4.8 Article

Tumour-suppression function of KLF12 through regulation of anoikis

Journal

ONCOGENE
Volume 35, Issue 25, Pages 3324-3334

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/onc.2015.394

Keywords

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Funding

  1. Cancer Research UK, from the European Commission [259770]
  2. European Research Council Advanced Grant RASTARGET
  3. Cancer Research UK [15680] Funding Source: researchfish
  4. The Francis Crick Institute [10070, 10071, 10074, 10002] Funding Source: researchfish

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Suppression of detachment-induced cell death, known as anoikis, is an essential step for cancer metastasis to occur. We report here that expression of KLF12, a member of the Kruppel-like family of transcription factors, is downregulated in lung cancer cell lines that have been selected to grow in the absence of cell adhesion. Knockdown of KLF12 in parental cells results in decreased apoptosis following cell detachment from matrix. KLF12 regulates anoikis by promoting the cell cycle transition through S phase and therefore cell proliferation. Reduced expression levels of KLF12 results in increased ability of lung cancer cells to form tumours in vivo and is associated with poorer survival in lung cancer patients. We therefore identify KLF12 as a novel metastasis-suppressor gene whose loss of function is associated with anoikis resistance through control of the cell cycle.

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