# The pro-tumorigenic roles of granzyme B: mechanisms and therapeutic implications

**Authors:** Yubi Zhang, Han Huang, Linjun Xie, Chunhong Li, Xiangyu Zhou

PMC · DOI: 10.3389/fimmu.2025.1733793 · Frontiers in Immunology · 2026-01-06

## TL;DR

Granzyme B, once seen as a tumor fighter, is now known to help tumors grow through various mechanisms, suggesting new ways to target it in cancer treatment.

## Contribution

This paper identifies the pro-tumorigenic roles of GZMB beyond immune cells, offering new insights into its therapeutic implications.

## Key findings

- GZMB from multiple immune and tumor cells promotes tumor initiation and progression.
- GZMB contributes to tumor growth via extracellular matrix remodeling, epithelial-mesenchymal transition, and angiogenesis.
- The paper highlights the clinical significance of GZMB for developing holistic anti-tumor therapies.

## Abstract

Granzyme B (GZMB) is an effector molecule primarily expressed by cytotoxic T lymphocytes (CTLs) and natural killer (NK) cells. Historically, GZMB expression levels have served as a marker of immune activity, indicative of the potency of anti-tumor immunity. However, recent evidence increasingly demonstrates that GZMB also exerts immunosuppressive effects within the tumor microenvironment. Beyond CTLs and NK cells, GZMB derived from multiple immune and tumor cells promotes tumor initiation and progression by regulating biological processes such as extracellular matrix remodeling, epithelial-mesenchymal transition, and angiogenesis. This paper summarizes the pro-tumor sources and mechanisms of GZMB, providing a comprehensive understanding of its clinical significance to guide more holistic GZMB-based anti-tumor therapies.

## Linked entities

- **Genes:** GZMB (granzyme B) [NCBI Gene 3002]

## Full-text entities

- **Genes:** GZMB (granzyme B) [NCBI Gene 3002] {aka C11, CCPI, CGL-1, CGL1, CSP-B, CSPB}
- **Diseases:** tumor (MESH:D009369), tumorigenic (MESH:D002471)

## Full text

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## Figures

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## References

103 references — full list in the complete paper: https://tomesphere.com/paper/PMC12816280/full.md

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Source: https://tomesphere.com/paper/PMC12816280