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首页> 外文期刊>Frontiers in Cell and Developmental Biology >Integrated Profiles Analysis Identified a Coding-Non-Coding Signature for Predicting Lymph Node Metastasis and Prognosis in Cervical Cancer
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Integrated Profiles Analysis Identified a Coding-Non-Coding Signature for Predicting Lymph Node Metastasis and Prognosis in Cervical Cancer

机译:集成型材分析确定了用于预测宫颈癌淋巴结转移和预后的编码 - 非编码签名

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摘要

Accumulating evidence has shown that lymph node metastasis (LNM) is not only an important prognostic factor but also an indicator of the need for postoperative chemoradiotherapy. Therefore, identifying risk factors or molecular markers related to LNM is critical for predicting the prognosis and guiding individualized treatment of patients with cervical cancer. In this study, we used the machine learning-based feature selection approach to identify eight optimal biomarkers from the list of 250 differentially expressed mRNAs and lncRNAs in the TCGA cohort. Then a coding-non-coding signature (named CNC8SIG) was developed using the elastic-net logistic regression approach based on the expression levels of eight optimal biomarkers, which is useful in discriminating patients with LNM from those without LNM in the discovery cohort. The predictive performance of the CNC8SIG was further validated in two independent patient cohorts. Moreover, the CNC8SIG was significantly associated with patient's survival in different patient cohorts. In silico functional analysis suggested that the CNC8SIG-associated mRNAs are enriched in known cancer-related biological pathways such as the Wnt signaling pathway, the Ras signaling pathway, Rap1 signaling pathway, and PI3K-Akt signaling pathway.
机译:累积证据表明,淋巴结转移(LNM)不仅是一个重要的预后因素,而且还是术后化学疗法需要的指标。因此,鉴定与LNM相关的危险因素或分子标记对于预测宫颈癌患者的预后和指导个体化治疗至关重要。在这项研究中,我们使用了基于机器学习的特征选择方法来识别来自TCGA队列中的250个差异表达的MRNA和LNCRNA列表的八个最佳生物标志物。然后,使用基于八个最佳生物标志物的表达水平的弹性净物流回归方法开发了编码 - 非编码签名(命名CNC8SIG),这对于在发现队列中的没有LNM的那些中,可用于区分LNM的患者。 CNC8SIG的预测性能在两个独立的患者队列中进一步验证。此外,CNC8SIG与患者在不同患者队列中的存活中显着相关。在硅功能分析中,提出CNC8SIG相关的MRNA在已知的癌症相关的生物途径中富集,例如WNT信号通路,RAS信号通路,RAP1信号通路和PI3K-AKT信号通路。

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