Gα13 mediates human cytomegalovirus‐encoded chemokine receptor US28‐induced cell death in melanoma. Issue 6 (16th March 2015)

• Record Type: Journal Article
• Authors: Joshi, Shripad; Wels, Christian; Beham‐Schmid, Christine; Fukunaga‐Kalabis, Mizuho; Holmen, Sheri L.; Otte, Marcus; Herlyn, Meenhard; Waldhoer, Maria; Schaider, Helmut
• Is Part Of: International journal of cancer. Volume 137:Issue 6(2015:Sep. 15)
• Page Start: 1503
• Page End: 1508
• Publication Date: 2015-03-16
• Subjects: Cancer -- Periodicals; Cancer -- Prevention -- Periodicals; 616.994
• DOI: 10.1002/ijc.29506
• Languages: English
• ISSNs: 0020-7136

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>US28, a constitutively active G‐protein‐coupled receptor encoded by the human cytomegalovirus, leads to mechanistically unknown programmed cell death. Here we show that expression of wild‐type US28 in human melanoma cells leads to apoptotic cell death via caspase 3 activation along with reduced cell proliferation. Reduced tumor growth upon US28 expression was observed in a xenograft mouse model. The signaling mute US28R129A showed a reduced antiproliferative effect. On evaluating different G‐proteins coupled to US28 for signal transduction, Gα13 was identified as the main G‐protein executing the apoptotic effect. Silencing of Gα13 but not Gαq resulted in a substantial increase in cell survival. Overexpression of Gα13 but not Gαq and their GTPase deficient forms Gα13Q226L and GαqQ209L, respectively, confirmed the requirement of Gα13 for US28 mediated cell death. Increasing expression of Gα13 alone induced cell death underscoring its relay function for US28 mediated decreased cell viability. Further reduced expression of Gα13 in melanoma cell lines isolated from advanced lesions and melanoma tissue was observed. These findings identified Gα13 as crucial for US28‐induced cell death, substantiating that the effect of US28 on cell fate depends on preferred G‐protein binding.</p> </abstract>