# The multifaceted role of kallistatin in human diseases: mechanistic insights and translational potential

**Authors:** Minrong Yu, Yanqing Feng, Zhiyan Wu, Suchun Li

PMC · DOI: 10.3389/fcvm.2025.1701235 · Frontiers in Cardiovascular Medicine · 2026-01-05

## TL;DR

Kallistatin is a versatile protein with potential roles in diagnosing and treating various diseases by regulating multiple biological functions.

## Contribution

This review provides a comprehensive synthesis of kallistatin's mechanisms and therapeutic potential across multiple disease contexts.

## Key findings

- Kallistatin protects against cardiovascular diseases by improving endothelial function and reducing inflammation.
- It shows dual roles in inflammatory diseases, both reducing and promoting inflammation depending on the context.
- Lower kallistatin expression in tumors is linked to cancer progression, suggesting its potential as a cancer biomarker.

## Abstract

Kallistatin, a multifunctional serine protease inhibitor, is widely distributed with tissue-specific effects. It may serve as a new diagnostic biomarker and therapeutic target for human diseases. Through binding to its two structural elements and specific receptors, it regulates differential signaling cascades, and thus has a wide spectrum of biological functions. In cardiovascular diseases like hypertension, atherosclerosis, and heart failure, it exerts protective effects by improving endothelial function, anti-inflammation, and regulating lipid metabolism. In liver diseases, high hepatic expression correlates with nonalcoholic fatty liver disease, while decreased serum levels indicate severe cirrhosis or liver fibrosis. In metabolic diseases, it regulates insulin resistance, glucose metabolism, angiogenesis and inflammation. In inflammatory diseases, its role is dual: it attenuates inflammation in rheumatoid arthritis, sepsis, etc., but exacerbates chronic rhinosinusitis and autoimmune uveitis by promoting inflammatory cytokines secretion. In cancer, it inhibits tumor cell proliferation, angiogenesis, and metastasis, with lower tumor tissue expression linked to cancer development. Kallistatin also serves as a potential biomarker for chronic kidney disease, preterm birth, neurodegenerative diseases, and other diseases. This review synthesizes current knowledge on kallistatin's mechanisms in organ injury and repair, emphasizes its therapeutic potential across disease contexts, and discusses challenges and future directions for clinical translation, including organ-targeted strategies and combination therapies.

## Linked entities

- **Proteins:** SERPINA4 (serpin family A member 4)
- **Diseases:** atherosclerosis (MONDO:0005311), heart failure (MONDO:0005252), nonalcoholic fatty liver disease (MONDO:0013209), cirrhosis (MONDO:0005155), rheumatoid arthritis (MONDO:0008383), chronic rhinosinusitis (MONDO:0006031), autoimmune uveitis (MONDO:0031012), cancer (MONDO:0004992), chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** SERPINA4 (serpin family A member 4) [NCBI Gene 5267] {aka KAL, KLST, KST, PI-4, PI4, kallistatin}
- **Diseases:** hypertension (MESH:D006973), neurodegenerative diseases (MESH:D019636), liver fibrosis (MESH:D008103), cancer (MESH:D009369), sepsis (MESH:D018805), cirrhosis (MESH:D005355), rheumatoid arthritis (MESH:D001172), rhinosinusitis (MESH:D000092562), cardiovascular diseases (MESH:D002318), heart failure (MESH:D006333), liver diseases (MESH:D008107), autoimmune uveitis (MESH:D014605), metastasis (MESH:D009362), atherosclerosis (MESH:D050197), preterm birth (MESH:D047928), insulin resistance (MESH:D007333), nonalcoholic fatty liver disease (MESH:D065626), inflammation (MESH:D007249), metabolic diseases (MESH:D008659), chronic kidney disease (MESH:D051436)
- **Chemicals:** glucose (MESH:D005947), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12812646/full.md

## References

122 references — full list in the complete paper: https://tomesphere.com/paper/PMC12812646/full.md

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Source: https://tomesphere.com/paper/PMC12812646