芝麻中的胸腺醌对小细胞肺癌的抗肿瘤作用:体外和体内研究。

Mahjabin Khan, Sze-Kwan Lam, Sheng Yan, Yuqian Feng, Caoyang Chen, Frankie Chi-Fat Ko, James Chung-Man Ho
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引用次数: 0

摘要

目的:小细胞肺癌(SCLC)具有恶性和侵袭性,约占所有确诊肺癌病例的 15%。由于化疗等主要治疗方法都会产生令人衰弱的副作用,人们对草药治疗能力的兴趣日益高涨。黑麦草有益特性背后的药理学驱动力是醌类化合物胸腺醌(TQ)。人们已经广泛研究了 TQ 对不同癌症的抗癌作用。然而,在整个美国国家生物技术信息中心(NCBI)数据库中,只有一篇论文介绍了 TQ 对 SCLC 的作用。需要进行更详细的调查:本研究在体外研究了 TQ 对五种 SCLC 细胞系的影响,并在体内研究了裸鼠异种移植模型。评估了 TQ 在体外对 SCLC 的以下影响:(a) 细胞活力;(b) 细胞凋亡;(c) 细胞周期停滞;(d) 细胞内活性氧 (ROS) 水平;(e) 相关信号通路的蛋白表达。关于TQ对SCLC的体内效应,(a)测量肿瘤体积,(b)通过Western印迹法测定某些相关信号通路中的蛋白质表达:结果:总的来说,TQ能降低细胞活力,诱导细胞凋亡和细胞周期停滞,消耗ROS,并改变相关信号通路的蛋白质表达。此外,在 H446 SCLC 异种移植模型中,TQ 表现出抑制肿瘤的作用:结论:本研究阐明了 TQ 从抗癌机制中产生的细胞毒性影响。本研究获得的积极结果值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The anti-neoplastic impact of thymoquinone from Nigella sativa on small cell lung cancer: In vitro and in vivo investigations.

Purpose: Malignant and aggressive, small cell lung cancer (SCLC) constitutes about 15% of all diagnosed lung cancer cases. With primary therapeutic options such as chemotherapy accompanied by debilitating side effects, interest has been soaring in the therapeutic competencies of herbs. The pharmacological driving force behind the beneficial properties of Nigella sativa is the quinone, thymoquinone (TQ). The anti-cancer effects of TQ on different cancers have been extensively studied. Nonetheless, only one paper in the entire National Center for Biotechnology Information (NCBI) database describes its effects on SCLC. A more detailed investigation is required.

Methods: The current study examined the impact of TQ in vitro on five SCLC cell lines and in vivo in a nude mouse xenograft model. The following in vitro effects of TQ on SCLC were evaluated: (a) cell viability; (b) apoptosis; (c) cell cycle arrest; (d) intracellular reactive oxygen species (ROS) levels, and (e) protein expression in concomitant signaling pathways. For the in vivo effects of TQ on SCLC, (a) tumor volume was measured, and (b) selected protein expression in selected concomitant signaling pathways was determined by Western blotting.

Result: In general, TQ reduced cell viability, induced apoptosis and cell cycle arrest, depleted ROS, and altered protein expression in associated signaling pathways. Furthermore, TQ exhibited a tumor-suppressive effect in an H446 SCLC xenograft model.

Conclusion: The cytotoxic impact of TQ arising from anti-cancer mechanisms was elucidated. The positive results obtained in this study warrant further investigation.

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