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晚期糖基化终末产物受体(RAGE)可能作为一种肿瘤抑制因子来调节肺癌的发展。

RAGE may act as a tumour suppressor to regulate lung cancer development.

作者信息

Wu Shuangshuang, Mao Liping, Li Yan, Yin Yuan, Yuan Weiwei, Chen Yujia, Ren Wenlong, Lu Xiao, Li Yue, Chen Lei, Chen Bo, Xu Wei, Tian Tian, Lu Yihua, Jiang Liying, Zhuang Xun, Chu Minjie, Wu Jianqing

机构信息

Jiangsu Provincial Key Laboratory of Geriatrics, Department of Geriatrics, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.

Department of Oncology, The Sixth People's Hospital of Nantong, Nantong, China.

出版信息

Gene. 2018 Apr 20;651:86-93. doi: 10.1016/j.gene.2018.02.009. Epub 2018 Feb 5.

Abstract

Although the correlation of the RAGE rs2070600 polymorphism and cancer risk has been confirmed, detailed studies with functional and experimental evaluations are lacking. In this study, we first aimed to examine whether this polymorphism is associated with cancer risk based on the latest published data, and consistent with previous meta-analyses, a significant association between the rs2070600 polymorphism and cancer risk was observed (A versus G: OR = 1.25; 95% CI = 1.12-1.40). In additional stratified analyses based on cancer type, rs2070600 was significantly associated with an increased risk of lung cancer (A versus G: OR = 1.20; 95% CI = 1.09-1.33). Moreover, TCGA database showed that the expression level of RAGE was significantly lower in lung cancer tumour tissues than in adjacent non-tumour tissues, which was validated in the GEO database. Additionally, eQTL analysis indicated that the rs2070600 polymorphism may modify the expression level of RAGE in lung squamous cell carcinoma tissues (P = 0.09). Finally, we performed functional experiments in lung cancer cells and preliminarily demonstrated that RAGE may act as a tumour suppressor in lung cancer development. These findings provide evidence that the variant A allele of rs2070600 may decrease the expression of the tumour suppressor gene RAGE, thereby increasing lung cancer risk.

摘要

尽管晚期糖基化终末产物受体(RAGE)基因rs2070600多态性与癌症风险之间的相关性已得到证实,但缺乏功能和实验评估的详细研究。在本研究中,我们首先旨在根据最新发表的数据研究这种多态性是否与癌症风险相关,并且与之前的荟萃分析一致,观察到rs2070600多态性与癌症风险之间存在显著关联(A与G比较:优势比[OR]=1.25;95%置信区间[CI]=1.12-1.40)。在基于癌症类型的额外分层分析中,rs2070600与肺癌风险增加显著相关(A与G比较:OR=1.20;95%CI=1.09-1.33)。此外,癌症基因组图谱(TCGA)数据库显示,肺癌肿瘤组织中RAGE的表达水平显著低于相邻的非肿瘤组织,这在基因表达综合数据库(GEO)中得到了验证。另外,表达定量性状位点(eQTL)分析表明,rs2070600多态性可能会改变肺鳞状细胞癌组织中RAGE的表达水平(P=0.09)。最后,我们在肺癌细胞中进行了功能实验,并初步证明RAGE可能在肺癌发生发展中起到肿瘤抑制作用。这些发现提供了证据,表明rs2070600的变异A等位基因可能会降低肿瘤抑制基因RAGE的表达,从而增加肺癌风险。

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