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Published on: December 30, 2025
Integration of interferon-alpha/beta signalling to p53 responses in tumour suppression and antiviral defence
Akinori Takaoka1, Sumio Hayakawa, Hideyuki Yanai
1Department of Immunology, Faculty of Medicine and Graduate School of Medicine, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
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.
Insights
Interferon-alpha/beta (IFN-alpha/beta) enhances the tumor suppressor p53
Area of Science:
- Immunology
- Molecular Biology
- Cancer Research
Background:
- The tumor suppressor p53 and interferon-alpha/beta (IFN-alpha/beta) are critical for eliminating cancerous and virally infected cells.
- The precise relationship between p53 and IFN-alpha/beta in these processes remains largely undefined.
Purpose of the Study:
- To investigate the interrelationship between p53 and IFN-alpha/beta signaling.
- To elucidate the role of this interaction in tumor suppression and antiviral immunity.
Main Methods:
- Analysis of p53 gene transcription and protein levels following IFN-alpha/beta treatment.
- Assessment of p53 activation in response to stress signals in the presence of IFN-alpha/beta.
- Evaluation of the impact of p53 induction by IFN-alpha/beta on tumor suppression and antiviral defense.
Main Results:
- IFN-alpha/beta treatment significantly induces p53 gene transcription and increases p53 protein levels.
- IFN-alpha/beta signaling potentiates p53 responses to cellular stress signals, rather than directly activating p53.
- p53 activation by IFN-alpha/beta contributes to tumor suppression and is crucial for effective antiviral immune responses.
Conclusions:
- A novel link exists between p53 and IFN-alpha/beta, highlighting their synergistic roles in tumor suppression and antiviral immunity.
- This interplay between p53 and IFN-alpha/beta offers potential therapeutic strategies for cancer and viral infections.
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