In vitro: anticancer effect of oily and methanolic extracts of Al-Zahdi (Phoenix dactylifera L.) from dry dates and leaves on AMN3, Hela and Ref cancer cell cultures

S. S. M. Al-zeiny, K. Alyaqubi, D. A. Abbas
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引用次数: 2

Abstract

The antioxidant and anti-tumor effects of extracts from various herbs and medicinal plants were measured using various in vitro and in vivo methods. The current study investigates and compare the anticancer effects of the two palm part extracts against cancer cell line in cultured cell line of AMN3, Hela and Ref. The results showed a concentration dependent inhibitory cytotoxic effects during 72 hrs of exposure for methanolic and oily crude extracts of date and leaves on AMN3, Hela and Ref cell lines. The highest significant effect of both dry date and leave methanolic extracts were achieved at concentration 2500 μg/ ml that causing highest growth inhibition percentage (GIP) of (73.3 %, 66.4%) for AMN3 and (76.7 %, 55.4%) for Hela respectively. The concentration 5000 μg/ ml showed nearly less effect after 72 hrs exposure. Both methanolic extracts tested concentrations didn’t cause   any inhibitory effect on the REF cell line. The effect of date and leaves oily extracts at different concentrations caused on tumor Cell Line AMN3, Hela and Ref highly significant in difference at exposure periods 72   hrs for concentrations gradient ranged from (15.62- 250 μg/ml). The concentration 125 µg/ml showed higher inhibition percentage compared to the higher concentration of 2500 µg/ ml causing   on AMN3 (85.1%, 66%), Hela (79.1%, 77%), and Ref (76%, 61.7%), respectively.  Plateau were noticed for all highest palm extracts concentrations GIP effect on all cell line cultures. The study concluded that the superiority of oil extract for both date and leave over alcoholic extracts one in inhibition of in vitro the same cell lines AMN3, Hela, Ref.
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体外:干枣和叶片Al-Zahdi (Phoenix dactylifera L.)油脂和甲醇提取物对AMN3、Hela和Ref癌细胞培养的抗癌作用
采用各种体外和体内实验方法测定了各种中草药提取物的抗氧化和抗肿瘤作用。本研究在AMN3、Hela和Ref培养细胞系中比较了两种棕榈提取物对癌细胞的抗癌作用。结果表明,在暴露72 h时,枣和叶的甲醇和含油粗提物对AMN3、Hela和Ref细胞系具有浓度依赖性的抑制细胞毒作用。干枣和叶甲醇提取物在浓度为2500 μg/ ml时,对AMN3和Hela的生长抑制率(GIP)分别为73.3%和66.4%和76.7%和55.4%。浓度5000 μg/ ml暴露72 h后,影响基本减弱。两种浓度的甲醇提取物对REF细胞系均无抑制作用。在浓度梯度为(15.62 ~ 250 μg/ml)范围内,不同浓度的枣、叶油提取物对肿瘤细胞株AMN3、Hela和Ref的影响在暴露72 h时差异极显著。125µg/ml浓度对AMN3(85.1%, 66%)、Hela(79.1%, 77%)和Ref(76%, 61.7%)的抑制率分别高于2500µg/ml浓度。在所有细胞系培养中,最高棕榈提取物浓度的GIP效应均达到高原。结果表明,枣油提取物和香叶油提取物在体外对同一细胞系AMN3、Hela、Ref的抑制作用均优于酒精提取物。
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