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Updated: Jun 13, 2025

High-throughput Quantitative Real-time RT-PCR Assay for Determining Expression Profiles of Types I and III Interferon Subtypes
Published on: March 24, 2015
The curious case of type I interferon signaling in cancer
Abu Sufiyan Chhipa1, Valentina Boscaro2, Margherita Gallicchio2
1Department of Pharmacology, Institute of Pharmacy, Nirma University, 382481 Ahmedabad, India; Department of Drug Science and Technology, University of Turin, 10125 Turin, Italy.
Insights
Interferon-1 (IFN-1) cytokines have dual roles in cancer. Acute IFN-1 signaling suppresses tumors, while chronic signaling can promote tumor growth by altering cellular pathways.
Area of Science:
- Immunology
- Cancer Biology
- Molecular Signaling
Background:
- Cytokines mediate tumor microenvironment (TME) cell communication.
- Interferon-1 (IFN-1) cytokines exhibit known tumor suppressive mechanisms.
- IFN-1 can also promote tumor growth in certain contexts.
Purpose of the Study:
- To review the dual anti- and pro-tumor actions of IFN-1 signaling.
- To explore how acute versus chronic IFN-1 activation impacts TME.
- To identify strategies for leveraging IFN-1's anti-tumor potential.
Main Methods:
- Literature review of IFN-1 signaling in the TME.
- Analysis of downstream pathway alterations under acute and chronic IFN-1 activation.
- Discussion of therapeutic strategies targeting IFN-1 pathways.
Main Results:
- Acute IFN-1 signaling activation demonstrates tumor-inhibiting functions.
- Chronic IFN-1 signaling activation can lead to tumor-promoting protein expression.
- Downstream signaling changes mediate the pro-tumor effects of constitutive IFN-1 signaling.
Conclusions:
- The context of IFN-1 signaling activation (acute vs. chronic) dictates its role in cancer.
- Understanding these dual roles is crucial for effective cancer therapy.
- Strategies to overcome chronic IFN-1 detrimental effects are needed to harness its anti-tumor benefits.
Abstract:
Cytokines are the crucial signaling proteins that mediate the crosstalks between the cells of tumor microenvironment (TME). Interferon-1 (IFN-1) are the important cytokines that are widely known for their tumor suppressive roles comprising of cancer cell intrinsic and extrinsic mechanisms. Despite having known antitumor effects, IFN-1 are also reported to have tumor promoting functions under varying circumstances. This dichotomy in the functions of IFN-1 is largely attributed to the acute and chronic activation of IFN-1 signaling in TME. The chronic activation of IFN-1 signaling in tumor cells results in altered stimulation of downstream pathways that result in the expression of tumor promoting proteins, while the acute IFN-1 signaling activation maintains its tumor inhibiting functions. In the present review, we have discussed the anti- and pro-tumor actions of IFN-1 signaling under acute and chronic IFN-1 signaling activation. We have also discussed the downstream changes in signaling components that result in tumor supportive functions of a constitutive IFN-1 signaling. We have further discussed the possible strategies to overcome the detrimental effects of chronic IFN-1 pathway activation and to successfully employ IFN-1 for their beneficial anti-tumor effects.
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