| Literature DB >> 27278737 |
Hao Xue1, Jinsen Zhang1, Xing Guo1, Jian Wang2, Jiangbing Li3, Xiao Gao1, Xiaofan Guo1, Tong Li1, Shugang Xu1, Ping Zhang4, Qinglin Liu1, Gang Li1.
Abstract
Hypoxia induces protective autophagy in advanced glioblastoma cells, and targeting this process may improve the outcome for glioblastoma patients. Recent studies have suggested that the autophagic process is upregulated in glioblastoma cells in response to extensive hypoxia. Here, we describe a novel tumor suppressor in glioblastoma cells, whereby hypoxia downregulated CREBRF expression and acts as a potent inhibitor of autophagy in glioblastoma cells via the CREB3/ATG5 pathway. Our results demonstrate that CREBRF expression negatively correlates with autophagic and HIF-1α levels in different grade gliomas. Given that CREBRF is a negative regulator of CREB3, CREB3 knockdown also repressed hypoxia-induced autophagy in glioblastoma cells in vitro. Collectively, our findings provide new insight into the molecular mechanisms underlying hypoxia-induced glioblastoma cell autophagy and indicate that the hypoxia/CREBRF/CREB3/ATG5 pathway plays a central role in malignant glioma progression.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27278737 DOI: 10.3892/ijo.2016.3576
Source DB: PubMed Journal: Int J Oncol ISSN: 1019-6439 Impact factor: 5.650