Logotipo do repositório
 

Publicação:
Arthrospira (Spirulina) platensis feeding reduces the early stage of chemically-induced rat colon carcinogenesis

dc.contributor.authorAmadeu, Simone Oliveira [UNESP]
dc.contributor.authorSarmiento-Machado, Luis Manuel [UNESP]
dc.contributor.authorBartolomeu, Ariane Rocha [UNESP]
dc.contributor.authorChaves, María Angel García
dc.contributor.authorRomualdo, Guilherme Ribeiro [UNESP]
dc.contributor.authorMoura, Nelci Antunes de [UNESP]
dc.contributor.authorBarbisan, Luis Fernando [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversity of Granada
dc.date.accessioned2023-03-01T20:43:57Z
dc.date.available2023-03-01T20:43:57Z
dc.date.issued2022-01-01
dc.description.abstractColorectal cancer is the third most diagnosed cancer worldwide and linked to dietary/lifestyle factors. Arthrospira (Spirulina) platensis (AP) contains bioactive compounds with beneficial effects in vivo/in vitro. Thus, we evaluated the preventive effects of AP feeding against 1,2- dimethylhydrazine (DMH)-induced colon carcinogenesis. Male Sprague Dawley rats were given subcutaneous injections of DMH (4×40 mg/kg body weight) (G1-G3) or vehicle (G4-G5) twice a week (weeks 3-4). During weeks 1-4, animals were fed a diet containing 1% (G2) or 2% (G3-G4) AP powder (w/w) as a chemopreventive agent. After this period, all groups received a balanced diet until week 12. Some animals were euthanized after the last DMH injection (week 4) for histological, immunohistochemical (Ki-67, γ-H2AX and caspase-3) and molecular analyses (RT-PCR for 91 genes), while other animals were euthanized at week 12 for preneoplastic aberrant crypt foci (ACF) analysis. Both AP treatments (G2-G3) significantly decreased the DMH-induced increase in γ-H2AX (DNA damage) and caspase 3 (DNA damage-induced cell death) in colonic crypts at week 4. In addition, Cyp2e1 (Drug metabolism), Notch1, Notch2, and Jag1 genes (Notch pathway) and Atm, Wee1, Chek2, Mgmt, Ogg1 and Xrcc6 genes (DNA repair) were also down-regulated by 2% AP feeding (G3) at week 4. A significant reduction in ACF development was observed in both AP-treated groups (G2-G3) at week 12. In conclusion, findings indicate that AP feeding reduced acute colonic damage after DMH, resulting in fewer preneoplastic lesions. Our study provided mechanistic insights on dietary AP-preventive effects against early colon carcinogenesis.en
dc.description.affiliationProgram of General and Applied Biology Biosciences Institute Sao Paulo State University (UNESP), SP
dc.description.affiliationProgram of Pathology Botucatu Medical School Sao Paulo State University (UNESP), SP
dc.description.affiliationDepartment of Oncology Biosanitary Research Institute of Granada (Ibs.GRANADA) University Hospitals of Granada University of Granada
dc.description.affiliationDepartment of Structural and Functional Biology Institute of Biosciences Sao Paulo State University (UNESP), SP
dc.description.affiliationUnespProgram of General and Applied Biology Biosciences Institute Sao Paulo State University (UNESP), SP
dc.description.affiliationUnespProgram of Pathology Botucatu Medical School Sao Paulo State University (UNESP), SP
dc.description.affiliationUnespDepartment of Structural and Functional Biology Institute of Biosciences Sao Paulo State University (UNESP), SP
dc.identifierhttp://dx.doi.org/10.1017/S0007114522001350
dc.identifier.citationBritish Journal of Nutrition.
dc.identifier.doi10.1017/S0007114522001350
dc.identifier.issn1475-2662
dc.identifier.issn0007-1145
dc.identifier.scopus2-s2.0-85130579704
dc.identifier.urihttp://hdl.handle.net/11449/241031
dc.language.isoeng
dc.relation.ispartofBritish Journal of Nutrition
dc.sourceScopus
dc.subjectArthrospira (Spirulina) platensis
dc.subjectcolon cancer prevention
dc.subjectcolonic preneoplastic lesions
dc.subjectNotch and DNA repair genes
dc.subjecttumor initiation
dc.titleArthrospira (Spirulina) platensis feeding reduces the early stage of chemically-induced rat colon carcinogenesisen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0002-2180-1814[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentPatologia - FMBpt

Arquivos