Microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomas

被引:49
作者
Chapusot, C
Martin, L
Bouvier, AM
Bonithon-Kopp, C
Ecarnot-Laubriet, A
Rageot, D
Ponnelle, T
Puig, PL
Faivre, J
Piard, F
机构
[1] CHU Dijon, Serv Anat Pathol, Fac Med, F-21079 Dijon, France
[2] Fac Med, INSERM EPI 0106, IFR 100, F-21079 Dijon, France
[3] Lab Toxicol Med, U490, F-75006 Paris, France
关键词
colon carcinoma; right-sided colon; carcinogenesis; microsatellite instability; mismatch repair; intratumoural heterogeneity;
D O I
10.1038/sj.bjc.6600474
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Microsatellite instability has been proposed as an alternative pathway of colorectal carcinogenesis. The aim of this study was to evaluate the interest of immunohistochemistry as a new tool for highlighting mismatch repair deficiency and to compare the results with a PCR-based microsatellite assay. A total of 100 sporadic proximal colon adenocarcinomas were analysed, The expression of hMLH1, hMSH2 and hMSH6 proteins evaluated by immunohistochemistry was altered in 39% of the cancers, whereas microsatellite instability assessed by PCR was detected in 43%. There was discordance between the two methods in eight cases. After further analyses performed on other tumoural areas for these eight cases, total concordance between the two techniques was observed (Kappa=100%). Our results demonstrate that immunohistochemistry may be as efficient as microsatellite amplification in the detection of unstable phenotype provided that at least two samples of each carcinoma are screened, because of intratumoural heterogeneity. (C) 2002 Cancer Research UK.
引用
收藏
页码:400 / 404
页数:5
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