Moss Steven F, Lee Jin-Woo, Sabo Edmond, Rubin Anna K, Rommel John, Westley Bruce R, May Felicity E B, Gao John, Meitner Patricia A, Tavares Rose, Resnick Murray B
Department of Medicine, Gastroenterology Division, Rhode Island Hospital, 593 Eddy Street, APC 414, Providence, RI 02903, USA.
Clin Cancer Res. 2008 Jul 1;14(13):4161-7. doi: 10.1158/1078-0432.CCR-07-4381.
Transcriptional profiling showed decreased expression of gastrokine 1 (GKN1) and the related trefoil factor interacting protein (TFIZ1/GKN2) in Helicobacter pylori infection. Decreased GKN1 and GKN2 mRNA expression has been reported in gastric adenocarcinoma. We have examined GKN1 and GKN2 protein expression in a large gastric cancer series, correlated expression with tumor subtype, and evaluated their utility as prognostic biomarkers.
GKN1, GKN2, and the trefoil factors TFF1 and TFF3 were examined in tissue microarrays from 155 distal gastric adenocarcinomas. Immunohistochemical expression was correlated with clinical outcome. GKN1 and GKN2 expression was measured by real-time PCR and Western analysis in samples of gastric cancer and adjacent nonneoplastic mucosa.
GKN1 was lost in 78% of diffuse and 42% of intestinal cancers (P < 0.0001, diffuse versus intestinal). GKN2 expression was lost in 85% of diffuse and 54% of intestinal type cancers (P < 0.002). GKN1 and GKN2 down-regulation were confirmed by Western and real-time PCR analysis. Loss of either protein was associated with significantly worse outcome in intestinal-type tumors by univariate analysis; and GKN2 loss remained a predictor of poor outcome in multivariate analysis (P < 0.033). TFF1 was lost in >70%, and TFF3 was expressed in approximately 50% of gastric cancers.
Loss of GKN1 and GKN2 expression occurs frequently in gastric adenocarcinomas, especially in the diffuse subtype. GKN1 and GKN2 loss are associated with shorter overall survival in the intestinal subtype.
转录谱分析显示,幽门螺杆菌感染时胃动素1(GKN1)及相关三叶因子相互作用蛋白(TFIZ1/GKN2)的表达降低。已有报道称,胃腺癌中GKN1和GKN2 mRNA表达降低。我们在一个大型胃癌队列中检测了GKN1和GKN2蛋白表达,将其表达与肿瘤亚型相关联,并评估了它们作为预后生物标志物的效用。
在155例远端胃腺癌的组织芯片中检测GKN1、GKN2以及三叶因子TFF1和TFF3。免疫组化表达与临床结局相关。通过实时PCR和蛋白质印迹分析检测胃癌及相邻非肿瘤黏膜样本中GKN1和GKN2的表达。
78%的弥漫性癌和42%的肠型癌中GKN1缺失(P<0.0001,弥漫性癌与肠型癌相比)。85%的弥漫性癌和54%的肠型癌中GKN2表达缺失(P<0.002)。蛋白质印迹和实时PCR分析证实了GKN1和GKN2的下调。单因素分析显示,在肠型肿瘤中,任一蛋白的缺失都与显著更差的结局相关;多因素分析中,GKN2缺失仍是不良结局的一个预测指标(P<0.033)。超过70%的胃癌中TFF1缺失,约50%的胃癌中TFF3表达。
GKN1和GKN2表达缺失在胃腺癌中频繁发生,尤其是在弥漫性亚型中。GKN1和GKN2缺失与肠型亚型的总生存期缩短相关。