Mali Ajay K, Murugappan Sivasubramanian, Prasad Jayashree Rajesh, Tofail Syed A M, Thorat Nanasaheb D
Department of Physics and Bernal Institute, University of Limerick, Castletroy, Limerick, V94T9PX, Ireland.
Computer Science and Engineering, School of Computing, MIT Art Design and Technology University, Pune, Maharashtra, 412201, India.
Biol Methods Protoc. 2025 Apr 11;10(1):bpaf030. doi: 10.1093/biomethods/bpaf030. eCollection 2025.
Three-dimensional (3D) spheroid models have advanced cancer research by better mimicking the tumour microenvironment compared to traditional dimensional cell cultures. However, challenges persist in high-throughput analysis of morphological characteristics and cell viability, as traditional methods like manual fluorescence analysis are labour-intensive and inconsistent. Existing AI-based approaches often address segmentation or classification in isolation, lacking an integrated workflow. We propose a scalable, two-stage deep learning pipeline to address these gaps: (i) a U-Net model for precise detection and segmentation of 3D spheroids from microscopic images, achieving 95% prediction accuracy, and (ii) a CNN Regression Hybrid method for estimating live/dead cell percentages and classifying spheroids, with an value of 98%. This end-to-end pipeline automates cell viability quantification and generates key morphological parameters for spheroid growth kinetics. By integrating segmentation and analysis, our method addresses environmental variability and morphological characterization challenges, offering a robust tool for drug discovery, toxicity screening, and clinical research. This approach significantly improves efficiency and scalability of 3D spheroid evaluations, paving the way for advancements in cancer therapeutics.
与传统的二维细胞培养相比,三维(3D)球体模型通过更好地模拟肿瘤微环境推动了癌症研究。然而,在形态特征和细胞活力的高通量分析方面仍然存在挑战,因为像手动荧光分析这样的传统方法既耗费人力又不一致。现有的基于人工智能的方法通常孤立地处理分割或分类问题,缺乏一个集成的工作流程。我们提出了一个可扩展的两阶段深度学习管道来弥补这些差距:(i)一个U-Net模型,用于从显微镜图像中精确检测和分割3D球体,预测准确率达到95%;(ii)一种卷积神经网络回归混合方法,用于估计活/死细胞百分比并对球体进行分类, 值为98%。这个端到端的管道实现了细胞活力量化的自动化,并生成了球体生长动力学的关键形态学参数。通过整合分割和分析,我们的方法解决了环境变异性和形态学表征方面的挑战,为药物发现、毒性筛选和临床研究提供了一个强大的工具。这种方法显著提高了3D球体评估的效率和可扩展性,为癌症治疗的进步铺平了道路。