Suppr超能文献

基因rs3738067 A>G多态性降低中国儿童神经母细胞瘤风险:来自一项八中心病例对照研究的证据。

Gene rs3738067 A>G Polymorphism Decreases Neuroblastoma Risk in Chinese Children: Evidence From an Eight-Center Case-Control Study.

作者信息

Zeng Huijuan, Li Meng, Liu Jiabin, Zhu Jinhong, Cheng Jiwen, Li Yong, Zhang Jiao, Yang Zhonghua, Li Li, Zhou Haixia, Li Suhong, Xia Huimin, Zou Yan, He Jing, Yang Tianyou

机构信息

Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.

Department of Clinical Laboratory, Biobank, Harbin Medical University Cancer Hospital, Harbin, China.

出版信息

Front Med (Lausanne). 2021 Dec 14;8:797195. doi: 10.3389/fmed.2021.797195. eCollection 2021.

Abstract

Neuroblastoma is a primary malignancy mainly occurring in children. We have reported that polymorphisms of several N6-methyladenosine (m6A) RNA modification-related genes contributed to neuroblastoma risk in previous studies. YTHDF2, a "reader" of RNA m6A modification, is involved in cancer progression. Here, we estimated the association between a gene rs3738067 A>G polymorphism and neuroblastoma susceptibility in 898 neuroblastoma patients and 1,734 healthy individuals from China. We found that the rs3738067 A>G could decrease neuroblastoma risk [AG vs. AA: adjusted odds ratio (OR) = 0.76, 95% confidence interval (CI) = 0.64-0.90, = 0.002; AG/GG vs. AA: adjusted OR = 0.81, 95% CI = 0.69-0.95, = 0.011). Besides, the rs3738067 AG/GG genotype was related to reduced neuroblastoma risk in the following subgroups: children aged 18 months and under, boys, patients with tumors originating from retroperitoneal, patients at clinical stage IV, and cases at clinical stages III plus IV. Importantly, false-positive report probability analysis proved our significant results worthy of close attention of. The expression quantitative trait locus analysis results revealed that the rs3738067 was associated with the expression of .

摘要

神经母细胞瘤是一种主要发生于儿童的原发性恶性肿瘤。我们在先前的研究中报道,几个N6-甲基腺苷(m6A)RNA修饰相关基因的多态性与神经母细胞瘤风险有关。YTHDF2是RNA m6A修饰的“读取器”,参与癌症进展。在此,我们评估了中国898例神经母细胞瘤患者和1734名健康个体中基因rs3738067 A>G多态性与神经母细胞瘤易感性之间的关联。我们发现rs3738067 A>G可降低神经母细胞瘤风险[AG与AA相比:调整后的比值比(OR)=0.76,95%置信区间(CI)=0.64 - 0.90,P = 0.002;AG/GG与AA相比:调整后的OR = 0.81,95%CI = 0.69 - 0.95,P = 0.011]。此外,rs3738067 AG/GG基因型与以下亚组中神经母细胞瘤风险降低相关:18个月及以下儿童、男孩、肿瘤起源于腹膜后的患者、临床IV期患者以及临床III期加IV期病例。重要的是,假阳性报告概率分析证明我们的显著结果值得密切关注。表达数量性状位点分析结果显示rs3738067与[此处原文缺失相关基因名称]的表达相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e472/8712649/84e6961a4371/fmed-08-797195-g0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验