Key Laboratory of Cell Differentiation and Apoptosis of National Ministry of Education, Department of Pathophysiology, Shanghai Jiao Tong University School of Medicine, 200025 Shanghai, China.
Department of Pediatric Neurosurgery, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, 200092 Shanghai, China.
Proc Natl Acad Sci U S A. 2019 Jun 25;116(26):12986-12995. doi: 10.1073/pnas.1815780116. Epub 2019 Jun 10.
The aberrant hedgehog (Hh) pathway plays important roles in multiple cancer types, therefore serving as a promising drug target. Current clinically available hedgehog-targeted drugs act mostly by antagonizing the upstream component smoothened; however, both primary and acquired resistance to FDA-approved smoothened inhibitor (SMOi) drugs have been described. We have recently demonstrated that the BET inhibitor effectively suppresses SMOi-resistant Hh-driven cancers through antagonizing transcription of GLI1 and GLI2, the core transcriptional factors of Hh pathway, suggesting epigenetic or transcriptional targeted therapy represents an anti-Hh therapeutic strategy that can overcome SMOi resistance. Here we performed an unbiased screening of epigenetic or transcriptional targeted small molecules to test their inhibitory effects on GLI1 and GLI2 transcription or cell viability of Hh-driven tumor lines. THZ1, a covalent inhibitor of cyclin-dependent kinase 7 (CDK7), is identified as the top hit in our screening. We then confirmed that antagonizing CDK7 by either small-molecule inhibitors or the CRISPR-Cas9 approach causes substantial suppression of GLI1 and GLI2 transcription, resulting in effective inhibition of Hh-driven cancers in vitro and in vivo. More importantly, antagonizing CDK7 retains inhibitory activity against Hh-driven cancers with almost all so-far described primary or acquired SMOi resistance. Furthermore, we reveal a synergy between CDK7 inhibition and BET inhibition on antagonizing aberrant Hh pathway and Hh-driven cancers that are either responsive or resistant to SMOi. Our results illustrate transcriptional inhibition through targeting CDK7 as a promising therapeutic strategy for treating Hh-driven cancers, especially those with primary or acquired resistance to SMOi drugs.
异常的刺猬(Hh)信号通路在多种癌症类型中起着重要作用,因此成为有前途的药物靶点。目前临床上可用的 Hedgehog 靶向药物主要通过拮抗上游成分 smoothened 起作用;然而,已经描述了对 FDA 批准的 smoothened 抑制剂(SMOi)药物的原发性和获得性耐药。我们最近证明,BET 抑制剂通过拮抗 Hh 通路的核心转录因子 GLI1 和 GLI2 的转录,有效抑制 SMOi 耐药的 Hh 驱动型癌症,这表明表观遗传或转录靶向治疗代表了一种可以克服 SMOi 耐药的抗 Hh 治疗策略。在这里,我们进行了无偏筛选表观遗传或转录靶向小分子,以测试它们对 GLI1 和 GLI2 转录或 Hh 驱动肿瘤系细胞活力的抑制作用。THZ1 是一种周期蛋白依赖性激酶 7(CDK7)的共价抑制剂,是我们筛选中的最佳命中物。然后,我们证实通过小分子抑制剂或 CRISPR-Cas9 方法拮抗 CDK7 会导致 GLI1 和 GLI2 转录的大量抑制,从而在体外和体内有效抑制 Hh 驱动的癌症。更重要的是,拮抗 CDK7 对迄今为止几乎所有描述的原发性或获得性 SMOi 耐药的 Hh 驱动癌症仍具有抑制活性。此外,我们揭示了 CDK7 抑制与 BET 抑制在拮抗异常 Hh 通路和对 SMOi 有反应或耐药的 Hh 驱动癌症方面的协同作用。我们的结果表明,通过靶向 CDK7 进行转录抑制是治疗 Hh 驱动癌症的一种很有前途的治疗策略,特别是对 SMOi 药物具有原发性或获得性耐药的癌症。