bee venom induces unfolded protein response in a172 glioblastoma cell line

Authors

ali bazi cancer molecular pathology research center, faculty of medicine, imam reza hospital, mashhad university of medical sciences, mashhad, ir iran; faculty of allied medical sciences, zabol university of medical sciences, zabol, ir iran; faculty of allied medical sciences, zabol university of medical sciences, zabol, ir iran. tel/fax: +98-5432232166

mehran gholamin division of human genetics, immunology research center, avicenna research institute, mashhad university of medical sciences, mashhad, ir iran

mohsen sisakht department of biochemistry, faculty of medicine, mashhad university of medical sciences, mashhad, ir iran

mohammad reza keramati cancer molecular pathology research center, faculty of medicine, imam reza hospital, mashhad university of medical sciences, mashhad, ir iran

abstract

background 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. objectives 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. materials and methods we treated the a172 glioblastoma cell line with different bv doses, and assessed upr-related genes expression by real-time polymerase chain reaction (pcr). results 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. conclusions our results suggest the potential role of bv as a therapeutic agent for glioblastomas.

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Journal title:
journal of biotechnology and health sciences

جلد ۲، شماره ۲، صفحات ۰-۰

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