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Negative regulation of the deacetylase SIRT1 by DBC1

Author

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  • Wenhui Zhao

    (Institute for Cancer Genetics, Columbia University, 1130 St Nicholas Avenue, New York, New York 10032, USA)

  • Jan-Philipp Kruse

    (Institute for Cancer Genetics, Columbia University, 1130 St Nicholas Avenue, New York, New York 10032, USA)

  • Yi Tang

    (Institute for Cancer Genetics, Columbia University, 1130 St Nicholas Avenue, New York, New York 10032, USA)

  • Sung Yun Jung

    (Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA)

  • Jun Qin

    (Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA)

  • Wei Gu

    (Institute for Cancer Genetics, Columbia University, 1130 St Nicholas Avenue, New York, New York 10032, USA)

Abstract

Linking ageing and cancer The deacetylase SIRT1, the mammalian version of the Sir2 protein that plays a critical role in determining lifespan in yeast, has been implicated in various cellular functions and possibly in tumorigenesis and ageing. The factors regulating SIRT1 are not well known but two groups now report that the tumour suppressor DBC1 is a negative regulator of SIRT1. By inhibiting SIRT1, DBC1 promotes increased acetylation of the tumour suppressor p53 and p53-mediated apoptosis in human cells.

Suggested Citation

  • Wenhui Zhao & Jan-Philipp Kruse & Yi Tang & Sung Yun Jung & Jun Qin & Wei Gu, 2008. "Negative regulation of the deacetylase SIRT1 by DBC1," Nature, Nature, vol. 451(7178), pages 587-590, January.
  • Handle: RePEc:nat:nature:v:451:y:2008:i:7178:d:10.1038_nature06515
    DOI: 10.1038/nature06515
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    Cited by:

    1. Ana M Rojas & Anna Santamaria & Rainer Malik & Thomas Skøt Jensen & Roman Körner & Ian Morilla & David de Juan & Martin Krallinger & Daniel Aaen Hansen & Robert Hoffmann & Jonathan Lees & Adam Reid & , 2012. "Uncovering the Molecular Machinery of the Human Spindle—An Integration of Wet and Dry Systems Biology," PLOS ONE, Public Library of Science, vol. 7(3), pages 1-16, March.

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