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The G-protein Alpha Subunit Gsα Is A Tumor Suppressor In Sonic Hedgehog-driven Medulloblastoma

Medulloblastoma, the most common malignant childhood brain tumor, exhibits distinct molecular subtypes and cellular origins. Genetic alterations driving medulloblastoma initiation and progression remain poorly understood. Herein, we identify GNAS, encoding the G-protein Gsα, as a potent tumor suppre...

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Detalles Bibliográficos
Autores principales: He, Xuelian, Zhang, Liguo, Chen, Ying, Remke, Marc, Shih, David, Lu, Fanghui, Wang, Haibo, Deng, Yaqi, Yu, Yang, Xia, Yong, Wu, Xiaochong, Ramaswamy, Vijay, Hu, Tom, Wang, Fan, Zhou, Wenhao, Burns, Dennis K., Kim, Se Hoon, Kool, Marcel, Pfister, Stefan M., Weinstein, Lee S., Pomeroy, Scott L., Gilbertson, Richard J., Rubin, Joshua B., Hou, Yiping, Wechsler-Reya, Robert, Taylor, Michael D., Lu, Q. Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334261/
https://www.ncbi.nlm.nih.gov/pubmed/25150496
http://dx.doi.org/10.1038/nm.3666
Descripción
Sumario:Medulloblastoma, the most common malignant childhood brain tumor, exhibits distinct molecular subtypes and cellular origins. Genetic alterations driving medulloblastoma initiation and progression remain poorly understood. Herein, we identify GNAS, encoding the G-protein Gsα, as a potent tumor suppressor gene that defines a subset of aggressive Sonic Hedgehog (Shh)-driven human medulloblastomas. Ablation of the single Gnas gene in anatomically-distinct progenitors is sufficient to induce Shh-associated medulloblastomas, which recapitulate their human counterparts. Gsα is highly enriched at the primary cilium of granule neuron precursors and suppresses Shh-signaling by regulating both the cAMP-dependent pathway and ciliary trafficking of Hedgehog pathway components. Elevation of a Gsα effector, cAMP, effectively inhibits tumor cell proliferation and progression in Gnas mutants. Thus, our gain- and loss-of-function studies identify a previously unrecognized tumor suppressor function for Gsα that acts as a molecular link across Shh-group medulloblastomas of disparate cellular and anatomical origins, illuminating G-protein modulation as a potential therapeutic avenue.