Chen Lihong, Shultz Zachary P, Sansone Marianna, Fang Bin, Liu Xiang, Teng Mingxiang, Schonbrunn Ernst, Lopchuk Justin M, Chen Jiandong
Molecular Oncology Department, Moffitt Cancer Center, Tampa, Florida.
Drug Discovery Department, Moffitt Cancer Center, Tampa, Florida.
Mol Cancer Ther. 2025 May 16:OF1-OF10. doi: 10.1158/1535-7163.MCT-24-1091.
The bromodomain-containing protein, transcription factor IID subunit 1 (TAF1; transcription factor II-250), is the largest component of the multiprotein assembly transcription factor IID, a dynamic complex that serves as a general factor for transcription initiation. CRISPR and RNAi screens of pan-cancer cell lines revealed that TAF1 is broadly required for optimal cell growth and survival, but a subset of cell lines showed enhanced TAF1 dependence. These observations suggest that TAF1 has the potential to serve as a therapeutic target in sensitive tumors. Current approaches employed to target TAF1 are limited to monovalent small-molecule inhibitors of the bromodomain. However, recent studies showed that such inhibitors lack cancer cell kill potential. We applied a structure-guided approach to generate cereblon recruiting Proteolysis Targeting Chimera (PROTAC) degraders of TAF1 using the chemical scaffolds of ceralasertib and GNE371. We present evidence that GNE371-based PROTACs are effective in degradation of TAF1 at concentrations as low as 1 nmol/L. TAF1 depletion activated p53 and induced apoptosis in acute myeloid leukemia (AML) cell lines and certain solid tumor cells. An in vivo active TAF1 PROTAC inhibited the growth of AML tumor xenografts. The results showed that inhibition of the bromodomain is not sufficient to inactivate TAF1 functions, whereas a PROTAC approach induces strong biological effects. Furthermore, TAF1 PROTACs have therapeutic potential against AML and other sensitive tumors.
含溴结构域蛋白、转录因子IID亚基1(TAF1;转录因子II - 250)是多蛋白组装转录因子IID的最大组成部分,转录因子IID是一种动态复合物,作为转录起始的通用因子。对泛癌细胞系进行的CRISPR和RNAi筛选显示,TAF1是细胞最佳生长和存活广泛所需的,但有一部分细胞系对TAF1的依赖性增强。这些观察结果表明,TAF1有潜力作为敏感肿瘤的治疗靶点。目前用于靶向TAF1的方法仅限于溴结构域的单价小分子抑制剂。然而,最近的研究表明,这类抑制剂缺乏杀死癌细胞的潜力。我们采用结构导向方法,利用西拉司他和GNE371的化学支架生成TAF1的脑啡肽募集蛋白酶靶向嵌合体(PROTAC)降解剂。我们提供的证据表明,基于GNE371的PROTAC在低至1 nmol/L的浓度下就能有效降解TAF1。TAF1的缺失激活了p53,并在急性髓系白血病(AML)细胞系和某些实体瘤细胞中诱导了细胞凋亡。一种体内有活性的TAF1 PROTAC抑制了AML肿瘤异种移植的生长。结果表明,抑制溴结构域不足以使TAF1功能失活,而PROTAC方法能诱导强烈的生物学效应。此外,TAF1 PROTAC对AML和其他敏感肿瘤具有治疗潜力。