Epstein-Barr Virus-associated Gastric Carcinoma: A Distinct Carcinoma of Gastric Phenotype by Claudin Expression Profiling

Epstein-Barr Virus-associated Gastric Carcinoma: A Distinct Carcinoma of Gastric Phenotype by Claudin Expression Profiling
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DOI:
10.1369/jhc.2009.953810
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发表时间:
2009-08-01
影响因子:
3.2
通讯作者:
Fukayama, Masashi
Fukayama, Masashi
中科院分区:
生物学3区
文献类型:
--
作者:
Shinozaki, Aya;Ushiku, Tetsuo;Fukayama, Masashi

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EB病毒相关性胃癌是一种具有特征性临床病理特征的独特亚型。为了更好地描述其细胞特征,我们对43例EBV相关性胃癌、68例EBV阴性胃癌以及成人和胎儿的非肿瘤性胃粘膜进行了免疫组化检查。我们定量了主要紧密连接蛋白claudin(CLDN)-1、-3、-4、-7和-18以及胃粘蛋白(MUC 5AC和MUC 6)、肠粘蛋白(MUC 2)和CD 10的表达。EBV相关的GC显示CLDN 18表达的高频率(84%)和CLDN 3表达的低频率(5%)。该表达谱与成人和胎儿正常胃上皮的表达谱一致。几乎一半的EBV相关胃癌病例显示胃粘蛋白表达,而另一半缺乏粘蛋白或CD 10表达。相反,如CLDN 3和CLDN 18的表达谱所示,EBV阴性GC包括四种不同CLDN表型的异质组:胃、肠、混合和具有可变粘蛋白表达模式的未分化类型。这些结果表明,EBV相关的GC是相当同质的细胞分化方面,它很好地保留了原始细胞的性质。EBV相关的GC可能经历不同的致癌过程,这与EBV阴性的GC不同。(C)Histochem Cytochem 57:775-785,2009)
Epstein-Barr virus (EBV)-associated gastric carcinoma (GC) is a distinct subtype with characteristic clinicopathological features. To better characterize its cellular characteristics, 43 cases of EBV-associated GC, 68 cases of EBV-negative GC, and non-neoplastic gastric mucosa in adults and fetuses were examined immunohistochemically. We quantified the expression of the major tight-junction protein claudin (CLDN) -1, -3, -4, -7, and -18 together with gastric mucins (MUC5AC and MUC6), intestinal mucin (MUC2), and CD10. EBV-associated GC showed a high frequency of CLDN18 expression (84%) and a low frequency of CLDN3 expression (5%). This expression profile corresponded to that of normal gastric epithelium in adults and fetuses. Almost half of the EBV-associated GC cases demonstrated gastric mucin expression, whereas the other half lacked mucin or CD10 expression. In contrast, as demonstrated by the expression profiles of CLDN3 and CLDN18, EBV-negative GC comprised a heterogeneous group of four different CLDN phenotypes: gastric, intestinal, mixed, and an undifferentiated type with variable expression patterns of mucins. These results indicate that EBV-associated GC is considerably homogenous with regard to cellular differentiation and that it preserves well the nature of the cells of origin. EBV-associated GC may undergo distinct carcinogenic processes, which differ from those of EBV-negative GC. (C) Histochem Cytochem 57:775-785, 2009)