Enhancement of colon carcinogenesis by the combination of indole-3 carbinol and synbiotics in hemin-fed rats
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , |
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. |
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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 |