| Literature DB >> 31782573 |
Victor Pham1,2, Raymond Rendon1, Vinh X Le1, Matthew Tippin1, Dong-Jun Fu1, Thanh H Le1, Marvin Miller1, Ericka Agredano1, Jose Cedano1, Xiaolin Zi1,2.
Abstract
Gartanin, a 4-prenylated xanthone, has been identified from the purple mangosteen fruit as a potent growth inhibitor of various cancer cell lines, including prostate cancer. However, much of Gartanin's anticancer mechanism remains unknown. We have discovered that Gartanin docked onto the regulatory subunit of the precursor cell-expressed developmentally downregulated 8 (NEDD8)-activating enzyme (NAE) complex and next to the NEDD8 binding complex, which leads to inhibit NEDD8 conjugations to both Cullin1 and Ubc12 in prostate cancer cell lines and Ubc12 NEDDylation in an in vitro assay. The S phase kinase-associated protein (Skp2) and F-box and WD-repeat domain-containing 2 (FBXW2), the NEDD8 family members of E3 ubiqutin ligases, were also downregulated and upregulated by Gartainin, respectively. Knock-down of NEDD8 expression by short harpin (Sh) RNAs blocked or attenuated these effects of Gartainin. Finally, Gartanin demonstrated its ability to inhibit growth of prostate cancer lines via autophagy initiation. Our data support that Gartanin is a naturally occurring NEDDylation inhibitor and deserves further investigation for prostate cancer prevention and treatment.Entities:
Keywords: Gartanin; Skp2; chemoprevention; neddylation; prostate cancer
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Year: 2019 PMID: 31782573 PMCID: PMC6946862 DOI: 10.1002/mc.23140
Source DB: PubMed Journal: Mol Carcinog ISSN: 0899-1987 Impact factor: 4.784