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Optimization of a Multiplex RNA-based Expression Assay Using Breast Cancer Archival Material
Published on: August 1, 2018
Serum proteins in breast cancer
Summary
Plasma protein changes, including elevated beta 2 glycoprotein and ceruloplasmin, may indicate early breast cancer. These protein levels correlated with tumor spread, suggesting potential diagnostic value.
Area of Science:
- Oncology
- Biochemistry
- Medical Diagnostics
Background:
- Early detection of breast cancer is crucial for effective treatment.
- Plasma protein profiles are increasingly explored as potential biomarkers for various diseases.
- Distinguishing between malignant and benign breast conditions requires reliable diagnostic tools.
Purpose of the Study:
- To determine if plasma protein level changes are characteristic of early breast cancer.
- To compare protein profiles in breast cancer patients versus those with benign breast disease.
- To investigate correlations between plasma protein changes and breast cancer progression.
Main Methods:
- Sequential follow-up of 39 women (18 with breast cancer, 21 with benign disease) for six months.
- Measurement of 10 serum proteins preoperatively and at 3 and 6 months postoperatively.
- Correlation analysis of serum protein levels with clinical scores of tumor spread.
Main Results:
- Breast cancer patients showed significantly higher preoperative beta 2 glycoprotein and six-month postoperative ceruloplasmin levels compared to benign disease patients.
- Significant correlations were observed between serum protein levels and breast cancer progression.
- Specific proteins like ceruloplasmin, prealbumin, hemopexin, alpha 1 antitrypsin, and beta 2 glycoprotein demonstrated correlations with disease status and progression.
Conclusions:
- Specific plasma protein changes, including beta 2 glycoprotein and ceruloplasmin, may serve as indicators for early breast cancer.
- Serum protein levels show correlations with tumor progression, highlighting their potential as prognostic markers.
- Further long-term studies are needed to validate the predictive value of these protein changes for metastasis development.

