Ciaccio Mark F, Chen Vincent C, Jones Richard B, Bagheri Neda
Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL 60208, USA.
Integr Biol (Camb). 2015 Jul;7(7):776-91. doi: 10.1039/c5ib00065c.
Many drug candidates fail in clinical trials due to an incomplete understanding of how small-molecule perturbations affect cell phenotype. Cellular responses can be non-intuitive due to systems-level properties such as redundant pathways caused by co-activation of multiple receptor tyrosine kinases. We therefore created a scalable algorithm, DIONESUS, based on partial least squares regression with variable selection to reconstruct a cellular signaling network in a human carcinoma cell line driven by EGFR overexpression. We perturbed the cells with 26 diverse growth factors and/or small molecules chosen to activate or inhibit specific subsets of receptor tyrosine kinases. We then quantified the abundance of 60 phosphosites at four time points using a modified microwestern array, a high-confidence assay of protein abundance and modification. DIONESUS, after being validated using three in silico networks, was applied to connect perturbations, phosphorylation, and cell phenotype from the high-confidence, microwestern dataset. We identified enhancement of STAT1 activity as a potential strategy to treat EGFR-hyperactive cancers and PTEN as a target of the antioxidant, N-acetylcysteine. Quantification of the relationship between drug dosage and cell viability in a panel of triple-negative breast cancer cell lines validated proposed therapeutic strategies.
许多候选药物在临床试验中失败,原因是对小分子扰动如何影响细胞表型的理解不完整。由于系统层面的特性,如多种受体酪氨酸激酶共同激活导致的冗余途径,细胞反应可能是非直观的。因此,我们基于带有变量选择的偏最小二乘回归创建了一种可扩展算法DIONESUS,以重建由表皮生长因子受体(EGFR)过表达驱动的人癌细胞系中的细胞信号网络。我们用26种不同的生长因子和/或小分子对细胞进行扰动,这些因子和小分子被选择用来激活或抑制受体酪氨酸激酶的特定子集。然后,我们使用改良的微 Western 阵列在四个时间点对60个磷酸化位点的丰度进行定量,这是一种对蛋白质丰度和修饰的高可信度检测方法。在使用三个计算机网络进行验证后,DIONESUS被应用于连接来自高可信度微 Western 数据集的扰动、磷酸化和细胞表型。我们确定增强信号转导和转录激活因子1(STAT1)的活性是治疗EGFR高活性癌症的潜在策略,并确定磷酸酶和张力蛋白同源物(PTEN)是抗氧化剂N-乙酰半胱氨酸的作用靶点。在一组三阴性乳腺癌细胞系中对药物剂量与细胞活力之间的关系进行定量,验证了所提出的治疗策略。