Hepsin colocalizes with desmosomes and induces progression of ovarian cancer in a mouse model

✍ Scribed by Jiangyong Miao; David Mu; Burce Ergel; Rajasekhar Singavarapu; Zhenfeng Duan; Scott Powers; Esther Oliva; Sandra Orsulic

• Book ID: 102270271
• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: French
• Weight: 350 KB
• Volume: 123
• Category: Article
• ISSN: 0020-7136
• DOI: 10.1002/ijc.23726

✦ Synopsis

Abstract

Hepsin is a serine protease that is widely expressed in different tissues and cell types, most prominently in the normal liver and kidney. Overexpression of hepsin has been associated with prostate cancers, ovarian cancers and renal cell carcinomas. The physiological functions of hepsin in normal tissues and tumors are poorly understood. To gain insight into its function in ovarian cancer, we analyzed the expression and subcellular localization of hepsin protein in ovarian cancer cell lines and tumors. We showed that the membrane‐associated hepsin protein is present at desmosomal junctions, where it colocalizes with its putative proteolytic substrate hepatocyte growth factor. Consistent with the growing evidence that desmosomal junctions and their constituents play a role in cancer progression, we demonstrated that overexpression of hepsin promotes ovarian tumor growth in a mouse model. The ability of ectopic hepsin to induce tumor growth in mice is abrogated by the mutation of 3 critical residues in the catalytic domain, thus implicating the enzymatic activity of hepsin in promoting tumor progression. © 2008 Wiley‐Liss, Inc.