{"title":"蜂毒诱导A172胶质母细胞瘤细胞系的未折叠蛋白反应","authors":"A. Bazi, M. Gholamin, M. Sisakht, M. Keramati","doi":"10.17795/BHS-27547","DOIUrl":null,"url":null,"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. \nObjectives: 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. \nMaterials 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). \nResults: 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. \nConclusions: Our results suggest the potential role of Bv as a therapeutic agent for glioblastomas. \nKeywords: Glioblastoma; A172 Cell Line; Unfolded Protein Response; Bee Venom","PeriodicalId":8849,"journal":{"name":"Biotechnology and Health Sciences","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2015-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bee Venom Induces Unfolded Protein Response in A172 Glioblastoma Cell Line\",\"authors\":\"A. Bazi, M. Gholamin, M. Sisakht, M. Keramati\",\"doi\":\"10.17795/BHS-27547\",\"DOIUrl\":null,\"url\":null,\"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. \\nObjectives: 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. \\nMaterials 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). \\nResults: 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. \\nConclusions: Our results suggest the potential role of Bv as a therapeutic agent for glioblastomas. \\nKeywords: Glioblastoma; A172 Cell Line; Unfolded Protein Response; Bee Venom\",\"PeriodicalId\":8849,\"journal\":{\"name\":\"Biotechnology and Health Sciences\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-05-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biotechnology and Health Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.17795/BHS-27547\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnology and Health Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17795/BHS-27547","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:胶质母细胞瘤是一种对现有治疗反应较差且死亡率高的脑肿瘤。尽管我们对胶质母细胞瘤的细胞遗传学和病理生理特征的了解取得了显著进展,但目前的治疗策略主要基于细胞毒性药物;然而,由于胶质母细胞瘤的耐药性,这些治疗方法正面临着逐渐失败。然而,近年来,由于针对癌细胞内部分子途径的靶向治疗,出现了令人鼓舞的结果。未折叠蛋白反应(Unfolded Protein Response, UPR)是一种重要的信号通路,可触发细胞内的凋亡和存活通路,因此可通过内质网应激诱导剂诱导癌细胞中UPR相关的凋亡通路。目的:蜂毒(Bv)含有强大的生物活性肽,近年来发现其在肿瘤细胞中诱导凋亡的作用。然而,目前还没有关于Bv在胶质母细胞瘤中诱导UPR凋亡途径的潜在能力的报道。本研究的目的是评估蜜蜂毒液在A172胶质母细胞瘤细胞系中诱导UPR通路的可能作用。材料与方法:用不同剂量的Bv处理A172胶质母细胞瘤细胞系,采用实时聚合酶链反应(PCR)检测uprr相关基因的表达。结果:Bv的IC50为28 μg/mL。此外,我们观察到Bv通过剂量依赖机制诱导UPR靶基因(Grp94和Gadd153)过表达。结论:我们的研究结果提示Bv作为胶质母细胞瘤治疗剂的潜在作用。关键词:胶质母细胞瘤;A172细胞系;未折叠蛋白反应;蜂毒
Bee Venom Induces Unfolded Protein Response in A172 Glioblastoma Cell Line
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.
Keywords: Glioblastoma; A172 Cell Line; Unfolded Protein Response; Bee Venom