食管癌前病变的p53组织病理学/遗传学综合分析。

Cancer detection and prevention Pub Date : 2000-01-01
A V Safatle-Ribeiro, U Ribeiro, P Sakai, M R Clarke, S N Fylyk, S Ishioka, J Gama-Rodrigues, S D Finkelstein, J C Reynolds
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引用次数: 0

摘要

未标示:食管癌常见于长期贲门失弛缓症患者。目的:探讨p53改变和PCNA在食管肥大患者中的作用。方法:采用免疫组化方法对恰加斯病贲门失弛缓症患者的4个肿瘤及相应邻区切片进行p53和PCNA蛋白检测。此外,前瞻性地收集了16例晚期贲门失禁患者的128份活检,并评估了炎症、增生、不典型增生以及p53和PCNA蛋白的等级。所有显示p53免疫反应性的标本均采用显微解剖、PCR扩增和p53外显子5-8的直接测序进行地形基因分型。结果:2/4肿瘤中p53呈弥漫性强免疫反应性。1例患者邻近粘膜也显示强p53。在邻近粘膜中,p53过表达的相同区域也有PCNA阳性细胞。在前瞻性组中,7/16(43.7%)患者或53/128(41.4%)活检组织表达p53。炎症程度与p53阳性的存在显著相关,在患者中,p = 0.004,在活检中,p < 0.00001。PCNA表达于粘膜基底层,PCNA升高与p53过表达相关,p = 0.00018。1例(1/16,6.2%)患者基因分型检测到外显子6,密码子213 RG突变。结论:(1)p53的改变、过表达和突变改变是贲门失弛缓症患者的早期事件;(2)。在这些患者中常见的炎症似乎与p53蛋白的改变有关;(3)。肿瘤抑制基因的表达在显示增殖的区域增加。
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Integrated p53 histopathologic/genetic analysis of premalignant lesions of the esophagus.

Unlabelled: Esophageal carcinoma frequently occurs in patients with long-standing achalasia.

Aim: To examine the role of p53 alterations and PCNA in patients with megaesophagus.

Methods: Sections of four tumors, and corresponding adjacent areas, from patients with achalasia due to Chagas' disease were examined by immunohistochemistry for p53 and PCNA proteins. Furthermore, 128 biopsies from 16 advanced achalasic patients were prospectively collected and evaluated for grades of inflammation, hyperplasia, dysplasia and also for p53 and PCNA proteins. All specimens showing p53 immunoreactivity were topographically genotyped using microdissection, PCR amplification and direct sequencing of p53 exons 5-8.

Results: Diffuse strong immunoreactivity of p53 was observed in 2/4 tumors. In one patient, the adjacent mucosa also showed strong p53. In the adjacent mucosa, the same areas showing p53 overexpression also had PCNA positive cells. In the prospective group, 7/16 (43.7%) patients or 53/128 (41.4%) biopsies expressed p53. The grade of inflammation was significantly correlated with the presence of positive p53, in patients, p = 0.004 and in biopsies, p < 0.00001. PCNA expression was found in the basal layer of the mucosa, and increased PCNA was associated with p53 overexpression, p = 0.00018. Genotyping detected mutation in exon 6, codon 213 RG, in one patient (1/16, 6.2%).

Conclusions: (1.) p53 alterations, overexpression and mutational change, are an early event in patients with achalasia; (2.) The inflammation frequently seen in these patients appears to be associated with alterations of the p53 protein; (3.) Expression of the tumor suppressor gene is increased in areas showing proliferation.

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