多组学分析揭示了3P医学背景下线粒体相关细胞死亡基因中肝细胞癌预后和治疗反应的潜在生物标志物

IF 6.5 2区 医学 Q1 Medicine Epma Journal Pub Date : 2024-05-03 DOI:10.1007/s13167-024-00362-8
Dingtao Hu, Xu Shen, Peng Gao, Tiantian Mao, Yuan Chen, Xiaofeng Li, Weifeng Shen, Yugang Zhuang, Jin Ding
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引用次数: 0

摘要

背景癌细胞生长、转移和耐药性是治疗肝细胞肝癌(LIHC)的主要挑战。方法我们利用线粒体细胞死亡(MCD)的七种不同模式,对MCD相关基因进行了多组学筛选。我们开发了一个新颖的机器学习框架,将 10 种机器学习算法与 67 种不同的算法组合在一起,建立了一个共识线粒体细胞死亡指数(MCDI)。该指数经过了训练、验证和内部临床队列的严格评估。为了更深入地了解所构建的特征,我们采用了一项全面的多组学分析,其中包括体细胞、单细胞和空间转录组学。对风险亚组对免疫疗法和靶向疗法的反应进行了评估和验证。结果在 LIHC 中发现了九个关键的差异表达 MCD 相关基因。基于67个组合的机器学习计算框架构建了共识的MCDI,在预测预后和临床转化方面表现突出。MCDI与免疫浸润、肿瘤免疫功能障碍和排斥(TIDE)评分以及索拉非尼敏感性相关。实验验证了这些发现。此外,我们还发现 PAK1IP1 是预测 LIHC 预后的最重要基因,并在内部临床队列中验证了其作为预后和索拉非尼反应指标的潜力。将 MCDI 纳入 PPPM 框架将改善临床决策过程,优化 LIHC 患者的个体化治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Multi-omic profiling reveals potential biomarkers of hepatocellular carcinoma prognosis and therapy response among mitochondria-associated cell death genes in the context of 3P medicine

Background

Cancer cell growth, metastasis, and drug resistance are major challenges in treating liver hepatocellular carcinoma (LIHC). However, the lack of comprehensive and reliable models hamper the effectiveness of the predictive, preventive, and personalized medicine (PPPM/3PM) strategy in managing LIHC.

Methods

Leveraging seven distinct patterns of mitochondrial cell death (MCD), we conducted a multi-omic screening of MCD-related genes. A novel machine learning framework was developed, integrating 10 machine learning algorithms with 67 different combinations to establish a consensus mitochondrial cell death index (MCDI). This index underwent rigorous evaluation across training, validation, and in-house clinical cohorts. A comprehensive multi-omics analysis encompassing bulk, single-cell, and spatial transcriptomics was employed to achieve a deeper insight into the constructed signature. The response of risk subgroups to immunotherapy and targeted therapy was evaluated and validated. RT-qPCR, western blotting, and immunohistochemical staining were utilized for findings validation.

Results

Nine critical differentially expressed MCD-related genes were identified in LIHC. A consensus MCDI was constructed based on a 67-combination machine learning computational framework, demonstrating outstanding performance in predicting prognosis and clinical translation. MCDI correlated with immune infiltration, Tumor Immune Dysfunction and Exclusion (TIDE) score and sorafenib sensitivity. Findings were validated experimentally. Moreover, we identified PAK1IP1 as the most important gene for predicting LIHC prognosis and validated its potential as an indicator of prognosis and sorafenib response in our in-house clinical cohorts.

Conclusion

This study developed a novel predictive model for LIHC, namely MCDI. Incorporating MCDI into the PPPM framework will enhance clinical decision-making processes and optimize individualized treatment strategies for LIHC patients.

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来源期刊
Epma Journal
Epma Journal Medicine-Biochemistry (medical)
CiteScore
11.30
自引率
23.10%
发文量
0
期刊介绍: PMA Journal is a journal of predictive, preventive and personalized medicine (PPPM). The journal provides expert viewpoints and research on medical innovations and advanced healthcare using predictive diagnostics, targeted preventive measures and personalized patient treatments. The journal is indexed by PubMed, Embase and Scopus.
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