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Diagnostic value of cyclin-dependent kinase/cyclin-dependent kinase inhibitor expression ratios as biomarkers of locoregional and hematogenous dissemination risks in oral squamous cell carcinoma

机译:细胞周期蛋白依赖性激酶/细胞周期蛋白依赖性激酶抑制剂表达比作为口腔鳞状细胞局部和血源性传播危险的生物标志物的诊断价值

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摘要

The aim of the present study was to investigate the diagnostic value of cell cycle-related genes in oral squamous cell carcinoma (OSCC) by examining the expression of the following genes in 77 OSCC tissues by quantitative polymerase chain reaction: Cyclin genes (CCNA1, CCND1, CCND2 and CCNE1), cyclin-dependent kinase (CDK) genes (CDK1, CDK2 and CDK4), CDK inhibitor genes (CDKN2A, CDKN1A, CDKN1B and CDKN1C), and integrin and associated genes that we previously reported (ITGA3, ITGB4, CD9 and JUP). The expression ratios of 66 combinations of the 11 cell cycle-related genes were analyzed to examine their associations with major clinical events using Mann-Whitney U and log-rank tests. Three expression ratios (CDK1/CDKN1B, CDK2/CDKN1A and CCNE1/CDK2) showed associations on univariate analyses and their diagnostic value was re-analyzed with integrin gene expression biomarkers (ITGA3/CD9 and ITGB4/JUP) using the Cox proportional hazards model and Kaplan-Meier estimates. Lymph node metastasis occurred in >90% of double-positive cases (high-ITGA3/CD9 and high-CDK1/CDKN1B) irrespective of tumor size (P<0.0001). Primary site recurrence was found in >30% of double-positive cases (high-ITGA3/CD9 and high-CDK2/CDKN1A) with tumors >20 mm (P=0.003). Triple-positive (high-ITGB4/JUP, high-ITGA3/CD9 and high-CDK2/CDKN1A) was associated with distant metastasis (P<0.0001), but not with other clinical parameters. Disease-specific death occurred in 55% of double-positive cases (high-ITGA3/CD9 and high-CDK2/CDKN1A) (P<0.0001) and a positive surgical margin was a significant factor for fatality in these cases. Reliable prediction of locoregional and hematogenous dissemination risks in OSCC using the four CDK and integrin gene expression ratios is a promising biomarker system. Clinical use of these parameters may improve the control rate with the use of new therapeutic strategies.
机译:本研究的目的是通过定量聚合酶链反应检测77个OSCC组织中以下基因的表达,从而研究细胞周期相关基因在口腔鳞状细胞癌(OSCC)中的诊断价值:Cyclin基因(CCNA1,CCND1 ,CCND2和CCNE1),细胞周期蛋白依赖性激酶(CDK)基因(CDK1,CDK2和CDK4),CDK抑制剂基因(CDKN2A,CDKN1A,CDKN1B和CDKN1C),整联蛋白和我们先前报道的相关基因(ITGA3,ITGB4,CD9和JUP)。使用Mann-Whitney U和log-rank检验分析了11种细胞周期相关基因的66种组合的表达比率,以检查它们与主要临床事件的关联。三种表达率(CDK1 / CDKN1B CDK2 / CDKN1A CCNE1 / CDK2 )显示出单因素分析的相关性,并用整联蛋白基因表达生物标志物( ITGA3 / CD9 ITGB4 / JUP )使用Cox比例风险模型和Kaplan-Meier估计。淋巴结转移发生率超过90%的双阳性病例(高 ITGA3 / CD9 和高 CDK1 / CDKN1B < / em>),与肿瘤大小无关(P <0.0001)。在> 30%的双阳性病例中发现原发部位复发(高 ITGA3 / CD9 和高 CDK2 / CDKN1A ),肿瘤大于20毫米(P = 0.003)。三重阳性(高- ITGB4 / JUP ,高- ITGA3 / CD9 和高- CDK2 / CDKN1A )与远处转移相关(P <0.0001),但与其他临床参数无关。 55%的双重阳性病例(高 ITGA3 / CD9 和高 CDK2 / CDKN1A < / em>)(P <0.0001)和手术切缘阳性是导致这些患者死亡的重要因素。使用四种CDK和整联蛋白基因表达比率可靠预测OSCC的局部和血源性传播风险是一种有前途的生物标记系统。这些参数的临床使用可通过使用新的治疗策略来提高控制率。

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