Competing endogenous RNA in colorectal cancer : an analysis for colon, rectum, and rectosigmoid junction

Detalhes bibliográficos
Autor(a) principal: Vieira, Lucas Maciel
Data de Publicação: 2021
Outros Autores: Jorge, Natasha Andressa Nogueira, Sousa, João Batista, Setubal, João Carlos, Stadler, Peter Florian, Walter, Maria Emília Machado Telles
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UnB
Texto Completo: http://repositorio2.unb.br/jspui/handle/10482/48102
https://doi.org/10.3389/fonc.2021.681579
Resumo: Background: Colorectal cancer (CRC) is a heterogeneous cancer. Its treatment depends on its anatomical site and distinguishes between colon, rectum, and rectosigmoid junction cancer. This study aimed to identify diagnostic and prognostic biomarkers using networks of CRC-associated transcripts that can be built based on competing endogenous RNAs (ceRNA). Methods: RNA expression and clinical information data of patients with colon, rectum, and rectosigmoid junction cancer were obtained from The Cancer Genome Atlas (TCGA). The RNA expression profiles were assessed through bioinformatics analysis, and a ceRNA was constructed for each CRC site. A functional enrichment analysis was performed to assess the functional roles of the ceRNA networks in the prognosis of colon, rectum, and rectosigmoid junction cancer. Finally, to verify the ceRNA impact on prognosis, an overall survival analysis was performed. Results: The study identified various CRC site-specific prognosis biomarkers: hsa-miR-1271-5p, NRG1, hsa-miR-130a-3p, SNHG16, and hsa-miR-495-3p in the colon; E2F8 in the rectum and DMD and hsa-miR-130b-3p in the rectosigmoid junction. We also identified different biological pathways that highlight differences in CRC behavior at different anatomical sites, thus reinforcing the importance of correctly identifying the tumor site. Conclusions: Several potential prognostic markers for colon, rectum, and rectosigmoid junction cancer were found. CeRNA networks could provide better understanding of the differences between, and common factors in, prognosis of colon, rectum, and rectosigmoid junction cancer.
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spelling Competing endogenous RNA in colorectal cancer : an analysis for colon, rectum, and rectosigmoid junctionColón (Anatomia) - câncerReto - câncerRNA endógeno concorrenteRNAs não-codificadoresmiRNABackground: Colorectal cancer (CRC) is a heterogeneous cancer. Its treatment depends on its anatomical site and distinguishes between colon, rectum, and rectosigmoid junction cancer. This study aimed to identify diagnostic and prognostic biomarkers using networks of CRC-associated transcripts that can be built based on competing endogenous RNAs (ceRNA). Methods: RNA expression and clinical information data of patients with colon, rectum, and rectosigmoid junction cancer were obtained from The Cancer Genome Atlas (TCGA). The RNA expression profiles were assessed through bioinformatics analysis, and a ceRNA was constructed for each CRC site. A functional enrichment analysis was performed to assess the functional roles of the ceRNA networks in the prognosis of colon, rectum, and rectosigmoid junction cancer. Finally, to verify the ceRNA impact on prognosis, an overall survival analysis was performed. Results: The study identified various CRC site-specific prognosis biomarkers: hsa-miR-1271-5p, NRG1, hsa-miR-130a-3p, SNHG16, and hsa-miR-495-3p in the colon; E2F8 in the rectum and DMD and hsa-miR-130b-3p in the rectosigmoid junction. We also identified different biological pathways that highlight differences in CRC behavior at different anatomical sites, thus reinforcing the importance of correctly identifying the tumor site. Conclusions: Several potential prognostic markers for colon, rectum, and rectosigmoid junction cancer were found. CeRNA networks could provide better understanding of the differences between, and common factors in, prognosis of colon, rectum, and rectosigmoid junction cancer.Faculdade de Medicina (FM)FrontiersUniversity of Brasília, Instituto de Ciência Exatas, Departamento de Ciência da ComputaçãoBioinformatics Group, Department of Computer Science, and Interdisciplinary Center for Bioinformatics, Leipzig, GermanyBioinformatics Group, Department of Computer Science, and Interdisciplinary Center for Bioinformatics, Leipzig, GermanyUniversity of Brasília School of Medicine, Department of Surgery, Division of ColoproctologyUniversity of São Paulo, Institute of Chemistry, Department of BiochemistryBioinformatics Group, Department of Computer Science, and Interdisciplinary Center for Bioinformatics, Leipzig, GermanyMax Planck Institute for Mathematics in the Science, Leipzig, GermanyInstitute for Theoretical Chemistry, University of Vienna, Wien, AustriaFacultad de Ciencias, Universidad National de Colombia, Sede Bogotá, ColombiaSanta Fe Institute, Santa Fe, CA, United StatesUniversity of Brasília, Instituto de Ciência Exatas, Departamento de Ciência da ComputaçãoVieira, Lucas MacielJorge, Natasha Andressa NogueiraSousa, João BatistaSetubal, João CarlosStadler, Peter FlorianWalter, Maria Emília Machado Telles2024-05-20T12:30:52Z2024-05-20T12:30:52Z2021info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfVIEIRA, Lucas Maciel et al. Competing endogenous RNA in colorectal cancer: an analysis for colon, rectum, and rectosigmoid junction. Frontiers in oncology, 09 jun. 2021. DOI: https://doi.org/10.3389/fonc.2021.681579. Disponível em: https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2021.681579/full0. Acesso em: 20 maio 2024.http://repositorio2.unb.br/jspui/handle/10482/48102https://doi.org/10.3389/fonc.2021.681579engCopyright © 2021 Vieira, Jorge, de Sousa, Setubal, Stadler and Walter. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UnBinstname:Universidade de Brasília (UnB)instacron:UNB2024-05-20T12:39:07Zoai:repositorio.unb.br:10482/48102Repositório InstitucionalPUBhttps://repositorio.unb.br/oai/requestrepositorio@unb.bropendoar:2024-05-20T12:39:07Repositório Institucional da UnB - Universidade de Brasília (UnB)false
dc.title.none.fl_str_mv Competing endogenous RNA in colorectal cancer : an analysis for colon, rectum, and rectosigmoid junction
title Competing endogenous RNA in colorectal cancer : an analysis for colon, rectum, and rectosigmoid junction
spellingShingle Competing endogenous RNA in colorectal cancer : an analysis for colon, rectum, and rectosigmoid junction
Vieira, Lucas Maciel
Colón (Anatomia) - câncer
Reto - câncer
RNA endógeno concorrente
RNAs não-codificadores
miRNA
title_short Competing endogenous RNA in colorectal cancer : an analysis for colon, rectum, and rectosigmoid junction
title_full Competing endogenous RNA in colorectal cancer : an analysis for colon, rectum, and rectosigmoid junction
title_fullStr Competing endogenous RNA in colorectal cancer : an analysis for colon, rectum, and rectosigmoid junction
title_full_unstemmed Competing endogenous RNA in colorectal cancer : an analysis for colon, rectum, and rectosigmoid junction
title_sort Competing endogenous RNA in colorectal cancer : an analysis for colon, rectum, and rectosigmoid junction
author Vieira, Lucas Maciel
author_facet Vieira, Lucas Maciel
Jorge, Natasha Andressa Nogueira
Sousa, João Batista
Setubal, João Carlos
Stadler, Peter Florian
Walter, Maria Emília Machado Telles
author_role author
author2 Jorge, Natasha Andressa Nogueira
Sousa, João Batista
Setubal, João Carlos
Stadler, Peter Florian
Walter, Maria Emília Machado Telles
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv University of Brasília, Instituto de Ciência Exatas, Departamento de Ciência da Computação
Bioinformatics Group, Department of Computer Science, and Interdisciplinary Center for Bioinformatics, Leipzig, Germany
Bioinformatics Group, Department of Computer Science, and Interdisciplinary Center for Bioinformatics, Leipzig, Germany
University of Brasília School of Medicine, Department of Surgery, Division of Coloproctology
University of São Paulo, Institute of Chemistry, Department of Biochemistry
Bioinformatics Group, Department of Computer Science, and Interdisciplinary Center for Bioinformatics, Leipzig, Germany
Max Planck Institute for Mathematics in the Science, Leipzig, Germany
Institute for Theoretical Chemistry, University of Vienna, Wien, Austria
Facultad de Ciencias, Universidad National de Colombia, Sede Bogotá, Colombia
Santa Fe Institute, Santa Fe, CA, United States
University of Brasília, Instituto de Ciência Exatas, Departamento de Ciência da Computação
dc.contributor.author.fl_str_mv Vieira, Lucas Maciel
Jorge, Natasha Andressa Nogueira
Sousa, João Batista
Setubal, João Carlos
Stadler, Peter Florian
Walter, Maria Emília Machado Telles
dc.subject.por.fl_str_mv Colón (Anatomia) - câncer
Reto - câncer
RNA endógeno concorrente
RNAs não-codificadores
miRNA
topic Colón (Anatomia) - câncer
Reto - câncer
RNA endógeno concorrente
RNAs não-codificadores
miRNA
description Background: Colorectal cancer (CRC) is a heterogeneous cancer. Its treatment depends on its anatomical site and distinguishes between colon, rectum, and rectosigmoid junction cancer. This study aimed to identify diagnostic and prognostic biomarkers using networks of CRC-associated transcripts that can be built based on competing endogenous RNAs (ceRNA). Methods: RNA expression and clinical information data of patients with colon, rectum, and rectosigmoid junction cancer were obtained from The Cancer Genome Atlas (TCGA). The RNA expression profiles were assessed through bioinformatics analysis, and a ceRNA was constructed for each CRC site. A functional enrichment analysis was performed to assess the functional roles of the ceRNA networks in the prognosis of colon, rectum, and rectosigmoid junction cancer. Finally, to verify the ceRNA impact on prognosis, an overall survival analysis was performed. Results: The study identified various CRC site-specific prognosis biomarkers: hsa-miR-1271-5p, NRG1, hsa-miR-130a-3p, SNHG16, and hsa-miR-495-3p in the colon; E2F8 in the rectum and DMD and hsa-miR-130b-3p in the rectosigmoid junction. We also identified different biological pathways that highlight differences in CRC behavior at different anatomical sites, thus reinforcing the importance of correctly identifying the tumor site. Conclusions: Several potential prognostic markers for colon, rectum, and rectosigmoid junction cancer were found. CeRNA networks could provide better understanding of the differences between, and common factors in, prognosis of colon, rectum, and rectosigmoid junction cancer.
publishDate 2021
dc.date.none.fl_str_mv 2021
2024-05-20T12:30:52Z
2024-05-20T12:30:52Z
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 VIEIRA, Lucas Maciel et al. Competing endogenous RNA in colorectal cancer: an analysis for colon, rectum, and rectosigmoid junction. Frontiers in oncology, 09 jun. 2021. DOI: https://doi.org/10.3389/fonc.2021.681579. Disponível em: https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2021.681579/full0. Acesso em: 20 maio 2024.
http://repositorio2.unb.br/jspui/handle/10482/48102
https://doi.org/10.3389/fonc.2021.681579
identifier_str_mv VIEIRA, Lucas Maciel et al. Competing endogenous RNA in colorectal cancer: an analysis for colon, rectum, and rectosigmoid junction. Frontiers in oncology, 09 jun. 2021. DOI: https://doi.org/10.3389/fonc.2021.681579. Disponível em: https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2021.681579/full0. Acesso em: 20 maio 2024.
url http://repositorio2.unb.br/jspui/handle/10482/48102
https://doi.org/10.3389/fonc.2021.681579
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Frontiers
publisher.none.fl_str_mv Frontiers
dc.source.none.fl_str_mv reponame:Repositório Institucional da UnB
instname:Universidade de Brasília (UnB)
instacron:UNB
instname_str Universidade de Brasília (UnB)
instacron_str UNB
institution UNB
reponame_str Repositório Institucional da UnB
collection Repositório Institucional da UnB
repository.name.fl_str_mv Repositório Institucional da UnB - Universidade de Brasília (UnB)
repository.mail.fl_str_mv repositorio@unb.br
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