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Updated: Mar 3, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Triple-negative breast cancer: New therapeutic options via signalling transduction cascades
Ulrich Andergassen1, Alexandra C Kölbl1, Jan-Niclas Mumm1
1Department of Obstetrics and Gynaecology, Ludwig-Maximilians University of Munich, 80337 Munich, Germany.
Abstract:
Triple-negative breast cancer is a highly aggressive type of mammalian carcinoma. It is defined by a rather weak expression of estrogen-, progesterone- and Her2-receptor, and is thus difficult to treat, resulting in low disease-free and overall survival rates of the affected patients. Hence it is important to find new therapeutic options. To this aim we analysed the incidence of some molecules from different signal transduction cascades by immunohistochemistry, which are known to correlate with triple-negative breast cancer, and correlated the expression of these molecules to different tumour traits, such as size, grading, menopausal stage, histology, lymph node affection, remote metastasis formation, and to the incidence of local and lymph node recurrence and metastasis by statistical analysis. Statistically significant correlations were found for a number of tumour characteristics and signalling molecules: HIF1α is correlated to tumour grading, β-catenin to the menopausal state of the patient, and for Notch1 a relation to lymph node affection is seen. In terms of different recurrences, a correlation of β-catenin to metastasis formation and lymph node affection could be shown, as well as coherences between XBP1 and lymph node recurrence, Notch1 and metastasis formation and FOXP3 and the occurrence of local recurrence. The presented results are in accordance with formerly published studies and therefore might comprise opportunities to develop new therapeutical strategies, which could help to handle this aggressive form of breast cancer in a manner, by which side effects would be reduced and therapeutical efficiency is increased.
Insights
New research identifies key signaling molecules linked to triple-negative breast cancer progression. Understanding these molecular correlations may lead to more effective treatments with fewer side effects for this aggressive cancer.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Triple-negative breast cancer (TNBC) is an aggressive carcinoma with limited treatment options.
- TNBC is characterized by the absence of estrogen, progesterone, and Her2 receptors.
- Low survival rates underscore the need for novel therapeutic strategies.
Purpose of the Study:
- To investigate correlations between signaling molecules and TNBC tumor traits.
- To identify potential therapeutic targets for TNBC management.
- To analyze the relationship between molecular markers and disease recurrence.
Main Methods:
- Immunohistochemistry was used to analyze the incidence of signaling molecules.
- Statistical analysis correlated molecule expression with tumor characteristics (size, grading, etc.).
- Associations with lymph node status, metastasis, and recurrence were examined.
Main Results:
- HIF1α correlated with tumor grading.
- β-catenin showed correlations with menopausal state, metastasis, and lymph node affection.
- Notch1 was linked to lymph node affection and metastasis.
- XBP1 correlated with lymph node recurrence.
- FOXP3 was associated with local recurrence.
Conclusions:
- Identified significant correlations between specific signaling molecules and TNBC characteristics.
- Findings align with previous studies, suggesting potential for new therapeutic strategies.
- These insights may improve treatment efficacy and reduce side effects for TNBC patients.
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