Department of Ultrasound, Shaanxi Provincial People's Hospital, Xi'an, 710068, China.
Department of Radiology, Xi'an Central Hospital Affiliated to Xi'an Jiaotong University, No. 161, Xiwu Road, Xincheng District, Xi'an, 710003, Shaanxi, PR China.
Biomed Eng Online. 2020 Sep 1;19(1):68. doi: 10.1186/s12938-020-00812-0.
Increasing evidence has demonstrated the correlation between hepatocellular carcinoma (HCC) prognosis and RNA binding proteins (RBPs) dysregulation. Thus, we aimed to develop and validate a reliable prognostic signature that can estimate the prognosis for HCC.
Gene expression profiling and clinical information of 374 HCC patients were derived from the TCGA data portal. The survival-related RBP pairs were determined using univariate cox-regression analysis and the signature was built based on LASSO analysis. All patients were divided patients into high-and low-risk groups according to the optimal cut off of the signature score determined by time-dependent receiver operating characteristic (ROC) curve analysis. The predictive value of the signature was further validated in an independent cohort.
A 37-RBP pairs signature consisting of 61 unique genes was constructed which was significantly associated with the survival. The RBP-related signature accurately predicted the prognosis of HCC patients, and patients in high-risk groups showed poor survival in two cohorts. The novel signature was an independent prognostic factor of HCC in two cohorts (all P < 0.001). Furthermore, the C-index of the prognostic model was 0.799, which was higher than that of many established risk models. Pathway and process enrichment analysis showed that the 61 unique genes were mainly enriched in translation, ncRNA metabolic process, RNA splicing, RNA modification, and translational termination.
The novel proposed RBP-related signature based on relative expression orderings could serve as a promising independent prognostic biomarker for patients with HCC, and could improve the individualized survival prediction in HCC.
越来越多的证据表明肝癌(HCC)的预后与 RNA 结合蛋白(RBPs)失调有关。因此,我们旨在开发和验证一个可靠的预后标志,以估计 HCC 的预后。
从 TCGA 数据门户中获得了 374 名 HCC 患者的基因表达谱和临床信息。使用单变量 cox 回归分析确定与生存相关的 RBP 对,然后基于 LASSO 分析构建该标志。根据时间依赖性接受者操作特征(ROC)曲线分析确定的最佳截断值,将所有患者分为高风险和低风险组。进一步在独立队列中验证该标志的预测价值。
构建了一个由 61 个独特基因组成的 37-RBP 对标志,该标志与生存显著相关。RBP 相关标志准确预测了 HCC 患者的预后,高风险组患者在两个队列中均表现出较差的生存。该新标志是两个队列中 HCC 的独立预后因素(均 P<0.001)。此外,该预后模型的 C 指数为 0.799,高于许多已建立的风险模型。通路和过程富集分析表明,这 61 个独特基因主要富集在翻译、ncRNA 代谢过程、RNA 剪接、RNA 修饰和翻译终止过程中。
基于相对表达顺序提出的新型 RBP 相关标志可以作为 HCC 患者有前途的独立预后生物标志物,可改善 HCC 患者的个体化生存预测。