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Evaluation of Efficacy of Curcumin and Caffeic Acid Phenethyl Ester in Breast Cancer by Preclinical Studies
被引:0
|作者:
Verma, Sumit Singh
[1
,7
]
Srivastava, Ankit
[1
]
Shekher, Anusmita
[1
,2
]
Dhasmana, Anupam
[3
,4
,8
]
Narula, Acharan Singh
[5
]
Gupta, Subash Chandra
[1
,6
]
机构:
[1] Banaras Hindu Univ, Inst Sci, Dept Biochem, Varanasi 221005, India
[2] Banaras Hindu Univ, Inst Med Sci, Dept Gen Surg, Varanasi 221005, India
[3] Swami Rama Himalayan Univ, Himalayan Inst Med Sci, Dept Biosci, Dehra Dun 248016, India
[4] Swami Rama Himalayan Univ, Canc Res Inst, Himalayan Inst Med Sci, Dehra Dun 248016, India
[5] Narula Res LLC, 107 Boulder Bluff, Chapel Hill, NC 27516 USA
[6] All India Inst Med Sci, Dept Biochem, Gauhati, India
[7] Indiana Univ Sch Med, Indiana Ctr Regenerat Med & Engn, Dept Surg, Indianapolis, IN 46202 USA
[8] Univ Texas Rio Grande Valley, Sch Med, Dept Immunol & Microbiol, Edinburg, TX USA
关键词:
Apoptosis;
breast cancer;
caffeic acid phenethyl ester;
curcumin;
ROS;
NF-kappa B;
NF-KAPPA-B;
ACTIVATION;
TRANSCRIPTION;
CELLS;
INHIBITION;
EXPRESSION;
APOPTOSIS;
ENZYME;
D O I:
10.2174/0109298673284600231230093955
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Aims The aim of this study was to evaluate the combined and comparative efficacy of Caffeic acid phenethyl ester (CAPE) and curcumin in breast cancer.Background CAPE and curcumin are a class of phenolics. While curcumin is obtained from turmeric, CAPE is found in Baccharis sarothroides and Populus deltoides. Both agents are reported to produce activities in some cancer types. The combined and comparative effects of the two agents in breast cancer have not yet reported.Objective We evaluated the potential of CAPE and curcumin in both in vitro and in vivo breast cancer models.Methods Human breast cancer cell lines, MDA-MB-231 and MCF-7, were exposed to CAPE and curcumin, followed by functional assays such as cell cytotoxicity, cell proliferation and colony formation, cell cycle, mitochondrial membrane potential, apoptosis, and monodansylcadaverine (MDC) staining for autophagy. Computational analyses and mouse models were also used.Results Employing computational analyses, both agents were found to exhibit drug-like properties. Both molecules interacted with the key molecules of the NF-kappa B pathway. CAPE and curcumin inhibited cell proliferation, colony formation, and invasion, triggering apoptosis in breast cancer cells. CAPE was found to be more effective than curcumin. Two agents working together were more effective than each agent working alone. Both agents suppressed the expression of survivin, Bcl-xL and GLUT-1. The level of cleaved PARP was increased by both agents. Both phenolics observed an induction in ROS generation. Further, both molecules triggered a dissipation in mitochondrial membrane potential. In mice models implanted with Ehrlich-Lettre ascites carcinoma (EAC) cells, both drugs inhibited the growth of the tumour. The phenolics also modulated the metabolic parameters in tumour-bearing mice.Conclusion The observations suggest that the combination of curcumin plus CAPE may be better in comparison to individual molecules.Other The study opens a window for analysing the efficacy of the combination of CAPE and curcumin in animal studies. This will provide a basis for examining the combined efficacy of two agents in a clinical trial.
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