发育毒性:人工智能驱动的评估。

IF 13.9 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Tong Wang, Xuelian Jia, Lauren M Aleksunes, Hui Shen, Hong-Wen Deng, Hao Zhu
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引用次数: 0

摘要

监管机构要求对产前药物接触进行全面毒性测试,包括开发中的新药,以减少对发育毒性的关注,即药物引起的毒性和对孕妇和胎儿的不利影响。然而,定义发育毒性终点和相关公共大数据的优化分析仍然具有挑战性。最近,人工智能(AI)方法在分析复杂的高维数据,揭示化学品暴露与相关发育风险之间的微妙关系方面发挥了关键作用。在这里,我们概述了主要的大数据资源和数据驱动模型,重点是预测各种毒性终点。我们还重点介绍了新兴的、可解释的人工智能模型,这些模型集成了多模态数据和领域知识,以揭示复杂端点背后的毒性机制,并概述了一个利用多种可解释模型来全面评估化学诱导的发育毒性的潜在框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Developmental toxicity: artificial intelligence-powered assessments.

Regulatory agencies require comprehensive toxicity testing for prenatal drug exposure, including new drugs in development, to reduce concerns about developmental toxicity, that is, drug-induced toxicity and adverse effects in pregnant women and fetuses. However, defining developmental toxicity endpoints and optimal analysis of associated public big data remain challenging. Recently, artificial intelligence (AI) approaches have had a critical role in analyzing complex, high-dimensional data, uncovering subtle relationships between chemical exposures and associated developmental risks. Here, we present an overview of major big data resources and data-driven models that focus on predicting various toxicity endpoints. We also highlight emerging, interpretable AI models that integrate multimodal data and domain knowledge to reveal toxic mechanisms underlying complex endpoints, and outline a potential framework that leverages multiple interpretable models to comprehensively evaluate chemical-induced developmental toxicity.

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来源期刊
CiteScore
23.90
自引率
0.70%
发文量
132
审稿时长
6-12 weeks
期刊介绍: Trends in Pharmacological Sciences (TIPS) is a monthly peer-reviewed reviews journal that focuses on a wide range of topics in pharmacology, pharmacy, pharmaceutics, and toxicology. Launched in 1979, TIPS publishes concise articles discussing the latest advancements in pharmacology and therapeutics research. The journal encourages submissions that align with its core themes while also being open to articles on the biopharma regulatory landscape, science policy and regulation, and bioethics. Each issue of TIPS provides a platform for experts to share their insights and perspectives on the most exciting developments in the field. Through rigorous peer review, the journal ensures the quality and reliability of published articles. Authors are invited to contribute articles that contribute to the understanding of pharmacology and its applications in various domains. Whether it's exploring innovative drug therapies or discussing the ethical considerations of pharmaceutical research, TIPS provides a valuable resource for researchers, practitioners, and policymakers in the pharmacological sciences.
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