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首页> 外文期刊>International journal of oncology >Loss of NKX3-1 as a potential marker for an increased risk of occult lymph node metastasis and poor prognosis in oral squamous cell carcinoma
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Loss of NKX3-1 as a potential marker for an increased risk of occult lymph node metastasis and poor prognosis in oral squamous cell carcinoma

机译:NKX3-1丢失可能是口腔鳞状细胞癌隐匿性淋巴结转移风险增加和预后不良的潜在标志

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The prognosis of oral squamous cell carcinoma (OSCC) is significantly dependent on the existence of cervical lymph node metastasis (LNM), with the overall survival rate being much lower in patients with LNM. Primary causes and molecular mechanisms of LNM are still largely unclear. We hypothesized that factors related with cancer progress and/or prognosis in OSCC are revealed by genome-wide investigation of DNA copy number aberrations (CNAs). In order to find biomarkers for occult LNM of OSCC, we comprehensively investigated genomic DNAs from 60?OSCC patients using Affymetrix mapping arrays and statistically analyzed correlations between CNAs of genes and the presence of occult LNM in the patients. The genome-wide CNA study indicated significant correlations between the presence of occult LNM and CNAs of certain genes. Through a literature survey, we narrowed down the candidates and focused on loss of NKX3-1, which is a homeodomain-containing transcription factor. NKX3-1 is known as a tumor suppressor gene in prostate cancer but has never been reported in OSCC. Quantitative RT-PCR and immunohistochemistry (IHC) analyses also showed significantly lower expression of NKX3-1 in the cases with occult LNM, which was further validated by IHC analysis in independent cases. The survival analyses indicated that NKX3-1 loss is a significant risk factor to decrease the disease-free survival (DFS) and the overall survival (OS) rates. This is the first time that the significant association of NKX3-1 loss and occult LNM was indicated in OSCC. The present results suggest that loss of NKX3-1 may be a potential biomarker for occult LNM of OSCC.
机译:口腔鳞状细胞癌(OSCC)的预后很大程度上取决于颈淋巴结转移(LNM)的存在,而LNM患者的总生存率要低得多。 LNM的主要原因和分子机制仍不清楚。我们假设与OSCC的癌症进展和/或预后有关的因素是通过DNA拷贝数畸变(CNA)的全基因组调查揭示的。为了找到OSCC隐匿性LNM的生物标记,我们使用Affymetrix定位阵列对60例OSCC患者的基因组DNA进行了全面研究,并统计分析了基因的CNA与患者隐匿性LNM存在之间的相关性。全基因组的CNA研究表明,隐匿性LNM与某些基因的CNA之间存在显着相关性。通过文献调查,我们缩小了候选范围,并专注于NKX3-1的丢失,NKX3-1是一种含同源结构域的转录因子。 NKX3-1在前列腺癌中被称为抑癌基因,但在OSCC中尚未见报道。定量RT-PCR和免疫组织化学(IHC)分析还显示,在隐匿性LNM患者中NKX3-1的表达明显降低,这在独立病例中通过IHC分析得到了进一步验证。生存分析表明,NKX3-1丢失是降低无病生存(DFS)和总体生存(OS)率的重要危险因素。这是第一次在OSCC中显示NKX3-1丢失和隐匿性LNM的显着关联。目前的结果表明,NKX3-1的丢失可能是OSCC隐匿性LNM的潜在生物标记。

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