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

被引:1
|
作者
Attia, Eman Zekry [1 ]
Abdel-Rahman, Iman A. M. [2 ]
Aly, Omar M. [3 ]
Saber, Hani [4 ]
Rushdi, Mohammed I. [2 ]
Abdelmohsen, Usama Ramadan [1 ,5 ]
机构
[1] Minia Univ, Fac Pharm, Dept Pharmacognosy, Al Minya 61519, Egypt
[2] South Valley Univ, Fac Pharm, Dept Pharmacognosy, Qena 83523, Egypt
[3] Port Said Univ, Fac Pharm, Dept Med Chem, Port Said 42526, Egypt
[4] South Valley Univ, Fac Sci, Dept Bot & Microbiol, Qena, Egypt
[5] Deraya Univ, Fac Pharm, Dept Pharmacognosy, Univ Zone, New Minia City 61111, Egypt
关键词
Marine algae; Natural products; Metabolic profiling; Cytotoxicity; EGFR; VEGF; SESQUITERPENES; HYDROQUINONES; DIVARICATA;
D O I
10.1007/s43450-023-00474-8
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Ethanol extracts of Caulerpa racemose (Forsskal) 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 IC50 values of 11.65, 9.28, and 16.86 mu g/ml, respectively, in comparison to doxorubicin as a positive control (IC50 5.72, 5.17, and 5.81 mu g/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 (IC50 0.11 mu g/ml) compared to lapatinib as a positive control (IC50 0.03 mu g/ml), and against vascular endothelial growth factor (IC50 0.276 mu g/ml) compared to sorafenib as a positive control (IC50 0.049 mu g/ml).
引用
收藏
页码:212 / 216
页数:5
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