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High frequency of microsatellite instability and loss of mismatch-repair protein expression in patients with double primary tumors of the endometrium and colorectum

机译:子宫内膜和结直肠双原发肿瘤患者微卫星不稳定性高,错配修复蛋白表达缺失

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摘要

BACKGROUND. Patients with the familial syndrome hereditary nonpolyposis colorectal carcinoma (HNPCC) exhibit air increased risk for several tumor types, of which the greatest lifetime risk is for colorectal and endometrial carcinoma. HNPCC is caused by a germline mutation in one of several identified mismatch repair (MMR) genes and typically presents with microsatellite instability (MSI) and frequent loss of NMR protein expression in the tumor tissue. The objective of this study was to estimate the proportion of double primary tumors of the endometrium and colorectum that displays tumor characteristics suggestive of MMR deficiency. METHODS. The authors used the southern Sweden regional population-based Cancer Registry to identify women who developed double primary tumors of tire endometrium and colorectum. Of the 256 women who were diagnosed with carcinoma at both of these sites during the period 1958-1998, 39 women had developed their first tumor before age 50 years. The authors successfully retrieved 67 tumors from 36 of these patients and analyzed them for MSI and immunohistochemical expression of the MMR genes, MLH1, MSH2, and MSH6. RESULTS. The MSI status of the 67 tumors was high MSI in 37 tumors, low MSI in 13 tumors, and microsatellite stable (MSS) in 17 tumors. Immunohistochemical loss of MMR protein expression was correlated with MSI status and was demonstrated in 29 high MSI turners, in 1 low MSI tumor, and in 1 MSS tumor. A concordant loss of the same MMR protein in both tumors was found in 12 of 27 patients. CONCLUSIONS. The authors demonstrated a high frequency of MSI (75%) in tumors from women with endometrial and colorectal carcinoma who had their first tumor diagnosed before age 50 years and observed concordant immunohistochemical loss of MMR protein expression, suggestive of a possible underlying germline mutation, in 12 of 27 patients (44%). They concluded that double primary malignancies of the colorectum and endometrium at a young age should make the clinician suspect (C) 2002 American Cancer Society.
机译:背景。家族性综合征遗传性非息肉病性大肠癌(HNPCC)患者表现出空气增加的几种肿瘤类型的风险,其中最大的终生风险是大肠癌和子宫内膜癌。 HNPCC是由几个已识别的错配修复(MMR)基因之一中的种系突变引起的,通常表现为微卫星不稳定性(MSI)和肿瘤组织中NMR蛋白表达的频繁丢失。这项研究的目的是估计子宫内膜和结直肠双重原发肿瘤的比例,这些肿瘤表现出提示MMR缺乏的肿瘤特征。方法。作者使用瑞典南部地区以人口为基础的癌症登记处来鉴定那些患有轮胎子宫内膜和结直肠双重原发性肿瘤的妇女。在1958年至1998年期间,在这两个地点被诊断出患有癌症的256名妇女中,有39名妇女在50岁之前出现了第一个肿瘤。作者成功地从这些患者中的36个中检索出67个肿瘤,并分析了它们的MSI以及MMR基因MLH1,MSH2和MSH6的免疫组织化学表达。结果。 67个肿瘤的MSI状态为:37个肿瘤中的MSI高,13个肿瘤中的MSI低,17个肿瘤中的微卫星稳定(MSS)。 MMR蛋白表达的免疫组织化学损失与MSI状态相关,并在29个高MSI肿瘤,1个低MSI肿瘤和1个MSS肿瘤中得到证实。在27名患者中的12名患者中,发现两种肿瘤中相同的MMR蛋白均出现一致减少。结论。作者证明,子宫内膜和大肠癌女性的肿瘤中MSI的发生率很高(75%),这些女性在50岁之前被诊断出第一个肿瘤,并且观察到MMR蛋白表达的免疫组织化学一致丧失,提示可能存在潜在的种系突变。 27名患者中的12名(44%)。他们得出的结论是,年轻时大肠癌和子宫内膜的双重原发性恶性肿瘤应使临床医生怀疑(C)2002 American Cancer Society。

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