Yamachika T, Nakanishi H, Inada K, Kitoh K, Kato T, Irimura T, Tatematsu M
Laboratory of Pathology, Aichi Cancer Center Research Institute, Nagoya, Japan.
Virchows Arch. 1997 Jul;431(1):25-30. doi: 10.1007/s004280050065.
Histochemical reports claim that sulfomucins decrease and sialylated mucins increase during colon carcinogenesis. We examined the expression of colon-specific sulfomucins and sialosyl Tn antigen (STN) in normal small intestine, normal colorectal mucosa and colorectal tumours at different stages of progression immunohistochemically, using MAb 91.9H specific for colonic sulfomucins and MAb TKH-2 for STN. No expression of sulfomucins recognized by MAb 91.9H was found in normal small intestine, whereas STN staining was pronounced. The converse was the case in normal colorectal mucosa. Sulfomucins were still found in adenomas, but the amounts decreased with depth of invasion in cancers (P < 0.001). In contrast, no STN could be detected in benign lesions, but staining became increasingly evident with invasion (P < 0.001). This reciprocal control of expression of colon-specific sulfomucins and STN evident in tumour progression indicates that the mucous phenotype shifts from the colonic to the small intestinal type.
组织化学报告称,在结肠癌发生过程中,硫酸黏蛋白减少,而唾液酸化黏蛋白增加。我们使用对结肠硫酸黏蛋白特异的单克隆抗体91.9H和对唾液酸Tn抗原(STN)的单克隆抗体TKH-2,通过免疫组织化学方法检测了正常小肠、正常结直肠黏膜以及不同进展阶段的结直肠肿瘤中结肠特异性硫酸黏蛋白和STN抗原的表达。在正常小肠中未发现单克隆抗体91.9H识别的硫酸黏蛋白表达,而STN染色明显。正常结直肠黏膜情况则相反。在腺瘤中仍可发现硫酸黏蛋白,但在癌组织中其含量随浸润深度而减少(P < 0.001)。相反,在良性病变中未检测到STN,但随着浸润其染色变得越来越明显(P < 0.001)。在肿瘤进展过程中结肠特异性硫酸黏蛋白和STN表达的这种相互调控表明,黏液表型从结肠型转变为小肠型。