Related Experiment Video
Updated: Dec 13, 2025

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
TGFβ biology in cancer progression and immunotherapy
Rik Derynck1,2,3, Shannon J Turley4, Rosemary J Akhurst5,6
1Department of Cell and Tissue Biology, University of California at San Francisco (UCSF), San Francisco, CA, USA. rik.derynck@ucsf.edu.
Abstract:
TGFβ signalling has key roles in cancer progression: most carcinoma cells have inactivated their epithelial antiproliferative response and benefit from increased TGFβ expression and autocrine TGFβ signalling through effects on gene expression, release of immunosuppressive cytokines and epithelial plasticity. As a result, TGFβ enables cancer cell invasion and dissemination, stem cell properties and therapeutic resistance. TGFβ released by cancer cells, stromal fibroblasts and other cells in the tumour microenvironment further promotes cancer progression by shaping the architecture of the tumour and by suppressing the antitumour activities of immune cells, thus generating an immunosuppressive environment that prevents or attenuates the efficacy of anticancer immunotherapies. The repression of TGFβ signalling is therefore considered a prerequisite and major avenue to enhance the efficacy of current and forthcoming immunotherapies, including in tumours comprising cancer cells that are not TGFβ responsive. Herein, we introduce the mechanisms underlying TGFβ signalling in tumours and their microenvironment and discuss approaches to inhibit these signalling mechanisms as well as the use of these approaches in cancer immunotherapies and their potential adverse effects.
Insights
Transforming growth factor beta (TGFβ) signaling fuels cancer progression and hinders immunotherapy. Inhibiting TGFβ signaling is crucial for enhancing cancer treatments and overcoming therapeutic resistance.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- Transforming growth factor beta (TGFβ) signaling is implicated in cancer progression.
- TGFβ signaling promotes tumor cell invasion, stemness, and therapeutic resistance.
- TGFβ in the tumor microenvironment creates an immunosuppressive environment, limiting immunotherapy efficacy.
Purpose of the Study:
- To elucidate the mechanisms of TGFβ signaling in tumors and their microenvironment.
- To discuss strategies for inhibiting TGFβ signaling.
- To explore the application of TGFβ inhibition in cancer immunotherapies.
Main Methods:
- Review of literature on TGFβ signaling pathways in cancer.
- Analysis of TGFβ's role in tumor microenvironment modulation.
- Discussion of therapeutic strategies targeting TGFβ signaling.
Main Results:
- TGFβ signaling supports cancer cell proliferation, invasion, and stem cell properties.
- Tumor-associated TGFβ suppresses anti-tumor immune responses.
- Inhibition of TGFβ signaling can enhance anti-cancer immunity and immunotherapy efficacy.
Conclusions:
- Targeting TGFβ signaling is a promising strategy to improve cancer immunotherapy.
- Understanding TGFβ mechanisms is key to developing effective combination therapies.
- Inhibiting TGFβ signaling may overcome resistance in various cancer types.
Related Concept Videos
TGF - β Signaling Pathway
Tumor Immunotherapy
The Tumor Microenvironment
Mitogens and the Cell Cycle
Tumor Progression
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...

