Oncotarget

Research Papers:

ACYP2 polymorphisms are associated with the risk of liver cancer in a Han Chinese population

Zhong Chen, Yu Sun, Zhenxiong Xu, Junnv Xu, Jingjie Li, Mengdan Yan, Jing Li, Tianbo Jin and Haifeng Lin _

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Oncotarget. 2017; 8:67723-67731. https://doi.org/10.18632/oncotarget.18574

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Abstract

Zhong Chen1, Yu Sun2, Zhenxiong Xu2, Junnv Xu3, Jingjie Li4, Mengdan Yan4, Jing Li4, Tianbo Jin4,5 and Haifeng Lin3

1Department of Thoracic Surgery, Second People’s Hospital of Hainan Province, Hainan, 572200, China

2Department of General Surgery, Second People’s Hospital of Hainan Province, Hainan, 572200, China

3Department of Internal Medicine-Oncology, Agricultural Reclamation General Hospital of Hainan Province, Hainan, 570311, China

4Key Laboratory of Resource Biology and Biotechnology in Western China, Northwest University, Ministry of Education, School of Life Sciences, Northwest University, Shaanxi, 710069, China

5Xi’an Tiangen Precision Medical Institute, Shaanxi, 710075, China

Correspondence to:

Haifeng Lin, email: 13322060949@163.com

Keywords: ACYP2, polymorphism, liver cancer, case-control, Han Chinese population

Received: October 24, 2016     Accepted: April 05, 2017     Published: June 19, 2017

ABSTRACT

We explored the association between single nucleotide polymorphisms (SNPs) in ACYP2 and liver cancer risk. Thirteen SNPs were genotyped in 473 cases and 564 controls. Genetic model, linkage disequilibrium, and haplotype analyses were performed to evaluate the association between ACPY2 SNPs and liver cancer risk. We found that rs6713088 (G allele: odds ratio [OR] = 1.27, 95% confidence interval [CI]: 1.07−1.52, P = 0.007; GG vs. CC: OR = 1.49, 95% CI: 1.02−2.1, P = 0.038), rs843711 (T allele: OR = 1.29, 95% CI: 1.09−1.54, P = 0.004; TT vs. CC: OR = 1.62, 95% CI: 1.13−2.31, P = 0.008), rs843706 (A allele: OR = 1.30, 95% CI: 1.09−1.55, P = 0.003; AA vs. CC: OR = 1.62, 95% CI: 1.13−2.31, P = 0.008), and rs843645 (GG vs. AG: OR = 1.40, 95% CI: 1.07−1.82, P = 0.014) were associated with an increased risk of liver cancer. In contrast, rs1682111 (A allele: OR = 0.77, 95% CI: 0.640−0.94, P = 0.007; AT vs. TT: OR = 0.69, 95% CI: 0.53−0.91, P = 0.007), rs843720 (additive model: OR = 0.82, 95% CI: 0.68−1.00, P = 0.049), ATATCGCC and CG haplotypes (OR = 0.76, 95% CI: 0.62−0.92, P = 0.006; OR = 0.78, 95% CI: 0.65−0.93, P = 0.006, respectively) were significantly decreased liver cancer risk. Our results confirmed that rs6713088, rs843645, rs843711 and rs843706 were significantly increased liver cancer risk, but rs1682111, rs843720 and haplotypes (ATATCGCC and CG) were significantly decreased liver cancer risk in a Han Chinese population.


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