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Updated: Nov 22, 2025

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
Recent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy
1Department of Biochemistry, Lee Gil Ya Cancer and Diabetes Institute, Gachon University College of Medicine, Incheon, Korea.
Abstract:
TGF-β is a multifunctional cytokine that plays an important role in both physiologic and pathologic processes, including cancer. Importantly, TGF-β has a dual role in tumorigenesis, acting as a tumor suppressor or a tumor promoter, depending on the stage of tumor development. The aberrantly upregulated production of TGF-β has been strongly implicated in tumor progression, angiogenesis, and metastasis, as well as immune evasion. Therefore, hyperactivated TGF-β signaling is considered a potential therapeutic target for cancer therapy. Numerous inhibitors of overactivated TGF-β signaling have been developed, and some of them are currently in clinical trials. This review focuses on the TGF-β signaling that contributes to tumor progression and immune evasion in the tumor microenvironment and presents recent achievements on TGF-β signaling inhibition as a single or combined therapeutic approach in cancer therapy.
Insights
Transforming growth factor-beta (TGF-β) has a dual role in cancer. This review highlights TGF-β signaling in tumor progression and immune evasion, exploring therapeutic inhibition strategies for cancer treatment.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- Transforming growth factor-beta (TGF-β) is a key cytokine involved in physiological and pathological processes, including cancer.
- TGF-β exhibits a dual role in tumorigenesis, acting as either a tumor suppressor or promoter based on cancer stage.
- Aberrant TGF-β upregulation is linked to tumor progression, angiogenesis, metastasis, and immune evasion.
Purpose of the Study:
- To review the role of TGF-β signaling in promoting tumor progression and immune evasion within the tumor microenvironment.
- To present recent advancements in TGF-β signaling inhibition as a therapeutic strategy for cancer.
Main Methods:
- Literature review focusing on TGF-β signaling pathways in cancer.
- Analysis of preclinical and clinical studies on TGF-β inhibitors.
Main Results:
- Hyperactivated TGF-β signaling is a significant driver of tumor progression and immune evasion.
- Inhibitors targeting TGF-β signaling show promise as single or combination therapies.
- Several TGF-β inhibitors are currently undergoing clinical trials for cancer treatment.
Conclusions:
- Targeting hyperactivated TGF-β signaling represents a promising therapeutic avenue for cancer.
- Further research into TGF-β inhibition strategies is crucial for developing effective cancer treatments.
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