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Immunohistochemical Pattern of MLH1/MSH2 Expression Is Related to Clinical and Pathological Features in Colorectal Adenocarcinomas with Microsatellite Instability

机译:MLH1 / MSH2表达的免疫组织化学模式与微卫星不稳定性大肠腺癌的临床和病理特征有关

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Detection of colorectal carcinomas with high-frequency microsatellite instability (MSI-H) is clinically important for several reasons. Recent studies suggested that immunohistochemical analysis of MLH1 and MSH2 expression is a rapid and accurate method for identifying large bowel tumors of the MSI-H phenotype. In this study, we evaluated by immunohistochemistry MLH1 and MSH2 protein expression in 132 MSI-H, 23 MSI-L (low-frequency MSI), and 150 microsatellite stable (MSS) colorectal adenocarcinomas. Loss of MLH1 or MSH2 expression was detected in 120 (90.9%) MSI-H carcinomas, whereas all MSI-L and MSS tumors showed normal expression of both proteins. Lack of MLH1 nuclear staining was observed much more often than absence of MSH2 nuclear staining (106 and 14 cases, respectively). Among MSI-H carcinomas, MLH1/MSH2 pattern of expression was significantly related to several clinical and pathological variables. In particular, MSI-H MLH1/MSH2-positive carcinomas were more often located in the distal colon, were more frequently classified as ordinary adenocarcinomas, and were more likely to be well or moderately differentiated, p53 positive, and <7 cm in diameter than were MLH1-negative and MSH2-negative carcinomas. In addition, MLH1-negative carcinomas were less common among patients with hereditary nonpolyposis colorectal cancer (HNPCC) or suspected HNPCC and in the group of patients aged <50 years. Patients with MLH1-negative carcinomas more frequently died of disease than did patients with MLH1/MSH2-positive and MSH2-negative MSI-H tumors, but the difference was not statistically significant. The results of the present investigation strongly indicate that immunohistochemical analysis of MLH1 and MSH2 expression is a practical and reliable method for the routine detection of the vast majority of MSI-H large bowel adenocarcinomas. Our data also point out that MSI-H MLH1/MSH2-positive colorectal carcinomas are characterized by distinctive pathological features.
机译:由于多种原因,具有高频微卫星不稳定性(MSI-H)的大肠癌检测在临床上很重要。最近的研究表明,MLH1和MSH2表达的免疫组织化学分析是鉴定MSI-H表型大肠肿瘤的一种快速而准确的方法。在这项研究中,我们通过免疫组化评估了132 MSI-H,23 MSI-L(低频MSI)和150个微卫星稳定(MSS)大肠腺癌中MLH1和MSH2蛋白的表达。在120个(90.9%)MSI-H癌中检测到MLH1或MSH2表达缺失,而所有MSI-L和MSS肿瘤均显示两种蛋白均正常表达。缺少MLH1核染色的频率比没有MSH2核染色的频率更高(分别为106和14例)。在MSI-H癌症中,MLH1 / MSH2的表达模式与几种临床和病理变量显着相关。特别是,MSI-H MLH1 / MSH2阳性癌更常位于远端结肠,被更频繁地分类为普通腺癌,并且与之相比,其分化程度更好或中等,p53阳性且直径小于7 cm是MLH1阴性和MSH2阴性的癌症。此外,在遗传性非息肉性结直肠癌(HNPCC)或疑似HNPCC的患者中以及年龄在<50岁的患者组中,MLH1阴性的癌症较少见。与MLH1 / MSH2阳性和MSH2阴性的MSI-H肿瘤患者相比,MLH1阴性癌患者死于疾病的几率更高,但差异无统计学意义。本研究的结果强烈表明,MLH1和MSH2表达的免疫组织化学分析是常规检测绝大多数MSI-H大肠腺癌的一种实用且可靠的方法。我们的数据还指出,MSI-H MLH1 / MSH2阳性结直肠癌的特征在于独特的病理特征。

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