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Updated: Jul 8, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
The TGFBeta pathway as a therapeutic target in cancer
1Vall d'Hebron Research Institute, Barcelona, Spain. jseoane@ir.vhebron.net
Abstract:
The TGFBeta pathway has recently emerged as a putative therapeutic target against cancer. However, TGFBeta has a complex and dual role in cancer. In normal epithelial cells and early tumours, TGFBeta acts as a tumour suppressor. In contrast, during tumour progression TGFBeta becomes an oncogenic factor inducing proliferation, angiogenesis, invasion and metastasis, as well as suppressing the anti-tumoral immune response. The role of TGFBeta in oncogenesis requires the precise understanding of the TGFBeta pathway in order to design optimal therapeutic approaches and select the patient population that may benefit from an anti-TGFBeta therapy. Here we review the rationale for evaluating TGFBeta signalling inhibitors as cancer therapeutics, and the progress made in the preclinical and clinical testing of anti- TGFBeta compounds.
Insights
Transforming growth factor beta (TGF-β) has a dual role in cancer, acting as a tumor suppressor early on but becoming oncogenic later. Understanding this complex pathway is key for developing effective TGF-β cancer therapies.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Therapeutics
Background:
- The Transforming Growth Factor Beta (TGF-β) pathway plays a complex, context-dependent role in cancer development.
- Initially, TGF-β acts as a tumor suppressor in normal epithelial cells and early-stage tumors.
- However, during tumor progression, TGF-β can promote oncogenesis, driving proliferation, angiogenesis, invasion, and metastasis, while also suppressing anti-tumor immunity.
Purpose of the Study:
- To review the rationale for targeting the TGF-β signaling pathway in cancer therapy.
- To summarize the progress in preclinical and clinical investigations of anti-TGF-β compounds.
Main Methods:
- Literature review of studies on TGF-β signaling in oncogenesis.
- Analysis of preclinical data for TGF-β inhibitors.
- Overview of ongoing and completed clinical trials for anti-TGF-β therapies.
Main Results:
- TGF-β's dual role necessitates careful consideration for therapeutic intervention.
- Preclinical studies show promise for TGF-β inhibitors in specific cancer contexts.
- Clinical trials are evaluating the efficacy and safety of various anti-TGF-β agents.
Conclusions:
- Precise understanding of TGF-β pathway dynamics in oncogenesis is crucial for effective cancer treatment.
- Targeting TGF-β signaling represents a promising therapeutic strategy, requiring patient stratification for optimal benefit.
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