Tissue factor pathway inhibitor-2 is specifically expressed in ovarian clear cell carcinoma tissues in the nucleus, cytoplasm and extracellular matrix

被引:19
|
作者
Ota, Yukihide [1 ,2 ]
Koizume, Shiro [1 ]
Nakamura, Yoshiyasu [1 ]
Yoshihara, Mitsuyo [1 ]
Takahashi, Tomoko [1 ]
Sato, Shinya [1 ]
Myoba, Shohei [3 ]
Ohtake, Norihisa [3 ]
Kato, Hisamori [4 ]
Yokose, Tomoyuki [5 ]
Miyagi, Etsuko [2 ]
Miyagi, Yohei [1 ]
机构
[1] Kanagawa Canc Ctr Res Inst, Mol Pathol & Genet Div, Yokohama, Kanagawa 2418515, Japan
[2] Yokohama City Univ, Dept Obstet & Gynecol, Grad Sch Med, Yokohama, Kanagawa 2360004, Japan
[3] Tosoh Corp, Biosci Div, Reagent Dev Dept, Ayase, Kanagawa 2521123, Japan
[4] Kanagawa Canc Ctr, Dept Gynecol Oncol, Yokohama, Kanagawa 2418515, Japan
[5] Kanagawa Canc Ctr, Dept Pathol, Yokohama, Kanagawa 2418515, Japan
关键词
TFPI-2; ovarian clear cell carcinoma; immunohistochemistry; biomarker; subcellular localization; TUMOR-MARKERS; CDNA CLONING; TFPI-2; GENE; INVASION; IDENTIFICATION; LOCALIZATION; PREECLAMPSIA; PROGRESSION; SURVIVAL;
D O I
10.3892/or.2021.7944
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:1023 / 1032
页数:10
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