GPR54 is a target for suppression of metastasis in endometrial cancer.


Journal Article

Invasion into deep myometrium and/or lymphovascular space is a well-known risk factor for endometrial cancer metastasis, resulting in poor prognosis. It is therefore clinically important to identify novel molecules that suppress tumor invasion. Reduced expression of the metastasis suppressor, kisspeptin (KISS1), and its endogenous receptor, GPR54, has been reported in several cancers, but the significance of the KISS1/GPR54 axis in endometrial cancer metastasis has not been clarified. Metastin-10 is the minimal bioactive sequence of genetic products of KISS1. Clinicopathological analysis of 92 endometrial cancers revealed overall survival is improved in cancers with high expression of GPR54 (P < 0.05) and that GPR54 expression is associated with known prognostic factors including FIGO stage, grade, and deep myometrial invasion. Through RNAi and microarray analyses, metastin-10 was predicted to suppress metastasis of GPR54-expressing endometrial cancers in vivo. Methylation analysis revealed GPR54 is epigenetically regulated. Metastin-GPR54 axis function was restored following treatment with the DNA hypomethylating agent 5-aza-DC. These data suggest that metastin-10 may be effective at inhibiting the metastatic spread of endometrial cancers in combination with demethylating agents to induce GPR54 expression.

Full Text

Duke Authors

Cited Authors

  • Kang, HS; Baba, T; Mandai, M; Matsumura, N; Hamanishi, J; Kharma, B; Kondoh, E; Yoshioka, Y; Oishi, S; Fujii, N; Murphy, SK; Konishi, I

Published Date

  • April 2011

Published In

Volume / Issue

  • 10 / 4

Start / End Page

  • 580 - 590

PubMed ID

  • 21282360

Pubmed Central ID

  • 21282360

Electronic International Standard Serial Number (EISSN)

  • 1538-8514

Digital Object Identifier (DOI)

  • 10.1158/1535-7163.MCT-10-0763


  • eng

Conference Location

  • United States