ReviewFrontiers in oncology2026
Exercise-responsive microRNA networks and extracellular vesicle-mediated microRNA signaling in breast cancer: linking tumor signaling, systemic crosstalk, and clinical relevance.
Review in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
3 authors.
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Abstract
Breast cancer is increasingly recognized as a systemic disease shaped by dynamic interactions between tumor-intrinsic signaling and host physiology. MicroRNAs (miRNAs), as post-transcriptional regulators, extend beyond canonical gene silencing to coordinate oncogenic pathways, tumor microenvironment remodeling, and inter-organ communication. In parallel, exercise has emerged as a systemic modulator capable of influencing immune, metabolic, and circulatory processes relevant to tumor progression. This review integrates current evidence on the interplay between miRNAs and exercise in breast cancer. We examine how miRNA-mediated networks regulate key processes including oncogenic signaling, angiogenesis, hypoxia responses, immune modulation, and metabolic adaptation. Particular attention is given to circulating and extracellular vesicle-associated miRNAs as mediators of systemic signaling, including muscle-tumor crosstalk. Emerging clinical data further support the role of circulating miRNAs as minimally invasive biomarkers for early detection and diagnosis, risk stratification, and monitoring of treatment response, with growing relevance to physical activity, overall health status, and lifestyle-based interventions that integrate exercise and behavioral modification strategies. Overall, this review proposes a systems-oriented framework in which miRNAs may link exercise-induced physiological adaptation to breast cancer biology, providing a foundation for future translational and precision oncology strategies.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.