Title of article :
Bee Venom Induces Unfolded Protein Response in A172 Glioblastoma Cell Line
Author/Authors :
Bazi، Ali نويسنده Cancer Molecular Pathology Research Center, Faculty of Medicine, Imam Reza Hospital, Mashhad University of Medical Sciences, Mashhad, IR Iran , , Gholamin، Mehran نويسنده Division of Human Genetics, Immunology Research Center, Avicenna Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran , , Sisakht، Mohsen نويسنده Department of Biochemistry, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, IR Iran , , Keramati، Mohammad Reza نويسنده ,
Issue Information :
فصلنامه با شماره پیاپی 0 سال 2015
Pages :
1
From page :
0
To page :
0
Abstract :
Glioblastoma is a type of brain tumor with poor response to available therapies, and shows high rate of mortality. Despite remarkable advancements in our knowledge about cytogenetic and pathophysiologic features of glioblastoma, current treatment strategies are mainly based on cytotoxic drugs; however, these therapeutic approaches are facing progressive failure because of the resistant nature of glioblastomas. In the recent years, however, promising results have emerged owing to targeted therapies toward molecular pathways within cancerous cells. Unfolded Protein Response (UPR) is a remarkable signaling pathway that triggers both apoptosis and survival pathways within cells, and therefore induces UPR-related apoptotic pathways in cancer cells by ER stress inducers. Recently, the role of Bee venom (Bv), which contains powerful bioactive peptides, in inducing UPR-related apoptosis was revealed in cancer cell lines. Nevertheless, currently there are no reports of Bv potential ability in induction of UPR apoptotic routes in glioblastoma. The aim of current study was to evaluate possible role of Bee venome in inducing of UPR pathway within A172 glioblastoma cell line. We treated the A172 glioblastoma cell line with different Bv doses, and assessed UPR-related genes expression by real-time Polymerase Chain Reaction (PCR). The IC50 of Bv for the studied cell line was 28 μg/mL. Furthermore, we observed that Bv can induce UPR target genes (Grp94 and Gadd153) over-expression through a dose-dependent mechanism. Our results suggest the potential role of Bv as a therapeutic agent for glioblastomas.
Journal title :
Biotechnology and Health Sciences
Serial Year :
2015
Journal title :
Biotechnology and Health Sciences
Record number :
2234262
Link To Document :
بازگشت