hMSH2 coordinated with the expression of E2F1 promotes platinum response in epithelial ovarian cancer

J Int Med Res. 2023 Mar;51(3):3000605231163780. doi: 10.1177/03000605231163780.

Abstract

Objective: To explore underlying mechanisms that regulate hMSH2 expression and drug susceptibility in epithelial ovarian cancer (EOC).

Methods: Using data from the Cancer Genome Atlas (TCGA) we used bioinformatical analysis to predict transcription factors (TFs) that potentially regulate hMSH2. RT-qPCR, Western blot, and luciferase assays were undertaken using ovarian cancer cell lines to verify the identified TF. Expressions of the TF were modulated using overexpression or knockdown, and the corresponding cellular responses to cisplatin were examined.

Results: The TF, E2F1, was found to regulate the hMSH2 gene. The expression level of E2F1 correlated with cisplatin susceptibility in vitro. Kaplan-Meier analysis of 77 patients with EOC showed that low E2F1 expression was associated with worse survival.

Conclusions: To our knowledge, this is the first report of E2F1 regulated MSH2 expression playing a role in drug resistance of platinum-based treatments for patients with EOC. Further work is need to confirm our results.

Keywords: E2F1; Mismatch repair; Platinum resistance; Transcription factors; hMSH2.

MeSH terms

  • Carcinoma, Ovarian Epithelial* / drug therapy
  • Carcinoma, Ovarian Epithelial* / genetics
  • Cell Line, Tumor
  • Cisplatin* / pharmacology
  • Drug Resistance, Neoplasm / genetics
  • E2F1 Transcription Factor* / genetics
  • E2F1 Transcription Factor* / metabolism
  • Female
  • Humans
  • Kaplan-Meier Estimate
  • MutS Homolog 2 Protein* / genetics
  • MutS Homolog 2 Protein* / metabolism
  • Ovarian Neoplasms* / drug therapy
  • Ovarian Neoplasms* / genetics
  • Ovarian Neoplasms* / metabolism
  • Platinum / pharmacology

Substances

  • Cisplatin
  • E2F1 protein, human
  • E2F1 Transcription Factor
  • Platinum
  • MSH2 protein, human
  • MutS Homolog 2 Protein