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麦冬皂苷D,一种甾体糖苷,可消除STAT3信号级联反应,并通过导致肺癌中谷胱甘肽/氧化型谷胱甘肽失衡发挥抗癌活性。

Ophiopogonin D, a Steroidal Glycoside Abrogates STAT3 Signaling Cascade and Exhibits Anti-Cancer Activity by Causing GSH/GSSG Imbalance in Lung Carcinoma.

作者信息

Lee Jong Hyun, Kim Chulwon, Lee Seok-Geun, Sethi Gautam, Ahn Kwang Seok

机构信息

Department of Science in Korean Medicine, College of Korean Medicine, Kyung Hee University, 24 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Korea.

Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600, Singapore.

出版信息

Cancers (Basel). 2018 Nov 8;10(11):427. doi: 10.3390/cancers10110427.

Abstract

Natural medicinal plants are multi-targeted in nature and their anti-cancer activities are also complex and varied, thus requiring a more systematic analysis of their modes of action. Since the activation of signal transducer and activator of transcription 3 (STAT3) is often deregulated in non-small cell lung carcinoma (NSCLC) cells and tissue specimens, its negative regulation can form the basis for identification of targeted therapy. In this report, we analyzed the possible anti-cancer effects of ophiopogonin D (OP-D) and the underlying mechanisms by which OP-D exerts its actions in NSCLC. OP-D exhibited substantial suppressive activity on STAT3 signaling and this effect was found to be mediated via oxidative stress phenomena caused by disturbance in GSH/GSSG ratio. In addition, OP-D induced apoptosis, activated caspase mediated apoptotic cascade and decreased expression of various oncogenic genes. Consistently, OP-D treatment significantly reduced NSCLC tumor growth in preclinical mouse model with via decreasing levels of p-STAT3. OP-D was also found to attenuate the expression of STAT3-regulated anti-apoptosis, cell cycle regulator, and angiogenesis biomarkers. Our findings suggest that OP-D can induce apoptosis and exert anti-tumor effects by inhibition of STAT3 signaling pathways in NSCLC.

摘要

天然药用植物本质上具有多靶点特性,其抗癌活性也复杂多样,因此需要对其作用方式进行更系统的分析。由于信号转导和转录激活因子3(STAT3)的激活在非小细胞肺癌(NSCLC)细胞和组织标本中常常失调,对其进行负调控可为靶向治疗的识别奠定基础。在本报告中,我们分析了麦冬皂苷D(OP-D)可能的抗癌作用以及OP-D在NSCLC中发挥作用的潜在机制。OP-D对STAT3信号传导表现出显著的抑制活性,且发现这种作用是通过谷胱甘肽(GSH)/氧化型谷胱甘肽(GSSG)比例紊乱引起的氧化应激现象介导的。此外,OP-D诱导细胞凋亡,激活半胱天冬酶介导的凋亡级联反应,并降低各种致癌基因的表达。同样,在临床前小鼠模型中,OP-D治疗通过降低p-STAT3水平显著减少了NSCLC肿瘤的生长。还发现OP-D可减弱STAT3调节的抗凋亡、细胞周期调节因子和血管生成生物标志物的表达。我们的研究结果表明,OP-D可通过抑制NSCLC中的STAT3信号通路诱导细胞凋亡并发挥抗肿瘤作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0874/6265752/0170fcc7b69b/cancers-10-00427-g001.jpg

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