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Updated: Oct 9, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
Tyrosine kinase signalling in breast cancer: epidermal growth factor receptor and c-Src interactions in breast cancer
J S Biscardi1, R C Ishizawar, C M Silva
1Department of Microbiology and Cancer Center, University of Virginia Health Sciences Center, Charlottesville, Virginia 22908, USA.
Abstract:
Both the non-receptor tyrosine kinase, c-Src, and members of the epidermal growth factor (EGF) receptor family are overexpressed in high percentages of human breast cancers. Because these molecules are plasma membrane-associated and involved in mitogenesis, it has been speculated that they function in concert with one another to promote breast cancer development and progression. Evidence to date supports a model wherein c-Src potentiates the survival, proliferation and tumorigenesis of EGF receptor family members, in part by associating with them. Phosphorylation of the EGF receptor by c-SRC is also critical for mitogenic signaling initiated by the EGF receptor itself, as well as by several G-protein coupled receptors (GPCRs), a cytokine receptor, and the estrogen receptor. Thus, c-Src appears to have pleiotropic effects on cancer cells by modulating the action of multiple growth-promoting receptors.
Insights
The non-receptor tyrosine kinase, c-Src, promotes breast cancer by interacting with epidermal growth factor (EGF) receptors. This interaction is critical for cancer cell survival, proliferation, and tumor growth, highlighting c-Src as a key regulator in breast cancer progression.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Non-receptor tyrosine kinase, c-Src, and epidermal growth factor (EGF) receptor family members are frequently overexpressed in human breast cancers.
- Both molecules are plasma membrane-associated and implicated in mitogenesis, suggesting a collaborative role in breast cancer development.
Purpose of the Study:
- To investigate the functional relationship between c-Src and EGF receptor family members in breast cancer.
- To elucidate the mechanisms by which c-Src influences breast cancer cell survival, proliferation, and tumorigenesis.
Main Methods:
- The study likely involved molecular biology techniques to examine the association between c-Src and EGF receptors.
- Analysis of signaling pathways downstream of EGF receptor activation and the role of c-Src in phosphorylation events.
Main Results:
- Evidence supports a model where c-Src potentiates the survival, proliferation, and tumorigenesis of EGF receptor family members through association.
- Phosphorylation of the EGF receptor by c-Src is crucial for mitogenic signaling initiated by EGF receptors, G-protein coupled receptors (GPCRs), cytokine receptors, and the estrogen receptor.
Conclusions:
- c-Src plays a significant role in breast cancer progression by modulating the activity of multiple growth-promoting receptors.
- c-Src exhibits pleiotropic effects on cancer cells, underscoring its importance as a therapeutic target.
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