Expanding pharmacological modalities for targeted cancer therapy

扩大癌症靶向治疗的药理学模式

• 批准号: 10416087
• 负责人: Hojong Yoon
• 金额: $ 9.66万
• 依托单位: BROAD INSTITUTE, INC.
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-06-01 至 2025-05-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10416087
• 关键词: Address; Affect; Antineoplastic Agents; Attenuated; B-Cell Lymphoma 6 Protein; BCL6 gene; BTB/POZ Domain; Binding; Biological Assay; CRISPR screen; Cancer Biology; Cell Cycle; Cell Line; Cells; Chemicals; Clinical; Clustered Regularly Interspaced Short Palindromic Repeats; Complex; Cryoelectron Microscopy; DNA; DNA Damage; Development; Disease; Distal; Dose; Drug Binding Site; Drug Targeting; Engineering; Filament; Gene Expression; Gene Expression Regulation; Genes; Genetic Transcription; Glues; Goals; Growth; Human; Immunomodulators; In Vitro; Intervention; Knock-in; Lead; Libraries; Ligands; Lymphoma cell; Malignant Neoplasms; Mediating; Methods; Modality; Modeling; Molecular; Multiprotein Complexes; Oncogenic; Pharmacology; Phase; Polymers; Proteins; Proteome; Research; Research Project Grants; Scaffolding Protein; Site; Structure; Substrate Specificity; Testing; Thalidomide; Therapeutic Intervention; Transcription Factor Oncogene; Transcription Repressor; Ubiquitination; Validation; Work; analog; clinical development; experimental study; functional genomics; genome sequencing; genome-wide; improved; in vivo; inhibitor; innovation; insight; large cell Diffuse non-Hodgkin' s lymphoma; multicatalytic endopeptidase complex; novel; polymerization; protein degradation; protein protein interaction; recruit; response; small molecule; structural biology; success; targeted cancer therapy; targeted treatment; tool; transcription factor; transcriptome; tumorigenesis; ubiquitin ligase; ubiquitin-protein ligase

Project Summary/Abstract Targeted cancer therapy requires complete and sustained pharmacological inhibition of the respective target, which is often challenging to achieve due to the lack of amenable sites in non-enzyme cancer targets such as transcription factors. The clinical success of thalidomide analogs demonstrates that small molecules that promote targeted protein degradation can overcome this limitation, providing a new pharmacologic toolbox. Most small molecule degraders induce new protein–protein interaction through a ‘molecular glue’ mechanism that bridges a ubiquitin E3 ligase and the target protein. Over 600 ubiquitin E3 ligases exist in the human proteome, allowing many points of intervention to tune their substrate specificity to degrade neo-substrates, However, directly re-wiring ubiquitin ligase to degrade target protein is still challenging; only few E3 ligases such as CRBN, VHL, and DCAF15 have been repurposed for targeted protein degradation. In order to devise general strategies for degrader discovery, it is important to acquire comprehensive mechanistic understanding of how chemical ligands facilitate the degradation of neo-substrates. A recently described small molecule, BI-3802 induces rapid ubiquitination and degradation of BCL6, an oncogenic transcription factor that drives diffuse large B cell lymphoma (DLBCL). BCL6 degradation by BI-3802 treatment results in superior anti-proliferative effects on DLBCL cells, but the mechanism and molecular machinery that are involved remain elusive. In the F99-phase of this proposed research, Hojong Yoon will use the combination of functional genomics and structural biology approaches to dissect the molecular mechanism of BI-3802-induced BCL6 degradation. In the K00-phase of this proposed research, Hojong Yoon will employ his new finding of chemically-inducible polymerization from the F99-phase to develop a novel method of pharmacological intervention. The proposed work will provide a better understanding of small molecule-induced protein degradation to enable the optimization of current small molecule degraders and the development of degraders for new targets. Ultimately, the new insights from this research will lead the development of innovative pharmacological modalities that can be tailored and applied to currently intractable cancers.

项目摘要/摘要 靶向癌症治疗需要对相应靶点进行完全和持续的药物抑制， 这通常是具有挑战性的，因为在非酶类癌症靶点中缺乏顺应性位点，例如 转录因子。沙利度胺类似物的临床成功表明，小分子 促进靶向蛋白质降解可以克服这一限制，提供一个新的药理学工具箱。多数 小分子降解物通过分子胶机制诱导新的蛋白质-蛋白质相互作用 连接泛素E3连接酶和目标蛋白。人类蛋白质组中存在600多种泛素E3连接酶， 然而，允许许多干预点调整其底物专一性以降解新底物， 直接重新连接泛素连接酶以降解靶蛋白仍然具有挑战性；只有少数E3连接酶，如CRBN， VHL和DCAF15已被重新用于靶向蛋白质降解。为了制定总体战略 对于降解物的发现，重要的是要全面了解化学物质是如何 配体促进了新底物的降解。 最近发现的一种小分子BI-3802可诱导BCL6的快速泛素化和降解 导致弥漫性大B细胞淋巴瘤(DLBCL)的致癌转录因子。BI-3802菌株降解BCl6的研究 治疗对DLBCL细胞有较好的抗增殖作用，但其机制和分子机制 涉及的机械设备仍然难以捉摸。 在这项拟议的研究的F99阶段，尹浩宗将使用功能基因组学和 用结构生物学方法剖析BI-3802诱导BCL6降解的分子机制。 在这项拟议研究的K00阶段，尹浩宗将采用他的新发现--化学诱导 从F99相聚合发展出一种新的药理干预方法。 拟议的工作将提供对小分子诱导的蛋白质降解的更好的理解，以使 现有小分子降解剂的优化和新靶点降解剂的开发。 最终，这项研究的新见解将引领创新药理学的发展 可以量身定做并应用于目前难以治愈的癌症的模式。