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 language | English |
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Pages (from-to) | 246-254 |
Number of pages | 9 |
Journal | Cell Death and Differentiation |
Volume | 17 |
Issue number | 2 |
DOIs | |
Publication status | Published - Feb 2010 |
Keywords
- Apoptosis
- Cell proliferation
- ER-a
- Human BC
- MiR-145
- TP53
ASJC Scopus subject areas
- Cell Biology
- Molecular Biology