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胃泌酸调节素 1 基因在胃腺瘤和癌中的失活。

Inactivation of the Gastrokine 1 gene in gastric adenomas and carcinomas.

机构信息

Department of Pathology, College of Medicine, The Catholic University of Korea, 505 Banpo-dong, Seocho-gu, Seoul, Korea.

出版信息

J Pathol. 2011 Apr;223(5):618-25. doi: 10.1002/path.2838. Epub 2011 Feb 21.

DOI:10.1002/path.2838
PMID:21341273
Abstract

Gastrokine 1 (GKN1) plays a role in the gastric mucosal defence mechanism and may be a gastric tumour suppressor. We have investigated whether inactivation of the GKN1 gene is involved in the development and/or progression of gastric cancers. GKN1 protein expression was examined in gastric adenomas and cancer and we also analysed GKN1 mutation and epigenetic alteration, DNA copy number change and mRNA transcript expression. The effect of GKN1 on cell proliferation and death was examined in wild-type GKN1-transfected AGS gastric cancer cells. Reduced or loss of GKN1 expression was detected in 36 (90%) and 170 (89.5%) of 40 adenomas and 190 gastric cancers, respectively. Statistically, there was no significant relationship between altered expression of GKN1 protein and clinicopathological parameters, including depth of invasion, location and lymph node metastasis (χ(2) test, p > 0.05). In western blot analysis, absence or reduced expression was found in 21 (84.0%) of 25 gastric carcinomas. No mutation was detected in gastric tumours, and hypermethylation of GKN1 gene was found in two tumours. DNA copy number and mRNA transcript of GKN1 were significantly decreased in gastric cancers. In functional analysis, AGS gastric cancer cells transfected with GKN1 wild-type showed marked inhibition of cell proliferation and induction of cell death. These data suggest that inactivation of the GKN1 gene may play an important role in the development of sporadic gastric cancers, as an early event.

摘要

胃动蛋白 1(GKN1)在胃黏膜防御机制中发挥作用,可能是胃肿瘤的抑制因子。我们研究了 GKN1 基因失活是否参与了胃癌的发生和/或进展。我们检测了胃腺瘤和癌组织中 GKN1 蛋白的表达情况,同时分析了 GKN1 突变和表观遗传改变、DNA 拷贝数变化以及 mRNA 转录表达。我们在野生型 GKN1 转染的 AGS 胃癌细胞中研究了 GKN1 对细胞增殖和死亡的影响。结果显示,在 40 个腺瘤中有 36 个(90%)和在 190 个胃癌中有 170 个(89.5%)存在 GKN1 表达减少或缺失。统计学分析表明,GKN1 蛋白表达改变与临床病理参数(包括浸润深度、部位和淋巴结转移)之间无显著相关性(卡方检验,p>0.05)。在 Western blot 分析中,25 个胃癌中有 21 个(84.0%)存在 GKN1 缺失或低表达。在胃癌组织中未检测到突变,有两个肿瘤存在 GKN1 基因的超甲基化。GKN1 的 DNA 拷贝数和 mRNA 转录均显著降低。功能分析显示,AGS 胃癌细胞转染野生型 GKN1 后,细胞增殖明显受到抑制,细胞死亡明显增加。这些数据表明,GKN1 基因失活可能在散发型胃癌的发生中发挥重要作用,是一个早期事件。

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