Liu Juan, Ping Wei, Zu Yukun, Sun Wei
Department of Geriatrics, Wuhan University, Renmin Hospital Wuhan 430060, Hubei Province, P.R.C.
Department of Thoracic Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan, Hubei, China.
Int J Clin Exp Pathol. 2014 Aug 15;7(9):6040-7. eCollection 2014.
Lysyl oxidase (LOX) has been reported to regulate tumor metastasis and has been found to involve in modification of extracellular matrix (ECM) in the context of tumorigenesis. The aim of this study is to determine the prognostic significance of LOX in non-small cell lung cancer (NSCLC) patients and to examine the correlation between LOX expression and ECM remodeling-associated MMP2/MMP9 in NSCLC tissues. The mRNA expression of LOX, MMP2 and MMP9 was investigated by quantitative real-time reverse transcriptase-polymerase chain reaction (qRT-PCR) in 30 NSCLC patients. The protein expression of LOX was measured by immunohistochemistry (IHC) in 110 paraffin-embedded tissues with NSCLC and the protein expression of MMP2/MMP9 was measured by in 30 NSCLC patients. The correlation between LOX expression and clinical parameters and MMP2/MMP9 was analyzed by appropriate statistics. The Kaplan-Meier method, univariate and multivariate regression analysis was used to analyze the correlation between LOX expression and overall survival (OS). The relative mRNA expression or protein expression of LOX were significantly higher in NSCLC tumor tissues than in the corresponding noncancerous tissues (P < 0.05). High LOX expression was significantly associated with MMP2, MMP9, tumor size, lymph node metastasis, pathological stage and OS (P < 0.05). Univariate and multivariate analysis showed that LOX was an independent prognostic factor for OS. Our results indicate that LOX may play a role in the metastasis of NSCLC by promoting MMP2/MMP9 expression. LOX expression is an independent prognostic factor in OS in NSCLC.
据报道,赖氨酰氧化酶(LOX)可调节肿瘤转移,并且在肿瘤发生过程中参与细胞外基质(ECM)的修饰。本研究的目的是确定LOX在非小细胞肺癌(NSCLC)患者中的预后意义,并研究NSCLC组织中LOX表达与ECM重塑相关的基质金属蛋白酶2/基质金属蛋白酶9(MMP2/MMP9)之间的相关性。采用定量实时逆转录聚合酶链反应(qRT-PCR)检测30例NSCLC患者中LOX、MMP2和MMP9的mRNA表达。采用免疫组织化学(IHC)检测110例NSCLC石蜡包埋组织中LOX的蛋白表达,并检测30例NSCLC患者中MMP2/MMP9的蛋白表达。采用适当的统计学方法分析LOX表达与临床参数及MMP2/MMP9之间的相关性。采用Kaplan-Meier法、单因素和多因素回归分析来分析LOX表达与总生存期(OS)之间的相关性。NSCLC肿瘤组织中LOX的相对mRNA表达或蛋白表达显著高于相应的癌旁组织(P<0.05)。高LOX表达与MMP2、MMP9、肿瘤大小、淋巴结转移、病理分期和OS显著相关(P<0.05)。单因素和多因素分析表明,LOX是OS的独立预后因素。我们的结果表明,LOX可能通过促进MMP2/MMP9表达在NSCLC转移中发挥作用。LOX表达是NSCLC患者OS的独立预后因素。