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p53蛋白过表达与大肠腺瘤发育异常的组织学分级

Overexpression of p53 protein and histologic grades of dysplasia in colorectal adenomas.

作者信息

Sameshima S, Kubota Y, Sawada T, Watanabe T, Kuroda T, Tsuno N, Higuchi Y, Shinozaki M, Sunouchi K, Masaki T, Saito Y, Muto T

机构信息

Department of Surgery, Faculty of Medicine, University of Tokyo, Japan.

出版信息

Dis Colon Rectum. 1996 May;39(5):562-7. doi: 10.1007/BF02058712.

Abstract

PURPOSE

To clarify the relation between tumor-suppressor gene p53 expression and histologic grades of dysplasia in colorectal adenomas, we performed immunohistochemical analysis in a series of 59 colorectal polyps and 40 advanced carcinomas.

METHODS

Adenomatous polyps were stained by hematoxylin and eosin and classified into mild, moderate, and severe dysplasia (intramucosal carcinoma), according to the World Health Organization's classification.

RESULTS

p53 was positive in 7.1 percent (2/28) of mild, 29.4 percent (5/17) of moderate, and 62.5 percent (5/8) of severe dysplasia. In submucosal and advanced carcinomas, positivity rates were 75 percent (3/4) and 47.5 percent (19/40), respectively. Different staining patterns were found, according to grades of dysplasia. In the adenomas with mild or moderate dysplasia, a few focal crypts showed localized p53-positive staining. Adenomas with severe dysplasia had two different staining types. One was a focal staining type as shown in mild or moderate dysplasia; the other was a diffuse staining type, in which glands with mild or moderate dysplasia, surrounding severe dysplasia area, were also stained. Submucosal and advanced carcinomas showed a strong positive staining in cancer cells only.

CONCLUSIONS

Overexpression of p53 protein in adenomas with mild or moderate dysplasia and existence of two types of expression in adenomas with severe dysplasia were observed. These facts suggested the possible existence of different pathways in the adenoma to carcinoma progression.

摘要

目的

为阐明肿瘤抑制基因p53表达与大肠腺瘤发育异常的组织学分级之间的关系,我们对59例大肠息肉和40例进展期癌进行了免疫组化分析。

方法

腺瘤性息肉经苏木精和伊红染色,根据世界卫生组织的分类标准分为轻度、中度和重度发育异常(黏膜内癌)。

结果

p53在轻度发育异常中阳性率为7.1%(2/28),中度为29.4%(5/17),重度为62.5%(5/8)。在黏膜下癌和进展期癌中,阳性率分别为75%(3/4)和47.5%(19/40)。根据发育异常的分级发现了不同的染色模式。在轻度或中度发育异常的腺瘤中,少数局灶性隐窝显示局部p53阳性染色。重度发育异常的腺瘤有两种不同的染色类型。一种是如轻度或中度发育异常中所见的局灶性染色类型;另一种是弥漫性染色类型,其中围绕重度发育异常区域的轻度或中度发育异常的腺体也被染色。黏膜下癌和进展期癌仅在癌细胞中显示强阳性染色。

结论

观察到轻度或中度发育异常的腺瘤中p53蛋白过表达,以及重度发育异常的腺瘤中存在两种表达类型。这些事实提示腺瘤向癌进展过程中可能存在不同途径。

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