Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats

Detalhes bibliográficos
Autor(a) principal: de Moura, Nelci A. [UNESP]
Data de Publicação: 2018
Outros Autores: Caetano, Brunno F.R. [UNESP], de Moraes, Leonardo N. [UNESP], Carvalho, Robson F. [UNESP], Rodrigues, Maria A.M. [UNESP], Barbisan, Luis F. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
DOI: 10.1016/j.fct.2017.12.029
Texto Completo: http://dx.doi.org/10.1016/j.fct.2017.12.029
http://hdl.handle.net/11449/175909
Resumo: The risk of developing colorectal cancer (CRC) could be associated with red and processed meat intake. Experimental data supports that hemin iron, found abundantly in red meat, promotes CRC in mice and rats, while indole-3 carbinol (I3C) and synbiotics (syn) exert anti-carcinogenic activities in most studies of colon carcinogenesis. This study aimed to investigate the modifying effects of I3C and syn (inulin + Bifidobacterium lactis), given separately or together, on dimethylhidrazine (DMH)-induced colon carcinogenesis in hemin-fed rats. All animals were given four subcutaneous DMH injections and then, two weeks after carcinogen exposure, they began a basal diet containing hemin, hemin + I3C, hemin + syn, or hemin + I3C + syn for 23 weeks. The combination of I3C + syn significantly increased fecal water genotoxicity, tumor volume and invasiveness when compared to the hemin-fed control group. The groups fed I3C or syn alone had a significant reduction in the number of preneoplastic aberrant crypt foci (ACF) lesions compared to the hemin-fed group. Dietary I3C also reduced fecal water genotoxicity. Gene expression analysis of colorectal tumors demonstrated that the combination of dietary I3C + syn increased transcript levels for Raf1 and decreased tumor progression and invasiveness related to the genes Cdh1 and Appl1. This analysis also revealed that the Tnf and Cdh1 genes were significantly up- and down-regulated, respectively, in tumors of rats that received I3C, in comparison with the hemin-fed group. These findings reveal that the joint administration of I3C and syn enhanced the development of colon tumors induced by DMH in hemin-fed rats, while they potentially reduced ACF development when given alone.
id UNSP_b5cfca2cbedac2ef5c4a6057a82d9762
oai_identifier_str oai:repositorio.unesp.br:11449/175909
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed ratsChemopreventionColorectal cancerHeminIndole 3-carbinolSynbiotcsThe risk of developing colorectal cancer (CRC) could be associated with red and processed meat intake. Experimental data supports that hemin iron, found abundantly in red meat, promotes CRC in mice and rats, while indole-3 carbinol (I3C) and synbiotics (syn) exert anti-carcinogenic activities in most studies of colon carcinogenesis. This study aimed to investigate the modifying effects of I3C and syn (inulin + Bifidobacterium lactis), given separately or together, on dimethylhidrazine (DMH)-induced colon carcinogenesis in hemin-fed rats. All animals were given four subcutaneous DMH injections and then, two weeks after carcinogen exposure, they began a basal diet containing hemin, hemin + I3C, hemin + syn, or hemin + I3C + syn for 23 weeks. The combination of I3C + syn significantly increased fecal water genotoxicity, tumor volume and invasiveness when compared to the hemin-fed control group. The groups fed I3C or syn alone had a significant reduction in the number of preneoplastic aberrant crypt foci (ACF) lesions compared to the hemin-fed group. Dietary I3C also reduced fecal water genotoxicity. Gene expression analysis of colorectal tumors demonstrated that the combination of dietary I3C + syn increased transcript levels for Raf1 and decreased tumor progression and invasiveness related to the genes Cdh1 and Appl1. This analysis also revealed that the Tnf and Cdh1 genes were significantly up- and down-regulated, respectively, in tumors of rats that received I3C, in comparison with the hemin-fed group. These findings reveal that the joint administration of I3C and syn enhanced the development of colon tumors induced by DMH in hemin-fed rats, while they potentially reduced ACF development when given alone.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Department of Morphology Institute of Biosciences of Botucatu Sao Paulo State University (UNESP)Department of Pathology School of Medicine Sao Paulo State University (UNESP)Department of Morphology Institute of Biosciences of Botucatu Sao Paulo State University (UNESP)Department of Pathology School of Medicine Sao Paulo State University (UNESP)FAPESP: 2011/23699-4FAPESP: 2012/12631-2FAPESP: 2013/08033-5CNPq: 303928/2012-3Universidade Estadual Paulista (Unesp)de Moura, Nelci A. [UNESP]Caetano, Brunno F.R. [UNESP]de Moraes, Leonardo N. [UNESP]Carvalho, Robson F. [UNESP]Rodrigues, Maria A.M. [UNESP]Barbisan, Luis F. [UNESP]2018-12-11T17:18:05Z2018-12-11T17:18:05Z2018-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article11-18application/pdfhttp://dx.doi.org/10.1016/j.fct.2017.12.029Food and Chemical Toxicology, v. 112, p. 11-18.1873-63510278-6915http://hdl.handle.net/11449/17590910.1016/j.fct.2017.12.0292-s2.0-850422256132-s2.0-85042225613.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengFood and Chemical Toxicology1,144info:eu-repo/semantics/openAccess2023-12-30T06:18:56Zoai:repositorio.unesp.br:11449/175909Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:41:40.956742Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
title Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
spellingShingle Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
de Moura, Nelci A. [UNESP]
Chemoprevention
Colorectal cancer
Hemin
Indole 3-carbinol
Synbiotcs
de Moura, Nelci A. [UNESP]
Chemoprevention
Colorectal cancer
Hemin
Indole 3-carbinol
Synbiotcs
title_short Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
title_full Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
title_fullStr Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
title_full_unstemmed Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
title_sort Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
author de Moura, Nelci A. [UNESP]
author_facet de Moura, Nelci A. [UNESP]
de Moura, Nelci A. [UNESP]
Caetano, Brunno F.R. [UNESP]
de Moraes, Leonardo N. [UNESP]
Carvalho, Robson F. [UNESP]
Rodrigues, Maria A.M. [UNESP]
Barbisan, Luis F. [UNESP]
Caetano, Brunno F.R. [UNESP]
de Moraes, Leonardo N. [UNESP]
Carvalho, Robson F. [UNESP]
Rodrigues, Maria A.M. [UNESP]
Barbisan, Luis F. [UNESP]
author_role author
author2 Caetano, Brunno F.R. [UNESP]
de Moraes, Leonardo N. [UNESP]
Carvalho, Robson F. [UNESP]
Rodrigues, Maria A.M. [UNESP]
Barbisan, Luis F. [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv de Moura, Nelci A. [UNESP]
Caetano, Brunno F.R. [UNESP]
de Moraes, Leonardo N. [UNESP]
Carvalho, Robson F. [UNESP]
Rodrigues, Maria A.M. [UNESP]
Barbisan, Luis F. [UNESP]
dc.subject.por.fl_str_mv Chemoprevention
Colorectal cancer
Hemin
Indole 3-carbinol
Synbiotcs
topic Chemoprevention
Colorectal cancer
Hemin
Indole 3-carbinol
Synbiotcs
description The risk of developing colorectal cancer (CRC) could be associated with red and processed meat intake. Experimental data supports that hemin iron, found abundantly in red meat, promotes CRC in mice and rats, while indole-3 carbinol (I3C) and synbiotics (syn) exert anti-carcinogenic activities in most studies of colon carcinogenesis. This study aimed to investigate the modifying effects of I3C and syn (inulin + Bifidobacterium lactis), given separately or together, on dimethylhidrazine (DMH)-induced colon carcinogenesis in hemin-fed rats. All animals were given four subcutaneous DMH injections and then, two weeks after carcinogen exposure, they began a basal diet containing hemin, hemin + I3C, hemin + syn, or hemin + I3C + syn for 23 weeks. The combination of I3C + syn significantly increased fecal water genotoxicity, tumor volume and invasiveness when compared to the hemin-fed control group. The groups fed I3C or syn alone had a significant reduction in the number of preneoplastic aberrant crypt foci (ACF) lesions compared to the hemin-fed group. Dietary I3C also reduced fecal water genotoxicity. Gene expression analysis of colorectal tumors demonstrated that the combination of dietary I3C + syn increased transcript levels for Raf1 and decreased tumor progression and invasiveness related to the genes Cdh1 and Appl1. This analysis also revealed that the Tnf and Cdh1 genes were significantly up- and down-regulated, respectively, in tumors of rats that received I3C, in comparison with the hemin-fed group. These findings reveal that the joint administration of I3C and syn enhanced the development of colon tumors induced by DMH in hemin-fed rats, while they potentially reduced ACF development when given alone.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:18:05Z
2018-12-11T17:18:05Z
2018-02-01
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/10.1016/j.fct.2017.12.029
Food and Chemical Toxicology, v. 112, p. 11-18.
1873-6351
0278-6915
http://hdl.handle.net/11449/175909
10.1016/j.fct.2017.12.029
2-s2.0-85042225613
2-s2.0-85042225613.pdf
url http://dx.doi.org/10.1016/j.fct.2017.12.029
http://hdl.handle.net/11449/175909
identifier_str_mv Food and Chemical Toxicology, v. 112, p. 11-18.
1873-6351
0278-6915
10.1016/j.fct.2017.12.029
2-s2.0-85042225613
2-s2.0-85042225613.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Food and Chemical Toxicology
1,144
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 11-18
application/pdf
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
_version_ 1822182252381995008
dc.identifier.doi.none.fl_str_mv 10.1016/j.fct.2017.12.029