Tsukamoto Sachiko
Department of Natural Medicines, Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-Honmachi, Kumamoto, 862-0973, Japan.
J Nat Med. 2025 Apr 28. doi: 10.1007/s11418-025-01906-6.
Wild-type p53 acts as a tumor suppressor, but p53 is frequently mutated and inactivated in tumor cells, promoting cancer progression, invasion, and metastasis. Thus, compounds that reactivate p53 may be leveraged for cancer treatment, and the development of drugs targeting p53 reactivation is actively progressing. Notably, natural products exhibit diverse structures and biological activities and are used as therapeutic agents for various diseases worldwide. This review discusses the natural products that inhibit p53 degradation through p53-Mdm2 interaction, promote p53 reactivation by inducing conformational changes, and exhibit p53-dependent growth inhibition.
野生型p53作为一种肿瘤抑制因子,但p53在肿瘤细胞中经常发生突变并失活,从而促进癌症进展、侵袭和转移。因此,可利用能重新激活p53的化合物进行癌症治疗,并且针对p53重新激活的药物研发正在积极推进。值得注意的是,天然产物具有多样的结构和生物活性,在全球范围内被用作各种疾病的治疗药物。本综述讨论了通过p53-Mdm2相互作用抑制p53降解、通过诱导构象变化促进p53重新激活以及表现出p53依赖性生长抑制作用的天然产物。