利用卷积神经网络图像解码胶质母细胞瘤单球体培养物的纵向药物协同作用评估

IF 3.7 Q1 CLINICAL NEUROLOGY Neuro-oncology advances Pub Date : 2023-11-05 DOI:10.1093/noajnl/vdad134
Anna Giczewska, Krzysztof Pastuszak, Megan Houweling, U Kulsoom Abdul, Noa Faaij, Laurine Wedekind, David Noske, Thomas Wurdinger, Anna Supernat, Bart A Westerman
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引用次数: 0

摘要

近年来,药物联合治疗越来越受欢迎,以改善各种疾病的治疗效果,包括难以治愈的癌症,如脑癌胶质母细胞瘤。随着时间的推移,评估药物之间的相互作用对于预测药物联合有效性和最小化治疗耐药风险至关重要。然而,由于药物联合实验的活力读数通常作为细胞裂解的终点,因此目前只能通过联合终点分析来进行纵向药物相互作用监测。我们提供了一种方法,在18天的时间框架内,对三种胶质母细胞瘤模型中16种药物组合的药物相互作用进行大规模平行监测。在我们的实验中,单个神经球的生存能力是根据在不同时间点拍摄的图像信息来估计的。最后一天(第18天)拍摄的神经球图像与当天CellTiter-Glo 3D测量的各自活力相匹配。这允许使用机器学习将图像信息解码为第18天以及更早时间点(第8,11,15天)的活力值。结果我们的研究表明,神经球图像可以通过外推的生存能力来预测细胞的生存能力。这使得在18天的时间窗口内评估药物相互作用成为可能。我们的研究结果表明,随着时间的推移,几种药物组合具有明确而持久的协同相互作用。我们的方法促进了药物相互作用的纵向评估,为三维神经球中药物联合的时间动态效应提供了新的见解,有助于确定更有效的胶质母细胞瘤治疗方法。
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Longitudinal drug synergy assessment using convolutional neural network image-decoding of glioblastoma single-spheroid cultures
Abstract Background In recent years, drug combinations have become increasingly popular to improve therapeutic outcomes in various diseases, including difficult to cure cancers such as the brain cancer glioblastoma. Assessing the interaction between drugs over time is critical for predicting drug combination effectiveness and minimizing the risk of therapy resistance. However, as viability readouts of drug combination experiments are commonly performed as an endpoint where cells are lysed, longitudinal drug-interaction monitoring is currently only possible through combined endpoint assays. Methods We provide a method for massive parallel monitoring of drug interactions for 16 drug combinations in three glioblastoma models over a time frame of 18 days. In our assay, viabilities of single neurospheres are to be estimated based on image information taken at different time points. Neurosphere images taken at the final day (day 18) were matched to the respective viability measured by CellTiter-Glo 3D at the same day. This allowed to use machine learning to decode image information to viability values at day 18 as well as for the earlier time points (at day 8, 11, 15). Results Our study shows that neurosphere images allow to predict cell viability from extrapolated viabilities. This enables to assess the drug interactions in a time-window of 18 days. Our results show a clear and persistent synergistic interaction for several drug combinations over time. Conclusions Our method facilitates longitudinal drug-interaction assessment, providing new insights into the temporal-dynamic effects of drug combinations in 3D neurospheres which can help to identify more effective therapies against glioblastoma.
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CiteScore
6.20
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审稿时长
12 weeks
期刊最新文献
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