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A two-antibody mismatch repair protein immunohistochemistry screening approach for colorectal carcinomas, skin sebaceous tumors, and gynecologic tract carcinomas

机译:两种抗体错配修复蛋白免疫组化的筛查方法用于大肠癌,皮肤皮脂瘤和妇科癌

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Mismatch repair protein immunohistochemistry is a widely used method for detecting patients at risk for Lynch syndrome. Recent data suggest that a two-antibody panel approach using PMS2 and MSH6 is an effective screening protocol for colorectal carcinoma, but there are limited data concerning this approach for extraintestinal tumors. The purpose of this study was to review the utility of a two-antibody panel approach in colorectal carcinoma and extraintestinal tumors. We evaluated mismatch repair protein expression in two cohorts: (1) a retrospective analysis of intestinal and extraintestinal tumors (n=334) tested for mismatch repair protein immunohistochemistry and (2) a prospectively accrued series of intestinal, gynecologic tract, and skin sebaceous neoplasms (n=98). A total of 432 cases were analyzed, including 323 colorectal, 50 gynecologic tract, 49 skin sebaceous, and 10 other neoplasms. Overall, 102/432 tumors (24%) demonstrated loss of at least one mismatch repair protein. Concurrent loss of MLH1 and PMS2 was the most common pattern of abnormal expression (50/432, 12%) followed by concurrent loss of MSH2 and MSH6 (33/432, 8%). Of 55 cases with abnormal PMS2 expression, 5 (9%) demonstrated isolated loss of PMS2 expression. Of 47 cases with abnormal MSH6 expression, 14 (30%) demonstrated isolated loss of MSH6 expression. Isolated loss of MLH1 or MSH2 was not observed. Colorectal carcinomas more frequently demonstrated abnormal expression of PMS2 (39/59, 66%). Skin sebaceous neoplasms more frequently demonstrated abnormal expression of MSH6 (18/24, 75%, respectively). A total of 65 tumors with abnormal mismatch repair protein expression were tested for microsatellite instability (MSI): 47 (72%) MSI high, 9 (14%) MSI low, and 9 (14%) microsatellite stable (MSS). Abnormal MSH6 expression accounted for 14/18 (78%) cases that were MSS or MSI low. Our findings confirm the utility of a two-antibody approach using PMS2 and MSH6 in colorectal carcinoma and indicate that this approach is effective in extraintestinal neoplasms associated with Lynch syndrome.
机译:错配修复蛋白免疫组化是一种广泛用于检测有Lynch综合征风险的患者的方法。最近的数据表明,使用PMS2和MSH6的二抗体小组方法是一种有效的结肠直肠癌筛查方案,但是有关这种方法用于肠外肿瘤的数据有限。这项研究的目的是审查两种抗体面板方法在大肠癌和肠外肿瘤中的实用性。我们在两个队列中评估了失配修复蛋白的表达:(1)对失配修复蛋白免疫组织化学测试的肠道和肠外肿瘤(n = 334)的回顾性分析,以及(2)肠道,妇科和皮肤皮脂瘤的前瞻性累积系列(n = 98)。共分析了432例病例,包括323例大肠,50例妇科,49例皮脂腺和10例其他肿瘤。总体而言,有102/432个肿瘤(占24%)表现出至少一种错配修复蛋白的缺失。 MLH1和PMS2并发丢失是最常见的异常表达模式(50/432,12 %),其次是MSH2和MSH6并发丢失(33/432,8 %)。在55例PMS2表达异常的病例中,有5例(9%)表现出单独的PMS2表达缺失。在47例MSH6表达异常的病例中,有14例(30%)表现出单独的MSH6表达缺失。未观察到MLH1或MSH2的单独丢失。大肠癌更频繁地表现出PMS2的异常表达(39 / 59,66%)。皮肤皮脂瘤更频繁地表现出MSH6的异常表达(分别为18 / 24、75%)。测试了总共65个错配修复蛋白表达异常的肿瘤的微卫星不稳定性(MSI):47(72 %)MSI高,9(14 %)MSI低和9(14 %)微卫星稳定(MSS) 。 MSH6表达异常占MSS或MSI低的14/18(78%)。我们的发现证实了使用PMS2和MSH6的两种抗体方法在结直肠癌中的实用性,并表明该方法在与Lynch综合征相关的肠外肿瘤中有效。

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