Chakri Naruebodindra Medical Institute, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bang Pla, Bang Phli, Samut Prakan 10540, Thailand.
Molecules. 2022 Mar 24;27(7):2086. doi: 10.3390/molecules27072086.
Cancer is a leading cause of morbidity and mortality worldwide. The development of cancer involves aberrations in multiple pathways, representing promising targets for anti-cancer drug discovery. Natural products are regarded as a rich source for developing anti-cancer therapies due to their unique structures and favorable pharmacology and toxicology profiles. Deoxyelephantopin and isodeoxyelephantopin, sesquiterpene lactone compounds, are major components of and , which have long been used as traditional medicines to treat multiple ailments, including liver diseases, diabetes, bronchitis, fever, diarrhea, dysentery, cancer, renal disorders, and inflammation-associated diseases. Recently, deoxyelephantopin and isodeoxyelephantopin have been extensively explored for their anti-cancer activities. This review summarizes and discusses the anti-cancer activities of deoxyelephantopin and isodeoxyelephantopin, with an emphasis on their modes of action and molecular targets. Both compounds disrupt several processes involved in cancer progression by targeting multiple signaling pathways deregulated in cancers, including cell cycle and proliferation, cell survival, autophagy, and invasion pathways. Future directions of research on these two compounds towards anti-cancer drug development are discussed.
癌症是全球发病率和死亡率的主要原因。癌症的发展涉及多个途径的异常,这些途径代表了抗癌药物发现的有前途的靶点。由于其独特的结构和良好的药理学和毒理学特性,天然产物被认为是开发抗癌疗法的丰富来源。去氧土大黄素和异去氧土大黄素是 和 的主要成分,它们一直被用作传统药物来治疗多种疾病,包括肝病、糖尿病、支气管炎、发热、腹泻、痢疾、癌症、肾脏疾病和炎症相关疾病。最近,去氧土大黄素和异去氧土大黄素的抗癌活性得到了广泛的研究。本综述总结和讨论了去氧土大黄素和异去氧土大黄素的抗癌活性,重点讨论了它们的作用机制和分子靶点。这两种化合物通过靶向癌症中失调的多种信号通路,破坏了癌症进展中涉及的几个过程,包括细胞周期和增殖、细胞存活、自噬和侵袭途径。讨论了这两种化合物在抗癌药物开发方面的未来研究方向。