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MiR-145 participates with TP53 in a death-promoting regulatory loop and targets estrogen receptor-α in human breast cancer cells

  • R. Spizzo
  • , M. S. Nicoloso
  • , L. Lupini
  • , Y. Lu
  • , J. Fogarty
  • , S. Rossi
  • , B. Zagatti
  • , M. Fabbri
  • , A. Veronese
  • , X. Liu
  • , R. Davuluri
  • , C. M. Croce
  • , G. Mills
  • , M. Negrini
  • , G. A. Calin
  • University of Texas Health Science Center at Houston
  • University of Ferrara
  • Ohio State University

Research output: Contribution to journalArticlepeer-review

237 Scopus citations

Abstract

Understanding the consequences of miR-145 reintroduction in human breast cancer (BC) could reveal its tumor-suppressive functions and may disclose new aspects of BC biology. Therefore, we characterized the effects of miR-145 re-expression in BC cell lines by using proliferation and apoptosis assays. As a result, we found that miR-145 exhibited a pro-apoptotic effect, which is dependent on TP53 activation, and that TP53 activation can, in turn, stimulate miR-145 expression, thus establishing a death-promoting loop between miR-145 and TP53. We also found that miR-145 can downregulate estrogen receptor-α (ER-α) protein expression through direct interaction with two complementary sites within its coding sequence. In conclusion, we described a tumor suppression function of miR-145 in BC cell lines, and we linked miR-145 to TP53 and ER-α. Moreover, our findings support a view that miR-145 re-expression therapy could be mainly envisioned in the specific group of patients with ER-α-positive and/or TP53 wild-type tumors.

Original languageEnglish
Pages (from-to)246-254
Number of pages9
JournalCell Death and Differentiation
Volume17
Issue number2
DOIs
StatePublished - Feb 2010

Keywords

  • Apoptosis
  • Cell proliferation
  • ER-a
  • Human BC
  • MiR-145
  • TP53

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