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Emerging Roles of P53 and Other Tumour-suppressor Genes in Immune Regulation

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Journal Nat Rev Immunol
Date 2016 Nov 8
PMID 27667712
Citations 198
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Abstract

Tumour-suppressor genes are indispensable for the maintenance of genomic integrity. Recently, several of these genes, including those encoding 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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References
1.
Sharma P, Allison J . Immune checkpoint targeting in cancer therapy: toward combination strategies with curative potential. Cell. 2015; 161(2):205-14. PMC: 5905674. DOI: 10.1016/j.cell.2015.03.030. View

2.
He X, Xiang C, Zhang C, Xie Y, Chen L, Zhang G . p53 in the Myeloid Lineage Modulates an Inflammatory Microenvironment Limiting Initiation and Invasion of Intestinal Tumors. Cell Rep. 2015; 13(5):888-97. DOI: 10.1016/j.celrep.2015.09.045. View

3.
Jones R, Plas D, Kubek S, Buzzai M, Mu J, Xu Y . AMP-activated protein kinase induces a p53-dependent metabolic checkpoint. Mol Cell. 2005; 18(3):283-93. DOI: 10.1016/j.molcel.2005.03.027. View

4.
Menendez D, Shatz M, Resnick M . Interactions between the tumor suppressor p53 and immune responses. Curr Opin Oncol. 2012; 25(1):85-92. DOI: 10.1097/CCO.0b013e32835b6386. View

5.
Sherr C . Divorcing ARF and p53: an unsettled case. Nat Rev Cancer. 2006; 6(9):663-73. DOI: 10.1038/nrc1954. View