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HIPK2 as a Novel Regulator of Fibrosis
Alessia Garufi1, Giuseppa Pistritto2, Gabriella D'Orazi1,3
1Unit of Cellular Networks, Department of Research and Advanced Technologies, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
Abstract:
Fibrosis is an unmet medical problem due to a lack of evident biomarkers to help develop efficient targeted therapies. Fibrosis can affect almost every organ and eventually induce organ failure. Homeodomain-interacting protein kinase 2 (HIPK2) is a protein kinase that controls several molecular pathways involved in cell death and development and it has been extensively studied, mainly in the cancer biology field. Recently, a role for HIPK2 has been highlighted in tissue fibrosis. Thus, HIPK2 regulates several pro-fibrotic pathways such as Wnt/β-catenin, TGF-β and Notch involved in renal, pulmonary, liver and cardiac fibrosis. These findings suggest a wider role for HIPK2 in tissue physiopathology and highlight HIPK2 as a promising target for therapeutic purposes in fibrosis. Here, we will summarize the recent studies showing the involvement of HIPK2 as a novel regulator of fibrosis.
Insights
Homeodomain-interacting protein kinase 2 (HIPK2) is emerging as a key regulator in fibrosis, impacting multiple organs. Targeting HIPK2 offers a promising therapeutic strategy for treating fibrotic diseases and preventing organ failure.
Area of Science:
- Molecular Biology
- Cellular Biology
- Pathophysiology
Background:
- Fibrosis is a significant unmet medical need, often leading to organ failure due to a lack of targeted therapies and biomarkers.
- Homeodomain-interacting protein kinase 2 (HIPK2) is a protein kinase with established roles in cell death and development, primarily studied in cancer biology.
Purpose of the Study:
- To summarize recent findings on the involvement of HIPK2 in regulating tissue fibrosis.
- To highlight HIPK2 as a potential therapeutic target for fibrotic diseases.
Main Methods:
- Review of recent scientific literature and studies.
- Analysis of HIPK2's role in established pro-fibrotic molecular pathways.
Main Results:
- HIPK2 has been recently identified as a novel regulator in tissue fibrosis.
- HIPK2 modulates key pro-fibrotic pathways including Wnt/β-catenin, TGF-β, and Notch.
- HIPK2's influence extends to renal, pulmonary, liver, and cardiac fibrosis.
Conclusions:
- HIPK2 plays a significant role in the pathophysiology of various fibrotic conditions.
- HIPK2 represents a promising therapeutic target for developing novel anti-fibrotic treatments.
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