机器学习识别与肝细胞癌相关的外泌体特征。

Frontiers in Cell and Developmental Biology Pub Date : 2022-09-19 eCollection Date: 2022-01-01 DOI:10.3389/fcell.2022.1020415
Kai Zhu, Qiqi Tao, Jiatao Yan, Zhichao Lang, Xinmiao Li, Yifei Li, Congcong Fan, Zhengping Yu
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引用次数: 3

摘要

背景:肝细胞癌(HCC)是预后较差的恶性肿瘤之一。目前仍缺乏有效的生物标志物来预测其预后。外泌体参与细胞间通讯,在癌症的发生和发展中发挥重要作用。方法:本研究采用单变量特征选择和随机森林(RF)算法两种机器学习方法,选择13个外显体相关基因(ERGs)并构建ERG特征。基于ERG签名评分和ERG签名相关通路评分,生成新的射频签名。采用实时定量聚合酶链反应和免疫组织化学检测13个ERGs成员BSG和SFN的表达。最后,采用细胞计数试剂盒-8 (CCK-8)检测BSG和SFN对细胞增殖的抑制作用。结果:ERG特征具有良好的预测性能,ERG评分被确定为HCC总生存的独立预测因子。我们的射频信号显示了良好的预后能力,TCGA的曲线下面积(AUC)在1年为0.845,2年为0.811,3年为0.801,优于ERG信号。值得注意的是,RF标记在预测高外泌体评分和高NK评分患者的HCC预后方面表现良好。与邻近正常组织相比,HCC组织中BSG和SFN水平升高。抑制BSG和SFN可抑制Huh7细胞的增殖。结论:射频信号能准确预测HCC患者的预后,具有潜在的临床价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Machine learning identifies exosome features related to hepatocellular carcinoma.

Machine learning identifies exosome features related to hepatocellular carcinoma.

Machine learning identifies exosome features related to hepatocellular carcinoma.

Machine learning identifies exosome features related to hepatocellular carcinoma.

Background: Hepatocellular carcinoma (HCC) is one of the most malignant tumors with a poor prognosis. There is still a lack of effective biomarkers to predict its prognosis. Exosomes participate in intercellular communication and play an important role in the development and progression of cancers. Methods: In this study, two machine learning methods (univariate feature selection and random forest (RF) algorithm) were used to select 13 exosome-related genes (ERGs) and construct an ERG signature. Based on the ERG signature score and ERG signature-related pathway score, a novel RF signature was generated. The expression of BSG and SFN, members of 13 ERGs, was examined using real-time quantitative polymerase chain reaction and immunohistochemistry. Finally, the effects of the inhibition of BSG and SFN on cell proliferation were examined using the cell counting kit-8 (CCK-8) assays. Results: The ERG signature had a good predictive performance, and the ERG score was determined as an independent predictor of HCC overall survival. Our RF signature showed an excellent prognostic ability with the area under the curve (AUC) of 0.845 at 1 year, 0.811 at 2 years, and 0.801 at 3 years in TCGA, which was better than the ERG signature. Notably, the RF signature had a good performance in the prediction of HCC prognosis in patients with the high exosome score and high NK score. Enhanced BSG and SFN levels were found in HCC tissues compared with adjacent normal tissues. The inhibition of BSG and SFN suppressed cell proliferation in Huh7 cells. Conclusion: The RF signature can accurately predict prognosis of HCC patients and has potential clinical value.

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