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Meta-analysis of miR-34 target mRNAs using an integrative online application

Members of the microRNA-34/miR-34 family are induced by the p53 tumor suppressor and themselves possess tumor suppressive properties, as they inhibit the translation of mRNAs that encode proteins involved in processes, such as proliferation, migration, invasion, and metastasis. Here we performed a c...

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Detalles Bibliográficos
Autores principales: Rokavec, Matjaz, Huang, Zekai, Hermeking, Heiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764205/
https://www.ncbi.nlm.nih.gov/pubmed/36582442
http://dx.doi.org/10.1016/j.csbj.2022.12.003
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author Rokavec, Matjaz
Huang, Zekai
Hermeking, Heiko
author_facet Rokavec, Matjaz
Huang, Zekai
Hermeking, Heiko
author_sort Rokavec, Matjaz
collection PubMed
description Members of the microRNA-34/miR-34 family are induced by the p53 tumor suppressor and themselves possess tumor suppressive properties, as they inhibit the translation of mRNAs that encode proteins involved in processes, such as proliferation, migration, invasion, and metastasis. Here we performed a comprehensive integrative meta-analysis of multiple computational and experimental miR-34 related datasets and developed tools to identify and characterize novel miR-34 targets. A miR-34 target probability score was generated for every mRNA to estimate the likelihood of representing a miR-34 target. Experimentally validated miR-34 targets were strongly enriched among mRNAs with the highest scores providing a proof of principle for our analysis. We integrated the results from the meta-analysis in a user-friendly METAmiR34TARGET website (www.metamir34target.com/) that allows to graphically represent the meta-analysis results for every mRNA. Moreover, the website harbors a screen function, which allows to select multiple miR-34-related criteria/analyses and cut-off values to facilitate the stringent and comprehensive prediction of relevant miR-34 targets in expression data obtained from cell lines and tumors/tissues. Furthermore, information on more than 200 miR-34 target mRNAs, that have been experimentally validated so far, has been integrated in the web-tool. The website and datasets provided here should facilitate further investigation into the mechanisms of tumor suppression by the p53/miR-34 connection and identification of potential cancer drug targets.
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spelling pubmed-97642052022-12-28 Meta-analysis of miR-34 target mRNAs using an integrative online application Rokavec, Matjaz Huang, Zekai Hermeking, Heiko Comput Struct Biotechnol J Research Article Members of the microRNA-34/miR-34 family are induced by the p53 tumor suppressor and themselves possess tumor suppressive properties, as they inhibit the translation of mRNAs that encode proteins involved in processes, such as proliferation, migration, invasion, and metastasis. Here we performed a comprehensive integrative meta-analysis of multiple computational and experimental miR-34 related datasets and developed tools to identify and characterize novel miR-34 targets. A miR-34 target probability score was generated for every mRNA to estimate the likelihood of representing a miR-34 target. Experimentally validated miR-34 targets were strongly enriched among mRNAs with the highest scores providing a proof of principle for our analysis. We integrated the results from the meta-analysis in a user-friendly METAmiR34TARGET website (www.metamir34target.com/) that allows to graphically represent the meta-analysis results for every mRNA. Moreover, the website harbors a screen function, which allows to select multiple miR-34-related criteria/analyses and cut-off values to facilitate the stringent and comprehensive prediction of relevant miR-34 targets in expression data obtained from cell lines and tumors/tissues. Furthermore, information on more than 200 miR-34 target mRNAs, that have been experimentally validated so far, has been integrated in the web-tool. The website and datasets provided here should facilitate further investigation into the mechanisms of tumor suppression by the p53/miR-34 connection and identification of potential cancer drug targets. Research Network of Computational and Structural Biotechnology 2022-12-06 /pmc/articles/PMC9764205/ /pubmed/36582442 http://dx.doi.org/10.1016/j.csbj.2022.12.003 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Rokavec, Matjaz
Huang, Zekai
Hermeking, Heiko
Meta-analysis of miR-34 target mRNAs using an integrative online application
title Meta-analysis of miR-34 target mRNAs using an integrative online application
title_full Meta-analysis of miR-34 target mRNAs using an integrative online application
title_fullStr Meta-analysis of miR-34 target mRNAs using an integrative online application
title_full_unstemmed Meta-analysis of miR-34 target mRNAs using an integrative online application
title_short Meta-analysis of miR-34 target mRNAs using an integrative online application
title_sort meta-analysis of mir-34 target mrnas using an integrative online application
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764205/
https://www.ncbi.nlm.nih.gov/pubmed/36582442
http://dx.doi.org/10.1016/j.csbj.2022.12.003
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