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血栓调节蛋白表达降低与非小细胞肺癌肿瘤细胞侵袭性和不良预后相关。

Decreased expression of thrombomodulin is correlated with tumor cell invasiveness and poor prognosis in nonsmall cell lung cancer.

机构信息

Department of Respiratory Therapy, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.

出版信息

Mol Carcinog. 2010 Oct;49(10):874-81. doi: 10.1002/mc.20663.

Abstract

Thrombomodulin (TM) plays a role in coagulation, inflammation, and cell adhesion. Reduction of TM expression plays an important role in the tumor metastatic process; however, insufficient information is available regarding the expression of TM in nonsmall cell lung cancer (NSCLC). Sixty NSCLC patients who underwent surgery were reviewed for TM expression and multiple variables were assessed by univariate and multivariate analyses. The expression level of TM and its metastatic ability were examined in vitro using the human NSCLC A549 cell line. TM expression in NSCLC was significantly correlated with survival; the 5-yr survival rates of patients with high and low TM expression were 23% and 18% (P < 0.01), respectively. Distribution of TM was detected predominantly in the normal lung tissue compared with lung cancer tissue. Western blot analysis showed, on average, decreased expression levels of TM protein in the lung cancer tissues of patients with NSCLC. An in vitro study also showed that overexpression of TM can inhibit the invasiveness and migration ability of the A549 cell line, whereas silencing of TM significantly enhanced these processes. This inhibition of cellular migration by overexpression of TM was significantly prevented by the selective inhibitors of PI3K and Akt, but not by MAPK inhibitors. This study demonstrates that a decrease in TM expression may be an indicator in the prognosis of NSCLC patients and provides new insights into the molecular mechanisms of TM in the metastasis of NSCLC.

摘要

血栓调节蛋白(TM)在凝血、炎症和细胞黏附中发挥作用。TM 表达的减少在肿瘤转移过程中起着重要作用;然而,关于非小细胞肺癌(NSCLC)中 TM 的表达情况,信息还不够充分。回顾了 60 名接受手术的 NSCLC 患者的 TM 表达情况,并通过单因素和多因素分析评估了多个变量。使用人非小细胞肺癌 A549 细胞系在体外检查 TM 的表达及其转移能力。TM 在 NSCLC 中的表达与生存显著相关;高表达和低表达 TM 的患者 5 年生存率分别为 23%和 18%(P<0.01)。与肺癌组织相比,TM 在正常肺组织中的分布更为明显。Western blot 分析显示,非小细胞肺癌患者的肺癌组织中 TM 蛋白表达水平平均降低。体外研究还表明,TM 的过表达可抑制 A549 细胞系的侵袭和迁移能力,而 TM 的沉默则显著增强了这些过程。过表达 TM 对细胞迁移的抑制作用可被 PI3K 和 Akt 的选择性抑制剂显著阻止,但不能被 MAPK 抑制剂阻止。本研究表明,TM 表达的降低可能是非小细胞肺癌患者预后的一个指标,并为 TM 在非小细胞肺癌转移中的分子机制提供了新的见解。

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