The Genomic Atlas of Breast Cancer — the non-coding theme

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  • GABC update 2020.06.15
  • GABC update 2019.03.20
  • GABC online 2018.08.09
  • Data collection 2018.04.09

About Us

  • Steven Xi Chen:
    steven.chen@miami.edu
  • Yunpeng Zhang:
    YXZ1418@med.miami.edu
  • Peng Wang:
    wpgqy@163.com
  • Shangwei Ning:
    ningsw@ems.hrbmu.edu.cn
  • Xia Li:
    lixia@hrbmu.edu.cn

Detail


Chr chr1
start 150515757
end 150518032
lncRNA name FAL1
entrez id 100874054
hgnc id HGNC:43713
ensg id ENSG00000228126
refseq id NR_051960
methods qPCR, RNA pull-down assay etc.
regulated up-regulated
function description We identified an oncogene, FAL1, we measured the copy number of FAL1 in 99 cancer cell lines using qPCR and observed FAL1 copy-number gain in 46% of the cell lines. We then extracted the FAL1 RNA expression data from the aforementioned custom RNA array containing 40 cancer cell lines and found a significant and positive correlation between the genomic copy-number and RNA expression of FAL1. FAL1 associates with the epigenetic repressor BMI1 and regulates its stability in order to modulate the transcription of a number of genes including CDKN1A. The oncogenic activity of FAL1 is partially attributable to its repression of p21. FAL1-specific siRNAs significantly inhibit tumor growth in vivo.
pubmed id 25203321
year 2014
title A functional genomic approach identifies FAL1 as an oncogenic long noncoding RNA that associates with BMI1 and represses p22 expression in cancer.
drug X
circulating X
survival V

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