Department of Molecular Genetics, Ahar Branch, Islamic Azad University, Ahar, Iran.
Mol Biol Rep. 2020 Oct;47(10):7421-7427. doi: 10.1007/s11033-020-05797-6. Epub 2020 Sep 8.
LncRNAs are of functional long non-coding RNAs, which have been shown to be involved in critical pathways in cancer development. LncRNA-HOTAIR gene overexpression has been reported in several cancers. The aim of this study was to evaluate the associations between two variants of lncRNA-HOTAIR (rs1899663 G>T and rs4759314 A>G) gene polymorphisms and the risk of ovarian cancer (OC) susceptibility. We performed a case and control analysis on two hundred individuals consisting of 100 cases with OC and 100 women cancer-free in East Azerbaijan of Iranian population. To evaluate the association between two SNPs of lncRNA-HOTAIR with the risk of OC susceptibility used the polymerase chain reaction-restriction fragment-length polymorphism (PCR-RFLP) method. We revealed that two SNPs in the lncRNA-HOTAIR gene were significantly associated with the risk of OC. The dominant model of rs4759314 in lncRNA-HOTAIR (AA vs. GA/GG) showed a significantly increased risk with an OR of 10.036 (CI 2.253-44.712, P = 0.000); the recessive model of rs1899663 (TT vs. GT/GG) revealed a significantly increased risk with OR of 0.910 (CI 0.856-0.968; P = 0.002). In addition, our findings demonstrated that the 4759314G (OR 13.500; CI 3.146-57.940; P = 0.000) and 1899663T (OR 3.273; CI 1.433-7.475; P = 0.003) alleles are increased the risk of OC susceptibility. Our findings provide evidence that the specific genetic variants in lncRNA-HOTAIR gene may affect OC susceptibility in an Iranian population.
LncRNAs 是具有功能的长非编码 RNA,已被证明参与了癌症发展的关键途径。lncRNA-HOTAIR 基因的过表达已在几种癌症中报道。本研究旨在评估 lncRNA-HOTAIR 基因的两个变体(rs1899663 G>T 和 rs4759314 A>G)基因多态性与卵巢癌(OC)易感性风险之间的关联。我们对来自伊朗东阿塞拜疆的 200 名个体(100 例 OC 患者和 100 名无癌妇女)进行了病例对照分析。为了评估 lncRNA-HOTAIR 中两个 SNP 与 OC 易感性风险之间的关联,我们使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法。结果显示,lncRNA-HOTAIR 基因中的两个 SNP 与 OC 风险显著相关。lncRNA-HOTAIR 中 rs4759314 的显性模型(AA 对 GA/GG)显示出显著增加的风险,OR 为 10.036(95%CI:2.253-44.712,P=0.000);rs1899663 的隐性模型(TT 对 GT/GG)显示出显著增加的风险,OR 为 0.910(95%CI:0.856-0.968;P=0.002)。此外,我们的研究结果表明,4759314G(OR 13.500;95%CI:3.146-57.940;P=0.000)和 1899663T(OR 3.273;95%CI:1.433-7.475;P=0.003)等位基因增加了 OC 易感性的风险。本研究结果提供了证据表明,lncRNA-HOTAIR 基因的特定遗传变异可能会影响伊朗人群的 OC 易感性。