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January 15, 2026BMC Cancer9 citationsOpen Access

Identification of novel exosomal miRNAs and their role in diagnosis and prognosis of triple negative breast cancer

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ACAnanya ChoudharySPSatish S. PoojaryPJPriyanka Jain

Key Points

  • This research aims to identify novel exosomal miRNAs associated with triple negative breast cancer for use as biomarkers.
  • Identification of five exosomal miRNAs in TNBC through integrated meta-analysis and in-vitro validation.
  • Assessment of miRNA expression levels in cancer cells and tissue samples.
  • Functional assays to evaluate effects of miRNAs on cell migration and invasion.
  • Found five exosomal miRNAs consistently overexpressed in TNBC cells and tissues.
  • Elevated expression of miRNAs correlated with poorer overall survival.
  • hsa-miR-1180 and hsa-miR-4728 enhanced cell migration and invasion, implicating oncogenic pathways.

Abstract

Triple-negative breast cancer (TNBC) is a clinically aggressive subtype characterized by poor prognosis and limited therapeutic options. Exosomal microRNAs (miRNAs), enclosed within secretory vesicles, have emerged as promising non-invasive biomarkers for cancer detection and disease monitoring. In this study, we identify a panel of five exosomal miRNAs: hsa-miR-6803, hsa-miR-1180, hsa-miR-4728, hsa-miR-1915, and hsa-miR-940, that are consistently overexpressed in TNBC cells, stem-like subpopulations, and patient tumor tissues. Integrated meta-analysis of public datasets combined with in-vitro validation revealed that elevated expression of these miRNAs correlates with poor overall survival. Functional assays further demonstrated that hsa-miR-1180 and hsa-miR-4728 enhance TNBC cell migration and invasion, implicating them in key oncogenic pathways such as Wnt, Notch, and EGFR. The consistent enrichment of these miRNAs in exosomes underscores their potential as exploratory biomarkers for future liquid-biopsy–based applications. To our knowledge, this discovery-phase investigation is the first to associate this exosomal miRNA panel with TNBC and its stem-like subpopulations, providing a preliminary framework for subsequent mechanistic and translational validation.

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Cite This Study

Choudhary et al. (2026) studied this question.

synapsesocial.com/papers/69683e135818e7dbd7c631aehttps://doi.org/10.1186/s12885-025-15499-6
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