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      Emerging roles of p53 and other tumour-suppressor genes in immune regulation

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          Abstract

          Tumour-suppressor genes are indispensable for the maintenance of genomic integrity. Recently, several of these genes, including p53, PTEN, RB1 and ARF, have been implicated in immune responses and inflammatory diseases. In particular, the p53 tumour-suppressor pathway is involved in crucial aspects of tumour immunology and in homeostatic regulation of immune responses. Other studies have identified roles for p53 in various cellular processes, including metabolism and stem cell maintenance. Here, we discuss the emerging roles of p53 and other tumour-suppressor genes in tumour immunology as well as in additional immunological settings, such as virus infection. This relatively unexplored area could yield important insights into the homeostatic control of immune cells in health and disease, and facilitate the development of more effective immunotherapies. Consequently, tumour-suppressor genes are emerging as potential guardians of immune integrity.

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          Author and article information

          Journal
          101124169
          27017
          Nat Rev Immunol
          Nat. Rev. Immunol.
          Nature reviews. Immunology
          1474-1733
          1474-1741
          25 January 2017
          26 September 2016
          December 2016
          24 February 2017
          : 16
          : 12
          : 741-750
          Affiliations
          [1 ]Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Martinistrasse 52, 20251 Hamburg, Germany
          [2 ]Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Building 149 13 th Street, Charlestown, Massachusetts 02129, USA
          [3 ]Harvard Stem Cell Institute, 7 Divinity Avenue Cambridge, MA 02138, USA
          [4 ]Department of Oncological Sciences, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, New York 10029, USA
          [5 ]Broad Institute of Harvard and MIT, 7 Cambridge Center, Cambridge, MA 02142, USA
          Author notes
          Article
          PMC5325695 PMC5325695 5325695 nihpa845193
          10.1038/nri.2016.99
          5325695
          27667712
          973e3b38-5f73-4474-88b2-d1a531304c70
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