Department of Breast Medicine 1, Cancer Hospital of China Medical University, Liaoning Cancer Hospital, Shenyang 110042, China.
Department of Pharmacology, Cancer Hospital of China Medical University, Liaoning Cancer Hospital, Shenyang 110042, China.
Biomolecules. 2024 Jul 10;14(7):831. doi: 10.3390/biom14070831.
Cancer poses a severe threat to human health. Although conventional chemotherapy remains a cornerstone of cancer treatment, its significant side effects and the growing issue of drug resistance necessitate the urgent search for more efficient and less toxic anticancer drugs. In recent years, bacteriocins, antimicrobial peptides of microbial origin, have garnered significant attention due to their targeted antitumor activity. This unique activity is mainly attributed to their cationic and amphiphilic nature, which enables bacteriocins to specifically kill tumor cells without harming normal cells. When involving non-membrane-disrupting mechanisms, such as apoptosis induction, cell cycle blockade, and metastasis inhibition, the core mechanism of action is achieved by disrupting cell membranes, which endows bacteriocins with low drug resistance and high selectivity. However, the susceptibility of bacteriocins to hydrolysis and hemolysis in vivo limits their clinical application. To overcome these challenges, structural optimization of bacteriocins or their combination with nanotechnology is proposed for future development. This review aims to study the mechanism of action and current research status of bacteriocins as anticancer treatments, thus providing new insights for their clinical development and application.
癌症严重威胁人类健康。尽管传统化疗仍然是癌症治疗的基石,但它的显著副作用和日益严重的耐药性问题需要迫切寻找更有效、毒性更低的抗癌药物。近年来,源于微生物的抗菌肽类细菌素由于其靶向抗肿瘤活性而受到广泛关注。这种独特的活性主要归因于其阳离子和两亲性,使细菌素能够特异性地杀死肿瘤细胞而不伤害正常细胞。当涉及非破坏细胞膜的机制,如诱导细胞凋亡、细胞周期阻滞和抑制转移时,通过破坏细胞膜来实现其核心作用机制,这使细菌素具有低耐药性和高选择性。然而,细菌素在体内易被水解和溶血,限制了其临床应用。为了克服这些挑战,提出了对细菌素进行结构优化或与纳米技术结合,以用于未来的发展。本综述旨在研究细菌素作为抗癌治疗的作用机制和当前研究状况,为其临床开发和应用提供新的思路。