Molecular Pathology and Genetics Division, Kanagawa Cancer Center Research Institute, 2-3-2 Nakao, Asahi Ward, Yokohama, Kanagawa, 241-8515, Japan; Department of Obstetrics and Gynecology, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa Ward, Yokohama, Kanagawa, 236-0004, Japan; Cancer Biology Division, Kanagawa Cancer Center Research Institute, 2-3-2 Nakao, Asahi Ward, Yokohama, Kanagawa, 241-8515, Japan.
Molecular Pathology and Genetics Division, Kanagawa Cancer Center Research Institute, 2-3-2 Nakao, Asahi Ward, Yokohama, Kanagawa, 241-8515, Japan; Department of Obstetrics and Gynecology, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa Ward, Yokohama, Kanagawa, 236-0004, Japan.
Biochem Biophys Res Commun. 2024 Dec 3;736:150890. doi: 10.1016/j.bbrc.2024.150890. Epub 2024 Oct 24.
Tissue factor pathway inhibitor-2 (TFPI2) is a Kunitz-type serine protease inhibitor and an ovarian clear cell carcinoma (CCC) biomarker. TFPI2 is expressed in several cancers and exerts tumor-suppressive effects; however, the role of TFPI2 in the CCC cell phenotype remains unclear. Therefore, in this study, we investigated the function of TFPI2 by establishing a gene knockout (KO) in ES-2 CCC cells and observed the change in phenotypes in vitro and in vivo. TFPI2 KO inhibited ES-2 cell proliferation, increased extracellular matrix protein adhesion, enhanced focal adhesion formation and activated integrin β1 cell surface clustering in vitro, and markedly increased ES-2 tumor growth and dissemination in the peritoneal cavity of a mouse xenograft model. These findings suggest a novel function of TFPI2 expression in suppressing the formation of focal adhesions in CCC cells, potentially by activating integrin β1. This function plays a role in the peritoneal growth characteristics of CCC cells.
组织因子途径抑制剂-2(TFPI2)是一种 Kunitz 型丝氨酸蛋白酶抑制剂,也是卵巢透明细胞癌(CCC)的生物标志物。TFPI2 在几种癌症中表达,并发挥肿瘤抑制作用;然而,TFPI2 在 CCC 细胞表型中的作用尚不清楚。因此,在这项研究中,我们通过在 ES-2 CCC 细胞中建立基因敲除(KO)来研究 TFPI2 的功能,并观察体外和体内表型的变化。TFPI2 KO 抑制 ES-2 细胞增殖,增加细胞外基质蛋白黏附,增强黏着斑形成,并激活整合素 β1 细胞表面聚集,显著增加 ES-2 肿瘤在小鼠异种移植模型腹腔中的生长和扩散。这些发现表明 TFPI2 表达在抑制 CCC 细胞黏着斑形成方面具有新的功能,可能通过激活整合素 β1。该功能在 CCC 细胞的腹膜生长特性中发挥作用。