通过机器学习策略预测双类型的肝毒性
Ying Zhao1, Xueer Zhang1, Zhendong Zhang1
1Key Laboratory of Modern Toxicology of Ministry of Education, School of Public Health, Nanjing Medical University, Nanjing, China; Department of Microbiology and Infection, School of Public Health, Nanjing Medical University, Nanjing, China.
这项研究提出了一种新的计算方法,使用网络分析和机器学习来预测新兴双相似物 (BPs) 的肝毒性. 这种方法有助于快速评估这些内分泌干扰物的危险性.
科学领域:
- 环境毒理学环境毒理学
- 计算化学计算化学
- 基因组学就是基因组学.
背景情况:
- 双相似物 (BPs) 是已知会引起肝毒性的内分泌干扰物.
- 负面结果途径 (AOPs) 有助于风险评估,但对于新兴BP存在数据缺口.
- 预测肝毒性对于评估新型合成化学品的风险至关重要.
研究的目的:
- 开发一种快速的策略来预测新兴双相似物 (BPs) 的肝毒性.
- 利用网络分析和机器学习进行危险评估.
- 为BP提供有限实验数据的结构-活动关系的见解.
主要方法:
- 将肝病基因集成到双A (BPA) - 基因-表型-肝毒性网络中.
- 应用计算AOP (cAOP) 和机器学习模型来得分肝毒性.
- 使用分子对接来评估BP和ESR1.1之间的相互作用.
主要成果:
- 成功预测了20个新出现的BP的肝毒性.
- 确定了对生物功能的结构特征贡献.
- 提出了一个AOP框架,ESR1作为分子启动事件.
结论:
- 这项研究为预测BP肝毒性提供了有价值的计算工具.
- 这种方法解决了新兴BP的数据限制.
- 它提高了对BP毒理机制和风险评估的理解.
更多相关视频
08:25Advanced 3D Liver Models for In vitro Genotoxicity Testing Following Long-Term Nanomaterial Exposure
Published on: June 5, 2020
08:28Assessment of the Effects of Endocrine Disrupting Compounds on the Development of Vertebrate Neural Network Function Using Multi-electrode Arrays
Published on: April 26, 2018
相关概念视频
Physiological Pharmacokinetic Models: Incorporating Hepatic Transporter-Mediated Clearance
A recent model describes pravastatin's hepatobiliary excretion,...
Pharmacokinetic Models: Comparison and Selection Criterion
Physiological models take a detailed approach by considering specific molecular processes. They can predict drug distribution, metabolism, and elimination changes, providing a comprehensive understanding of how drugs interact with the body.
Mechanistic Models: Overview of Compartment Models
Pharmacokinetic Models: Overview
There are three primary types of models: empirical, compartment, and physiological. Empirical models, with minimal...
Mechanistic Models: Compartment Models in Individual and Population Analysis
