Arai Tomio, Sugai Tamotsu, Kasahara Ichiro, Sawabe Motoji, Honma Naoko, Aida Junko, Nakamura Shin-Ichi, Takubo Kaiyo
Department of Pathology, Tokyo Metropolitan Geriatric Hospital, Tokyo, Japan.
Pathol Int. 2006 Oct;56(10):597-603. doi: 10.1111/j.1440-1827.2006.02014.x.
Microsatellite instability (MSI) is present in approximately 15-20% of sporadic colorectal cancers. However, despite the increased prevalence of absent hMLH1 expression and MSI in colorectal cancer in the elderly, few attempts have been made to define it in detail. The aim of the present paper was to correlate age-related alterations in absent hMLH1 expression and MSI with various histological types of colorectal carcinoma. hMLH1 expression and microsatellite status were studied in 184 colorectal carcinomas (49 well-differentiated, 49 moderately differentiated, 49 poorly differentiated adenocarcinomas, and 37 mucinous carcinomas). The prevalence of absent hMLH1 expression was higher in poorly differentiated adenocarcinoma (63%) and mucinous carcinoma (43%) than in well- (8%) and moderately (12%) differentiated adenocarcinomas. MSI was found more frequently in poorly differentiated adenocarcinoma (69%) and mucinous carcinoma (41%) than in well- and moderately differentiated adenocarcinomas (8% and 6%, respectively). Age-related differences in absent hMLH1 expression and MSI were found only in poorly differentiated adenocarcinoma, in which the prevalence of medullary-type carcinoma increased with advancing age. These results indicate that an age-related increase of medullary-type tumors in poorly differentiated adenocarcinoma may play an important role in the increase of absent hMLH1 expression and MSI in colorectal carcinoma.
微卫星不稳定性(MSI)存在于约15%-20%的散发性结直肠癌中。然而,尽管老年结直肠癌中hMLH1表达缺失和MSI的患病率有所增加,但很少有人尝试对其进行详细定义。本文的目的是将hMLH1表达缺失和MSI的年龄相关变化与各种组织学类型的结直肠癌相关联。对184例结直肠癌(49例高分化、49例中分化、49例低分化腺癌和37例黏液癌)进行了hMLH1表达和微卫星状态研究。低分化腺癌(63%)和黏液癌(43%)中hMLH1表达缺失的患病率高于高分化腺癌(8%)和中分化腺癌(12%)。低分化腺癌(占69%)和黏液癌(占41%)中MSI的发生率高于高分化腺癌和中分化腺癌(分别为8%和6%)。仅在低分化腺癌中发现hMLH1表达缺失和MSI的年龄相关差异,其中髓样癌的患病率随年龄增长而增加。这些结果表明,低分化腺癌中髓样型肿瘤的年龄相关增加可能在结直肠癌中hMLH1表达缺失和MSI的增加中起重要作用。