Majdalawieh Amin F, Al-Samaraie Saud, Terro Tala M
Department of Biology, Chemistry, and Environmental Sciences, College of Arts and Sciences, American University of Sharjah, Sharjah P.O. Box 26666, United Arab Emirates.
School of Medicine, University College Dublin, Belfield, D04 V1W8 Dublin, Ireland.
Molecules. 2024 Dec 14;29(24):5907. doi: 10.3390/molecules29245907.
Thymoquinone (TQ), a bioactive compound derived from , has garnered significant attention for its potential as a natural anti-cancer agent, particularly in the context of colorectal cancer. This review provides a detailed synthesis of the current literature on the anti-cancer properties of TQ in colorectal cancer cells, exploring both in vitro and in vivo studies to elucidate its mechanisms of action. TQ effectively induces apoptosis, inhibits cell proliferation, and reduces metastasis in colorectal cancer cells by modulating key molecular pathways such as PI3K/AKT/mTOR, NF-κB, STAT3, and MAPK. It causes mitochondrial dysfunction and activates caspases, contributing to its pro-apoptotic effects. TQ also regulates EMT and targets cancer stem cells, reducing the likelihood of metastasis. Moreover, its antioxidant properties contribute to its protective role against cancer progression. While preclinical studies provide strong evidence of TQ's efficacy, further clinical studies are essential to establish its therapeutic potential in humans. This review underscores TQ's promising role as a natural agent with the potential to significantly improve colorectal cancer treatment outcomes.
百里醌(TQ)是一种从[具体来源未给出]中提取的生物活性化合物,因其作为天然抗癌剂的潜力,特别是在结直肠癌方面,而备受关注。本综述详细综合了当前关于TQ在结直肠癌细胞中的抗癌特性的文献,探讨了体外和体内研究以阐明其作用机制。TQ通过调节PI3K/AKT/mTOR、NF-κB、STAT3和MAPK等关键分子途径,有效诱导结直肠癌细胞凋亡、抑制细胞增殖并减少转移。它导致线粒体功能障碍并激活半胱天冬酶,促成其促凋亡作用。TQ还调节上皮-间质转化并靶向癌症干细胞,降低转移的可能性。此外,其抗氧化特性有助于其对癌症进展的保护作用。虽然临床前研究提供了TQ疗效的有力证据,但进一步的临床研究对于确定其在人类中的治疗潜力至关重要。本综述强调了TQ作为一种天然药物的有前景的作用,有可能显著改善结直肠癌的治疗效果。