4.5 Article

LINC00473 mediates cyclin D1 expression through a balance between activation and repression signals in breast cancer cells

Journal

FEBS LETTERS
Volume 593, Issue 7, Pages 751-759

Publisher

WILEY
DOI: 10.1002/1873-3468.13353

Keywords

breast cancer; CCND1; FUS; LINC00473; ncRNA(CCND1)s

Funding

  1. Ministry of Science and Technology
  2. National Natural Science Foundation of China [2016YFA0100502, 31471226]
  3. Major/Innovative Program of Development Foundation of Hefei Center for Physical Science and Technology [2018CXFX006]
  4. Fundamental Research Funds for The Central Universities [WK2070000044, WK2070000034]

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Long noncoding RNAs (lncRNAs) are critical regulators in tumorigenesis. However, their roles in breast cancer remain unclear. Here, we found that lncRNA LINC00473 is significantly upregulated in breast cancer cells. Loss- or gain-of-function experiments show that LINC00473 promotes cell proliferation. Mechanistically, LINC00473 is required for the activation of cyclin D1 (CCND1) expression through recruitment of phosphorylated CREB and histone acetylation to the CCND1 promoter. Interestingly, we found that LINC00473 is also required for maintaining the expression levels of the noncoding RNA(CCND1)s and recruiting corepressor FUS to the CCND1 promoter. Altogether, the activation effect of LINC00473 on CCND1 is a net effect of two antagonistic regulatory pathways. Our finding provides a novel lncRNA-mediated precise transcriptional control of CCND1.

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