Caffeine and Chlorogenic Acid Combination Attenuate Early-Stage Chemically Induced Colon Carcinogenesis in Mice: Involvement of oncomiR miR-21a-5p

Detalhes bibliográficos
Autor(a) principal: Bartolomeu, Ariane Rocha [UNESP]
Data de Publicação: 2022
Outros Autores: Romualdo, Guilherme Ribeiro [UNESP], Lisón, Carmen Griñán, Besharat, Zein Mersini, Corrales, Juan Antonio Marchal, Chaves, Maria Ángel García, Barbisan, Luís Fernando [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/ijms23116292
http://hdl.handle.net/11449/241091
Resumo: Colorectal cancer (CRC) is one of most common cancers worldwide, with high rates of mortality. Epidemiological findings demonstrate that coffee consumption reduces the risk of developing CRC by ~13%. In general, in vivo and in vitro findings demonstrate the antiproliferative, antioxidant and proapoptotic effects of brewed coffee or major bioavailable coffee compounds. Thus, it was assessed whether caffeine (CAF) and/or chlorogenic acid (CGA) attenuates the early-stage of chemically induced mouse colon carcinogenesis. Male Swiss mice were submitted to a 1,2-dimethylhydrazine/deoxycholic acid (DMH/DCA)-induced colon carcinogenesis model. These animals received CAF (50 mg/kg), CGA (25 mg/kg) or CAF+CGA (50 + 25 mg/kg) intragastrically for five times/week for ten weeks. CAF+CGA had the most pronounced effects on decreasing epithelial cell proliferation (Ki-67) and increasing apoptosis (cleaved caspase-3) in colonic crypts. This treatment also decreased the levels of proinflammatory cytokines IL-6, IL-17 and TNF-α, and downregulated the oncomiR miR-21a-5p in the colon. Accordingly, the analysis of miR-21a-5p targets demonstrated the genes involved in the negative regulation of proliferation and inflammation, and the positive regulation of apoptosis. Ultimately, CAF+CGA attenuated preneoplastic aberrant crypt foci (ACF) development. Our findings suggest that a combination of coffee compounds reduces early-stage colon carcinogenesis by the modulation of miR-21a-5p expression, highlighting the importance of coffee intake to prevent CRC.
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spelling Caffeine and Chlorogenic Acid Combination Attenuate Early-Stage Chemically Induced Colon Carcinogenesis in Mice: Involvement of oncomiR miR-21a-5pcaffeinechemically induced colon carcinogenesischlorogenic acidmicemiRNA expressionColorectal cancer (CRC) is one of most common cancers worldwide, with high rates of mortality. Epidemiological findings demonstrate that coffee consumption reduces the risk of developing CRC by ~13%. In general, in vivo and in vitro findings demonstrate the antiproliferative, antioxidant and proapoptotic effects of brewed coffee or major bioavailable coffee compounds. Thus, it was assessed whether caffeine (CAF) and/or chlorogenic acid (CGA) attenuates the early-stage of chemically induced mouse colon carcinogenesis. Male Swiss mice were submitted to a 1,2-dimethylhydrazine/deoxycholic acid (DMH/DCA)-induced colon carcinogenesis model. These animals received CAF (50 mg/kg), CGA (25 mg/kg) or CAF+CGA (50 + 25 mg/kg) intragastrically for five times/week for ten weeks. CAF+CGA had the most pronounced effects on decreasing epithelial cell proliferation (Ki-67) and increasing apoptosis (cleaved caspase-3) in colonic crypts. This treatment also decreased the levels of proinflammatory cytokines IL-6, IL-17 and TNF-α, and downregulated the oncomiR miR-21a-5p in the colon. Accordingly, the analysis of miR-21a-5p targets demonstrated the genes involved in the negative regulation of proliferation and inflammation, and the positive regulation of apoptosis. Ultimately, CAF+CGA attenuated preneoplastic aberrant crypt foci (ACF) development. Our findings suggest that a combination of coffee compounds reduces early-stage colon carcinogenesis by the modulation of miR-21a-5p expression, highlighting the importance of coffee intake to prevent CRC.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Pathology Botucatu Medical School São Paulo State University (UNESP), SPDepartment of Structural and Functional Biology Biosciences Institute São Paulo State University (UNESP), SPBiosanitary Research Institute of Granada (ibs.GRANADA) University Hospitals of Granada University of GranadaGENYO (Centre for Genomics and Oncological Research) Pfizer/University of Granada/Andalusian Regional GovernmentUGC de Oncología Médica Complejo Hospitalario de JaenDepartment of Experimental Medicine Sapienza University of RomeDepartment of Human Anatomy and Embryology School of Medicine University of GranadaDepartment of Biochemistry and Molecular Biology III and Immunology University of GranadaDepartment of Pathology Botucatu Medical School São Paulo State University (UNESP), SPDepartment of Structural and Functional Biology Biosciences Institute São Paulo State University (UNESP), SPFAPESP: #2016/12015–0FAPESP: #2016/14420–0FAPESP: #2017/26217-7Universidade Estadual Paulista (UNESP)University of GranadaPfizer/University of Granada/Andalusian Regional GovernmentComplejo Hospitalario de JaenSapienza University of RomeBartolomeu, Ariane Rocha [UNESP]Romualdo, Guilherme Ribeiro [UNESP]Lisón, Carmen GriñánBesharat, Zein MersiniCorrales, Juan Antonio MarchalChaves, Maria Ángel GarcíaBarbisan, Luís Fernando [UNESP]2023-03-01T20:46:42Z2023-03-01T20:46:42Z2022-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/ijms23116292International Journal of Molecular Sciences, v. 23, n. 11, 2022.1422-00671661-6596http://hdl.handle.net/11449/24109110.3390/ijms231162922-s2.0-85131179138Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Journal of Molecular Sciencesinfo:eu-repo/semantics/openAccess2024-09-03T13:18:24Zoai:repositorio.unesp.br:11449/241091Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T13:18:24Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Caffeine and Chlorogenic Acid Combination Attenuate Early-Stage Chemically Induced Colon Carcinogenesis in Mice: Involvement of oncomiR miR-21a-5p
title Caffeine and Chlorogenic Acid Combination Attenuate Early-Stage Chemically Induced Colon Carcinogenesis in Mice: Involvement of oncomiR miR-21a-5p
spellingShingle Caffeine and Chlorogenic Acid Combination Attenuate Early-Stage Chemically Induced Colon Carcinogenesis in Mice: Involvement of oncomiR miR-21a-5p
Bartolomeu, Ariane Rocha [UNESP]
caffeine
chemically induced colon carcinogenesis
chlorogenic acid
mice
miRNA expression
title_short Caffeine and Chlorogenic Acid Combination Attenuate Early-Stage Chemically Induced Colon Carcinogenesis in Mice: Involvement of oncomiR miR-21a-5p
title_full Caffeine and Chlorogenic Acid Combination Attenuate Early-Stage Chemically Induced Colon Carcinogenesis in Mice: Involvement of oncomiR miR-21a-5p
title_fullStr Caffeine and Chlorogenic Acid Combination Attenuate Early-Stage Chemically Induced Colon Carcinogenesis in Mice: Involvement of oncomiR miR-21a-5p
title_full_unstemmed Caffeine and Chlorogenic Acid Combination Attenuate Early-Stage Chemically Induced Colon Carcinogenesis in Mice: Involvement of oncomiR miR-21a-5p
title_sort Caffeine and Chlorogenic Acid Combination Attenuate Early-Stage Chemically Induced Colon Carcinogenesis in Mice: Involvement of oncomiR miR-21a-5p
author Bartolomeu, Ariane Rocha [UNESP]
author_facet Bartolomeu, Ariane Rocha [UNESP]
Romualdo, Guilherme Ribeiro [UNESP]
Lisón, Carmen Griñán
Besharat, Zein Mersini
Corrales, Juan Antonio Marchal
Chaves, Maria Ángel García
Barbisan, Luís Fernando [UNESP]
author_role author
author2 Romualdo, Guilherme Ribeiro [UNESP]
Lisón, Carmen Griñán
Besharat, Zein Mersini
Corrales, Juan Antonio Marchal
Chaves, Maria Ángel García
Barbisan, Luís Fernando [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
University of Granada
Pfizer/University of Granada/Andalusian Regional Government
Complejo Hospitalario de Jaen
Sapienza University of Rome
dc.contributor.author.fl_str_mv Bartolomeu, Ariane Rocha [UNESP]
Romualdo, Guilherme Ribeiro [UNESP]
Lisón, Carmen Griñán
Besharat, Zein Mersini
Corrales, Juan Antonio Marchal
Chaves, Maria Ángel García
Barbisan, Luís Fernando [UNESP]
dc.subject.por.fl_str_mv caffeine
chemically induced colon carcinogenesis
chlorogenic acid
mice
miRNA expression
topic caffeine
chemically induced colon carcinogenesis
chlorogenic acid
mice
miRNA expression
description Colorectal cancer (CRC) is one of most common cancers worldwide, with high rates of mortality. Epidemiological findings demonstrate that coffee consumption reduces the risk of developing CRC by ~13%. In general, in vivo and in vitro findings demonstrate the antiproliferative, antioxidant and proapoptotic effects of brewed coffee or major bioavailable coffee compounds. Thus, it was assessed whether caffeine (CAF) and/or chlorogenic acid (CGA) attenuates the early-stage of chemically induced mouse colon carcinogenesis. Male Swiss mice were submitted to a 1,2-dimethylhydrazine/deoxycholic acid (DMH/DCA)-induced colon carcinogenesis model. These animals received CAF (50 mg/kg), CGA (25 mg/kg) or CAF+CGA (50 + 25 mg/kg) intragastrically for five times/week for ten weeks. CAF+CGA had the most pronounced effects on decreasing epithelial cell proliferation (Ki-67) and increasing apoptosis (cleaved caspase-3) in colonic crypts. This treatment also decreased the levels of proinflammatory cytokines IL-6, IL-17 and TNF-α, and downregulated the oncomiR miR-21a-5p in the colon. Accordingly, the analysis of miR-21a-5p targets demonstrated the genes involved in the negative regulation of proliferation and inflammation, and the positive regulation of apoptosis. Ultimately, CAF+CGA attenuated preneoplastic aberrant crypt foci (ACF) development. Our findings suggest that a combination of coffee compounds reduces early-stage colon carcinogenesis by the modulation of miR-21a-5p expression, highlighting the importance of coffee intake to prevent CRC.
publishDate 2022
dc.date.none.fl_str_mv 2022-06-01
2023-03-01T20:46:42Z
2023-03-01T20:46:42Z
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/10.3390/ijms23116292
International Journal of Molecular Sciences, v. 23, n. 11, 2022.
1422-0067
1661-6596
http://hdl.handle.net/11449/241091
10.3390/ijms23116292
2-s2.0-85131179138
url http://dx.doi.org/10.3390/ijms23116292
http://hdl.handle.net/11449/241091
identifier_str_mv International Journal of Molecular Sciences, v. 23, n. 11, 2022.
1422-0067
1661-6596
10.3390/ijms23116292
2-s2.0-85131179138
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv International Journal of Molecular Sciences
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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 repositoriounesp@unesp.br
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