4.5 Article Proceedings Paper

The mitochondrial p53 pathway

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
Volume 1787, Issue 5, Pages 414-420

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbabio.2008.10.005

Keywords

p53; Mitochondria; Apoptosis; Transcription; Bcl-2 family; Pathophysiology; Radiosensitivity; Ischemia

Funding

  1. NCI NIH HHS [R01 CA060664-14A1, R01 CA060664] Funding Source: Medline

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p53 is one of the most mutated tumor suppressors in human cancers and as such has been intensively studied for a long time. p53 is a major orchestrator of the cellular response to a broad array of stress types by regulating apoptosis, cell cycle arrest, senescence, DNA repair and genetic stability. For a long time it was thought that these functions of p53 solely rely on its function as a transcription factor, and numerous p53 target genes have been identified [1]. In the last 8 years however, a novel transcription-independent proapoptotic function mediated by the cytoplasmic pool of p53 has been revealed. p53 participates directly in the intrinsic apoptosis pathway by interacting with the multidomain members of the Bcl-2 family to induce mitochondrial outer membrane permeabilization. Our review will discuss these studies, focusing on recent advances in the field. (C) 2008 Elsevier B.V. All rights reserved.

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