Assessment of microsatellite instability in colorectal cancer patients from Brazil

被引:0
|
作者
Sinara M. O. Leite
Karina B. Gomes
Victor C. Pardini
Alessandro C. S. Ferreira
Vanessa C. Oliveira
Geraldo M. G. Cruz
机构
[1] Department of Coloproctology,Department of Human Genetics
[2] COLTEC,undefined
[3] Federal University of Minas Gerais,undefined
[4] Instituto H. Pardini,undefined
来源
Molecular Biology Reports | 2010年 / 37卷
关键词
Amsterdam II; Bethesda; Colorectal cancer; Microsatellite instability; Replication error status;
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学科分类号
摘要
The replication error status analysis of DNA, through microsatellite instability detection, has become an indispensable tool for hereditary non-polyposis colorectal cancer screening. This study investigated the microsatellite instability in Brazilian individuals presenting colorectal cancer. In this study, 66 patients were clinically analyzed according to Amsterdam II and Bethesda guidelines. Normal and tumour tissues were collected and analyzed for MSI degree according to molecular markers BAT25, BAT26, BAT40, APC–D5S346, D2S123, and D17S250. Eight patients (12.1%) fulfilled the Amsterdam II guidelines, and 15 (22.7%) met the Bethesda guidelines. BAT25 was the most sensitive marker (86.7%), while BAT26 was the least sensitive (66.7%). The specificity of both markers was 100%, but all of the markers must be used since the contribution of each marker to the sensitivity and specificity of the test is complementary. Proximal tumours were significantly predominant among RER+ patients. Conclusions: Patients with a family history of colorectal cancer with the tumour in the proximal colon must be screened to replication error status as early as possible in order to avoid the progression of the disease.
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页码:375 / 380
页数:5
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