| Literature DB >> 30567972 |
Dominic Lapadula1, Eduardo Farias2,3,4, Clinita E Randolph1, Timothy J Purwin5, Dougan McGrath1, Thomas H Charpentier1, Lihong Zhang6, Shihua Wu6, Mizue Terai7, Takami Sato7, Gregory G Tall8, Naiming Zhou6, Philip B Wedegaertner1, Andrew E Aplin5, Julio Aguirre-Ghiso2,3,4, Jeffrey L Benovic9.
Abstract
Uveal melanoma is the most common intraocular tumor in adults and often metastasizes to the liver, leaving patients with few options. Recurrent activating mutations in the G proteins, Gαq and Gα11, are observed in approximately 93% of all uveal melanomas. Although therapeutic intervention of downstream Gαq/11 targets has been unsuccessful in treating uveal melanoma, we have found that the Gαq/11 inhibitor, FR900359 (FR), effectively inhibits oncogenic Gαq/11 signaling in uveal melanoma cells expressing either mutant Gαq or Gα11. Inhibition of oncogenic Gαq/11 by FR results in cell-cycle arrest and induction of apoptosis. Furthermore, colony formation is prevented by FR treatment of uveal melanoma cells in 3D-cell culture, providing promise for future in vivo studies. This suggests direct inhibition of activating Gαq/11 mutants may be a potential means of treating uveal melanoma. IMPLICATIONS: Oncogenic Gαq/11 inhibition by FR900359 may be a potential treatment option for those with uveal melanoma. ©2018 American Association for Cancer Research.Entities:
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Year: 2018 PMID: 30567972 PMCID: PMC6445713 DOI: 10.1158/1541-7786.MCR-18-0574
Source DB: PubMed Journal: Mol Cancer Res ISSN: 1541-7786 Impact factor: 5.852