The Bioflavonoid Galangin Suppresses the Growth of Ehrlich Ascites Carcinoma in Swiss Albino Mice: A Molecular Insight

被引:14
|
作者
Jaiswal, Jai V. [1 ]
Wadegaonkar, Prasad A. [1 ]
Hajare, Sunil W. [2 ]
机构
[1] St Gadge Baba Amravati Univ, Dept Biotechnol, Amravati, India
[2] PG Inst Vet Sci, Dept Vet Pharmacol & Toxicol, Akola, India
关键词
Bioflavonoid; Galangin; Erhlich ascites carcinoma; Apoptosis; Animal model; ADMET; Docking; FLAVONOID GALANGIN; INDUCE APOPTOSIS; DRUG ABSORPTION; FRAGMENTS PRIOR; CANCER; CELLS; INHIBITION; PERMEABILITY; VEGETABLES; PROPOLIS;
D O I
10.1007/s12010-012-9646-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bioflavonoids are plant compounds touted for their potential to treat or prevent several diseases including cancer caused by various stress conditions. Galangin (4H-1-Benzopyran-4-one, 3, 5, 7-trihydroxy-2-phenyl-), a flavonoid, is a polyphenolic compound found primarily in medicinal herb, Alpinia galanga. This study aims to demonstrate the galangin as a pharmacological lead compound using in vitro, in vivo, and in silico model targeting specific cancer condition and proteins. The proliferation of MCF-7 and Ehrlich ascites carcinoma (EAC) cells was significantly inhibited with an IC50 of 34.11 and 22.29 mu g/ml, respectively. In an animal model system, galangin has inhibited the tumor growth by 73.51% +/- 4.742 in EAC-induced Swiss Albino mice with no evidences of mortality as compared to standard drug, 5-fluorouracil. The effectiveness of galangin is proven in an animal system suggesting its pharmacokinetics behavior in an animal model which is also complemented by outcome of in silico analysis with more than 88 % of human intestinal absorption and significant Caco-2 cell, MDCK cell, and skin permeability as predicted by in silico methods. Galangin was docked against 19 different proteins involved in tumorogenesis and apoptosis; the energetic analysis indicates that it exhibits higher predicted binding free energy of -12.7 kcal/mol with Bcl-xL protein.
引用
收藏
页码:1325 / 1339
页数:15
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