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PMID: 12872134 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Integration of interferon-alpha/beta signalling to p53 responses in tumour suppression and antiviral defence.

Nature ·Vol. 424 ·No. 6948 ·2003-07-31 ·Pages 516-23

Takaoka A, Hayakawa S, Yanai H, Stoiber D, Negishi H, Kikuchi H, Sasaki S, Imai K, Shibue T, Honda K, Taniguchi T

Abstract

Swift elimination of undesirable cells is an important feature in tumour suppression and immunity. The tumour suppressor p53 and interferon-alpha and -beta (IFN-alpha/beta) are essential for the induction of apoptosis in cancerous cells and in antiviral immune responses, respectively, but little is known about their interrelationship. Here we show that transcription of the p53 gene is induced by IFN-alpha/beta, accompanied by an increase in p53 protein level. IFN-alpha/beta signalling itself does not activate p53; rather, it contributes to boosting p53 responses to stress signals. We show examples in which p53 gene induction by IFN-alpha/beta contributes to tumour suppression. Furthermore, we show that p53 is activated in virally infected cells to evoke an apoptotic response and that p53 is critical for antiviral defence of the host. Our study reveals a hitherto unrecognized link between p53 and IFN-alpha/beta in tumour suppression and antiviral immunity, which may have therapeutic implications.

MeSH Terms
Animals Apoptosis Cell Transformation, Neoplastic DNA-Binding Proteins/metabolism Gene Expression Regulation, Neoplastic Humans Interferon-Stimulated Gene Factor 3 Interferon-Stimulated Gene Factor 3, gamma Subunit Interferon-alpha/metabolism Interferon-beta/metabolism Mice Mice, Inbred C57BL Neoplasms/immunology,pathology RNA, Messenger/genetics,metabolism Response Elements/genetics Signal Transduction Transcription Factors/metabolism Transcription, Genetic/genetics Transcriptional Activation Tumor Cells, Cultured Tumor Suppressor Protein p53/biosynthesis,genetics,metabolism Vesicular stomatitis Indiana virus/immunology,physiology
Chemicals
DNA-Binding Proteins IRF9 protein, human Interferon-Stimulated Gene Factor 3 Interferon-Stimulated Gene Factor 3, gamma Subunit Interferon-alpha Isgf3g protein, mouse RNA, Messenger Transcription Factors Tumor Suppressor Protein p53 Interferon-beta
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Takaoka Akinori
Department of Immunology, Faculty of Medicine and Graduate School of Medicine, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
Hayakawa Sumio
Yanai Hideyuki
Stoiber Dagmar
Negishi Hideo
Kikuchi Hideaki
Sasaki Shigeru
Imai Kohzoh
Shibue Tsukasa
Honda Kenya
Taniguchi Tadatsugu
Article Info
Journal
Nature
Abbr.
Nature
ISSN
1476-4687
Published
2003-07-31
Pages
516-23
Language
English
Region
England
NLM ID
0410462
Subset
IM
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