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Updated: Jul 17, 2026

Quantification of Breast Cancer Cell Invasiveness Using a Three-dimensional (3D) Model
Published on: June 11, 2014
Expression of Syk in invasive breast cancer: correlation to proliferation and invasiveness
Katerina Repana1, Konstantinos Papazisis, Periklis Foukas
1Laboratory of Biochemistry, Department of Chemistry, Aristotle University of Thessaloniki, 54124, Thessaloniki, Greece.
Background:
Spleen tyrosine kinase (Syk) kinase has recently been considered as a tumor suppressor gene in breast cancer.
Materials And Methods:
Syk expression in patients with invasive breast cancer was immunohistochemically assessed.
Results:
Decreased expression was found in 26% of the specimens examined. In cases with vascular invasion, expression of Syk was lost in the intravascular emboli. A significant relationship between increased proliferation levels (as estimated by the proliferative index, Ki67) and decreased Syk expression (p <0.05) was found.
Conclusion:
Our data suggest that Syk protein expression inversely correlates with the proliferation and invasive capacity of breast cancer.
Insights
Spleen tyrosine kinase (Syk) expression is decreased in invasive breast cancer, correlating with higher proliferation and invasive capacity. This suggests Syk may act as a tumor suppressor in breast cancer.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Spleen tyrosine kinase (Syk) is emerging as a potential tumor suppressor in breast cancer.
- Understanding Syk's role is crucial for developing targeted breast cancer therapies.
Purpose of the Study:
- To investigate the expression levels of Syk in invasive breast cancer specimens.
- To determine the correlation between Syk expression and key indicators of tumor aggressiveness, such as proliferation and vascular invasion.
Main Methods:
- Immunohistochemistry was utilized to assess Syk protein expression in patient samples.
- Proliferative index (Ki67) was used to quantify tumor cell proliferation.
Main Results:
- Reduced Syk expression was observed in 26% of invasive breast cancer cases.
- Loss of Syk expression was noted in intravascular emboli, indicating a link to vascular invasion.
- A statistically significant inverse correlation was found between high proliferation (Ki67) and decreased Syk expression (p <0.05).
Conclusions:
- Syk protein expression is inversely associated with tumor proliferation and invasive potential in breast cancer.
- These findings support the hypothesis that Syk functions as a tumor suppressor in breast cancer progression.
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