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The Study Of Microsatellite Alterations On Chromsome 18q In Sporadic Colorectal Cancer

Posted on:2003-05-06Degree:MasterType:Thesis
Country:ChinaCandidate:Y Z ZhanFull Text:PDF
GTID:2144360062496480Subject:Genetics
Abstract/Summary:PDF Full Text Request
Objective To detect the frequency of MA on 18q, to investigate the function of MA during the progress of pathogenesis in sporadic colorectal cancer. Methods By PCR, polyacrylamide gel-electrophoresis and silver staining, MA was detected at 4 microsatellite loci on chromsome 18q in tumor tissues,adjacent tissues and normal colorectum tissues excised from 34 cases with sporadic colorectal cancer . Results 12 cases demonstrated MA at one or more loci ,the total frequency was 35.29% (12/34). The frequency of MA on D18S34, D18S473 . D18S487, D18S58 was 20.59% (7/34), 17.64% ( 6/34), 11.76% (4/34X 17.64% (6/34) , respectively. In only one patieftfr adjacent tissues , MA was detected at one selected locus. The freguency of MA of poorly differentiated carcinomas and mucoid carcinomas (56.25%, 9/16) was significantly higher than that of well differentiated ones(16.67%, 3/18) , and the frequency in right colon( 61.53%, 8/13) was significantly higher than that in left colorectum (19.05%, 4/21). MA-positive cases were youngerthan negative ones ; there were no statistic significance ( P>0.05) in the frequency of MA between male (38.64%,7/19) and female(33.33%, 5/15) . Conclusions The most common MA occurrence at the 4 loci might imply the existence of the potential genes related to the carci nogenesis of colorectal cancer. and provide a effective index for early diagnosis of colonrectal cancer. Between MA positive and negative cases , some events were found as follows: tendency towards younger patients (usually<50 years in age), more frequentcy in right colon and more frequency in poorly differentiated carcinomas.
Keywords/Search Tags:Colorectal carcinoma, Microsatellite instability, Loss of heterozygosity, Polymerase chain reaction (PCR), Tumor suppressor gene
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