B-raf protein immunoexpression in hepatocellular carcinoma due to hepatitis c virus related cirrhosis

Detalhes bibliográficos
Autor(a) principal: Paula Piedade Garcia
Data de Publicação: 2021
Outros Autores: Ronniel Morais Albuquerque, Fernanda Maria Farage Osório, Cláudia Alves Couto, Agnaldo Soares Lima, Paula Vieira Teixeira Vidigal
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFMG
Texto Completo: http://hdl.handle.net/1843/60754
Resumo: Background – Hepatocarcinogenesis is a multistep process that lead to genetic changes in hepatocytes resulting in neoplasia. However, the mechanisms of malignant transformation seem to differ widely. To know carcinogenesis mechanisms is essential to develop new treatment and prevention methods. Objective – The aim of this study is to analyze B-Raf protein immunoexpression in explants with hepatocellular carcinoma (HCC) related to hepatitis C (HCV), in adjacent cirrhotic tissue and in normal livers. We also associated the immunoexpression with known HCC related histopathogical prognostic features. Methods – Livers from 35 patients with HCV related cirrhosis and HCC that underwent liver transplantation or hepatectomy at Clinical Hospital – UFMG and 25 normal livers from necropsy archives were studied. Tumors were classified according to: tumor size, vascular invasion and differentiation grade. B-Raf protein expression was determined by immunohistochemistry. Results – B-Raf was strongly expressed in the HCV cirrhotic parenchyma cytoplasm of 17.1% cases and in 62.9% of HCC samples. Strong B-Raf protein staining was associated with tumor tissue (P<0.0001; OR=8.18 (2.62–26.63)). All normal livers showed weak or negative expression for B-Raf. There was no significant association among B-Raf scores and tumor differentiation grade (P=0.9485), tumor size (P=0.4427) or with vascular invasion (P=0.2666). Conclusion – We found B-Raf protein immunostaining difference in normal livers, in the areas of HCV cirrhosis and in the hepatocarcinoma. We did not find association between B-Raf expression and histopathological markers of tumor progression. Our data suggests that B-Raf may play an important role in initial HCC carcinogenesis. Larger studies are needed to validate these observation.
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spelling 2023-11-09T22:11:02Z2023-11-09T22:11:02Z2021-1058441942310.1590/s0004-2803.202100000-7616784219http://hdl.handle.net/1843/60754Background – Hepatocarcinogenesis is a multistep process that lead to genetic changes in hepatocytes resulting in neoplasia. However, the mechanisms of malignant transformation seem to differ widely. To know carcinogenesis mechanisms is essential to develop new treatment and prevention methods. Objective – The aim of this study is to analyze B-Raf protein immunoexpression in explants with hepatocellular carcinoma (HCC) related to hepatitis C (HCV), in adjacent cirrhotic tissue and in normal livers. We also associated the immunoexpression with known HCC related histopathogical prognostic features. Methods – Livers from 35 patients with HCV related cirrhosis and HCC that underwent liver transplantation or hepatectomy at Clinical Hospital – UFMG and 25 normal livers from necropsy archives were studied. Tumors were classified according to: tumor size, vascular invasion and differentiation grade. B-Raf protein expression was determined by immunohistochemistry. Results – B-Raf was strongly expressed in the HCV cirrhotic parenchyma cytoplasm of 17.1% cases and in 62.9% of HCC samples. Strong B-Raf protein staining was associated with tumor tissue (P<0.0001; OR=8.18 (2.62–26.63)). All normal livers showed weak or negative expression for B-Raf. There was no significant association among B-Raf scores and tumor differentiation grade (P=0.9485), tumor size (P=0.4427) or with vascular invasion (P=0.2666). Conclusion – We found B-Raf protein immunostaining difference in normal livers, in the areas of HCV cirrhosis and in the hepatocarcinoma. We did not find association between B-Raf expression and histopathological markers of tumor progression. Our data suggests that B-Raf may play an important role in initial HCC carcinogenesis. Larger studies are needed to validate these observation.engUniversidade Federal de Minas GeraisUFMGBrasilMED - DEPARTAMENTO DE CLÍNICA MÉDICAArquivos de GastroenterologiaCarcinoma, HepatocellularProto-Oncogene Proteins B-rafHepacivirusHepatocellular carcinomaB-Rafhepatitis C virusB-raf protein immunoexpression in hepatocellular carcinoma due to hepatitis c virus related cirrhosisinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.1590/S0004-2803.202100000-76Paula Piedade GarciaRonniel Morais AlbuquerqueFernanda Maria Farage OsórioCláudia Alves CoutoAgnaldo Soares LimaPaula Vieira Teixeira Vidigalapplication/pdfinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMGLICENSELicense.txtLicense.txttext/plain; charset=utf-82042https://repositorio.ufmg.br/bitstream/1843/60754/1/License.txtfa505098d172de0bc8864fc1287ffe22MD51ORIGINALB-RAF PROTEIN IMMUNOEXPRESSION IN HEPATOCELLULAR CARCINOMA DUE TO HEPATITIS C VIRUS RELATED CIRRHOSIS pdfa.pdfB-RAF PROTEIN IMMUNOEXPRESSION IN HEPATOCELLULAR CARCINOMA DUE TO HEPATITIS C VIRUS RELATED CIRRHOSIS pdfa.pdfapplication/pdf487093https://repositorio.ufmg.br/bitstream/1843/60754/2/B-RAF%20PROTEIN%20IMMUNOEXPRESSION%20IN%20HEPATOCELLULAR%20CARCINOMA%20DUE%20TO%20HEPATITIS%20C%20VIRUS%20RELATED%20CIRRHOSIS%20pdfa.pdf242000c480c3ba6a732d5e0e01da21ffMD521843/607542023-11-09 20:49:57.174oai:repositorio.ufmg.br:1843/60754Repositório de PublicaçõesPUBhttps://repositorio.ufmg.br/oaiopendoar:2023-11-09T23:49:57Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false
dc.title.pt_BR.fl_str_mv B-raf protein immunoexpression in hepatocellular carcinoma due to hepatitis c virus related cirrhosis
title B-raf protein immunoexpression in hepatocellular carcinoma due to hepatitis c virus related cirrhosis
spellingShingle B-raf protein immunoexpression in hepatocellular carcinoma due to hepatitis c virus related cirrhosis
Paula Piedade Garcia
Hepatocellular carcinoma
B-Raf
hepatitis C virus
Carcinoma, Hepatocellular
Proto-Oncogene Proteins B-raf
Hepacivirus
title_short B-raf protein immunoexpression in hepatocellular carcinoma due to hepatitis c virus related cirrhosis
title_full B-raf protein immunoexpression in hepatocellular carcinoma due to hepatitis c virus related cirrhosis
title_fullStr B-raf protein immunoexpression in hepatocellular carcinoma due to hepatitis c virus related cirrhosis
title_full_unstemmed B-raf protein immunoexpression in hepatocellular carcinoma due to hepatitis c virus related cirrhosis
title_sort B-raf protein immunoexpression in hepatocellular carcinoma due to hepatitis c virus related cirrhosis
author Paula Piedade Garcia
author_facet Paula Piedade Garcia
Ronniel Morais Albuquerque
Fernanda Maria Farage Osório
Cláudia Alves Couto
Agnaldo Soares Lima
Paula Vieira Teixeira Vidigal
author_role author
author2 Ronniel Morais Albuquerque
Fernanda Maria Farage Osório
Cláudia Alves Couto
Agnaldo Soares Lima
Paula Vieira Teixeira Vidigal
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Paula Piedade Garcia
Ronniel Morais Albuquerque
Fernanda Maria Farage Osório
Cláudia Alves Couto
Agnaldo Soares Lima
Paula Vieira Teixeira Vidigal
dc.subject.por.fl_str_mv Hepatocellular carcinoma
B-Raf
hepatitis C virus
topic Hepatocellular carcinoma
B-Raf
hepatitis C virus
Carcinoma, Hepatocellular
Proto-Oncogene Proteins B-raf
Hepacivirus
dc.subject.other.pt_BR.fl_str_mv Carcinoma, Hepatocellular
Proto-Oncogene Proteins B-raf
Hepacivirus
description Background – Hepatocarcinogenesis is a multistep process that lead to genetic changes in hepatocytes resulting in neoplasia. However, the mechanisms of malignant transformation seem to differ widely. To know carcinogenesis mechanisms is essential to develop new treatment and prevention methods. Objective – The aim of this study is to analyze B-Raf protein immunoexpression in explants with hepatocellular carcinoma (HCC) related to hepatitis C (HCV), in adjacent cirrhotic tissue and in normal livers. We also associated the immunoexpression with known HCC related histopathogical prognostic features. Methods – Livers from 35 patients with HCV related cirrhosis and HCC that underwent liver transplantation or hepatectomy at Clinical Hospital – UFMG and 25 normal livers from necropsy archives were studied. Tumors were classified according to: tumor size, vascular invasion and differentiation grade. B-Raf protein expression was determined by immunohistochemistry. Results – B-Raf was strongly expressed in the HCV cirrhotic parenchyma cytoplasm of 17.1% cases and in 62.9% of HCC samples. Strong B-Raf protein staining was associated with tumor tissue (P<0.0001; OR=8.18 (2.62–26.63)). All normal livers showed weak or negative expression for B-Raf. There was no significant association among B-Raf scores and tumor differentiation grade (P=0.9485), tumor size (P=0.4427) or with vascular invasion (P=0.2666). Conclusion – We found B-Raf protein immunostaining difference in normal livers, in the areas of HCV cirrhosis and in the hepatocarcinoma. We did not find association between B-Raf expression and histopathological markers of tumor progression. Our data suggests that B-Raf may play an important role in initial HCC carcinogenesis. Larger studies are needed to validate these observation.
publishDate 2021
dc.date.issued.fl_str_mv 2021-10
dc.date.accessioned.fl_str_mv 2023-11-09T22:11:02Z
dc.date.available.fl_str_mv 2023-11-09T22:11:02Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/1843/60754
dc.identifier.doi.pt_BR.fl_str_mv 10.1590/s0004-2803.202100000-76
dc.identifier.issn.pt_BR.fl_str_mv 16784219
identifier_str_mv 10.1590/s0004-2803.202100000-76
16784219
url http://hdl.handle.net/1843/60754
dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.none.fl_str_mv Arquivos de Gastroenterologia
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dc.publisher.none.fl_str_mv Universidade Federal de Minas Gerais
dc.publisher.initials.fl_str_mv UFMG
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv MED - DEPARTAMENTO DE CLÍNICA MÉDICA
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFMG
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