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Bioinformatics analysis of circulating miRNAs related to cancer following spinal cord injury

Patients with spinal cord injury (SCI) have an increased risk of developing esophageal, bladder and hematologic malignancies compared with the normal population. In the present study, we aimed to identify, through in silico analysis, miRNAs and their target genes related to the three most frequent t...

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Autores principales: Lopes, Elisangela C.P., Paim, Layde R., Matos-Souza, José R., Calegari, Décio R., Gorla, José I., Cliquet, Alberto, Lima, Carmen S.P., McDonald, John F., Nadruz, Wilson, Schreiber, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753324/
https://www.ncbi.nlm.nih.gov/pubmed/31444279
http://dx.doi.org/10.1042/BSR20190989
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author Lopes, Elisangela C.P.
Paim, Layde R.
Matos-Souza, José R.
Calegari, Décio R.
Gorla, José I.
Cliquet, Alberto
Lima, Carmen S.P.
McDonald, John F.
Nadruz, Wilson
Schreiber, Roberto
author_facet Lopes, Elisangela C.P.
Paim, Layde R.
Matos-Souza, José R.
Calegari, Décio R.
Gorla, José I.
Cliquet, Alberto
Lima, Carmen S.P.
McDonald, John F.
Nadruz, Wilson
Schreiber, Roberto
author_sort Lopes, Elisangela C.P.
collection PubMed
description Patients with spinal cord injury (SCI) have an increased risk of developing esophageal, bladder and hematologic malignancies compared with the normal population. In the present study, we aimed to identify, through in silico analysis, miRNAs and their target genes related to the three most frequent types of cancer in individuals with SCI. In a previous study, we reported a pattern of expression of miRNAs in 17 sedentary SCI males compared with 22 healthy able-bodied males by TaqMan OpenArray. This list of miRNAs deregulated in SCI patients was uploaded to miRWALK2.0 to predict the target genes and pathways of selected miRNAs. We used Cytoscape software to construct the network displaying the miRNAs and their gene targets. Among the down-regulated miRNAs in SCI, 21, 19 and 20 miRNAs were potentially associated with hematological, bladder and esophageal cancer, respectively, and three target genes (TP53, CCND1 and KRAS) were common to all three types of cancer. The three up-regulated miRNAs were potentially targeted by 18, 15 and 10 genes associated with all three types of cancer. Our current bioinformatics analysis suggests the potential influence of several miRNAs on the development of cancer in SCI. In general, these data may provide novel information regarding potential molecular mechanisms involved in the development of cancer among individuals with SCI. Further studies aiming at understanding how miRNAs contribute to the development of the major cancers that affect patients after SCI may help elucidate the role of these molecules in the pathophysiology of the disease.
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spelling pubmed-67533242019-09-25 Bioinformatics analysis of circulating miRNAs related to cancer following spinal cord injury Lopes, Elisangela C.P. Paim, Layde R. Matos-Souza, José R. Calegari, Décio R. Gorla, José I. Cliquet, Alberto Lima, Carmen S.P. McDonald, John F. Nadruz, Wilson Schreiber, Roberto Biosci Rep Research Articles Patients with spinal cord injury (SCI) have an increased risk of developing esophageal, bladder and hematologic malignancies compared with the normal population. In the present study, we aimed to identify, through in silico analysis, miRNAs and their target genes related to the three most frequent types of cancer in individuals with SCI. In a previous study, we reported a pattern of expression of miRNAs in 17 sedentary SCI males compared with 22 healthy able-bodied males by TaqMan OpenArray. This list of miRNAs deregulated in SCI patients was uploaded to miRWALK2.0 to predict the target genes and pathways of selected miRNAs. We used Cytoscape software to construct the network displaying the miRNAs and their gene targets. Among the down-regulated miRNAs in SCI, 21, 19 and 20 miRNAs were potentially associated with hematological, bladder and esophageal cancer, respectively, and three target genes (TP53, CCND1 and KRAS) were common to all three types of cancer. The three up-regulated miRNAs were potentially targeted by 18, 15 and 10 genes associated with all three types of cancer. Our current bioinformatics analysis suggests the potential influence of several miRNAs on the development of cancer in SCI. In general, these data may provide novel information regarding potential molecular mechanisms involved in the development of cancer among individuals with SCI. Further studies aiming at understanding how miRNAs contribute to the development of the major cancers that affect patients after SCI may help elucidate the role of these molecules in the pathophysiology of the disease. Portland Press Ltd. 2019-09-20 /pmc/articles/PMC6753324/ /pubmed/31444279 http://dx.doi.org/10.1042/BSR20190989 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Lopes, Elisangela C.P.
Paim, Layde R.
Matos-Souza, José R.
Calegari, Décio R.
Gorla, José I.
Cliquet, Alberto
Lima, Carmen S.P.
McDonald, John F.
Nadruz, Wilson
Schreiber, Roberto
Bioinformatics analysis of circulating miRNAs related to cancer following spinal cord injury
title Bioinformatics analysis of circulating miRNAs related to cancer following spinal cord injury
title_full Bioinformatics analysis of circulating miRNAs related to cancer following spinal cord injury
title_fullStr Bioinformatics analysis of circulating miRNAs related to cancer following spinal cord injury
title_full_unstemmed Bioinformatics analysis of circulating miRNAs related to cancer following spinal cord injury
title_short Bioinformatics analysis of circulating miRNAs related to cancer following spinal cord injury
title_sort bioinformatics analysis of circulating mirnas related to cancer following spinal cord injury
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753324/
https://www.ncbi.nlm.nih.gov/pubmed/31444279
http://dx.doi.org/10.1042/BSR20190989
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