通过多组学单细胞整合孟德尔分析阐明硬脂酰代谢和ncoa4介导的胃癌肝转移中的铁凋亡:推进个性化免疫治疗策略。

IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Discover. Oncology Pub Date : 2025-01-15 DOI:10.1007/s12672-025-01769-z
Zhongqiu Yang, Yuquan Chen, Yaping Miao, Haisheng Yan, Kexin Chen, Yaoqin Xu, Lanqian Su, Lanyue Zhang, Yalan Yan, Hao Chi, Jin Fu, Lexin Wang
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引用次数: 0

摘要

背景:硬脂酰gpe代谢在胃癌肝转移中起关键作用。本研究深入探讨了胃癌伴肝转移(LMGC)中硬脂酰代谢引发的复杂肿瘤微环境(TME)异质性的机制,为LMGC研究提供了新的视角。目的:利用孟德尔随机化,我们确定硬脂酰代谢显著促进胃癌(GC)的进展。在此之后,大量转录组分析和单细胞多组学技术研究了硬脂酰gpe代谢相关基因,特别是NCOA4,在调节LMGC TME中的作用。结果:我们的分析强调了硬脂酰代谢在调节LMGC复杂微环境中的关键作用,特别是对单核细胞的影响。通过单细胞测序和空间转录组学,我们已经确定了单核细胞群中硬脂酰代谢的关键代谢基因,包括NCOA4。关于铁下垂、硬脂酰代谢和LMGC发现之间的关系,似乎硬脂酰代谢和LMGC途径与铁下垂相关的机制相互交叉。铁下垂以铁依赖性脂质过氧化为特征,是一种受调控的细胞死亡形式。硬脂酰辅酶a去饱和酶(SCD)是硬脂酰代谢的关键酶,其活性与脂质组成的调节和对铁死亡的易感性有关。此外,LMGC在与氧化应激和脂质代谢相关的细胞过程中是不可或缺的,这两者都是铁下垂的重要因素。结论:本研究增强了对硬脂酰代谢与铁上吊在促进胃癌肝转移中的关系及其在肿瘤异质性调节中的作用的认识。此外,本研究有助于更深入地了解胃癌肿瘤微环境(TME)的动态,为制定更好的干预措施来对抗胃癌转移提供依据。
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Elucidating stearoyl metabolism and NCOA4-mediated ferroptosis in gastric cancer liver metastasis through multi-omics single-cell integrative mendelian analysis: advancing personalized immunotherapy strategies.

Background: The metabolism of stearoyl-GPE plays a key role in the liver metastasis of gastric cancer. This investigation delves into the mechanisms underlying the intricate tumor microenvironment (TME) heterogeneity triggered by stearoyl metabolism in gastric cancer with liver metastasis (LMGC), offering novel perspectives for LMGC.

Objective: Utilizing Mendelian randomization, we determined that stearoyl metabolism significantly contributes to the progression of gastric cancer (GC). Following this, bulk transcriptome analyses and single-cell multiomics techniques to investigate the roles of stearoyl-GPE metabolism-related genes, particularly NCOA4, in regulating LMGC TME.

Results: Our analysis highlights the crucial role of stearoyl metabolism in modulating the complex microenvironment of LMGC, particularly impacting monocyte cells. Through single-cell sequencing and spatial transcriptomics, we have identified key metabolic genes specific to stearoyl metabolism within the monocyte cell population, including NCOA4. Regarding the relationship between ferroptosis, stearoyl metabolism, and LMGC findings, it is plausible that stearoyl metabolism and LMGC pathways intersect with mechanisms involved in ferroptosis. Ferroptosis, characterized by iron-dependent lipid peroxidation, represents a regulated form of cell death. The activity of Stearoyl-CoA desaturase (SCD), a critical enzyme in stearoyl metabolism, has been associated with the modulation of lipid composition and susceptibility to ferroptosis. Furthermore, the LMGC is integral to cellular processes related to oxidative stress and lipid metabolism, both of which are significant factors in the context of ferroptosis.

Conclusion: This study enhances the understanding of the relationship between stearoyl metabolism and ferroptosis in promoting liver metastasis of gastric cancer and its role in the regulation of tumor heterogeneity. In addition, this study contributes to a deeper understanding of the dynamics of gastric cancer tumor microenvironment (TME) and provides a basis for the development of better interventions to combat cancer metastasis.

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来源期刊
Discover. Oncology
Discover. Oncology Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.40
自引率
9.10%
发文量
122
审稿时长
5 weeks
期刊最新文献
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