Polycomb Protein BMI-1 as a Potential Therapeutic Target in Mucinous Ovarian Cancer

Anticancer Res. 2022 Apr;42(4):1739-1747. doi: 10.21873/anticanres.15650.

Abstract

Background/aim: Mucinous ovarian carcinoma (mOC) is a rare subtype with distinct clinical characteristics and biological behavior that differentiate them from other epithelial ovarian cancers. This study aimed to evaluate BMI-1 expression as a potential target for therapeutic approaches in advanced stage mOC.

Materials and methods: We performed gene set, as well as transcription factor enrichment analysis and immunohistochemistry assessing of the BMI-1 protein levels in tissue specimens of eighteen mucinous ovarian cancer patients. To validate the clinical relevance of the findings, we performed cell viability assays and western blot analysis utilizing high-grade serous (HGSC) and mOC cell lines.

Results: BMI1 expression was not significantly associated with patient age, FIGO stage, lymph node status, and family history. With regard to progression-free survival, there was also no significant association (p=0.418). Cell viability was significant decreased in response to carboplatin in HGSC cells TYK-nu and OVHASO, and in mOC cell lines COV644 and EFO-27. Western blot analysis demonstrated various expression levels across all cell lines.

Conclusion: BMI-1 could be a useful potential therapeutic target in some ovarian cancer patients, including mOC patients.

Keywords: BMI-1; Polycomb protein; cancer stem cell; chemoresistance; mucinous ovarian carcinoma.

MeSH terms

  • Adenocarcinoma, Mucinous* / drug therapy
  • Adenocarcinoma, Mucinous* / genetics
  • Body Mass Index
  • Carcinoma, Ovarian Epithelial / drug therapy
  • Carcinoma, Ovarian Epithelial / genetics
  • Female
  • Humans
  • Ovarian Neoplasms* / drug therapy
  • Ovarian Neoplasms* / genetics
  • Polycomb Repressive Complex 1* / genetics

Substances

  • BMI1 protein, human
  • Polycomb Repressive Complex 1