In Vitro Cytotoxic Potential of Ethanol Extract of Dictyopteris acrostichoides Against Human Cancer Cells

Eman Zekry Attia, Iman A. M. Abdel-Rahman, Omar M. Aly, Hani Saber, Mohammed I. Rushdi, Usama Ramadan Abdelmohsen
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Abstract

Abstract Ethanol extracts of Caulerpa racemose (Forsskål) J.Agardh, 1873, Dictyopteris acrostichoides (J.Agardh) Bornet, 1885, Halimeda opuntia (Linnaeus) J.V.Lamouroux, 1816, and Polycladia myrica (S.G.Gmelin) Draima, Ballesteros, F.Rousseau & T.Thibaut, 2010, were tested for their cytotoxicity against human hepatoma, human breast adenocarcinoma, and human colon adenocarcinoma cell lines. Dictyopteris acrostichoides displayed cytotoxicity against human hepatoma, human breast adenocarcinoma, and human colon adenocarcinoma with IC 50 values of 11.65, 9.28, and 16.86 µg/ml, respectively, in comparison to doxorubicin as a positive control (IC 50 5.72, 5.17, and 5.81 µg/ml, respectively). Metabolic profiling of the D. acrostichoides extract characterized seventeen metabolites. In silico analysis indicated 1-(3-oxo-undecyldisulfanyl)-undecan-3-one was the most active epidermal growth factor receptor inhibitor, while 1-(3-oxo-undecyldisulfanyl)-undecan-3-one and di(3-acetoxy-5-undecenyl) disulfide were the most active vascular endothelial growth factor inhibitors. Furthermore, the ethanol extract of D. acrostichoides was tested against epidermal growth factor receptor kinase (IC 50 0.11 µg/ml) compared to lapatinib as a positive control (IC 50 0.03 µg/ml), and against vascular endothelial growth factor (IC 50 0.276 µg/ml) compared to sorafenib as a positive control (IC 50 0.049 µg/ml). Graphical Abstract
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双翼蝶醇提物对人癌细胞的体外细胞毒性研究
摘要:总状茎叶(Caulerpa racemose) (forssk) j.a agardh), 1873, Dictyopteris acrostichoides (j.a agardh) Bornet, 1885, haalimeda opuntia (Linnaeus) J.V.Lamouroux, 1816, Polycladia myrica (S.G.Gmelin) Draima, Ballesteros, f.l usau等的乙醇提取物;T.Thibaut, 2010,对其对人肝癌、人乳腺腺癌和人结肠腺癌细胞系的细胞毒性进行了测试。与阳性对照多柔比星(ic50分别为5.72、5.17和5.81µg/ml)相比,多柔比星对人肝癌、人乳腺腺癌和人结肠腺癌的ic50分别为11.65、9.28和16.86µg/ml。花楸提取物代谢谱分析表征了17种代谢物。结果表明,1-(3-氧-十一烷基二磺胺基)-十一烷-3- 1是活性最高的表皮生长因子受体抑制剂,而1-(3-氧-十一烷基二磺胺基)-十一烷-3- 1和二(3-乙酰氧基-5-十一烷基)二硫化物是活性最高的血管内皮生长因子抑制剂。此外,我们还测试了荆刺草乙醇提取物对表皮生长因子受体激酶(IC 50 0.11µg/ml)的抑制作用(IC 50 0.03µg/ml),和对血管内皮生长因子(IC 50 0.276µg/ml)的抑制作用(IC 50 0.049µg/ml),分别比阳性对照拉帕替尼(50 0.03µg/ml)进行了比较。图形抽象
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