miRNome 图谱分析揭示了新型肝细胞癌诊断、预后和治疗相关候选生物标记物:SORAMIC 试验的事后分析。

IF 2 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Egidijus Morkūnas, E. Vaitkeviciute, R. Inciuraite, J. Kupčinskas, Alexander Link, J. Skieceviciene, Marianna Alunni-Fabbroni, Kerstin Schütte, Peter Malfertheiner, G. Varkalaite, Jens Ricke
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Hepatocellular carcinoma patients underwent collection of plasma samples before and 7-9 weeks after the beginning of the treatment. Isolation of circulating miRNAs, preparation of small RNA sequencing libraries and next-generation sequencing were performed. Association analysis for novel diagnostic, prognostic and treatment-related candidate biomarkers was performed. Results A total of 42 differentially expressed (16 up-regulated and 26 down-regulated) miRNAs were identified comparing baseline and control group plasma samples. hsa-miR-215-5p and hsa-miR-192-5p were down-regulated, while hsa-miR-483-5p and hsa-miR-23b-3p were up-regulated comparing baseline and 7-9 weeks post-sorafenib monotherapy samples. hsa-miR-215-5p was the sole down-regulated miRNA in the same combination therapy comparison. hsa-miR-183-5p, hsa-miR-28-3p and hsa-miR-1246 were found to be significantly up-regulated comparing non-responders versus responders to sorafenib. 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引用次数: 0

摘要

引言 由于缺乏特异性非侵入性生物标志物,肝细胞癌的早期诊断、预后评估和疗效预测仍面临挑战。本研究旨在确定疾病特异性微 RNA(miRNA)模式,以诊断、预测肝细胞癌(HCC)患者的预后和治疗反应。方法 研究对象包括 42 名来自 SORAMIC 临床试验的肝细胞癌患者:22 名患者接受索拉非尼单药治疗,20 名患者接受 90Y 放射性栓塞与索拉非尼联合治疗。对照组包括 20 人。肝细胞癌患者在治疗前和治疗开始后 7-9 周采集血浆样本。研究人员进行了循环 miRNAs 分离、小 RNA 测序文库制备和新一代测序。对新型诊断、预后和治疗相关的候选生物标志物进行了关联分析。与基线样本和索拉非尼单药治疗后7-9周的样本相比,hsa-miR-215-5p和hsa-miR-192-5p下调,而hsa-miR-483-5p和hsa-miR-23b-3p上调。hsa-miR-183-5p 、hsa-miR-28-3p 和 hsa-miR-1246 在索拉非尼治疗无应答者与应答者的比较中被显著上调。hsa-miR-215-5p的高表达与HCC患者的预后明显相关。结论 对 SORAMIC 研究的高特征样本进行系统的 miRNA 分析,发现了一些潜在的 miRNA 生物标志物,可用于诊断肝细胞癌和索拉非尼治疗患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
miRNome profiling analysis reveals novel hepatocellular carcinoma diagnostic, prognostic and treatment-related candidate biomarkers: post-hoc analysis of SORAMIC trial.
Introduction Early diagnosis of hepatocellular carcinoma as well as evaluation of prognosis and prediction of treatment efficacy remain challenging due to the missing specific non-invasive biomarkers. The aim of this study is to identify disease-specific microRNA (miRNA) patterns for diagnosis, prediction of prognosis and treatment response in patients with hepatocellular carcinoma (HCC). Methods The study population included 42 HCC patients from SORAMIC clinical trial: 22 patients received sorafenib monotherapy, 20 patients underwent 90Y radioembolization in combination with sorafenib. 20 individuals were included in the control group. Hepatocellular carcinoma patients underwent collection of plasma samples before and 7-9 weeks after the beginning of the treatment. Isolation of circulating miRNAs, preparation of small RNA sequencing libraries and next-generation sequencing were performed. Association analysis for novel diagnostic, prognostic and treatment-related candidate biomarkers was performed. Results A total of 42 differentially expressed (16 up-regulated and 26 down-regulated) miRNAs were identified comparing baseline and control group plasma samples. hsa-miR-215-5p and hsa-miR-192-5p were down-regulated, while hsa-miR-483-5p and hsa-miR-23b-3p were up-regulated comparing baseline and 7-9 weeks post-sorafenib monotherapy samples. hsa-miR-215-5p was the sole down-regulated miRNA in the same combination therapy comparison. hsa-miR-183-5p, hsa-miR-28-3p and hsa-miR-1246 were found to be significantly up-regulated comparing non-responders versus responders to sorafenib. High hsa-miR-215-5p expression was significantly associated with worse HCC patients' prognosis. Conclusions Systematic miRNA profiling of highly characterized samples from SORAMIC study revealed a subset of potential miRNA biomarkers for hepatocellular carcinoma diagnosis and prognosis of sorafenib-treated patients' survival.
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来源期刊
Digestive Diseases
Digestive Diseases 医学-胃肠肝病学
CiteScore
4.80
自引率
0.00%
发文量
58
审稿时长
2 months
期刊介绍: Each issue of this journal is dedicated to a special topic of current interest, covering both clinical and basic science topics in gastrointestinal function and disorders. The contents of each issue are comprehensive and reflect the state of the art, featuring editorials, reviews, mini reviews and original papers. These individual contributions encompass a variety of disciplines including all fields of gastroenterology. ''Digestive Diseases'' bridges the communication gap between advances made in the academic setting and their application in patient care. The journal is a valuable service for clinicians, specialists and physicians-in-training.
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