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肿瘤组织 ANG-1 表达和 Ang-1 浓度对非小细胞肺癌患者的预后价值。

Prognostic value of tumour tissue ANG-1 expression and Ang-1 concentration in patients with non-small-cell lung cancer.

机构信息

Chair and Department of Medical and Molecular Biology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland.

Department of Basic Medical Sciences, Faculty of Health Sciences in Bytom, Medical University of Silesia, Katowice, Poland.

出版信息

Pol J Pathol. 2022;73(1):6-13. doi: 10.5114/pjp.2022.117176.

Abstract

Tumor cells stimulate local angiogenesis, resulting in their further multiplication and spread. Angiogenesis is a multifaceted process in which angiopoietins parti- cipate. Angiopoietin-1 (Ang-1) through its receptor Tie2 stimulates endothelial cell survival and the maintenance of the endothelial barrier. These phenomena can support tumour growth by promoting angiogenesis. On the other hand, overproduction of Ang-1 triggers endothelium stability and can lead to angiogenesis inhibition. Because of the ambiguous role of Ang-1, we decided to determine its clinical significance in patients with resectable NSCLC. In a group of 47 patients, tumours and the adjacent non-cancerous tissues were assessed for ANG-1 mRNA expression (using Q-RT-PCR analysis) and Ang-1 concentration (by enzyme-linked immunosorbent assay) together with clinical parameters and the five-year survival rate. ANG-1 expression and Ang-1 concentration were higher in tumour-free tissue, showing no differences between histological types of NSCLC, clinical stage or grading and seemed not to determine the five-year survival. ANG-1 expression and Ang-1 concentration in tumour and tumour-free tissues in patients with NSCLC seem not to be useful as factors supporting either diagnostics or prognosis.

摘要

肿瘤细胞刺激局部血管生成,导致其进一步增殖和扩散。血管生成是一个多方面的过程,其中血管生成素参与其中。血管生成素-1(Ang-1)通过其受体 Tie2 刺激内皮细胞存活和内皮屏障的维持。这些现象可以通过促进血管生成来支持肿瘤生长。另一方面,Ang-1 的过度产生引发内皮稳定性,并可能导致血管生成抑制。由于 Ang-1 的作用不明确,我们决定确定其在可切除 NSCLC 患者中的临床意义。在一组 47 名患者中,使用 Q-RT-PCR 分析评估了肿瘤和相邻非癌组织中的 ANG-1 mRNA 表达(使用 Q-RT-PCR 分析)以及 Ang-1 浓度(通过酶联免疫吸附测定),并结合临床参数和五年生存率。无肿瘤组织中的 ANG-1 表达和 Ang-1 浓度较高,NSCLC 的组织学类型、临床分期或分级之间无差异,似乎不能决定五年生存率。非小细胞肺癌患者肿瘤和无肿瘤组织中的 ANG-1 表达和 Ang-1 浓度似乎不能作为支持诊断或预后的因素。

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