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Updated: Aug 19, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
Role of transforming growth factor Beta in human cancer
Rebecca L Elliott1, Gerard C Blobe
1Department of Medicine and Pharmacology and Cancer Biology, Duke University Medical Center, 221 BMSRB Research Drive, Box 2631 DUMC, Durham, NC 27710, USA.
Abstract:
Transforming growth factor beta (TGF-beta) is a ubiquitous and essential regulator of cellular and physiologic processes including proliferation, differentiation, migration, cell survival, angiogenesis, and immunosurveillance. Alterations in the TGF-beta signaling pathway, including mutation or deletion of members of the signaling pathway and resistance to TGF-beta-mediated inhibition of proliferation are frequently observed in human cancers. Although these alterations define a tumor suppressor role for the TGF-beta pathway in human cancer, TGF-beta also mediates tumor-promoting effects, either through differential effects on tumor and stromal cells or through a fundamental alteration in the TGF-beta responsiveness of the tumor cells themselves. TGF-beta and members of the TGF-beta signaling pathway are being evaluated as prognostic or predictive markers for cancer patients. Ongoing advances in understanding the TGF-beta signaling pathway will enable targeting of this pathway for the chemoprevention and treatment of human cancers.
Insights
Transforming growth factor beta (TGF-beta) signaling is crucial for cell regulation but is altered in cancer. Understanding its dual role is key for developing new cancer treatments.
Area of Science:
- Cell Biology
- Molecular Biology
- Oncology
Background:
- Transforming growth factor beta (TGF-beta) is a critical regulator of fundamental cellular processes like proliferation, differentiation, migration, cell survival, angiogenesis, and immunosurveillance.
- Dysregulation of the TGF-beta signaling pathway, including mutations and resistance to its inhibitory effects, is common in human cancers, implicating it in tumor suppression.
Purpose of the Study:
- To explore the multifaceted role of TGF-beta signaling in cancer, considering both its tumor-suppressive and tumor-promoting functions.
- To evaluate the potential of TGF-beta pathway components as prognostic and predictive markers in cancer patients.
- To highlight the implications of ongoing research in targeting the TGF-beta pathway for cancer chemoprevention and therapy.
Main Methods:
- Review and synthesis of existing literature on TGF-beta signaling in cellular physiology and cancer.
- Analysis of studies investigating alterations in the TGF-beta pathway in various human cancers.
- Examination of research on the dual role of TGF-beta in tumor progression and suppression.
- Evaluation of current and emerging therapeutic strategies targeting the TGF-beta pathway.
Main Results:
- Alterations in the TGF-beta pathway are frequently observed in human cancers, often associated with a loss of its tumor suppressor functions.
- TGF-beta exhibits a complex, context-dependent role in cancer, mediating both tumor suppression and promotion through differential effects on tumor and stromal cells.
- Components of the TGF-beta pathway are being investigated as valuable prognostic and predictive biomarkers for cancer patients.
Conclusions:
- The TGF-beta signaling pathway plays a complex and often contradictory role in cancer development and progression.
- Targeting the TGF-beta pathway holds significant promise for the future chemoprevention and treatment of human cancers.
- Further research into the intricate mechanisms of TGF-beta signaling is essential for optimizing therapeutic strategies.
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