Related Experiment Video
Updated: May 2, 2026

Characterize Disease-related Mutants of RAF Family Kinases by Using a Set of Practical and Feasible Methods
Published on: July 17, 2019
Cardiotoxicity of BRAF/MEK inhibitors
Katharina Seuthe1, Valerie Lohner2, Kevin Terre3
1Faculty of Medicine and University Hospital Cologne, Clinic III for Internal Medicine, University of Cologne, Cologne, Germany.
BRAF and MEK inhibitors improve cancer therapy but can cause heart problems like heart failure and arrhythmias. Early detection and management are key to safe treatment and preserving heart health.
Area of Science:
- Cardio-oncology
- Molecular oncology
- Pharmacology
Background:
- BRAF and MEK inhibitors have revolutionized cancer treatment, especially for melanoma.
- Cardiovascular toxicities associated with these inhibitors are a growing concern in clinical practice.
Purpose of the Study:
- To review the mechanisms and clinical implications of BRAF and MEK inhibitor-induced cardiotoxicity.
- To provide guidance on risk assessment, surveillance, and management of cardiotoxicity.
Main Methods:
- Literature review synthesizing biological rationale, clinical trial data, and observational cohort studies.
- Analysis of reported cardiovascular events, including heart failure, hypertension, thromboembolism, and arrhythmias.
- Development of management algorithms based on current cardio-oncology guidelines.
Main Results:
- Cardiotoxicity manifests as left ventricular dysfunction, heart failure, hypertension, thromboembolism, and arrhythmias.
- Mechanisms are multifactorial, involving on-target and off-target effects on cardiomyocytes and endothelium.
- Risk profiles differ between combination and monotherapy.
Conclusions:
- Proactive understanding, detection, and management of cardiotoxicity are crucial.
- These strategies enable safe administration of BRAF/MEK inhibitor therapy.
- Preserving cardiovascular health is paramount during cancer treatment.
More Related Videos
06:44Author Spotlight: Integrating BRET-Based Assays and Rare Mutation Analysis to Decipher RAF Kinase Regulation in Live Cells
Published on: March 1, 2024
09:32Drug-Induced Senescence in Liver Cells Promotes M2 Macrophage Polarization: Implications for Tyrosine Kinase Inhibitor-Associated Hepatotoxicity
Published on: October 17, 2025
Related Concept Videos
MAPK Signaling Cascades
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Mitogens and the Cell Cycle
Targeted Cancer Therapies
There are several types of targeted therapies against...
Inhibition of Cdk Activity
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...