结肠腺癌铜代谢相关分子亚型和预后风险分层的综合多组学分析

IF 4.2
Xi Sun, Jingfei Tong, Xiaojie Fang, Miaojiong Lu, Chunhui Rao, Yanyan Li
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引用次数: 0

摘要

结肠腺癌(COAD)是最常见的结直肠癌亚型,起源于结肠的腺细胞。尽管诊断和治疗取得了进步,但其预后仍然很差。铜是一种必需的微量营养素,参与肿瘤发生和其他生物过程。在本研究中,我们从TCGA和GEO数据库中鉴定出与COAD预后相关的铜代谢相关基因(copper metabolism-related genes, CMRG),并构建了基于CMRG的风险模型。我们通过分析免疫浸润、免疫治疗反应和药物敏感性来评估其临床意义。单细胞测序揭示了CMRG在COAD组织中的空间和细胞分布,从而深入了解了它们在肿瘤微环境中的作用。选择COX19进行进一步验证,体外实验(western blot、PCR、siRNA、菌落形成和Transwell实验)证实了其促进COAD细胞侵袭和增殖的作用。这些发现强调了铜代谢在COAD进展中的作用,并提出了潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comprehensive Multi-Omics Analysis of Copper Metabolism Related Molecular Subtypes and Prognostic Risk Stratification in Colon Adenocarcinoma

Comprehensive Multi-Omics Analysis of Copper Metabolism Related Molecular Subtypes and Prognostic Risk Stratification in Colon Adenocarcinoma

Colon adenocarcinoma (COAD) is the most common subtype of colorectal cancer, originating from glandular cells in the colon. Despite diagnostic and therapeutic advances, its prognosis remains poor. Copper, an essential micronutrient, is involved in tumorigenesis and other biological processes. In this study, we identified copper metabolism-related genes (CMRG) associated with COAD prognosis from TCGA and GEO databases and constructed a CMRG-based risk model. We assessed its clinical relevance through analyses of immune infiltration, immunotherapy response, and drug sensitivity. Single-cell sequencing revealed the spatial and cellular distribution of CMRG in COAD tissues, providing insight into their roles in the tumour microenvironment. COX19 was selected for further validation, and in vitro experiments (western blot, PCR, siRNA, colony formation, and Transwell assays) confirmed its role in promoting COAD cell invasion and proliferation. These findings highlight the involvement of copper metabolism in COAD progression and suggest potential targets for therapy.

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来源期刊
CiteScore
11.50
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0.00%
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期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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