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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...

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Autores principales: Juvvuna, Prasanna Kumar, Mondal, Tanmoy, Di Marco, Mirco, Kosalai, Subazini Thankaswamy, Kanduri, Meena, Kanduri, Chandrasekhar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
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.
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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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