# Molecular Imaging Advances in Endometriosis: The Promise of Radiopharmaceuticals

**Authors:** Rebecca Napolitano, Giorgia Speltri, Petra Martini, Francesca Porto, Lorenza Marvelli, Alessandro Niorettini, Licia Uccelli, Luca Urso, Luca Filippi, Hatice Uslu, Burak Canitez, Hamza Alperen Kösem, Alessandra Boschi

PMC · DOI: 10.3390/molecules31010093 · Molecules · 2025-12-25

## TL;DR

This paper reviews how new radiopharmaceuticals targeting Fibroblast Activation Protein (FAP) could improve the diagnosis of endometriosis, a chronic gynecological condition.

## Contribution

The paper introduces FAP-targeting radiopharmaceuticals as a novel molecular imaging approach for endometriosis, contrasting them with traditional imaging methods.

## Key findings

- FAP is overexpressed in endometriotic lesions and correlates with fibrosis and immune infiltration.
- Traditional PET tracers like FDG and Ga-DOTATATE have limited effectiveness for endometriosis imaging.
- FAP inhibitors (FAPI) show promise as specific and non-invasive imaging agents for endometriosis.

## Abstract

Endometriosis is a highly prevalent, chronic gynecological disorder characterized by the ectopic presence of endometrial-like tissue, driving significant morbidity and chronic pelvic pain. Pathologically, it is increasingly recognized as a fibro-inflammatory condition involving extensive tissue remodeling and fibrosis. Current conventional imaging modalities, including ultrasound and MRI, are primarily morphological, while standard molecular imaging using Positron Emission Tomography (PET) tracers has shown limited diagnostic utility. [18F]Fluorodeoxyglucose (FDG) suffers from high physiological uptake in pelvic organs and inconsistent detection of lesions. Receptor-based tracers like [68Ga]Ga-DOTATATE have demonstrated uncertain efficacy. In contrast, radiopharmaceuticals targeting the Fibroblast Activation Protein (FAP) offer a promising molecular approach. FAP is specifically overexpressed by activated fibroblasts present in the stroma of endometriotic lesions, correlating significantly with tissue fibrosis (collagen content) and local immune infiltration (e.g., CD68 macrophages). This comprehensive review analyzes the landscape of radiopharmaceuticals for endometriosis imaging, contrasting the specific limitations of traditional metabolic and receptor agents with the molecular rationale and emerging evidence supporting the use of FAP Inhibitors (FAPI), positioning them as crucial, non-invasive tools for the future diagnosis and management of this challenging disease.

## Linked entities

- **Proteins:** FAP (fibroblast activation protein alpha), CD68 (CD68 molecule)
- **Chemicals:** [18F]Fluorodeoxyglucose (PubChem CID 68614), FDG (PubChem CID 68614)
- **Diseases:** endometriosis (MONDO:0005133)

## Full-text entities

- **Genes:** FAP (fibroblast activation protein alpha) [NCBI Gene 2191] {aka DPPIV, FAPA, FAPalpha, SIMP}, CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}
- **Diseases:** fibro-inflammatory (MESH:D009810), endometriotic lesions (MESH:D009059), fibrosis (MESH:D005355), Endometriosis (MESH:D004715), pelvic pain (MESH:D017699), chronic (MESH:D002908), gynecological disorder (MESH:D005831)
- **Chemicals:** [68Ga]Ga-DOTATATE (-), 18F]Fluorodeoxyglucose (MESH:D019788)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12786799/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786799/full.md

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Source: https://tomesphere.com/paper/PMC12786799