scholarly journals Methylenetetrahydrofolate reductase C677T polymorphism predicts response and time to progression to gemcitabine-based chemotherapy for advanced non-small cell lung cancer in a Chinese Han population

2013 ◽  
Vol 14 (3) ◽  
pp. 207-215 ◽  
Author(s):  
Wei Hong ◽  
Kai Wang ◽  
Yi-ping Zhang ◽  
Jun-yan Kou ◽  
Dan Hong ◽  
...  
2019 ◽  
Author(s):  
Kun huang ◽  
Erqiang Hu ◽  
Wan Li ◽  
Junjie Lv ◽  
Yuehan He ◽  
...  

Abstract Introduction Lung cancer is a leading cause of death from cancer worldwide, especially non-small cell lung cancer (NSCLC). The marker of progression in lung adenocarcinoma has been rarely studied. PD-1 is an effective drug target for the treatment of non-small cell lung cancer. The study of the effect of polymorphism on the progression of lung adenocarcinoma in the Han population of Northeast China may provide a valuable reference for the research and application of these drugs. Methods Chi-square test, Wilcoxon rank sum test, and classification efficacy assessment were used to teste SNPs of PD-1 in 287 patients and combined with clinical information. Results We successfully identified biomarkers (rs2227981, rs2227982, and rs3608432) that could distinguish the early stages and late stages of lung adenocarcinoma. Multiple clinical indicators showed significant differences among different SNP typing and cancer stages. Furthermore, this gene was confirmed to effectively distinguish the staging of lung adenocarcinoma with RNA-seq data in TCGA. Conclusions This indicated that the PD-1 gene and the SNPs on it could be used as markers for distinguishing lung adenocarcinoma staging in the Northeast Han population.


2018 ◽  
Vol Volume 10 ◽  
pp. 1487-1495
Author(s):  
Chuanyin Li ◽  
Xiaona Wang ◽  
Yingfu Li ◽  
Xinwen Zhang ◽  
Mingbo Sun ◽  
...  

2021 ◽  
pp. 1-10
Author(s):  
Miao Li ◽  
Rong Chen ◽  
Baoyan Ji ◽  
Chunmei Fan ◽  
Guanying Wang ◽  
...  

<b><i>Background:</i></b> We aimed to explore the relation of <i>XPD</i> and <i>XPF</i> variants with non-small cell lung cancer (NSCLC) risk and the effect of these variants on the sensitivity to cisplatin-based chemotherapy among the Chinese Han population in high-altitude areas. <b><i>Methods:</i></b> Eight single-nucleotide polymorphisms (SNPs) in <i>XPD</i> and <i>XPF</i> were genotyped by Agena MassARRAY platform among 506 NSCLC cases and 510 healthy controls. Correlation of <i>XPD</i> and <i>XPF</i> gene polymorphisms with NSCLC susceptibility and the response of cis­platin-based chemotherapy were analyzed with logistic regression by calculating odds ratios (ORs) and 95% confidence intervals (CIs). <b><i>Results:</i></b> <i>XPD</i> rs13181 (OR = 1.53, 95% CI: 1.04–2.24, <i>p</i> = 0.029) and rs1052555 (OR = 1.63, 95% CI: 1.05–2.53, <i>p</i> = 0.029) possibly contributed to the increased risk of lung adenocarcinoma, while <i>XPD</i> rs238406 (OR = 0.63, 95% CI: 0.43–0.94, <i>p</i> = 0.024) was a protective factor for lung squamous cell carcinoma. Age, gender, BMI, smoking, and drinking might affect the correlation of <i>XPD</i> and <i>XPF</i> polymorphisms with NSCLC risk. More importantly, <i>XPD</i> rs13181 (OR = 2.91, <i>p</i> = 0.015), <i>XPD</i> rs1052555 (OR = 2.67, <i>p</i> = 0.022), and <i>XPF</i> rs231127 (OR = 4.15, <i>p</i> = 0.008) were associated with treatment response in NSCLC patients underwent cisplatin-based chemotherapy. <b><i>Conclusion:</i></b> This study found that <i>XPD</i> and <i>XPF</i> variants might contribute to NSCLC risk and the response of cisplatin-based chemotherapy among the Chinese Han population in high-altitude areas.


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