Dango Sebastian, Sienel Wulf, Schreiber Moritz, Stremmel Christian, Kirschbaum Andreas, Pantel Klaus, Passlick Bernward
Department of Thoracic Surgery, Albert-Ludwigs-University Freiburg, 79106 Freiburg, Germany.
Lung Cancer. 2008 Jun;60(3):426-33. doi: 10.1016/j.lungcan.2007.11.015. Epub 2008 Jan 22.
Recent studies have challenged the previously postulated concept of a tumor-suppressive effect of carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM-1). A possible angiogenic influence of CEACAM-1 in non-small-cell lung cancer (NSCLC) has not been investigated so far. Therefore, we examined microvessel density (MVD) and CEACAM-1 expression in primary NSCLC and analyzed their possible correlations under consideration of their prognostic effects. Specimens from 82 consecutive patients with completely resected NSCLC were stained immunohistochemically using the monoclonal anti-CEACAM-1 antibody 4D1/C2 and the monoclonal anti-CD31 antibody JC70A. The prognostic relevance of CEACAM-1 expression and MVD was evaluated by univariate Kaplan-Meier and multivariate Cox regression analysis. The median follow-up period was 75 months (range 10-156 months). A high MVD (i.e., > or =31microvessels/400x microscopic field) was observed more frequently in tumors with high CEACAM-1 expression (i.e., >/=66% stained tumor cells) than in tumors with low CEACAM-1 expression (61.8% vs. 33.3%, respectively; p=0.01). In univariate survival analyses, high CEACAM-1 expression and high MVD were associated with development of distant metastasis (p=0.011 and 0.022, respectively) and decreased cancer-related survival (p=0.046 and 0.006, respectively). Multivariate Cox regression analysis demonstrated that the prognostic impact of CEACAM-1 depended on the prognostic influence of MVD, while MVD itself represented an independent prognosticator for unfavorable cancer-related survival (p=0.021; relative risk 2.1; 95% confidence interval, 1.1-4.0). Here we show for the first time that high CEACAM-1 expression is associated with an increased angiogenic activity in NSCLC, and that the prognostic influence of CEACAM-1 might be derived from this association.
近期研究对先前假定的癌胚抗原相关细胞黏附分子1(CEACAM-1)具有肿瘤抑制作用的概念提出了挑战。迄今为止,尚未对CEACAM-1在非小细胞肺癌(NSCLC)中可能的血管生成影响进行研究。因此,我们检测了原发性NSCLC中的微血管密度(MVD)和CEACAM-1表达,并在考虑其预后作用的情况下分析了它们之间可能的相关性。对82例连续的NSCLC完全切除患者的标本,使用单克隆抗CEACAM-1抗体4D1/C2和单克隆抗CD31抗体JC70A进行免疫组织化学染色。通过单变量Kaplan-Meier分析和多变量Cox回归分析评估CEACAM-1表达和MVD的预后相关性。中位随访期为75个月(范围10 - 156个月)。与低CEACAM-1表达的肿瘤相比,高CEACAM-1表达的肿瘤(即≥66%的肿瘤细胞染色)中更频繁地观察到高MVD(即≥31个微血管/400倍显微镜视野)(分别为61.8%和33.3%;p = 0.01)。在单变量生存分析中,高CEACAM-1表达和高MVD与远处转移的发生相关(分别为p = 0.011和0.022),以及与癌症相关生存率降低相关(分别为p = 0.046和0.006)。多变量Cox回归分析表明,CEACAM-1的预后影响取决于MVD的预后影响,而MVD本身是癌症相关生存不良的独立预后因素(p = 0.021;相对风险2.1;95%置信区间,1.1 - 4.0)。我们首次表明,高CEACAM-1表达与NSCLC中血管生成活性增加相关,并且CEACAM-1的预后影响可能源于这种关联。