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Long non-coding RNA profiling of pediatric Medulloblastoma

BACKGROUND: Medulloblastoma (MB) is one of the most common malignant cancers in children. MB is primarily classified into four subgroups based on molecular and clinical characteristics as (1) WNT (2) Sonic-hedgehog (SHH) (3) Group 3 (4) Group 4. Molecular characteristics used for MB classification a...

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Autores principales: Kesherwani, Varun, Shukla, Mamta, Coulter, Don W., Sharp, J. Graham, Joshi, Shantaram S., Chaturvedi, Nagendra K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318516/
https://www.ncbi.nlm.nih.gov/pubmed/32591022
http://dx.doi.org/10.1186/s12920-020-00744-7
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author Kesherwani, Varun
Shukla, Mamta
Coulter, Don W.
Sharp, J. Graham
Joshi, Shantaram S.
Chaturvedi, Nagendra K.
author_facet Kesherwani, Varun
Shukla, Mamta
Coulter, Don W.
Sharp, J. Graham
Joshi, Shantaram S.
Chaturvedi, Nagendra K.
author_sort Kesherwani, Varun
collection PubMed
description BACKGROUND: Medulloblastoma (MB) is one of the most common malignant cancers in children. MB is primarily classified into four subgroups based on molecular and clinical characteristics as (1) WNT (2) Sonic-hedgehog (SHH) (3) Group 3 (4) Group 4. Molecular characteristics used for MB classification are based on genomic and mRNAs profiles. MB subgroups share genomic and mRNA profiles and require multiple molecular markers for differentiation from each other. Long non-coding RNAs (lncRNAs) are more than 200 nucleotide long RNAs and primarily involve in gene regulation at epigenetic and post-transcriptional levels. LncRNAs have been recognized as diagnostic and prognostic markers in several cancers. However, the lncRNA expression profile of MB is unknown. METHODS: We used the publicly available gene expression datasets for the profiling of lncRNA expression across MB subgroups. Functional analysis of differentially expressed lncRNAs was accomplished by Ingenuity pathway analysis (IPA). RESULTS: In the current study, we have identified and validated the lncRNA expression profile across pediatric MB subgroups and associated molecular pathways. We have also identified the prognostic significance of lncRNAs and unique lncRNAs associated with each MB subgroup. CONCLUSIONS: Identified lncRNAs can be used as single biomarkers for molecular identification of MB subgroups that warrant further investigation and functional validation.
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spelling pubmed-73185162020-06-29 Long non-coding RNA profiling of pediatric Medulloblastoma Kesherwani, Varun Shukla, Mamta Coulter, Don W. Sharp, J. Graham Joshi, Shantaram S. Chaturvedi, Nagendra K. BMC Med Genomics Research Article BACKGROUND: Medulloblastoma (MB) is one of the most common malignant cancers in children. MB is primarily classified into four subgroups based on molecular and clinical characteristics as (1) WNT (2) Sonic-hedgehog (SHH) (3) Group 3 (4) Group 4. Molecular characteristics used for MB classification are based on genomic and mRNAs profiles. MB subgroups share genomic and mRNA profiles and require multiple molecular markers for differentiation from each other. Long non-coding RNAs (lncRNAs) are more than 200 nucleotide long RNAs and primarily involve in gene regulation at epigenetic and post-transcriptional levels. LncRNAs have been recognized as diagnostic and prognostic markers in several cancers. However, the lncRNA expression profile of MB is unknown. METHODS: We used the publicly available gene expression datasets for the profiling of lncRNA expression across MB subgroups. Functional analysis of differentially expressed lncRNAs was accomplished by Ingenuity pathway analysis (IPA). RESULTS: In the current study, we have identified and validated the lncRNA expression profile across pediatric MB subgroups and associated molecular pathways. We have also identified the prognostic significance of lncRNAs and unique lncRNAs associated with each MB subgroup. CONCLUSIONS: Identified lncRNAs can be used as single biomarkers for molecular identification of MB subgroups that warrant further investigation and functional validation. BioMed Central 2020-06-26 /pmc/articles/PMC7318516/ /pubmed/32591022 http://dx.doi.org/10.1186/s12920-020-00744-7 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article
Kesherwani, Varun
Shukla, Mamta
Coulter, Don W.
Sharp, J. Graham
Joshi, Shantaram S.
Chaturvedi, Nagendra K.
Long non-coding RNA profiling of pediatric Medulloblastoma
title Long non-coding RNA profiling of pediatric Medulloblastoma
title_full Long non-coding RNA profiling of pediatric Medulloblastoma
title_fullStr Long non-coding RNA profiling of pediatric Medulloblastoma
title_full_unstemmed Long non-coding RNA profiling of pediatric Medulloblastoma
title_short Long non-coding RNA profiling of pediatric Medulloblastoma
title_sort long non-coding rna profiling of pediatric medulloblastoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318516/
https://www.ncbi.nlm.nih.gov/pubmed/32591022
http://dx.doi.org/10.1186/s12920-020-00744-7
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