Abstract
Regulator of G Protein Signaling 6 (RGS6), a Novel Suppressor of Bladder Carcinogenesis
The FASEB journal, Vol.29(S1)
04/2015
DOI: 10.1096/fasebj.29.1_supplement.618.12
Abstract
Abstract only Urinary bladder cancer, the fifth most common cancer in the United States, is largely caused by exposure to toxic chemicals including those from smoking. Polymorphisms in the RGS6 gene leading to increased RGS6 translation are associated with a pronounced reduction in the risk of bladder cancer, especially among smokers. We employed a RGS6 ‐/‐ mouse line to interrogate the role of RGS6 in BBN‐induced bladder carcinogenesis, a model that closely resembles human invasive bladder cancer. RGS6 is highly expressed in mouse bladders, including urothelium where transitional cell carcinoma originates. Ablation of RGS6 greatly shortened the time needed for BBN‐induced bladder tumor formation (12 wks vs 20 wks in wild type (WT) mice). Consistently, WT mice treated with BBN showed a marked down‐regulation of RGS6 and Gβ5 as well as a transient activation of p53 (phosphorylation of S15), the latter of which was greatly blunted in RGS6 ‐/‐ mice. Loss of RGS6, either in BBN‐treated WT mice or RGS6 ‐/‐ mice, also resulted in an increase in DNMT1 in bladder urothelium, consistent with our recent evidence that RGS6 functions as a scaffold to promote DNMT1 degradation. Consequently, expression of tumor suppressor RASSF1A, a direct downstream target of DNMT1, was greatly repressed in RGS6 ‐/‐ urothelium. Our findings show that RGS6 is a previously unrecognized, but critical repressor of bladder carcinogenesis. Loss of RGS6, observed during BBN‐induced mouse bladder carcinogenesis and in human bladder tumors, would be expected to drive carcinogenesis through impaired p53 activation and increased expression of DNMT1. (Supported by AHA 11SDG7580008 (JY) and NIH CA161882 (RAF))
Details
- Title: Subtitle
- Regulator of G Protein Signaling 6 (RGS6), a Novel Suppressor of Bladder Carcinogenesis
- Creators
- Jianqi Yang - University of IowaLance Platt - University of IowaBiswanath Maity - University of IowaStella‐Rita Ibeawuchi - University of IowaAdele Stewart - University of IowaJie Huang - University of IowaSimon Anderegg - University of IowaRory Fisher - University of Iowa
- Resource Type
- Abstract
- Publication Details
- The FASEB journal, Vol.29(S1)
- DOI
- 10.1096/fasebj.29.1_supplement.618.12
- ISSN
- 0892-6638
- eISSN
- 1530-6860
- Language
- English
- Date published
- 04/2015
- Academic Unit
- Neuroscience and Pharmacology; Internal Medicine; Iowa Neuroscience Institute
- Record Identifier
- 9984618499102771
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