A Comprehensive Prognostic Model for Colon Adenocarcinoma Depending on Nuclear-Mitochondrial-Related Genes.

IF 2.7 4区 医学 Q3 ONCOLOGY
Lingling Lv, Yuqing Huang, Qiong Li, Yuan Wu, Lan Zheng
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引用次数: 0

Abstract

Background: Colon adenocarcinoma (COAD) has increasing incidence and is one of the most common malignant tumors. The mitochondria involved in cell energy metabolism, oxygen free radical generation, and cell apoptosis play important roles in tumorigenesis and progression. The relationship between mitochondrial genes and COAD remains largely unknown. Methods: COAD data including 512 samples were set out from the UCSC Xena database. The nuclear mitochondrial-related genes (NMRGs)-related risk prognostic model and prognostic nomogram were constructed, and NMRGs-related gene mutation and the immune environment were analyzed using bioinformatics methods. Then, a liver metastasis model of colorectal cancer was constructed and protein expression was detected using Western blot assay. Results: A prognostic model for COAD was constructed. Comparing the prognostic model dataset and the validation dataset showed considerable correlation in both risk grouping and prognosis. Based on the risk score (RS) model, the samples of the prognostic dataset were divided into high risk group and low risk group. Moreover, pathologic N and T stage and tumor recurrence in the two risk groups were significantly different. The four prognostic factors, including age and pathologic T stage in the nomogram survival model also showed excellent predictive performance. An optimal combination of nine differentially expressed NMRGs was finally obtained, including LARS2, PARS2, ETHE1, LRPPRC, TMEM70, AARS2, ACAD9, VARS2, and ATP8A2. The high-RS group had more inflamed immune features, including T and CD4+ memory cell activation. Besides, mitochondria-associated LRPPRC and LARS2 expression levels were increased in vivo xenograft construction and liver metastases assays. Conclusion: This study established a comprehensive prognostic model for COAD, incorporating nine genes associated with nuclear-mitochondrial functions. This model demonstrates superior predictive performance across four prognostic factors: age, pathological T stage, tumor recurrence, and overall prognosis. It is anticipated to be an effective model for enhancing the prognosis and treatment of COAD.

基于核-线粒体相关基因的结肠腺癌综合预后模型
背景:结肠腺癌(COAD)的发病率越来越高,是最常见的恶性肿瘤之一。参与细胞能量代谢、氧自由基生成和细胞凋亡的线粒体在肿瘤发生和发展过程中发挥着重要作用。线粒体基因与 COAD 之间的关系在很大程度上仍然未知。研究方法从加州大学圣地亚哥分校 Xena 数据库中收集了包括 512 个样本的 COAD 数据。构建了线粒体相关基因(NMRGs)相关风险预后模型和预后提名图,并利用生物信息学方法分析了NMRGs相关基因突变和免疫环境。然后,构建了结直肠癌肝转移模型,并利用 Western 印迹法检测了蛋白表达。结果构建了 COAD 的预后模型。预后模型数据集与验证数据集的比较显示,在风险分组和预后方面都有相当大的相关性。根据风险评分(RS)模型,预后数据集中的样本被分为高风险组和低风险组。此外,两个风险组的病理 N 和 T 分期以及肿瘤复发率也有显著差异。在提名图生存模型中,包括年龄和病理 T 分期在内的四个预后因素也显示出卓越的预测性能。最终得到了九个差异表达 NMRGs 的最佳组合,包括 LARS2、PARS2、ETHE1、LRPPRC、TMEM70、AARS2、ACAD9、VARS2 和 ATP8A2。高RS组有更多的炎症免疫特征,包括T细胞和CD4+记忆细胞活化。此外,在体内异种移植和肝转移试验中,线粒体相关 LRPPRC 和 LARS2 的表达水平也有所增加。结论本研究建立了一个全面的 COAD 预后模型,纳入了 9 个与核-线粒体功能相关的基因。该模型在年龄、病理 T 分期、肿瘤复发和总体预后这四个预后因素上都表现出了卓越的预测能力。预计它将成为改善 COAD 预后和治疗的有效模型。
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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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
202
审稿时长
2 months
期刊介绍: Technology in Cancer Research & Treatment (TCRT) is a JCR-ranked, broad-spectrum, open access, peer-reviewed publication whose aim is to provide researchers and clinicians with a platform to share and discuss developments in the prevention, diagnosis, treatment, and monitoring of cancer.
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