Microsatellite instability in solitary and sporadic gastric cancer

Detalhes bibliográficos
Autor(a) principal: Perez,Rodrigo Oliva
Data de Publicação: 2004
Outros Autores: Jacob,Carlos Eduardo, D'Ottaviano,Fabricio L'ofreddo, Alvarenga,Conrado, Ribeiro,Adriana Safatle, Ribeiro Jr.,Ulysses, Bresciani,Cláudio José Caldas, Zilberstein,Bruno, Krieger,José Eduardo, Habr-Gama,Angelita, Gama-Rodrigues,Joaquim José
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista do Hospital das Clínicas
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0041-87812004000500010
Resumo: Recently, the presence of microsatellite instability (MSI) has been reported in gastric cancer and associated with older age of presentation, distal tumor location, early disease staging, and better overall prognosis. Different characteristics in presentation and in tumor behavior may be explained by different genetic alterations during carcinogenesis of gastric cancer. Identification of specific genetic pathways in gastric cancer may have direct impact on prognosis and selection of treatment strategies. PATIENTS AND METHODS: All 24 patients were treated by radical surgery. Fragments of normal and tumor tissues were extracted from the specimen and stored at -80ºC before DNA purification and extraction. PCR amplification utilizing microsatellite markers was performed. Tumors presenting PCR products of abnormal sizes were considered positive for microsatellite instability (MSI+). RESULTS: Five patients (21%) had tumors that were MSI+ in at least 1 marker. In the group of patients with Lauren's intestinal-type gastric carcinoma, 3 had tumors that were MSI+ (23%), while in the group of diffuse-type gastric cancer, 2 patients had tumors that were MSI+ (19%). The mean age of presentation and the male:female ratio was similar in both groups. Tumors that were MSI+ were more frequently located in proximal portion of the stomach compared to microsatellite-stable (MSS) tumors (40% vs. 16%). Although there was a trend of patients with MSI+ tumors towards a proximal gastric tumor location, early staging, and negative lymph node metastasis, there was no statistical significance compared to those with MSS tumors (P >.1). Comparison of overall and disease-free survival between gastric tumors that were MSI+ and those that were MSS found no statistically significant differences (P >.1). CONCLUSIONS: Microsatellite instability is a frequent event in gastric carcinogenesis and shows a trend towards distinct clinical and pathological characteristics of gastric cancer.
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spelling Microsatellite instability in solitary and sporadic gastric cancerGastric cancerGeneticsMicrosatellite instabilityRecently, the presence of microsatellite instability (MSI) has been reported in gastric cancer and associated with older age of presentation, distal tumor location, early disease staging, and better overall prognosis. Different characteristics in presentation and in tumor behavior may be explained by different genetic alterations during carcinogenesis of gastric cancer. Identification of specific genetic pathways in gastric cancer may have direct impact on prognosis and selection of treatment strategies. PATIENTS AND METHODS: All 24 patients were treated by radical surgery. Fragments of normal and tumor tissues were extracted from the specimen and stored at -80ºC before DNA purification and extraction. PCR amplification utilizing microsatellite markers was performed. Tumors presenting PCR products of abnormal sizes were considered positive for microsatellite instability (MSI+). RESULTS: Five patients (21%) had tumors that were MSI+ in at least 1 marker. In the group of patients with Lauren's intestinal-type gastric carcinoma, 3 had tumors that were MSI+ (23%), while in the group of diffuse-type gastric cancer, 2 patients had tumors that were MSI+ (19%). The mean age of presentation and the male:female ratio was similar in both groups. Tumors that were MSI+ were more frequently located in proximal portion of the stomach compared to microsatellite-stable (MSS) tumors (40% vs. 16%). Although there was a trend of patients with MSI+ tumors towards a proximal gastric tumor location, early staging, and negative lymph node metastasis, there was no statistical significance compared to those with MSS tumors (P >.1). Comparison of overall and disease-free survival between gastric tumors that were MSI+ and those that were MSS found no statistically significant differences (P >.1). CONCLUSIONS: Microsatellite instability is a frequent event in gastric carcinogenesis and shows a trend towards distinct clinical and pathological characteristics of gastric cancer.Faculdade de Medicina / Universidade de São Paulo - FM/USP2004-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0041-87812004000500010Revista do Hospital das Clínicas v.59 n.5 2004reponame:Revista do Hospital das Clínicasinstname:Universidade de São Paulo (USP)instacron:USP10.1590/S0041-87812004000500010info:eu-repo/semantics/openAccessPerez,Rodrigo OlivaJacob,Carlos EduardoD'Ottaviano,Fabricio L'ofreddoAlvarenga,ConradoRibeiro,Adriana SafatleRibeiro Jr.,UlyssesBresciani,Cláudio José CaldasZilberstein,BrunoKrieger,José EduardoHabr-Gama,AngelitaGama-Rodrigues,Joaquim Joséeng2004-10-29T00:00:00Zoai:scielo:S0041-87812004000500010Revistahttp://www.scielo.br/rhcPUBhttps://old.scielo.br/oai/scielo-oai.php||revista.hc@hcnet.usp.br1678-99030041-8781opendoar:2004-10-29T00:00Revista do Hospital das Clínicas - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Microsatellite instability in solitary and sporadic gastric cancer
title Microsatellite instability in solitary and sporadic gastric cancer
spellingShingle Microsatellite instability in solitary and sporadic gastric cancer
Perez,Rodrigo Oliva
Gastric cancer
Genetics
Microsatellite instability
title_short Microsatellite instability in solitary and sporadic gastric cancer
title_full Microsatellite instability in solitary and sporadic gastric cancer
title_fullStr Microsatellite instability in solitary and sporadic gastric cancer
title_full_unstemmed Microsatellite instability in solitary and sporadic gastric cancer
title_sort Microsatellite instability in solitary and sporadic gastric cancer
author Perez,Rodrigo Oliva
author_facet Perez,Rodrigo Oliva
Jacob,Carlos Eduardo
D'Ottaviano,Fabricio L'ofreddo
Alvarenga,Conrado
Ribeiro,Adriana Safatle
Ribeiro Jr.,Ulysses
Bresciani,Cláudio José Caldas
Zilberstein,Bruno
Krieger,José Eduardo
Habr-Gama,Angelita
Gama-Rodrigues,Joaquim José
author_role author
author2 Jacob,Carlos Eduardo
D'Ottaviano,Fabricio L'ofreddo
Alvarenga,Conrado
Ribeiro,Adriana Safatle
Ribeiro Jr.,Ulysses
Bresciani,Cláudio José Caldas
Zilberstein,Bruno
Krieger,José Eduardo
Habr-Gama,Angelita
Gama-Rodrigues,Joaquim José
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Perez,Rodrigo Oliva
Jacob,Carlos Eduardo
D'Ottaviano,Fabricio L'ofreddo
Alvarenga,Conrado
Ribeiro,Adriana Safatle
Ribeiro Jr.,Ulysses
Bresciani,Cláudio José Caldas
Zilberstein,Bruno
Krieger,José Eduardo
Habr-Gama,Angelita
Gama-Rodrigues,Joaquim José
dc.subject.por.fl_str_mv Gastric cancer
Genetics
Microsatellite instability
topic Gastric cancer
Genetics
Microsatellite instability
description Recently, the presence of microsatellite instability (MSI) has been reported in gastric cancer and associated with older age of presentation, distal tumor location, early disease staging, and better overall prognosis. Different characteristics in presentation and in tumor behavior may be explained by different genetic alterations during carcinogenesis of gastric cancer. Identification of specific genetic pathways in gastric cancer may have direct impact on prognosis and selection of treatment strategies. PATIENTS AND METHODS: All 24 patients were treated by radical surgery. Fragments of normal and tumor tissues were extracted from the specimen and stored at -80ºC before DNA purification and extraction. PCR amplification utilizing microsatellite markers was performed. Tumors presenting PCR products of abnormal sizes were considered positive for microsatellite instability (MSI+). RESULTS: Five patients (21%) had tumors that were MSI+ in at least 1 marker. In the group of patients with Lauren's intestinal-type gastric carcinoma, 3 had tumors that were MSI+ (23%), while in the group of diffuse-type gastric cancer, 2 patients had tumors that were MSI+ (19%). The mean age of presentation and the male:female ratio was similar in both groups. Tumors that were MSI+ were more frequently located in proximal portion of the stomach compared to microsatellite-stable (MSS) tumors (40% vs. 16%). Although there was a trend of patients with MSI+ tumors towards a proximal gastric tumor location, early staging, and negative lymph node metastasis, there was no statistical significance compared to those with MSS tumors (P >.1). Comparison of overall and disease-free survival between gastric tumors that were MSI+ and those that were MSS found no statistically significant differences (P >.1). CONCLUSIONS: Microsatellite instability is a frequent event in gastric carcinogenesis and shows a trend towards distinct clinical and pathological characteristics of gastric cancer.
publishDate 2004
dc.date.none.fl_str_mv 2004-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0041-87812004000500010
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0041-87812004000500010
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0041-87812004000500010
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Faculdade de Medicina / Universidade de São Paulo - FM/USP
publisher.none.fl_str_mv Faculdade de Medicina / Universidade de São Paulo - FM/USP
dc.source.none.fl_str_mv Revista do Hospital das Clínicas v.59 n.5 2004
reponame:Revista do Hospital das Clínicas
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Revista do Hospital das Clínicas
collection Revista do Hospital das Clínicas
repository.name.fl_str_mv Revista do Hospital das Clínicas - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||revista.hc@hcnet.usp.br
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