Abstract：
:The nuclear receptor PPAR-β/δ (PPARD) has essential roles in fatty acid catabolism and energy homeostasis as well as cell differentiation, inflammation, and metabolism. However, its contributions to tumorigenesis are uncertain and have been disputed. Here, we provide evidence of tumor suppressive activity of PPARD in prostate cancer through a noncanonical and ligand-independent pathway. PPARD was downregulated in prostate cancer specimens. In murine prostate epithelium, PPARD gene deletion resulted in increased cellularity. Genetic modulation of PPARD in human prostate cancer cell lines validated the tumor suppressive activity of this gene in vitro and in vivo Mechanistically, PPARD exerted its activity in a DNA binding-dependent and ligand-independent manner. We identified a novel set of genes repressed by PPARD that failed to respond to ligand-mediated activation. Among these genes, we observed robust regulation of the secretory trefoil factor family (TFF) members, including a causal and correlative association of TFF1 with prostate cancer biology in vitro and in patient specimens. Overall, our results illuminate the oncosuppressive function of PPARD and understanding of the pathogenic molecular pathways elicited by this nuclear receptor.Significance: These findings challenge the presumption that the function of the nuclear receptor PPARβ/δ in cancer is dictated by ligand-mediated activation. Cancer Res; 78(2); 399-409. ©2017 AACR.
journal_name
Cancer Resjournal_title
Cancer researchauthors
Martín-Martín N,Zabala-Letona A,Fernández-Ruiz S,Arreal L,Camacho L,Castillo-Martin M,Cortazar AR,Torrano V,Astobiza I,Zúñiga-García P,Ugalde-Olano A,Loizaga-Iriarte A,Unda M,Valcárcel-Jiménez L,Arruabarrena-Aristorena A,Pidoi
10.1158/0008-5472.CAN-17-0908subject
Has Abstractpub_date
2018-01-15 00:00:00pages
399-409issue
2eissn
0008-5472issn
1538-7445pii
0008-5472.CAN-17-0908journal_volume
78pub_type
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