基质金属蛋白酶与膀胱癌患者上皮-间质转化的正相关及其与临床预后的关系

Q2 Medicine Cancer Microenvironment Pub Date : 2018-06-01 Epub Date: 2018-01-18 DOI:10.1007/s12307-017-0199-4
R Singh, A Mandhani, V Agrawal, Minal Garg
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引用次数: 17

摘要

基质金属蛋白酶(MMPs)参与尿路上皮癌的发病机制使其成为临床和预后意义的敏感标志物。MMPs通过诱导上皮细胞向间充质转化(epithelial-to-mesenchymal transition, EMT)调节肿瘤生长和侵袭,EMT以上皮细胞的复杂重编程为特征,最终导致膀胱尿路上皮结构组织发生重大变化。本研究旨在评估MMPs在两种不同类型膀胱癌疾病中的临床相关性。MMP-2、MMP-7、MMP-9和上皮标志物、E-cadherin等EMT标志物的表达分析;间充质标志物,n -钙粘蛋白和Vimentin;采用实时定量聚合酶链反应(RT-qPCR)对64例膀胱肿瘤组织[{非肌性浸润性膀胱癌(NMIBC) 35例}和{肌性浸润性膀胱癌(MIBC) 29例}]进行emt激活转录因子(EMT-ATFs)、Snail、Slug、Twist和Zeb的检测。采用免疫组化(IHC)染色方法检测配对膀胱肿瘤组织中E-cadherin、N-cadherin、Vimentin、Snail和Slug的蛋白表达和定位。我们的数据显示,在32.8%、25%和37.5%的膀胱肿瘤病例中,MMP-2、MMP-7和MMP-9在转录组水平上过表达。肿瘤组织间质标志物(N-cadherin和Vimentin) mRNA和蛋白水平均有较高表达,且与肿瘤分期和肿瘤分级有统计学相关性(p = 0.02, p = 0.04, Mann-Whitney检验)。在MMPs过表达的肿瘤组织中,转录因子的增加和E-cadherin的弱表达也与肿瘤分期、分级、性别、患者是否有血尿和吸烟史存在显著的统计学相关性。MMPs过表达膀胱肿瘤中EMT标记物的基因表达模式及其与临床特征的显著相关性证实了MMPs在膀胱尿路上皮癌(UCB)发病中的重要作用。特异性MMPs表达的增加可能会影响一些下游EMT计划,从而可能提高其在临床环境中的诊断和预后效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Positive Correlation between Matrix Metalloproteinases and Epithelial-to-Mesenchymal Transition and its Association with Clinical Outcome in Bladder Cancer Patients.

Involvement of matrix metalloproteinases (MMPs) in the pathogenesis of urothelial carcinoma elects them to be sensitive marker for clinical and prognostic implications. MMPs regulate tumor growth and invasion by inducing epithelial-to-mesenchymal transition (EMT) which is characterized by the complex reprogramming of epithelial cells and ultimately bring about major changes in the structural organization of bladder urothelium. The present study has been undertaken to evaluate the clinical relevance of MMPs in two distinct types of bladder cancer disease. Expression analysis of MMPs namely MMP-2, MMP-7, MMP-9 and EMT markers including epithelial marker, E-cadherin; mesenchymal markers, N-cadherin and Vimentin; and EMT-activating transcriptional factors (EMT-ATFs), Snail, Slug, Twist and Zeb was done in 64 cases of bladder tumor tissues [{Non-muscle invasive bladder cancer (NMIBC): 35 cases} and {Muscle invasive bladder cancer (MIBC): 29 cases}] by real-time quantitative polymerase chain reaction (RT-qPCR). Immunohistochemistry (IHC) staining was done in matched bladder tumor tissues to evaluate the protein expression and localization of E-cadherin, N-cadherin, Vimentin, Snail, and Slug. Our data showed overexpression of MMP-2, MMP-7 and MMP-9 at transcriptome level in 32.8%, 25% and 37.5% bladder tumor cases respectively. These tumor tissues were examined for higher expression of mesenchymal markers (N-cadherin and Vimentin) at mRNA and protein level and exhibited statistical association with tumor stage and tumor grade (p = 0.02, p = 0.04, Mann-Whitney test). Significant statistical correlation in tumor tissues with overexpressed MMPs has also been observed between gain of transcriptional factors and weak expression of E-cadherin with tumor stage, grade, gender, presence of hematuria and smoking history of the patients. Gene expression patterns of EMT markers in bladder tumors with overexpressed MMPs and their significant association with clinical profile validate the important role of MMPs in the pathogenesis of urothelial carcinoma of bladder (UCB). Increased expression of specific MMPs may affect several downstream EMT programs and thus may improve its diagnostic and prognostic utility in clinical setting.

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来源期刊
Cancer Microenvironment
Cancer Microenvironment Medicine-Oncology
CiteScore
4.90
自引率
0.00%
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期刊介绍: Cancer Microenvironment is the official journal of the International Cancer Microenvironment Society (ICMS). It publishes original studies in all aspects of basic, clinical and translational research devoted to the study of cancer microenvironment. It also features reports on clinical trials. Coverage in Cancer Microenvironment includes: regulation of gene expression in the cancer microenvironment; innate and adaptive immunity in the cancer microenvironment, inflammation and cancer; tumor-associated stroma and extracellular matrix, tumor-endothelium interactions (angiogenesis, extravasation), cancer stem cells, the metastatic niche, targeting the tumor microenvironment: preclinical and clinical trials.
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