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Additional data support the role of LINC00673 rs11655237 CT in the development of neuroblastoma

机译:其他数据支持LINC​​00673 rs11655237 C T在神经母细胞瘤发展中的作用

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摘要

Neuroblastoma is the most frequently diagnosed neural tumor of childhood. Abnormal function of the long intergenic non-coding RNA (lincRNA) LINC00673 has been implicated in various human malignancies. Genome-wide association studies revealed the LINC00673 rs11655237 C>T polymorphism to be associated with the risk of neuroblastoma, though the effect was not well defined, in part due to the small sample size in our earlier study. Herein, we verified the impact of LINC00673 rs11655237 C>T on the risk of neuroblastoma in 700 cases and 1516 controls from six centers in China. After pooling all enrolled patients, we observed a significant association between LINC00673 rs11655237 C>T and risk of neuroblastoma (TT vs. CC: adjusted odds ratio [OR]=1.58, 95% confidence interval [CI]=1.06–2.35, P=0.024; additive model: adjusted OR=1.20, 95% CI=1.03–1.39, P=0.020; recessive model: adjusted OR=1.50, 95% CI=1.02–2.22, P=0.040). Stratification analysis revealed a significant relationship between rs11655237 CT/TT and neuroblastoma risk in subgroups of males, patients whose tumor originated in the adrenal gland, and patients with clinical stage IV disease. These findings add new evidence of the importance of LINC00673 rs11655237 C>T to the risk of developing neuroblastoma.
机译:神经母细胞瘤是儿童中最常见的神经瘤。长的基因间非编码RNA(lincRNA)LINC00673的异常功能与各种人类恶性肿瘤有关。全基因组关联研究表明,LINC00673 rs11655237 C> T多态性与神经母细胞瘤的风险有关,尽管这种作用尚未明确定义,部分原因是我们早期研究的样本量较小。本文中,我们验证了来自中国六个中心的700例病例和1516例对照的LINC00673 rs11655237 C> T对神经母细胞瘤风险的影响。汇总所有入组患者后,我们观察到LINC00673 rs11655237 C> T与神经母细胞瘤的风险之间存在显着相关性(TT与CC:调整后的优势比[OR] = 1.58,95%置信区间[CI] = 1.06–2.35,P = 0.024;附加模型:调整后的OR = 1.20,95%CI = 1.03–1.39,P = 0.020;隐性模型:调整后的OR = 1.50,95%CI = 1.02–2.22,P = 0.040)。分层分析显示,rs11655237 CT / TT与男性亚组,肿瘤起源于肾上腺的患者以及患有临床IV期疾病的患者的神经母细胞瘤风险之间存在显着相关性。这些发现为LINC00673 rs11655237 C> T在发展成神经母细胞瘤的风险中的重要性提供了新的证据。

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