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血清血管生成素-2作为肺癌的临床标志物。

Serum angiopoietin-2 as a clinical marker for lung cancer.

作者信息

Park Joo Hun, Park Kwang Joo, Kim Young Sun, Sheen Seung Soo, Lee Keu Sung, Lee Hyoung No, Oh Yoon Jung, Hwang Sung Chul

机构信息

Department of Pulmonary and Critical Care Medicine, Ajou University School of Medicine, San 5, Wonchon-dong, Yeongtong-gu, Suwon, Gyeonggi-do 443-721, South Korea.

出版信息

Chest. 2007 Jul;132(1):200-6. doi: 10.1378/chest.06-2915. Epub 2007 May 15.

Abstract

BACKGROUND

Angiopoietins play a critical role in the angiogenesis related to tumor growth in concert with vascular endothelial growth factor (VEGF), and enhanced expression of angiopoietin-2 has been reported in lung cancer tissue.

METHODS

Patients with lung cancer (n = 136) and healthy volunteers (n = 40) were enrolled. Serum angiopoietin-2 and VEGF concentrations were measured using enzyme-linked immunosorbent assay.

RESULTS

Patients with lung cancer had higher serum angiopoietin-2 (2,046.3 +/- 1,171.3 pg/mL vs 1,269.8 +/- 494.1 pg/mL, p < 0.001) and VEGF (542.9 +/- 445.8 pg/mL vs 364.7 +/- 185.9 pg/mL, p < 0.05) [mean +/- SD] levels than the control group. Serum angiopoietin-2 and VEGF levels correlated with each other in patients with lung cancer (Spearman r = 0.30, p < 0.001), specifically in non-small cell lung cancer (NSCLC) [n = 110; r = 0.34; p < 0.001] but not in small cell lung cancer (n = 26). With stage progression in NSCLC, serum angiopoietin-2 levels increased, and patients with distant metastasis had higher levels than those without metastasis (p < 0.005). By contrast, serum VEGF level did not increase with stage progression, and only had a trend toward elevation in distant metastasis (p = 0.05). In NSCLC, the low angiopoietin-2 group (< 1,605.5 pg/mL) had a better overall survival compared to the high angiopoietin-2 group (> or = 1,605.5 pg/mL; p < 0.05), although this survival benefit was not maintained after controlling for stage in a multivariate analysis. The angiopoietin-2 levels were higher in NSCLC patients with postoperative recurrence than in those without.

CONCLUSIONS

Our study suggests that serum angiopoietin-2 is a useful clinical marker for detecting NSCLC with distant metastasis and is of potential prognostic value.

摘要

背景

血管生成素与血管内皮生长因子(VEGF)协同作用,在与肿瘤生长相关的血管生成中起关键作用,且有报道称肺癌组织中血管生成素-2的表达增强。

方法

纳入肺癌患者(n = 136)和健康志愿者(n = 40)。采用酶联免疫吸附测定法测量血清血管生成素-2和VEGF浓度。

结果

肺癌患者的血清血管生成素-2(2,046.3±1,171.3 pg/mL vs 1,269.8±494.1 pg/mL,p < 0.001)和VEGF(542.9±445.8 pg/mL vs 364.7±185.9 pg/mL,p < 0.05)[均值±标准差]水平高于对照组。肺癌患者血清血管生成素-2和VEGF水平相互相关(Spearman相关系数r = 0.30,p < 0.001),特别是在非小细胞肺癌(NSCLC)[n = 110;r = 0.34;p < 0.001]中,但在小细胞肺癌(n = 26)中不相关。在NSCLC中,随着分期进展,血清血管生成素-2水平升高,远处转移患者的水平高于无转移患者(p < 0.005)。相比之下,血清VEGF水平不随分期进展而升高,仅在远处转移时有升高趋势(p = 0.05)。在NSCLC中,血管生成素-2低水平组(< 1,605.5 pg/mL)的总生存期优于血管生成素-2高水平组(≥1,605.5 pg/mL;p < 0.05),尽管在多变量分析中校正分期后这种生存获益未得到维持。NSCLC术后复发患者的血管生成素-2水平高于未复发患者。

结论

我们的研究表明,血清血管生成素-2是检测伴有远处转移的NSCLC的有用临床标志物,具有潜在的预后价值。

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