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Repression of miR-17-5p with elevated expression of E2F-1 and c-MYC in non-metastatic hepatocellular carcinoma and enhancement of cell growth upon reversing this expression pattern

  • H. M. El Tayebi
  • , K. Omar
  • , S. Hegy
  • , M. El Maghrabi
  • , M. El Brolosy
  • , K. A. Hosny
  • , G. Esmat
  • , A. I. Abdelaziz
  • German University in Cairo
  • Cairo University

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

E2F-1, c-MYC, and miR-17-5p is a triad of two regulatory loops: a negative and a positive loop, where c-MYC induces the expression of E2F-1 that induces the expression of miR-17-5p which in turn reverses the expression of E2F-1 to close the loop. In this study, we investigated this triad for the first time in hepatocellular carcinoma (HCC), where miR-17-5p showed a significant down-regulation in 23 non-metastatic HCC biopsies compared to 10 healthy tissues; however, E2F-1 and c-MYC transcripts were markedly elevated. Forced over-expression of miR-17-5p in HuH-7 cells resulted in enhanced cell proliferation, growth, migration and clonogenicity with concomitant inhibition of E2F-1 and c-MYC transcripts expressions, while antagomirs of miR-17-5p reversed these events. In conclusion, this study revealed a unique pattern of expression for miR-17-5p in non-metastatic HCC patients in contrast to metastatic HCC patients. In addition we show that miR-17-5p is the key player among the triad that tumor growth and spread.

Original languageEnglish
Pages (from-to)421-427
Number of pages7
JournalBiochemical and Biophysical Research Communications
Volume434
Issue number3
DOIs
StatePublished - May 10 2013

Keywords

  • c-MYC
  • E2F-1
  • miR-17-5p
  • Non-metastatic hepatocellular carcinoma

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