Hepatocellular oncofetal protein, glypican 3 is a sensitive marker for α-fetoprotein-producing gastric carcinoma

被引:59
作者
Hishinuma, M.
Ohashi, K-I
Yamauchi, N.
Kashima, T.
Uozaki, H.
Ota, S.
Kodama, T.
Aburatani, H.
Fukayama, M.
机构
[1] Univ Tokyo, Grad Sch Med, Dept Pathol, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Toranomon Hosp, Dept Pathol, Tokyo, Japan
[3] Univ Tokyo, Genome Sci Div, Adv Sci & Technol Res Ctr, Tokyo, Japan
关键词
AFP; gastric carcinoma; glypican; 3; hepatoid adenocarcinoma; immunohistochemistry;
D O I
10.1111/j.1365-2559.2006.02522.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Glypican 3 (GPC3) is a cell surface heparan sulphate proteoglycan expressed specifically in the fetal liver and malignant neoplasms of hepatocyte lineage. The aim was to evaluate the significance of GPC3 in alpha-fetoprotein (AFP)-producing gastric carcinoma (GC) and other forms of GC. We immunohistochemically evaluated GPC3 expression in representative cases of AFP-producing GC and in a tissue microarray of a consecutive series of GCs with other markers of hepatocyte lineage (AFP, PIVKA-II and hepatocyte antigen, HEP). In a series of 10 cases of AFP-producing GC, we observed immunohistochemical positivity for GPC3, PIVKA-II and HEP in 10, three and three cases in components with a hepatoid pattern and in nine, two and five cases in components with a non-hepatoid pattern, respectively. In a series of 118 cases of GC, we observed positivity for AFP, GPC3, PIVKA-II and HEP in one (0.8%), four (3.4%), six (5.1%) and 26 cases (22%), respectively. GPC3 was observed concurrently with AFP and discordantly with PIVKA-II and HEP. GPC3 positivity was clearly stronger in a larger area compared with immunoreactivity for AFP. GPC3 is a sensitive marker for AFP-producing GC and its hepatoid component and is therefore useful to identify this aggressive subgroup of GC.
引用
收藏
页码:479 / 486
页数:8
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