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NBAT1/CASC15-003/USP36 control MYCN expression and its downstream pathway genes in neuroblastoma
BACKGROUND: MYCN has been an attractive therapeutic target in neuroblastoma considering the widespread amplification of the MYCN locus in neuroblastoma, and its established role in neuroblastoma development and progression. Thus, understanding neuroblastoma-specific control of MYCN expression at the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156975/ https://www.ncbi.nlm.nih.gov/pubmed/34056606 http://dx.doi.org/10.1093/noajnl/vdab056 |
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author | Juvvuna, Prasanna Kumar Mondal, Tanmoy Di Marco, Mirco Kosalai, Subazini Thankaswamy Kanduri, Meena Kanduri, Chandrasekhar |
author_facet | Juvvuna, Prasanna Kumar Mondal, Tanmoy Di Marco, Mirco Kosalai, Subazini Thankaswamy Kanduri, Meena Kanduri, Chandrasekhar |
author_sort | Juvvuna, Prasanna Kumar |
collection | PubMed |
description | BACKGROUND: MYCN has been an attractive therapeutic target in neuroblastoma considering the widespread amplification of the MYCN locus in neuroblastoma, and its established role in neuroblastoma development and progression. Thus, understanding neuroblastoma-specific control of MYCN expression at the transcriptional and post-transcriptional level would lead to identification of novel MYCN-dependent oncogenic pathways and potential therapeutic strategies. METHODS: By performing loss- and gain-of-function experiments of the neuroblastoma hotspot locus 6p22.3 derived lncRNAs CASC15-003 and NBAT1, together with coimmunoprecipitation and immunoblotting of MYCN, we have shown that both lncRNAs post-translationally control the expression of MYCN through regulating a deubiquitinase enzyme USP36. USP36 oncogenic properties were investigated using cancer cell lines and in vivo models. RNA-seq analysis of loss-of-function experiments of CASC15-003/NBAT1/MYCN/USP36 and JQ1-treated neuroblastoma cells uncovered MYCN-dependent oncogenic pathways. RESULTS: We show that NBAT1/CASC15-003 control the stability of MYCN protein through their common interacting protein partner USP36. USP36 harbors oncogenic properties and its higher expression in neuroblastoma patients correlates with poor prognosis, and its downregulation significantly reduces tumor growth in neuroblastoma cell lines and xenograft models. Unbiased integration of RNA-seq data from CASC15-003, NBAT1, USP36, and MYCN knockdowns and neuroblastoma cells treated with MYCN inhibitor JQ1, identified genes that are jointly regulated by the NBAT1/CASC15-003/USP36/MYCN pathway. Functional experiments on one of the target genes, COL18A1, revealed its role in the NBAT1/CASC15-003-dependent cell adhesion feature in neuroblastoma cells. CONCLUSION: Our data show post-translational regulation of MYCN by NBAT1/CASC15-003/USP36, which represents a new regulatory layer in the complex multilayered gene regulatory network that controls MYCN expression. |
format | Online Article Text |
id | pubmed-8156975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81569752021-05-28 NBAT1/CASC15-003/USP36 control MYCN expression and its downstream pathway genes in neuroblastoma Juvvuna, Prasanna Kumar Mondal, Tanmoy Di Marco, Mirco Kosalai, Subazini Thankaswamy Kanduri, Meena Kanduri, Chandrasekhar Neurooncol Adv Basic and Translational Investigations BACKGROUND: MYCN has been an attractive therapeutic target in neuroblastoma considering the widespread amplification of the MYCN locus in neuroblastoma, and its established role in neuroblastoma development and progression. Thus, understanding neuroblastoma-specific control of MYCN expression at the transcriptional and post-transcriptional level would lead to identification of novel MYCN-dependent oncogenic pathways and potential therapeutic strategies. METHODS: By performing loss- and gain-of-function experiments of the neuroblastoma hotspot locus 6p22.3 derived lncRNAs CASC15-003 and NBAT1, together with coimmunoprecipitation and immunoblotting of MYCN, we have shown that both lncRNAs post-translationally control the expression of MYCN through regulating a deubiquitinase enzyme USP36. USP36 oncogenic properties were investigated using cancer cell lines and in vivo models. RNA-seq analysis of loss-of-function experiments of CASC15-003/NBAT1/MYCN/USP36 and JQ1-treated neuroblastoma cells uncovered MYCN-dependent oncogenic pathways. RESULTS: We show that NBAT1/CASC15-003 control the stability of MYCN protein through their common interacting protein partner USP36. USP36 harbors oncogenic properties and its higher expression in neuroblastoma patients correlates with poor prognosis, and its downregulation significantly reduces tumor growth in neuroblastoma cell lines and xenograft models. Unbiased integration of RNA-seq data from CASC15-003, NBAT1, USP36, and MYCN knockdowns and neuroblastoma cells treated with MYCN inhibitor JQ1, identified genes that are jointly regulated by the NBAT1/CASC15-003/USP36/MYCN pathway. Functional experiments on one of the target genes, COL18A1, revealed its role in the NBAT1/CASC15-003-dependent cell adhesion feature in neuroblastoma cells. CONCLUSION: Our data show post-translational regulation of MYCN by NBAT1/CASC15-003/USP36, which represents a new regulatory layer in the complex multilayered gene regulatory network that controls MYCN expression. Oxford University Press 2021-04-09 /pmc/articles/PMC8156975/ /pubmed/34056606 http://dx.doi.org/10.1093/noajnl/vdab056 Text en © The Author(s) 2021. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Basic and Translational Investigations Juvvuna, Prasanna Kumar Mondal, Tanmoy Di Marco, Mirco Kosalai, Subazini Thankaswamy Kanduri, Meena Kanduri, Chandrasekhar NBAT1/CASC15-003/USP36 control MYCN expression and its downstream pathway genes in neuroblastoma |
title | NBAT1/CASC15-003/USP36 control MYCN expression and its downstream pathway genes in neuroblastoma |
title_full | NBAT1/CASC15-003/USP36 control MYCN expression and its downstream pathway genes in neuroblastoma |
title_fullStr | NBAT1/CASC15-003/USP36 control MYCN expression and its downstream pathway genes in neuroblastoma |
title_full_unstemmed | NBAT1/CASC15-003/USP36 control MYCN expression and its downstream pathway genes in neuroblastoma |
title_short | NBAT1/CASC15-003/USP36 control MYCN expression and its downstream pathway genes in neuroblastoma |
title_sort | nbat1/casc15-003/usp36 control mycn expression and its downstream pathway genes in neuroblastoma |
topic | Basic and Translational Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156975/ https://www.ncbi.nlm.nih.gov/pubmed/34056606 http://dx.doi.org/10.1093/noajnl/vdab056 |
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