An integrative approach to characterize the early phases of dimethylhydrazine-induced colorectal carcinogenesis in the rat

Detalhes bibliográficos
Autor(a) principal: Silva-Reis, Carla
Data de Publicação: 2022
Outros Autores: Castro-Ribeiro, C, Gonçalves, M, Ferreira, T, Pires, MJ, Iglesias-Aguirre, CE, Cortés-Martín, A, Selma, MV, Espín, JC, Nascimento-Gonçalves, E, Moreira-Pais, A, Neuparth, MJ, Peixoto, F, Rosa, E, Gama, A, Ferreira, R, Oliveira, PA
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10174/32791
https://doi.org/10.3390/biomedicines10020409
Resumo: This study aimed to characterize an animal model of colorectal cancer (CRC) in the early stages of disease development. Twenty-nine male Wistar rats were divided into two control groups (CTRL1 and CTRL2), receiving EDTA–saline injections and two induced groups (CRC1 and CRC2), receiving 1,2-dimethylhydrazine (DMH) injections for seven consecutive weeks. CRC1 and CTRL1 were euthanized at the 11th week, while CRC2 and CTRL2 were euthanized at the 17th week. DMH treatment decreased microhematocrit values and IL-6, ghrelin, and myostatin serum levels. Histopathological analysis of intestinal sections showed that DMH-treated rats were characterized by moderate to severe epithelial dysplasia. An adenoma was observed in one animal (CRC2 group), and the presence of inflammatory infiltrate at the intestinal level was primarily observed in DMH-treated animals. DMH also induced Ki-67 immunoexpression. The gut microbiota analysis showed a higher abundance of Firmicutes, Clostridia, Clostridiales, Peptostreptococcaceae, Blautia, Romboutsia, and Clostridium sensu stricto in CRC than CTRL rats, whereas Prevotellaceae, Prevotella, Akkermansia, and Lactobacillus levels were more prevalent in CTRL animals. Our results suggest that this model could be helpful to investigate chemoprevention in the early stages of CRC.
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spelling An integrative approach to characterize the early phases of dimethylhydrazine-induced colorectal carcinogenesis in the ratThis study aimed to characterize an animal model of colorectal cancer (CRC) in the early stages of disease development. Twenty-nine male Wistar rats were divided into two control groups (CTRL1 and CTRL2), receiving EDTA–saline injections and two induced groups (CRC1 and CRC2), receiving 1,2-dimethylhydrazine (DMH) injections for seven consecutive weeks. CRC1 and CTRL1 were euthanized at the 11th week, while CRC2 and CTRL2 were euthanized at the 17th week. DMH treatment decreased microhematocrit values and IL-6, ghrelin, and myostatin serum levels. Histopathological analysis of intestinal sections showed that DMH-treated rats were characterized by moderate to severe epithelial dysplasia. An adenoma was observed in one animal (CRC2 group), and the presence of inflammatory infiltrate at the intestinal level was primarily observed in DMH-treated animals. DMH also induced Ki-67 immunoexpression. The gut microbiota analysis showed a higher abundance of Firmicutes, Clostridia, Clostridiales, Peptostreptococcaceae, Blautia, Romboutsia, and Clostridium sensu stricto in CRC than CTRL rats, whereas Prevotellaceae, Prevotella, Akkermansia, and Lactobacillus levels were more prevalent in CTRL animals. Our results suggest that this model could be helpful to investigate chemoprevention in the early stages of CRC.Biomedicines2022-11-17T17:36:47Z2022-11-172022-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10174/32791http://hdl.handle.net/10174/32791https://doi.org/10.3390/biomedicines10020409porndndndndndndndndndndndndndndndndndSilva-Reis, CarlaCastro-Ribeiro, CGonçalves, MFerreira, TPires, MJIglesias-Aguirre, CECortés-Martín, ASelma, MVEspín, JCNascimento-Gonçalves, EMoreira-Pais, ANeuparth, MJPeixoto, FRosa, EGama, AFerreira, ROliveira, PAinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-01-03T19:33:33Zoai:dspace.uevora.pt:10174/32791Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T01:21:35.816020Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv An integrative approach to characterize the early phases of dimethylhydrazine-induced colorectal carcinogenesis in the rat
title An integrative approach to characterize the early phases of dimethylhydrazine-induced colorectal carcinogenesis in the rat
spellingShingle An integrative approach to characterize the early phases of dimethylhydrazine-induced colorectal carcinogenesis in the rat
Silva-Reis, Carla
title_short An integrative approach to characterize the early phases of dimethylhydrazine-induced colorectal carcinogenesis in the rat
title_full An integrative approach to characterize the early phases of dimethylhydrazine-induced colorectal carcinogenesis in the rat
title_fullStr An integrative approach to characterize the early phases of dimethylhydrazine-induced colorectal carcinogenesis in the rat
title_full_unstemmed An integrative approach to characterize the early phases of dimethylhydrazine-induced colorectal carcinogenesis in the rat
title_sort An integrative approach to characterize the early phases of dimethylhydrazine-induced colorectal carcinogenesis in the rat
author Silva-Reis, Carla
author_facet Silva-Reis, Carla
Castro-Ribeiro, C
Gonçalves, M
Ferreira, T
Pires, MJ
Iglesias-Aguirre, CE
Cortés-Martín, A
Selma, MV
Espín, JC
Nascimento-Gonçalves, E
Moreira-Pais, A
Neuparth, MJ
Peixoto, F
Rosa, E
Gama, A
Ferreira, R
Oliveira, PA
author_role author
author2 Castro-Ribeiro, C
Gonçalves, M
Ferreira, T
Pires, MJ
Iglesias-Aguirre, CE
Cortés-Martín, A
Selma, MV
Espín, JC
Nascimento-Gonçalves, E
Moreira-Pais, A
Neuparth, MJ
Peixoto, F
Rosa, E
Gama, A
Ferreira, R
Oliveira, PA
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Silva-Reis, Carla
Castro-Ribeiro, C
Gonçalves, M
Ferreira, T
Pires, MJ
Iglesias-Aguirre, CE
Cortés-Martín, A
Selma, MV
Espín, JC
Nascimento-Gonçalves, E
Moreira-Pais, A
Neuparth, MJ
Peixoto, F
Rosa, E
Gama, A
Ferreira, R
Oliveira, PA
description This study aimed to characterize an animal model of colorectal cancer (CRC) in the early stages of disease development. Twenty-nine male Wistar rats were divided into two control groups (CTRL1 and CTRL2), receiving EDTA–saline injections and two induced groups (CRC1 and CRC2), receiving 1,2-dimethylhydrazine (DMH) injections for seven consecutive weeks. CRC1 and CTRL1 were euthanized at the 11th week, while CRC2 and CTRL2 were euthanized at the 17th week. DMH treatment decreased microhematocrit values and IL-6, ghrelin, and myostatin serum levels. Histopathological analysis of intestinal sections showed that DMH-treated rats were characterized by moderate to severe epithelial dysplasia. An adenoma was observed in one animal (CRC2 group), and the presence of inflammatory infiltrate at the intestinal level was primarily observed in DMH-treated animals. DMH also induced Ki-67 immunoexpression. The gut microbiota analysis showed a higher abundance of Firmicutes, Clostridia, Clostridiales, Peptostreptococcaceae, Blautia, Romboutsia, and Clostridium sensu stricto in CRC than CTRL rats, whereas Prevotellaceae, Prevotella, Akkermansia, and Lactobacillus levels were more prevalent in CTRL animals. Our results suggest that this model could be helpful to investigate chemoprevention in the early stages of CRC.
publishDate 2022
dc.date.none.fl_str_mv 2022-11-17T17:36:47Z
2022-11-17
2022-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10174/32791
http://hdl.handle.net/10174/32791
https://doi.org/10.3390/biomedicines10020409
url http://hdl.handle.net/10174/32791
https://doi.org/10.3390/biomedicines10020409
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dc.publisher.none.fl_str_mv Biomedicines
publisher.none.fl_str_mv Biomedicines
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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