# TGF-β in hematologic malignancies: molecular functions and clinical applications

**Authors:** Ruiyang Li, Fang Wei, Mengbo Yang

PMC · DOI: 10.3389/fimmu.2026.1728730 · Frontiers in Immunology · 2026-02-26

## TL;DR

This review explores how TGF-β contributes to blood cancers and how targeting it could improve immunotherapy.

## Contribution

The paper provides a comprehensive overview of TGF-β's role in hematologic malignancies and its therapeutic potential.

## Key findings

- TGF-β is highly expressed in leukemia, lymphoma, and multiple myeloma.
- TGF-β promotes immunosuppression and drug resistance in cancer cells.
- Targeting TGF-β signaling shows promise in preclinical and early clinical studies.

## Abstract

Transforming growth factor-β (TGF-β) represents a family of multifunctional cytokines, primarily secreted by megakaryocytes, monocytes, T lymphocytes, bone marrow stromal cells, and other cell types. TGF-β plays an essential role in various physiological processes, including the regulation of cell proliferation, differentiation, apoptosis, and immune homeostasis. As a key immunoregulatory cytokine, TGF-β contributes to an immunosuppressive network within the microenvironment of hematologic malignancies by modulating the functions of both adaptive and innate immune cells. Current studies have shown that TGF-β is often highly expressed in major hematologic malignancies such as leukemia, lymphoma, and multiple myeloma (MM). It not only enhances immunosuppression by inhibiting effector T cell activation but also regulates tumor cell proliferation, apoptosis, and drug resistance. Meanwhile, strategies targeting the TGF-β signaling pathway have shown potential to improve immunotherapy responses in preclinical models of hematologic malignancies. Several such agents have now entered early-phase clinical trials, offering a promising direction for enhancing the efficacy of immunotherapy in these diseases. In this review, we outline the molecular mechanisms of TGF-β biosynthesis, activation, and signal transduction, discuss its functions across various immune cell types, and summarize recent progress and challenges in clinical research on TGF-β targeted therapies for hematologic disorders, with the aim of providing new perspectives for related treatment strategies.

## Linked entities

- **Proteins:** TGFB1 (transforming growth factor beta 1)
- **Diseases:** leukemia (MONDO:0004355), lymphoma (MONDO:0003659), multiple myeloma (MONDO:0009693)

## Full-text entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}
- **Diseases:** MM (MESH:D009101), leukemia (MESH:D007938), hematologic disorders (MESH:D006402), tumor (MESH:D009369), lymphoma (MESH:D008223), hematologic malignancies (MESH:D019337)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12979174/full.md

## References

134 references — full list in the complete paper: https://tomesphere.com/paper/PMC12979174/full.md

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Source: https://tomesphere.com/paper/PMC12979174