Plasminogen activators in breast-cancer cells
J Yamashita1, K Inada, M Ogawa
1KUMAMOTO UNIV,SCH MED,DEPT SURG 2,HONJO 1-1-1,KUMAMOTO 860,JAPAN.
International Journal of Oncology
|May 18, 2011
Summary
This review examines plasminogen activators (PAs) in breast cancer. Urokinase-type PA (u-PA) indicates poor prognosis and metastasis, while tissue-type PA (t-PA) suggests a good prognosis but may drive bone metastasis.
Area of Science:
- Oncology
- Biochemistry
- Molecular Biology
Background:
- Plasminogen activators (PAs) play critical roles in cancer progression.
- Urokinase-type PA (u-PA) and tissue-type PA (t-PA) exhibit distinct functions in breast cancer.
- Estrogen receptor signaling influences t-PA production.
Purpose of the Study:
- To review experimental and clinical studies on PA expression in breast cancer.
- To elucidate the differential roles of u-PA and t-PA in breast cancer.
- To evaluate PAs as potential prognostic markers.
Main Methods:
- Review of experimental and clinical studies.
- Analysis of PA expression patterns.
- Correlation of PA levels with patient survival and metastasis.
Main Results:
- High u-PA levels correlate with poor disease-free and overall survival, indicating its role as a prognostic marker for breast cancer.
- t-PA production is estrogen-regulated, suggesting its utility as a marker for estrogen action.
- While generally associated with a good prognosis, t-PA may contribute to bone-only metastasis.
Conclusions:
- u-PA is a significant negative prognostic marker in breast cancer, linked to invasion and metastasis.
- t-PA serves as a marker for estrogen action and is generally associated with favorable outcomes, despite a role in bone metastasis.
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