Yu Wei-Ling, Yao Jin-Jian, Xie Zong-Zhou, Huang Yan-Jing, Xiao Sha
Oncology Department of Haikou City People's Hospital, Haikou 570208, Hainan, People's Republic of China.
Key Laboratory of Emergency and Trauma, Ministry of Education of Hainan Medical University, Haikou 571199, Hainan, People's Republic of China.
Int J Gen Med. 2021 Jan 25;14:255-266. doi: 10.2147/IJGM.S290997. eCollection 2021.
Long noncoding RNA single nucleotide polymorphisms (lncRNA-SNPs) PCAT1 rs710886, PRNCR1 rs1456315 and CCAT2 rs6983267 on 8q24 region present generalizability in the susceptibility to multiple cancers, however, the influence of rs710886, rs1456315 and rs6983267 on lung cancer has not been assessed. The aim of this study was to investigate associations between three lncRNA-SNPs and lung cancer.
A case-control study was performed on 438 patients with lung cancer and 456 healthy controls in the Han population from southern China. The collected samples were genotyped by the TaqMan genotyping, and the association with clinical characteristics, including age, gender, drinking status, smoking status, pathological types and clinical stages were analyzed. And the SNP function prediction was based on lncRNASNP2, RNAfold and GTEx.
The rs1456315 T allele increased the risk of lung cancer [OR=1.95, 95% CI (1.58-2.43), =0.003] compared to the rs1456315 C allele, and rs1456315 significantly increased the risk of lung cancer in the dominant model [OR=1.86, 95% CI (1.16-3.00), =0.002]. The rs6983267 G allele, compared with the T allele, increased the risk of lung cancer [OR=1.29, 95% CI (1.07-1.57), =0.007], and rs6983267 was identified as a risk factor for lung cancer [OR=1.28, 95% CI (1.06-1.55), =0.003] in the additive model. Both rs1456315 and rs6983267 demonstrated significance after adjusting for the smoking status, drinking status and age. The structure prediction found rs6983267 and rs1456315 influence the secondary structure of its lncRNA. The results from lncRNASNP2 indicated that rs6983267 and rs1456315 change gain/loss target of miRNAs.
rs1456315 and rs6983267 on 8q24 region are significantly associated with lung cancer in the Han population of southern China and alter the potential biological function in bioinformatic analysis, and the results further extended generalism of the susceptibility of cancer-associated lncRNA-SNPs to lung cancer and underlying mechanism involved in lung cancer.
8q24区域的长链非编码RNA单核苷酸多态性(lncRNA-SNPs)PCAT1 rs710886、PRNCR1 rs1456315和CCAT2 rs6983267在多种癌症易感性方面具有普遍性,然而,rs710886、rs1456315和rs6983267对肺癌的影响尚未得到评估。本研究旨在探讨这三种lncRNA-SNPs与肺癌之间的关联。
对来自中国南方汉族人群的438例肺癌患者和456例健康对照进行病例对照研究。通过TaqMan基因分型对收集的样本进行基因分型,并分析其与年龄、性别、饮酒状况、吸烟状况、病理类型和临床分期等临床特征的关联。SNP功能预测基于lncRNASNP2、RNAfold和GTEx。
与rs1456315 C等位基因相比,rs1456315 T等位基因增加了肺癌风险[比值比(OR)=1.95,95%置信区间(CI)(1.58 - 2.43),P = 0.003],且rs1456315在显性模型中显著增加了肺癌风险[OR = 1.86,95% CI(1.16 - 3.00),P = 0.002]。与T等位基因相比,rs6983267 G等位基因增加了肺癌风险[OR = 1.29,95% CI(1.07 - 1.57),P = 0.007],并且在加性模型中rs6983267被确定为肺癌的危险因素[OR = 1.28,95% CI(1.06 - 1.55),P = 0.003]。在调整吸烟状况、饮酒状况和年龄后,rs1456315和rs6983267均显示出显著性。结构预测发现rs6983267和rs1456315影响其lncRNA的二级结构。lncRNASNP2的结果表明rs6983267和rs1456315改变了miRNA的靶标增减。
8q24区域的rs1456315和rs6983267与中国南方汉族人群的肺癌显著相关,并在生物信息学分析中改变了潜在生物学功能,该结果进一步扩展了癌症相关lncRNA-SNPs对肺癌易感性及肺癌潜在机制的普遍性。