Imanishi K, Tabuchi Y, Saitoh Y
First Department of Surgery, Kobe University School of Medicine, Japan.
Nihon Geka Gakkai Zasshi. 1988 Oct;89(10):1632-40.
Intracellular distribution of CEA, lectin binding sites including PNA, DBA and UEA-1, and quantity of nuclear DNA content were examined in 54 adenomas and 29 carcinomas of the colorectum. CEA was found in 40% and 60% of adenomas with mild and moderate dysplasia, and all carcinomas. In particular CEA which was diffusely distributed in the cytoplasm was found in 9% and 26% of adenomas with mild and moderate dysplasia, and in 79% of carcinomas. Both PNA and DBA were shown to have different binding sites in non-tumorous mucosa, adenoma and carcinoma. However, no difference was found in the binding sites of adenomas with different grades of dysplasia. Whereas, the binding sites of UEA-1 were demonstrated to differ with the degree of dysplasia in adenomas and also carcinomas: UEA-1 binding in the brush border was found to be 29%, 63%, and 80% in adenomas with mild and moderate dysplasia, and carcinomas respectively. Nuclear Feulgen DNA content increased in parallel with the grade of cellular dysplasia. All carcinomas exhibited polyploid cell over 4C greater than 8%. Thirty percent of adenomas with moderate dysplasia also showed the same polyploid cells as carcinomas. These results suggest that the changes of CEA distribution, binding sites of lectins and of nuclear Feulgen DNA in adenoma may indicate its malignant potential in the colorectum, and that these changes may occur before any histological malignant transformation.
对54例结肠直肠腺瘤和29例结肠癌进行了癌胚抗原(CEA)的细胞内分布、包括花生凝集素(PNA)、双花扁豆凝集素(DBA)和荆豆凝集素-1(UEA-1)的凝集素结合位点以及核DNA含量的检测。在轻度和中度发育异常的腺瘤中,分别有40%和60%发现了CEA,而在所有癌中均发现有CEA。特别是,在轻度和中度发育异常的腺瘤中,分别有9%和26%的细胞中发现CEA呈弥漫性细胞质分布,而在癌中这一比例为79%。结果显示,PNA和DBA在非肿瘤性黏膜、腺瘤和癌中的结合位点不同。然而,不同发育异常等级的腺瘤在结合位点上未发现差异。而UEA-1的结合位点在腺瘤和癌中均随发育异常程度不同而有差异:在轻度和中度发育异常的腺瘤以及癌中,UEA-1在刷状缘的结合率分别为29%、63%和80%。核福尔根DNA含量随细胞发育异常等级的升高而增加。所有癌中均有超过8%的细胞出现多倍体(大于4C)。30%中度发育异常的腺瘤也出现了与癌相同的多倍体细胞。这些结果提示,腺瘤中CEA分布、凝集素结合位点以及核福尔根DNA的变化可能提示其在结肠直肠中的恶性潜能,并且这些变化可能在任何组织学上的恶性转化之前就已发生。