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Updated: Jun 6, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
Transforming growth factor-β regulates the sphere-initiating stem cell-like feature in breast cancer through
1Division of Tumor Cell Biology, Beckman Research Institute of City of Hope, Duarte, CA 91010, USA.
Abstract:
Recent studies indicate that a subset of cancer cells possessing stem cell properties, referred to as cancer-initiating or cancer stem cells (CSCs), have crucial roles in tumor initiation, metastasis and resistance to anticancer therapies. Transforming growth factor (TGF)-β and their family members have been implicated in both normal (embryonic and somatic) stem cells and CSCs. In this study, we observed that exposure to TGF-β increased the population of breast cancer (BC) cells that can form mammospheres in suspension, a feature endowed by stem cells. This was mediated by the micro (mi)RNA family miR-181, which was upregulated by TGF-β at the post-transcriptional level. Levels of the miR-181 family members were elevated in mammospheres grown in undifferentiating conditions, compared with cells grown in two-dimensional conditions. Ataxia telangiectasia mutated (ATM), a target gene of miR-181, exhibited reduced expression in mammospheres and upon TGF-β treatment. Overexpression of miR-181a/b, or depletion of ATM or its substrate CHK2, was sufficient to induce sphere formation in BC cells. Finally, knockdown of ATM enhanced in vivo tumorigenesis of the MDA361 BC cells. Our results elucidate a novel mechanism through which the TGF-β pathway regulates the CSC property by interfering with the tumor suppressor ATM, providing insights into the cellular and environmental factors regulating CSCs, which may guide future studies on therapeutic strategies targeting these cells.
Insights
Transforming growth factor-beta (TGF-β) promotes cancer stem cell (CSC) properties in breast cancer by upregulating miR-181, which suppresses the tumor suppressor ATM. This pathway highlights a novel mechanism regulating CSCs and potential therapeutic targets.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Cancer stem cells (CSCs) drive tumor initiation, metastasis, and therapy resistance.
- Transforming growth factor-beta (TGF-β) signaling is implicated in both normal and cancer stem cells.
Purpose of the Study:
- To investigate the role of TGF-β in regulating breast cancer stem cell properties.
- To elucidate the molecular mechanisms by which TGF-β influences CSCs.
Main Methods:
- Exposure of breast cancer cells to TGF-β and assessment of mammosphere formation.
- Quantification of miR-181 family members and ATM expression.
- Genetic manipulation of miR-181, ATM, and CHK2.
- In vivo tumorigenesis assays.
Main Results:
- TGF-β increased mammosphere formation in breast cancer cells, mediated by miR-181 upregulation.
- miR-181 levels were elevated in mammospheres, correlating with decreased ATM expression.
- Overexpression of miR-181 or depletion of ATM/CHK2 induced sphere formation.
- ATM knockdown enhanced in vivo tumorigenesis.
Conclusions:
- The TGF-β pathway regulates CSC properties by downregulating the tumor suppressor ATM via miR-181.
- This mechanism provides insights into CSC regulation and potential therapeutic strategies targeting CSCs.
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