Driessen Ann, Landuyt Willy, Pastorekova Sylvia, Moons Johnny, Goethals Laurence, Haustermans Karin, Nafteux Philippe, Penninckx Freddy, Geboes Karel, Lerut Toni, Ectors Nadine
Department of Pathology, University Hospital Maastricht, Maastricht, The Netherlands.
Ann Surg. 2006 Mar;243(3):334-40. doi: 10.1097/01.sla.0000201452.09591.f3.
To evaluate the expression of carbonic anhydrase IX (CA IX) and vascular-endothelial growth factor (VEGF) in esophageal and gastric adenocarcinomas and in turn with the histologic subtype.
Tumor hypoxia is an important factor in therapy resistance. A low oxygen concentration in tumors stimulates a.o. the expression of CA IX, a marker of hypoxia, and VEGF, a pro-angiogenic factor.
We evaluated the immunohistochemical expression of CA IX and VEGF on paraffin-embedded material of 154 resection specimens: 39 esophageal, 73 cardiac, and 42 distal gastric adenocarcinomas (UICC classification). The adenocarcinomas were subtyped according to the Lauren classification (intestinal- and diffuse-type).
chi test, Kaplan-Meier survival analysis, log-rank test, and Cox proportional hazards model.
CA IX and VEGF expression were independent of the localization of the tumor. However, intestinal-type adenocarcinomas showed a significantly higher expression of CA IX as well as VEGF than diffuse-type tumors. VEGF expression was associated with a high microvessel density. Although survival analysis showed that CA IX expression (P = 0.008) as well as the coexpression of CA IX and VEGF (P = 0.008) correlate with a poor outcome, only CA IX expression is an independent prognostic factor for overall survival and metastasis-free survival.
The difference in expression of CA IX and VEGF between intestinal- and diffuse-type adenocarcinomas may possibly explain the different clinical behavior of these tumors. CA IX expression, rather than VEGF positivity in tumors, enables the identification of a subpopulation, characterized by a more aggressive behavior and a poorer prognosis.
评估碳酸酐酶IX(CA IX)和血管内皮生长因子(VEGF)在食管腺癌和胃腺癌中的表达情况,并探讨其与组织学亚型的关系。
肿瘤缺氧是导致治疗抵抗的重要因素。肿瘤内低氧浓度会刺激多种因子的表达,如缺氧标志物CA IX以及促血管生成因子VEGF。
我们评估了154例切除标本石蜡包埋材料中CA IX和VEGF的免疫组化表达情况,其中包括39例食管腺癌、73例贲门腺癌和42例远端胃腺癌(根据国际抗癌联盟(UICC)分类)。腺癌根据劳伦分类法(肠型和弥漫型)进行亚型分类。
采用卡方检验、Kaplan-Meier生存分析、对数秩检验和Cox比例风险模型。
CA IX和VEGF的表达与肿瘤的位置无关。然而,肠型腺癌中CA IX和VEGF的表达明显高于弥漫型肿瘤。VEGF表达与高微血管密度相关。虽然生存分析显示CA IX表达(P = 0.008)以及CA IX和VEGF的共表达(P = 0.008)与不良预后相关,但只有CA IX表达是总生存和无转移生存的独立预后因素。
肠型和弥漫型腺癌中CA IX和VEGF表达的差异可能解释了这些肿瘤不同的临床行为。CA IX的表达而非肿瘤中的VEGF阳性,能够识别出具有更侵袭性行为和更差预后特征的亚群。