TY - JOUR
T1 - Hepatocellular oncofetal protein, glypican 3 is a sensitive marker for α-fetoprotein-producing gastric carcinoma
AU - Hishinuma, M.
AU - Ohashi, K. I.
AU - Yamauchi, N.
AU - Kashima, T.
AU - Uozaki, H.
AU - Ota, S.
AU - Kodama, T.
AU - Aburatani, H.
AU - Fukayama, M.
PY - 2006/11
Y1 - 2006/11
N2 - Aims: 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 α-fetoprotein (AFP)-producing gastric carcinoma (GC) and other forms of GC. Methods and results: 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. Conclusions: GPC3 is a sensitive marker for AFP-producing GC and its hepatoid component and is therefore useful to identify this aggressive subgroup of GC.
AB - Aims: 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 α-fetoprotein (AFP)-producing gastric carcinoma (GC) and other forms of GC. Methods and results: 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. Conclusions: GPC3 is a sensitive marker for AFP-producing GC and its hepatoid component and is therefore useful to identify this aggressive subgroup of GC.
KW - AFP
KW - Gastric carcinoma
KW - Glypican 3
KW - Hepatoid adenocarcinoma
KW - Immunohistochemistry
UR - https://www.scopus.com/pages/publications/33748548525
U2 - 10.1111/j.1365-2559.2006.02522.x
DO - 10.1111/j.1365-2559.2006.02522.x
M3 - 記事
C2 - 17064293
AN - SCOPUS:33748548525
SN - 0309-0167
VL - 49
SP - 479
EP - 486
JO - Histopathology
JF - Histopathology
IS - 5
ER -