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Microsatellite Instability in Korean Patients with Gastric Adenocarcinoma

OBJECTIVES: Microsatellites are short repeated oligonucleotide sequences found throughout the human genome. High mutation rates in microsatellite sequences have been found in tumors from patients with hereditary non-polyposis colorectal carcinoma and some sporadic carcinomas. However, little informa...

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Autores principales: Jee, Mi Seon, Koo, Cheol, Kim, Mi Hwa, Choi, Chan, Lee, Kwang Min, Choi, Sung Kyu, Rew, Jong Sun, Yoon, Chong Mann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531980/
https://www.ncbi.nlm.nih.gov/pubmed/9439149
http://dx.doi.org/10.3904/kjim.1997.12.2.144
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author Jee, Mi Seon
Koo, Cheol
Kim, Mi Hwa
Choi, Chan
Lee, Kwang Min
Choi, Sung Kyu
Rew, Jong Sun
Yoon, Chong Mann
author_facet Jee, Mi Seon
Koo, Cheol
Kim, Mi Hwa
Choi, Chan
Lee, Kwang Min
Choi, Sung Kyu
Rew, Jong Sun
Yoon, Chong Mann
author_sort Jee, Mi Seon
collection PubMed
description OBJECTIVES: Microsatellites are short repeated oligonucleotide sequences found throughout the human genome. High mutation rates in microsatellite sequences have been found in tumors from patients with hereditary non-polyposis colorectal carcinoma and some sporadic carcinomas. However, little information is available regarding RER-positive phenotype in gastric carcinomas, particularly in terms of age of onset and other pathologic features, such as histologic types, degree of differentiation, location or stage of the carcinoma. METHODS: To obtain a better understanding of the molecular mechanism of gastric carcinogenesis, microsatellite instability was examined at 6 gene loci (D2S71, D2S119, D3S1067, D6S87, D8S87, D11S905) in 77 gastric carcinomas (40 cases of young patients and 37 cases of elderly patients). RESULTS: RER-positive phenotypes were found in 17 (22.1%) of 77 cases. In young patients (under 40 years) RER-positive phenotype was found in 9 (22.5%) of 40 cases, and in elderly patients 8 (21.6%) of 37 cases. Moderately differentiated carcinoma revealed a significantly high frequency of RER-positive phenotype than well differentiated carcinoma (p<0.001). Tumors arising from the middle third (p<0.001) or lower third (p<0.001) revealed higher frequency of RER-positive phenotype than the tumors arising from the upper third of the stomach. The RER-positive phenotype was not significantly affected by the sex, histologic type or stage of carcinoma. CONCLUSION: RER-positive phenotype occurs frequently in gastric carcinoma, although the frequency of RER-positive phenotype between young and elderly patient was not significantly different. Thus, the acquisition of RER-positive phenotype might be an early event in gastric carcinogenesis.
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spelling pubmed-45319802015-10-02 Microsatellite Instability in Korean Patients with Gastric Adenocarcinoma Jee, Mi Seon Koo, Cheol Kim, Mi Hwa Choi, Chan Lee, Kwang Min Choi, Sung Kyu Rew, Jong Sun Yoon, Chong Mann Korean J Intern Med Original Article OBJECTIVES: Microsatellites are short repeated oligonucleotide sequences found throughout the human genome. High mutation rates in microsatellite sequences have been found in tumors from patients with hereditary non-polyposis colorectal carcinoma and some sporadic carcinomas. However, little information is available regarding RER-positive phenotype in gastric carcinomas, particularly in terms of age of onset and other pathologic features, such as histologic types, degree of differentiation, location or stage of the carcinoma. METHODS: To obtain a better understanding of the molecular mechanism of gastric carcinogenesis, microsatellite instability was examined at 6 gene loci (D2S71, D2S119, D3S1067, D6S87, D8S87, D11S905) in 77 gastric carcinomas (40 cases of young patients and 37 cases of elderly patients). RESULTS: RER-positive phenotypes were found in 17 (22.1%) of 77 cases. In young patients (under 40 years) RER-positive phenotype was found in 9 (22.5%) of 40 cases, and in elderly patients 8 (21.6%) of 37 cases. Moderately differentiated carcinoma revealed a significantly high frequency of RER-positive phenotype than well differentiated carcinoma (p<0.001). Tumors arising from the middle third (p<0.001) or lower third (p<0.001) revealed higher frequency of RER-positive phenotype than the tumors arising from the upper third of the stomach. The RER-positive phenotype was not significantly affected by the sex, histologic type or stage of carcinoma. CONCLUSION: RER-positive phenotype occurs frequently in gastric carcinoma, although the frequency of RER-positive phenotype between young and elderly patient was not significantly different. Thus, the acquisition of RER-positive phenotype might be an early event in gastric carcinogenesis. Korean Association of Internal Medicine 1997-06 /pmc/articles/PMC4531980/ /pubmed/9439149 http://dx.doi.org/10.3904/kjim.1997.12.2.144 Text en Copyright © 1997 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jee, Mi Seon
Koo, Cheol
Kim, Mi Hwa
Choi, Chan
Lee, Kwang Min
Choi, Sung Kyu
Rew, Jong Sun
Yoon, Chong Mann
Microsatellite Instability in Korean Patients with Gastric Adenocarcinoma
title Microsatellite Instability in Korean Patients with Gastric Adenocarcinoma
title_full Microsatellite Instability in Korean Patients with Gastric Adenocarcinoma
title_fullStr Microsatellite Instability in Korean Patients with Gastric Adenocarcinoma
title_full_unstemmed Microsatellite Instability in Korean Patients with Gastric Adenocarcinoma
title_short Microsatellite Instability in Korean Patients with Gastric Adenocarcinoma
title_sort microsatellite instability in korean patients with gastric adenocarcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531980/
https://www.ncbi.nlm.nih.gov/pubmed/9439149
http://dx.doi.org/10.3904/kjim.1997.12.2.144
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