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非小细胞肺癌患者淋巴管生成和血管生成的临床意义。

The clinical significance of lymphangiogenesis and angiogenesis in non-small cell lung cancer patients.

作者信息

Kadota Kyuichi, Huang Cheng-Long, Liu Dage, Ueno Masaki, Kushida Yoshio, Haba Reiji, Yokomise Hiroyasu

机构信息

Department of General Thoracic Surgery, Breast and Endocrinological Surgery, Faculty of Medicine, Kagawa University, 1750-1 Miki-cho, Kita-gun, Kagawa 761-0793, Japan.

出版信息

Eur J Cancer. 2008 May;44(7):1057-67. doi: 10.1016/j.ejca.2008.03.012. Epub 2008 Apr 8.

Abstract

BACKGROUND

Angiogenesis and lymphangiogenesis have been reported to affect malignant phenotype.

METHOD

We investigated 147 patients with non-small cell lung cancer (NSCLC). Immunohistochemistry using D2-40 was performed to evaluate lymphatic vessel density (LVD), including Micro-LVD (without lumen), Tubal-LVD (with lumen) and lymphatic vessel invasion (LVI). The intratumoural microvessel density (MVD) was evaluated by CD-34 immunostaining. The expressions of vascular endothelial growth factor-A (VEGF-A) and VEGF-C were also studied.

RESULTS

Lymphangiogenesis was significantly associated with Micro-LVD (p=0.0003). The VEGF-C expression was significantly associated with the Micro-LVD (p=0.0057). In contrast, the VEGF-A expression was significantly associated with the MVD (p=0.0092). The survival was significantly lower in patients with Micro-LVD-high tumours than in patients with Micro-LVD-low tumours (p=0.0397). Survival was also significantly lower in patients with MVD-high tumours than in patients with MVD-low tumours (p=0.0334). A multivariate analysis demonstrated that the Micro-LVD (p=0.0363) and the MVD (p=0.0232) were independent prognostic factors for NSCLC patients.

CONCLUSIONS

Lymphangiogenesis, specifically Micro-LVD and angiogenesis are independently associated with a poor prognosis in NSCLC patients.

摘要

背景

据报道,血管生成和淋巴管生成会影响恶性表型。

方法

我们研究了147例非小细胞肺癌(NSCLC)患者。采用D2-40进行免疫组织化学检测,以评估淋巴管密度(LVD),包括微淋巴管密度(无管腔)、管状淋巴管密度(有管腔)和淋巴管浸润(LVI)。通过CD-34免疫染色评估肿瘤内微血管密度(MVD)。还研究了血管内皮生长因子-A(VEGF-A)和VEGF-C的表达。

结果

淋巴管生成与微淋巴管密度显著相关(p = 0.0003)。VEGF-C表达与微淋巴管密度显著相关(p = 0.0057)。相比之下,VEGF-A表达与微血管密度显著相关(p = 0.0092)。微淋巴管密度高的肿瘤患者的生存率显著低于微淋巴管密度低的肿瘤患者(p = 0.0397)。微血管密度高的肿瘤患者的生存率也显著低于微血管密度低的肿瘤患者(p = 0.0334)。多因素分析表明,微淋巴管密度(p = 0.0363)和微血管密度(p = 0.0232)是NSCLC患者的独立预后因素。

结论

淋巴管生成,特别是微淋巴管密度和血管生成与NSCLC患者的不良预后独立相关。

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