STEAP: A prostate-specific cell-surface antigen highly expressed in human prostate tumors

René Hubert(Genesys (United States)), Igor Vivanco(Genesys (United States)), Emily Chen(Genesys (United States)), Shiva Rastegar(Genesys (United States)), Kahan Leong(Genesys (United States)), S.C. Mitchell(Genesys (United States)), Rashida Madraswala(Genesys (United States)), Yanhong Zhou(Genesys (United States)), James Kuo(Genesys (United States)), Arthur Raitano(Genesys (United States)), Aya Jakobovits(Genesys (United States)), Douglas C. Saffran(Genesys (United States)), Daniel Afar(Genesys (United States))
Proceedings of the National Academy of Sciences
December 7, 1999
Cited by 356Open Access

Abstract

In search of novel genes expressed in metastatic prostate cancer, we subtracted cDNA isolated from benign prostatic hypertrophic tissue from cDNA isolated from a prostate cancer xenograft model that mimics advanced disease. One novel gene that is highly expressed in advanced prostate cancer encodes a 339-amino acid protein with six potential membrane-spanning regions flanked by hydrophilic amino- and carboxyl-terminal domains. This structure suggests a potential function as a channel or transporter protein. This gene, named STEAP for six-transmembrane epithelial antigen of the prostate, is expressed predominantly in human prostate tissue and is up-regulated in multiple cancer cell lines, including prostate, bladder, colon, ovarian, and Ewing sarcoma. Immunohistochemical analysis of clinical specimens demonstrates significant STEAP expression at the cell-cell junctions of the secretory epithelium of prostate and prostate cancer cells. Little to no staining was detected at the plasma membranes of normal, nonprostate human tissues, except for bladder tissue, which expressed low levels of STEAP at the cell membrane. Protein analysis located STEAP at the cell surface of prostate-cancer cell lines. Our results support STEAP as a cell-surface tumor-antigen target for prostate cancer therapy and diagnostic imaging.


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