Zhang Chi, He Xiao-Juan, Li Li, Lu Cheng, Lu Ai-Ping
Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical SciencesNanxiaojie, Beijing, China.
School of Chinese Medicine, Hong Kong Baptist UniversityKowloon Tong, Hong Kong.
Front Pharmacol. 2017 Aug 25;8:490. doi: 10.3389/fphar.2017.00490. eCollection 2017.
Triptolide (TL), a natural product isolated from Tripterygium wilfordii Hook F (TwHF), shows potent anticancer effects and . We aimed to summary the biochemical mechanisms through which TL has been shown to induce apoptosis, autophagy and inhibit angiogenesis in pancreatic cancer (PC). We undertook a systematic review of preclinical evidence. We searched electronic databases. The potential mechanisms and the underlying signaling pathways have been accumulated as well. We screened 116 abstracts for eligibility and included 17 preclinical studies in the analysis. Details of the animals and cell lines were provided in 16 studies (94.1%). Six studies (75.0%) randomly assigned animals to treatment or control groups and only 1 study (12.5%) reported on blinding. The majority of the TL's research field has focused on its pro-apoptotic effects through downregulation of inhibitory pathways and upregulation of apoptotic pathways. The studies have shown that TL is effective both and against PC cells. This study provides a systematic summary of TL's anti-pancreatic cancer profile and the underlying mechanisms of with special emphasis on the apoptosis, autophagy, angiogenesis and related molecular pathways. Improved study quality in terms of treatment allocation methods reporting, randomization and blinding will accelerate needed progress toward trials.
雷公藤甲素(TL)是从雷公藤(Tripterygium wilfordii Hook F,TwHF)中分离出的一种天然产物,具有强大的抗癌作用。我们旨在总结雷公藤甲素在胰腺癌(PC)中诱导凋亡、自噬以及抑制血管生成的生化机制。我们对临床前证据进行了系统综述。我们检索了电子数据库。潜在机制和相关信号通路也已得到积累。我们筛选了116篇摘要以确定其是否符合条件,并纳入了17项临床前研究进行分析。16项研究(94.1%)提供了动物和细胞系的详细信息。6项研究(75.0%)将动物随机分配至治疗组或对照组,仅有1项研究(12.5%)报告了盲法情况。雷公藤甲素的大部分研究领域都集中在通过下调抑制性通路和上调凋亡通路来发挥促凋亡作用。研究表明,雷公藤甲素对胰腺癌细胞有效。本研究对雷公藤甲素的抗胰腺癌概况及其潜在机制进行了系统总结,特别强调了凋亡、自噬、血管生成及相关分子通路。在治疗分配方法报告、随机化和盲法方面提高研究质量将加速开展试验所需的进展。