石蒜碱通过激活STING通路和刺激抗肿瘤免疫反应抑制非小细胞肺癌的进展

IF 3.2 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ze-Bo Jiang, Cong Xu, Pan Xu, Dong-Hui Huang, Li-Ping Kang
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引用次数: 0

摘要

非小细胞肺癌(NSCLC)是全球癌症相关死亡的主要原因。石蒜碱(LYD)是一种天然存在于药用植物中的活性倍半萜,已被证明对多种癌细胞具有抗癌作用。然而,lyd诱导的非小细胞肺癌抗肿瘤的潜在机制尚不完全清楚。本研究表明,LYD通过增加细胞内ROS水平,显著降低NSCLC的增殖,诱导细胞凋亡。n -乙酰半胱氨酸(NAC)抑制ROS可消除LYD的凋亡作用,提高细胞活力。此外,LYD处理显著激活NSCLC的STING通路,诱导CXCL10、CXCL9和CCL5在NSCLC细胞中的表达。机制上,LYD发现显著降低P70S6K和S6K蛋白水平,这是参与细胞生长和存活的关键蛋白。值得注意的是,体内实验表明,LYD显著抑制H358异种移植物和LLC1肿瘤的生长,在NSCLC小鼠模型中通过提高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、调节STING通路和关键趋化因子诱导细胞凋亡,在非小细胞肺癌中具有强大的抗癌作用。此外,LYD还通过抑制参与细胞生长的关键蛋白来发挥其抗肿瘤作用。总的来说,LYD作为一种潜在的治疗非小细胞肺癌的药物显示出了希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Lycorine Suppresses Non-Small-Cell Lung Cancer Progression Through Activating STING Pathway and Stimulating an Antitumor Immune Response

Lycorine Suppresses Non-Small-Cell Lung Cancer Progression Through Activating STING Pathway and Stimulating an Antitumor Immune Response

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.

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来源期刊
Chemical Biology & Drug Design
Chemical Biology & Drug Design 医学-生化与分子生物学
CiteScore
5.10
自引率
3.30%
发文量
164
审稿时长
4.4 months
期刊介绍: Chemical Biology & Drug Design is a peer-reviewed scientific journal that is dedicated to the advancement of innovative science, technology and medicine with a focus on the multidisciplinary fields of chemical biology and drug design. It is the aim of Chemical Biology & Drug Design to capture significant research and drug discovery that highlights new concepts, insight and new findings within the scope of chemical biology and drug design.
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