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The low expression of miR-1976 in plasma samples indicating its biological functions in the progression of breast cancer.

AbstractBACKGROUND:
The incidence of breast cancer (BC) is the highest among women. Identification of miRNAs as biomarkers may help to improve the diagnosis of BC. The purpose of this study was to assess the expression levels of miR-1976 in plasma samples and the biological functions in the progression of BC.
METHODS:
The expression levels of miR-1976 in plasma samples and tissues were measured by quantitative real-time polymerase chain reaction (qRT-PCR). The associations between the expression levels and clinicopathological features were studied. Cell supernatants were used to simulate circulation. The biological functions of miR-1976 were assessed in vitro and in vivo.
RESULTS:
The expression levels of miR-1976 in plasma samples were found significantly lower in patients with BC than those in healthy controls, and were associated with Ki-67. The expression levels in BC tissues were lower than those in adjacent normal tissues, and were correlated with the number of lymph nodes and Ki-67. The expression levels in BC cell supernatants and cell lines were lower than that in normal human breast epithelial cell line HBL-100. miR-1976 knockdown promoted proliferation in vitro and in vivo.
CONCLUSION:
miR-1976 may serve as a promising non-invasive biomarker for the diagnosis of BC in the future.
AuthorsJ Wang, G Ma, X Han, M Liang, X Wang, T Xia, S Wang
JournalClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico (Clin Transl Oncol) Vol. 22 Issue 11 Pg. 2111-2120 (Nov 2020) ISSN: 1699-3055 [Electronic] Italy
PMID32419112 (Publication Type: Journal Article)
Chemical References
  • MIRN-1976 microRNA, human
  • MicroRNAs
Topics
  • Animals
  • Breast Neoplasms (etiology, genetics, pathology)
  • Cell Line, Tumor
  • Cell Proliferation
  • Disease Progression
  • Exosomes
  • Female
  • Humans
  • Mice
  • Mice, Inbred BALB C
  • MicroRNAs (blood, physiology)

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