Title of article :
Evaluation of Silibinin Effects on the Viability of HepG2 (Human hepatocellular liver carcinoma) and HUVEC (Human Umbilical Vein Endothelial) Cell Lines
Author/Authors :
Vakili Zahir, Niki Department of Toxicology and Pharmacology - school of Pharmacy - Shahid Beheshti University of Medical Science, Tehran, Iran , Nakhjavani, Maryam Department of Toxicology and Pharmacology - school of Pharmacy - Shahid Beheshti University of Medical Science, Tehran, Iran , Hajianb, Parastoo Cancer Research Center - Shohadae Tajrish Hospital - Department of Radiation Oncology - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Shirazi, Farshad H Department of Toxicology and Pharmacology - school of Pharmacy - Shahid Beheshti University of Medical Science, Tehran, Iran , Mirzaei, Hamidreza Cancer research Center - Shohadae Tajrish Hospital - Department of Radiation Oncology - Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract :
Human hepatocellular carcinoma is one of the most common recurrent malignancies since
there is no effective therapy for it. Silibinin, a widely used drug and supplement for various
liver disorders, demonstrated anti-cancer effects on human hepatocellular carcinoma, human
prostate adenocarcinoma cells, human breast carcinoma cells, human ectocervical carcinoma
cells, and human colon cancer cells. Considering the anti-hepatotoxic activity of silibinin and
its strong preventive and anti-cancer efficacy against various epithelial cancers, we investigated
the efficacy of silibinin against human HCC and HUVEC cell lines. Silibinin effects on the
growth and mode of cell death of these two cell lines are presented in this paper. HepG2 and
HUVEC cells were incubated with different doses of silibinin (12.5, 25, 50, 100, 150 and 200
μg/mL) at 24, 48, and 72 h. Cytotoxicity was assessed using MTT and Trypan blue assays.
Mode of cell death induced by silibinin was investigated using LDH assay and acridine orange/
PI double dye staining. The results showed that silibinin has dose-dependent inhibitory effect
on the viability of HepG2 and HUVEC cells. However, Silibinin causes a more continuous
dose-dependent cytotoxicity in HepG2 cells compared to the HUVEC cells in which some
degrees of resistance is apparent at the beginning. The mode of cell death looks also different
in these two cell lines with HepG2 cells being more in favor of apoptosis while necrosis is more
evident for the HUVEC cells.
Keywords :
HepG2 , HUVEC , Human hepatocellular carcinoma , Silibinin
Journal title :
Astroparticle Physics