Feng Hui, Yang Runyu, Du Yue, Liu Yi, Niu Fan
Department of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, No.277 Yanta West Road, Xi'an, Shaanxi, 710061, China.
Curr Med Chem. 2025;32(23):4713-4724. doi: 10.2174/0109298673273034231215190811.
Oridonin is a tetracyclic diterpenoid compound extracted from the medicinal herb Isodon and related species. Since 1976, studies have reported the significant anti-tumor activity of oridonin in vivo. Recently, an increasing number of studies have confirmed the anti-tumor effects of oridonin in various types of cancers, and its effect on hematological malignancies stands out. Herein, we have systematically reviewed the antitumor effects of oridonin and its specific mechanisms in hematological malignancies, including the regulation of cancer proteins, activation of intrinsic and extrinsic apoptosis signaling pathways, accumulation of reactive oxygen species (ROS), modulation of chaperone proteins and miRNA expression, combination therapy with chemotherapeutic drugs, and the development of its derivatives. Taken together, oridonin exhibits multiple anti-tumor activities and serves as a multi-target agent, making it worthy of further investigation.
冬凌草甲素是一种从药用植物冬凌草及其相关物种中提取的四环二萜类化合物。自1976年以来,已有研究报道冬凌草甲素在体内具有显著的抗肿瘤活性。最近,越来越多的研究证实了冬凌草甲素对各种癌症的抗肿瘤作用,其对血液系统恶性肿瘤的作用尤为突出。在此,我们系统地综述了冬凌草甲素在血液系统恶性肿瘤中的抗肿瘤作用及其具体机制,包括对癌蛋白的调节、内源性和外源性凋亡信号通路的激活、活性氧(ROS)的积累、伴侣蛋白和miRNA表达的调节、与化疗药物的联合治疗以及其衍生物的开发。综上所述,冬凌草甲素具有多种抗肿瘤活性,是一种多靶点药物,值得进一步研究。