| Literature DB >> 27424288 |
Li Zhang1, Jiling Feng2, Siyuan Kong2, Man Wu2, Zhichao Xi2, Baojun Zhang2, Wenwei Fu2, Yuanzhi Lao2, Hongsheng Tan3, Hongxi Xu4.
Abstract
Cervical cancer is among the most frequently diagnosed cancers in females worldwide. Nujiangexathone A (NJXA), a novel compound from Garcinia nujiangensis, has been shown to have anti-cancer potential. In this study, the anti-tumor effects and the underlying mechanisms of NJXA action were investigated. Our results suggested that NJXA induced G0/G1 cell cycle arrest in HeLa and SiHa cells by down-regulating cyclins B1, E1, and A and cyclin-dependent kinases 2, 4 and 6, while selectively restoring p27. Using two-dimensional gel electrophoresis, we showed that NJXA reduced the expression of heterogeneous nuclear ribonucleoprotein K (hnRNPK) by accelerating ubiquitin-proteasome-dependent hnRNPK degradation, which then induced cell cycle arrest through the c-Myc-cyclin/Cdk-Rb-E2F1 pathway. The loss-of-function study showed NJXA induced cell cycle arrest was mediated by down regulation of hnRNPK protein. In vivo results further confirmed the tumor inhibitory effect of NJXA via the down-regulation of hnRNPK, and NJXA induced no apparent toxicity. Our study suggests that NJXA may be a novel anti-cancer drug candidate, especially for treating cancers with abnormally high hnRNPK expression.Entities:
Keywords: Cell cycle; Cervical cancer; Garcinia species; Nujiangexathone A; hnRNPK
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Year: 2016 PMID: 27424288 DOI: 10.1016/j.canlet.2016.07.005
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679