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The identification of miRNA and mRNA expression profiles associated with pediatric atypical teratoid/rhabdoid tumor

BACKGROUND: Atypical teratoid/rhabdoid tumor (AT/RT) is a malignant pediatric tumor of the central nervous system (CNS) with high recurrence and low survival rates that is often misdiagnosed. MicroRNAs (miRNAs) are involved in the tumorigenesis of numerous pediatric cancers, but their roles in AT/RT...

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Autores principales: Xu, Xinke, Yuan, Hongyao, Pan, Junping, Chen, Wei, Chen, Cheng, Li, Yang, Li, Fangcheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074338/
https://www.ncbi.nlm.nih.gov/pubmed/35524230
http://dx.doi.org/10.1186/s12885-022-09549-6
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author Xu, Xinke
Yuan, Hongyao
Pan, Junping
Chen, Wei
Chen, Cheng
Li, Yang
Li, Fangcheng
author_facet Xu, Xinke
Yuan, Hongyao
Pan, Junping
Chen, Wei
Chen, Cheng
Li, Yang
Li, Fangcheng
author_sort Xu, Xinke
collection PubMed
description BACKGROUND: Atypical teratoid/rhabdoid tumor (AT/RT) is a malignant pediatric tumor of the central nervous system (CNS) with high recurrence and low survival rates that is often misdiagnosed. MicroRNAs (miRNAs) are involved in the tumorigenesis of numerous pediatric cancers, but their roles in AT/RT remain unclear. METHODS: In this study, we used miRNA sequencing and gene expression microarrays from patient tissue to study both the miRNAome and transcriptome traits of AT/RT. RESULTS: Our findings demonstrate that 5 miRNAs were up-regulated, 16 miRNAs were down-regulated, 179 mRNAs were up-regulated and 402 mRNAs were down-regulated in AT/RT. qPCR revealed that hsa-miR-17-5p and MAP7 mRNA were the most significantly differentially expressed miRNA and mRNA in AT/RT tissues. Furthermore, the results from analyses using the miRTarBase database identified MAP7 mRNA as a target gene of hsa-miR-17-5p. CONCLUSIONS: Our findings suggest that the dysregulation of hsa-miR-17-5p may be a pivotal event in AT/RT and miRNAs that may represent potential therapeutic targets and diagnostic biomarkers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09549-6.
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spelling pubmed-90743382022-05-07 The identification of miRNA and mRNA expression profiles associated with pediatric atypical teratoid/rhabdoid tumor Xu, Xinke Yuan, Hongyao Pan, Junping Chen, Wei Chen, Cheng Li, Yang Li, Fangcheng BMC Cancer Research BACKGROUND: Atypical teratoid/rhabdoid tumor (AT/RT) is a malignant pediatric tumor of the central nervous system (CNS) with high recurrence and low survival rates that is often misdiagnosed. MicroRNAs (miRNAs) are involved in the tumorigenesis of numerous pediatric cancers, but their roles in AT/RT remain unclear. METHODS: In this study, we used miRNA sequencing and gene expression microarrays from patient tissue to study both the miRNAome and transcriptome traits of AT/RT. RESULTS: Our findings demonstrate that 5 miRNAs were up-regulated, 16 miRNAs were down-regulated, 179 mRNAs were up-regulated and 402 mRNAs were down-regulated in AT/RT. qPCR revealed that hsa-miR-17-5p and MAP7 mRNA were the most significantly differentially expressed miRNA and mRNA in AT/RT tissues. Furthermore, the results from analyses using the miRTarBase database identified MAP7 mRNA as a target gene of hsa-miR-17-5p. CONCLUSIONS: Our findings suggest that the dysregulation of hsa-miR-17-5p may be a pivotal event in AT/RT and miRNAs that may represent potential therapeutic targets and diagnostic biomarkers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09549-6. BioMed Central 2022-05-06 /pmc/articles/PMC9074338/ /pubmed/35524230 http://dx.doi.org/10.1186/s12885-022-09549-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Xu, Xinke
Yuan, Hongyao
Pan, Junping
Chen, Wei
Chen, Cheng
Li, Yang
Li, Fangcheng
The identification of miRNA and mRNA expression profiles associated with pediatric atypical teratoid/rhabdoid tumor
title The identification of miRNA and mRNA expression profiles associated with pediatric atypical teratoid/rhabdoid tumor
title_full The identification of miRNA and mRNA expression profiles associated with pediatric atypical teratoid/rhabdoid tumor
title_fullStr The identification of miRNA and mRNA expression profiles associated with pediatric atypical teratoid/rhabdoid tumor
title_full_unstemmed The identification of miRNA and mRNA expression profiles associated with pediatric atypical teratoid/rhabdoid tumor
title_short The identification of miRNA and mRNA expression profiles associated with pediatric atypical teratoid/rhabdoid tumor
title_sort identification of mirna and mrna expression profiles associated with pediatric atypical teratoid/rhabdoid tumor
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074338/
https://www.ncbi.nlm.nih.gov/pubmed/35524230
http://dx.doi.org/10.1186/s12885-022-09549-6
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