Analysis of ANRIL gene polymorphism rs4977574 association with kidney cancer development in Ukrainian population.

A. Volkogon, V. Harbuzova, A. Ataman
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引用次数: 3

Abstract

ANRIL (Antisense Non-coding RNA in the INK4 Locus, also known as CDKN2B-AS1) – 3.8-kb long non-coding RNA transcribed from the antisense strand of INK4b-ARF-INK4a gene cluster. It is known that ANRIL overexpression is associated with development of oncological pathologies of different localization. In addition, there are a number of studies devoted to role of ANRIL genetic polymorphism in emergence and progression of tumors, including tumors of genitourinary system. The aim of the study was to check the possible association between ANRIL gene polymorphism rs4977574 and kidney cancer development in representatives of Ukrainian population. Whole venous blood of 101 patients with clear cell renal cell carcinoma (CCRCC) (42 women and 59 men) and 100 patients without oncology history (34 women and 66 men) was used in the study. DNA from blood white cells was extracted using GeneJET Whole Blood Genomic DNA Purification Mini Kit (Thermo Fisher Scientific, USA). Genotyping of rs4977574 ANRIL gene polymorphic locus was performed using real-time polymerase chain reaction (real-time PCR) method in the presence of TaqMan assay C_31720978_30. The mathematical data were processed using the SPSS software package (version 17.0). P values <0.05 were considered as statistically significant. It was found that difference in rs4977574-genotype distribution between patients with CCRCC and control persons was absent in general group (P=0.216). At the same time, the statistical analysis stratified by gender showed that both in female and male subjects rs4977574-genotypes frequency also did not differ significantly between comparison groups (P=0.526 and P=0.160, respectively). However, after adjusting for age, body mass index, and smoking habits statistically significant association between rs4977574 ANRIL gene polymorphism and risk of kidney cancer development was detected in male subjects under superdominant inheritance model (P=0.049). It was revealed that heterozygotes (AG-genotype) have 2.17-fold  higher risk of CCRCC development (95% CI=1.005-4.695) compared to patients with AA- and GG-genotypes. In summary, this is the first report about ANRIL gene polymorphisms association with kidney cancer. Obtained results revealed that rs4977574 is related to kidney cancer risk only in Ukrainian men. Male individuals with AG-genotype have higher risk of CCRCC development compared to AA- and GG-genotypes carriers.
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乌克兰人群ANRIL基因多态性rs4977574与肾癌发展的相关性分析
ANRIL (Antisense Non-coding RNA in INK4 Locus,又称CDKN2B-AS1)是INK4b-ARF-INK4a基因簇的反义链转录的3.8 kb长的非编码RNA。已知ANRIL过表达与不同部位肿瘤病理的发展有关。此外,有大量研究致力于ANRIL基因多态性在包括泌尿生殖系统肿瘤在内的肿瘤发生和发展中的作用。该研究的目的是检查ANRIL基因多态性rs4977574与乌克兰人群中肾癌发展之间可能的关联。101例透明细胞肾细胞癌(CCRCC)患者(女性42例,男性59例)和100例无肿瘤史患者(女性34例,男性66例)的全静脉血用于研究。使用GeneJET全血基因组DNA纯化迷你试剂盒(Thermo Fisher Scientific, USA)从白细胞中提取DNA。在TaqMan检测C_31720978_30的条件下,采用实时聚合酶链反应(real-time PCR)方法对rs4977574 ANRIL基因多态性位点进行分型。数学数据采用SPSS软件包(17.0版)处理。P值<0.05认为有统计学意义。结果发现,普通组CCRCC患者与对照组rs4977574基因型分布无差异(P=0.216)。同时,按性别分层的统计分析显示,女性和男性受试者rs4977574基因型频率在对照组之间也无显著差异(P=0.526和P=0.160)。然而,在超显性遗传模型下,调整年龄、体重指数、吸烟习惯等因素后,男性受试者rs4977574 ANRIL基因多态性与肾癌发生风险之间存在统计学意义(P=0.049)。结果显示,杂合子(ag -基因型)发生CCRCC的风险是AA-和gg -基因型患者的2.17倍(95% CI=1.005-4.695)。总之,这是关于ANRIL基因多态性与肾癌相关的第一篇报道。获得的结果显示,rs4977574仅与乌克兰男性的肾癌风险相关。与AA-和gg基因型携带者相比,ag基因型男性个体发生CCRCC的风险更高。
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