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星形胶质细胞上调基因-1在非小细胞肺癌中过度表达,并与肿瘤血管生成增加相关。

Astrocyte elevated gene-1 is overexpressed in non-small-cell lung cancer and associated with increased tumour angiogenesis.

作者信息

Ding Qiuping, Chen Yingrong, Dong Shunli, Xu Xuting, Liu Jin, Song Pengtao, Yu Caihua, Ma Zhihong

机构信息

Department of Surgery, Huzhou Central Hospital, Huzhou, Zhejiang, China.

Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, China.

出版信息

Interact Cardiovasc Thorac Surg. 2018 Mar 1;26(3):395-401. doi: 10.1093/icvts/ivx340.

Abstract

OBJECTIVES

Astrocyte elevated gene-1 (AEG-1) functions to mediate angiogenesis, and its upregulation is responsible for tumour angiogenesis during cancer development. This study analysed AEG-1 expression in non-small-cell lung cancer (NSCLC) for association with NSCLC clinicopathological features and tumour angiogenesis.

METHODS

The expression of AEG-1, vascular endothelial growth factor and intratumoural microvessel density (assessed using the expression of CD105) was detected by immunohistochemistry in 88 paired tumour tissue and adjacent normal tissue specimens obtained from NSCLC patients. The Kaplan-Meier curves were used for survival analysis through an online tool (http://kmplot.com/analysis/).

RESULTS

AEG-1 was overexpressed in 61.3% of NSCLC tissues vs 6.8% (6/88) of normal tissues (P < 0.001). AEG-1 expression in NSCLC was significantly associated with advanced pTNM stage (P = 0.021), tumour dedifferentiation (P = 0.034), vascular invasion (P = 0.035), lymph node metastasis (P < 0.001) and poor overall survival (P = 0.024). Moreover, the expression of AEG-1 in NSCLC was associated with tumour angiogenesis; that is, vascular endothelial growth factor overexpression (P < 0.001) and intratumoural microvessel density (P < 0.001).

CONCLUSIONS

This study demonstrates that AEG-1 expression is associated with NSCLC development, angiogenesis, progression and poor prognosis, indicating that the adjuvant therapy with antiangiogenic agent be adopted for the early postoperative period before the start of conventional chemotherapy in patients with AEG-1 overexpressed NSCLC.

摘要

目的

星形胶质细胞上调基因1(AEG-1)具有介导血管生成的功能,其上调是癌症发展过程中肿瘤血管生成的原因。本研究分析了非小细胞肺癌(NSCLC)中AEG-1的表达情况,及其与NSCLC临床病理特征和肿瘤血管生成的关系。

方法

采用免疫组织化学法检测了88例NSCLC患者的配对肿瘤组织和癌旁正常组织标本中AEG-1、血管内皮生长因子的表达以及肿瘤内微血管密度(通过CD105表达进行评估)。通过在线工具(http://kmplot.com/analysis/)使用Kaplan-Meier曲线进行生存分析。

结果

61.3%的NSCLC组织中AEG-1呈过表达,而正常组织中这一比例为6.8%(6/88)(P<0.001)。NSCLC中AEG-1的表达与pTNM晚期(P=0.021)、肿瘤去分化(P=0.034)、血管侵犯(P=0.035)、淋巴结转移(P<0.001)及总生存期差(P=0.024)显著相关。此外,NSCLC中AEG-1的表达与肿瘤血管生成相关,即与血管内皮生长因子过表达(P<0.001)和肿瘤内微血管密度(P<0.001)相关。

结论

本研究表明,AEG-1的表达与NSCLC的发生、血管生成、进展及预后不良相关,提示对于AEG-1过表达的NSCLC患者,在术后早期、常规化疗开始前应采用抗血管生成药物进行辅助治疗。

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