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State of homeobox A10 expression as a putative prognostic marker for oral squamous cell carcinoma.

机译:同源盒A10表达水平作为口腔鳞状细胞癌的预后标志物的状态。

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摘要

Homeobox (HOX) A10, the regulator of embryonic morphogenesis and differentiation, is aberrantly expressed in several cancer types. Our previous study using microarray technology showed that significant up-regulation of HOXA10 occurs in oral squamous cell carcinoma (OSCC)-derived cell lines compared to human normal oral keratinocytes (HNOKs). The aim of the current study was to examine the status of HOXA10 mRNA and protein expression in OSCC-derived cell lines and human primary OSCCs. HOXA10 mRNA was up-regulated in six OSCC-derived cell lines compared with HNOKs and in primary OSCCs by using real-time quantitative reverse transcriptase-polymerase chain reaction. Immunohistochemistry data indicated that HOXA10 protein expression levels were consistent with mRNA expression status in OSCC-derived cell lines and primary OSCCs. Furthermore, HOXA10 expression status was correlated with the TNM stage (P<0.05). These results indicate that HOXA10 expression could contribute to cancer progression and prognosis and that HOXA10 may be a potential diagnostic marker and a therapeutic target for OSCCs.
机译:同源形态(HOX)A10,胚胎形态发生和分化的调节剂,在几种癌症类型中异常表达。我们先前使用微阵列技术的研究表明,与人类正常的口腔角质形成细胞(HNOK)相比,口腔鳞状细胞癌(OSCC)衍生的细胞系中HOXA10明显上调。本研究的目的是检查在OSCC衍生的细胞系和人类原发性OSCC中HOXA10 mRNA和蛋白表达的状态。通过使用实时定量逆转录酶-聚合酶链反应,与HNOK和原代OSCC相比,HOXA10 mRNA在六个OSCC衍生的细胞系中被上调。免疫组织化学数据表明,HOXA10蛋白表达水平与OSCC来源的细胞系和原发性OSCC中的mRNA表达状态一致。此外,HOXA10表达状态与TNM分期相关(P <0.05)。这些结果表明,HOXA10的表达可能有助于癌症的进展和预后,并且HOXA10可能是OSCC的潜在诊断标记和治疗靶标。

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