Ajwa Date (Phoenix dactylifera L.) Extract Inhibits Human Breast Adenocarcinoma (MCF7) Cells In Vitro by Inducing Apoptosis and Cell Cycle Arrest

被引:55
作者
Khan, Fazal [1 ,2 ,3 ]
Ahmed, Farid [2 ]
Pushparaj, Peter Natesan [2 ]
Abuzenadah, Adel [3 ]
Kumosani, Taha [1 ,4 ]
Barbour, Elie [1 ,5 ]
AlQahtani, Mohammed [2 ]
Gauthaman, Kalamegam [2 ]
机构
[1] King Abdulaziz Univ, Fac Sci, Dept Biochem, Jeddah, Saudi Arabia
[2] King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah, Saudi Arabia
[3] King Abdulaziz Univ, King Fahd Med Res Ctr, Ctr Innovat Personalized Med, Jeddah, Saudi Arabia
[4] King Abdulaziz Univ, King Fahd Med Res Ctr, Biochem Unit, Jeddah, Saudi Arabia
[5] Amer Univ Beirut, Fac Agr & Food Sci, Dept Agr, Beirut, Lebanon
关键词
CYTOCHROME-C; CANCER; QUERCETIN; PROLIFERATION; MYRICETIN; MITOCHONDRIA; ANTIOXIDANT; ACTIVATION; FLAVONOIDS; INDUCTION;
D O I
10.1371/journal.pone.0158963
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Introduction Phoenix dactylifera L (Date palm) is a native plant of the Kingdom of Saudi Arabia (KSA) and other Middle Eastern countries. Ajwa date has been described in the traditional and alternative medicine to provide several health benefits including anticholesteremic, antioxidant, hepatoprotective and anticancer effects, but most remains to be scientifically validated. Herein, we evaluated the anticancer effects of the Methanolic Extract of Ajwa Date (MEAD) on human breast adenocarcinoma (MCF7) cells in vitro. Methods MCF7 cells were treated with various concentrations (5, 10, 15, 20 and 25 mg/ml) of MEAD for 24, 48 and 72 h and changes in cell morphology, cell cycle, apoptosis related protein and gene expression were studied. Results Phase contrast microscopy showed various morphological changes such as cell shrinkage, vacuolation, blebbing and fragmentation. MTT (2-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay demonstrated statistically significant dose-dependent inhibitions of MCF7 cell proliferation from 35% to 95%. Annexin V-FITC and TUNEL assays showed positive staining for apoptosis of MCF7 cells treated with MEAD (15 mg and 25 mg for 48 h). Flow cytometric analyses of MCF7 cells with MEAD (15 mg/ml and 20 mg/ml) for 24 h demonstrated cell cycle arrest at 'S' phase; increased p53, Bax protein expression; caspase 3activation and decreased the mitochondrial membrane potential (MMP). Quantitative real time PCR (qRT-PCR) analysis showed up-regulation of p53, Bax, Fas, and FasL and downregulation of Bcl-2. Conclusions MEAD inhibited MCF7 cells in vitro by the inducing cell cycle arrest and apoptosis. Our results indicate the anticancer effects of Ajwa dates, which therefore may be used as an adjunct therapy with conventional chemotherapeutics to achieve a synergistic effect against breast cancer.
引用
收藏
页数:17
相关论文
共 43 条
[1]
Abhishek Bhanot Abhishek Bhanot, 2011, International Journal of Phytomedicine, V3, P9
[2]
Ali A, 2011, FUNCT FOODS HEALTH D, V1, P118
[3]
American Cancer Society, 2016, CANC FACTS FIG 2016
[4]
[Anonymous], EUR SCI J
[5]
[Anonymous], 2015, J MICROBIAL BIOCH TE, DOI DOI 10.4172/1948-5948.1000180
[6]
[Anonymous], 2013, J Environ Anal Toxicol
[7]
[Anonymous], 2011, FOOD NUTR SCI
[8]
A review of the chemistry and pharmacology of the date fruits (Phoenix dactylifera L.) [J].
Baliga, Manjeshwar Shrinath ;
Baliga, Bantwal Raghavendra Vittaldas ;
Kandathil, Shaun Mathew ;
Bhat, Harshith P. ;
Vayalil, Praveen Kumar .
FOOD RESEARCH INTERNATIONAL, 2011, 44 (07) :1812-1822
[9]
Growth Inhibition and Induction of Apoptosis in SHG-44 Glioma Cells by Chinese Medicine Formula "Pingliu Keli" [J].
Cao, Peng ;
Cai, Xueting ;
Lu, Wuguang ;
Zhou, Fei ;
Huo, Jiege .
EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2011, 2011 :1-9
[10]
Quercetin-induced apoptosis acts through mitochondrial- and caspase-3-dependent pathways in human breast cancer MDA-MB-231 cells [J].
Chien, Su-Yu ;
Wu, Yao-Chung ;
Chung, Jing-Gung ;
Yang, Jai-Sing ;
Lu, Hsu-Feng ;
Tsou, Mei-Fen ;
Wood, W. G. ;
Kuo, Shou-Jen ;
Chen, Dar-Ren .
HUMAN & EXPERIMENTAL TOXICOLOGY, 2009, 28 (08) :493-503