human lung adenocarcinoma cells to chemotherapy by targeting glutathione S-transferase P1 (GSTP1). Here, we found that x-ray induced the apoptosis of BEAS-2B and miR-513a-3p expression in a dose- and time-dependent manner, and miR-513a-3p-mimic significantly increased x-ray induced apoptosis, while miR-513a-3p-inhibitor significantly decreased x-ray induced apoptosis. Dual luciferase gene reporter system showed that miR-513a-3p targeted to inhibit the expression of GSTP1 in BEAS-2B cells. Moreover, knockdown of GSTP1 significantly increased, while overexpression of GSTP1 decreased the apoptosis of BEAS-2B induced by x-ray. Importantly, overexpression of GSTP1 significantly reduced miR-513a-3p-mimic elevated x-ray -induced apoptosis in BEAS-2B cells. In conclusion, x-ray caused increased expression of miR-513a-3p, and miR-513a-3p promoted x-ray-induced apoptosis of human lung cells by inhibiting GSTP1.

MeSH terms

  • Apoptosis* / genetics
  • Cell Proliferation
  • Glutathione Transferase* / metabolism
  • Humans
  • Lung / metabolism
  • Lung Neoplasms* / genetics
  • Lung Neoplasms* / radiotherapy
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Quality of Life

Substances

  • MIRN513A1 microRNA, human
  • MicroRNAs
  • Glutathione Transferase