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Updated: May 5, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
The microRNA networks of TGFβ signaling in cancer
1Laboratory of Cell Cycle Regulation & Molecular Oncology, Division of Cancer Research, Regional Cancer Centre, Thiruvananthapuram, 695011, Kerala, India.
Abstract:
In metazoans, the transforming growth factor β (TGFβ) signaling regulates a host of activities ranging from embryonic development to tissue homeostasis. The normal as well as tumor cells respond to this cytokine signaling pathway in a highly context-dependent manner. It acts as a potent tumor suppressor initially by inducing cell cycle arrest and apoptosis. But advanced tumors often misuse TGFβ signaling for tumor progression by selectively disabling the tumor suppressor arm and using other properties of TGFβ signaling such as induction of angiogenesis, epithelial to mesenchymal transition, and metastases. This dual role of TGFβ in cancer remained a mystery until recently. But recent advances in the field of microRNA provided a deeper understanding about this dual nature of TGFβ signaling in cancers. In the present review, we present an account of the role of microRNAs in deregulating TGFβ signaling and modulating cancer cell behavior during tumor initiation and cancer progression. This review also includes a discussion on the recent advances in the deregulation of TGFβ signaling in carcinogenesis.
Insights
MicroRNAs (miRNAs) explain the dual role of transforming growth factor β (TGFβ) signaling in cancer. These small RNAs regulate TGFβ, influencing both tumor suppression and progression.
Area of Science:
- Molecular Biology
- Cancer Research
- Cell Signaling
Background:
- Transforming growth factor β (TGFβ) signaling is crucial for metazoan development and tissue homeostasis.
- TGFβ exhibits context-dependent roles in cancer, initially suppressing tumors but later promoting progression in advanced stages.
- The dual nature of TGFβ in cancer has been a long-standing question in the field.
Purpose of the Study:
- To review the role of microRNAs (miRNAs) in modulating TGFβ signaling in cancer.
- To elucidate how miRNAs contribute to the dual functions of TGFβ during tumor initiation and progression.
- To discuss recent advancements in understanding TGFβ signaling deregulation in carcinogenesis.
Main Methods:
- Literature review focusing on microRNAs and TGFβ signaling in cancer.
- Analysis of studies investigating miRNA-mediated regulation of TGFβ pathways.
- Synthesis of current knowledge on TGFβ's role in tumor suppression and progression.
Main Results:
- MicroRNAs play a significant role in deregulating TGFβ signaling in cancer cells.
- Specific miRNAs can either inhibit or promote TGFβ-driven processes relevant to cancer.
- Understanding miRNA-TGFβ interactions provides insights into cancer cell behavior.
Conclusions:
- MicroRNAs are key regulators that explain the paradoxical roles of TGFβ in cancer.
- Targeting miRNA-TGFβ interactions may offer novel therapeutic strategies for cancer treatment.
- Further research into miRNA-mediated regulation of TGFβ signaling is essential for cancer research.
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