解密坏死相关长非编码 RNA 在肝细胞癌中的作用:基于坏死相关 lncRNA 标志预测肝细胞癌的预后

IF 3.1 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Applied Biochemistry and Biotechnology Pub Date : 2024-08-08 DOI:10.1007/s12010-024-05014-1
Gao-Qi Ye, Ming-Da Wang, Yong-Kang Diao, Chao Li, Lan-Qing Yao, Li-Hui Gu, Jia-Hao Xu, Tian Yang, Xiang-Min Tong
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引用次数: 0

摘要

肝细胞癌(HCC)是最常见的肝癌类型,具有发病率高的特点。长非编码 RNA(lncRNA)在调控包括癌症在内的各种细胞过程和疾病中发挥着重要作用。然而,它们在 HCC 中的具体作用和机制尚不完全清楚。本研究采用多队列设计研究了HCC患者中与坏死相关的lncRNAs(NRLs)。我们筛选出了 1095 个 NRLs 和 838 个在肿瘤和正常组织间有差异表达的基因。其中,我们发现 105 个 NRL 与 HCC 患者的预后密切相关。通过LASSO-Cox回归分析产生的10个lncRNA(AC100803.3、AC027237.2、AL158166.1、LINC02870、AC026412.3、LINC02159、AC027097.1、AC139887.4、AC007405.1、AL023583.1)被用于建立HCC预后风险模型,并根据风险将患者分组。KEGG 分析显示,高风险(H-R)亚组和低风险(L-R)亚组的通路富集程度不同。根据GO分析,该研究发现了230个差异表达基因(DEG),它们在特定的生物过程中被显著富集。对 H-R 和 L-R 患者的免疫检查点相关基因(MCPGs)进行比较后发现了明显的差异。此外,我们还确定了肝癌患者的风险评分与其对 16 种化疗药物的敏感性之间的相关性。通过蛋白-蛋白相互作用(PPI)分析,我们发现了 10 个可能调控 HCC 发病分子网络的枢纽基因。这项研究是研究 NRL 在 HCC 中作用的一项开创性工作。它为潜在的靶向治疗开辟了一条新途径,并为了解 HCC 的分子机制提供了见解。
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Deciphering the Role of Necroptosis-Related Long Non-coding RNAs in Hepatocellular Carcinoma: A Necroptosis-Related lncRNA-Based Signature to Predict the Prognosis of Hepatocellular Carcinoma.

Hepatocellular carcinoma (HCC) is the most common type of liver cancer, characterized by a high morbidity rate. Long non-coding RNAs (lncRNAs) play an important role in regulating various cellular processes and diseases, including cancer. However, their specific roles and mechanisms in HCC are not fully understood. This study used a multi-cohort design to investigate necroptosis-related lncRNAs (NRLs) in patients with HCC. We curated a list of 1095 NRLs and 838 genes showing differential expression between tumor and normal tissues. Among them, we found 105 NRLs closely associated with the prognosis of HCC patients. The 10 lncRNAs (AC100803.3, AC027237.2, AL158166.1, LINC02870, AC026412.3, LINC02159, AC027097.1, AC139887.4, AC007405.1, AL023583.1) generated by LASSO-Cox regression analysis were used to create a prognostic risk model for HCC and group patients into groups based on risk. The KEGG analysis revealed distinct pathway enrichments in high-risk (H-R) and low-risk (L-R) subgroups. According to GO analysis, this study identified 230 differentially expressed genes (DEGs) that were significantly enriched in specific biological processes. Comparison of immune checkpoint-related genes (MCPGs) between H-R and L-R patients revealed significant differences. Moreover, we established a correlation between the risk scores of patients with liver cancer and their sensitivity to 16 chemotherapeutic agents. Employing protein-protein interaction (PPI) analysis, we identified 10 hub genes that potentially regulate the molecular networks involved in HCC development. This study is a pioneering effort to investigate the roles of NRLs in HCC. It opens a new avenue for potential targeted therapies and provides insights into the molecular mechanisms of HCC.

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来源期刊
Applied Biochemistry and Biotechnology
Applied Biochemistry and Biotechnology 工程技术-生化与分子生物学
CiteScore
5.70
自引率
6.70%
发文量
460
审稿时长
5.3 months
期刊介绍: This journal is devoted to publishing the highest quality innovative papers in the fields of biochemistry and biotechnology. The typical focus of the journal is to report applications of novel scientific and technological breakthroughs, as well as technological subjects that are still in the proof-of-concept stage. Applied Biochemistry and Biotechnology provides a forum for case studies and practical concepts of biotechnology, utilization, including controls, statistical data analysis, problem descriptions unique to a particular application, and bioprocess economic analyses. The journal publishes reviews deemed of interest to readers, as well as book reviews, meeting and symposia notices, and news items relating to biotechnology in both the industrial and academic communities. In addition, Applied Biochemistry and Biotechnology often publishes lists of patents and publications of special interest to readers.
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