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A novel multi-omics data analysis of dose-dependent and temporal changes in regulatory pathways due to chemical
Yufan Liu1, Guoping Lian1,2, Tao Chen1
1School of Chemistry and Chemical Engineering, University of Surrey, Guildford, UK.
Abstract:
Comprehensive analysis of multi-omics data can reveal alterations in regulatory pathways induced by cellular exposure to chemicals by characterizing biological processes at the molecular level. Data-driven omics analysis, conducted in a dose-dependent or dynamic manner, can facilitate comprehending toxicity mechanisms. This study introduces a novel multi-omics data analysis designed to concurrently examine dose-dependent and temporal patterns of cellular responses to chemical perturbations. This analysis, encompassing preliminary exploration, pattern deconstruction, and network reconstruction of multi-omics data, provides a comprehensive perspective on the dynamic behaviors of cells exposed to varying levels of chemical stimuli. Importantly, this analysis is adaptable to any number of omics layers, including site-specific phosphoproteomics. We implemented this analysis on multi-omics data obtained from HepG2 cells exposed to a range of caffeine doses over varying durations and identified six response patterns, along with their associated biomolecules and pathways. Our study demonstrates the effectiveness of the proposed multi-omics data analysis in capturing multidimensional patterns of cellular response to chemical perturbation, enhancing understanding of pathway regulation for chemical risk assessment.
Insights
This study presents a new multi-omics data analysis to understand cellular responses to chemical exposure. It reveals dose-dependent and temporal patterns, aiding in chemical toxicity mechanism comprehension.
Area of Science:
- Toxicology
- Systems Biology
- Bioinformatics
Background:
- Chemical exposure can alter cellular regulatory pathways.
- Understanding molecular-level biological processes is key to characterizing toxicity.
- Multi-omics data analysis offers insights into dose-dependent and dynamic cellular responses.
Purpose of the Study:
- To introduce a novel multi-omics data analysis method.
- To concurrently examine dose-dependent and temporal patterns of cellular responses to chemical perturbations.
- To provide a comprehensive perspective on dynamic cellular behaviors under chemical stimuli.
Main Methods:
- The study employed a multi-omics data analysis approach.
- This included preliminary exploration, pattern deconstruction, and network reconstruction.
- The method was applied to HepG2 cells exposed to varying doses and durations of caffeine.
Main Results:
- Six distinct cellular response patterns were identified.
- Associated biomolecules and regulatory pathways for each pattern were determined.
- The analysis captured multidimensional patterns of cellular response to chemical perturbation.
Conclusions:
- The proposed multi-omics analysis effectively captures dynamic cellular responses to chemical exposure.
- This approach enhances the understanding of pathway regulation in chemical risk assessment.
- The method is adaptable to various omics layers, including phosphoproteomics.
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