An integrative approach to characterize the early phases of dimethylhydrazine-induced colorectal carcinogenesis in the rat
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , , , , , , , , |
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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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 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
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 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
nd nd nd nd nd nd nd nd nd nd nd nd nd nd nd nd nd |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799136697373425664 |