Developments in the anticancer activity of structurally modified curcumin: An up-to-date review

被引:115
作者
Rodrigues, Fiona C. [1 ]
Kumar, N. V. Anil [2 ]
Thakur, Goutam [1 ]
机构
[1] Manipal Acad Higher Educ, Manipal Inst Technol, Dept Biomed Engn, Manipal 576104, Karnataka, India
[2] Manipal Acad Higher Educ, Manipal Inst Technol, Dept Chem, Manipal 576104, Karnataka, India
关键词
Curcumin; Analogue; Derivative; Structural modification; Anticancer; NF-KAPPA-B; DEPENDENT KINASE INHIBITOR; CELL-CYCLE ARREST; BIOLOGICAL EVALUATION; IN-VITRO; ANTIOXIDANT ACTIVITY; GOLDEN SPICE; CANCER CELLS; CURRY SPICE; ANALOGS;
D O I
10.1016/j.ejmech.2019.04.058
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Curcumin is a pharmacologically active polyphenol derived from the popular spice element-Turmeric. The therapeutic activity of curcumin has been extensively investigated over the last few decades and reports suggest the role of curcumin in a large number of biological activities, particularly its prominent anticancer activity. Curcumin, being a pleiotropic molecule, is a regulator of multiple molecular targets which play crucial roles in various cell signaling pathways. It is known to suppress transformation, inhibit proliferation as well as induce apoptosis. However, despite all these benefits, the efficacy of curcumin remains limited due to its poor bioavailability, poor absorption within the systemic circulation and rapid elimination from the body. To overcome these limiting factors, researchers all around the world are working towards designing a synthetic and superior curcuminoid by making suitable structural modifications to the parent skeleton. These curcuminoids, mainly analogues and derivatives, will not only improve the physicochemical properties but also enhance the efficacy simultaneously. The present review will provide a comprehensive account of the analogues and derivatives of curcumin that have been reported since 2014 which have indicated a better anticancer activity than curcumin. (C) 2019 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:76 / 104
页数:29
相关论文
共 130 条
[1]  
Aggarwal BB, 2003, ANTICANCER RES, V23, P363
[2]   RETRACTED: Curcumin induces the degradation of cyclin E expression through ubiquitin-dependent pathway and up-regulates cyclin-dependent kinase inhibitors p21 and p27 in multiple human tumor cell lines (Retracted article. See vol. 102, pg. 147, 2016) [J].
Aggarwal, Bharat B. ;
Banerjee, Sanjeev ;
Bharadwaj, Uddalak ;
Sung, Bokyung ;
Shishodia, Shishir ;
Sethi, Gautam .
BIOCHEMICAL PHARMACOLOGY, 2007, 73 (07) :1024-1032
[3]   Curcumin and Its Analogues: Potential Anticancer Agents [J].
Agrawal, Dinesh Kumar ;
Mishra, Pushpesh Kumar .
MEDICINAL RESEARCH REVIEWS, 2010, 30 (05) :818-860
[4]   Synthesis of diethylamino-curcumin mimics with substituted triazolyl groups and their sensitization effect of TRAIL against brain cancer cells [J].
Ahn, Yongchel ;
Oh, Sangtae ;
Lee, Seong Jun ;
Park, Byong-Gon ;
Park, Yoon-Sun ;
Shin, Woon-Seob ;
Jang, Hyuk Jai ;
Park, Jin Hoon ;
Kwon, Daeho ;
Lee, Seokjoon .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2014, 24 (15) :3346-3350
[5]   Antioxidant and radical scavenging properties of curcumin [J].
Ak, Tuba ;
Gulcin, Ilhami .
CHEMICO-BIOLOGICAL INTERACTIONS, 2008, 174 (01) :27-37
[6]  
American Cancer Society, 2018, FACTS FIG 2018
[7]  
Anchal S, 2017, INT CONF COMMUN SYST, P47, DOI 10.1109/COMSNETS.2017.7945357
[8]  
Anthwal A., 2014, BIOMED RES INT, V2014, P1
[9]   Evaluation of Anticancer Activity of Water-Soluble Curcumin through the Induction of Apoptosis by p53 and p21 Modulation [J].
Banuppriya, Govindharasu ;
Shakambari, Ganeshan ;
Sribalan, Rajendran ;
Varalakshmi, Perumal ;
Padmini, Vediappen .
CHEMISTRYSELECT, 2018, 3 (11) :2976-2981
[10]   Synthesis and characterization of curcumin-sulfonamide hybrids: Biological evaluation and molecular docking studies [J].
Banuppriya, Govindharasu ;
Sribalan, Rajendran ;
Padmini, Vediappen .
JOURNAL OF MOLECULAR STRUCTURE, 2018, 1155 :90-100