Tian Tian, Li Chunjian, Xiao Jing, Shen Yi, Lu Yihua, Jiang Liying, Zhuang Xun, Chu Minjie
Department of Epidemiology and Biostatistics, School of Public Health, Nantong University, Nantong, Jiangsu, China.
Analysis and Testing Center of Nantong University, Nantong, Jiangsu, China.
PLoS One. 2016 Mar 24;11(3):e0152296. doi: 10.1371/journal.pone.0152296. eCollection 2016.
HOX transcript antisense intergenic RNA (HOTAIR) is a long non-coding RNA (lncRNA) that functions as an oncogenic molecule in different cancer cells. Genetic variants of HOTAIR may affect the activity of certain regulatory factors and further regulate the aberrant expression of HOTAIR, which might be underlying mechanisms that affect tumour susceptibility and prognosis. Recently, several studies have been performed to examine the possible link between polymorphisms in HOTAIR and cancer risk; however, the results have been inconclusive. Therefore, we performed a meta-analysis to estimate the associations between HOTAIR polymorphisms (rs920778, rs4759314 and rs1899663) and cancer risk. Eight studies comprising 7,151 cases and 8,740 controls were included in our study. Overall, no significant associations between the HOTAIR polymorphisms (rs920778, rs4759314 and rs1899663) and cancer risk were observed. However, in further stratified analyses, the variant T allele of rs920778 exhibited a significant increased risk of developing digestive cancers (dominant model: OR = 1.44; 95% CI = 1.31-1.59). These findings provided evidence that HOTAIR rs920778 may modify the susceptibility to certain cancer types. Further studies incorporating subjects with different ethnic backgrounds combined with re-sequencing of the marked region and functional evaluations are warranted.
HOX转录本反义基因间RNA(HOTAIR)是一种长链非编码RNA(lncRNA),在不同癌细胞中作为致癌分子发挥作用。HOTAIR的基因变异可能影响某些调节因子的活性,并进一步调节HOTAIR的异常表达,这可能是影响肿瘤易感性和预后的潜在机制。最近,已经进行了几项研究来检验HOTAIR多态性与癌症风险之间的可能联系;然而,结果尚无定论。因此,我们进行了一项荟萃分析,以评估HOTAIR多态性(rs920778、rs4759314和rs1899663)与癌症风险之间的关联。我们的研究纳入了八项研究,共7151例病例和8740例对照。总体而言,未观察到HOTAIR多态性(rs920778、rs4759314和rs1899663)与癌症风险之间存在显著关联。然而,在进一步的分层分析中,rs920778的变异T等位基因显示出患消化系统癌症的风险显著增加(显性模型:OR = 1.44;95% CI = 1.31 - 1.59)。这些发现提供了证据,表明HOTAIR rs920778可能改变对某些癌症类型的易感性。有必要开展进一步的研究,纳入不同种族背景的受试者,并结合对标记区域的重新测序和功能评估。