Cytotoxicity of Nigella Sativa Seed Oil and Extract Against Human Lung Cancer Cell Line

被引:51
作者
Al-Sheddi, Ebtesam Saad [1 ]
Farshori, Nida Nayyar [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
Nigella sativa; A-549; cells; cytotoxicity; cellular morphology; IN-VITRO; ANTICANCER ACTIVITY; ANTITUMOR-ACTIVITY; OXIDATIVE STRESS; THYMOQUINONE; L; CARCINOGENESIS; INHIBITION; BLACKSEED; APOPTOSIS;
D O I
10.7314/APJCP.2014.15.2.983
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nigella sativa (N sativa), commonly known as black seed, has been used in traditional medicine to treat many diseases. The antioxidant, anti-inflammatory, and antibacterial activities of N sativa extracts are well known. Therefore, the present study was designed to investigate the anticancer activity of seed extract (NSE) and seed oil (NSO) of N sativa against a human lung cancer cell line. Cells were exposed to 0.01 to 1 mg/ml of NSE and NSO for 24 h, then percent cell viability was assessed 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 NSE and NSO significantly reduce the cell viability and alter the cellular morphology of A-549 cells in a concentration dependent manner. The percent cell viability was recorded as 75%, 50%, and 26% at 0.25, 0.5, and 1 mg/ml of NSE by MTT assay and 73%, 48%, and 23% at 0.25, 0.5, and 1 mg/ml of NSE by NRU assay. Exposure to NSO concentrations of 0.1 mg/ml and above for 24 h was also found to be cytotoxic. The decrease in cell viability at 0.1, 0.25, 0.5, and 1 mg/ml of NSO was recorded to be 89%, 52%, 41%, and 13% by MTT assay and 85%, 52%, 38%, and 11% by NRU assay, respectively. A-549 cells exposed to 0.25, 0.5 and 1 mg/ml of NSE and NSO lost their typical morphology and appeared smaller in size. The data revealed that the treatment of seed extract (NSE) and seed oil (NSO) of Nigella sativa significantly reduce viability of human lung cancer cells.
引用
收藏
页码:983 / 987
页数:5
相关论文
共 42 条
  • [1] Ahmad Aftab, 2013, Asian Pacific Journal of Tropical Biomedicine, V3, P337, DOI 10.1016/S2221-1691(13)60075-1
  • [2] Al-Khalaf M. I., 2013, Australian Journal of Basic and Applied Sciences, V7, P505
  • [3] In Vitro Cytotoxic Activity of Seed Oil of Fenugreek Against Various Cancer Cell Lines
    Al-Oqail, Mai Mohammad
    Farshori, Nida Nayyar
    Al-Sheddi, Ebtesam Saad
    Musarrat, Javed
    Al-Khedhairy, Abdulaziz Ali
    Siddiqui, Maqsood Ahmed
    [J]. ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2013, 14 (03) : 1829 - 1832
  • [4] Pharmacological and toxicological properties of Nigella sativa
    Ali, BH
    Blunden, G
    [J]. PHYTOTHERAPY RESEARCH, 2003, 17 (04) : 299 - 305
  • [5] [Anonymous], INT J PHARM SCI
  • [6] In vitro decreases of the fibrinolytic potential of cultured human fibrosarcoma cell line, HT1080, by Nigella sativa oil
    Awad, EM
    [J]. PHYTOMEDICINE, 2005, 12 (1-2) : 100 - 107
  • [7] ANTIOXIDANT, ANTI-INFLAMMATORY, ANTICANCER AND ANTIBACTERIAL ACTIVITIES OF EXTRACTS FROM NIGELLA SATIVA (BLACK CUMIN) PLANT PARTS
    Bourgou, Soumaya
    Pichette, Andre
    Marzouk, Brahim
    Legault, Jean
    [J]. JOURNAL OF FOOD BIOCHEMISTRY, 2012, 36 (05) : 539 - 546
  • [8] Anti-inflammatory effects of the Nigella sativa seed extract, thymoquinone, in pancreatic cancer cells
    Chehl, Navdeep
    Chipitsyna, Galina
    Gong, Qiaoke
    Yeo, Charles J.
    Arafat, Hwyda A.
    [J]. HPB, 2009, 11 (05) : 373 - 381
  • [9] Antiproliferative Properties of Methanolic Extract of Nigella sativa against the MDA-MB-231 Cancer Cell Line
    Dilshad, Ahmad
    Abulkhair, Omalkhair
    Nemenqani, Dalal
    Tamimi, Waleed
    [J]. ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2012, 13 (11) : 5839 - 5842
  • [10] Terpene Conjugates of the Nigella sativa Seed-Oil Constituent Thymoquinone with Enhanced Efficacy in Cancer Cells
    Effenberger, Katharina
    Breyer, Sandra
    Schobert, Rainer
    [J]. CHEMISTRY & BIODIVERSITY, 2010, 7 (01) : 129 - 139