Journal of Clinical & Experimental Pharmacology

Regucalcin protects HepG2 cells from Doxorubicin-induced apoptosis and autophagy

2^nd International Conference and Exhibition on Pharmacology and Ethnopharmacology

May 02-04, 2016 Chicago, USA

Noor Mohammed, Frank Michelangeli and Nikolas Hodges

University of Birmingham School of Bioscience, UK

Scientific Tracks Abstracts: Clin Exp Pharmacol

Abstract:

Regucalcin (RGN) is a cytosolic Ca2+-binding protein that was discovered in 1978 and is known to be a multi-functional protein involved in number of cellular processes including �?? calcium homeostasis by regulating Ca²+ binding protein activity such as Ca2+-ATPases, calmodulin kinase and PKC. This protein is mostly found in liver and kidney tissues. Furthermore, RGN also plays a defence role in Ca2+-mediated stress protection and apoptosis. Doxorubicin (DOX) is a potent anti-cancer drug that is used either in isolation or in combination with other drugs for treating variety of cancers. Several studies have shown that DOX induces p53 activation leading to apoptosis in both normal and tumour endothelial cardiomyocytes cells; by causing cytochrome c release from the mitochondria, resulting in caspase 3 activation and induction of apoptosis. Moreover, this drug has the ability to damage DNA by producing reactive oxygen species. A major problem of DOX treatment is that it is highly cardio- and hepato-toxic. In the current study we have investigated the molecular mechanisms of DOX-induced hepatic cell death and show that DOX can induce cell death in human HepG2 liver cells through a number of different mechanisms including; apoptosis, DNA damage and autophagy. However, necrosis does not appear to be involved in this process. Furthermore, over-expression of RGN in HepG2 cells was found to protect against the toxicity by DOX. Therefore increased expression of RGN in the liver could be a mechanism for protection against DOXinduced toxicity.

Biography :

Noor Mohammed has completed her Master degree (MSc) in Histology on March 2010 from University of Duhok (Kurdistan Region Government of Iraq) and has published her master thesis as two papers in local university journal. She worked as an Assistant Lecturer in biology department, University of Duhok since 2010, and then she started her PhD on September 2013 focusing on the mechanism effect of chemotherapy drugs on liver and kidney cell line.

Email: nam274@bham.ac.uk