Griffiths E A, Pritchard S A, Valentine H R, Whitchelo N, Bishop P W, Ebert M P, Price P M, Welch I M, West C M L
Academic Radiation Oncology, Division of Cancer Studies, The University of Manchester, Christie Hospital, Wilmslow Road, Manchester M20 4BX, UK.
Br J Cancer. 2007 Jan 15;96(1):95-103. doi: 10.1038/sj.bjc.6603524. Epub 2006 Dec 19.
Hypoxia-inducible factor-1 (HIF-1)alpha 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-1alpha expression and prognosis was assessed in resection specimens from 177 patients with gastric and gastro-oesophageal junction adenocarcinoma. Hypoxia-inducible factor-1alpha expression was not observed in normal gastric mucosa but increased in density (P<0.01) and intensity (P<0.01) with progression from H. 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-1alpha, 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-1alpha lost prognostic significance in multivariate analysis. The results suggest HIF-1alpha is involved in gastric carcinogenesis and disease progression, but is only a weak prognostic factor for survival.
研究了缺氧诱导因子-1(HIF-1)α在胃癌发生序列中的表达情况,并将其作为手术切除的胃癌和胃食管交界肿瘤的预后因素进行研究。采用免疫组织化学方法检测了正常黏膜(n=20)、幽门螺杆菌相关性胃炎(n=24)、肠化生(n=24)、发育异常(n=12)以及肠型(n=19)和弥漫型(n=21)腺癌的福尔马林固定活检标本中的蛋白表达。在177例胃癌和胃食管交界腺癌患者的切除标本中评估了HIF-1α表达与预后的关系。正常胃黏膜中未观察到缺氧诱导因子-1α表达,但随着从幽门螺杆菌相关性胃炎、肠化生、发育异常发展到腺癌,其表达密度(P<0.01)和强度(P<0.01)均增加。切除标本中的染色模式在49例(28%)中呈局灶性阳性,在41例(23%)中在肿瘤浸润边缘呈阳性。浸润边缘表达与淋巴结转移(P=0.034)、TNM分期较晚(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)。在单因素分析中,与未表达HIF-1α的肿瘤相比,浸润边缘染色的风险比为1.6(95%CI 1.0-2.5),局灶性阳性染色的风险比为0.7(95%CI 0.5-1.2)。在多因素分析中,缺氧诱导因子-1α失去了预后意义。结果表明,HIF-1α参与胃癌发生和疾病进展,但仅是生存的弱预后因素。