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Hypoxia-inducible factor-1|[alpha]| expression in the gastric carcinogenesis sequence and its prognostic role in gastric and gastro-oesophageal adenocarcinomas

机译:缺氧诱导因子-1 |α|在胃癌发生序列中的表达及其在胃和胃食管腺癌中的预后作用

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Hypoxia-inducible factor-1 (HIF-1)α expression was studied in the gastric carcinogenesis sequence and as a prognostic factor in surgically resected gastric and gastro-oesophageal junction tumours. Protein expression was examined using immunohistochemistry on formalin-fixed biopsies of normal mucosa (n=20), Helicobacter pylori associated gastritis (n=24), intestinal metaplasia (n=24), dysplasia (n=12) and intestinal (n=19) and diffuse (n=21) adenocarcinoma. The relationship between HIF-1α expression and prognosis was assessed in resection specimens from 177 patients with gastric and gastro-oesophageal junction adenocarcinoma. Hypoxia-inducible factor-1α expression was not observed in normal gastric mucosa but increased in density (PPH. pylori-associated gastritis, intestinal metaplasia, dysplasia to adenocarcinoma. The pattern of staining in the resection specimens was focally positive in 49 (28%) and at the invasive tumour edge in 41 (23%). Invasive edge expression was associated with lymph node metastases (P=0.034), advanced TNM stage (P=0.001) and was an adverse prognostic factor for cancer-specific survival (P=0.019). In univariate analysis and in comparison with tumours not expressing HIF-1α, invasive edge staining was associated with a hazard ratio of 1.6 (95% CI 1.0?2.5) and focally positive staining a hazard ratio of 0.7 (95% CI 0.5?1.2). Hypoxia-inducible factor-1α lost prognostic significance in multivariate analysis. The results suggest HIF-1α is involved in gastric carcinogenesis and disease progression, but is only a weak prognostic factor for survival.
机译:在胃癌发生过程中研究了缺氧诱导因子-1(HIF-1)α的表达,并将其作为手术切除的胃和胃-食管连接处肿瘤的预后因素。使用福尔马林固定的正常黏膜活检(n = 20),幽门螺杆菌相关性胃炎(n = 24),肠化生(n = 24),不典型增生(n = 12)和肠(n = 19),通过免疫组织化学检查蛋白表达)和弥漫性(n = 21)腺癌。在177例胃和胃-食管连接腺癌患者的切除标本中评估了HIF-1α表达与预后的关系。在正常胃粘膜中未观察到缺氧诱导因子-1α的表达,但其密度增加(PPH。幽门相关胃炎,肠化生,异型增生至腺癌。切除标本的染色模式在49例中呈局部阳性(28%)。 )和41例(占23%)的浸润性肿瘤边缘。浸润性边缘表达与淋巴结转移(P = 0.034),晚期TNM分期(P = 0.001)相关,并且是癌症特异性生存的不良预后因素( P = 0.019)。在单变量分析中,与不表达HIF-1α的肿瘤相比,侵入性边缘染色的危险比为1.6(95 %CI 1.0?2.5),而灶性阳性染色的危险比为0.7(95 %CI 0.5?1.2)。缺氧诱导因子-1α在多因素分析中失去了预后意义,结果表明HIF-1α参与胃癌的发生和疾病进展,但仅是生存的弱预后因子。

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