New regulatory mechanisms of TGF-beta receptor function
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Updated: Jun 21, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
Jong Seok Kang1, Cheng Liu, Rik Derynck
1Department of Cell and Tissue Biology, University of California - San Francisco, San Francisco, CA 94143, USA.
Abstract:
Transforming growth factor-beta (TGF-beta) regulates cell proliferation, differentiation and apoptosis, and TGF-beta-related proteins have key roles in development, tissue homeostasis and disease. Upon binding to their cell surface receptors, TGF-beta family proteins signal through Smads to induce changes in gene expression. TGF-beta-induced Smad signaling and additional non-Smad pathways have been studied extensively in an effort to understand the complex and versatile responses to TGF-beta family proteins. Recently, it has become increasingly apparent that the signaling responses are also extensively defined by regulatory mechanisms at the level of the receptors themselves. Here, we discuss recent insights into the effects of post-translational modifications, protein associations and mode of internalization on the functions of the TGF-beta receptors and their signaling responses.
Insights
Transforming growth factor-beta (TGF-beta) regulates cell functions via its receptors. Recent research reveals post-translational modifications, protein associations, and internalization significantly impact TGF-beta receptor signaling pathways.
Area of Science:
- Cellular biology
- Molecular signaling
- Biochemistry
Background:
- Transforming growth factor-beta (TGF-beta) is crucial for cell proliferation, differentiation, and apoptosis.
- TGF-beta signaling pathways are vital in development, tissue homeostasis, and disease.
- Smad and non-Smad pathways mediate TGF-beta's diverse cellular responses.
Purpose of the Study:
- To explore how regulatory mechanisms at the TGF-beta receptor level influence signaling.
- To discuss recent findings on post-translational modifications, protein associations, and receptor internalization.
- To provide insights into the complex regulation of TGF-beta receptor function.
Main Methods:
- Review of recent scientific literature on TGF-beta receptor signaling.
- Analysis of studies investigating post-translational modifications of TGF-beta receptors.
- Examination of research on protein-protein interactions involving TGF-beta receptors.
- Evaluation of studies on the role of receptor internalization in TGF-beta signaling.
Main Results:
- Post-translational modifications critically affect TGF-beta receptor activity and downstream signaling.
- Interactions with other proteins modulate TGF-beta receptor complex assembly and signal transduction.
- The mode of TGF-beta receptor internalization influences the nature and duration of signaling responses.
- These receptor-level regulations add complexity to the understanding of TGF-beta's versatile roles.
Conclusions:
- TGF-beta receptor regulation through modifications, associations, and internalization is key to understanding its diverse functions.
- These mechanisms provide critical layers of control over TGF-beta-mediated cellular processes.
- Further research into these regulatory aspects is essential for comprehending TGF-beta's role in health and disease.
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