Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA, USA.
Institute for Neurodegenerative Diseases, University of California, San Francisco, San Francisco, CA, USA.
Commun Biol. 2024 Sep 15;7(1):1149. doi: 10.1038/s42003-024-06865-4.
Chemical probes interrogate disease mechanisms at the molecular level by linking genetic changes to observable traits. However, comprehensive chemical screens in diverse biological models are impractical. To address this challenge, we develop ChemProbe, a model that predicts cellular sensitivity to hundreds of molecular probes and drugs by learning to combine transcriptomes and chemical structures. Using ChemProbe, we infer the chemical sensitivity of cancer cell lines and tumor samples and analyze how the model makes predictions. We retrospectively evaluate drug response predictions for precision breast cancer treatment and prospectively validate chemical sensitivity predictions in new cellular models, including a genetically modified cell line. Our model interpretation analysis identifies transcriptome features reflecting compound targets and protein network modules, identifying genes that drive ferroptosis. ChemProbe is an interpretable in silico screening tool that allows researchers to measure cellular response to diverse compounds, facilitating research into molecular mechanisms of chemical sensitivity.
化学探针通过将遗传变化与可观察的特征联系起来,在分子水平上探究疾病机制。然而,在不同的生物模型中进行全面的化学筛选是不切实际的。为了解决这个挑战,我们开发了 ChemProbe,这是一种通过学习组合转录组和化学结构来预测数百种分子探针和药物对细胞敏感性的模型。我们使用 ChemProbe 推断癌细胞系和肿瘤样本的化学敏感性,并分析模型如何进行预测。我们对精准乳腺癌治疗的药物反应预测进行了回顾性评估,并在新的细胞模型中前瞻性验证了化学敏感性预测,包括一个基因修饰的细胞系。我们的模型解释分析确定了反映化合物靶标和蛋白质网络模块的转录组特征,鉴定了驱动铁死亡的基因。ChemProbe 是一种可解释的计算筛选工具,允许研究人员测量细胞对多种化合物的反应,促进对化学敏感性的分子机制的研究。