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高丽红参提取物通过废除肾细胞癌细胞中 CREB 和 c-Jun 的激活增强索拉非尼的抗癌作用。

Korean Red Ginseng Extract Enhances the Anticancer Effects of Sorafenib through Abrogation of CREB and c-Jun Activation in Renal Cell Carcinoma.

机构信息

College of Korean Medicine, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul, 130-701, Korea.

College of Korean Medicine, Woosuk University, Wanju, Jeonbuk, 55338, Korea.

出版信息

Phytother Res. 2017 Jul;31(7):1078-1089. doi: 10.1002/ptr.5829. Epub 2017 May 22.

DOI:10.1002/ptr.5829
PMID:28544385
Abstract

Although application of sorafenib in the treatment of human renal cell carcinoma (RCC) remains one of the best examples of successful targeted therapy, majority of RCC patients suffer from its side effects as well as develop resistance to this targeted therapy. Thus, there is a need to promote novel alternative therapies for the treatment of RCC. In this study, we investigated whether Korean red ginseng extract (KRGE) could inhibit the proliferation and induce chemosensitization in human renal cancer cells. Also, we used a human phospho-antibody array containing 46 antibodies against signaling molecules to examine a subset of phosphorylation events after KRGE and sorafenib combination treatment. Korean red ginseng extract suppressed the proliferation of two RCC cell lines; activated caspase-3; caused poly(ADP-ribose) polymerase cleavage; abrogated the expression of B-cell lymphoma 2, B-cell lymphoma extra large, survivin, inhibitors of apoptosis proteins-1/2, cyclooxygenase-2, cyclin D1, matrix metallopeptidase-9, and vascular endothelial growth factor; and upregulated pro-apoptotic gene products. Interestingly, KRGE enhanced the cytotoxic and apoptotic effects of sorafenib in RCC cells. The combination treatment of KRGE and sorafenib more clearly suppressed cyclic adenosine monophosphate response element-binding protein and c-Jun phosphorylation and induced phosphorylation of p53 than did the individual treatment regimen. Our results clearly demonstrate that KRGE can enhance the anticancer activity of sorafenib and may have a substantial potential in the treatment of RCC. Copyright © 2017 John Wiley & Sons, Ltd.

摘要

虽然索拉非尼在治疗人类肾细胞癌(RCC)中的应用仍然是成功靶向治疗的最佳范例之一,但大多数 RCC 患者都遭受其副作用的困扰,并且对这种靶向治疗产生耐药性。因此,需要促进用于治疗 RCC 的新的替代疗法。在这项研究中,我们研究了高丽红参提取物(KRGE)是否可以抑制人肾癌细胞的增殖并诱导化学增敏作用。此外,我们使用了包含针对信号分子的 46 种抗体的人磷酸化抗体阵列,以检查 KRGE 和索拉非尼联合治疗后亚磷酸化事件的子集。高丽红参提取物抑制了两种 RCC 细胞系的增殖;激活了 caspase-3;引起聚(ADP-核糖)聚合酶切割;阻断了 B 细胞淋巴瘤 2、B 细胞淋巴瘤大、存活素、凋亡蛋白抑制剂-1/2、环氧化酶-2、细胞周期蛋白 D1、基质金属蛋白酶-9 和血管内皮生长因子的表达;并上调了促凋亡基因产物。有趣的是,KRGE 增强了 RCC 细胞中索拉非尼的细胞毒性和促凋亡作用。与单独治疗方案相比,KRGE 和索拉非尼的联合治疗更明显地抑制了环磷酸腺苷反应元件结合蛋白和 c-Jun 的磷酸化,并诱导了 p53 的磷酸化。我们的研究结果清楚地表明,KRGE 可以增强索拉非尼的抗癌活性,并且在治疗 RCC 方面具有很大的潜力。版权所有©2017 年 John Wiley & Sons, Ltd.

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