Joshi Priyanka, Joshi Sushil, Semwal Deepak, Bisht Akansha, Paliwal Sarvesh, Dwivedi Jaya, Sharma Swapnil
Department of Pharmacy, Banasthali Vidyapith, Banasthali, Rajasthan, India.
R&D, Patanjali Ayurved Ltd, Patanjali Food and Herbal Park, Haridwar, Uttarakhand, India.
Mini Rev Med Chem. 2021;21(17):2420-2457. doi: 10.2174/1389557521666210122153823.
Curcuma longa has been mentioned in the Indian system of medicine for the management of a wide range of diseases. C. longa and its metabolites like curcumin, ar-turmerone, methylcurcumin, demethoxy-curcumin, and bisdemethoxycurcumin have also been reported to be beneficial in various types of cancer. Curcumin elicits anticancer properties chiefly by triggering apoptotic pathways in cancer cells. The properties are facilitated through diverse signaling pathways viz. pathways mediated by NF-kB, WNT/β-catenin pathway COX-2, LOX, STAT3, prostaglandin E2, phosphorylase kinase, VEGF, AKT, AP1, STAT3, PI3K, Akt, mTOR, ERK5, AP-1, TGF-b, PPARc, EBPa, NLRP3 inflammasome, p38MAPK, Nrf2, Notch-1, AMPK, TLR-4, etc. The present article highlights curcumin biosynthesis, phytochemistry and diverse molecular pathways involved in regulating several types of secondary messengers to exhibit anticancer activity in almost all the forms of cancer.
姜黄在印度医学体系中被提及可用于治疗多种疾病。姜黄及其代谢产物如姜黄素、莪术酮、甲基姜黄素、去甲氧基姜黄素和双去甲氧基姜黄素也被报道对多种类型的癌症有益。姜黄素主要通过触发癌细胞的凋亡途径发挥抗癌特性。这些特性通过多种信号通路来实现,即由NF-κB、WNT/β-连环蛋白途径、COX-2、LOX、STAT3、前列腺素E2、磷酸化酶激酶、VEGF、AKT、AP1、STAT3、PI3K、Akt、mTOR、ERK5、AP-1、TGF-β、PPARγ、EBPa、NLRP3炎性小体、p38MAPK、Nrf2、Notch-1、AMPK、TLR-4等介导的途径。本文重点介绍了姜黄素的生物合成、植物化学以及参与调节多种类型二级信使以在几乎所有癌症形式中展现抗癌活性的不同分子途径。