Grant: Discovery Grants Program - Individual
Université d'Ottawa
$50,000.00
Characterizing mechanisms of toxicological action for data-poor priority pollutants in Canada using novel model systems and transcriptomic methodologies
FY 2024-25
Summary
There are thousands of chemicals in our environment that have never been subject to toxicological testing (referred to as `data-poor'). The root cause of this is reliance on traditional tests that are not high-throughput or economical. These tests also do not reveal toxicological mechanisms that inform species relevance and individual susceptibility.
Transcriptomics (global gene expression profiling) provides a rich source of information to understand and predict toxicological effects. Transcriptomics has yet to be fully harnessed for use in regulatory decision-making and risk assessment.
Objectives
The overarching goal of my research and training program is to modernize regulatory evaluation of chemical toxicity testing. We aim to develop and apply pragmatic approaches to efficiently identify toxicological mechanisms and predict hazards from transcriptomic data.
Specific objectives
We will apply high-throughput transcriptomics and bioinformatics in human in vitro models to address knowledge gaps in data-poor chemicals of high concern. Projects will focus on two chemical families, per- and poly-fluorinated alkyl substances and bisphenols, because of their widespread use and the large number of data-poor chemicals within these families. The work will be broken into three phases:
Phase 1a - Hypothesis generation. Deeply mine existing and new genomic data sets to decipher mechanisms of toxicity and identify physico-chemical drivers of toxicity;
Phase 1b - Methods development. Apply/develop machine-learning tools to predict toxicological effects from transcriptomic profiles to increase the efficiency and reproducibility of data interpretation;
Phase 2 - Hypothesis testing and methods validation. Conduct validation experiments to confirm molecular, biochemical and phenotypic predictions from Phase 1;
Phase 3 - Discovery. Apply single-cell RNA-sequencing to identify cell type- and individual-specific mechanisms, potencies, and effects.
The program supports 5 graduate students each year, for a total of 4 MSc, 3 PhD completed, and 2 MSc, 3 PhD initiated. The program provides a unique training ground focused on translation of research innovation into regulatory decision-making, policy and practice.
Novelty and significance
The work will provide critical information on the toxicity of data-poor chemicals and reveal how new models and artificial intelligence can be used to predict toxicological effects. The analytical approaches can be applied in green-chemistry development pipelines to reduce the probability of regrettable replacements. The work will impact policy related to priority chemical categories and use of genomic data in regulatory decision-making. The tools provide new approaches that increase analytical throughput and save cost/time for chemical evaluations, which impacts industry and regulatory agencies. Importantly, the training program will produce the next-generation of toxicologists and risk assessment specialists for Canada.
Program
Discovery Grants Program - Individual
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
RGPIN-2021-02806
Name nom
Yauk, Carole
Department département
Biology
Organization id
28
Institution établissement
Université d'Ottawa
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2024
Competition year année de concours
2021
Award amount
50000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
406
Area of application group en
Environment
Area of application group fr
Environnement
Area of application en
Pollutants and toxic agents (waste, use 902)
Area of application fr
Polluants et agents toxiques (déchets, utiliser 902)
Research subject code
5000
Research subject group en
Genetics
Research subject group fr
Génétique
Research subject en
Genetics
Research subject fr
Génétique
Field of research list names en
Not available
Field of research list names fr
Non disponible
Socioeconomic objective list names en
Not available
Socioeconomic objective list names fr
Non disponible
Application title
Characterizing mechanisms of toxicological action for data-poor priority pollutants in Canada using novel model systems and transcriptomic methodologies
Keywords
transcriptomics; toxicology; mechanisms of action; in vitro models; single-cell transcriptomics; biomarkers; benchmark dose modeling; bioinformatics; adverse outcome pathways; toxicogenomics
Application summary
There are thousands of chemicals in our environment that have never been subject to toxicological testing (referred to as `data-poor'). The root cause of this is reliance on traditional tests that are not high-throughput or economical. These tests also do not reveal toxicological mechanisms that inform species relevance and individual susceptibility.
Transcriptomics (global gene expression profiling) provides a rich source of information to understand and predict toxicological effects. Transcriptomics has yet to be fully harnessed for use in regulatory decision-making and risk assessment.
Objectives
The overarching goal of my research and training program is to modernize regulatory evaluation of chemical toxicity testing. We aim to develop and apply pragmatic approaches to efficiently identify toxicological mechanisms and predict hazards from transcriptomic data.
Specific objectives
We will apply high-throughput transcriptomics and bioinformatics in human in vitro models to address knowledge gaps in data-poor chemicals of high concern. Projects will focus on two chemical families, per- and poly-fluorinated alkyl substances and bisphenols, because of their widespread use and the large number of data-poor chemicals within these families. The work will be broken into three phases:
Phase 1a - Hypothesis generation. Deeply mine existing and new genomic data sets to decipher mechanisms of toxicity and identify physico-chemical drivers of toxicity;
Phase 1b - Methods development. Apply/develop machine-learning tools to predict toxicological effects from transcriptomic profiles to increase the efficiency and reproducibility of data interpretation;
Phase 2 - Hypothesis testing and methods validation. Conduct validation experiments to confirm molecular, biochemical and phenotypic predictions from Phase 1;
Phase 3 - Discovery. Apply single-cell RNA-sequencing to identify cell type- and individual-specific mechanisms, potencies, and effects.
The program supports 5 graduate students each year, for a total of 4 MSc, 3 PhD completed, and 2 MSc, 3 PhD initiated. The program provides a unique training ground focused on translation of research innovation into regulatory decision-making, policy and practice.
Novelty and significance
The work will provide critical information on the toxicity of data-poor chemicals and reveal how new models and artificial intelligence can be used to predict toxicological effects. The analytical approaches can be applied in green-chemistry development pipelines to reduce the probability of regrettable replacements. The work will impact policy related to priority chemical categories and use of genomic data in regulatory decision-making. The tools provide new approaches that increase analytical throughput and save cost/time for chemical evaluations, which impacts industry and regulatory agencies. Importantly, the training program will produce the next-generation of toxicologists and risk assessment specialists for Canada.