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High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential Biomarkers

机译:miRNA的高通量测序揭示了胃癌的组织特征并提出了新的潜在生物标志物

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摘要

Gastric cancer has a high incidence and mortality rate worldwide; however, the use of biomarkers for its clinical diagnosis remains limited. The microRNAs (miRNAs) are biomarkers with the potential to identify the risk and prognosis as well as therapeutic targets. We performed the ultradeep miRnomes sequencing of gastric adenocarcinoma and gastric antrum without tumor samples. We observed that a small set of those samples were responsible for approximately 80% of the total miRNAs expression, which might represent a miRNA tissue signature. Additionally, we identified seven miRNAs exhibiting significant differences, and, of these, hsa-miR-135b and hsa-miR-29c were able to discriminate antrum without tumor from gastric cancer regardless of the histological type. These findings were validated by quantitative real-time polymerase chain reaction. The results revealed that hsa-miR-135b and hsa-miR-29c are potential gastric adenocarcinoma occurrence biomarkers with the ability to identify individuals at a higher risk of developing this cancer, and could even be used as therapeutic targets to allow individualized clinical management.
机译:胃癌在全球范围内具有很高的发病率和死亡率。然而,将生物标志物用于其临床诊断仍然受到限制。 microRNA(miRNA)是生物标志物,具有识别风险和预后以及治疗目标的潜力。我们对没有肿瘤标本的胃腺癌和胃窦进行了超深miRnomes测序。我们观察到这些样品中的一小部分约占总miRNA表达的80%,这可能代表了miRNA组织的特征。此外,我们鉴定出七个显示出显着差异的miRNA,其中hsa-miR-135b和hsa-miR-29c能够区分无肿瘤的胃窦与胃癌,而与组织学类型无关。通过定量实时聚合酶链反应验证了这些发现。结果表明,hsa-miR-135b和hsa-miR-29c是潜在的胃腺癌发生生物标志物,具有识别罹患这种癌症的较高风险的个体的能力,甚至可以用作治疗靶点,以进行个性化的临床管理。

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