4.8 Article

Downregulation of the Mitochondrial Calcium Uniporter by Cancer-Related miR-25

Journal

CURRENT BIOLOGY
Volume 23, Issue 1, Pages 58-63

Publisher

CELL PRESS
DOI: 10.1016/j.cub.2012.11.026

Keywords

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Funding

  1. Italian Association for Cancer Research (AIRC)
  2. Telethon [GGP09128, GGP11139B]
  3. University of Ferrara
  4. Italian Ministry of Education, University and Research (COFIN, FIRB, and Futuro in Ricerca)
  5. Italian Cystic Fibrosis Research Foundation
  6. Italian Ministry of Health
  7. Italian Ministry of Health and Ministry of Education, University and Research
  8. European Union (ERC mitoCalcium) [294777, 223576]
  9. National Institutes of Health [1P01AG025532-01A1]
  10. Cariparo Foundation (Padua)
  11. AIRC
  12. Telethon-Italy [GPP1005A, GGP11082]
  13. Italian Ministry of Education, University and Research, FIRB program [RBAP11BYNP]
  14. Regione Emilia Romagna
  15. FIRC fellowship

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The recently discovered mitochondrial calcium uniporter (MCU) promotes Ca2+ accumulation into the mitochondrial matrix [1, 2] We identified in silico miR-25 as a cancer-related MCU-targeting microRNA family and demonstrate that its overexpression in HeLa cells drastically reduces MCU levels and mitochondria! Ca2+ uptake, while leaving other mitochondrial parameters and cytosolic Ca2+ signals unaffected. In human colon cancers and cancer-derived cells, miR-25 is overexpressed and MCU accordingly silenced. miR-25-dependent reduction of mitochondria! Ca2+ uptake correlates with resistance to apoptotic challenges and can be reversed by anti-miR-25 overexpression. Overall, the data demonstrate that microRNA targeting of mitochondrial Ca2+ signaling favors cancer cell survival, thus providing mechanistic insight into the role of mitochondria in tumorigenesis and identifying a novel therapeutic target in neoplasia.

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