Anticancer Activity of Petroselinum sativum Seed Extracts on MCF-7 Human Breast Cancer Cells

被引:27
|
作者
Farshori, Nida Nayyar [1 ]
Al-Sheddi, Ebtesam Saad [1 ]
Al-Oqail, Mai Mohammad [1 ]
Musarrat, Javed [2 ]
Al-Khedhairy, Abdulaziz Ali [2 ]
Siddiqui, Maqsood Ahmed [2 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmacognosy, Riyadh, Saudi Arabia
[2] King Saud Univ, Coll Sci, Dept Zool, Riyadh 11451, Saudi Arabia
关键词
MCF-7; cells; Petroselinum sativum; cellular morphology; cytotoxicity; PLANT-EXTRACTS; APOPTOSIS; LINES; OIL;
D O I
10.7314/APJCP.2013.14.10.5719
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pharmacological and preventive properties of Petroselinum sativum seed extracts are well known, but the anticancer activity of alcoholic extracts and oil of Petroselinum sativum seeds on human breast cancer cells have not been explored so far. Therefore, the present study was designed to investigate the cytotoxic activities of these extracts against MCF-7 cells. Cells were exposed to 10 to 1000 mu g/ml of alcoholic seed extract (PSA) and seed oil (PSO) of Petroselinum sativum for 24 h. Post-treatment, percent cell viability was studied by 3-(4, 5-dimethylthiazol-2yl)-2, 5-biphenyl tetrazolium bromide (MTT) and neutral red uptake (NRU) assays, and cellular morphology by phase contrast inverted microscopy. The results showed that PSA and PSO significantly reduced cell viability, and altered the cellular morphology of MCF-7 cells in a concentration dependent manner. Concentrations of 50 mu g/ml and above of PSA and 100 mu g/ml and above of PSO were found to be cytotoxic in MCF-7 cells. Cell viability at 50, 100, 250, 500 and 1000 mu g/ml of PSA was recorded as 81%, 57%, 33%, 8% and 5%, respectively, whereas at 100, 250, 500, and 1000 mu g/ml of PSO values were 90%, 78%, 62%, and 8%, respectively by MTT assay. MCF-7 cells exposed to 250, 500 and 1000 mu g/ml of PSA and PSO lost their typical morphology and appeared smaller in size. The data revealed that the treatment with PSA and PSO of Petroselinum sativum induced cell death in MCF-7 cells.
引用
收藏
页码:5719 / 5723
页数:5
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