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Updated: Aug 15, 2025

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
TGF-β: A novel predictor and target for anti-PD-1/PD-L1 therapy
Ming Yi1,2, Tianye Li3, Mengke Niu1
1Department of Oncology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Abstract:
Transforming growth factor-β (TGF-β) signaling regulates multiple physiological processes, such as cell proliferation, differentiation, immune homeostasis, and wound healing. Besides, TGF-β plays a vital role in diseases, including cancer. Accumulating evidence indicates that TGF-β controls the composition and behavior of immune components in the tumor microenvironment (TME). Advanced cancers leverage TGF-β to reshape the TME and escape immune surveillance. TGF-β-mediated immune evasion is an unfavorable factor for cancer immunotherapy, especially immune checkpoint inhibitors (ICI). Numerous preclinical and clinical studies have demonstrated that hyperactive TGF-β signaling is closely associated with ICI resistance. It has been validated that TGF-β blockade synergizes with ICI and overcomes treatment resistance. TGF-β-targeted therapies, including trap and bispecific antibodies, have shown immense potential for cancer immunotherapy. In this review, we summarized the predictive value of TGF-β signaling and the prospects of TGF-β-targeted therapies for cancer immunotherapy.
Insights
Transforming growth factor-β (TGF-β) signaling promotes cancer immune evasion and resistance to immune checkpoint inhibitors (ICI). Blocking TGF-β with targeted therapies can overcome this resistance, improving cancer immunotherapy outcomes.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- Transforming growth factor-β (TGF-β) signaling is crucial for normal physiological processes.
- Dysregulated TGF-β signaling contributes to various diseases, notably cancer.
- TGF-β influences the tumor microenvironment (TME) and immune cell behavior.
Purpose of the Study:
- To review the role of TGF-β in cancer immune evasion.
- To explore the association between TGF-β signaling and resistance to immune checkpoint inhibitors (ICI).
- To discuss the therapeutic potential of targeting TGF-β in cancer immunotherapy.
Main Methods:
- Literature review of preclinical and clinical studies.
- Analysis of TGF-β's impact on the tumor microenvironment.
- Evaluation of TGF-β blockade strategies in combination with ICI.
Main Results:
- Hyperactive TGF-β signaling is linked to resistance to ICI therapy.
- TGF-β blockade demonstrates synergy with ICI, overcoming treatment resistance.
- Targeted TGF-β therapies show promise for enhancing cancer immunotherapy.
Conclusions:
- TGF-β signaling is a key mechanism for cancer immune evasion.
- Targeting TGF-β represents a promising strategy to improve the efficacy of cancer immunotherapy, particularly for ICI-resistant tumors.
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