Tumor-Suppressor Functions of the TP53 Pathway

  1. Gemma L. Kelly1,2
  1. 1The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia
  2. 2Department of Medical Biology, University of Melbourne, Parkville, Victoria 3050, Australia
  3. 3Department of Clinical Haematology and Bone Marrow Transplant Service, The Royal Melbourne Hospital, Parkville, Victoria 3050, Australia
  1. Correspondence: strasser{at}wehi.edu.au; gkelly{at}wehi.edu.au

Abstract

The fundamental biological importance of the Tp53 gene family is highlighted by its evolutionary conservation for more than one billion years dating back to the earliest multicellular organisms. The TP53 protein provides essential functions in the cellular response to diverse stresses and safeguards maintenance of genomic integrity, and this is manifest in its critical role in tumor suppression. The importance of Tp53 in tumor prevention is exemplified in human cancer where it is the most frequently detected genetic alteration. This is confirmed in animal models, in which a defective Tp53 gene leads inexorably to cancer development, whereas reinstatement of TP53 function results in regression of established tumors that had been initiated by loss of TP53. Remarkably, despite extensive investigation, the specific mechanisms by which TP53 acts as a tumor suppressor are yet to be fully defined. We review the history and current standing of efforts to understand these mechanisms and how they complement each other in tumor suppression.

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