Caffeine and Chlorogenic Acid Combination Attenuate Early-Stage Chemically Induced Colon Carcinogenesis in Mice: Involvement of oncomiR miR-21a-5p
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , |
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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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 |
_version_ |
1810021414182322176 |