The programmed death-1 gene polymorphism (PD-1.5 C/T) is associated with non-small cell lung cancer risk in a Chinese Han population.
Yin Liu, Huishu Guo, Lei Zhao, Jinguang Wang
Abstract
Yin Liu, Huishu Guo, Lei Zhao, Jinguang Wang
Abstract
It has been proposed that genetic factors contribute to the susceptibility of non-small cell lung cancer (NSCLC). The programmed death-1 (PD1) is an immunoinhibitory receptor belonging to the CD28/B7 family. The aim of this study is to investigate the relationship between PD-1.5 C/T and NSCLC risk in a Chinese population. A population-based case-control study was conducted in 324 NSCLC patients and 330 cancer-free controls. The genotype of the PD-1.5 C/T was determined by using a polymerase chain reaction assay. Statistically significant difference was observed when the patients and controls were compared according to CC+CT versus TT (OR=2.34, 95% CI 1.35-4.06, P=0.003). The C allele was significantly associated with NSCLC risk (OR=1.421, 95% CI 1.10-1.82, P=0.006). Compared to TNM stage I+II, PD-1.5 C/T significantly increased advanced NSCLC risk (OR=2.66, 95% CI 1.07-6.63, P=0.03). The results from this study suggested that PD-1.5 C/T was potentially related to NSCLC susceptibility in Chinese Han population.
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It has been proposed that genetic factors contribute to the susceptibility of non-small cell lung cancer (NSCLC). The programmed death-1 (PD1) is an immunoinhibitory receptor belonging to the CD28/B7 family. The aim of this study is to investigate the relationship between PD-1.5 C/T and NSCLC risk in a Chinese population. A population-based case-control study was conducted in 324 NSCLC patients and 330 cancer-free controls. The genotype of the PD-1.5 C/T was determined by using a polymerase chain reaction assay. Statistically significant difference was observed when the patients and controls were compared according to CC+CT versus TT (OR=2.34, 95% CI 1.35-4.06, P=0.003). The C allele was significantly associated with NSCLC risk (OR=1.421, 95% CI 1.10-1.82, P=0.006). Compared to TNM stage I+II, PD-1.5 C/T significantly increased advanced NSCLC risk (OR=2.66, 95% CI 1.07-6.63, P=0.03). The results from this study suggested that PD-1.5 C/T was potentially related to NSCLC susceptibility in Chinese Han population.
Key concepts: Medicine, Lung cancer, Internal medicine, Genotype, Oncology, Allele, Gastroenterology, Han chinese