Evaluation of the C3435T polymorphism in the MDR1 gene in patients with hepatocellular carcinoma

Detalhes bibliográficos
Autor(a) principal: Baldissera, Vanessa Dido
Data de Publicação: 2012
Outros Autores: Mattos, Angelo Alves de, Coral, Gabriela Perdomo, Araújo, Fernanda Schild Branco de, Marroni, Claudio Augusto, Brandao, Ajacio Bandeira de Mello, Fontes, Paulo Roberto Ott, Cerski, Carlos Thadeu Schmidt, Hartmann, Antonio Atalibio, Kretzmann Filho, Nelson Alexandre
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/267225
Resumo: Introduction. Considering the high prevalence of liver tumors and the impact on patient survival, a greater understanding of the biological behavior of those tumors if of great importance. The multidrug resistance gene (MDR1) may present as single nucleotide polymorphism (SNP) which can affect the expression and activity of P-glycoprotein (Pgp), and high expression of Pgp has been associated with a worse prognosis in affected patients. Objective. To correlate the C3435T polymorphism in the MDR1 gene with the immunohistochemical expression of Pgp. Material and methods. A total of 67 samples from patients with diagnosis of hepatocellular carcinoma (HCC), collected in the period from 2000 to 2009, were analyzed. The polymorphism in the MDR1 gene was determined by the technique of allele-specific real time PCR using TaqMan assay, and the expression of protein Pgp was evaluated by immunohistochemistry. Results. Among the samples evaluated, 56 (83.6%) were from male patients and 11 (16.4%) from females. Mean age was 60.6 years (± 8.8), ranging from 37 to 85 years. The etiology of the HCC was related to hepatitis C virus infection (HCV) in 31 (46.3%) of cases, followed by hepatitis C virus infection + alcohol in 24 cases (35.8%), alcohol in 4 cases (6)%, hepatitis B virus (HBV) in 4 cases (6%) and other factors in 4 cases (6%). Liver transplantation was performed in 48 cases (71.6%) and hepatectomia in 19 cases (28.4%). The genotypes CC, CT and TT showed frequencies of 25.4%, 41.8% and 32.8%, respectively, and the allele frequencies were 46.3% for allele C and 53.7% for allele T. The expression of Pgp in over 75% of the cells was significantly more frequent in tumor tissue. On the other hand, a low expression of Pgp, in less than 25% of the cells, was significantly more frequent in non-tumor tissue. The Pgp expression in more than 50% of tumor cells of individuals with genotypes CC, CT and TT was 15.7%, 51.0% and 33.3%, respectively, and was significantly higher when in the presence of allele T (p = 0.002). Conclusion. The presence of the polymorphic allele T is related to increased expression of Pgp protein in patients with HCC.
id UFRGS-2_8f5f2f2c9badab897d0512a253799faf
oai_identifier_str oai:www.lume.ufrgs.br:10183/267225
network_acronym_str UFRGS-2
network_name_str Repositório Institucional da UFRGS
repository_id_str
spelling Baldissera, Vanessa DidoMattos, Angelo Alves deCoral, Gabriela PerdomoAraújo, Fernanda Schild Branco deMarroni, Claudio AugustoBrandao, Ajacio Bandeira de MelloFontes, Paulo Roberto OttCerski, Carlos Thadeu SchmidtHartmann, Antonio AtalibioKretzmann Filho, Nelson Alexandre2023-11-18T03:24:59Z20121665-2681http://hdl.handle.net/10183/267225001186702Introduction. Considering the high prevalence of liver tumors and the impact on patient survival, a greater understanding of the biological behavior of those tumors if of great importance. The multidrug resistance gene (MDR1) may present as single nucleotide polymorphism (SNP) which can affect the expression and activity of P-glycoprotein (Pgp), and high expression of Pgp has been associated with a worse prognosis in affected patients. Objective. To correlate the C3435T polymorphism in the MDR1 gene with the immunohistochemical expression of Pgp. Material and methods. A total of 67 samples from patients with diagnosis of hepatocellular carcinoma (HCC), collected in the period from 2000 to 2009, were analyzed. The polymorphism in the MDR1 gene was determined by the technique of allele-specific real time PCR using TaqMan assay, and the expression of protein Pgp was evaluated by immunohistochemistry. Results. Among the samples evaluated, 56 (83.6%) were from male patients and 11 (16.4%) from females. Mean age was 60.6 years (± 8.8), ranging from 37 to 85 years. The etiology of the HCC was related to hepatitis C virus infection (HCV) in 31 (46.3%) of cases, followed by hepatitis C virus infection + alcohol in 24 cases (35.8%), alcohol in 4 cases (6)%, hepatitis B virus (HBV) in 4 cases (6%) and other factors in 4 cases (6%). Liver transplantation was performed in 48 cases (71.6%) and hepatectomia in 19 cases (28.4%). The genotypes CC, CT and TT showed frequencies of 25.4%, 41.8% and 32.8%, respectively, and the allele frequencies were 46.3% for allele C and 53.7% for allele T. The expression of Pgp in over 75% of the cells was significantly more frequent in tumor tissue. On the other hand, a low expression of Pgp, in less than 25% of the cells, was significantly more frequent in non-tumor tissue. The Pgp expression in more than 50% of tumor cells of individuals with genotypes CC, CT and TT was 15.7%, 51.0% and 33.3%, respectively, and was significantly higher when in the presence of allele T (p = 0.002). Conclusion. The presence of the polymorphic allele T is related to increased expression of Pgp protein in patients with HCC.application/pdfengAnnals of hepatology. México. Vol. 11, NO. 6 (2012), p. 899-906Polimorfismo genéticoCarcinoma hepatocelularPolimorfismo de nucleotídeo únicoGenes MDRLiver tumorsSingle nucleotide polymorphismMultidrug resistance geneP-glycoproteinEvaluation of the C3435T polymorphism in the MDR1 gene in patients with hepatocellular carcinomaEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001186702.pdf.txt001186702.pdf.txtExtracted Texttext/plain34091http://www.lume.ufrgs.br/bitstream/10183/267225/2/001186702.pdf.txt18a5cc93c738945504c7d036fce0e88dMD52ORIGINAL001186702.pdfTexto completo (inglês)application/pdf197108http://www.lume.ufrgs.br/bitstream/10183/267225/1/001186702.pdfa60dfb1492a27ba6f58ccdc873c76690MD5110183/2672252023-11-19 04:21:14.167645oai:www.lume.ufrgs.br:10183/267225Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-11-19T06:21:14Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Evaluation of the C3435T polymorphism in the MDR1 gene in patients with hepatocellular carcinoma
title Evaluation of the C3435T polymorphism in the MDR1 gene in patients with hepatocellular carcinoma
spellingShingle Evaluation of the C3435T polymorphism in the MDR1 gene in patients with hepatocellular carcinoma
Baldissera, Vanessa Dido
Polimorfismo genético
Carcinoma hepatocelular
Polimorfismo de nucleotídeo único
Genes MDR
Liver tumors
Single nucleotide polymorphism
Multidrug resistance gene
P-glycoprotein
title_short Evaluation of the C3435T polymorphism in the MDR1 gene in patients with hepatocellular carcinoma
title_full Evaluation of the C3435T polymorphism in the MDR1 gene in patients with hepatocellular carcinoma
title_fullStr Evaluation of the C3435T polymorphism in the MDR1 gene in patients with hepatocellular carcinoma
title_full_unstemmed Evaluation of the C3435T polymorphism in the MDR1 gene in patients with hepatocellular carcinoma
title_sort Evaluation of the C3435T polymorphism in the MDR1 gene in patients with hepatocellular carcinoma
author Baldissera, Vanessa Dido
author_facet Baldissera, Vanessa Dido
Mattos, Angelo Alves de
Coral, Gabriela Perdomo
Araújo, Fernanda Schild Branco de
Marroni, Claudio Augusto
Brandao, Ajacio Bandeira de Mello
Fontes, Paulo Roberto Ott
Cerski, Carlos Thadeu Schmidt
Hartmann, Antonio Atalibio
Kretzmann Filho, Nelson Alexandre
author_role author
author2 Mattos, Angelo Alves de
Coral, Gabriela Perdomo
Araújo, Fernanda Schild Branco de
Marroni, Claudio Augusto
Brandao, Ajacio Bandeira de Mello
Fontes, Paulo Roberto Ott
Cerski, Carlos Thadeu Schmidt
Hartmann, Antonio Atalibio
Kretzmann Filho, Nelson Alexandre
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Baldissera, Vanessa Dido
Mattos, Angelo Alves de
Coral, Gabriela Perdomo
Araújo, Fernanda Schild Branco de
Marroni, Claudio Augusto
Brandao, Ajacio Bandeira de Mello
Fontes, Paulo Roberto Ott
Cerski, Carlos Thadeu Schmidt
Hartmann, Antonio Atalibio
Kretzmann Filho, Nelson Alexandre
dc.subject.por.fl_str_mv Polimorfismo genético
Carcinoma hepatocelular
Polimorfismo de nucleotídeo único
Genes MDR
topic Polimorfismo genético
Carcinoma hepatocelular
Polimorfismo de nucleotídeo único
Genes MDR
Liver tumors
Single nucleotide polymorphism
Multidrug resistance gene
P-glycoprotein
dc.subject.eng.fl_str_mv Liver tumors
Single nucleotide polymorphism
Multidrug resistance gene
P-glycoprotein
description Introduction. Considering the high prevalence of liver tumors and the impact on patient survival, a greater understanding of the biological behavior of those tumors if of great importance. The multidrug resistance gene (MDR1) may present as single nucleotide polymorphism (SNP) which can affect the expression and activity of P-glycoprotein (Pgp), and high expression of Pgp has been associated with a worse prognosis in affected patients. Objective. To correlate the C3435T polymorphism in the MDR1 gene with the immunohistochemical expression of Pgp. Material and methods. A total of 67 samples from patients with diagnosis of hepatocellular carcinoma (HCC), collected in the period from 2000 to 2009, were analyzed. The polymorphism in the MDR1 gene was determined by the technique of allele-specific real time PCR using TaqMan assay, and the expression of protein Pgp was evaluated by immunohistochemistry. Results. Among the samples evaluated, 56 (83.6%) were from male patients and 11 (16.4%) from females. Mean age was 60.6 years (± 8.8), ranging from 37 to 85 years. The etiology of the HCC was related to hepatitis C virus infection (HCV) in 31 (46.3%) of cases, followed by hepatitis C virus infection + alcohol in 24 cases (35.8%), alcohol in 4 cases (6)%, hepatitis B virus (HBV) in 4 cases (6%) and other factors in 4 cases (6%). Liver transplantation was performed in 48 cases (71.6%) and hepatectomia in 19 cases (28.4%). The genotypes CC, CT and TT showed frequencies of 25.4%, 41.8% and 32.8%, respectively, and the allele frequencies were 46.3% for allele C and 53.7% for allele T. The expression of Pgp in over 75% of the cells was significantly more frequent in tumor tissue. On the other hand, a low expression of Pgp, in less than 25% of the cells, was significantly more frequent in non-tumor tissue. The Pgp expression in more than 50% of tumor cells of individuals with genotypes CC, CT and TT was 15.7%, 51.0% and 33.3%, respectively, and was significantly higher when in the presence of allele T (p = 0.002). Conclusion. The presence of the polymorphic allele T is related to increased expression of Pgp protein in patients with HCC.
publishDate 2012
dc.date.issued.fl_str_mv 2012
dc.date.accessioned.fl_str_mv 2023-11-18T03:24:59Z
dc.type.driver.fl_str_mv Estrangeiro
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://hdl.handle.net/10183/267225
dc.identifier.issn.pt_BR.fl_str_mv 1665-2681
dc.identifier.nrb.pt_BR.fl_str_mv 001186702
identifier_str_mv 1665-2681
001186702
url http://hdl.handle.net/10183/267225
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Annals of hepatology. México. Vol. 11, NO. 6 (2012), p. 899-906
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Repositório Institucional da UFRGS
collection Repositório Institucional da UFRGS
bitstream.url.fl_str_mv http://www.lume.ufrgs.br/bitstream/10183/267225/2/001186702.pdf.txt
http://www.lume.ufrgs.br/bitstream/10183/267225/1/001186702.pdf
bitstream.checksum.fl_str_mv 18a5cc93c738945504c7d036fce0e88d
a60dfb1492a27ba6f58ccdc873c76690
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv
_version_ 1815447845161926656