Impact of CD151 overexpression on prognosis and therapy in non-small cell lung cancer patients lacking EGFR mutations.
Amanda Huee-Ping WongMin En NgaChin Yein ChinYee Kit TaiHung Chew WongRoss SooOmer AnHenry YangJu Ee SeetYaw Chyn LimJohn Kit Chung TamThai TranPublished in: Cell proliferation (2024)
This 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.
Keyphrases
- epidermal growth factor receptor
- small cell lung cancer
- tyrosine kinase
- advanced non small cell lung cancer
- cell proliferation
- poor prognosis
- growth factor
- end stage renal disease
- randomized controlled trial
- chronic kidney disease
- nk cells
- newly diagnosed
- signaling pathway
- prognostic factors
- case report
- gene expression
- bone marrow
- young adults
- oxidative stress
- radiation therapy
- dna methylation
- stem cells
- brain metastases
- systematic review
- papillary thyroid
- mesenchymal stem cells
- risk assessment
- patient reported
- drug induced
- single cell
- ultrasound guided
- diabetic rats
- rectal cancer
- high throughput
- lymph node metastasis
- stress induced
- squamous cell
- replacement therapy