Tissue factor pathway inhibitor‑2 is specifically expressed in ovarian clear cell carcinoma tissues in the nucleus,

Yukihide Ota1, Shiro Koizume1, Yoshiyasu Nakamura1

  • 1Molecular Pathology and Genetics Division, Kanagawa Cancer Center Research Institute, Yokohama 241‑8515, Japan.

Oncology Reports
|March 2, 2021
PubMed

Insights

Tissue factor pathway inhibitor-2 (TFPI-2) is found in ovarian clear cell carcinoma (OCCC) tissues. Its high specificity suggests TFPI-2 could aid in diagnosing OCCC, a subtype of epithelial ovarian cancer.

Area of Science:

  • Oncology
  • Biochemistry
  • Molecular Biology

Background:

  • Tissue factor pathway inhibitor-2 (TFPI-2) is a secreted serine protease inhibitor with potential roles in cancer progression.
  • Previous research indicated nuclear TFPI-2 may act as a transcriptional repressor of matrix metalloproteinase-2 (MMP-2).
  • TFPI-2 is being investigated as a serum biomarker for ovarian clear cell carcinoma (OCCC), but its expression in OCCC tissues was unexamined.

Purpose of the Study:

  • To investigate the expression and localization of TFPI-2 in OCCC cell lines and patient tissues.
  • To evaluate TFPI-2's diagnostic potential for OCCC compared to other epithelial ovarian cancer (EOC) subtypes.

Main Methods:

  • Western blotting and enzyme-linked immune assay were used to analyze TFPI-2 expression in 11 OCCC cell lines.
  • Immunohistochemistry was employed to examine TFPI-2 levels and distribution in 77 OCCC tumors and 65 other EOC tissues.

Main Results:

  • TFPI-2 was detected in the nucleus, cytoplasm, and extracellular matrix in 67.5% of OCCC tumors.
  • TFPI-2 expression was absent in other EOC subtypes, yielding 100% specificity.
  • TFPI-2 expression distinguished OCCC from other EOCs with 67.5% sensitivity.

Conclusions:

  • TFPI-2 is expressed in the nucleus, cytoplasm, and extracellular matrix of OCCC tissues.
  • The high specificity of TFPI-2 for OCCC supports its potential use in diagnostic panels.
  • Further research may explore TFPI-2's role in OCCC pathogenesis and its combination with other markers for improved diagnosis.