Wang Qi, Liu Zhile, Du Kunpeng, Liang Min, Zhu Xiongjie, Yu Zhongjian, Chen Rui, Qin Lingyu, Li Ying, Zheng Yanfang
Department of Oncology, Zhujiang Hospital of Southern Medical University Gugangzhou 510282, China.
Department of Oncology, The Fifth Affiliated Hospital of Guangzhou Medical University Gugangzhou 510700, China.
Am J Transl Res. 2019 Aug 15;11(8):5272-5283. eCollection 2019.
Babaodan capsule (BBD), a traditional Chinese (TCM) formula, has been widely used as an alternative remedy for multiple types of malignancies, clinically. However, the underlying mechanisms behind the efficacy of BBD remain poorly understood, particularly in regard to lung cancer. Herein, we demonstrate that BBD induced autophagic death in A549 and A549DDP cells without apoptosis. Treatment with autophagic inhibitor 3-MA, Baf-A1 and PI3K agonist, IGF-1, fully proved our conclusion, as well as uncovered the potential downregulated signaling pathway, PI3K/AKT/mTOR. The study additionally found that BBD could downregulate the expression of MDR1 and increase the chemosensitivity of cisplatin. Collectively, our results, both and , demonstrate that BBD leads to autophagic cell death through downregulating the PI3K/AKT/mTOR signaling pathway and improved the antitumor effects of cisplatin in non-small cell lung cancer (NSCLC).
八宝丹胶囊(BBD)是一种中药配方,在临床上已被广泛用作多种恶性肿瘤的替代疗法。然而,BBD疗效背后的潜在机制仍知之甚少,尤其是在肺癌方面。在此,我们证明BBD在A549和A549DDP细胞中诱导自噬性死亡而无凋亡。用自噬抑制剂3-MA、巴佛洛霉素A1(Baf-A1)和PI3K激动剂胰岛素样生长因子-1(IGF-1)进行处理,充分证明了我们的结论,同时也揭示了潜在的下调信号通路PI3K/AKT/mTOR。该研究还发现BBD可下调多药耐药蛋白1(MDR1)的表达并增加顺铂的化学敏感性。总体而言,我们的结果表明,BBD通过下调PI3K/AKT/mTOR信号通路导致自噬性细胞死亡,并提高了顺铂在非小细胞肺癌(NSCLC)中的抗肿瘤作用。