Open AccessCYTOTOXIC EFFECT OF CORCHORUS DEPRESSUS AGAINST HEPG2 AND HLE HUMAN LIVER CANCER CELLS
Author(s) -
Purvi Harishkumar Kakrani,
Harish N. Kakrani,
Manan Raval
Publication year - 2018
Publication title -
asian journal of pharmaceutical and clinical research
Language(s) - English
Resource type - Journals
eISSN - 2455-3891
pISSN - 0974-2441
DOI - 10.22159/ajpcr.2018.v11i12.27937
Subject(s) - chloroform , ethyl acetate , ic50 , cytotoxicity , chemistry , hepatocellular carcinoma , cytotoxic t cell , mtt assay , cell culture , hepatic carcinoma , traditional medicine , liver cancer , viability assay , chromatography , cell growth , in vitro , biochemistry , biology , medicine , genetics , cancer research
Objective: The present study was designed to examine the cytotoxic effects of methanolic extract of aerial parts of Corchorus depressus and hexane, chloroform, ethyl acetate, and aqueous fractions of the same extract in the human hepatocellular carcinoma (HCC) (HepG2) and invasive hepatocellular carcinoma cell lines (HLE).Methods: Anti-proliferative effects were evaluated using 3-(4,5-dimethythiazol2-yl)-2,5-diphenyl tetrazolium bromide (MTT) and neutral red uptake (NRU) assay. Human HCC (HepG2) and invasive hepatocellular carcinoma cell lines (HLE) were treated with different concentrations of methanolic extract (10, 25, 50, 100, 200, 300, 400, and 500 μg/mL) of aerial parts of C. depressus as well as hexane, chloroform, ethyl acetate, and aqueous fractions (200 μg/mL) for 24 and 48 h. The cell viability and the half maximal inhibitory concentration (IC50) were determined.Results: The maximum cytotoxic effect was noticed with a maximum dose of methanolic extract (500 μg/mL) and alkaloidal fraction (200 μg) in this study with an IC50 value of about 200 μg.Conclusion: The set of studies showed that methanolic extract of aerial parts of C. depressus and alkaloidal, chloroform and ethyl acetate fractions fractions was capable of inhibiting cell growth and cell proliferation by inducing cytotoxicity of HepG2 and HLE cells.