Impact of CD151 overexpression on prognosis and therapy in non‐small cell lung cancer patients lacking EGFR mutations

Author:

Wong Amanda Huee‐Ping1ORCID,Nga Min En23,Chin Chin Yein1,Tai Yee Kit1,Wong Hung Chew4,Soo Ross5,An Omer6ORCID,Yang Henry6,Seet Ju Ee2,Lim Yaw Chyn36,Tam John Kit Chung78ORCID,Tran Thai19ORCID

Affiliation:

1. Department of Physiology, Yong Loo Lin School of Medicine National University of Singapore Singapore Singapore

2. Department of Pathology National University Hospital Singapore Singapore

3. Department of Pathology, Yong Loo Lin School of Medicine National University of Singapore Singapore Singapore

4. Department of Biostatistics, Yong Loo Lin School of Medicine National University of Singapore Singapore Singapore

5. Department of Haematology‐Oncology National University Hospital Singapore Singapore

6. Cancer Science Institute of Singapore National University of Singapore Singapore Singapore

7. Department of Surgery, Yong Loo Lin School of Medicine National University of Singapore Singapore Singapore

8. Department of Cardiac, Thoracic and Vascular Surgery, National University Heart Centre, Singapore National University Health System Singapore Singapore

9. Infectious Disease Translational Research Programme, Yong Loo Lin School of Medicine National University of Singapore Singapore Singapore

Abstract

AbstractThis study investigates CD151, a protein linked to cancer progression, in non‐small cell lung cancer (NSCLC) patients without epidermal growth factor receptor (EGFR) mutations. These patients often have limited treatment options. The study used retrospective analysis to examine 157 adenocarcinoma biopsy specimens and 199 patient cases from The Cancer Genome Atlas, correlating CD151 expression with patient survival. Cellular studies revealed that CD151 interacts with EGFR, influencing epidermal growth factor (EGF)‐induced cell proliferation and the effectiveness of the EGFR inhibitor, erlotinib. A strong association was found between CD151 expression and EGFR mutation status. High CD151 expression in the absence of EGFR mutations is correlated with poorer survival outcomes. Biological assays showed that CD151 colocalizes and associates with EGFR, playing a crucial role in regulating EGF‐induced cell proliferation via the AKT and ERK1/2 pathways. Importantly, CD151 expression was found to influence the anti‐proliferative effects of the EGFR tyrosine kinase inhibitor, erlotinib. High CD151 expression, in the absence of EGFR mutations, was associated with poorer survival outcomes. It could serve as a potential prognostic marker and influence cellular responses to EGFR‐targeted treatments. This study highlights CD151 as a potential novel target for therapeutic intervention in NSCLC, especially in populations lacking EGFR mutations.

Publisher

Wiley

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