Li Zhongxiao, Napolitano Antonella, Fedele Monica, Gao Xin, Napolitano Francesco
Computer Science Program, Computer, Electrical and Mathematical Sciences and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955, Saudi Arabia.
Computational Bioscience Research Center, King Abdullah University of Science and Technology, Thuwal, 23955, Saudi Arabia.
Brief Bioinform. 2024 Mar 27;25(3). doi: 10.1093/bib/bbae207.
Cancer stem cells (CSCs) are a subpopulation of cancer cells within tumors that exhibit stem-like properties and represent a potentially effective therapeutic target toward long-term remission by means of differentiation induction. By leveraging an artificial intelligence approach solely based on transcriptomics data, this study scored a large library of small molecules based on their predicted ability to induce differentiation in stem-like cells. In particular, a deep neural network model was trained using publicly available single-cell RNA-Seq data obtained from untreated human-induced pluripotent stem cells at various differentiation stages and subsequently utilized to screen drug-induced gene expression profiles from the Library of Integrated Network-based Cellular Signatures (LINCS) database. The challenge of adapting such different data domains was tackled by devising an adversarial learning approach that was able to effectively identify and remove domain-specific bias during the training phase. Experimental validation in MDA-MB-231 and MCF7 cells demonstrated the efficacy of five out of six tested molecules among those scored highest by the model. In particular, the efficacy of triptolide, OTS-167, quinacrine, granisetron and A-443654 offer a potential avenue for targeted therapies against breast CSCs.
癌症干细胞(CSCs)是肿瘤内癌细胞的一个亚群,具有干细胞样特性,通过诱导分化可能成为实现长期缓解的有效治疗靶点。本研究仅基于转录组学数据,利用人工智能方法,根据小分子诱导干细胞样细胞分化的预测能力,对一个小分子大文库进行了评分。具体而言,使用从处于不同分化阶段的未处理人类诱导多能干细胞获得的公开单细胞RNA测序数据训练了一个深度神经网络模型,随后用于筛选基于综合网络的细胞特征库(LINCS)数据库中的药物诱导基因表达谱。通过设计一种对抗学习方法解决了适应如此不同数据域的挑战,该方法能够在训练阶段有效识别并消除特定域偏差。在MDA-MB-231和MCF7细胞中的实验验证表明,模型评分最高的六个测试分子中有五个有效。特别是,雷公藤内酯醇、OTS-167、奎纳克林、格拉司琼和A-443654的有效性为针对乳腺癌干细胞的靶向治疗提供了一条潜在途径。