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The functions and regulation of the PTEN tumour suppressor

Journal

NATURE REVIEWS MOLECULAR CELL BIOLOGY
Volume 13, Issue 5, Pages 283-296

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrm3330

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Funding

  1. Canadian Institutes of Health Research
  2. Human Frontier Science Program
  3. US National Institutes of Health (NIH) [R01 CA-82328-09]

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The importance of the physiological function of phosphatase and tensin homologue (PTEN) is illustrated by its frequent disruption in cancer. By suppressing the phosphoinositide 3-kinase (PI3K)-AKT-mammalian target of rapamycin (mTOR) pathway through its lipid phosphatase activity, PTEN governs a plethora of cellular processes including survival, proliferation, energy metabolism and cellular architecture. Consequently, mechanisms regulating PTEN expression and function, including transcriptional regulation, post-transcriptional regulation by non-coding RNAs, post-translational modifications and protein-protein interactions, are all altered in cancer. The repertoire of PTEN functions has recently been expanded to include phosphatase-independent activities and crucial functions within the nucleus. Our increasing knowledge of PTEN and pathologies in which its function is altered will undoubtedly inform the rational design of novel therapies.

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