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Updated: Apr 23, 2026

Modeling Paracrine Noncanonical Wnt Signaling In Vitro
Published on: December 10, 2021
Intersection of AHR and Wnt signaling in development, health, and disease
Andrew J Schneider1, Amanda M Branam2, Richard E Peterson3
1School of Pharmacy and Molecular and Environmental Toxicology Center University of Wisconsin, Madison, WI 53705, USA. ajschnei@wisc.edu.
Abstract:
The AHR (aryl hydrocarbon receptor) and Wnt (wingless-related MMTV integration site) signaling pathways have been conserved throughout evolution. Appropriately regulated signaling through each pathway is necessary for normal development and health, while dysregulation can lead to developmental defects and disease. Though both pathways have been vigorously studied, there is relatively little research exploring the possibility of crosstalk between these pathways. In this review, we provide a brief background on (1) the roles of both AHR and Wnt signaling in development and disease, and (2) the molecular mechanisms that characterize activation of each pathway. We also discuss the need for careful and complete experimental evaluation of each pathway and describe existing research that explores the intersection of AHR and Wnt signaling. Lastly, to illustrate in detail the intersection of AHR and Wnt signaling, we summarize our recent findings which show that 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-induced disruption of Wnt signaling impairs fetal prostate development.
Insights
Aryl hydrocarbon receptor (AHR) and Wnt signaling pathways are crucial for development. This review explores their crosstalk, finding that TCDD-induced AHR activation disrupts Wnt signaling, impairing fetal prostate development.
Area of Science:
- Developmental Biology
- Molecular Signaling
- Toxicology
Background:
- Aryl hydrocarbon receptor (AHR) and Wnt signaling pathways are evolutionarily conserved pathways essential for normal development and health.
- Dysregulation of AHR and Wnt signaling is linked to developmental defects and various diseases.
- While individually well-studied, the crosstalk between AHR and Wnt signaling remains underexplored.
Purpose of the Study:
- To review the roles of AHR and Wnt signaling in development and disease.
- To elucidate the molecular mechanisms of AHR and Wnt pathway activation.
- To investigate the intersection and potential crosstalk between AHR and Wnt signaling pathways.
Main Methods:
- Literature review of AHR and Wnt signaling pathways.
- Analysis of existing research on AHR-Wnt pathway interactions.
- Summary of recent findings on TCDD's effect on Wnt signaling and fetal prostate development.
Main Results:
- Aryl hydrocarbon receptor (AHR) and Wnt signaling are critical for development.
- 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) exposure disrupts Wnt signaling.
- TCDD-induced disruption of Wnt signaling impairs fetal prostate development.
Conclusions:
- Understanding AHR and Wnt signaling crosstalk is vital for developmental biology and toxicology.
- Experimental evaluation of these pathways is necessary to uncover complex interactions.
- TCDD's adverse effects on fetal development highlight the importance of studying pathway intersections.
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