Jiang Ze-Bo, Xu Cong, Xu Pan, Huang Dong-Hui, Kang Li-Ping
Zhuhai Hospital of Integrated Traditional Chinese & Western Medicine, Zhuhai, Guangdong, China.
Department of Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, China.
Chem Biol Drug Des. 2024 Dec;104(6):e70036. doi: 10.1111/cbdd.70036.
Non-small-cell lung cancer (NSCLC) stands as a primary contributor to cancer-related deaths worldwide. It has been demonstrated that Lycorine (LYD), a naturally occurring active sesquiterpene present in Chinese medicinal plants, exhibits anti-cancer properties across various cancer cell lines. However, the underlying mechanisms of LYD-induced anti-tumor in NSCLC are not fully known. This study demonstrated that LYD significantly reduced the proliferation of NSCLC and induced apoptosis by increasing intracellular ROS levels. The inhibition of ROS using N-acetylcysteine (NAC) eliminated the apoptosis effects of LYD, resulting in increased cell viability. Additionally, LYD treatment significantly activated the STING pathway in NSCLC and induced the expression of CXCL10, CXCL9 and CCL5 in NSCLC cells. Mechanistically, LYD was found to significantly reduce the protein levels of P70S6K and S6K, which are key proteins involved in cell growth and survival. Notably, in vivo experiments demonstrated that LYD significantly inhibited the growth of H358 xenograft and LLC1 tumor, exhibiting anti-tumor activity by elevating CD8 T cells in the NSCLC mouse model. Our findings suggest that LYD possesses potent anti-cancer properties in NSCLC by inducing apoptosis through ROS generation and modulating the STING pathway and key chemokines. Furthermore, LYD also exerts its antitumor effects by inhibiting crucial proteins involved in cell growth. Overall, LYD shows promise as a potential therapeutic agent for NSCLC treatment.
非小细胞肺癌(NSCLC)是全球癌症相关死亡的主要原因。已证明,存在于中药中的天然活性倍半萜生物碱石蒜碱(LYD)在多种癌细胞系中均表现出抗癌特性。然而,LYD诱导NSCLC抗肿瘤的潜在机制尚不完全清楚。本研究表明,LYD通过提高细胞内活性氧(ROS)水平显著降低NSCLC的增殖并诱导细胞凋亡。使用N-乙酰半胱氨酸(NAC)抑制ROS消除了LYD的凋亡作用,导致细胞活力增加。此外,LYD处理显著激活了NSCLC中的干扰素基因刺激蛋白(STING)通路,并诱导了NSCLC细胞中趋化因子CXCL10、CXCL9和CCL5的表达。从机制上讲,发现LYD显著降低了细胞生长和存活的关键蛋白P70S6K和S6K的蛋白水平。值得注意的是,体内实验表明,LYD显著抑制H358异种移植瘤和LLC1肿瘤的生长,通过提高NSCLC小鼠模型中的CD8 T细胞表现出抗肿瘤活性。我们的研究结果表明,LYD通过ROS生成诱导细胞凋亡并调节STING通路和关键趋化因子,在NSCLC中具有强大的抗癌特性。此外,LYD还通过抑制参与细胞生长的关键蛋白发挥其抗肿瘤作用。总体而言,LYD有望成为NSCLC治疗的潜在治疗药物。