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BCAM (basal cell adhesion molecule) protein expression in different tumor populations
Sneha Burela1, Mengni He1, Ioannis P Trontzas1
1Department of Pathology, Yale School of Medicine, New Haven, CT, 06519, USA.
Discover Oncology
|August 29, 2024
Summary
Basal Cell Adhesion Molecule (BCAM) shows promise as a cancer biomarker. High BCAM expression correlates with better survival in lung cancer and may predict immunotherapy response independently of PD-L1.
Area of Science:
- Oncology
- Immunology
- Biomarker Discovery
Background:
- Basal Cell Adhesion Molecule (BCAM) is implicated in cancer pathogenesis.
- Low BCAM expression and hypermethylation at immune checkpoints suggest potential response to immune checkpoint inhibitors (ICIs).
Purpose of the Study:
- To evaluate BCAM expression patterns across diverse cancer types.
- To determine BCAM's potential as a predictive biomarker for immunotherapy response.
- To investigate the correlation between BCAM and PD-L1 expression.
Main Methods:
- Quantitative immunofluorescence (QIF) was used to assess BCAM expression.
- Analysis included 3114 patients across discovery and validation cohorts, covering seven cancer types.
- Correlation analysis between BCAM and PD-L1 expression was performed.
Main Results:
- BCAM was highly expressed in ovarian (79.2%) and lung (78.5%) tumors.
- Significant BCAM expression was also observed in breast, head and neck, and bladder-urothelial tumors.
- High BCAM expression correlated with improved overall survival (OS) in non-small cell lung cancer (NSCLC).
- BCAM expression showed no correlation with PD-L1 protein levels, indicating independent predictive potential.
Conclusions:
- BCAM is expressed across multiple tumor types, suggesting its broad relevance.
- BCAM's lack of correlation with PD-L1 highlights its potential as a novel, independent predictive biomarker for immunotherapy.
- BCAM warrants further investigation as a predictive biomarker for cancer immunotherapy response.
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