Buhimschi Alexandru D, Armstrong Haley A, Toure Momar, Jaime-Figueroa Saul, Chen Timothy L, Lehman Amy M, Woyach Jennifer A, Johnson Amy J, Byrd John C, Crews Craig M
Department of Molecular, Cellular, and Developmental Biology , Yale University , New Haven , Connecticut 06511 , United States.
Division of Pharmaceutics & Pharmaceutical Chemistry, College of Pharmacy , The Ohio State University , Columbus , Ohio 43210 , United States.
Biochemistry. 2018 Jul 3;57(26):3564-3575. doi: 10.1021/acs.biochem.8b00391. Epub 2018 Jun 14.
Inhibition of Bruton's tyrosine kinase (BTK) with the irreversible inhibitor ibrutinib has emerged as a transformative treatment option for patients with chronic lymphocytic leukemia (CLL) and other B-cell malignancies, yet >80% of CLL patients develop resistance due to a cysteine to serine mutation at the site covalently bound by ibrutinib (C481S). Currently, an effective treatment option for C481S patients exhibiting relapse to ibrutinib does not exist, and these patients have poor outcomes. To address this, we have developed a PROteolysis TArgeting Chimera (PROTAC) that induces degradation of both wild-type and C481S mutant BTK. We selected a lead PROTAC, MT-802, from several candidates on the basis of its potency to induce BTK knockdown. MT-802 recruits BTK to the cereblon E3 ubiquitin ligase complex to trigger BTK ubiquitination and degradation via the proteasome. MT-802 binds fewer off-target kinases than ibrutinib does and retains an equivalent potency (>99% degradation at nanomolar concentrations) against wild-type and C481S BTK. In cells isolated from CLL patients with the C481S mutation, MT-802 is able to reduce the pool of active, phosphorylated BTK whereas ibrutinib cannot. Collectively, these data provide a basis for further preclinical study of BTK PROTACs as a novel strategy for treatment of C481S mutant CLL.
使用不可逆抑制剂依鲁替尼抑制布鲁顿酪氨酸激酶(BTK)已成为慢性淋巴细胞白血病(CLL)和其他B细胞恶性肿瘤患者的一种变革性治疗选择,然而,超过80%的CLL患者会由于依鲁替尼共价结合位点(C481S)的半胱氨酸到丝氨酸突变而产生耐药性。目前,对于出现依鲁替尼复发的C481S患者不存在有效的治疗选择,且这些患者预后较差。为了解决这一问题,我们开发了一种蛋白酶靶向嵌合体(PROTAC),它可诱导野生型和C481S突变型BTK的降解。我们基于其诱导BTK敲低的效力从多个候选物中选择了一种先导PROTAC,即MT-802。MT-802将BTK招募到cereblon E3泛素连接酶复合物,以触发BTK的泛素化并通过蛋白酶体进行降解。与依鲁替尼相比,MT-802与脱靶激酶的结合更少,并且对野生型和C481S BTK保持同等效力(在纳摩尔浓度下>99%降解)。在从具有C481S突变的CLL患者中分离出的细胞中,MT-802能够减少活性磷酸化BTK的总量,而依鲁替尼则不能。总体而言,这些数据为进一步将BTK PROTAC作为治疗C481S突变型CLL的新策略进行临床前研究提供了依据。