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Updated: Jan 30, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Expression profile of CADM1 and CADM4 in triple negative breast cancer with primary systemic therapy
Yasuyuki Kanke1, Motonobu Saito1, Noriko Abe2
1Department of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine, Fukushima, Fukushima 960-1295, Japan.
Abstract:
Triple negative breast cancer (TNBC) is defined by a lack of ER, PgR, and HER2 expression, and to date there have been no significant advances in treatment by targeted therapies against those molecules. Therefore, primary systemic therapy (PST) followed by surgery is the standard therapy for patients with advanced TNBC. According to gene expression analysis, TNBC has a distinct profile when compared with non-TNBC, suggesting that a unique gene affects the treatment efficacy of PST. Cell adhesion molecule (CADM) genes encode an immunoglobulin superfamily molecule involved in cell-to-cell adhesion in a variety of human epithelial cells. While it has been reported that inactivation of CADM1 and CADM4 serves a pivotal role in the progression of breast cancer, a full analysis has not been completed for TNBC. Previous studies have reported that CADM1 and CADM4 expression is less likely to be decreased in TNBC than in non-TNBC. In the present study, CADM1 and CADM4 expression was evaluated in patients with TNBC who had received PST. The present study revealed that loss or weak expression of CADM1 was frequently observed in non-pathological complete response patients. Furthermore, while the majority of TNBC cases exhibited high CADM1 expression, a small number of cases exhibited low CADM1 expression and low therapeutic response of PST for TNBC. These results suggest that CADM1 has a pivotal role in anti-PST efficacy in patients with TNBC.
Insights
Loss of CADM1 expression in triple-negative breast cancer (TNBC) correlates with poor response to primary systemic therapy (PST). This finding suggests CADM1 may be a key factor in TNBC treatment efficacy.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Triple-negative breast cancer (TNBC) lacks ER, PgR, and HER2 expression, limiting targeted therapy options.
- Primary systemic therapy (PST) followed by surgery is the standard treatment for advanced TNBC.
- Distinct gene expression profiles in TNBC suggest unique genes influence PST efficacy.
Purpose of the Study:
- To investigate the role of Cell Adhesion Molecule 1 (CADM1) and CADM4 expression in TNBC patients undergoing PST.
- To determine if CADM1/CADM4 expression levels correlate with treatment response to PST in TNBC.
Main Methods:
- Evaluation of CADM1 and CADM4 gene expression in TNBC patient samples.
- Correlation analysis between CADM1/CADM4 expression levels and pathological complete response after PST.
Main Results:
- Loss or weak expression of CADM1 was frequently observed in TNBC patients who did not achieve a pathological complete response.
- While most TNBC cases showed high CADM1 expression, a subset with low CADM1 expression exhibited poor PST response.
- CADM1 expression levels appear distinct between TNBC and non-TNBC, with implications for treatment.
Conclusions:
- CADM1 expression plays a pivotal role in the efficacy of primary systemic therapy for triple-negative breast cancer.
- CADM1 may serve as a predictive biomarker for PST response in TNBC patients.
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