| Literature DB >> 31949827 |
Jiqiang Li1,2, Qianxue Chen2, Shuwen Xu3, Jinglei Wu1, Qiaochun Huang1, Ping Song1, Faliang Duan1.
Abstract
Bcl2-associated athanogene 3 (BAG3) belongs to the BAG family and regulates many biologic behaviors of tumors. When tumor cells are in a hypoxic condition, BAG3 protein expression level increases, as does HIF-1α which is an important transcription factor induced by hypoxia. Glioblastoma is one of the typical solid tumors existing in a hypoxic microenvironment that can activate expression of BAG3 and HIF-1α. This research aimed to reveal the relationship between BAG3 and HIF-1α and their effects in glioblastoma multiforme. We found that down-regulated BAG3 inhibited proliferation and promoted apoptosis of glioblastoma multiforme U87 and U251 cell lines by decreasing HIF-1α expression level. The mechanism of BAG3 regulating HIF-1α is mainly through increasing degradation of HIF-1α by HSP70. When HIF-1α was up-regulated, induced by HIF-1α plasmid transfection on the basis of down-regulation of BAG3, the proliferation inhibition and apoptosis promotion were partially reversed. This novel result showed, for the first time, that down-regulation of BAG3 resulted in a low expression of HIF-1α under both normoxic or hypoxic conditions and finally caused inhibited proliferation and promoted apoptosis in glioblastoma. The mechanism of down-regulated BAG3 decreased HIF-1α protein expression through enhancing formation of HSP70-HIF-1α complex and promoting degradation of HIF-1α by HSP70. IJCEPEntities:
Keywords: Bcl2-associated athanogene 3 (BAG3); apoptosis; glioblastoma multiforme; heat shock protein 70 (HSP70); hypoxia inducible factor 1 alpha (HIF-1α); proliferation
Year: 2018 PMID: 31949827
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625