# Role of Salivary MicroRNA as a Marker of Progesterone Resistance in Endometriosis: Preliminary Results from a Single-Institution Experience

**Authors:** Matilde Degano, Giorgia Vesca, Michela Bulfoni, Silvia Zermano, Stefano Restaino, Martina Arcieri, Errico Zupi, Renato Seracchioli, Lorenza Driul, Daniela Cesselli, Giovanni Scambia, Anna Biasioli, Giuseppe Vizzielli

PMC · DOI: 10.3390/biom15040493 · Biomolecules · 2025-03-27

## TL;DR

This study explores using saliva microRNAs to detect endometriosis and predict treatment response, offering a non-invasive diagnostic tool.

## Contribution

The study identifies specific salivary microRNAs as potential biomarkers for endometriosis and progesterone resistance.

## Key findings

- Salivary miRNA sequencing is feasible and reveals distinct profiles in endometriosis patients.
- Key miRNAs like mir-3168, mir-200a family, and mir-93-5p show significant differential expression.
- These miRNAs may serve as biomarkers for endometriosis and treatment response.

## Abstract

This feasibility study explores the potential of salivary microRNAs (miRNAs) as non-invasive biomarkers for diagnosing endometriosis and assessing treatment response. Almost one-third of patients with endometriosis do not respond to the standard progestin treatment due to various mechanisms of progesterone resistance. MiRNAs, recognized for their stability in body fluids and role in gene regulation, may offer new diagnostic and prognostic opportunities as they are involved in the pathogenic pathways of endometriosis and progesterone resistance. We sequenced salivary miRNAs in three cohorts of patients: control women without endometriosis and patients with endometriosis who responded and did not respond to standard progestin treatment. This aims to identify the differential miRNA expression profiles associated with therapeutic response to dienogest. The preliminary results demonstrate the feasibility of miRNA sequencing from saliva and reveal distinct miRNA profiles between responders, non-responders, and controls. Key miRNAs, including mir-3168, the mir-200a family, and mir-93-5p, emerged as potential biomarkers, showing significant differential expression linked to both endometriosis presence and treatment response. Further validation of these findings in larger cohorts could pave the way for miRNA-based diagnostic and prognostic tools, potentially reducing diagnostic delays and personalizing treatment approaches for endometriosis patients, also with new target therapies.

## Linked entities

- **Chemicals:** dienogest (PubChem CID 68861)
- **Diseases:** endometriosis (MONDO:0005133)

## Full-text entities

- **Genes:** MIR200A (microRNA 200a) [NCBI Gene 406983] {aka MIRN200A, mir-200a}, MIR935 (microRNA 935) [NCBI Gene 100126325] {aka MIRN935, hsa-mir-935, mir-935}, MIR3168 (microRNA 3168) [NCBI Gene 100422878]
- **Diseases:** progesterone (MESH:C564871), Endometriosis (MESH:D004715)
- **Chemicals:** dienogest (MESH:C023635), Progesterone (MESH:D011374)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

13 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12025187/full.md

## References

71 references — full list in the complete paper: https://tomesphere.com/paper/PMC12025187/full.md

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Source: https://tomesphere.com/paper/PMC12025187