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铜死亡相关基因(CAGs)有助于肝细胞癌的预后预测和潜在治疗靶点。

Cuproptosis-associated genes (CAGs) contribute to the prognosis prediction and potential therapeutic targets in hepatocellular carcinoma.

作者信息

Shi Xiaoli, Shi Dongmin, Yin Yefeng, Wu Yuxiao, Chen Wenwei, Yu Yue, Wang Xuehao

机构信息

School of Medicine, Southeast University, Nanjing, Jiangsu Province 210009, China; Hepatobiliary/Liver Transplantation Center, The First Affiliated Hospital of Nanjing Medical University, Key Laboratory of Living Donor Transplantation, Chinese Academy of Medical Sciences, Nanjing, Jiangsu Province 210029, China.

Department of Medical Oncology, Shanghai Changzheng Hospital, Shanghai 200072, China.

出版信息

Cell Signal. 2024 May;117:111072. doi: 10.1016/j.cellsig.2024.111072. Epub 2024 Feb 1.

Abstract

BACKGROUND

Cuproptosis is a novel form of cell death that exhibits close association with mitochondrial respiration and occurs through distinct mechanisms compared to previously characterized forms of cell death. However, the precise impact of cuproptosis-associated genes (CAGs) on prognosis, immune profiles, and treatment efficacy in hepatocellular carcinomas (HCC) remains poorly understood.

METHODS

A comprehensive analysis of CAGs in hepatocellular carcinoma (HCC) prognosis was conducted using genomic data from HCC patients. Consensus clustering analysis was performed to determine molecular subtypes related to cuproptosis in HCC. The single-sample gene set enrichment analysis (ssGSEA) algorithm was applied to quantify the infiltration levels of immune cells, while the "ESTIMATE" package was employed to calculate tumor purity, stromal scores, and immune scores in the tumor microenvironment (TME). Principal component analysis (PCA) algorithm was utilized to construct a risk score related to CAGs. Finally, CCK8, wound healing, Transwell migration/invasion, EDU and xenograft model were employed to explore the potential oncogenic role of MTF1.

RESULTS

Three distinct patterns of cuproptosis modification were identified, each associated with unique functional enrichments, clinical characteristics, immune cell infiltration, immune checkpoints, tumor microenvironment (TME), and prognosis. A CAGs-related risk score (Cuscore) was developed to predict prognosis in TCGA and validated in GSE76427 and ICGC datasets. Notably, patients with a low Cuscore had better prognoses and were more likely to benefit from immunotherapy.Additionally, the high Cuscore group in HCC also revealed three potential therapeutic targets (TUBA1B, CDC25B, and CSNK2A1) as well as several therapeutic compounds. Moreover, the experiment measured the expression levels of six prognosis-related CAGs, wherein knockdown of MTF1 exhibited suppression of proliferation, invasion, and migration formation in HCC cell lines.

CONCLUSION

The findings have enhanced our comprehension of the cuproptosis characteristics in HCC, and stratification based on CuScore may potentially enhance the prediction of patients' prognosis and facilitate the development of effective and innovative treatment strategies.

摘要

背景

铜死亡是一种新型细胞死亡形式,与线粒体呼吸密切相关,且其发生机制与先前已明确的细胞死亡形式不同。然而,铜死亡相关基因(CAGs)对肝细胞癌(HCC)预后、免疫特征及治疗效果的确切影响仍知之甚少。

方法

利用HCC患者的基因组数据对CAGs在肝细胞癌(HCC)预后中的作用进行全面分析。进行共识聚类分析以确定HCC中与铜死亡相关的分子亚型。应用单样本基因集富集分析(ssGSEA)算法量化免疫细胞浸润水平,同时使用“ESTIMATE”软件包计算肿瘤微环境(TME)中的肿瘤纯度、基质评分和免疫评分。利用主成分分析(PCA)算法构建与CAGs相关的风险评分。最后,采用CCK8、伤口愈合实验、Transwell迁移/侵袭实验、EDU实验和异种移植模型来探究MTF1的潜在致癌作用。

结果

确定了三种不同的铜死亡修饰模式,每种模式都与独特的功能富集、临床特征、免疫细胞浸润、免疫检查点、肿瘤微环境(TME)及预后相关。开发了一种与CAGs相关的风险评分(Cuscore)来预测TCGA中的预后,并在GSE76427和ICGC数据集中进行了验证。值得注意的是,Cuscore低的患者预后较好,且更有可能从免疫治疗中获益。此外,HCC中高Cuscore组还揭示了三个潜在治疗靶点(TUBA1B、CDC25B和CSNK2A1)以及几种治疗化合物靶点。此外,实验检测了六个与预后相关的CAGs的表达水平,其中MTF1的敲低表现出对HCC细胞系增殖、侵袭和迁移形成的抑制作用。

结论

这些发现加深了我们对HCC中铜死亡特征的理解,基于CuScore的分层可能会增强对患者预后的预测,并有助于制定有效且创新的治疗策略。

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