McKenzie K J, Purnell D M, Shamsuddin A M
Department of Pathology, University of Maryland School of Medicine, Baltimore 21201.
Hum Pathol. 1987 Dec;18(12):1282-6. doi: 10.1016/s0046-8177(87)80414-8.
Several crypt abnormalities have been demonstrated in the mucosa of neoplastic and preneoplastic lesions of the large intestine. In addition, certain tumor markers are expressed in large intestinal carcinoma but not in normal mucosa. To determine whether any correlation exists between tumor marker expression and crypt abnormalities and at what stage markers are expressed, we studied specimens of large intestinal mucosa from 13 patients with preneoplastic conditions (adenomatous polyp, familial polyposis, Crohn's disease, and ulcerative colitis). The tumor markers examined include carcinoembryonic antigen (CEA), the ras gene products p21 and p21ser (mutated form), and beta-D-galactosyl-(1----3)-alpha-N-acetyl-D-galactosamine (gal--gal NAc, also known as T-antigen). Results were compared to those of five cases of adenocarcinoma of colon and three control cases of colonic mucosa obtained at immediate autopsy. All four markers were expressed in three of the five cases of adenocarcinoma, but none were expressed in the control cases. Variable expression of each marker was demonstrated in the dilated, distorted crypts of preneoplastic lesions. CEA and gal--gal NAc appeared to be expressed most frequently, suggesting that these are common markers or are expressed at an earlier stage in the neoplastic process than p21 or p21ser. Demonstration of such markers in preneoplastic conditions may be of use in determining the malignant potential and in monitoring these lesions.
在大肠肿瘤性和肿瘤前病变的黏膜中已证实存在几种隐窝异常。此外,某些肿瘤标志物在大肠癌中表达,但在正常黏膜中不表达。为了确定肿瘤标志物表达与隐窝异常之间是否存在任何相关性以及标志物在哪个阶段表达,我们研究了13例肿瘤前疾病(腺瘤性息肉、家族性息肉病、克罗恩病和溃疡性结肠炎)患者的大肠黏膜标本。所检测的肿瘤标志物包括癌胚抗原(CEA)、ras基因产物p21和p21ser(突变形式)以及β-D-半乳糖基-(1→3)-α-N-乙酰-D-半乳糖胺(gal--gal NAc,也称为T抗原)。将结果与5例结肠癌和3例尸检时立即获取的结肠黏膜对照病例的结果进行比较。在5例腺癌病例中的3例中所有4种标志物均有表达,但对照病例中均无表达。在肿瘤前病变扩张、变形的隐窝中显示出每种标志物的可变表达。CEA和gal--gal NAc似乎表达最为频繁,这表明这些是常见标志物,或者在肿瘤形成过程中比p21或p21ser更早表达。在肿瘤前疾病中证实这些标志物可能有助于确定恶性潜能并监测这些病变。