Age-related alteration in the association of microsatellite instability with absent hMLH1 expression and histological types of colorectal carcinoma

被引:6
作者
Arai, Tomio
Sugai, Tamotsu
Kasahara, Ichiro
Sawabe, Motoji
Honma, Naoko
Aida, Junko
Nakamura, Shin-ichi
Takubo, Kaiyo
机构
[1] Tokyo Metropolitan Geriatr Hosp, Dept Pathol, Itabashi Ku, Tokyo 173, Japan
[2] Tokyo Metropolitan Inst Gerontol, Res Team Geriatr Dis, Tokyo, Japan
[3] Iwate Med Univ, Sch Med, Cent Clin Lab, Div Pathol, Morioka, Iwate 020, Japan
关键词
colorectal carcinoma; elderly; histological type; hMLH1; microsatellite instability;
D O I
10.1111/j.1440-1827.2006.02014.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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.
引用
收藏
页码:597 / 603
页数:7
相关论文
共 28 条
[1]   CLUES TO THE PATHOGENESIS OF FAMILIAL COLORECTAL-CANCER [J].
AALTONEN, LA ;
PELTOMAKI, P ;
LEACH, FS ;
SISTONEN, P ;
PYLKKANEN, L ;
MECKLIN, JP ;
JARVINEN, H ;
POWELL, SM ;
JEN, J ;
HAMILTON, SR ;
PETERSEN, GM ;
KINZLER, KW ;
VOGELSTEIN, B ;
DELACHAPELLE, A .
SCIENCE, 1993, 260 (5109) :812-816
[2]   Pathologic characteristics of colorectal cancer in the elderly [J].
Arai, T ;
Takubo, K ;
Sawabe, M ;
Esaki, Y .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 2000, 31 (01) :67-72
[3]   Hypermethylation of the hMLH1 promoter with absent hMLH1 expression in medullary-type poorly differentiated colorectal adenocarcinoma in the elderly [J].
Arai, T ;
Esaki, Y ;
Sawabe, M ;
Honma, N ;
Nakamura, K ;
Takubo, K .
MODERN PATHOLOGY, 2004, 17 (02) :172-179
[4]   Immunohistochemical pattern of hMSH2/hMLH1 in familial and sporadic colorectal, gastric, endometrial and ovarian carcinomas with instability in microsatellite sequences [J].
Chiaravalli, AM ;
Furlan, D ;
Facco, C ;
Tibiletti, MG ;
Dionigi, A ;
Casati, B ;
Albarello, L ;
Riva, C ;
Capella, C .
VIRCHOWS ARCHIV, 2001, 438 (01) :39-48
[5]  
Cravo M, 1999, J PATHOL, V188, P252, DOI 10.1002/(SICI)1096-9896(199907)188:3<252::AID-PATH354>3.0.CO
[6]  
2-3
[7]  
Gafà R, 2000, CANCER, V89, P2025, DOI 10.1002/1097-0142(20001115)89:10<2025::AID-CNCR1>3.0.CO
[8]  
2-S
[9]   Microsatellite instability of papillary subtype of human gastric adenocarcinoma and hMLH1 promoter hypermethylation in the surrounding mucosa [J].
Guo, RJ ;
Arai, H ;
Kitayama, Y ;
Igarashi, H ;
Hemmi, H ;
Arai, T ;
Hanai, H ;
Sugimura, H .
PATHOLOGY INTERNATIONAL, 2001, 51 (04) :240-247
[10]   Microsatellite instability testing in colorectal carcinoma: Choice of markers affects sensitivity of detection of mismatch repair-deficient tumors [J].
Hatch, SB ;
Lightfoot, HM ;
Garwacki, CP ;
Moore, DT ;
Calvo, BF ;
Woosley, JT ;
Sciarrotta, J ;
Funkhouser, WK ;
Farber, RA .
CLINICAL CANCER RESEARCH, 2005, 11 (06) :2180-2187