Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma
Autor(a) principal: | |
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Data de Publicação: | 2006 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.3748/WJG.v12.i38.6207 http://repositorio.unifesp.br/handle/11600/45742 |
Resumo: | AIM: To investigate chromosome 8 numerical aberrations, C-MYC oncogene alterations and its expression in gastric cancer and to correlate these findings with histopathological characteristics of gastric tumors.METHODS: Specimens were collected surgically from seven patients with gastric adenocarcinomas. Immunostaining for C-MYC and dual-color fluorescence in situ hybridization (FISH) for C-MYC gene and chromosome 8 centromere were performed.RESULTS: All the cases showed chromosome 8 aneuploidy and C-MYC amplification, in both the diffuse and intestinal histopathological types of Lauren. No significant difference (P < 0.05) was observed between the level of chromosome 8 ploidy and the site, stage or histological type of the adenocarcinomas. C-MYC high amplification, like homogeneously stained regions (HSRs) and double minutes (DMs), was observed only in the intestinal-type. Structural rearrangement of C-MYC, like translocation, was observed only in the diffuse type. Regarding C-MYC gene, a significant difference (P < 0.05) was observed between the two histological types. The C-MYC protein was expressed in all the studied cases. In the intestinal-type the C-MYC immunoreactivity was localized only in the nucleus and in the diffuse type in the nucleus and cytoplasm.CONCLUSION: Distinct patterns of alterations between intestinal and diffuse types of gastric tumors support the hypothesis that these types follow different genetic pathways. (C) 2006 The WJG Press. All rights reserved. |
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Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinomachromosome 8 aneuploidyC-MYC amplificationimmunostaininggastric adenocarcinomaAIM: To investigate chromosome 8 numerical aberrations, C-MYC oncogene alterations and its expression in gastric cancer and to correlate these findings with histopathological characteristics of gastric tumors.METHODS: Specimens were collected surgically from seven patients with gastric adenocarcinomas. Immunostaining for C-MYC and dual-color fluorescence in situ hybridization (FISH) for C-MYC gene and chromosome 8 centromere were performed.RESULTS: All the cases showed chromosome 8 aneuploidy and C-MYC amplification, in both the diffuse and intestinal histopathological types of Lauren. No significant difference (P < 0.05) was observed between the level of chromosome 8 ploidy and the site, stage or histological type of the adenocarcinomas. C-MYC high amplification, like homogeneously stained regions (HSRs) and double minutes (DMs), was observed only in the intestinal-type. Structural rearrangement of C-MYC, like translocation, was observed only in the diffuse type. Regarding C-MYC gene, a significant difference (P < 0.05) was observed between the two histological types. The C-MYC protein was expressed in all the studied cases. In the intestinal-type the C-MYC immunoreactivity was localized only in the nucleus and in the diffuse type in the nucleus and cytoplasm.CONCLUSION: Distinct patterns of alterations between intestinal and diffuse types of gastric tumors support the hypothesis that these types follow different genetic pathways. (C) 2006 The WJG Press. All rights reserved.Fed Univ Para, Ctr Ciencias Biol, Dept Biol, Lab Citogenet Humana & Genet Toxicol, BR-66075900 Belem, Para, BrazilUniv Fed Sao Paulo, Dept Morphol, Div Genet, Sao Paulo, BrazilFed Univ Para, Dept Pathol, BR-66059 Belem, Para, BrazilFed Univ Para, Surg Serv, BR-66059 Belem, Para, BrazilFed Univ Para, Joao de Barros Barreto Univ Hosp, BR-66059 Belem, Para, BrazilFed Univ Ceara, Sch Med, Dept Pathol, Genet Mol Lab, Fortaleza, Ceara, BrazilUniv Fed Sao Paulo, Dept Morphol, Div Genet, Sao Paulo, BrazilWeb of ScienceW J G PressFed Univ ParaUniversidade Federal de São Paulo (UNIFESP)Fed Univ CearaCalcagno, Danielle Queiroz [UNIFESP]Leal, Mariana Ferreira [UNIFESP]Seabra, Aline DamacenoKhayat, Andre SalimChen, Elizabeth Suchi [UNIFESP]Demachki, SamiaAssumpção, Paulo Pimentel [UNIFESP]Girao Faria, Mario HenriqueRabenhorst, Silvia Helena BaremFerreira, Márcia Valéria PitombeiraCardoso Smith, Marilia de Arruda [UNIFESP]Burbano, Rommel Rodriguez [UNIFESP]2018-06-18T12:15:15Z2018-06-18T12:15:15Z2006-10-14info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion6207-6211http://dx.doi.org/10.3748/WJG.v12.i38.6207World Journal Of Gastroenterology. Beijing: W J G Press, v. 12, n. 38, p. 6207-6211, 2006.10.3748/WJG.v12.i34.5544WOS000241371400021.pdf1007-9327http://repositorio.unifesp.br/handle/11600/45742WOS:000241371400021engWorld Journal Of Gastroenterologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-05-02T13:59:32Zoai:repositorio.unifesp.br/:11600/45742Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-05-02T13:59:32Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma |
title |
Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma |
spellingShingle |
Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma Calcagno, Danielle Queiroz [UNIFESP] chromosome 8 aneuploidy C-MYC amplification immunostaining gastric adenocarcinoma |
title_short |
Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma |
title_full |
Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma |
title_fullStr |
Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma |
title_full_unstemmed |
Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma |
title_sort |
Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma |
author |
Calcagno, Danielle Queiroz [UNIFESP] |
author_facet |
Calcagno, Danielle Queiroz [UNIFESP] Leal, Mariana Ferreira [UNIFESP] Seabra, Aline Damaceno Khayat, Andre Salim Chen, Elizabeth Suchi [UNIFESP] Demachki, Samia Assumpção, Paulo Pimentel [UNIFESP] Girao Faria, Mario Henrique Rabenhorst, Silvia Helena Barem Ferreira, Márcia Valéria Pitombeira Cardoso Smith, Marilia de Arruda [UNIFESP] Burbano, Rommel Rodriguez [UNIFESP] |
author_role |
author |
author2 |
Leal, Mariana Ferreira [UNIFESP] Seabra, Aline Damaceno Khayat, Andre Salim Chen, Elizabeth Suchi [UNIFESP] Demachki, Samia Assumpção, Paulo Pimentel [UNIFESP] Girao Faria, Mario Henrique Rabenhorst, Silvia Helena Barem Ferreira, Márcia Valéria Pitombeira Cardoso Smith, Marilia de Arruda [UNIFESP] Burbano, Rommel Rodriguez [UNIFESP] |
author2_role |
author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Fed Univ Para Universidade Federal de São Paulo (UNIFESP) Fed Univ Ceara |
dc.contributor.author.fl_str_mv |
Calcagno, Danielle Queiroz [UNIFESP] Leal, Mariana Ferreira [UNIFESP] Seabra, Aline Damaceno Khayat, Andre Salim Chen, Elizabeth Suchi [UNIFESP] Demachki, Samia Assumpção, Paulo Pimentel [UNIFESP] Girao Faria, Mario Henrique Rabenhorst, Silvia Helena Barem Ferreira, Márcia Valéria Pitombeira Cardoso Smith, Marilia de Arruda [UNIFESP] Burbano, Rommel Rodriguez [UNIFESP] |
dc.subject.por.fl_str_mv |
chromosome 8 aneuploidy C-MYC amplification immunostaining gastric adenocarcinoma |
topic |
chromosome 8 aneuploidy C-MYC amplification immunostaining gastric adenocarcinoma |
description |
AIM: To investigate chromosome 8 numerical aberrations, C-MYC oncogene alterations and its expression in gastric cancer and to correlate these findings with histopathological characteristics of gastric tumors.METHODS: Specimens were collected surgically from seven patients with gastric adenocarcinomas. Immunostaining for C-MYC and dual-color fluorescence in situ hybridization (FISH) for C-MYC gene and chromosome 8 centromere were performed.RESULTS: All the cases showed chromosome 8 aneuploidy and C-MYC amplification, in both the diffuse and intestinal histopathological types of Lauren. No significant difference (P < 0.05) was observed between the level of chromosome 8 ploidy and the site, stage or histological type of the adenocarcinomas. C-MYC high amplification, like homogeneously stained regions (HSRs) and double minutes (DMs), was observed only in the intestinal-type. Structural rearrangement of C-MYC, like translocation, was observed only in the diffuse type. Regarding C-MYC gene, a significant difference (P < 0.05) was observed between the two histological types. The C-MYC protein was expressed in all the studied cases. In the intestinal-type the C-MYC immunoreactivity was localized only in the nucleus and in the diffuse type in the nucleus and cytoplasm.CONCLUSION: Distinct patterns of alterations between intestinal and diffuse types of gastric tumors support the hypothesis that these types follow different genetic pathways. (C) 2006 The WJG Press. All rights reserved. |
publishDate |
2006 |
dc.date.none.fl_str_mv |
2006-10-14 2018-06-18T12:15:15Z 2018-06-18T12:15:15Z |
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://dx.doi.org/10.3748/WJG.v12.i38.6207 World Journal Of Gastroenterology. Beijing: W J G Press, v. 12, n. 38, p. 6207-6211, 2006. 10.3748/WJG.v12.i34.5544 WOS000241371400021.pdf 1007-9327 http://repositorio.unifesp.br/handle/11600/45742 WOS:000241371400021 |
url |
http://dx.doi.org/10.3748/WJG.v12.i38.6207 http://repositorio.unifesp.br/handle/11600/45742 |
identifier_str_mv |
World Journal Of Gastroenterology. Beijing: W J G Press, v. 12, n. 38, p. 6207-6211, 2006. 10.3748/WJG.v12.i34.5544 WOS000241371400021.pdf 1007-9327 WOS:000241371400021 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
World Journal Of Gastroenterology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
6207-6211 |
dc.publisher.none.fl_str_mv |
W J G Press |
publisher.none.fl_str_mv |
W J G Press |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268294712000512 |