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Updated: Jan 22, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Prognostic impact of PIK3CA protein expression in triple negative breast cancer and its subtypes
C Elfgen1,2, K Reeve3, L Moskovszky4
1Breast Center Zurich, Seefeldstrasse 214, 8008, Zurich, Switzerland. c.elfgen@brust-zentrum.ch.
Background:
Triple negative breast cancer (TNBC) harbors a heterogeneous group of carcinomas with poor prognosis and high genetic variability. As a potential aim for targeted therapy, genetic mutations leading to an activation of the phosphoinositide 3-kinase pathway in a catalytic subunit (PIK3CA) in breast cancer have been analyzed currently. Little is known about the clinical impact and prognostic or predictive value of this marker in TNBC subtypes.
Methods:
Samples from 119 TNBC cases were submitted to immunohistochemical PIK3CA protein expression analysis and scored semi-quantitatively as negative, weak (1 +), or strongly expressed (2 +). Expression scores were correlated to patient's characteristics, imaging features, and TNBC subtypes. TNBC subtypes were categorized into four subtypes: basal like, mesenchymal like, luminal androgen receptor (LAR), and immunomodulatory.
Results:
We did not observe differences in clinical aspects and imaging features between TNBC with and without PIK3CA expression. PIK3CA expression was in general higher in the LAR subtype. The disease-free survival and overall survival were significantly better in TNBC with PIK3CA protein expression, independent of TNBC subtypes.
Conclusion:
Despite conflicting results in the literature, our study clearly shows a better outcome of PIK3CA-expressing TNBC, independent of TNBC subtypes. PIK3CA expression in TNBC is not associated with specific clinical or diagnostic features. Further molecular studies and meta-analysis are warranted to clarify the prognostic and predictive role of PIK3CA protein expression.
Insights
Phosphoinositide 3-kinase catalytic subunit alpha (PIK3CA) expression in triple negative breast cancer (TNBC) is linked to better patient outcomes, regardless of subtype. This finding offers new insights into TNBC prognosis and potential therapeutic targets.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Triple negative breast cancer (TNBC) is a heterogeneous group of aggressive carcinomas with poor prognosis and significant genetic variability.
- Activating mutations in phosphoinositide 3-kinase catalytic subunit alpha (PIK3CA) are potential therapeutic targets in breast cancer, but their role in TNBC subtypes is not well understood.
Purpose of the Study:
- To investigate the clinical impact and prognostic value of PIK3CA protein expression in different subtypes of triple negative breast cancer.
- To correlate PIK3CA expression with patient characteristics, imaging features, and survival outcomes in TNBC.
Main Methods:
- Immunohistochemical analysis of PIK3CA protein expression in 119 TNBC samples, with semi-quantitative scoring (negative, weak, strong).
- Categorization of TNBC into four subtypes: basal-like, mesenchymal-like, luminal androgen receptor (LAR), and immunomodulatory.
- Correlation of PIK3CA expression scores with clinical data, imaging features, and TNBC subtypes.
Main Results:
- No significant differences in clinical aspects or imaging features were observed between TNBC with and without PIK3CA expression.
- PIK3CA expression was generally higher in the Luminal Androgen Receptor (LAR) subtype of TNBC.
- TNBC cases with PIK3CA protein expression demonstrated significantly better disease-free survival and overall survival, independent of TNBC subtype.
Conclusions:
- PIK3CA protein expression in triple negative breast cancer is associated with a better patient outcome, irrespective of TNBC subtype.
- PIK3CA expression does not appear to be linked to specific clinical or diagnostic features within TNBC.
- Further research, including molecular studies and meta-analyses, is needed to fully elucidate the prognostic and predictive significance of PIK3CA protein expression in TNBC.
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