Aberrant epithelialization: A plausible factor for the development of endometrial polyps

Pathare, A. D. S.; Lawarde, A.; Täär, K.; Vela Moreno, S.; Apostolov, A.; Modhukur, V.; Tarassova, D.; Sola-Leyva, A.; Salumets, A.; Saare, M.; Peters, M.

doi:10.1101/2025.08.18.670791

bioRxiv · 10.1101/2025.08.18.670791

Aberrant epithelialization: A plausible factor for the development of endometrial polyps

Pathare, A. D. S.·Lawarde, A.·Täär, K.·Vela Moreno, S.·Apostolov, A.·Modhukur, V.·Tarassova, D.·Sola-Leyva, A.·Salumets, A.·Saare, M.·Peters, M.

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Abstract

Endometrial polyps (EPs) are localized overgrowths of endometrial glands and stroma, common in reproductive-age and postmenopausal women, and can cause abnormal uterine bleeding and infertility. Here, we investigated the cellular heterogeneity and molecular mechanisms of EPs by integrating bulk and single-cell RNA sequencing (scRNA-seq) of EPs and adjacent endometrial tissues (adENs) from 12 women. Bulk RNA-seq revealed high transcriptional similarity, with few differentially expressed genes including upregulated KMT2B and DLEC1 and downregulated COL9A1 and RAB3C. ScRNA-seq identified eight major cell clusters, such as stromal, epithelial, endothelial, immune, perivascular, macrophage, B, and ciliated cells. Pseudotime analysis showed aberrant stromal-to-epithelial transitions in EPs, marked by MECOM and EYA2 intermediate clusters, indicating incomplete epithelial maturation. These altered differentiation trajectories may disrupt perivascular and endothelial cell development, contributing to abnormal vascular remodeling in EPs, despite minimal overall transcriptomic changes compared with adENs.

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Pathare, A. D. S., Lawarde, A., Täär, K., Vela Moreno, S., Apostolov, A., Modhukur, V., Tarassova, D., Sola-Leyva, A., Salumets, A., Saare, M., Peters, M.. 2025-08-22. Aberrant epithelialization: A plausible factor for the development of endometrial polyps. https://doi.org/10.1101/2025.08.18.670791

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