| Literature DB >> 29762656 |
Wei Wang1,2,3, Jiang-Jiang Qin1,3, Xin Li1,3, Guanyu Tao1,3, Qiang Wang3,4, Xuming Wu5, Jianwei Zhou4, Xiaolin Zi6,7, Ruiwen Zhang1,2,3.
Abstract
Prostate cancer remains a major health problem in the USA and worldwide. There is an urgent need to develop novel approaches to preventing primary and metastatic prostate cancer. We have identified 25-OCH3-protopanaxadiol (GS25), the most active ginsenoside that has been identified so far; it has potent activity against human cancers, including prostate cancer. However, it has not been proven if GS25 could be a safe and effective agent for cancer prevention. In this study, we used the TRAMP model and clearly demonstrated that GS25 inhibited prostate tumorigenesis and metastasis with minimal host toxicity. Mechanistically, GS25 directly bound to the RING domain of MDM2, disrupted MDM2-MDMX binding and induced MDM2 protein degradation, resulting in strong inhibition of prostate cancer cell growth and metastasis, independent of p53 and androgen receptor status. In conclusion, our in vitro and in vivo data support the potential use of GS25 in prevention of primary and metastatic prostate cancer.Entities:
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Year: 2018 PMID: 29762656 PMCID: PMC6067121 DOI: 10.1093/carcin/bgy063
Source DB: PubMed Journal: Carcinogenesis ISSN: 0143-3334 Impact factor: 4.944