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Homeobox gene expression profile indicates HOXA5 as a candidate prognostic marker in oral squamous cell carcinoma

机译:同源盒基因表达谱表明HOXA5是口腔鳞状细胞癌的预后标志物

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摘要

The search for molecular markers to improve diagnosis, individualize treatment and predict behavior of tumors has been the focus of several studies. This study aimed to analyze homeobox gene expression profile in oral squamous cell carcinoma (OSCC) as well as to investigate whether some of these genes are relevant molecular markers of prognosis and/or tumor aggressiveness. Homeobox gene expression levels were assessed by microarrays and qRT-PCR in OSCC tissues and adjacent non-cancerous matched tissues (margin), as well as in OSCC cell lines. Analysis of microarray data revealed the expression of 147 homeobox genes, including one set of six at least 2-fold up-regulated, and another set of 34 at least 2-fold down-regulated homeobox genes in OSCC. After qRT-PCR assays, the three most up-regulated homeobox genes (HOXA5, HOXD10 and HOXD11) revealed higher and statistically significant expression levels in OSCC samples when compared to margins. Patients presenting lower expression of HOXA5 had poorer prognosis compared to those with higher expression (P=0.03). Additionally, the status of HOXA5, HOXD10 and HOXD11 expression levels in OSCC cell lines also showed a significant up-regulation when compared to normal oral keratinocytes. Results confirm the presence of three significantly upregulated (>4-fold) homeobox genes (HOXA5, HOXD10 and HOXD11) in OSCC that may play a significant role in the pathogenesis of these tumors. Moreover, since lower levels of HOXA5 predict poor prognosis, this gene may be a novel candidate for development of therapeutic strategies in OSCC.
机译:寻找分子标记以改善诊断,个体化治疗和预测肿瘤行为一直是数项研究的重点。这项研究旨在分析口腔鳞状细胞癌(OSCC)中同源异型盒基因的表达谱,并研究其中某些基因是否是预后和/或肿瘤侵袭性的相关分子标记。通过微阵列和qRT-PCR在OSCC组织和邻近的非癌性匹配组织(边缘)以及OSCC细胞系中评估了同源盒基因的表达水平。对微阵列数据的分析揭示了OSCC中147个同源盒基因的表达,包括一组至少六个上调2倍的上调基因,和另一组34个至少2倍下调的同源盒基因。经过qRT-PCR分析后,与边缘相比,三个最上调的同源异型盒基因(HOXA5,HOXD10和HOXD11)显示出OSCC样品中较高的和统计学上显着的表达水平。与高表达HOXA5的患者相比,低表达HOXA5的患者的预后较差(P = 0.03)。此外,与正常的口腔角质形成细胞相比,OSCC细胞系中HOXA5,HOXD10和HOXD11表达水平的状态也显示出明显的上调。结果证实在OSCC中存在三个显着上调(> 4倍)同源盒基因(HOXA5,HOXD10和HOXD11),这些基因可能在这些肿瘤的发病机理中发挥重要作用。而且,由于较低水平的HOXA5预测不良预后,因此该基因可能是OSCC治疗策略发展的新候选者。

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