Tundis Rosa, Patra Jayanta Kumar, Bonesi Marco, Das Subrata, Nath Rajat, Das Talukdar Anupam, Das Gitishree, Loizzo Monica Rosa
Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, Italy.
Research Institute of Integrative Life Sciences, Dongguk University-Seoul, Goyangsi 10326, Republic of Korea.
Plants (Basel). 2023 May 12;12(10):1969. doi: 10.3390/plants12101969.
In spite of the progress in treatment strategies, cancer remains a major cause of death worldwide. Therefore, the main challenge should be the early diagnosis of cancer and the design of an optimal therapeutic strategy to increase the patient's life expectancy as well as the continuation of the search for increasingly active and selective molecules for the treatment of different forms of cancer. In the recent decades, research in the field of natural compounds has increasingly shifted towards advanced and molecular level understandings, thus leading to the development of potent anti-cancer agents. Among them is the diterpene lactone andrographolide, isolated from (Burm.f.) Wall. ex Nees that showed shows a plethora of biological activities, including not only anti-cancer activity, but also anti-inflammatory, anti-viral, anti-bacterial, neuroprotective, hepatoprotective, hypoglycemic, and immunomodulatory properties. Andrographolide has been shown to act as an anti-tumor drug by affecting specific molecular targets that play a part in the development and progression of several cancer types including breast, lung, colon, renal, and cervical cancer, as well as leukemia and hepatocarcinoma. This review comprehensively and systematically summarized the current research on the potential anti-cancer properties of andrographolide highlighting its mechanisms of action, pharmacokinetics, and potential side effects and discussing the future perspectives, challenges, and limitations of use.
尽管治疗策略取得了进展,但癌症仍然是全球主要的死亡原因。因此,主要挑战应该是癌症的早期诊断以及设计最佳治疗策略以提高患者的预期寿命,同时继续寻找治疗不同类型癌症的活性越来越高、选择性越来越强的分子。近几十年来,天然化合物领域的研究越来越多地转向先进的分子水平理解,从而导致了强效抗癌药物的开发。其中包括从穿心莲(学名:Andrographis paniculata (Burm.f.) Wall. ex Nees)中分离出的二萜内酯穿心莲内酯,它具有多种生物活性,不仅包括抗癌活性,还具有抗炎、抗病毒、抗菌、神经保护、肝脏保护、降血糖和免疫调节特性。穿心莲内酯已被证明通过影响在包括乳腺癌、肺癌、结肠癌、肾癌和宫颈癌以及白血病和肝癌在内的几种癌症类型的发生和发展中起作用的特定分子靶点,从而发挥抗肿瘤药物的作用。这篇综述全面系统地总结了目前关于穿心莲内酯潜在抗癌特性的研究,重点介绍了其作用机制、药代动力学以及潜在的副作用,并讨论了其未来的前景、挑战和使用局限性。