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Updated: Jun 29, 2025

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
Unboxing the network among long non-coding RNAs and TGF-β signaling in cancer
Dorival Mendes Rodrigues-Junior1, Aristidis Moustakas1
1Department of Medical Biochemistry and Microbiology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Abstract:
Deeper analysis of molecular mechanisms arising in tumor cells is an unmet need to provide new diagnostic and therapeutic strategies to prevent and treat tumors. The transforming growth factor β (TGF-β) signaling has been steadily featured in tumor biology and linked to poor prognosis of cancer patients. One pro-tumorigenic mechanism induced by TGF-β is the epithelial-to-mesenchymal transition (EMT), which can initiate cancer dissemination, enrich the tumor stem cell population, and increase chemoresistance. TGF-β signals via SMAD proteins, ubiquitin ligases, and protein kinases and modulates the expression of protein-coding and non-coding RNA genes, including those encoding larger than 500 nt transcripts, defined as long non-coding RNAs (lncRNAs). Several reports have shown lncRNAs regulating malignant phenotypes by directly affecting epigenetic processes, transcription, and post-transcriptional regulation. Thus, this review aims to update and summarize the impact of TGF-β signaling on the expression of lncRNAs and the function of such lncRNAs as regulators of TGF-β signaling, and how these networks might impact specific hallmarks of cancer.
Insights
Transforming growth factor beta (TGF-β) signaling influences tumor progression by altering long non-coding RNA (lncRNA) expression. This review details how lncRNAs regulate TGF-β signaling and cancer hallmarks.
Area of Science:
- Molecular biology
- Cancer research
- Genomics
Background:
- Transforming growth factor beta (TGF-β) signaling is crucial in tumor biology and associated with poor cancer prognosis.
- TGF-β induces epithelial-to-mesenchymal transition (EMT), promoting cancer spread, stemness, and chemoresistance.
- Long non-coding RNAs (lncRNAs) are increasingly recognized for their roles in regulating gene expression and cellular processes.
Purpose of the Study:
- To review the impact of TGF-β signaling on lncRNA expression.
- To summarize the regulatory functions of lncRNAs in TGF-β signaling pathways.
- To explore how these TGF-β-lncRNA networks influence cancer hallmarks.
Main Methods:
- Literature review and synthesis of existing research on TGF-β signaling and lncRNAs in cancer.
- Analysis of molecular mechanisms involving SMAD proteins, ubiquitin ligases, and protein kinases in TGF-β pathways.
- Examination of lncRNA-mediated epigenetic, transcriptional, and post-transcriptional regulation.
Main Results:
- TGF-β signaling modulates the expression of numerous lncRNAs.
- lncRNAs act as both suppressors and enhancers of TGF-β signaling.
- Specific lncRNAs are implicated in regulating key cancer hallmarks like proliferation, migration, and chemoresistance.
Conclusions:
- The interplay between TGF-β signaling and lncRNAs represents a critical regulatory network in cancer.
- Targeting TGF-β-regulated lncRNAs offers potential for novel cancer diagnostics and therapeutics.
- Further research into these molecular mechanisms is essential for developing effective anti-cancer strategies.
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