Chemopreventive activity of systemically administered curcumin on oral cancer in the 4-nitroquinoline 1-oxide model

Detalhes bibliográficos
Autor(a) principal: De Paiva Gonçalves, Vinícius [UNESP]
Data de Publicação: 2015
Outros Autores: Ortega, Adriana Alicia C. [UNESP], Guimarães, Morgana R. [UNESP], Curylofo, Fabiana Almeida [UNESP], Junior, Carlos Rossa [UNESP], Ribeiro, Daniel Araki, Spolidorio, Luis C. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1002/jcb.25035
http://hdl.handle.net/11449/227941
Resumo: Curcumin has therapeutic potential in preventing several types of cancer, including colon, liver, prostate, and breast. The goal of this study was to evaluate the chemopreventive activity of systemically administered curcumin on oral carcinogenesis induced by 4-nitroquinolone-1-oxide (4-NQO). A total of 50 male albino rats, Rattus norvegicus, (Holtzman), were divided into five groups (n = 10 per group). Four of these groups were exposed to 50 ppm 4-NQO in their drinking water ad libitum for 8 or 12 weeks, two groups were treated with curcumin by oral gavage at 30 or 100 mg/kg per day, and one group was treated with corn oil (vehicle) only. The negative control group was euthanized at baseline. Tongues of all animals were removed after euthanasia and used in the subsequent analysis because the tongue is the primary site of carcinogenesis in this model. Descriptive histological analysis and immunohistochemistry for PCNA, Bcl-2, SOCS1 e-3, and STAT3 were performed to assess the oncogenic process. The gene expression of Vimentin, E-cadherin, N-cadherin, or TWIST1 was assessed using RT-qPCR as a representative of epithelial-mesenchymal transition (EMT) events. The administration of curcumin at 100 mg/kg during the 12 weeks markedly decreased the expression of PCNA, Bcl-2, SOCS1 e -3, and STAT3. Curcumin also minimized the cellular atypia under microscopic analysis and diminished the expression of the genes associated with EMT. These findings demonstrate that the systemic administration of curcumin has chemopreventive activity during oral carcinogenesis induced by 4-NQO. J. Cell. Biochem. 116: 787-796, 2015.
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spelling Chemopreventive activity of systemically administered curcumin on oral cancer in the 4-nitroquinoline 1-oxide model4-NITROQUINOLINE-1-OXIDECHEMOPREVENTIONCURCUMINRATTONGUECurcumin has therapeutic potential in preventing several types of cancer, including colon, liver, prostate, and breast. The goal of this study was to evaluate the chemopreventive activity of systemically administered curcumin on oral carcinogenesis induced by 4-nitroquinolone-1-oxide (4-NQO). A total of 50 male albino rats, Rattus norvegicus, (Holtzman), were divided into five groups (n = 10 per group). Four of these groups were exposed to 50 ppm 4-NQO in their drinking water ad libitum for 8 or 12 weeks, two groups were treated with curcumin by oral gavage at 30 or 100 mg/kg per day, and one group was treated with corn oil (vehicle) only. The negative control group was euthanized at baseline. Tongues of all animals were removed after euthanasia and used in the subsequent analysis because the tongue is the primary site of carcinogenesis in this model. Descriptive histological analysis and immunohistochemistry for PCNA, Bcl-2, SOCS1 e-3, and STAT3 were performed to assess the oncogenic process. The gene expression of Vimentin, E-cadherin, N-cadherin, or TWIST1 was assessed using RT-qPCR as a representative of epithelial-mesenchymal transition (EMT) events. The administration of curcumin at 100 mg/kg during the 12 weeks markedly decreased the expression of PCNA, Bcl-2, SOCS1 e -3, and STAT3. Curcumin also minimized the cellular atypia under microscopic analysis and diminished the expression of the genes associated with EMT. These findings demonstrate that the systemic administration of curcumin has chemopreventive activity during oral carcinogenesis induced by 4-NQO. J. Cell. Biochem. 116: 787-796, 2015.Department of Diagnosis and Surgery Araraquara School of Dentistry University of São Paulo State UNESPSPDepartment of Biosciences Federal University of São Paulo UNIFESPSPDepartment of Physiology and Pathology Araraquara School of Dentistry University of São Paulo State UNESPSPDepartment of Diagnosis and Surgery Araraquara School of Dentistry University of São Paulo State UNESPSPDepartment of Physiology and Pathology Araraquara School of Dentistry University of São Paulo State UNESPSPUniversidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)De Paiva Gonçalves, Vinícius [UNESP]Ortega, Adriana Alicia C. [UNESP]Guimarães, Morgana R. [UNESP]Curylofo, Fabiana Almeida [UNESP]Junior, Carlos Rossa [UNESP]Ribeiro, Daniel ArakiSpolidorio, Luis C. [UNESP]2022-04-29T07:25:54Z2022-04-29T07:25:54Z2015-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article787-796http://dx.doi.org/10.1002/jcb.25035Journal of Cellular Biochemistry, v. 116, n. 5, p. 787-796, 2015.1097-46440730-2312http://hdl.handle.net/11449/22794110.1002/jcb.250352-s2.0-84924303224Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Cellular Biochemistryinfo:eu-repo/semantics/openAccess2022-04-29T07:25:54Zoai:repositorio.unesp.br:11449/227941Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-04-29T07:25:54Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Chemopreventive activity of systemically administered curcumin on oral cancer in the 4-nitroquinoline 1-oxide model
title Chemopreventive activity of systemically administered curcumin on oral cancer in the 4-nitroquinoline 1-oxide model
spellingShingle Chemopreventive activity of systemically administered curcumin on oral cancer in the 4-nitroquinoline 1-oxide model
De Paiva Gonçalves, Vinícius [UNESP]
4-NITROQUINOLINE-1-OXIDE
CHEMOPREVENTION
CURCUMIN
RAT
TONGUE
title_short Chemopreventive activity of systemically administered curcumin on oral cancer in the 4-nitroquinoline 1-oxide model
title_full Chemopreventive activity of systemically administered curcumin on oral cancer in the 4-nitroquinoline 1-oxide model
title_fullStr Chemopreventive activity of systemically administered curcumin on oral cancer in the 4-nitroquinoline 1-oxide model
title_full_unstemmed Chemopreventive activity of systemically administered curcumin on oral cancer in the 4-nitroquinoline 1-oxide model
title_sort Chemopreventive activity of systemically administered curcumin on oral cancer in the 4-nitroquinoline 1-oxide model
author De Paiva Gonçalves, Vinícius [UNESP]
author_facet De Paiva Gonçalves, Vinícius [UNESP]
Ortega, Adriana Alicia C. [UNESP]
Guimarães, Morgana R. [UNESP]
Curylofo, Fabiana Almeida [UNESP]
Junior, Carlos Rossa [UNESP]
Ribeiro, Daniel Araki
Spolidorio, Luis C. [UNESP]
author_role author
author2 Ortega, Adriana Alicia C. [UNESP]
Guimarães, Morgana R. [UNESP]
Curylofo, Fabiana Almeida [UNESP]
Junior, Carlos Rossa [UNESP]
Ribeiro, Daniel Araki
Spolidorio, Luis C. [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv De Paiva Gonçalves, Vinícius [UNESP]
Ortega, Adriana Alicia C. [UNESP]
Guimarães, Morgana R. [UNESP]
Curylofo, Fabiana Almeida [UNESP]
Junior, Carlos Rossa [UNESP]
Ribeiro, Daniel Araki
Spolidorio, Luis C. [UNESP]
dc.subject.por.fl_str_mv 4-NITROQUINOLINE-1-OXIDE
CHEMOPREVENTION
CURCUMIN
RAT
TONGUE
topic 4-NITROQUINOLINE-1-OXIDE
CHEMOPREVENTION
CURCUMIN
RAT
TONGUE
description Curcumin has therapeutic potential in preventing several types of cancer, including colon, liver, prostate, and breast. The goal of this study was to evaluate the chemopreventive activity of systemically administered curcumin on oral carcinogenesis induced by 4-nitroquinolone-1-oxide (4-NQO). A total of 50 male albino rats, Rattus norvegicus, (Holtzman), were divided into five groups (n = 10 per group). Four of these groups were exposed to 50 ppm 4-NQO in their drinking water ad libitum for 8 or 12 weeks, two groups were treated with curcumin by oral gavage at 30 or 100 mg/kg per day, and one group was treated with corn oil (vehicle) only. The negative control group was euthanized at baseline. Tongues of all animals were removed after euthanasia and used in the subsequent analysis because the tongue is the primary site of carcinogenesis in this model. Descriptive histological analysis and immunohistochemistry for PCNA, Bcl-2, SOCS1 e-3, and STAT3 were performed to assess the oncogenic process. The gene expression of Vimentin, E-cadherin, N-cadherin, or TWIST1 was assessed using RT-qPCR as a representative of epithelial-mesenchymal transition (EMT) events. The administration of curcumin at 100 mg/kg during the 12 weeks markedly decreased the expression of PCNA, Bcl-2, SOCS1 e -3, and STAT3. Curcumin also minimized the cellular atypia under microscopic analysis and diminished the expression of the genes associated with EMT. These findings demonstrate that the systemic administration of curcumin has chemopreventive activity during oral carcinogenesis induced by 4-NQO. J. Cell. Biochem. 116: 787-796, 2015.
publishDate 2015
dc.date.none.fl_str_mv 2015-01-01
2022-04-29T07:25:54Z
2022-04-29T07:25:54Z
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/10.1002/jcb.25035
Journal of Cellular Biochemistry, v. 116, n. 5, p. 787-796, 2015.
1097-4644
0730-2312
http://hdl.handle.net/11449/227941
10.1002/jcb.25035
2-s2.0-84924303224
url http://dx.doi.org/10.1002/jcb.25035
http://hdl.handle.net/11449/227941
identifier_str_mv Journal of Cellular Biochemistry, v. 116, n. 5, p. 787-796, 2015.
1097-4644
0730-2312
10.1002/jcb.25035
2-s2.0-84924303224
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Cellular Biochemistry
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 787-796
dc.source.none.fl_str_mv Scopus
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
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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