Bouhoudan Assia, Bakkach Joaira, Khaddor Mustapha, Mourabit Nadira
Department of Biology, Laboratory of Research and Development in Engineering Sciences, Faculty of Sciences and Techniques of Al-Hoceima, Abdelmalek Essaadi University, Tetouan 93000, Al-Hoceima, Morocco.
Department of Biology, Higher Institute of Nursing Professions and Health Techniques of Tetouan, Al-Hoceima 93000, Morocco.
Int J Microbiol. 2024 Dec 5;2024:5553860. doi: 10.1155/ijm/5553860. eCollection 2024.
Research into biologically natural substances with antitumor properties, known for their potential to induce fewer side effects and exhibit specificity toward cancerous cells, remains imperative. The pressing demand for novel agents in cancer therapy underscores the intensive investigation of natural products from microorganisms. , frequently isolated from food and feed, emerges as a promising candidate against pathogenic bacteria and fungi. This species harbors numerous mycotoxins that warrant extensive clinical study due to their potential in cancer treatment. Identifying mycotoxins with anticancer properties produced by could unveil novel therapeutic targets and enrich the pharmacological landscape. This review provides a comprehensive overview of the utilization of mycotoxins in cancer research and elucidates therapeutic agents' advantages and limitations. produces at least 15 mycotoxins with potent anticancer effects mediated through diverse mechanisms, including enzyme inhibition (e.g., pseurotin), induction of apoptosis (e.g., auranthine, aurantiamides A, aurantiomides A-C, penicillic acid, penitrem, verrucisidinol, acetate verrucosidinol, and chaetoglobosin A), and cell-cycle arrest (e.g., anicequol, aurantiamine, and Taxol). Although certain mycotoxins, such as Taxol, Anacin, and Compactin, are used in commerce, many others remain relatively unexplored. The mycotoxins derived from hold considerable potential for cancer treatment, offering novel therapeutic avenues and enhancing current treatments through synergistic combinations and advanced delivery systems.
对具有抗肿瘤特性的生物天然物质进行研究仍然势在必行,这些物质以其诱导较少副作用和对癌细胞具有特异性的潜力而闻名。癌症治疗中对新型药物的迫切需求凸显了对微生物天然产物的深入研究。,通常从食物和饲料中分离出来,成为对抗病原菌和真菌的有希望的候选物。该物种含有多种霉菌毒素,由于其在癌症治疗中的潜力,值得进行广泛的临床研究。鉴定由产生的具有抗癌特性的霉菌毒素可以揭示新的治疗靶点并丰富药理学领域。这篇综述全面概述了霉菌毒素在癌症研究中的应用,并阐明了治疗药物的优点和局限性。产生至少15种具有强大抗癌作用的霉菌毒素,其作用机制多样,包括酶抑制(如假丝菌素)、诱导凋亡(如金橙素、金橙酰胺A、金橙酰胺A-C、青霉酸、青霉震颤素、疣孢菌素醇、醋酸疣孢菌素醇和毛壳菌素A)以及细胞周期阻滞(如茴香脑、金橙胺和紫杉醇)。虽然某些霉菌毒素,如紫杉醇、阿纳辛和康帕丁,已用于商业用途,但许多其他霉菌毒素仍相对未被探索。源自的霉菌毒素在癌症治疗方面具有相当大的潜力,通过协同组合和先进的递送系统提供新的治疗途径并增强当前的治疗方法。