CTLA-4 Expression and Polymorphisms in Lung Tissue of Patients with Diagnosed Non-Small-Cell Lung Cancer

• Published in: BioMed research international 2013-01, Vol.2013 (2013), p.1-8
• Main Authors: Brzeziańska, Ewa, Kordiak, Jacek, Czarnecka, Karolina, Migdalska-Sęk, Monika, Domańska, Daria, Górski, Paweł, Pastuszak-Lewandoska, Dorota, Antczak, Adam, Nawrot, Ewa
• Format: Article
• Language: English
• Subjects: Aged; Alleles; Antitumor activity; Carcinoma, Non-Small-Cell Lung - genetics; Carcinoma, Non-Small-Cell Lung - metabolism; Carcinoma, Non-Small-Cell Lung - pathology; Cell growth; CTLA-4 Antigen - biosynthesis; CTLA-4 Antigen - genetics; CTLA-4 Antigen - immunology; Cytotoxicity; Diagnosis; Disease; Female; Gene expression; Gene Expression Regulation, Neoplastic; Genetic aspects; Genetic polymorphisms; Genetic Predisposition to Disease; Genotype; Genotype & phenotype; Hospitals; Humans; Lung - metabolism; Lung cancer; Lung cancer, Non-small cell; Lymphocytes; Male; Middle Aged; Mortality; Polymerase chain reaction; Polymorphism, Genetic; Risk Factors; Studies; Surgery; Thoracic surgery; Tumor Necrosis Factor Receptor Superfamily, Member 7 - genetics; Tumor Necrosis Factor Receptor Superfamily, Member 7 - immunology
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2013/576486

Cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) is a potent immunoregulatory molecule that downregulates T-cell activation and thus influences the antitumor immune response. CTLA-4 polymorphisms are associated with various cancers, and CTLA-4 mRNA/protein increased expression is found in several tumor types. However, most of the studies are based on peripheral blood mononuclear cells, and much less is known about the relationship between CTLA-4 expression, especially gene expression, and its polymorphic variants in cancer tissue. In our study we assessed the distribution of CTLA-4 two polymorphisms (+49A/G and −318C/T), using TaqMan probes (rs231775 and rs5742909, resp.), and CTLA-4 gene expression in real-time PCR assay in non-small-cell lung cancer (NSCLC) tissue samples. The increased CTLA-4 expression was observed in the majority of NSCLC patients, and it was significantly correlated with TT genotype (−318C/T) and with tumor size (T2 versus T3 + T4). The presence of G allele and GG genotype in cancer tissue (+49A/G) was significantly associated with the increased NSCLC risk. Additionally, we compared genotype distributions in the corresponding tumor and blood samples and found statistically significant differences. The shift from one genotype in the blood to another in the tumor may confirm the complexity of gene functionality in cancer tissue.