Ohe Y, Hinoda Y, Irimura T, Imai K, Yachi A
Department of Internal Medicine (Section 1), Sapporo Medical University School of Medicine.
Jpn J Cancer Res. 1994 Apr;85(4):400-8. doi: 10.1111/j.1349-7006.1994.tb02373.x.
Expression of sulfated carbohydrate chains in intestinal metaplasia (IM) and gastric cancer tissues was immunohistochemically evaluated by using a monoclonal antibody (MAb) 91.9H. While normal gastric tissues were negative for MAb 91.9H, IM and cancer tissues were positively stained with high frequency. The incidence was 67% for IM with chronic gastritis (n = 12), 95% for IM with gastric cancer (n = 21), 77% for well and moderately differentiated adenocarcinoma (n = 13), 48% for poorly differentiated adenocarcinoma (n = 23), 89% for signet-ring cell carcinoma (n = 9) and 100% for mucinous adenocarcinoma (n = 7). When poorly differentiated adenocarcinoma cases were divided into two groups, solid (n = 13) and non-solid types (n = 10), the incidences were 8% and 100%, respectively. These data suggest that MAb 91.9H could be of practical use as a new marker for IM and gastric cancer, and may be valuable for subgrouping poorly differentiated adenocarcinomas. Analyses of the core proteins for 91.9H epitope were then carried out. Comparison of immunostaining of ten poorly differentiated adenocarcinoma cases by MAb MUSE11 against MUC1 gene product with that by MAb 91.9H suggested that 91.9H epitope is not expressed on MUC1. Northern blot analysis of 10 pairs of gastric cancer and adjacent normal tissues with a MUC2 cDNA probe showed that the expression level of MUC2 mRNA was below the limit of detection. Thus, 91.9H epitope may be expressed on other proteins than MUC1 or MUC2 core proteins in gastric cancer.
使用单克隆抗体(MAb)91.9H通过免疫组织化学方法评估肠化生(IM)和胃癌组织中硫酸化碳水化合物链的表达。正常胃组织对MAb 91.9H呈阴性,而IM和癌组织高频呈阳性染色。慢性胃炎伴IM的发生率为67%(n = 12),胃癌伴IM的发生率为95%(n = 21),高分化和中分化腺癌的发生率为77%(n = 13),低分化腺癌的发生率为48%(n = 23),印戒细胞癌的发生率为89%(n = 9),黏液腺癌的发生率为100%(n = 7)。当将低分化腺癌病例分为实体型(n = 13)和非实体型(n = 10)两组时,发生率分别为8%和100%。这些数据表明,MAb 91.9H可作为IM和胃癌的一种新的实用标志物,对低分化腺癌的亚组分类可能有价值。随后对91.9H表位的核心蛋白进行了分析。MAb MUSE11针对MUC1基因产物与MAb 91.9H对10例低分化腺癌病例的免疫染色比较表明,91.9H表位在MUC1上不表达。用MUC2 cDNA探针对10对胃癌及相邻正常组织进行Northern印迹分析显示,MUC2 mRNA的表达水平低于检测限。因此,91.9H表位可能在胃癌中表达于MUC1或MUC2核心蛋白以外的其他蛋白上。