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The miR-183∼96∼182 cluster promotes tumorigenesis in a mouse model of medulloblastoma

Medulloblastoma is the most common malignant pediatric brain tumor. Some are thought to originate from cerebellar granule neuron progenitors (CGNPs) that fail to undergo normal cell cycle exit and differentiation. The contribution of microRNAs to the initiation and progression of medulloblastoma rem...

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Detalles Bibliográficos
Autores principales: Zhang, Zengdi, Li, Sanen, Cheng, Steven Y
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841474/
https://www.ncbi.nlm.nih.gov/pubmed/24285947
http://dx.doi.org/10.7555/JBR.27.20130010
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author Zhang, Zengdi
Li, Sanen
Cheng, Steven Y
author_facet Zhang, Zengdi
Li, Sanen
Cheng, Steven Y
author_sort Zhang, Zengdi
collection PubMed
description Medulloblastoma is the most common malignant pediatric brain tumor. Some are thought to originate from cerebellar granule neuron progenitors (CGNPs) that fail to undergo normal cell cycle exit and differentiation. The contribution of microRNAs to the initiation and progression of medulloblastoma remains poorly understood. Increased expression of the miR-183∼96∼182 cluster of microRNAs has been noted in several aggressive subgroups. We identified that expression of miR-183∼96∼182 was higher in medulloblastomas with Pten gene loss in the background of the activated sonic hedgehog (Shh) signaling pathway. Ectopic miR-183∼96∼182 expression in CGNPs synergized with exogenous Shh to increase proliferation and its role depended on hedgehog signaling activation. Our findings suggest a new microRNA cluster, the miR-183∼96∼182, functionally collaborates with the Shh signaling pathway in the development of medulloblastomas in mice.
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spelling pubmed-38414742013-11-27 The miR-183∼96∼182 cluster promotes tumorigenesis in a mouse model of medulloblastoma Zhang, Zengdi Li, Sanen Cheng, Steven Y J Biomed Res Research Paper Medulloblastoma is the most common malignant pediatric brain tumor. Some are thought to originate from cerebellar granule neuron progenitors (CGNPs) that fail to undergo normal cell cycle exit and differentiation. The contribution of microRNAs to the initiation and progression of medulloblastoma remains poorly understood. Increased expression of the miR-183∼96∼182 cluster of microRNAs has been noted in several aggressive subgroups. We identified that expression of miR-183∼96∼182 was higher in medulloblastomas with Pten gene loss in the background of the activated sonic hedgehog (Shh) signaling pathway. Ectopic miR-183∼96∼182 expression in CGNPs synergized with exogenous Shh to increase proliferation and its role depended on hedgehog signaling activation. Our findings suggest a new microRNA cluster, the miR-183∼96∼182, functionally collaborates with the Shh signaling pathway in the development of medulloblastomas in mice. Editorial Department of Journal of Biomedical Research 2013-11 2013-07-10 /pmc/articles/PMC3841474/ /pubmed/24285947 http://dx.doi.org/10.7555/JBR.27.20130010 Text en © 2013 by the Journal of Biomedical Research. All rights reserved.
spellingShingle Research Paper
Zhang, Zengdi
Li, Sanen
Cheng, Steven Y
The miR-183∼96∼182 cluster promotes tumorigenesis in a mouse model of medulloblastoma
title The miR-183∼96∼182 cluster promotes tumorigenesis in a mouse model of medulloblastoma
title_full The miR-183∼96∼182 cluster promotes tumorigenesis in a mouse model of medulloblastoma
title_fullStr The miR-183∼96∼182 cluster promotes tumorigenesis in a mouse model of medulloblastoma
title_full_unstemmed The miR-183∼96∼182 cluster promotes tumorigenesis in a mouse model of medulloblastoma
title_short The miR-183∼96∼182 cluster promotes tumorigenesis in a mouse model of medulloblastoma
title_sort mir-183∼96∼182 cluster promotes tumorigenesis in a mouse model of medulloblastoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841474/
https://www.ncbi.nlm.nih.gov/pubmed/24285947
http://dx.doi.org/10.7555/JBR.27.20130010
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