多组学分析显示,RNA聚合酶II降解是PF-3758309抗肿瘤活性的新机制。

IF 7 2区 生物学 Q1 CELL BIOLOGY
Xinglong Jia, Jingdan Zhang, Lulu Pan, Jingliang He, Mingrui Zhu, Lei Zhao, Xingyu Zhang, Wensi Zhao, Dong Xie, Xiaoyan Shen, Bin Liu, Minjia Tan
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引用次数: 0

摘要

PF-3758309是一种基于吡咯嘧啶的p21活化激酶4 (PAK4)抑制剂,具有临床前抗肿瘤活性。然而,由于药代动力学差和脱靶效应,尚未进入临床应用。本研究通过蛋白质组学、转录组学、泛素组学等综合多组学分析,探讨了PF-3758309在HCT116细胞中的作用机制。结果表明,PF-3758309通过cullin-RING连接酶途径促进RNA聚合酶II亚基蛋白(POLR2A/B/E)的降解。该过程由E3泛素连接酶DNA损伤结合蛋白2 (DDB2)介导,不依赖于PAK4。此外,阻断nedd8活化酶的小分子抑制剂MLN4924逆转了POLR2A/B/E的降解,支持泛素-蛋白酶体途径在这一过程中的作用。功能实验证实,PF-3758309通过促进泛素化依赖性降解POLR2A/B/E来抑制肿瘤细胞的生长和迁移。这些发现揭示了PF-3758309抗肿瘤活性的机制,为进一步研究其治疗潜力提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-omics analysis reveals RNA polymerase II degradation as a novel mechanism of PF-3758309's anti-tumor activity.

PF-3758309, a pyrrolopyrimidine-based inhibitor of p21-activated kinase 4 (PAK4), has demonstrated preclinical anti-tumor activity. However, due to poor pharmacokinetics and off-target effects, it has not advanced to clinical use. In this study, we conducted a comprehensive multi-omics analysis, including proteomics, transcriptomics, and ubiquitinomics, to investigate the mechanism of PF-3758309 in HCT116 cells. Our results revealed that PF-3758309 promotes the degradation of RNA polymerase II subunit proteins (POLR2A/B/E) via the cullin-RING ligase pathway. This process is mediated by the E3 ubiquitin ligase DNA damage-binding protein 2 (DDB2), and is independent of PAK4. Furthermore, the small-molecule inhibitor MLN4924, which blocks NEDD8-activating enzyme, reversed the degradation of POLR2A/B/E, supporting the role of ubiquitin-proteasome pathways in this process. Functional assays confirmed that PF-3758309 inhibits tumor cell growth and migration by promoting ubiquitination-dependent degradation of POLR2A/B/E. These findings uncover a previously unrecognized mechanism of PF-3758309's anti-tumor activity and provide a basis for further investigation into its therapeutic potential.

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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
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