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THERPA:一个与朊病毒蛋白调控和朊病毒疾病进展相关的小分子数据库。

THERPA: A small molecule database related to prion protein regulation and prion diseases progression.

作者信息

Lee Sol Moe, Lee Wonseok, Lee Yeong Seon, Yoo Jin-Soo, Park Soo-Jung, Kim Heebal, Kim Su Yeon

机构信息

a Division of Bacterial Disease Research, Center for Infectious Diseases Research , Korea National Institute of Health, Centers for Disease Control & Prevention , Cheongju-si , Chungcheongbuk-do , South Korea.

b Department of Agricultural Biotechnology and Research Institute of Agriculture and Life Sciences , Seoul National University , Seoul , South Korea.

出版信息

Prion. 2018 Mar 4;12(2):138-142. doi: 10.1080/19336896.2018.1461519. Epub 2018 May 4.

DOI:10.1080/19336896.2018.1461519
PMID:29633896
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6016511/
Abstract

Prion diseases are fatal neurodegenerative disorders that affect humans and animals. Although various small molecules have been evaluated for application in the treatment of prion diseases, none have been shown to be efficacious. Expanding our knowledge of these molecules is important for understanding of the complex mechanisms of prion diseases. To improve access to the scattered information on small molecules related to prion diseases, we built a database of therapeutic molecules associated with prion diseases (THERPA, therpa.pythonanywhere.com). THERPA includes 119 small molecules and their 283 relationships with prion diseases. THERPA is an interactive visual database and useful for improving search efficiency which can help researchers identify intrinsic small molecules that can be used for developing therapeutics for prion diseases.

摘要

朊病毒疾病是影响人类和动物的致命性神经退行性疾病。尽管已经评估了各种小分子用于治疗朊病毒疾病,但尚无一种被证明是有效的。扩展我们对这些分子的了解对于理解朊病毒疾病的复杂机制很重要。为了更方便地获取与朊病毒疾病相关的小分子的分散信息,我们建立了一个与朊病毒疾病相关的治疗性分子数据库(THERPA,therpa.pythonanywhere.com)。THERPA包含119种小分子及其与朊病毒疾病的283种关系。THERPA是一个交互式可视化数据库,有助于提高搜索效率,可帮助研究人员识别可用于开发朊病毒疾病治疗药物的内在小分子。

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本文引用的文献

1
Disruption of copper homeostasis due to a mutation of Atp7a delays the onset of prion disease.由于 Atp7a 突变导致铜稳态失衡会延迟朊病毒病的发作。
Proc Natl Acad Sci U S A. 2012 Aug 21;109(34):13733-8. doi: 10.1073/pnas.1211499109. Epub 2012 Aug 6.
2
Role of copper and manganese in prion disease progression.铜和锰在朊病毒疾病进展中的作用。
Brain Res. 2009 Oct 6;1292:155-64. doi: 10.1016/j.brainres.2009.07.051. Epub 2009 Jul 25.
3
Comparison of chloroquine, quinacrine (atabrine) and quinine in the treatment of acute attacks of sporozoite-induced vivax malaria, Chesson strain.氯喹、阿的平(奎纳克林)和奎宁治疗切森株子孢子诱发的间日疟急性发作的比较
J Clin Invest. 1948 May;27(3 Pt1):46-50.
4
Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report.与输血相关的变异型克雅氏病的临床表现及死前诊断:一例报告
Lancet. 2006 Dec 9;368(9552):2061-7. doi: 10.1016/S0140-6736(06)69835-8.
5
Role of copper in prion diseases: deleterious or beneficial?铜在朊病毒疾病中的作用:有害还是有益?
Curr Pharm Des. 2006;12(20):2587-95. doi: 10.2174/138161206777698873.
6
Creutzfeldt-Jakob disease acquired via a dural graft: failure of therapy with quinacrine and chlorpromazine.通过硬脑膜移植获得的克雅氏病:奎纳克林和氯丙嗪治疗失败
Surg Neurol. 2005 Dec;64(6):542-5, discussion 545. doi: 10.1016/j.surneu.2005.03.035.
7
Effect of metal ions on de novo aggregation of full-length prion protein.金属离子对全长朊病毒蛋白从头聚集的影响。
Biochem Biophys Res Commun. 2004 Aug 6;320(4):1240-6. doi: 10.1016/j.bbrc.2004.06.075.
8
Copper binding to PrPC may inhibit prion disease propagation.铜与朊蛋白(PrPC)结合可能会抑制朊病毒疾病的传播。
Brain Res. 2003 Dec 12;993(1-2):192-200. doi: 10.1016/j.brainres.2003.09.014.
9
Copper chelation delays the onset of prion disease.铜螯合作用可延缓朊病毒疾病的发病。
J Biol Chem. 2003 Nov 21;278(47):46199-202. doi: 10.1074/jbc.C300303200. Epub 2003 Sep 30.
10
Quinacrine-induced cytolytic hepatitis in sporadic Creutzfeldt-Jakob disease.散发性克雅氏病中奎纳克林诱导的细胞溶解性肝炎
Ann Neurol. 2003 Apr;53(4):546-7. doi: 10.1002/ana.10530.