Label-Free Machine Learning Prediction of Chemotherapy on Tumor Spheroids Using a Microfluidics Droplet Platform.

IF 8.3 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Small Science Pub Date : 2025-07-16 eCollection Date: 2025-09-01 DOI:10.1002/smsc.202500173
Caroline Parent, Hasti Honari, Tiziana Tocci, Franck Simon, Sakina Zaidi, Audric Jan, Vivian Aubert, Olivier Delattre, Hervé Isambert, Claire Wilhelm, Jean-Louis Viovy
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引用次数: 0

Abstract

An integrated approach is proposed to rapidly evaluate the effects of anticancer treatments in 3D models, combining a droplet-based microfluidic platform for spheroid formation and single-spheroid chemotherapy application, label-free morphological analysis, and machine learning to assess treatment response. Morphological features of spheroids, such as size and color intensity, are extracted and selected using the multivariate information-based inductive causation algorithm, and used to train a neural network for spheroid classification into viability classes, derived from metabolic assays performed within the same platform as a benchmark. The model is tested on Ewing sarcoma cell lines and patient-derived xenograft (PDX) cells, demonstrating robust performance across datasets. It accurately predicts spheroid viability, used to generate dose-response curves and to determine half maximal inhibitory concentration (IC50) values comparable to traditional biochemical assays. Notably, a model trained on cell line spheroids successfully classifies PDX spheroids, highlighting its adaptability. Compared to convolutional neural network-based approaches, this method works with smaller training datasets and provides greater interpretability by identifying key morphological features. The droplet platform further reduces cell requirements, while single-spheroid confinement enhances classification quality. Overall, this label-free experimental and analytical platform is confirmed as a scalable, efficient, and dynamic tool for drug screening.

使用微流体液滴平台的无标记机器学习预测肿瘤球体化疗。
提出了一种综合方法来快速评估三维模型中的抗癌治疗效果,结合基于液滴的微流控平台用于球体形成和单球体化疗应用,无标记形态分析和机器学习来评估治疗反应。球体的形态特征,如大小和颜色强度,使用基于多元信息的归纳因果算法进行提取和选择,并用于训练一个神经网络,将球体分类为活力类,这些分类来自于在同一平台上作为基准进行的代谢分析。该模型在尤文氏肉瘤细胞系和患者来源的异种移植(PDX)细胞上进行了测试,显示出跨数据集的稳健性能。它准确地预测球体活力,用于生成剂量-反应曲线,并确定一半最大抑制浓度(IC50)值,可与传统的生化分析相媲美。值得注意的是,一个基于细胞系椭球体训练的模型成功地对PDX椭球体进行了分类,突出了其适应性。与基于卷积神经网络的方法相比,该方法使用更小的训练数据集,并通过识别关键形态特征提供更大的可解释性。液滴平台进一步降低了对细胞的要求,而单球体约束提高了分类质量。总的来说,这种无标签的实验和分析平台被证实是一种可扩展、高效和动态的药物筛选工具。
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来源期刊
CiteScore
14.00
自引率
2.40%
发文量
0
期刊介绍: Small Science is a premium multidisciplinary open access journal dedicated to publishing impactful research from all areas of nanoscience and nanotechnology. It features interdisciplinary original research and focused review articles on relevant topics. The journal covers design, characterization, mechanism, technology, and application of micro-/nanoscale structures and systems in various fields including physics, chemistry, materials science, engineering, environmental science, life science, biology, and medicine. It welcomes innovative interdisciplinary research and its readership includes professionals from academia and industry in fields such as chemistry, physics, materials science, biology, engineering, and environmental and analytical science. Small Science is indexed and abstracted in CAS, DOAJ, Clarivate Analytics, ProQuest Central, Publicly Available Content Database, Science Database, SCOPUS, and Web of Science.
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