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  4. Intragenic homozygous deletions of MTS1 gene in gastric cancer in Taiwan
 
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Intragenic homozygous deletions of MTS1 gene in gastric cancer in Taiwan

Journal
Japanese Journal of Cancer Research
Journal Volume
87
Journal Issue
10
Pages
1052-1055
Date Issued
1996
Author(s)
MING-SHIANG WU  
Lin Y.-W.
JIN-CHUAN SHEU  
HSIU-PO WANG  
Wang, Jin-Town  
CHIA-TUNG SHUN  
Lee W.-J.
Wang T.-H.
Lin J.-T.
DOI
10.1111/j.1349-7006.1996.tb03109.x
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029826439&doi=10.1111%2fj.1349-7006.1996.tb03109.x&partnerID=40&md5=313e829dd17b16d0b2749da60278db74
https://scholars.lib.ntu.edu.tw/handle/123456789/417230
Abstract
The multiple tumor suppressor 1 (MTS1) and 2 (MTS2) genes, located on chromosome 9p21, have been reported to be deleted or mutated in many malignant cell lines and in a high percentage of some primary carcinomas. To determine whether these genes are altered, and if so, what is the nature of the alterations, in human gastric adenocarcinoma, we investigated their frequency of mutation by Southern blotting, polymerase chain reaction (PCR) and direct sequencing in 55 patients. Furthermore, loss of heterozygosity (LOH) of chromosome 9p21 at the IFNA locus and D9S171 was assessed. Homozygous deletions of exon 1 of the MTS1 gene were identified in 5 of 55 (9.1%) primary tumors. No deletion of MTS2 gene was noted. LOH was observed in 7 (14.3%) of 49 informative cases (5 cases at IFNA locus, 2 cases at D9S171 and one case with combined LOH at D9S171 and homozygous deletion at exon 1 of MTS1). Direct sequencing of PCR products of the MTS1 and MTS2 gene did not reveal any point mutation in these 55 patients. These data indicate that alterations of the MTS1 and MTS2 genes are infrequently encountered. Additional studies of LOH with more microsatellite markers near 9p21 are mandatory to elucidate whether another tumor suppressor gene exists in the vicinity of MTS2 in primary gastric adenocarcinoma.
SDGs

[SDGs]SDG3

Other Subjects
article; chromosome 9p; chromosome satellite; controlled study; deletion mutant; exon; heterozygosity; homozygosity; human; human cell; human tissue; major clinical study; mutation rate; nucleotide sequence; polymerase chain reaction; priority journal; Southern blotting; stomach adenocarcinoma; stomach cancer; Taiwan; tumor suppressor gene
Publisher
Japanese Cancer Association
Type
journal article

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