Department of Biology, Chemistry, and Environmental Sciences, College of Arts and Sciences, American University of Sharjah, Sharjah P.O. Box 26666, United Arab Emirates.
Biomolecules. 2024 Oct 30;14(11):1382. doi: 10.3390/biom14111382.
α-Mangostin, a xanthone derivative extracted from the pericarp of the mangosteen fruit ( L.), has garnered significant attention for its potential as a natural anti-cancer agent. This review provides a comprehensive analysis of the current literature on the anti-cancer properties of α-mangostin across various cancer types. Through an extensive analysis of in vitro and in vivo studies, this review elucidates the multifaceted mechanisms underlying α-mangostin's cytotoxicity, apoptosis induction through both intrinsic and extrinsic pathways, and modulation of key cellular processes implicated in cancer progression in a diverse array of cancer cells. It causes mitochondrial dysfunction, activates caspases, and regulates autophagy, endoplasmic reticulum stress, and oxidative stress, enhancing its anti-cancer efficacy. Moreover, α-mangostin exhibits synergistic effects with conventional chemotherapeutic agents, suggesting its utility in combination therapies. The ability of α-mangostin to inhibit cell proliferation, modulate cell cycle progression, and induce apoptosis is linked to its effects on key signaling pathways, including Akt, NF-κB, and p53. Preclinical studies highlight the therapeutic potential and safety profile of α-mangostin, demonstrating significant tumor growth inhibition without adverse effects on normal cells. In summary, understanding the molecular targets and mechanisms of action of α-mangostin is crucial for its development as a novel chemotherapeutic agent, and future clinical investigations are warranted to explore its clinical utility and efficacy in cancer prevention and therapy.
α-倒捻子素是从山竹果皮中提取的一种酮衍生物,具有成为天然抗癌剂的潜力,因此备受关注。本文对 α-倒捻子素在各种癌症类型中的抗癌特性的现有文献进行了全面分析。通过对体外和体内研究的广泛分析,本综述阐明了 α-倒捻子素细胞毒性的多方面机制,通过内在和外在途径诱导细胞凋亡,以及调节多种癌细胞中涉及癌症进展的关键细胞过程。它会导致线粒体功能障碍,激活半胱天冬酶,并调节自噬、内质网应激和氧化应激,从而增强其抗癌功效。此外,α-倒捻子素与常规化疗药物表现出协同作用,表明其在联合治疗中的应用潜力。α-倒捻子素抑制细胞增殖、调节细胞周期进程和诱导细胞凋亡的能力与其对关键信号通路的影响有关,包括 Akt、NF-κB 和 p53。临床前研究强调了 α-倒捻子素的治疗潜力和安全性,证明其在抑制肿瘤生长方面具有显著效果,而对正常细胞没有不良影响。综上所述,了解 α-倒捻子素的分子靶点和作用机制对于将其开发为新型化疗药物至关重要,需要进行未来的临床研究来探索其在癌症预防和治疗中的临床应用和疗效。