4.5 Review

PML tumour suppression and beyond: Therapeutic implications

Journal

FEBS LETTERS
Volume 588, Issue 16, Pages 2653-2662

Publisher

WILEY
DOI: 10.1016/j.febslet.2014.02.007

Keywords

Promyelocytic leukemia; Promyelocytic leukemia protein; PML nuclear bodies; Isoform; Tumour suppression

Funding

  1. NHMRC [1026990, 1026988, 1049179, 1063389]
  2. NHMRC Fellowship [9628426]
  3. VESKI award
  4. CASS Foundation
  5. National Health and Medical Research Council of Australia [1063389] Funding Source: NHMRC

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Recognition of the tumour suppressive capacity of the Promyelocytic Leukemia protein (PML) has emerged beyond its identification through APL, to a broad spectrum of tumors. This ability has chiefly been linked to its role as a core component of dynamic structures termed PML Nuclear Bodies (PML-NBs). In response to a variety of stresses, key factors and their molecular modifiers are recruited to PML-NBs, where activating modifications are facilitated, leading to a cellular stress response. PML was also found to perform anti-tumourigenic functions through cytoplasmic activities. Surprisingly, important recent research defined growth promoting capabilities of PML, which significantly challenges the notion of a 'classic' tumour suppressor. Through metabolic reprogramming, PML can afford a selective advantage for tumor cells in certain settings. The multiple forms in which PML exists are the likely explanation of this functional diversity. This behavioral ambiguity however raises a significant challenge to the design of strategies to therapeutically target PML In this review we discuss this change of paradigm in the PML field and its ramifications, particularly for tailoring cancer therapies. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

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