4.7 Article

Breast Cancer Subtype-Specific miRNAs: Networks, Impacts, and the Potential for Intervention

Journal

BIOMEDICINES
Volume 10, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/biomedicines10030651

Keywords

microRNA (miRNA); breast cancer; subtype specificity; triple negative breast cancer (TNBC); human epidermal growth factor receptor 2 (HER2); estrogen receptor (ER); progesterone receptor (PR); prognosis

Funding

  1. Cancer Research Training Program from the Beatrice Hunter Cancer Research Institute (BHCRI)
  2. Nova Scotia Graduate Studentship
  3. Canadian Institutes of Health Research (CHIR) [PJT 162313]
  4. Saunders Matthey

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The regulatory and functional roles of non-coding RNAs, especially microRNAs, in cancer are critical. Understanding the altered miRNA landscape in breast cancer is important for revealing breast cancer signaling and identifying potential therapeutic targets.
The regulatory and functional roles of non-coding RNAs are increasingly demonstrated as critical in cancer. Among non-coding RNAs, microRNAs (miRNAs) are the most well-studied with direct regulation of biological signals through post-transcriptional repression of mRNAs. Like the transcriptome, which varies between tissue type and disease condition, the miRNA landscape is also similarly altered and shows disease-specific changes. The importance of individual tumor-promoting or suppressing miRNAs is well documented in breast cancer; however, the implications of miRNA networks is less defined. Some evidence suggests that breast cancer subtype-specific cellular effects are influenced by distinct miRNAs and a comprehensive network of subtype-specific miRNAs and mRNAs would allow us to better understand breast cancer signaling. In this review, we discuss the altered miRNA landscape in the context of breast cancer and propose that breast cancer subtypes have distinct miRNA dysregulation. Further, given that miRNAs can be used as diagnostic and/or prognostic biomarkers, their impact as novel targets for subtype-specific therapy is also possible and suggest important implications for subtype-specific miRNAs.

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