Repurposing Artemisinin and its Derivatives as Anticancer Drugs: A Chance or Challenge?

被引:37
作者
Ma, Zhaowu [1 ]
Woon, Clariis Yi-Ning [2 ]
Liu, Chen-Guang [1 ]
Cheng, Jun-Ting [1 ]
You, Mingliang [3 ,4 ]
Sethi, Gautam [5 ]
Wong, Andrea Li-Ann [6 ,7 ]
Ho, Paul Chi-Lui [2 ]
Zhang, Daping [1 ]
Ong, Peishi [2 ]
Wang, Lingzhi [5 ,6 ]
Goh, Boon-Cher [5 ,6 ,7 ]
机构
[1] Yangtze Univ, Hlth Sci Ctr, Sch Basic Med, Jingzhou, Peoples R China
[2] Natl Univ Singapore, Fac Sci, Dept Pharm, Singapore, Singapore
[3] Hangzhou Canc Inst, Key Lab Clin Canc Pharmacol & Toxicol Res Zhejian, Hangzhou, Peoples R China
[4] Zhejiang Univ, Sch Med, Affiliated Hangzhou Canc Hosp, Hangzhou, Peoples R China
[5] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pharmacol, Singapore, Singapore
[6] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore, Singapore
[7] Natl Univ Canc Inst, Dept Haematol Oncol, Singapore, Singapore
基金
英国医学研究理事会;
关键词
artemisinin; artemisinin derivatives; drug repurposing; anticancer therapy; pharmacokinetics; signalling pathways; OVARIAN-CANCER CELLS; ENDOTHELIAL GROWTH-FACTOR; METASTATIC BREAST-CANCER; ADD-ON THERAPY; LINE IN-VITRO; ORAL ARTESUNATE; INDUCED-APOPTOSIS; PHASE-I; INHIBITS ANGIOGENESIS; COMBINATION TREATMENT;
D O I
10.3389/fphar.2021.828856
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cancer has become a global health problem, accounting for one out of six deaths. Despite the recent advances in cancer therapy, there is still an ever-growing need for readily accessible new therapies. The process of drug discovery and development is arduous and takes many years, and while it is ongoing, the time for the current lead compounds to reach clinical trial phase is very long. Drug repurposing has recently gained significant attention as it expedites the process of discovering new entities for anticancer therapy. One such potential candidate is the antimalarial drug, artemisinin that has shown anticancer activities in vitro and in vivo. In this review, major molecular and cellular mechanisms underlying the anticancer effect of artemisinin and its derivatives are summarised. Furthermore, major mechanisms of action and some key signaling pathways of this group of compounds have been reviewed to explore potential targets that contribute to the proliferation and metastasis of tumor cells. Despite its established profile in malaria treatment, pharmacokinetic properties, anticancer potency, and current formulations that hinder the clinical translation of artemisinin as an anticancer agent, have been discussed. Finally, potential solutions or new strategies are identified to overcome the bottlenecks in repurposing artemisinin-type compounds as anticancer drugs.
引用
收藏
页数:26
相关论文
共 139 条
[1]   Dihydroartemisinine Enhances Dictamnine-induced Apoptosis via a Caspase Dependent Pathway in Human Lung Adenocarcinoma A549 Cells [J].
An, Fu-Fei ;
Liu, Yuan-Chong ;
Zhang, Wei-Wei ;
Liang, Lei .
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2013, 14 (10) :5895-5900
[2]  
Ashton M, 1998, BIOPHARM DRUG DISPOS, V19, P245, DOI 10.1002/(SICI)1099-081X(199805)19:4<245::AID-BDD99>3.0.CO
[3]  
2-Z
[4]   Artemisinins as a novel anti-cancer therapy: Targeting a global cancer pandemic through drug repurposing [J].
Augustin, Yolanda ;
Staines, Henry M. ;
Krishna, Sanjeev .
PHARMACOLOGY & THERAPEUTICS, 2020, 216
[5]   Developing combination of artesunate with paclitaxel loaded into poly-D,L-lactic-co-glycolic acid nanoparticle for systemic delivery to exhibit synergic chemotherapeutic response [J].
Bao Ngoc Tran ;
Hanh Thuy Nguyen ;
Kim, Jong Oh ;
Yong, Chul Soon ;
Chien Ngoc Nguyen .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2017, 43 (12) :1952-1962
[6]   Relative bioavailability of artesunate and dihydroartemisinin: Investigations in the isolated perfused rat liver and in healthy Caucasian volunteers [J].
Batty, KT ;
Ilett, KF ;
Powell, SM ;
Martin, J ;
Davis, TME .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2002, 66 (02) :130-136
[7]   Artesunate induces ROS- and p38 MAPK-mediated apoptosis and counteracts tumor growth in vivo in embryonal rhabdomyosarcoma cells [J].
Beccafico, Sara ;
Morozzi, Giulio ;
Marchetti, Maria Cristina ;
Riccardi, Carlo ;
Sidoni, Angelo ;
Donato, Rosario ;
Sorci, Guglielmo .
CARCINOGENESIS, 2015, 36 (09) :1071-1083
[8]   Artesunate Induces Oxidative DNA Damage, Sustained DNA Double-Strand Breaks, and the ATM/ATR Damage Response in Cancer Cells [J].
Berdelle, Nicole ;
Nikolova, Teodora ;
Quiros, Steve ;
Efferth, Thomas ;
Kaina, Bernd .
MOLECULAR CANCER THERAPEUTICS, 2011, 10 (12) :2224-2233
[9]  
Berger TG, 2005, ONCOL REP, V14, P1599
[10]   Artesunate enhances the therapeutic response of glioma cells to temozolomide by inhibition of homologous recombination and senescence [J].
Berte, Nancy ;
Lokan, Stefanie ;
Eich, Marcus ;
Kim, Ella ;
Kaina, Bernd .
ONCOTARGET, 2016, 7 (41) :67235-67250