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The oncogenic circular RNA circ_63706 is a potential therapeutic target in sonic hedgehog-subtype childhood medulloblastomas
Medulloblastoma (MB) develops through various genetic, epigenetic, and non-coding (nc) RNA-related mechanisms, but the roles played by ncRNAs, particularly circular RNAs (circRNAs), remain poorly defined. CircRNAs are increasingly recognized as stable non-coding RNA therapeutic targets in many cance...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10007801/ https://www.ncbi.nlm.nih.gov/pubmed/36899402 http://dx.doi.org/10.1186/s40478-023-01521-0 |
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author | Katsushima, Keisuke Pokhrel, Rudramani Mahmud, Iqbal Yuan, Menglang Murad, Rabi Baral, Prabin Zhou, Rui Chapagain, Prem Garrett, Timothy Stapleton, Stacie Jallo, George Bettegowda, Chetan Raabe, Eric Wechsler-Reya, Robert J. Eberhart, Charles G. Perera, Ranjan J. |
author_facet | Katsushima, Keisuke Pokhrel, Rudramani Mahmud, Iqbal Yuan, Menglang Murad, Rabi Baral, Prabin Zhou, Rui Chapagain, Prem Garrett, Timothy Stapleton, Stacie Jallo, George Bettegowda, Chetan Raabe, Eric Wechsler-Reya, Robert J. Eberhart, Charles G. Perera, Ranjan J. |
author_sort | Katsushima, Keisuke |
collection | PubMed |
description | Medulloblastoma (MB) develops through various genetic, epigenetic, and non-coding (nc) RNA-related mechanisms, but the roles played by ncRNAs, particularly circular RNAs (circRNAs), remain poorly defined. CircRNAs are increasingly recognized as stable non-coding RNA therapeutic targets in many cancers, but little is known about their function in MBs. To determine medulloblastoma subgroup-specific circRNAs, publicly available RNA sequencing (RNA-seq) data from 175 MB patients were interrogated to identify circRNAs that differentiate between MB subgroups. circ_63706 was identified as sonic hedgehog (SHH) group-specific, with its expression confirmed by RNA-FISH analysis in clinical tissue samples. The oncogenic function of circ_63706 was characterized in vitro and in vivo. Further, circ_63706-depleted cells were subjected to RNA-seq and lipid profiling to identify its molecular function. Finally, we mapped the circ_63706 secondary structure using an advanced random forest classification model and modeled a 3D structure to identify its interacting miRNA partner molecules. Circ_63706 regulates independently of the host coding gene pericentrin (PCNT), and its expression is specific to the SHH subgroup. circ_63706-deleted cells implanted into mice produced smaller tumors, and mice lived longer than parental cell implants. At the molecular level, circ_63706-deleted cells elevated total ceramide and oxidized lipids and reduced total triglyceride. Our study implicates a novel oncogenic circular RNA in the SHH medulloblastoma subgroup and establishes its molecular function and potential as a future therapeutic target. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-023-01521-0. |
format | Online Article Text |
id | pubmed-10007801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100078012023-03-12 The oncogenic circular RNA circ_63706 is a potential therapeutic target in sonic hedgehog-subtype childhood medulloblastomas Katsushima, Keisuke Pokhrel, Rudramani Mahmud, Iqbal Yuan, Menglang Murad, Rabi Baral, Prabin Zhou, Rui Chapagain, Prem Garrett, Timothy Stapleton, Stacie Jallo, George Bettegowda, Chetan Raabe, Eric Wechsler-Reya, Robert J. Eberhart, Charles G. Perera, Ranjan J. Acta Neuropathol Commun Research Medulloblastoma (MB) develops through various genetic, epigenetic, and non-coding (nc) RNA-related mechanisms, but the roles played by ncRNAs, particularly circular RNAs (circRNAs), remain poorly defined. CircRNAs are increasingly recognized as stable non-coding RNA therapeutic targets in many cancers, but little is known about their function in MBs. To determine medulloblastoma subgroup-specific circRNAs, publicly available RNA sequencing (RNA-seq) data from 175 MB patients were interrogated to identify circRNAs that differentiate between MB subgroups. circ_63706 was identified as sonic hedgehog (SHH) group-specific, with its expression confirmed by RNA-FISH analysis in clinical tissue samples. The oncogenic function of circ_63706 was characterized in vitro and in vivo. Further, circ_63706-depleted cells were subjected to RNA-seq and lipid profiling to identify its molecular function. Finally, we mapped the circ_63706 secondary structure using an advanced random forest classification model and modeled a 3D structure to identify its interacting miRNA partner molecules. Circ_63706 regulates independently of the host coding gene pericentrin (PCNT), and its expression is specific to the SHH subgroup. circ_63706-deleted cells implanted into mice produced smaller tumors, and mice lived longer than parental cell implants. At the molecular level, circ_63706-deleted cells elevated total ceramide and oxidized lipids and reduced total triglyceride. Our study implicates a novel oncogenic circular RNA in the SHH medulloblastoma subgroup and establishes its molecular function and potential as a future therapeutic target. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-023-01521-0. BioMed Central 2023-03-10 /pmc/articles/PMC10007801/ /pubmed/36899402 http://dx.doi.org/10.1186/s40478-023-01521-0 Text en © The Author(s) 2023 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 Katsushima, Keisuke Pokhrel, Rudramani Mahmud, Iqbal Yuan, Menglang Murad, Rabi Baral, Prabin Zhou, Rui Chapagain, Prem Garrett, Timothy Stapleton, Stacie Jallo, George Bettegowda, Chetan Raabe, Eric Wechsler-Reya, Robert J. Eberhart, Charles G. Perera, Ranjan J. The oncogenic circular RNA circ_63706 is a potential therapeutic target in sonic hedgehog-subtype childhood medulloblastomas |
title | The oncogenic circular RNA circ_63706 is a potential therapeutic target in sonic hedgehog-subtype childhood medulloblastomas |
title_full | The oncogenic circular RNA circ_63706 is a potential therapeutic target in sonic hedgehog-subtype childhood medulloblastomas |
title_fullStr | The oncogenic circular RNA circ_63706 is a potential therapeutic target in sonic hedgehog-subtype childhood medulloblastomas |
title_full_unstemmed | The oncogenic circular RNA circ_63706 is a potential therapeutic target in sonic hedgehog-subtype childhood medulloblastomas |
title_short | The oncogenic circular RNA circ_63706 is a potential therapeutic target in sonic hedgehog-subtype childhood medulloblastomas |
title_sort | oncogenic circular rna circ_63706 is a potential therapeutic target in sonic hedgehog-subtype childhood medulloblastomas |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10007801/ https://www.ncbi.nlm.nih.gov/pubmed/36899402 http://dx.doi.org/10.1186/s40478-023-01521-0 |
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