Department of Pharmacology, Miller School of Medicine, University of Miami, Miami, USA.
Sylvester Comprehensive Cancer Center, University of Miami, Miami, USA.
Cell Rep Med. 2020 Oct 20;1(7):100128. doi: 10.1016/j.xcrm.2020.100128.
The approval of the first kinase inhibitor, Gleevec, ushered in a paradigm shift for oncological treatment-the use of genomic data for targeted, efficacious therapies. Since then, over 48 additional small-molecule kinase inhibitors have been approved, solidifying the case for kinases as a highly druggable and attractive target class. Despite the role deregulated kinase activity plays in cancer, only 8% of the kinome has been effectively "drugged." Moreover, 24% of the 634 human kinases are understudied. We have developed a comprehensive scoring system that utilizes differential gene expression, pathological parameters, overall survival, and mutational hotspot analysis to rank and prioritize clinically relevant kinases across 17 solid tumor cancers from The Cancer Genome Atlas. We have developed the clinical kinase index (CKI) app (http://cki.ccs.miami.edu) to facilitate interactive analysis of all kinases in each cancer. Collectively, we report that understudied kinases have potential clinical value as biomarkers or drug targets that warrant further study.
首个激酶抑制剂格列卫(Gleevec)的获批开创了肿瘤治疗的新纪元——利用基因组数据进行靶向、有效的治疗。自那时以来,已有超过 48 种额外的小分子激酶抑制剂获得批准,这进一步证实了激酶作为一个高度可成药和有吸引力的靶标类别。尽管激酶活性失调在癌症中起作用,但激酶组仅 8%得到了有效“靶向治疗”。此外,634 个人类激酶中有 24%研究不足。我们开发了一种综合评分系统,利用差异基因表达、病理参数、总生存期和突变热点分析对来自癌症基因组图谱(The Cancer Genome Atlas)的 17 种实体瘤癌症中的临床相关激酶进行排名和优先级划分。我们开发了临床激酶指数(clinical kinase index,CKI)应用程序(http://cki.ccs.miami.edu),以方便在每个癌症中对所有激酶进行交互式分析。总的来说,我们报告说,研究不足的激酶作为生物标志物或药物靶点具有潜在的临床价值,值得进一步研究。