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探讨 IGF1、IGF2BP2 和 IGFBP3 变异与淋巴结状态及食管胃结合部腺癌风险的关系。

Investigation of IGF1, IGF2BP2, and IGFBP3 variants with lymph node status and esophagogastric junction adenocarcinoma risk.

机构信息

Department of Cardiothoracic Surgery, Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.

Department of Thoracic Surgery, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.

出版信息

J Cell Biochem. 2019 Apr;120(4):5510-5518. doi: 10.1002/jcb.27834. Epub 2018 Oct 18.

Abstract

Esophagogastric junction adenocarcinoma (EGJA) may be associated with obesity and overweight. Thus, any variant in energy metabolism-related gene may influence the development of EGJA. In this study, we recruited 720 EGJA cases and 1541 noncancer controls. We selected IGF2BP2 rs4402960 G > T, rs1470579 A > C, IGF1 rs5742612 A > G and IGFBP3 rs3110697 G > A, rs2270628 C > T and rs6953668 G > A loci and assessed the relationship of these polymorphisms with lymph node status and susceptibility of EGJA. We found that IGF2BP2 rs1470579 A > C and IGFBP3 rs6953668 G > A polymorphisms were associated with the decreased risk of EGJA ( IGF2BP2 rs1470579: CC vs AA: adjusted odds ratio [OR] = 0.65, 95% confidence interval [CI] = 0.43-0.98, P = 0.041 and CC vs AA/AC: adjusted OR = 0.62, 95% CI = 0.41-0.93, P = 0.021 and IGFBP3 rs6953668: GA vs GG: adjusted OR = 0.66, 95% CI = 0.47-0.93, P = 0.019 and GA/AA vs GG: adjusted OR = 0.68, 95% CI = 0.48-0.95, P = 0.026). However, we also found that IGF1 rs5742612 A > G polymorphism increased the risk of LNM among patients with EGJA (GG vs AA: adjusted OR = 1.88, 95% CI = 1.02-3.46, P = 0.042 and GG vs AA/AG: adjusted OR = 1.92, 95% CI = 1.06-3.47, P = 0.032). This study suggests that IGF2BP2 rs1470579 A > C and IGFBP3 rs6953668 G > A polymorphisms may decrease genetic susceptibility to EGJA in eastern Chinese Han population. In addition, our findings also indicate that IGF1 rs5742612 A > G polymorphism may increase the susceptibility of LNM among patients with EGJA.

摘要

食管胃结合部腺癌(EGJA)可能与肥胖和超重有关。因此,能量代谢相关基因的任何变异都可能影响 EGJA 的发展。在这项研究中,我们招募了 720 例 EGJA 病例和 1541 名非癌症对照。我们选择了 IGF2BP2 rs4402960 G > T、rs1470579 A > C、IGF1 rs5742612 A > G 和 IGFBP3 rs3110697 G > A、rs2270628 C > T 和 rs6953668 G > A 位点,并评估了这些多态性与淋巴结状态和 EGJA 易感性的关系。我们发现,IGF2BP2 rs1470579 A > C 和 IGFBP3 rs6953668 G > A 多态性与 EGJA 风险降低相关(IGF2BP2 rs1470579:CC 与 AA:调整后的优势比 [OR] = 0.65,95%置信区间 [CI] = 0.43-0.98,P = 0.041 和 CC 与 AA/AC:调整后的 OR = 0.62,95%CI = 0.41-0.93,P = 0.021 和 IGFBP3 rs6953668:GA 与 GG:调整后的 OR = 0.66,95%CI = 0.47-0.93,P = 0.019 和 GA/AA 与 GG:调整后的 OR = 0.68,95%CI = 0.48-0.95,P = 0.026)。然而,我们还发现 IGF1 rs5742612 A > G 多态性增加了 EGJA 患者发生 LNM 的风险(GG 与 AA:调整后的 OR = 1.88,95%CI = 1.02-3.46,P = 0.042 和 GG 与 AA/AG:调整后的 OR = 1.92,95%CI = 1.06-3.47,P = 0.032)。这项研究表明,IGF2BP2 rs1470579 A > C 和 IGFBP3 rs6953668 G > A 多态性可能降低中国东部汉族人群对 EGJA 的遗传易感性。此外,我们的研究结果还表明,IGF1 rs5742612 A > G 多态性可能增加 EGJA 患者发生 LNM 的易感性。

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