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胃癌中的血管生成因子与生长因子

Angiogenic and growth factors in gastric cancer.

作者信息

Blank Susanne, Deck Catrin, Dreikhausen Lena, Weichert Wilko, Giese Natalia, Falk Christine, Schmidt Thomas, Ott Katja

机构信息

Department of Surgery, University Hospital of Heidelberg, Heidelberg, Germany.

Department of Surgery, University Hospital of Heidelberg, Heidelberg, Germany.

出版信息

J Surg Res. 2015 Apr;194(2):420-429. doi: 10.1016/j.jss.2014.11.028. Epub 2014 Nov 26.

Abstract

BACKGROUND

Antiangiogenic treatment is at the horizon in the palliative treatment of gastric cancer (GC), but data on proangiogenic biomarkers are still limited. The aim of this study was to analyze five proteins with a function in tumor angiogenesis: vascular endothelial growth factor (VEGF), angiopoietin-2 (Ang-2), follistatin, leptin, and platelet endothelial cell adhesion molecule 1 (CD31) in peripheral blood and corresponding tumor tissue.

MATERIAL AND METHODS

From 2008-2010, tumor tissue (n = 76) and corresponding preoperative serum (n = 69) of patients with localized GC were collected; 45 had perioperative chemotherapy. Protein serum or tumor lysate levels of these factors were measured by an angiogenesis multiplex immunoassay and correlated with response and survival.

RESULTS

Serum Ang-2 had prognostic relevance in the whole study population (P = 0.027). In subgroup analysis, serum VEGF and Ang-2 had prognostic relevance in primarily resected patients (P = 0.028; P = 0.048) but no association was found in neoadjuvantly treated patients. Follistatin concentration in the tumor tissue was associated with prognosis in all patients (P = 0.019). Tumor VEGF concentrations were correlated with histopathologic response (P = 0.011), with patients showing >50% remaining tumor having higher VEGF concentrations. The tissue Ang-2/VEGF ratio was significantly correlated with both clinical and histopathologic response (P = 0.029, P = 0.009). Additionally, the level of leptin in the tissue was associated with clinical response: nonresponding patients had higher leptin levels than those of responding patients (P = 0.032).

CONCLUSIONS

Our results show the importance of angiogenetic factors in serum and tumor tissue in GC for prognosis and treatment response. Further trials in larger patient populations are warranted for a further evaluation of proangiogenetic factors as biomarkers in gastrointestinal cancer.

摘要

背景

抗血管生成治疗即将应用于胃癌(GC)的姑息治疗,但有关促血管生成生物标志物的数据仍然有限。本研究的目的是分析外周血和相应肿瘤组织中五种具有肿瘤血管生成功能的蛋白质:血管内皮生长因子(VEGF)、血管生成素-2(Ang-2)、卵泡抑素、瘦素和血小板内皮细胞黏附分子1(CD31)。

材料与方法

收集2008年至2010年局部GC患者的肿瘤组织(n = 76)和相应的术前血清(n = 69);45例患者接受了围手术期化疗。通过血管生成多重免疫测定法测量这些因子的血清蛋白或肿瘤裂解物水平,并与反应和生存率相关联。

结果

血清Ang-2在整个研究人群中具有预后相关性(P = 0.027)。在亚组分析中,血清VEGF和Ang-2在主要接受手术切除的患者中具有预后相关性(P = 0.028;P = 0.048),但在接受新辅助治疗的患者中未发现相关性。肿瘤组织中的卵泡抑素浓度与所有患者的预后相关(P = 0.019)。肿瘤VEGF浓度与组织病理学反应相关(P = 0.011),肿瘤残留>50%的患者VEGF浓度较高。组织Ang-2/VEGF比值与临床和组织病理学反应均显著相关(P = 0.029,P = 0.009)。此外,组织中瘦素水平与临床反应相关:无反应患者的瘦素水平高于有反应患者(P = 0.032)。

结论

我们的结果表明,GC患者血清和肿瘤组织中的血管生成因子对预后和治疗反应具有重要意义。有必要在更大的患者群体中进行进一步试验,以进一步评估促血管生成因子作为胃肠道癌生物标志物的作用。

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