Lille Neuroscience and Cognition Research Center, University of Lille, INSERM, CHU Lille, UMR-S 1172, Lille, France.
Expert Opin Ther Pat. 2022 Aug;32(8):899-912. doi: 10.1080/13543776.2022.2096436. Epub 2022 Jul 5.
The Hippo pathway represents a new opportunity for the treatment of cancer. Overexpression of Yes-associated protein (YAP) or transcriptional coactivator with PDZ-binding motif (TAZ) or TEAD has been demonstrated in cancers and YAP mediates resistance to cancer drugs. Since 2018, the potential of this pathway has been illustrated by numerous articles and patents and the first drugs entering in clinical trial phase 1.
This review is limited to published patent applications that have disclosed direct small-molecule inhibitors of the YAP/TAZ-TEAD interaction.
The YAP/TAZ-TEAD transcriptional complex is a promising target for the treatment of cancer. Approximately 30 international patents (used database: Sci-finder, query: TEAD; documents: patents; period: from 2017-January 2022) that disclose TEAD transcriptional inhibitors have been filled since 2018. The mechanism of action is not always described in the patents, we can divide the drugs into three different categories: (i) external TEAD ligands; (ii) non-covalent TEAD ligands of the palmitate pocket; (iii) covalent TEAD ligands, which bind into the palmitate pocket. The first molecules in clinical trial phase 1 are non-covalent TEAD ligands. The selective TEAD ligand have also been patented, published and selectivity could be of great interest for personalized medicine.
Hippo 通路为癌症治疗提供了新的机会。在癌症中已经证实 Yes 相关蛋白 (YAP) 或转录共激活因子与 PDZ 结合基序 (TAZ) 或 TEAD 的过表达,并且 YAP 介导了癌症药物耐药性。自 2018 年以来,大量的文章和专利表明了该通路的潜力,并且首批药物已经进入临床试验 1 期。
本综述仅限于已披露 YAP/TAZ-TEAD 相互作用直接小分子抑制剂的已发表专利申请。
YAP/TAZ-TEAD 转录复合物是治疗癌症的有前途的靶点。自 2018 年以来,已经提交了大约 30 项国际专利(使用数据库:Sci-finder,查询:TEAD;文献:专利;期限:2017 年 1 月至 2022 年 1 月),这些专利披露了 TEAD 转录抑制剂。自 2018 年以来,已经提交了大约 30 项国际专利(使用数据库:Sci-finder,查询:TEAD;文献:专利;期限:2017 年 1 月至 2022 年 1 月),这些专利披露了 TEAD 转录抑制剂。作用机制在专利中并不总是描述的,我们可以将药物分为三类:(i)外部 TEAD 配体;(ii)棕榈酸口袋的非共价 TEAD 配体;(iii)结合棕榈酸口袋的共价 TEAD 配体。首个处于临床试验 1 期的分子是非共价 TEAD 配体。选择性 TEAD 配体也已获得专利、发表,并可能对个性化医学具有重要意义。