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Perspectives for Synthetic Curcumins in Chemoprevention and Treatment of Cancer: An Update with Promising Analogues

Overview
Journal Eur J Pharmacol
Specialty Pharmacology
Date 2021 Jun 19
PMID 34146588
Citations 10
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Abstract

Curcumin, a pure compound extracted from the flowering plant, turmeric (Curcuma longa. Zingiberaceae), is a common dietary ingredient found in curry powder. It has been studied extensively for its anti-inflammatory, antioxidant, antimicrobial and anti-tumour activities. Evidence is accumulating demonstrating its potential in chemoprevention and as an anti-tumour agent for the treatment of cancer. Despite demonstrated safety and tolerability, the clinical application of curcumin is frustrated by its poor solubility, metabolic instability and low oral bioavailability. Consequently researchers have tried novel techniques of formulation and delivery as well as synthesis of analogues with enhanced properties to overcome these barriers. This review presents the synthetic analogues of curcumin that have proven their anticancer potential from different studies. It also highlights studies that combined these analogues with approved chemotherapies and delivered them via novel techniques. Currently, there are no reports of clinical studies on any of the synthetic congeners of curcumin and this presents an opportunity for future research. This review presents the synthetic analogues of curcumin and makes a compelling argument for their potential application in the management of cancerous disease.

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References
1.
Zhu S, Moore T, Lin X, Morii N, Mancini A, Howard R . Synthetic curcumin analog EF31 inhibits the growth of head and neck squamous cell carcinoma xenografts. Integr Biol (Camb). 2012; 4(6):633-40. PMC: 3734847. DOI: 10.1039/c2ib20007d. View

2.
Yang C, Yue J, Sims M, Pfeffer L . The curcumin analog EF24 targets NF-κB and miRNA-21, and has potent anticancer activity in vitro and in vivo. PLoS One. 2013; 8(8):e71130. PMC: 3737134. DOI: 10.1371/journal.pone.0071130. View

3.
Haque A, Rahman M, Fuchs J, Chen Z, Khuri F, Shin D . FLLL12 induces apoptosis in lung cancer cells through a p53/p73-independent but death receptor 5-dependent pathway. Cancer Lett. 2015; 363(2):166-75. PMC: 4433807. DOI: 10.1016/j.canlet.2015.04.017. View

4.
Kesharwani P, Xie L, Banerjee S, Mao G, Padhye S, Sarkar F . Hyaluronic acid-conjugated polyamidoamine dendrimers for targeted delivery of 3,4-difluorobenzylidene curcumin to CD44 overexpressing pancreatic cancer cells. Colloids Surf B Biointerfaces. 2015; 136:413-23. DOI: 10.1016/j.colsurfb.2015.09.043. View

5.
Liang G, Shao L, Wang Y, Zhao C, Chu Y, Xiao J . Exploration and synthesis of curcumin analogues with improved structural stability both in vitro and in vivo as cytotoxic agents. Bioorg Med Chem. 2009; 17(6):2623-31. DOI: 10.1016/j.bmc.2008.10.044. View