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Prognostic microRNA signatures derived from The Cancer Genome Atlas for head and neck squamous cell carcinomas

机译:源自癌症基因组图谱的预后性microRNA签名,可用于头颈部鳞状细胞癌

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Abstract Identification of novel prognostic biomarkers typically requires a large dataset which provides sufficient statistical power for discovery research. To this end, we took advantage of the high-throughput data from The Cancer Genome Atlas (TCGA) to identify a set of prognostic biomarkers in head and neck squamous cell carcinomas (HNSCC) including oropharyngeal squamous cell carcinoma (OPSCC) and other subtypes. In this study, we analyzed miRNA-seq data obtained from TCGA patients to identify prognostic biomarkers for OPSCC. The identified miRNAs were further tested with an independent cohort. miRNA-seq data from TCGA was also analyzed to identify prognostic miRNAs in oral cavity squamous cell carcinoma (OSCC) and laryngeal squamous cell carcinoma (LSCC). Our study identified that miR-193b-3p and miR-455-5p were positively associated with survival, and miR-92a-3p and miR-497-5p were negatively associated with survival in OPSCC. A combined expression signature of these four miRNAs was prognostic of overall survival in OPSCC, and more importantly, this signature was validated in an independent OPSCC cohort. Furthermore, we identified four miRNAs each in OSCC and LSCC that were prognostic of survival, and combined signatures were specific for subtypes of HNSCC. A robust 4-miRNA prognostic signature in OPSCC, as well as prognostic signatures in other subtypes of HNSCC, was developed using sequencing data from TCGA as the primary source. This demonstrates the power of using TCGA as a potential resource to develop prognostic tools for improving individualized patient care.
机译:摘要鉴定新的预后生物标志物通常需要一个大型数据集,该数据集可为发现研究提供足够的统计能力。为此,我们利用了癌症基因组图谱(TCGA)的高通量数据来鉴定一组包括口咽鳞状细胞癌(OPSCC)和其他亚型的头颈部鳞状细胞癌(HNSCC)的预后生物标志物。在这项研究中,我们分析了从TCGA患者获得的miRNA-seq数据,以确定OPSCC的预后生物标志物。所鉴定的miRNA与独立队列进一步测试。还分析了来自TCGA的miRNA-seq数据,以鉴定口腔鳞状细胞癌(OSCC)和喉鳞状细胞癌(LSCC)的预后性miRNA。我们的研究确定,miR-193b-3p和miR-455-5p与生存呈正相关,而miR-92a-3p和miR-497-5p与OPSCC生存呈负相关。这四个miRNA的组合表达特征可预测OPSCC的总体生存,更重要的是,该特征已在独立的OPSCC队列中得到验证。此外,我们在OSCC和LSCC中分别鉴定了4个可预后的miRNA,并且组合的特征对于HNSCC的亚型具有特异性。使用来自TCGA的测序数据作为主要来源,开发了OPSCC中强大的4-miRNA预后签名以及HNSCC其他亚型中的预后签名。这证明了将TCGA用作开发预后工具以改善个性化患者护理的潜在资源的力量。

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