首页> 美国卫生研究院文献>Experimental and Therapeutic Medicine >Aurora kinase A (AURKA) and never in mitosis gene A-related kinase 6 (NEK6) genes are upregulated in erosive esophagitis and esophageal adenocarcinoma
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Aurora kinase A (AURKA) and never in mitosis gene A-related kinase 6 (NEK6) genes are upregulated in erosive esophagitis and esophageal adenocarcinoma

机译:糜烂性食管炎和食管腺癌中的Aurora激酶A(AURKA)且从未在有丝分裂基因中表达A相关激酶6(NEK6)基因上调

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摘要

Gastroesophageal reflux disease is a risk factor for esophageal adenocarcinoma yet studies that have investigated the relationship between erosive esophagitis and esophageal adenocarcinoma have usually focused on symptom-related evidence or polymorphisms. There are no epigenetic gene expression studies on this topic. In this study, we aimed to evaluate the relationship between erosive esophagitis and esophageal adenocarcinoma to identify whether there is a genetic predisposition for esophageal adenocarcinoma. The Human Epigenetic Chromatin Modification Enzyme RT2 Profiler PCR array (PAHS-085A) was used to detect the expression of 84 key genes encoding enzymes. This was carried out prospectively for samples from 60 patients (20 patients as a control group, 20 patients with erosive esophagitis and 20 patients with esophageal adenocarcinoma). AURKA, AURKB, NEK6 were expressed at significantly higher levels in esophageal adenocarcinoma compared to the control group. MBD2 was expressed at significantly lower levels in the esophageal adenocarcinoma group compared to the control group. AURKA, AURKC, HDAC9 and NEK6 were expressed at significantly higher levels in erosive esophagitis compared to the control group. There was no difference in upregulated gene expression between the erosive esophagitis and esophageal adenocarcinoma. MBD2 was significantly downregulated in esophageal adenocarcinoma compared to erosive esophagitis. NEK6 and AURKA were significantly upregulated in esophageal adenocarcinoma and erosive esophagitis compared to the control group. This is a novel study on the genetic predisposition for erosive esophagitis and esophageal adenocarcinoma. AURKA and NEK6 are two promising genetic markers for erosive esophagitis and esophageal adenocarcinoma.
机译:胃食管反流病是食管腺癌的危险因素,然而研究侵蚀性食管炎与食管腺癌之间关系的研究通常集中在症状相关证据或多态性上。没有关于此主题的表观遗传基因表达研究。在这项研究中,我们旨在评估糜烂性食管炎与食管腺癌之间的关系,以确定是否存在食管腺癌的遗传易感性。使用人类表观遗传染色质修饰酶RT 2 Profiler PCR阵列(PAHS-085A)检测84种编码酶的关键基因的表达。前瞻性地对60例患者(对照组为20例,糜烂性食管炎为20例,食管腺癌为20例)进行了采样。与对照组相比,食管腺癌中AURKA,AURKB,NEK6的表达水平明显升高。与对照组相比,食管腺癌组中MBD2的表达水平明显降低。与糜烂性食管炎相比,AURKA,AURKC,HDAC9和NEK6的表达水平明显高于对照组。糜烂性食管炎和食管腺癌之间的基因表达上调没有差异。与糜烂性食管炎相比,MBD2在食管腺癌中显着下调。与对照组相比,食管腺癌和糜烂性食管炎中NEK6和AURKA明显上调。这是关于糜烂性食管炎和食管腺癌的遗传易感性的新研究。 AURKA和NEK6是糜烂性食管炎和食道腺癌的两个有前途的遗传标记。

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