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Microrna Cluster 7/17/155 As a Potential Driver for High-Grade Breast Tumors Transformation Through Egfr-Associated Emt Publisher



Khodayari S ; Khodayari H ; Jalali H ; Saeedi E ; Muhammadnejad A ; Dashtkoohi M ; Emami Razavi A ; Yeganeh M ; Shirkoohi R ; Miri S R ; Omranipour R ; Mahmoodzadeh H
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Source: Frontiers in Cell and Developmental Biology Published:2026


Abstract

Background – Breast tumor dedifferentiation and progression onto high-grade states with stem-like fea-tures are governed by complex regulatory networks within the tumor microenvironment. This study aimed to identify a potential microRNA (miRNA) cluster associated with breast tumor stemness and in-vestigate its regulatory functions inspired by mammary gland development (MGD). Methods – We reana-lyzed microarray data and identified differentially expressed mRNAs and miRNAs in breast cancer of various grades. High-throughput transcriptomic datasets were incorporated to strengthen the discovery framework. Spatial mRNA–miRNA interactions in each breast cancer grade were identified, and a series of q-PCR, immunohistochemical analysis of epidermal growth factor receptor (EGFR) expression, and Single-cell RNA sequencing were used to validate findings. Results – MGD-related regulatory mecha-nisms correlated with well- and moderately-differentiated tumors but were absent in high-grade tumors. miRNAs 7, 17, and 155 were significantly upregulated in undifferentiated high-grade tumors. These tu-mors also showed marked activation of EGFR-mediated epithelial-mesenchymal transition (EMT) and elevated histological EGFR levels. scRNA-seq revealed a stem cell-like and undifferentiated cellular pop-ulation characterized by miRNAs 7, 17, and 155, as well as EGFR-associated EMT activation. Pseudotemporal trajectory analysis indicated this cluster as a potential origin of malignant breast tumor heterogeneity and stemness. Conclusion – The miRNA cluster 7/17/155 may act as a potential driver of breast tumor dedifferentiation and acquisition of stem-like properties via EGFR-mediated EMT. This cluster represents a promising target for therapies to reverse tumor dedifferentiation and a biomarker for molecular classification of breast tumor differentiation status. Copyright © 2026 Khodayari, Khodayari, Jalali, Saeedi, Muhammadnejad, Dashtkoohi, Emami Razavi, Yeganeh, Shirkoohi, Miri, Omranipour and Mahmoodzadeh.
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