# Looking at endometriosis–diagnosis and disease mechanisms through a mechanical lens

**Authors:** Taylor Thomsen, Emilie Petite, Corrine A. Pierce, Trinity Ellis, Pritika Acharya, Lydia Sohn

PMC · DOI: 10.3389/fmed.2026.1716836 · Frontiers in Medicine · 2026-02-05

## TL;DR

This paper explores how mechanical properties of cells could help diagnose endometriosis, a painful gynecological condition, and improve understanding of its progression.

## Contribution

The paper introduces a novel mechanobiological perspective for diagnosing endometriosis using cellular biophysical properties.

## Key findings

- Cell stiffness, deformability, and contractility may serve as functional biomarkers for endometriosis.
- Menstrual effluent is proposed as a non-invasive sample for mechanical profiling of endometriosis-related cells.

## Abstract

Endometriosis is a chronic gynecological disorder marked by the growth of endometrial-like tissue outside the uterus, often resulting in pain and infertility and affecting overall quality of life. Despite its prevalence, diagnostic delays persist due to reliance on invasive laparoscopy and the lack of sensitive, specific, non-invasive biomarkers. Current molecular and imaging tools have improved detection but remain limited, underscoring the need for new diagnostic strategies. This review introduces a mechanobiological perspective, exploring how cellular biophysical properties such as cell stiffness, deformability, and contractility can potentially serve as functional biomarkers for endometriosis. We examine lesion subtypes, menstrual cycle dynamics, and key biological processes such as decidualization, epithelial–mesenchymal transition (EMT), and stromal remodeling through a mechanical lens. Parallels are drawn between endometriosis and cancer to underscore the diagnostic potential of tissue and cell mechanics. We specifically highlight menstrual effluent as a promising non-invasive, cell-rich sample uniquely suited for mechanical profiling. Together, these insights suggest that viewing endometriosis with a mechanical lens may accelerate diagnostic innovation and uncover new mechanisms driving disease development and progression.

## Linked entities

- **Diseases:** endometriosis (MONDO:0005133)

## Full-text entities

- **Genes:** MYH14 (myosin heavy chain 14) [NCBI Gene 79784] {aka DFNA4, DFNA4A, FP17425, MHC16, MYH17, NMHC II-C}, SNAI1 (snail family transcriptional repressor 1) [NCBI Gene 6615] {aka SLUGH2, SNA, SNAH, SNAIL, SNAIL1, dJ710H13.1}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, SLTM (SAFB like transcription modulator) [NCBI Gene 79811] {aka Met}, CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, IGFBP1 (insulin like growth factor binding protein 1) [NCBI Gene 3484] {aka AFBP, IBP1, IGF-BP25, PP12, hIGFBP-1}, CDH2 (cadherin 2) [NCBI Gene 1000] {aka ACOGS, ADHD8, ARVD14, CD325, CDHN, CDw325}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, MME (membrane metalloendopeptidase) [NCBI Gene 4311] {aka CALLA, CD10, CMT2T, NEP, SCA43, SFE}, ALDH1A1 (aldehyde dehydrogenase 1 family member A1) [NCBI Gene 216] {aka ALDC, ALDH-E1, ALDH1, ALDH11, HEL-9, HEL-S-53e}, ITGB1 (integrin subunit beta 1) [NCBI Gene 3688] {aka CD29, FNRB, GPIIA, MDF2, MSK12, VLA-BETA}, IDO1 (indoleamine 2,3-dioxygenase 1) [NCBI Gene 3620] {aka IDO, IDO-1, INDO}, FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, RHOA (ras homolog family member A) [NCBI Gene 387] {aka ARH12, ARHA, EDFAOB, RHO12, RHOH12}, YAP1 (Yes1 associated transcriptional regulator) [NCBI Gene 10413] {aka COB1, YAP, YAP-1, YAP2, YAP65, YKI}, CD9 (CD9 molecule) [NCBI Gene 928] {aka BTCC-1, DRAP-27, MIC3, MRP-1, TSPAN-29, TSPAN29}, ROCK1 (Rho associated coiled-coil containing protein kinase 1) [NCBI Gene 6093] {aka P160ROCK, ROCK-I}, PDPN (podoplanin) [NCBI Gene 10630] {aka AGGRUS, D2-40, GP36, GP40, Gp38, HT1A-1}, ROCK2 (Rho associated coiled-coil containing protein kinase 2) [NCBI Gene 9475] {aka ROCK-II}, VIM (vimentin) [NCBI Gene 7431], COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}
- **Diseases:** endometrial lesions (MESH:D014591), irritable bowel syndrome (MESH:D043183), interstitial cystitis (MESH:D018856), fibroids (MESH:D007889), inflammatory bowel disease (MESH:D015212), gynecological disorder (MESH:D005831), chronic pain (MESH:D059350), depression (MESH:D003866), chocolate cysts (MESH:D003560), immune dysregulation (OMIM:614878), OMA (MESH:D010049), metastasis (MESH:D009362), infertility (MESH:D007246), pelvic inflammatory disease (MESH:D000292), endometriotic lesion (MESH:D009059), pain (MESH:D010146), DIE (MESH:D004715), E-MenSCs (MESH:D016751), Inflammation (MESH:D007249), fibrosis (MESH:D005355), anxiety (MESH:D001007), behavioral disorders (MESH:D001523), lung cancer (MESH:D008175), Cancer (MESH:D009369)
- **Chemicals:** DC (MESH:D003841), lipid (MESH:D008055), DHT (MESH:D013196), retinoic acid (MESH:D014212), cAMP (MESH:D000242), progesterone (MESH:D011374)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12916566/full.md

## References

120 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916566/full.md

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Source: https://tomesphere.com/paper/PMC12916566