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Evaluation of colonoscopic sized biopsies for microsatellite instability and adenomatous polyposis coli (APC) variants
Author(s) -
Shamik Sengupta,
Pearson pearson,
Yiu,
Boulos
Publication year - 2000
Publication title -
colorectal disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.029
H-Index - 89
eISSN - 1463-1318
pISSN - 1462-8910
DOI - 10.1046/j.1463-1318.2000.00163.x
Subject(s) - medicine , microsatellite instability , adenomatous polyposis coli , familial adenomatous polyposis , colonoscopy , gastroenterology , colorectal cancer , microsatellite , general surgery , genetics , cancer , gene , allele , biology
Objective Knowledge of certain genetic changes associated with the development of colorectal cancer may influence surgical treatment in the future. Cancers are known to show intratumoural genetic heterogeneity. The aim of this study was to determine whether colonoscopic sized biopsies provide enough tissue to overcome the effects of tumour heterogeneity for the results of genetic analysis to be representative of the tumour as a whole. Patients and methods Using colonoscopic biopsy forceps, samples were taken from 30 resected colorectal cancers and investigated for microsatellite instability (MSI) at five loci and changes in the adenomatous polyposis coli gene (APC) by single‐stranded conformational polymorphism analysis. Identical genetic analysis was carried out on larger specimens taken from each of these cancers to determine whether the molecular findings from the large specimen were the same as those from colonoscopic sized biopsies. Results The microsatellite instability and APC status of the colonoscopic sized biopsies and those from larger specimens were completely consistent. Conclusion These results suggest that colonoscopic sized biopsies are reliable in determining the MSI status and APC variants of individual colorectal cancers.