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Updated: May 29, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
Inhibitory machinery for the TGF-β family signaling pathway
1Laboratory of Biochemistry, Showa Pharmaceutical University, 3-3165 Higashi-Tamagawagakuen, Machida, Tokyo 194-8543, Japan. sitoh@ac.shoyaku.ac.jp
Abstract:
Transforming growth factor-β (TGF-β) family signaling regulates cell growth and differentiation of many different cell types and is widely involved in the regulation of homeostasis during both embryogenesis and adult life. Therefore, aberrant TGF-β family signal transduction is linked to congenital disorders, tumorigenicity, and fibrosis, which can be life-threatening. A specific receptor-ligand complex initiates transduction of TGF-β family signaling to the nucleus via intracellular signal molecules, mainly Smads, whereby a number of bioactivities such as wound healing, immunomodulation, apoptosis, and angiogenesis are controlled. To avoid an excess of TGF-β family signaling in cells, the duration and intensity of the TGF-β family signal appear to be subject to elaborate regulation. In this paper, we describe recent advances in the understanding of how TGF-β family signals are perturbed and terminated to maintain homeostasis in cells.
Insights
Transforming growth factor-β (TGF-β) signaling is crucial for cell regulation and homeostasis. This study reviews how TGF-β signals are controlled to prevent cellular dysfunction and disease.
Area of Science:
- Cellular biology
- Molecular signaling
- Physiology
Background:
- Transforming growth factor-β (TGF-β) family signaling regulates vital cellular processes including growth, differentiation, and homeostasis.
- Dysregulation of TGF-β signaling is implicated in serious health conditions such as congenital disorders, cancer, and fibrosis.
- TGF-β signal transduction involves receptor-ligand complexes and intracellular Smad molecules, controlling diverse biological activities.
Purpose of the Study:
- To review recent advancements in understanding the regulatory mechanisms of TGF-β family signaling.
- To elucidate how TGF-β signals are perturbed and terminated to maintain cellular homeostasis.
- To provide insights into the control of TGF-β signaling duration and intensity.
Main Methods:
- Literature review of recent research on TGF-β signaling pathways.
- Analysis of molecular mechanisms controlling TGF-β signal transduction and termination.
- Synthesis of current knowledge on homeostasis maintenance through TGF-β signal regulation.
Main Results:
- TGF-β signaling is tightly regulated to maintain cellular balance.
- Elaborate mechanisms exist to control the duration and intensity of TGF-β signals.
- Understanding these regulatory processes is key to addressing diseases linked to TGF-β dysregulation.
Conclusions:
- Proper regulation of TGF-β signaling is essential for preventing diseases like cancer and fibrosis.
- Further research into TGF-β signal termination pathways can offer therapeutic targets.
- Maintaining homeostasis through controlled TGF-β signaling is critical for overall health.
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