| Literature DB >> 32464323 |
Hui-Yao Li1, Yue Yuan1, Yu-Hong Fu1, Ying Wang1, Xin-Yuan Gao2.
Abstract
Diabetic retinopathy (DR) is a serious condition that can cause blindness in diabetic patients. It is a neurovascular disease, but the pathogenesis leading to the onset of this disease is still not completely understood. However, hypoxia with subsequent neovascularization is a characteristic phenomenon observed with DR. Cellular response to hypoxia is mediated by the transcriptional regulator hypoxia-inducible factor (HIF). Long-term research has shown that one isotype of HIF, HIF-1α, may play a pivotal role under hypoxic conditions, and an increasing number of studies have shown that HIF-1α and its target genes contribute to retinal neovascularization. Therefore, targeting HIF-1α may lead to more effective DR treatments. This review describes the possible mechanisms of HIF-1α in neovascularization of DR. Furthermore, various inhibitors of HIF-1α that may have viable potential in the treatment of DR are also discussed.Entities:
Keywords: Diabetic retinopathy; Hypoxia-inducible factor-1α; Inhibitor; Neovascularization; Vascular endothelial growth factor
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Year: 2020 PMID: 32464323 DOI: 10.1016/j.phrs.2020.104924
Source DB: PubMed Journal: Pharmacol Res ISSN: 1043-6618 Impact factor: 7.658