Chromosomal imbalances are uncommon in chagasic megaesophagus

Detalhes bibliográficos
Autor(a) principal: Bellini, Marilanda F. [UNESP]
Data de Publicação: 2010
Outros Autores: Manzato, Antonio J. [UNESP], Silva, Ana E. [UNESP], Varella-Garcia, Marileila
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1186/1471-230X-10-20
http://hdl.handle.net/11449/42380
Resumo: Background: Chagas' disease is a human tropical parasitic illness and a subset of the chronic patients develop megaesophagus or megacolon. The esophagus dilation is known as chagasic megaesophagus (CM) and one of the severe late consequences of CM is the increased risk for esophageal carcinoma (ESCC). Based on the association between CM and ESCC, we investigated whether genes frequently showing unbalanced copy numbers in ESCC were altered in CM by fluorescence in situ (FISH) technology.Methods: A total of 50 formalin-fixed, paraffin-embedded esophageal mucosa specimens (40 from Chagas megaesophagus-CM, and 10 normal esophageal mucosa-NM) were analyzed. DNA FISH probes were tested for FHIT, TP63, PIK3CA, EGFR, FGFR1, MYC, CDKN2A, YES1 and NCOA3 genes, and centromeric sequences from chromosomes 3, 7 and 9.Results: No differences between superficial and basal layers of the epithelial mucosa were found, except for loss of copy number of EGFR in the esophageal basal layer of CM group. Mean copy number of CDKN2A and CEP9 and frequency of nuclei with loss of PIK3CA were significantly different in the CM group compared with normal mucosa and marginal levels of deletions in TP63, FHIT, PIK3CA, EGFR, CDKN2A, YES and gains at PIK3CA, TP63, FGFR1, MYC, CDNK2A and NCOA3 were detected in few CM cases, mainly with dilation grades III and IV. All changes occurred at very low levels.Conclusions: Genomic imbalances common in esophageal carcinomas are not present in chagasic megaesophagus suggesting that these features will not be effective markers for risk assessment of ESCC in patients with chagasic megaesophagus.
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spelling Chromosomal imbalances are uncommon in chagasic megaesophagusBackground: Chagas' disease is a human tropical parasitic illness and a subset of the chronic patients develop megaesophagus or megacolon. The esophagus dilation is known as chagasic megaesophagus (CM) and one of the severe late consequences of CM is the increased risk for esophageal carcinoma (ESCC). Based on the association between CM and ESCC, we investigated whether genes frequently showing unbalanced copy numbers in ESCC were altered in CM by fluorescence in situ (FISH) technology.Methods: A total of 50 formalin-fixed, paraffin-embedded esophageal mucosa specimens (40 from Chagas megaesophagus-CM, and 10 normal esophageal mucosa-NM) were analyzed. DNA FISH probes were tested for FHIT, TP63, PIK3CA, EGFR, FGFR1, MYC, CDKN2A, YES1 and NCOA3 genes, and centromeric sequences from chromosomes 3, 7 and 9.Results: No differences between superficial and basal layers of the epithelial mucosa were found, except for loss of copy number of EGFR in the esophageal basal layer of CM group. Mean copy number of CDKN2A and CEP9 and frequency of nuclei with loss of PIK3CA were significantly different in the CM group compared with normal mucosa and marginal levels of deletions in TP63, FHIT, PIK3CA, EGFR, CDKN2A, YES and gains at PIK3CA, TP63, FGFR1, MYC, CDNK2A and NCOA3 were detected in few CM cases, mainly with dilation grades III and IV. All changes occurred at very low levels.Conclusions: Genomic imbalances common in esophageal carcinomas are not present in chagasic megaesophagus suggesting that these features will not be effective markers for risk assessment of ESCC in patients with chagasic megaesophagus.NCISão Paulo State Univ, UNESP, Dept Biol, São Paulo, BrazilUniv Colorado Denver, Dept Med Med Oncol, Aurora, CO USASão Paulo State Univ, UNESP, Dept Comp Sci & Stat, São Paulo, BrazilSão Paulo State Univ, UNESP, Dept Biol, São Paulo, BrazilSão Paulo State Univ, UNESP, Dept Comp Sci & Stat, São Paulo, BrazilNCI: U01CA85070NCI: P30-CA46934NCI: P50 CA58187Biomed Central Ltd.Universidade Estadual Paulista (Unesp)Univ Colorado DenverBellini, Marilanda F. [UNESP]Manzato, Antonio J. [UNESP]Silva, Ana E. [UNESP]Varella-Garcia, Marileila2014-05-20T15:33:59Z2014-05-20T15:33:59Z2010-02-17info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article10application/pdfhttp://dx.doi.org/10.1186/1471-230X-10-20Bmc Gastroenterology. London: Biomed Central Ltd., v. 10, p. 10, 2010.1471-230Xhttp://hdl.handle.net/11449/4238010.1186/1471-230X-10-20WOS:000276342000001WOS000276342000001.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBMC Gastroenterology2.731info:eu-repo/semantics/openAccess2023-10-10T06:09:43Zoai:repositorio.unesp.br:11449/42380Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-10-10T06:09:43Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Chromosomal imbalances are uncommon in chagasic megaesophagus
title Chromosomal imbalances are uncommon in chagasic megaesophagus
spellingShingle Chromosomal imbalances are uncommon in chagasic megaesophagus
Bellini, Marilanda F. [UNESP]
title_short Chromosomal imbalances are uncommon in chagasic megaesophagus
title_full Chromosomal imbalances are uncommon in chagasic megaesophagus
title_fullStr Chromosomal imbalances are uncommon in chagasic megaesophagus
title_full_unstemmed Chromosomal imbalances are uncommon in chagasic megaesophagus
title_sort Chromosomal imbalances are uncommon in chagasic megaesophagus
author Bellini, Marilanda F. [UNESP]
author_facet Bellini, Marilanda F. [UNESP]
Manzato, Antonio J. [UNESP]
Silva, Ana E. [UNESP]
Varella-Garcia, Marileila
author_role author
author2 Manzato, Antonio J. [UNESP]
Silva, Ana E. [UNESP]
Varella-Garcia, Marileila
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Univ Colorado Denver
dc.contributor.author.fl_str_mv Bellini, Marilanda F. [UNESP]
Manzato, Antonio J. [UNESP]
Silva, Ana E. [UNESP]
Varella-Garcia, Marileila
description Background: Chagas' disease is a human tropical parasitic illness and a subset of the chronic patients develop megaesophagus or megacolon. The esophagus dilation is known as chagasic megaesophagus (CM) and one of the severe late consequences of CM is the increased risk for esophageal carcinoma (ESCC). Based on the association between CM and ESCC, we investigated whether genes frequently showing unbalanced copy numbers in ESCC were altered in CM by fluorescence in situ (FISH) technology.Methods: A total of 50 formalin-fixed, paraffin-embedded esophageal mucosa specimens (40 from Chagas megaesophagus-CM, and 10 normal esophageal mucosa-NM) were analyzed. DNA FISH probes were tested for FHIT, TP63, PIK3CA, EGFR, FGFR1, MYC, CDKN2A, YES1 and NCOA3 genes, and centromeric sequences from chromosomes 3, 7 and 9.Results: No differences between superficial and basal layers of the epithelial mucosa were found, except for loss of copy number of EGFR in the esophageal basal layer of CM group. Mean copy number of CDKN2A and CEP9 and frequency of nuclei with loss of PIK3CA were significantly different in the CM group compared with normal mucosa and marginal levels of deletions in TP63, FHIT, PIK3CA, EGFR, CDKN2A, YES and gains at PIK3CA, TP63, FGFR1, MYC, CDNK2A and NCOA3 were detected in few CM cases, mainly with dilation grades III and IV. All changes occurred at very low levels.Conclusions: Genomic imbalances common in esophageal carcinomas are not present in chagasic megaesophagus suggesting that these features will not be effective markers for risk assessment of ESCC in patients with chagasic megaesophagus.
publishDate 2010
dc.date.none.fl_str_mv 2010-02-17
2014-05-20T15:33:59Z
2014-05-20T15:33:59Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/1471-230X-10-20
Bmc Gastroenterology. London: Biomed Central Ltd., v. 10, p. 10, 2010.
1471-230X
http://hdl.handle.net/11449/42380
10.1186/1471-230X-10-20
WOS:000276342000001
WOS000276342000001.pdf
url http://dx.doi.org/10.1186/1471-230X-10-20
http://hdl.handle.net/11449/42380
identifier_str_mv Bmc Gastroenterology. London: Biomed Central Ltd., v. 10, p. 10, 2010.
1471-230X
10.1186/1471-230X-10-20
WOS:000276342000001
WOS000276342000001.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv BMC Gastroenterology
2.731
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eu_rights_str_mv openAccess
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application/pdf
dc.publisher.none.fl_str_mv Biomed Central Ltd.
publisher.none.fl_str_mv Biomed Central Ltd.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
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