Zhang Jinwei
Institute of Biomedical and Clinical Sciences, Medical School, Faculty of Health and Life Sciences, Hatherly Laboratories, Streatham Campus, University of Exeter, Exeter EX4 4PS, UK.
State Key Laboratory of Chemical Biology, Research Center of Chemical Kinomics, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
Mar Drugs. 2025 Jul 9;23(7):283. doi: 10.3390/md23070283.
Marine-derived compounds represent a rich source of structurally diverse molecules with therapeutic potential for cancer, renal disorders, metabolic-associated fatty liver disease (MAFLD), and atherosclerosis. This review systematically evaluates recent advances, highlighting compounds such as Microcolin H, Benzosceptrin C, S14, HN-001, Equisetin, glycosides (e.g., cucumarioside A-2), ilimaquinone, and Aplidin (plitidepsin). Key mechanisms include autophagy modulation, immune checkpoint inhibition, anti-inflammatory effects, and mitochondrial homeostasis. Novel findings reveal glycosides' dual role in cytotoxicity and immunomodulation, ilimaquinone's induction of the DNA damage response, and Aplidin's disruption of protein synthesis via eEF1A2 binding. Pharmacokinetic challenges and structure-activity relationships are critically analyzed, emphasizing nanodelivery systems and synthetic analog development. This review bridges mechanistic insights with translational potential, offering a cohesive framework for future drug development.
海洋来源的化合物是结构多样的分子的丰富来源,对癌症、肾脏疾病、代谢相关脂肪性肝病(MAFLD)和动脉粥样硬化具有治疗潜力。本综述系统地评估了近期的进展,重点介绍了如微科林H、苯并截短侧耳素C、S14、HN-001、木贼菌素、糖苷(如海参苷A-2)、伊立替康酮和阿普利丁(普利替得辛)等化合物。关键机制包括自噬调节、免疫检查点抑制、抗炎作用和线粒体稳态。新发现揭示了糖苷在细胞毒性和免疫调节中的双重作用、伊立替康酮对DNA损伤反应的诱导以及阿普利丁通过结合eEF1A2对蛋白质合成的破坏。对药代动力学挑战和构效关系进行了批判性分析,强调了纳米递送系统和合成类似物的开发。本综述将机制见解与转化潜力联系起来,为未来的药物开发提供了一个连贯的框架。