E-cadherin、β-catenin、基质金属蛋白酶-2、基质金属蛋白酶-9生物标志物的表型评价及基因表达预测口腔鳞状细胞癌转移与临床相关性

Q1 Environmental Science
Journal of Carcinogenesis Pub Date : 2020-08-06 eCollection Date: 2020-01-01 DOI:10.4103/jcar.JCar_8_20
S V Sowmya, Roopa S Rao, Kavitha Prasad
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引用次数: 10

摘要

背景:关于上皮-间质转化(EMT)生物标志物在口腔鳞状细胞癌(OSCC)转移中的真正预测作用,目前存在争议。迄今为止,也有有限的研究在印度人群中同时研究了EMT生物标志物的蛋白质和基因表达。目的:本研究的目的是通过常规方法和MATLAB软件评估EMT生物标志物的基因表达和定量蛋白表达,并确定转移性和非转移性OSCCs的表达是否存在临床病理相关性差异。设置和设计:各从科室档案中获得20张转移性和非转移性OSCC组织切片。进行EMT标记物的基因表达和定量蛋白表达,并与临床参数进行相关性分析。对象和方法:采用半定量和定量(MATLAB)方法对免疫染色的EMT生物标志物切片进行评估。采用半定量逆转录-聚合酶链反应进行基因表达。这些发现与临床参数相关。统计方法:采用SPSS软件进行Pearson卡方检验、Student’st检验和单因素logistic回归分析。结果:E-cadherin和β-catenin的低表达和基质金属蛋白酶(MMP)-2和MMP-9的高表达与III期和IV期转移风险高相关。此外,MMP-2和MMP-9基因在临床晚期OSCC的表达上调具有较高的转移潜力。结论:本研究首次在MATLAB中使用纹理和颜色分割来客观评价EMT生物标志物的蛋白表达。本研究有助于研究EMT标志物的蛋白和基因表达与临床的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prediction of metastasis in oral squamous cell carcinoma through phenotypic evaluation and gene expression of E-cadherin, β-catenin, matrix metalloproteinase-2, and matrix metalloproteinase-9 biomarkers with clinical correlation.

Prediction of metastasis in oral squamous cell carcinoma through phenotypic evaluation and gene expression of E-cadherin, β-catenin, matrix metalloproteinase-2, and matrix metalloproteinase-9 biomarkers with clinical correlation.

Prediction of metastasis in oral squamous cell carcinoma through phenotypic evaluation and gene expression of E-cadherin, β-catenin, matrix metalloproteinase-2, and matrix metalloproteinase-9 biomarkers with clinical correlation.

Prediction of metastasis in oral squamous cell carcinoma through phenotypic evaluation and gene expression of E-cadherin, β-catenin, matrix metalloproteinase-2, and matrix metalloproteinase-9 biomarkers with clinical correlation.

Context: Controversies prevail regarding the true predictive role of epithelial-mesenchymal transition (EMT) biomarkers in metastasis of oral squamous cell carcinoma (OSCC). There is also limited research carried on till date wherein the protein and gene expression of EMT biomarkers have been investigated simultaneously in the Indian population.

Aim: The aim of this study was to assess the gene expression and quantitative protein expression of EMT biomarkers using conventional method and MATLAB software and to determine if there is any difference in the expression between metastatic and nonmetastatic OSCCs with clinicopathologic correlation.

Settings and design: Twenty metastatic and nonmetastatic OSCC tissue sections each were obtained from department archives. Gene expression and quantified protein expression of EMT markers were done and correlated with clinical parameters.

Subjects and methods: Sections immunostained for EMT biomarkers were evaluated using semi-quantitative and quantitative (MATLAB) methods. Gene expression using semi-quantitative reverse transcriptase-polymerase chain reaction was done. These findings were correlated with clinical parameters.

Statistical analysis used: Pearson's Chi-square test, Student's t-test, and univariate logistic regression analysis were performed using SPSS software.

Results: The low immunoexpression of E-cadherin and β-catenin and the high expression of matrix metalloproteinase (MMP)-2 and MMP-9 correlate with Stages III and IV showing high metastatic risk. Furthermore, the upregulated MMP-2 and MMP-9 gene expressions in advanced clinical stages of OSCC have high metastatic potential.

Conclusions: This study is the first of its kind to employ texture and color segmentation in MATLAB to objectively assess the protein expression of EMT biomarkers. This research is instrumental in studying the protein and gene expressions of EMT markers with clinical correlation.

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来源期刊
Journal of Carcinogenesis
Journal of Carcinogenesis Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
7.50
自引率
0.00%
发文量
0
审稿时长
15 weeks
期刊介绍: Journal of Carcinogenesis considers manuscripts in many areas of carcinogenesis and Chemoprevention. Primary areas of interest to the journal include: physical and chemical carcinogenesis and mutagenesis; processes influencing or modulating carcinogenesis, such as DNA repair; genetics, nutrition, and metabolism of carcinogens; the mechanism of action of carcinogens and modulating agents; epidemiological studies; and, the formation, detection, identification, and quantification of environmental carcinogens. Manuscripts that contribute to the understanding of cancer prevention are especially encouraged for submission
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