Journal of Biological Chemistry · 2019 · 24 citations · 20 references
MedicineMolecular BiologyUrologyCell SignalingProstate DiseaseSignal TransductionBenign Prostatic HyperplasiaProstate AnatomyProstate CancerProstate PhysiologyReceptor RegulationMuscle ContractionProstate Growth RegulationProstate MicroenvironmentProstate Smooth Muscle PhysiologyProstate Stromal PhysiologyProstate Stromal-epithelial InteractionsProstatic StromaSmooth Muscle Contraction
agonist U46619, or by high molar KCl were not inhibited. Correlation analyses suggested up-regulation of prostatic ARF6 expression with increasing degree of BPH, as ARF6 expression increased with the content of prostate-specific antigen (PSA) of prostate tissues. NAV2729 inhibited ARF6 activity but not other GTPases (ARF1, RhoA, Rac1) in prostate tissues and in WPMY-1 cells. Proliferation of WPMY-1 cells was inhibited concentration-dependently by NAV2726, as reflected by decreased viability, 5-ethynyl-2'-deoxyuridine (EdU) assay, colony formation assay, and expression of Ki-67. Silencing of ARF6 expression mimicked effects of NAV2729 on viability and in the EdU assay. Effects of NAV2729 on viability and proliferation were attenuated in cells with silenced ARF6 expression. Our findings suggest that a NAV2729-sensitive mechanism promotes adrenergic contraction and stromal cell growth in the human prostate, which is probably ARF6-mediated. Similar actions in other organs and urodynamic effects of NAV2729 appear possible.
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Luca Cindolo, Luisella Pirozzi, Caterina Fanizza et al. · European Urology · 2014 · 205 citations
Medicine, Pharmacotherapy, Urology +14
ARF6 Is an Actionable Node that Orchestrates Oncogenic GNAQ Signaling in Uveal Melanoma
Jae Hyuk Yoo, Dallas Shi, Allie H. Grossmann et al. · Cancer Cell · 2016 · 158 citations · Full text