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本文引用的文献

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Chaetomin, a New Antibiotic Substance Produced by Chaetomium cochliodes: II. Isolation and Concentration.毛壳菌素,一种由卷旋毛壳菌产生的新型抗生素物质:II. 分离与浓缩
J Bacteriol. 1944 Nov;48(5):531-6. doi: 10.1128/jb.48.5.531-536.1944.
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Chaetomin, a New Antibiotic Substance Produced by Chaetomium cochliodes: I. Formation and Properties.嗜卷毛壳菌产生的一种新抗生素物质——壳霉黄素:I. 形成与性质
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Phase I and pharmacologic study of 17-(allylamino)-17-demethoxygeldanamycin in adult patients with solid tumors.17-(烯丙胺基)-17-去甲氧基格尔德霉素在成年实体瘤患者中的I期及药理学研究。
J Clin Oncol. 2005 Mar 20;23(9):1885-93. doi: 10.1200/JCO.2005.12.085.
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Apigenin inhibits VEGF and HIF-1 expression via PI3K/AKT/p70S6K1 and HDM2/p53 pathways.芹菜素通过PI3K/AKT/p70S6K1和HDM2/p53信号通路抑制血管内皮生长因子(VEGF)和缺氧诱导因子-1(HIF-1)的表达。
FASEB J. 2005 Mar;19(3):342-53. doi: 10.1096/fj.04-2175com.
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Ras inhibition in glioblastoma down-regulates hypoxia-inducible factor-1alpha, causing glycolysis shutdown and cell death.在胶质母细胞瘤中抑制Ras可下调缺氧诱导因子-1α,导致糖酵解停止和细胞死亡。
Cancer Res. 2005 Feb 1;65(3):999-1006.
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Identification of a novel small-molecule inhibitor of the hypoxia-inducible factor 1 pathway.一种新型缺氧诱导因子1通路小分子抑制剂的鉴定。
Cancer Res. 2005 Jan 15;65(2):605-12.
7
Differential prognostic impact of hypoxia induced and diffuse HIF-1alpha expression in invasive breast cancer.缺氧诱导和弥漫性HIF-1α表达在浸润性乳腺癌中的差异预后影响
J Clin Pathol. 2005 Feb;58(2):172-7. doi: 10.1136/jcp.2004.019885.
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Histone deacetylase inhibitors.组蛋白去乙酰化酶抑制剂
Eur J Med Chem. 2005 Jan;40(1):1-13. doi: 10.1016/j.ejmech.2004.10.001.
9
2-methoxyestradiol inhibits hypoxia-inducible factor 1alpha, tumor growth, and angiogenesis and augments paclitaxel efficacy in head and neck squamous cell carcinoma.2-甲氧基雌二醇抑制缺氧诱导因子1α、肿瘤生长和血管生成,并增强紫杉醇在头颈部鳞状细胞癌中的疗效。
Clin Cancer Res. 2004 Dec 15;10(24):8665-73. doi: 10.1158/1078-0432.CCR-04-1393.
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Pseudolaric acid B inhibits angiogenesis and reduces hypoxia-inducible factor 1alpha by promoting proteasome-mediated degradation.土荆酸乙通过促进蛋白酶体介导的降解来抑制血管生成并降低缺氧诱导因子1α。
Clin Cancer Res. 2004 Dec 15;10(24):8266-74. doi: 10.1158/1078-0432.CCR-04-0951.

基于天然产物的缺氧诱导因子-1(HIF-1)抑制剂

Natural product-based inhibitors of hypoxia-inducible factor-1 (HIF-1).

作者信息

Nagle Dale G, Zhou Yu-Dong

机构信息

Department of Pharmacognosy, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, University, MS 38677-1848, USA.

出版信息

Curr Drug Targets. 2006 Mar;7(3):355-69. doi: 10.2174/138945006776054979.

DOI:10.2174/138945006776054979
PMID:16515532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2908043/
Abstract

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.

摘要

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。