Wang Xin-Zhi, Cheng Ying, Wang Kui-Long, Liu Rui, Yang Xiao-Lin, Wen Hong-Mei, Chai Chuan, Liang Jing-Yu, Wu Hao
College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, China.
Department of Natural Medicinal Chemistry, China Pharmaceutical University, Nanjing, China.
Cancer Sci. 2016 Oct;107(10):1506-1519. doi: 10.1111/cas.13029. Epub 2016 Oct 7.
Advanced lung cancer has poor prognosis owing to its low sensitivity to current chemotherapy agents. Therefore, discovery of new therapeutic agents is urgently needed. In this study, we investigated the antitumor effects of peperomin E, a secolignan isolated from Peperomia dindygulensis, a frequently used Chinese folk medicine for lung cancer treatment. The results indicate that peperomin E has antiproliferative effects, promoting apoptosis and cell cycle arrest in non-small-cell lung cancer (NSCLC) cell lines in a dose-dependent manner, while showing lower toxicity against normal human lung epidermal cells. Peperomin E inhibited tumor growth in A549 xenograft BALB/c nude mice without significant secondary adverse effects, indicating that it may be safely used to treat NSCLC. Furthermore, the mechanisms underlying the anticancer effects of peperomin E have been investigated. Using an in silico target fishing method, we observed that peperomin E directly interacts with the active domain of DNA methyltransferase 1 (DNMT1), potentially affecting its genome methylation activity. Subsequent experiments verified that peperomin E decreased DNMT1 activity and expression, thereby decreasing global methylation and reactivating the epigenetically silenced tumor suppressor genes including RASSF1A, APC, RUNX3, and p16INK4, which in turn activates their mediated pro-apoptotic and cell cycle regulatory signaling pathways in lung cancer cells. The observations herein report for the first time that peperomin E is a potential chemotherapeutic agent for NSCLC. The anticancer effects of peperomin E may be partly attributable to its ability to demethylate and reactivate methylation-silenced tumor suppressor genes through direct inhibition of the activity and expression of DNMT1.
晚期肺癌对当前化疗药物的敏感性较低,预后较差。因此,迫切需要发现新的治疗药物。在本研究中,我们研究了从胡椒科植物丁迪古勒草胡椒中分离得到的一种裂环木脂素——胡椒素E的抗肿瘤作用。结果表明,胡椒素E具有抗增殖作用,能以剂量依赖的方式促进非小细胞肺癌(NSCLC)细胞系的凋亡和细胞周期阻滞,同时对正常人肺表皮细胞的毒性较低。胡椒素E抑制A549异种移植BALB/c裸鼠的肿瘤生长,且无明显的继发性不良反应,表明它可安全用于治疗NSCLC。此外,还研究了胡椒素E抗癌作用的潜在机制。通过计算机模拟靶点筛选方法,我们观察到胡椒素E直接与DNA甲基转移酶1(DNMT1)的活性结构域相互作用,可能影响其基因组甲基化活性。随后的实验证实,胡椒素E降低了DNMT1的活性和表达,从而降低了整体甲基化水平,并使包括RASSF1A、APC、RUNX3和p16INK4在内的表观遗传沉默的肿瘤抑制基因重新激活,进而激活它们在肺癌细胞中介导的促凋亡和细胞周期调节信号通路。本文的观察结果首次报道胡椒素E是一种潜在的NSCLC化疗药物。胡椒素E的抗癌作用可能部分归因于其通过直接抑制DNMT1的活性和表达来使甲基化沉默的肿瘤抑制基因去甲基化并重新激活的能力。