4.8 Article

Multipolar mitosis of tetraploid cells: inhibition by p53 and dependency on Mos

Journal

EMBO JOURNAL
Volume 29, Issue 7, Pages 1272-1284

Publisher

WILEY
DOI: 10.1038/emboj.2010.11

Keywords

aneuploidy; apoptosis; centrosome; colon carcinoma; mitotic catastrophe

Funding

  1. Ligue Nationale contre le Cancer (Equipe labellisee)
  2. Agence Nationale pour la Recherche, European Commission (Apo-Sys, ChemoRes, ApopTrain)
  3. Fondation pour la Recherche Medicale
  4. Institut National du Cancer
  5. Canceropole Ile-de-France
  6. Association pour la Recherche sur le Cancer (ARC)
  7. European Union
  8. FRM
  9. EMBO

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Tetraploidy can constitute a metastable intermediate between normal diploidy and oncogenic aneuploidy. Here, we show that the absence of p53 is not only permissive for the survival but also for multipolar asymmetric divisions of tetraploid cells, which lead to the generation of aneuploid cells with a near-to-diploid chromosome content. Multipolar mitoses (which reduce the tetraploid genome to a sub-tetraploid state) are more frequent when p53 is down-regulated and the product of the Mos oncogene is upregulated. Mos inhibits the coalescence of supernumerary centrosomes that allow for normal bipolar mitoses of tetraploid cells. In the absence of p53, Mos knockdown prevents multipolar mitoses and exerts genome-stabilizing effects. These results elucidate the mechanisms through which asymmetric cell division drives chromosomal instability in tetraploid cells. The EMBO Journal (2010) 29, 1272-1284. doi:10.1038/emboj.2010.11; Published online 25 February 2010

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