Related Experiment Video
Updated: Jun 5, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
Switching TGFβ from a tumor suppressor to a tumor promoter
1Biomedical Research Institute, University of Dundee, Level 5, Ninewells Hospital and Medical School, Dundee, DD1 9SY, United Kingdom. g.j.inman@dundee.ac.uk
Abstract:
TGFβ acts as a potent tumor suppressor and tumor promoter in a context dependent manner. Tumor suppressive functions include inhibition of cell proliferation, induction of apoptosis and regulation of autophagy. As tumors develop they switch their response to TGFβ and utilise this factor as a potent promoter of cell motility, invasion, metastasis and tumor stem cell maintenance. These multifactorial tumor influencing actions of TGFβ involve regulation of an increasing number of signal transduction pathways employing a diverse range of signaling molecules. Understanding the molecular mechanisms of how tumor cells respond to TGFβ and switch their response to this cytokine during disease progression is vital for both the development and the informed use of potentially powerful TGFβ targeted therapeutics.
Insights
Transforming growth factor beta (TGFβ) initially suppresses tumors but later promotes cancer progression, including metastasis. Understanding this dual role is key for developing effective TGFβ-targeted cancer therapies.
Area of Science:
- Oncology
- Molecular Biology
- Cell Signaling
Background:
- Transforming growth factor beta (TGFβ) exhibits context-dependent roles in cancer, acting as both a tumor suppressor and promoter.
- Early tumor suppressive functions include inhibiting cell proliferation and inducing apoptosis.
- Advanced tumors hijack TGFβ signaling to enhance motility, invasion, metastasis, and cancer stem cell maintenance.
Purpose of the Study:
- To elucidate the molecular mechanisms underlying tumor cell responses to TGFβ.
- To understand how TGFβ signaling shifts during cancer progression.
- To inform the development and application of TGFβ-targeted therapeutics.
Main Methods:
- Analysis of TGFβ signaling pathways.
- Investigation of molecular mechanisms in tumor cells.
- Correlation of TGFβ response with disease progression.
Main Results:
- TGFβ's function transitions from tumor suppression to promotion as cancer develops.
- This transition involves complex regulation of multiple signal transduction pathways.
- Tumor cells utilize TGFβ for critical pro-metastatic and stemness functions.
Conclusions:
- Understanding the dynamic role of TGFβ is crucial for cancer therapy.
- Targeting TGFβ requires consideration of its context-dependent functions.
- Further research into molecular mechanisms will optimize TGFβ-targeted drug development.
Related Concept Videos
TGF - β Signaling Pathway
Loss of Tumor Suppressor Gene Functions
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
Loss of Tumor Suppressor Gene Functions
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
Cancer-Critical Genes II: Tumor Suppressor Genes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
Abnormal Proliferation
Cancer-Critical Genes I: Proto-oncogenes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
