基于 11 个抑郁相关基因的结肠腺癌预后风险预测模型的构建与验证

Yunchuan Yuan, Lili Xia, Xintong Wu, Hongjing Yang, Lu Dou
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引用次数: 0

摘要

背景:抑郁症对癌症的影响已引起学者们的关注。本研究旨在探讨抑郁症与结肠腺癌(COAD)之间的关系:方法:将 COAD 中的差异表达基因与抑郁相关基因(DRGs)重叠,得到 COAD-DRGs。通过单变量和多变量Cox回归分析,构建了预测总生存期(OS)的风险模型。GSE39582 数据集用于验证该模型。结果:结果:构建了一个包含 11 个基因的风险模型。接收者操作特征曲线分析结果显示,该模型能很好地预测OS。在高危人群中,浆细胞、静止/活化记忆 CD4 T 细胞和单核细胞的浸润水平降低,只有 CD8 T 细胞和调节性 T 细胞的浸润水平升高。Cox 回归分析表明,风险评分是一个独立的预后因素。最后,建立了综合风险评分、年龄和 pM 分期的提名图,该模型的预测结果与实际 OS 数据非常吻合:结论:利用 11 个 DRGs 成功构建了 COAD 风险预测模型。该模型有助于实施更有效的治疗和护理策略,提高 COAD 的临床疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Construction and Validation of a Risk Prediction Model for Colon Adenocarcinoma Prognosis Based on 11 Depression-Related Genes

Construction and Validation of a Risk Prediction Model for Colon Adenocarcinoma Prognosis Based on 11 Depression-Related Genes

Background: The influences of depression on cancer have noticeably attracted scholars’ attention. This study is aimed at exploring the relationships between depression and colon adenocarcinoma (COAD).

Methods: Differentially expressed genes in COAD were overlapped with depression-related genes (DRGs) to obtain COAD-DRGs. A risk model was constructed to predict overall survival (OS) using univariate and multivariate Cox regression analyses. GSE39582 dataset was utilized to validate the model. A nomogram was developed utilizing the clinical data.

Results: A risk model containing 11 genes was constructed. The results of receiver operating characteristic curve analysis revealed that the model could well predict the OS. In the high-risk group, the infiltration levels of plasma cells, resting/activated memory CD4 T cells, and monocytes were reduced, and only the infiltration levels of CD8 T cells and regulatory T cells were elevated. Cox regression analysis indicated that the risk score emerged as an independent prognostic factor. Finally, a nomogram of comprehensive risk score, age, and pM stage was established, and the predictions of this model aligned well with the actual OS data.

Conclusion: A COAD risk prediction model was successfully constructed utilizing 11 DRGs. This model assists in implementing more effective treatment and care strategies, enhancing the clinical outcomes for COAD.

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Comparative and Functional Genomics
Comparative and Functional Genomics 生物-生化与分子生物学
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