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Interrelationship between TP53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinoma

BACKGROUND: This study evaluates the existence of numerical alterations of chromosome 17 and TP53 gene deletion in gastric adenocarcinoma. The p53 protein expression was also evaluated, as well as, possible associations with clinicopathological characteristics. METHODS: Dual-color fluorescence in si...

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Autores principales: Khayat, André S, Guimarães, Adriana C, Calcagno, Danielle Q, Seabra, Aline D, Lima, Eleonidas M, Leal, Mariana F, Faria, Mário HG, Rabenhorst, Silvia HB, Assumpção, Paulo P, Demachki, Samia, Smith, Marília AC, Burbano, Rommel R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716360/
https://www.ncbi.nlm.nih.gov/pubmed/19619279
http://dx.doi.org/10.1186/1471-230X-9-55
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author Khayat, André S
Guimarães, Adriana C
Calcagno, Danielle Q
Seabra, Aline D
Lima, Eleonidas M
Leal, Mariana F
Faria, Mário HG
Rabenhorst, Silvia HB
Assumpção, Paulo P
Demachki, Samia
Smith, Marília AC
Burbano, Rommel R
author_facet Khayat, André S
Guimarães, Adriana C
Calcagno, Danielle Q
Seabra, Aline D
Lima, Eleonidas M
Leal, Mariana F
Faria, Mário HG
Rabenhorst, Silvia HB
Assumpção, Paulo P
Demachki, Samia
Smith, Marília AC
Burbano, Rommel R
author_sort Khayat, André S
collection PubMed
description BACKGROUND: This study evaluates the existence of numerical alterations of chromosome 17 and TP53 gene deletion in gastric adenocarcinoma. The p53 protein expression was also evaluated, as well as, possible associations with clinicopathological characteristics. METHODS: Dual-color fluorescence in situ hybridization and immunostaining were performed in twenty gastric cancer samples of individuals from Northern Brazil. RESULTS: Deletion of TP53 was found in all samples. TP53 was inactivated mainly by single allelic deletion, varying to 7–39% of cells/case. Aneusomy of chromosome 17 was observed in 85% of cases. Chromosome 17 monosomy and gain were both observed in about half of cases. Cells with gain of chromosome 17 frequently presented TP53 deletion. The frequency of cells with two chr17 and one TP53 signals observed was higher in diffuse than in intestinal-type GC. Immunoreactivity of p53 was found only in intestinal-type samples. The frequency of cells with two chr17 and two TP53 signals found was higher in samples with positive p53 expression than in negative cases in intestinal-type GC. CONCLUSION: We suggest that TP53 deletion and chromosome 17 aneusomy is a common event in GC and other TP53 alterations, as mutation, may be implicated in the distinct carcinogenesis process of diffuse and intestinal types.
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spelling pubmed-27163602009-07-28 Interrelationship between TP53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinoma Khayat, André S Guimarães, Adriana C Calcagno, Danielle Q Seabra, Aline D Lima, Eleonidas M Leal, Mariana F Faria, Mário HG Rabenhorst, Silvia HB Assumpção, Paulo P Demachki, Samia Smith, Marília AC Burbano, Rommel R BMC Gastroenterol Research Article BACKGROUND: This study evaluates the existence of numerical alterations of chromosome 17 and TP53 gene deletion in gastric adenocarcinoma. The p53 protein expression was also evaluated, as well as, possible associations with clinicopathological characteristics. METHODS: Dual-color fluorescence in situ hybridization and immunostaining were performed in twenty gastric cancer samples of individuals from Northern Brazil. RESULTS: Deletion of TP53 was found in all samples. TP53 was inactivated mainly by single allelic deletion, varying to 7–39% of cells/case. Aneusomy of chromosome 17 was observed in 85% of cases. Chromosome 17 monosomy and gain were both observed in about half of cases. Cells with gain of chromosome 17 frequently presented TP53 deletion. The frequency of cells with two chr17 and one TP53 signals observed was higher in diffuse than in intestinal-type GC. Immunoreactivity of p53 was found only in intestinal-type samples. The frequency of cells with two chr17 and two TP53 signals found was higher in samples with positive p53 expression than in negative cases in intestinal-type GC. CONCLUSION: We suggest that TP53 deletion and chromosome 17 aneusomy is a common event in GC and other TP53 alterations, as mutation, may be implicated in the distinct carcinogenesis process of diffuse and intestinal types. BioMed Central 2009-07-20 /pmc/articles/PMC2716360/ /pubmed/19619279 http://dx.doi.org/10.1186/1471-230X-9-55 Text en Copyright ©2009 Khayat et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Khayat, André S
Guimarães, Adriana C
Calcagno, Danielle Q
Seabra, Aline D
Lima, Eleonidas M
Leal, Mariana F
Faria, Mário HG
Rabenhorst, Silvia HB
Assumpção, Paulo P
Demachki, Samia
Smith, Marília AC
Burbano, Rommel R
Interrelationship between TP53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinoma
title Interrelationship between TP53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinoma
title_full Interrelationship between TP53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinoma
title_fullStr Interrelationship between TP53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinoma
title_full_unstemmed Interrelationship between TP53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinoma
title_short Interrelationship between TP53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinoma
title_sort interrelationship between tp53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716360/
https://www.ncbi.nlm.nih.gov/pubmed/19619279
http://dx.doi.org/10.1186/1471-230X-9-55
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