| Literature DB >> 12788060 |
Tetsuya Nakatsura1, Yoshihiro Yoshitake, Satoru Senju, Mikio Monji, Hiroyuki Komori, Yutaka Motomura, Seiji Hosaka, Toru Beppu, Takatoshi Ishiko, Hidenobu Kamohara, Hiroshi Ashihara, Toyomasa Katagiri, Yoichi Furukawa, Shigetoshi Fujiyama, Michio Ogawa, Yusuke Nakamura, Yasuharu Nishimura.
Abstract
With the global pandemic of hepatitis B and C infections, the incidence of Hepatocellular carcinoma (HCC) is rapidly increasing world wide. We identified glypican-3 (GPC3), a novel oncofetal gene over-expressed specifically in human HCC, as based on data of cDNA microarrays. As GPC3 is a GPI-anchored membrane protein and could be secreted, we attempted to detect secreted GPC3 protein in sera from HCC patients using Western blotting and ELISA. GPC3 protein was positive in sera of 40.0% (16/40) of HCC patients, and negative in sera from subjects with liver cirrhosis (LC) (0/13), chronic hepatitis (CH) (0/34), and healthy donors (0/60). All subjects were Japanese. Although 12 of 40 HCC patients were negative for both alpha-fetoprotein (AFP) and PIVKA-II well known tumor markers of HCC, four of these were GPC3-positive in the sera. We also observed vanishing GPC3 protein in the sera of three patients after the surgical treatment for HCC. On the other hand, immunohistochemical analysis revealed that HCC expressed GPC3 protein in all 14 HCC patients tested. In conclusion, GPC3, as defined in this study was shown to be a useful tumor marker for cancer-diagnosis for large numbers of patients with HCC.Entities:
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Year: 2003 PMID: 12788060 DOI: 10.1016/s0006-291x(03)00908-2
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575