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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.
Abstract:
Tissue factor pathway inhibitor‑2 (TFPI‑2) is a promising candidate as a serum biomarker of ovarian clear cell carcinoma (OCCC), a lethal histological subtype of epithelial ovarian cancer (EOC). TFPI‑2 is a secreted serine protease inhibitor that suppresses cancer progression through the inhibition of matrix protease activities. Previous studies have also identified TFPI‑2 in the nucleus, and a possible function of nuclear TFPI‑2 as a transcriptional repressor of matrix metalloproteinase‑2 (MMP‑2) was recently demonstrated. We are currently establishing TFPI‑2 as a serum biomarker for OCCC patients; however, TFPI‑2 expression in OCCC tissues has not been previously investigated. In the present study, we examined TFPI‑2 expression and its localization in 11 OCCC cell lines by western blotting and enzyme‑linked immune assay. Four cell lines expressed TFPI‑2 in the nucleus, cytoplasm and culture plate-attached extracellular fraction, while four other cell lines expressed TFPI‑2 only in the extracellular fraction. In the remaining three cell lines, TFPI‑2 was not identified in any fraction. The amount of secreted soluble TFPI‑2 showed similar trends to that of the plate‑attached fraction. We next investigated the expression levels and distribution of TFPI‑2 in surgically resected EOC tissues by immunohistochemistry. In 52 of the 77 (67.5%) OCCC tumors, TFPI‑2 expression was detected in at least one of the nuclear, cytoplasmic and extracellular matrix fractions. In contrast, we did not identify TFPI‑2 in the other EOC subtypes (n=65). TFPI‑2‑positive expression distinguished CCC from the other EOC tissues with a sensitivity of 67.5% and specificity of 100%. Although the inherent tumor suppressor function, statistical analyses failed to demonstrate correlations between TFPI‑2 expression and clinical parameters, including 5‑year overall survival, except for the patient age. In conclusion, we identified TFPI‑2 expression in the nucleus, cytoplasm and extracellular matrix in OCCC tissues. The high specificity of TFPI‑2 may support its use for diagnosis of OCCC in combination with existing markers.
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.
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