Department of Oncology, Haematology and Bone Marrow Transplantation with Section Pneumology, Hubertus Wald-Tumor Zentrum UCCH, University Hospital Eppendorf UKE, Hamburg, Germany.
PLoS One. 2013;8(1):e53668. doi: 10.1371/journal.pone.0053668. Epub 2013 Jan 9.
In drug discovery, the characterisation of the precise modes of action (MoA) and of unwanted off-target effects of novel molecularly targeted compounds is of highest relevance. Recent approaches for identification of MoA have employed various techniques for modeling of well defined signaling pathways including structural information, changes in phenotypic behavior of cells and gene expression patterns after drug treatment. However, efficient approaches focusing on proteome wide data for the identification of MoA including interference with mutations are underrepresented. As mutations are key drivers of drug resistance in molecularly targeted tumor therapies, efficient analysis and modeling of downstream effects of mutations on drug MoA is a key to efficient development of improved targeted anti-cancer drugs. Here we present a combination of a global proteome analysis, reengineering of network models and integration of apoptosis data used to infer the mode-of-action of various tyrosine kinase inhibitors (TKIs) in chronic myeloid leukemia (CML) cell lines expressing wild type as well as TKI resistance conferring mutants of BCR-ABL. The inferred network models provide a tool to predict the main MoA of drugs as well as to grouping of drugs with known similar kinase inhibitory activity patterns in comparison to drugs with an additional MoA. We believe that our direct network reconstruction approach, demonstrated on proteomics data, can provide a complementary method to the established network reconstruction approaches for the preclinical modeling of the MoA of various types of targeted drugs in cancer treatment. Hence it may contribute to the more precise prediction of clinically relevant on- and off-target effects of TKIs.
在药物发现中,精确作用模式(MoA)和新型分子靶向化合物的非预期脱靶效应的特征至关重要。最近用于鉴定 MoA 的方法采用了各种技术来模拟明确的信号通路,包括结构信息、药物处理后细胞表型行为的变化和基因表达模式。然而,针对包括干扰突变在内的全蛋白质组数据来鉴定 MoA 的有效方法还不够完善。由于突变是分子靶向肿瘤治疗中药物耐药性的关键驱动因素,因此有效分析和模拟突变对药物 MoA 的下游影响是开发改进的靶向抗癌药物的关键。在这里,我们提出了一种组合方法,即全局蛋白质组分析、网络模型重构和细胞凋亡数据的整合,用于推断在表达野生型和 TKI 耐药突变体的慢性髓性白血病(CML)细胞系中各种酪氨酸激酶抑制剂(TKI)的作用模式。推断的网络模型提供了一种工具,可用于预测药物的主要作用模式,以及将具有已知相似激酶抑制活性模式的药物与具有其他作用模式的药物进行分组。我们相信,我们在蛋白质组学数据上展示的直接网络重建方法可以为各种类型的靶向药物在癌症治疗中的 MoA 的临床前建模提供一种补充方法。因此,它可能有助于更精确地预测 TKI 的临床相关脱靶和靶内效应。