articleCancer ResearchOct 15, 2007Closed access

MicroRNA Let-7a Down-regulates MYC and Reverts MYC-Induced Growth in Burkitt Lymphoma Cells

Alfred I. duPont Hospital for Children · Qiagen (United States) · +2 more institutions

PubMed
Indexed incrossrefpubmed

Abstract

Regulation of the MYC oncogene remains unclear. Using 10058-F4, a compound that inhibits MYC-MAX transcription factor, MYC protein and gene expression were down-regulated in Namalwa cells, a Burkitt lymphoma. Compound 10058-F4 decreased MYC mRNA (45%), MYC protein (50%), and cell growth (32%). MYC-MAX transcription factor was disrupted 24 h after treatment, resulting in transcriptional inhibition of target genes. Because microRNAs (miRNA) disrupt mRNA translation, let-7a, let-7b, and mir-98 were selected using bioinformatics for targeting MYC. Inhibition of MYC-MAX transcription factor with 10058-F4 increased levels of members of the let-7 family. In inhibited cells at 24 h, let-7a, let-7b, and mir-98 were…

Citation impact

821
total citations
FWCI
30.25
Percentile
100%
References
52
Citations per year

Authors

9

Topics & keywords

Keywords
  • microRNA
  • Oncogene
  • Messenger RNA
  • Molecular biology
  • Transcription factor
  • Cancer research
  • Gene
  • Transcription (linguistics)
UN Sustainable Development Goals
  • Good health and well-being
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