Nagle Dale G, Zhou Yu-Dong
Department of Pharmacognosy, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, University, MS 38677-1848, USA.
Curr Drug Targets. 2006 Mar;7(3):355-69. doi: 10.2174/138945006776054979.
The transcription factor hypoxia-inducible factor-1 (HIF-1) regulates the expression of more than 70 genes involved in cellular adaptation and survival under hypoxic stress. Activation of HIF-1 is associated with numerous physiological and pathological processes that include tumorigenesis, vascular remodeling, inflammation, and hypoxia/ischemia-related tissue damage. Clinical studies suggested that HIF-1 activation correlates directly with advanced disease stages and treatment resistance among cancer patients. Preclinical studies support the inhibition of HIF-1 as a major molecular target for antitumor drug discovery. Considerable effort is underway, in government laboratories, industry and academia, to identify therapeutically useful small molecule HIF-1 inhibitors. Natural products (low molecular weight organic compounds produced by plants, microbes, and animals) continue to play a major role in modern antitumor drug discovery. Most of the compounds discovered to inhibit HIF-1 are natural products or synthetic compounds with structures that are based on natural product leads. Natural products have also served a vital role as molecular probes to elucidate the pathways that regulate HIF-1 activity. Natural products and natural product-derived compounds that inhibit HIF-1 are summarized in light of their biological source, chemical class, and effect on HIF-1 and HIF-mediated gene regulation. When known, the mechanism(s) of action of HIF-1 inhibitors are described. Many of the substances found to inhibit HIF-1 are non-druggable compounds that are too cytotoxic to serve as drug leads. The application of high-throughput screening methods, complementary molecular-targeted assays, and structurally diverse chemical libraries hold promise for the discovery of therapeutically useful HIF-1 inhibitors.
转录因子缺氧诱导因子-1(HIF-1)可调控70多个参与细胞在缺氧应激下适应和存活的基因的表达。HIF-1的激活与众多生理和病理过程相关,包括肿瘤发生、血管重塑、炎症以及缺氧/缺血相关的组织损伤。临床研究表明,HIF-1激活与癌症患者的晚期疾病阶段和治疗抗性直接相关。临床前研究支持将抑制HIF-1作为抗肿瘤药物发现的主要分子靶点。政府实验室、工业界和学术界正在付出巨大努力来鉴定具有治疗作用的小分子HIF-1抑制剂。天然产物(由植物、微生物和动物产生的低分子量有机化合物)在现代抗肿瘤药物发现中继续发挥着重要作用。大多数被发现可抑制HIF-1的化合物是天然产物或基于天然产物先导结构的合成化合物。天然产物还作为分子探针在阐明调控HIF-1活性的途径方面发挥了至关重要的作用。抑制HIF-1的天然产物和天然产物衍生化合物根据其生物来源、化学类别以及对HIF-1和HIF介导的基因调控的影响进行了总结。已知的HIF-1抑制剂的作用机制也进行了描述。许多被发现可抑制HIF-1的物质是不可成药的化合物,其细胞毒性太大,无法作为药物先导。高通量筛选方法、互补的分子靶向测定以及结构多样的化学文库的应用有望发现具有治疗作用的HIF-1抑制剂。