Ushiku Tetsuo, Uozaki Hiroshi, Shinozaki Aya, Ota Satoshi, Matsuzaka Keisuke, Nomura Sachiyo, Kaminishi Michio, Aburatani Hiroyuki, Kodama Tatsuhiko, Fukayama Masashi
Department of Pathology and Diagnostic Pathology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Cancer Sci. 2009 Apr;100(4):626-32. doi: 10.1111/j.1349-7006.2009.01108.x. Epub 2009 Feb 19.
Gypican-3 (GPC3) has been recognized as an oncofetal protein in hepatic neoplasms and yolk sac tumors. To characterize a distinct subgroup of gastric carcinoma (GC) expressing GPC3 (GPC3-GC), primary and metastatic GC tissues were evaluated by immunohistochemistry with special focus on their related entities: hepatoid, clear-cell, and alpha-fetoprotein-producing GC. GPC3-GC was defined as focal GPC3-GC when 10-49% of neoplastic cells were positive, and as diffuse GPC3-GC when more than 50% of cells were positive. Among 926 GC cases, 101 (11%) were GPC3-GC, of which 45 were diffuse and 56 were focal GPC3-GC. Specific histological patterns, such as the hepatoid and clear-cell patterns, were frequently observed in diffuse GPC3-GC (38 and 49%, respectively) and in focal GPC3-GC (4 and 25%, respectively), whereas these patterns were extremely rare in GPC3-negative GC. Immunoreactive alpha-fetoprotein was only identified in GPC3-GC (38% of diffuse and 14% of focal GPC3-GC). Both diffuse and focal GPC3-GC showed nodal metastasis more frequently (67 and 55%, respectively) than GPC3-negative GC (34%), and the diffuse GPC3-GC had significantly more T2-4 and M1 stage cases. GPC3 immunostaining was present in 57 out of 61 nodal metastases (93%) and in all four liver metastases examined. Importantly, diffuse GPC3 expression was observed in the liver metastasis, even if the primary tumor was focal GPC3-GC. GPC3-GC is a distinctive group of GC, which unifies hepatoid, clear-cell, and alpha-fetoprotein-producing GC. GPC3 is expected to be a target of forthcoming immunotherapy for a patient bearing this specific type of GC.
Gypican-3(GPC3)已被确认为肝脏肿瘤和卵黄囊瘤中的一种癌胚蛋白。为了表征表达GPC3的胃癌(GC)的一个独特亚组(GPC3-GC),通过免疫组织化学对原发性和转移性GC组织进行了评估,特别关注其相关实体:肝样、透明细胞和产生甲胎蛋白的GC。当10%-49%的肿瘤细胞呈阳性时,GPC3-GC被定义为局灶性GPC3-GC;当超过50%的细胞呈阳性时,则被定义为弥漫性GPC3-GC。在926例GC病例中,101例(11%)为GPC3-GC,其中45例为弥漫性,56例为局灶性GPC3-GC。特定的组织学模式,如肝样和透明细胞模式,在弥漫性GPC3-GC中经常观察到(分别为38%和49%),在局灶性GPC3-GC中也有观察到(分别为4%和25%),而这些模式在GPC3阴性的GC中极为罕见。免疫反应性甲胎蛋白仅在GPC3-GC中被鉴定出来(弥漫性GPC3-GC的38%和局灶性GPC3-GC的14%)。弥漫性和局灶性GPC3-GC发生淋巴结转移的频率均高于GPC3阴性的GC(分别为67%和55%比34%),并且弥漫性GPC3-GC的T2-4期和M1期病例明显更多。在61例淋巴结转移中有57例(93%)存在GPC3免疫染色,在所检查所有4例肝转移中也都存在。重要的是,即使原发性肿瘤是局灶性GPC3-GC,在肝转移中也观察到弥漫性GPC3表达。GPC3-GC是GC的一个独特组群,它统一了肝样、透明细胞和产生甲胎蛋白的GC。GPC3有望成为针对患有这种特定类型GC患者的未来免疫治疗的靶点。