PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
May 21, 2026Frontiers in Toxicology1 citationsOpen Access

Cardiotoxicity adverse outcome pathway network: towards mechanistic and quantitative modelling

LLLuiz LadeiraUniversity of LiègeDBDebra A. BarnesUtrecht UniversityRMRosalinde MasereeuwUtrecht University

Key Result

A comprehensive Adverse Outcome Pathway network analysis identified oxidative stress and mitochondrial dysfunction as the primary central biological drivers of chemical-induced cardiac injury.

Key Points

  • The aim is to explore the complex biological processes leading to chemical-induced heart toxicity and develop a predictive AOP network.
  • Constructed a network from OECD AOP-Wiki data showing 64 biological events and 94 relationships.
  • Identified central biological crossroads contributing to cardiac injury.
  • Developed a methods catalog linking biological events to laboratory assays.
  • Identified oxidative stress and mitochondrial dysfunction as primary drivers of cardiac injury.
  • Demonstrated systemic interactions, including with kidneys, impact cardiotoxicity.
  • Created an interactive platform for researchers to utilize in safety assessments.

Structured PICO

P
Population
Data from the OECD AOP-Wiki comprising 64 biological events and 94 documented relationships related to chemical-induced heart toxicity
I
Intervention
Development of a comprehensive Adverse Outcome Pathway (AOP) network and methods catalogue
O
Outcome
Identification of critical biological crossroads and primary drivers of cardiac injury

The development of a cardiotoxicity Adverse Outcome Pathway network provides a framework for understanding chemical-induced heart damage and supports animal-free testing strategies.

Limitations

  • The network is built from linear AOPs available in AOP-Wiki and is not intended to be the most comprehensive collection of mechanistic understanding.
  • Degree of quantitative understanding was limited, with only 37.2% of key event relationships associated with any quantitative level of understanding.

Abstract

Introduction Chemical-induced heart toxicity remains a major challenge in drug development and environmental safety, largely because current testing often relies on narrow, late-stage endpoints that miss the complex biological progression of the toxicities. To address this, we developed a comprehensive Adverse Outcome Pathway (AOP) network that maps how early (bio) chemical triggers evolve into organ-level dysfunction. Methods By integrating data from the OECD AOP-Wiki, we constructed a unified network of 64 biological events and 94 documented relationships that identifies the critical biological “crossroads” where different toxic chemicals converge to cause heart damage. Results/discussion Our analysis reveals a compact core of central biological events, such as oxidative stress and mitochondrial dysfunction, which act as the primary drivers of cardiac injury. This network approach moves beyond single, linear pathways to show how systemic factors, including interactions with other organs like the kidneys, contribute to cardiotoxicity. To translate these findings into a practical resource for the broader scientific community, we developed a methods catalogue that links these biological events to specific laboratory assays. To ensure this work is accessible and actionable, we hosted the network on an interactive, FAIRaligned web platform. By providing a clear scaffold for understanding heart safety, this resource enables the design of more human-relevant, animal-free testing strategies and helps prioritise the most impactful biomarkers for future safety assessments.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Ladeira et al. (2026) studied Cardiotoxicity. Adverse Outcome Pathway (AOP) network analysis was evaluated on Identification of critical biological events driving cardiotoxicity. A comprehensive Adverse Outcome Pathway network analysis identified oxidative stress and mitochondrial dysfunction as the primary central biological drivers of chemical-induced cardiac injury.

synapsesocial.com/papers/6a0ea02cbe05d6e3efb5f17chttps://doi.org/10.3389/ftox.2026.1781536
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Cardiac tissue engineering: Multiple approaches and potential applications2022 · 15 citations
  2. 2CellDesigner 3.5: A Versatile Modeling Tool for Biochemical Networks2008 · 475 citations
  3. 3Report of the 1st and 2nd Mystery of Reactive Oxygen Species Conferences2022 · 12 citations
  4. 4Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks2003 · 55,507 citations
  5. 5Microengineered platforms for characterizing the contractile function of in vitro cardiac models2022 · 76 citations