School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China; Institute of Arthritis Research, Shanghai Academy of Chinese Medical Sciences, Guanghua Integrative Medicine Hospital, Shanghai University of T.C.M, Shanghai 201203, China; Engineering Research Center of Shanghai Colleges for TCM New Drug Discovery, Shanghai 201203, China.
School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China; Engineering Research Center of Shanghai Colleges for TCM New Drug Discovery, Shanghai 201203, China.
Cancer Lett. 2016 Oct 1;380(2):447-456. doi: 10.1016/j.canlet.2016.07.005. Epub 2016 Jul 14.
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.
宫颈癌是全球女性最常见的癌症之一。来自怒江藤黄的新化合物 Nujiangexathone A(NJXA)已被证明具有抗癌潜力。在这项研究中,研究了 NJXA 的抗肿瘤作用及其作用机制。结果表明,NJXA 通过下调细胞周期蛋白 B1、E1 和 A 以及细胞周期蛋白依赖性激酶 2、4 和 6 来诱导 HeLa 和 SiHa 细胞的 G0/G1 细胞周期停滞,同时选择性地恢复 p27。通过二维凝胶电泳,我们表明 NJXA 通过加速泛素-蛋白酶体依赖性 hnRNPK 降解来减少异质性核核糖核蛋白 K(hnRNPK)的表达,从而通过 c-Myc-cyclin/Cdk-Rb-E2F1 通路诱导细胞周期停滞。功能丧失研究表明,NJXA 通过下调 hnRNPK 蛋白诱导细胞周期停滞。体内结果进一步证实了 NJXA 通过下调 hnRNPK 发挥肿瘤抑制作用,且 NJXA 诱导无明显毒性。我们的研究表明,NJXA 可能是一种新型的抗癌药物候选物,特别是用于治疗 hnRNPK 表达异常高的癌症。