# cAMP–PKA/EPAC signaling pathways: crucial regulators of lipid homeostasis

**Authors:** Caixia Chen, Hui Gao, Qi Tian, Junwei Cao

PMC · DOI: 10.1080/21623945.2025.2603605 · Adipocyte · 2026-01-07

## TL;DR

This review explores how cAMP-PKA and EPAC signaling pathways regulate lipid balance in adipose tissue and their interactions with the microenvironment in metabolic diseases.

## Contribution

The paper introduces a novel framework linking cAMP-PKA/EPAC signaling with the adipose microenvironment to explain metabolic disorders.

## Key findings

- cAMP-PKA and EPAC pathways regulate lipid metabolism and interact with immune and vascular cells in adipose tissue.
- Pharmacological modulation of these pathways may help restore adipose tissue homeostasis in diseases like obesity and diabetes.
- The review fills knowledge gaps by synthesizing studies on PKA and EPAC signaling in adipose metabolism.

## Abstract

Adipose omeostasishomoeostasis is maintained through the precise coordination of lipogenesis, lipolysis, and adipocyte differentiation, with microenvironmental components dynamically regulating lipid metabolism. Even though the classical cAMP-PKA pathway has been well-characterized for its function in lipid metabolism by phosphorylating transcription factors and lipolytic enzymes, little is known about how it collaborates with elements of the adipose tissue microenvironment, such as immune cells and the vascular endothelium, especially in pathological situations like obesity. EPAC, a newly discovered cAMP effector, has shown new signalingsignallingsignalling signalling pathways in the immune and cardiovascular systems by activating small G proteins. However, there are important understanding gaps regarding its roles in adipose metabolism, namely adipocyte development, microenvironmental interaction, and the pathophysiology of metabolic diseases. By bringing together disparate studies on PKA and EPAC, this review provides the first comprehensive synthesis of the cAMP-PKA/EPAC dual signaling signalling signallingcins signalling network, filling in knowledge gaps. The reciprocal regulation between this signaling signalling signalling signalling network and the adipose microenvironment establishes a novel ‘signaling-microenvironment-systemic metabolism’ framework for understanding metabolic disorders, including obesity, diabetes, and hepatic steatosis. Pharmacological modulation of the PKA/EPAC signalingsignalling signalling signalling pathways may therefore represent a viable therapeutic approach for restoring adipose tissue homeostasis homoeostasis.

## Linked entities

- **Proteins:** RAPGEF3 (Rap guanine nucleotide exchange factor 3)
- **Diseases:** obesity (MONDO:0011122), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** CAMP (cathelicidin antimicrobial peptide) [NCBI Gene 820] {aka CAP-18, CAP18, CRAMP, FALL-39, FALL39, HSD26}, RAPGEF3 (Rap guanine nucleotide exchange factor 3) [NCBI Gene 10411] {aka CAMP-GEFI, EPAC, EPAC1, HSU79275, bcm910}
- **Diseases:** diabetes (MESH:D003920), obesity (MESH:D009765), metabolic diseases (MESH:D008659), hepatic steatosis (MESH:D005234)
- **Chemicals:** lipid (MESH:D008055)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12785204/full.md

## References

330 references — full list in the complete paper: https://tomesphere.com/paper/PMC12785204/full.md

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Source: https://tomesphere.com/paper/PMC12785204