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通过差异显示逆转录聚合酶链反应对口腔鳞状细胞癌进行基因表达谱分析及肿瘤生物标志物的鉴定。

Gene expression profiling of oral squamous cell carcinoma by differential display rt-PCR and identification of tumor biomarkers.

作者信息

Chakraborty Sanjukta, Nagashri M N, Mohiyuddin S M Azeem, Gopinath K S, Kumar Arun

出版信息

Indian J Surg Oncol. 2010 Dec;1(4):284-93. doi: 10.1007/s13193-011-0054-x. Epub 2011 Feb 18.

Abstract

Oral squamous cell carcinoma (OSCC) is the sixth most common cancer worldwide. Despite progress in therapeutic and surgical treatments, its survival period at 5 years is the lowest among major cancers, and remains unchanged in the last two decades. The growing epidemiological relevance of oral cancer emphasizes the need to better understand the molecular mechanisms underlying this disease and identify predictive tumor markers and therapeutic targets. To this end, we have used the DDRT-PCR analysis to profile the oral tumor transcriptome and identify differentially regulated genes that may be used as potential biomarkers and therapeutic targets. Our DDRT-PCR analysis identified 51 differentially expressed fragments, of which 25 were revalidated by reverse Northern analysis. Northern blot analysis further corroborated these findings for a few genes. In order to ascertain the utility of some of the identified genes as molecular markers and therapeutic targets, semi-quantitative RT-PCR analysis was carried out in a panel of matched oral normal and tumor samples, that confirmed GLTP, PCNA, RBM28, C17orf75 and DIAPH1 as significantly upregulated, whereas TNKS2, PAM and TUBB2C showed significant downregulation in tumor samples. Taken together, our DDRT-PCR analysis has revealed several genes, belonging to diverse cellular pathways, that have been associated with OSCC for the first time. Thus, these genes could be investigated as biomarkers and therapeutic targets for OSCC.

摘要

口腔鳞状细胞癌(OSCC)是全球第六大常见癌症。尽管在治疗和手术治疗方面取得了进展,但其5年生存期在主要癌症中是最低的,并且在过去二十年中一直没有变化。口腔癌在流行病学上的相关性日益增加,这凸显了更好地了解该疾病潜在分子机制以及识别预测性肿瘤标志物和治疗靶点的必要性。为此,我们使用DDRT-PCR分析来描绘口腔肿瘤转录组,并识别可能用作潜在生物标志物和治疗靶点的差异调节基因。我们的DDRT-PCR分析鉴定出51个差异表达片段,其中25个通过反向Northern分析进行了重新验证。Northern印迹分析进一步证实了其中一些基因的这些发现。为了确定一些已鉴定基因作为分子标志物和治疗靶点的效用,我们在一组匹配的口腔正常和肿瘤样本中进行了半定量RT-PCR分析,结果证实GLTP、PCNA、RBM28、C17orf75和DIAPH1在肿瘤样本中显著上调,而TNKS2、PAM和TUBB2C则显著下调。综上所述,我们的DDRT-PCR分析首次揭示了几个属于不同细胞途径的基因,这些基因与OSCC相关。因此,可以将这些基因作为OSCC的生物标志物和治疗靶点进行研究。

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