Related Experiment Video
Updated: Apr 17, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
Molecular Mechanism of Activation of Transforming Growth Factor Beta/Smads Signaling Pathway in Ets Related
Jinbo Fang1, Huali Xu1, Chunshu Yang1
1Georgia Cancer Center for Excellence, Cancer Biology Program, Department of OB/GYN, Morehouse School of Medicine, Grady Health System, 80 Jesse Hill Jr. Drive, Atlanta, GA 30303, USA.
Abstract:
Transforming growth factor beta (TGF-β) signaling pathway is involved in diverse cellular processes, including cell proliferation, differentiation, adhesion, apoptosis, and some human diseases including cancer. Smad proteins function as mediators of intracellular signal transduction of TGF-β. Following their phosphorylation by TGF-β receptor I, Smad2 and Smad3 form a heteromeric complex with Smad4 and then are translocated into the nucleus where they bind to other co-factors and regulate the expression of target genes. ERG (Ets Related Gene) belongs to the ETS family of transcriptional factors. Chromosomal rearrangement of TMPRSS2 gene and ERG gene has been found in the majority of prostate cancers. Over-expression of full length or truncated ERG proteins is associated with a higher rate of recurrence and unfavorable prognosis. In this review, we focus on recent understanding of regulation of TGF-β/Smads signaling pathway by ERG proteins in prostate cancer.
Insights
This review explores how the Ets Related Gene (ERG) protein influences the Transforming Growth Factor beta (TGF-β)/Smads signaling pathway. Understanding this interaction is crucial for prostate cancer prognosis and treatment strategies.
Area of Science:
- Molecular Biology
- Cellular Signaling
- Oncology
Background:
- The Transforming Growth Factor beta (TGF-β) pathway regulates critical cellular functions like proliferation and differentiation.
- Smad proteins are key intracellular mediators of TGF-β signaling, translocating to the nucleus to control gene expression.
- The Ets Related Gene (ERG) is an ETS family transcription factor frequently altered in prostate cancer.
Purpose of the Study:
- To review the current understanding of ERG protein's role in regulating the TGF-β/Smads signaling pathway.
- To highlight the implications of this regulation in the context of prostate cancer development and progression.
Main Methods:
- Literature review of recent studies on ERG, TGF-β/Smads signaling, and prostate cancer.
- Analysis of molecular mechanisms linking ERG and TGF-β/Smads pathway components.
- Synthesis of findings related to ERG's impact on TGF-β/Smads activity in prostate cancer.
Main Results:
- ERG proteins can modulate the TGF-β/Smads signaling cascade.
- Overexpression of ERG is linked to adverse outcomes in prostate cancer.
- Specific interactions between ERG and components of the TGF-β/Smads pathway are identified.
Conclusions:
- ERG plays a significant role in regulating TGF-β/Smads signaling within prostate cancer cells.
- This regulatory interplay contributes to prostate cancer's aggressive behavior and recurrence.
- Targeting the ERG-mediated regulation of TGF-β/Smads signaling may offer therapeutic avenues for prostate cancer.
Related Concept Videos
TGF - β Signaling Pathway
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
MAPK Signaling Cascades
Mitogens and the Cell Cycle
The JAK-STAT Signaling Pathway
PI3K/mTOR/AKT Signaling Pathway

