根据 MED19 和临床分期建立肝细胞癌预后模型,并确定 MED19 为治疗靶点。

IF 2.7 3区 医学 Q3 ONCOLOGY Journal of Cancer Research and Clinical Oncology Pub Date : 2024-10-05 DOI:10.1007/s00432-024-05978-x
Xiaojun Jin, Yun Zhang, Wei Hu, Chang Liu, Danyang Cai, Jialin Sun, Qichun Wei, Qun Cai
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引用次数: 0

摘要

背景介绍介导复合体亚基19(MED19)是介导复合体的一个成员,已被证实参与了肝细胞癌(HCC)的肿瘤发生。方法:我们分析了癌症基因组图谱(The Cancer Genome Atlas)和其他数据库的数据,评估了MED19的表达及其对HCC预后和治疗靶点的影响:结果:与非肿瘤性肝组织相比,MED19在HCC组织中表达上调,且其上调与晚期临床病理特征呈正相关。多变量分析表明,MED19 是预测 HCC 预后的独立指标。体外实验显示,敲除 MED19 可抑制肝癌细胞的增殖、集落形成和侵袭,并诱导细胞凋亡。此外,MED19抑制还导致hepG2细胞G0/G1期停滞。我们筛选了 MED19 低表达组和高表达组之间的差异表达基因。富集分析表明,这些基因主要与核分裂和细胞周期有关。肿瘤浸润免疫的模式被证明与 HCC 中 MED19 的表达有关。TIDE分析显示,低表达组患者的免疫治疗效果明显更好。此外,我们还建立了一个预测 HCC 患者预后的模型。接收者操作特征分析表明,该模型在预测 HCC 患者预后方面表现良好。最后,建立了一个用于预测个别 HCC 患者生存概率的提名图:这些研究结果表明,MED19 是一种新型生物标志物,与 HCC 的免疫景观和免疫治疗反应有显著关联。由 MED19 和病理分期组成的预测模型在确定 HCC 的预后和分层方面具有更好的作用。
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Developing a prognostic model for hepatocellular carcinoma based on MED19 and clinical stage and determining MED19 as a therapeutic target.

Backgroud: Mediator complex subunit 19 (MED19), a member of the mediator complex, has been demonstrated to involve in tumorigenesis of hepatocellular carcinoma (HCC). However, the regulation mechanisms of MED19, the immune landscape linking MED19 to HCC and its predictive value of immunotherapy treatment in HCC are so far unknown.

Methods: Here, we analyzed data from The Cancer Genome Atlas and other databases to assess the expression of MED19 and its prognosis and therapeutical-targets impact in HCC.

Results: MED19 expression was upregulated in HCC tissues compared to non-tumorous liver tissues and that its upregulation was positively associated with advanced clinicopathology features. The multivariate analysis showed that MED19 was an independent predictor of outcome in HCC. In vitro experiments revealed that MED19 knockdown suppressed hepG2 cells proliferation, colony forming and invasion and induced apoptosis. Furthermore, MED19 inhibition resulted in G0/G1 phase arrest in hepG2 cells. We screened differentially expressed genes between low and high MED19 expression groups. Enrichment analyses showed that these genes were mainly linked to nuclear division and cell cycle. The pattern of tumor-infiltrating immune was demonstrated to be related with MED19 expression in HCC. TIDE analyses showed that patients in the low-expression group presented significantly better immunotherapy. Moreover, we developed a predicted model for HCC patient's prognosis. Receiver operating characteristic analyses revealed that this model processed a favorable performance in predicting the prognosis of HCC patients. Finally, a nomogram was built for predicting survival probability of individual HCC patient.

Conclusion: These findings suggest that MED19 as a novel biomarker that has significant association with immune landscape and immunotherapy response in HCC. The proposed prediction model composed of MED19 and pathological stage has a better role in determining prognosis and stratifying of HCC.

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来源期刊
CiteScore
4.00
自引率
2.80%
发文量
577
审稿时长
2 months
期刊介绍: The "Journal of Cancer Research and Clinical Oncology" publishes significant and up-to-date articles within the fields of experimental and clinical oncology. The journal, which is chiefly devoted to Original papers, also includes Reviews as well as Editorials and Guest editorials on current, controversial topics. The section Letters to the editors provides a forum for a rapid exchange of comments and information concerning previously published papers and topics of current interest. Meeting reports provide current information on the latest results presented at important congresses. The following fields are covered: carcinogenesis - etiology, mechanisms; molecular biology; recent developments in tumor therapy; general diagnosis; laboratory diagnosis; diagnostic and experimental pathology; oncologic surgery; and epidemiology.
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