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The G protein α subunit Gαs is a tumor suppressor in Sonic hedgehog-driven medulloblastoma.

Nature medicine | 2014

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 Gαs, as a potent tumor suppressor gene that, when expressed at low levels, defines a subset of aggressive Sonic hedgehog (SHH)-driven human medulloblastomas. Ablation of the single Gnas gene in anatomically distinct progenitors in mice is sufficient to induce Shh-associated medulloblastomas, which recapitulate their human counterparts. Gαs 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 in levels of a Gαs effector, cAMP, effectively inhibits tumor cell proliferation and progression in Gnas-ablated mice. Thus, our gain- and loss-of-function studies identify a previously unrecognized tumor suppressor function for Gαs that can be found consistently across Shh-group medulloblastomas of disparate cellular and anatomical origins, highlighting G protein modulation as a potential therapeutic avenue.

Pubmed ID: 25150496 RIS Download

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Associated grants

  • Agency: NINDS NIH HHS, United States
    Id: R01 NS078092
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS075243
  • Agency: CIHR, Canada
  • Agency: NCI NIH HHS, United States
    Id: R01 CA109467
  • Agency: NCI NIH HHS, United States
    Id: P01 CA096832
  • Agency: NCI NIH HHS, United States
    Id: R01 CA129541
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS072427

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