Small Molecules that Regulate Proteasome Activity

调节蛋白酶体活性的小分子

基本信息

批准号：
8204613
负责人：
Chin-Ho Chen
金额：
$ 29.89万
依托单位：
DUKE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-01-01 至 2013-11-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8204613
关键词：
Amino Acids Antineoplastic Agents Betulinic Acid Binding Biological Factors Bortezomib Cancer cell line Cell Cycle Cell model Cell physiology Chemical Structure Chemicals Collection Disease Drug Binding Site Drug Delivery Systems Exhibits Goals Growth Huntington Disease Induction of Apoptosis Inhibition of Cell Proliferation Label Lead Malignant Neoplasms Mediating Modification Molecular Molecular Probes Molecular Target Neoplasm Metastasis Neurodegenerative Disorders Neurons Pharmaceutical Preparations Pharmacologic Substance Play Process Proteasome Inhibition Proteasome Inhibitor Proteolysis Role Screening procedure Side Structure-Activity Relationship System Terpenes Testing Therapeutic Ubiquitin angiogenesis base cancer cell cancer therapy cancer type cell type design drug candidate drug discovery human disease improved inhibitor/antagonist interest multicatalytic endopeptidase complex nervous system disorder next generation novel scaffold small molecule tool tumor tumor growth

项目摘要

Title: Small molecules that regulate proteasome activity The ubiquitin-proteasome system plays an important role in regulating the cell cycle, cancer growth, and metastasis. Activation of the proteasome is a critical process that is required for optimal proteolytic activity. Inhibitors of the proteasome were shown to arrest tumor growth, tumor spread, and angiogenesis. On the other hand, drug-like proteasome activators are rare, and their biomedical applications remain to be determined. Although there is tremendous interest in developing drugs targeting the proteasome, currently there is only one clinically available proteasome inhibitor, Bortezomib, for anti-cancer therapy. The goal of this study is to identify and synthesize small molecules that can specifically and potently inhibit or activate the proteasome. Our preliminary results indicated that terpenoid natural products, such as betulinic acid, activated proteasome, and chemical modifications on betulinic acid turned it into proteasome inhibitors. We hypothesize that potent proteasome activators or inhibitors could be identified from terpenoid natural products and their potency can be further increased by chemical modifications. The goal will be achieved and the hypothesis will be tested by carrying out the following specific aims: 1) to discover new terpenoids that activate or inhibit the proteasome; 2) to obtain a next generation of potent proteasome inhibitors through lead optimization; 3) to determine the drug binding site and mode of action of the terpenoid proteasome inhibitors. We have established a panel of terpenoids and the strategies for lead optimization to achieve our goal in the discovery of potent proteasome activators and inhibitors that can regulate the proteasome activity at low nanomolar or sub-nanomolar concentrations. It is expected that a new class of novel proteasome regulators (activators and inhibitors) and the molecular target of the inhibitor will be identified upon completion of the proposed studies. Moreover, the study will also determine the therapeutic potential of the proposed proteasome regulators for diseases such as cancers and Huntington's disease. Discovery of novel proteasome activators and inhibitors would not only provide a very useful tool for dissecting the molecular mechanisms of proteasome-mediated cellular functions, but would also have the potential to be developed as therapeutics to treat diseases such as cancers.

标题：调节蛋白酶体活性的小分子泛素-蛋白酶体系统在调节细胞周期、癌症生长和转移。蛋白酶体的激活是最佳蛋白水解活性所需的关键过程。蛋白酶体抑制剂被证明可以阻止肿瘤生长、肿瘤扩散和血管生成。上另一方面，药物样蛋白酶体激活剂很少见，其生物医学应用仍有待进一步研究。决定。尽管人们对开发针对蛋白酶体的药物有着巨大的兴趣，但目前临床上只有一种蛋白酶体抑制剂可用于抗癌治疗，即硼替佐米。此举的目标研究的目的是识别和合成能够特异性地、有效地抑制或激活蛋白酶体。我们的初步结果表明，萜类天然产物，例如桦木酸，可以激活蛋白酶体，并对桦木酸进行化学修饰将其变成蛋白酶体抑制剂。我们假设可以从萜类天然产物中鉴定出有效的蛋白酶体激活剂或抑制剂并且它们的效力可以通过化学修饰进一步增强。目标一定会实现，并且将通过执行以下具体目标来检验假设：1）发现可激活的新萜类化合物或抑制蛋白酶体； 2）通过铅获得下一代强效蛋白酶体抑制剂优化; 3)确定萜类蛋白酶体抑制剂的药物结合位点和作用方式。我们已经建立了萜类化合物小组和先导化合物优化策略，以实现我们的目标发现可以在低浓度下调节蛋白酶体活性的有效蛋白酶体激活剂和抑制剂纳摩尔或亚纳摩尔浓度。预计一类新型蛋白酶体调节剂（激活剂和抑制剂）和抑制剂的分子靶标将在完成后确定拟议的研究。此外，该研究还将确定所提出的治疗潜力癌症和亨廷顿舞蹈病等疾病的蛋白酶体调节剂。小说的发现蛋白酶体激活剂和抑制剂不仅为剖析分子生物学提供了非常有用的工具蛋白酶体介导的细胞功能机制，但也有可能被开发为治疗癌症等疾病的疗法。