Lanza Giovanni, Gafà Roberta, Maestri Iva, Santini Alessandra, Matteuzzi Maurizio, Cavazzini Luigi
Department of Experimental and Diagnostic Medicine, Section of Anatomic Pathology, University of Ferrara, Ferrara, Italy.
Mod Pathol. 2002 Jul;15(7):741-9. doi: 10.1097/01.MP.0000018979.68686.B2.
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.
检测具有高频微卫星不稳定性(MSI-H)的结直肠癌具有重要的临床意义,原因如下。近期研究表明,对MLH1和MSH2表达进行免疫组化分析是识别MSI-H表型大肠肿瘤的一种快速且准确的方法。在本研究中,我们通过免疫组化评估了132例MSI-H、23例MSI-L(低频微卫星不稳定性)和150例微卫星稳定(MSS)的结直肠腺癌中MLH1和MSH2蛋白的表达。在120例(90.9%)MSI-H癌中检测到MLH1或MSH2表达缺失,而所有MSI-L和MSS肿瘤均显示这两种蛋白的正常表达。观察到MLH1核染色缺失的情况比MSH2核染色缺失更为常见(分别为106例和14例)。在MSI-H癌中,MLH1/MSH2表达模式与几个临床和病理变量显著相关。特别是,MSI-H MLH1/MSH2阳性癌更常位于结肠远端,更常被分类为普通腺癌,并且比MLH1阴性和MSH2阴性癌更可能为高分化或中分化、p53阳性且直径<7 cm。此外,MLH1阴性癌在遗传性非息肉病性结直肠癌(HNPCC)或疑似HNPCC患者以及年龄<50岁的患者组中较少见。MLH1阴性癌患者比MLH1/MSH2阳性和MSH2阴性MSI-H肿瘤患者更常死于疾病,但差异无统计学意义。本研究结果强烈表明,对MLH1和MSH2表达进行免疫组化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阳性结直肠癌具有独特的病理特征。