Bayram Süleyman, Sümbül Ahmet Taner, Dadaş Erdoğan
Department of Nursing, Adıyaman School of Health, Adıyaman University, 02040, Adıyaman, Turkey.
Department of Medical Oncology, Faculty of Medicine, Başkent University, 01250, Adana, Turkey.
Tumour Biol. 2016 Apr;37(4):5577-84. doi: 10.1007/s13277-015-4430-y. Epub 2015 Nov 14.
Hox transcript antisense intergenic RNA (HOTAIR), a long non-coding RNA (lncRNA), is pervasively overexpressed and correlated with tumor invasion, progression, metastasis, and poor prognosis in various human cancers including breast cancer (BC) that plays a role as an oncogenic molecule. A common functional single-nucleotide polymorphism (SNP) (rs12826786 C>T) at the HOTAIR promoter has been reported to influence HOTAIR expression and gastric adenocarcinoma susceptibility, but relation of HOTAIR rs12826786 C>T polymorphism with BC susceptibility and clinicopathological characteristics has yet to be reported. To explore the association of the HOTAIR rs12826786 C>T polymorphism with the risk of BC in a Turkish population, a hospital-based case-control study was carried out consisting of 123 BC patients and 122 age-matched healthy controls. HOTAIR rs12826786 C>T polymorphism was determined by real-time polymerase chain reaction (PCR) using TaqMan assay. We found that women carrying TT genotype of HOTAIR rs12826786 C>T polymorphism had an increased risk of developing BC in both codominant (odds ratio (OR) = 2.24, 95 % confidence interval (CI) 1.05-4.81, P = 0.02) and recessive (OR = 2.49, 95 % CI 1.25-4.97, P = 0.008) inheritance models. Moreover, TT genotype of HOTAIR rs12826786 C>T polymorphism was significantly related with multiple clinicopathological characteristics concerned with worse BC progression such as advanced TNM stage (III and IV), larger tumor size (T3 and T4), and distant metastasis (M1), as well as poor histological grade (III) (P < 0.05). Because of our results put forward for the first time that TT genotype of HOTAIR rs12826786 C>T polymorphism might play crucial roles in genetic susceptibility and poor prognosis for BC in Turkish population, further independent studies are needed to confirm our results in a larger series, as well as in patients of distinct populations.
Hox转录反义基因间RNA(HOTAIR)是一种长链非编码RNA(lncRNA),在包括乳腺癌(BC)在内的多种人类癌症中普遍过度表达,且与肿瘤侵袭、进展、转移及不良预后相关,其作为一种致癌分子发挥作用。据报道,HOTAIR启动子区一个常见的功能性单核苷酸多态性(SNP)(rs12826786 C>T)会影响HOTAIR表达及胃腺癌易感性,但HOTAIR rs12826786 C>T多态性与BC易感性及临床病理特征的关系尚未见报道。为探究土耳其人群中HOTAIR rs12826786 C>T多态性与BC风险的关联,开展了一项基于医院的病例对照研究,包括123例BC患者和122例年龄匹配的健康对照。采用TaqMan法通过实时聚合酶链反应(PCR)确定HOTAIR rs12826786 C>T多态性。我们发现,携带HOTAIR rs12826786 C>T多态性TT基因型的女性在共显性(优势比(OR)=2.24,95%置信区间(CI)1.05 - 4.81,P = 0.02)和隐性(OR = 2.49,95% CI 1.25 - 4.97,P = 0.008)遗传模型中患BC的风险均增加。此外,HOTAIR rs12826786 C>T多态性的TT基因型与多个与BC进展较差相关的临床病理特征显著相关,如晚期TNM分期(III和IV期)、更大的肿瘤大小(T3和T4)、远处转移(M1)以及较差的组织学分级(III级)(P < 0.05)。鉴于我们的结果首次提出HOTAIR rs12826786 C>T多态性的TT基因型可能在土耳其人群BC的遗传易感性和不良预后中起关键作用,需要进一步的独立研究在更大样本以及不同人群的患者中证实我们的结果。