The Sidney Kimmel Comprehensive Cancer Center, the Johns Hopkins School of Medicine, 4940 Eastern Avenue, 4th Floor, Asthma & Allergy Building, Baltimore, MD, 21224, USA.
Division of Pulmonary and Critical Care Medicine, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.
J Cancer Res Clin Oncol. 2024 Mar 15;150(3):130. doi: 10.1007/s00432-024-05648-y.
Psoralen is a family of naturally occurring photoactive compounds found in plants that acquire potential cytotoxicity when activated by specific frequencies of electromagnetic waves. Psoralens penetrate the phospholipid cellular membranes and insert themselves between the pyrimidines of deoxyribonucleic acid (DNA). Psoralens are initially biologically inert and acquire photoreactivity when exposed to certain classes of electromagnetic radiation, such as ultraviolet light. Once activated, psoralens form mono- and di-adducts with DNA, leading to marked cell apoptosis. This apoptotic effect is more pronounced in tumor cells due to their high rate of cell division. Moreover, photoactivated psoralen can inhibit tyrosine kinase signaling and influence the immunogenic properties of cells. Thus, the cytotoxicity of photoactivated psoralen holds promising clinical applications from its immunogenic properties to potential anti-cancer treatments. This narrative review aims to provide an overview of the current understanding and research on psoralen and to explore its potential future pharmacotherapeutic benefits in specific diseases.
补骨脂素是一类存在于植物中的天然光活性化合物,当被特定频率的电磁波激活时,会获得潜在的细胞毒性。补骨脂素穿透磷脂细胞膜,并插入脱氧核糖核酸(DNA)的嘧啶之间。补骨脂素最初在生物学上是惰性的,只有在暴露于某些类别的电磁辐射(如紫外线)时才具有光反应性。一旦被激活,补骨脂素就会与 DNA 形成单加合物和二加合物,导致明显的细胞凋亡。由于肿瘤细胞的细胞分裂率高,这种凋亡效应更为明显。此外,光激活的补骨脂素可以抑制酪氨酸激酶信号转导,并影响细胞的免疫原性。因此,光激活补骨脂素的细胞毒性从其免疫原性到潜在的抗癌治疗都具有有前途的临床应用。本综述旨在提供对补骨脂素的当前理解和研究的概述,并探讨其在特定疾病中的潜在未来药物治疗益处。