Graduate/PhD Degree Program in Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Department of Oral Biology, Faculty of Dentistry, Mahidol University, Bangkok 10400, Thailand.
Oncol Rep. 2020 Oct;44(4):1441-1454. doi: 10.3892/or.2020.7710. Epub 2020 Jul 31.
The high activation of protein kinase B (AKT)/nuclear factor‑κB (NF‑κB) signaling has often been associated with the induction of non‑small cell lung cancer (NSCLC) cell survival and resistance to cisplatin, which is one of the most widely used chemotherapeutic drugs in the treatment of NSCLC. The inhibition of AKT/NF‑κB can potentially be used as a molecular target for cancer therapy. Eurycomalactone (ECL), a quassinoid from Eurycoma longifolia Jack, has previously been revealed to exhibit strong cytotoxic activity against the human NSCLC A549 cell line, and can inhibit NF‑κB activity in TNF‑α‑activated 293 cells stably transfected with an NF‑κB luciferase reporter. The present study was the first to investigate whether ECL inhibits the activation of AKT/NF‑κB signaling, induces apoptosis and enhances chemosensitivity to cisplatin in human NSCLC cells. The anticancer activity of ECL was evaluated in two NSCLC cell lines, A549 and Calu‑1. ECL decreased the viability and colony formation ability of both cell lines by inducing cell cycle arrest and apoptosis through the activation of pro‑apoptotic caspase‑3 and poly (ADP‑ribose) polymerase, as well as the reduction of anti‑apoptotic proteins Bcl‑xL and survivin. In addition, ECL treatment suppressed the levels of AKT (phospho Ser473) and NF‑κB (phospho Ser536). Notably, ECL significantly enhanced cisplatin sensitivity in both assessed NSCLC cell lines. The combination treatment of cisplatin and ECL promoted cell apoptosis more effectively than cisplatin alone, as revealed by the increased cleaved caspase‑3, but decreased Bcl‑xL and survivin levels. Exposure to cisplatin alone induced the levels of phosphorylated‑AKT and phosphorylated‑NF‑κB, whereas co‑treatment with ECL inhibited the cisplatin‑induced phosphorylation of AKT and NF‑κB, leading to an increased sensitization effect on cisplatin‑induced apoptosis. In conclusion, ECL exhibited an anticancer effect and sensitized NSCLC cells to cisplatin through the inactivation of AKT/NF‑κB signaling. This finding provides a rationale for the combined use of chemotherapy drugs with ECL to improve their efficacy in NSCLC treatment.
蛋白激酶 B(AKT)/核因子-κB(NF-κB)信号的高度激活常与非小细胞肺癌(NSCLC)细胞的存活和对顺铂的耐药性有关,顺铂是治疗 NSCLC 最广泛使用的化疗药物之一。抑制 AKT/NF-κB 可能可作为癌症治疗的分子靶点。此前已证实,来自长叶土楠的三萜醌 Eurycomalactone(ECL)对人 NSCLC A549 细胞系具有很强的细胞毒性活性,并能抑制 TNF-α激活的 NF-κB 荧光素酶报告基因稳定转染的 293 细胞中 NF-κB 的活性。本研究首次探讨了 ECL 是否抑制 AKT/NF-κB 信号的激活,诱导人 NSCLC 细胞凋亡并增强顺铂化疗敏感性。在两种 NSCLC 细胞系 A549 和 Calu-1 中评估了 ECL 的抗癌活性。ECL 通过激活促凋亡 caspase-3 和多聚(ADP-核糖)聚合酶,以及降低抗凋亡蛋白 Bcl-xL 和 survivin,诱导细胞周期停滞和凋亡,从而降低两种细胞系的活力和集落形成能力。此外,ECL 处理还抑制了 AKT(磷酸化 Ser473)和 NF-κB(磷酸化 Ser536)的水平。值得注意的是,ECL 显著增强了两种评估的 NSCLC 细胞系对顺铂的敏感性。与单独使用顺铂相比,顺铂和 ECL 的联合治疗更有效地促进了细胞凋亡,这表现为 cleaved caspase-3 增加,而 Bcl-xL 和 survivin 水平降低。单独使用顺铂诱导磷酸化 AKT 和磷酸化 NF-κB 的水平,而 ECL 联合治疗抑制了顺铂诱导的 AKT 和 NF-κB 的磷酸化,从而增加了顺铂诱导凋亡的敏化作用。总之,ECL 通过失活 AKT/NF-κB 信号表现出抗癌作用,并使 NSCLC 细胞对顺铂敏感。这一发现为联合使用化疗药物和 ECL 以提高 NSCLC 治疗效果提供了依据。