ORIGINAL RESEARCH article
Front. Immunol.
Sec. Cancer Immunity and Immunotherapy
Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1619749
This article is part of the Research TopicMicrobiota-Immunity Dynamics in Cancer: Mechanisms and Implications for Treatment StrategiesView all 6 articles
Role of Necroptosis-Related Genes in Immune Activity and Prognosis of Colorectal Cancer
Provisionally accepted- 1First Affiliated Hospital of Zhengzhou University, Zhengzhou, China
- 2China Three Gorges University, Yichang, China
- 3The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China
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Background: Necroptosis plays a critical role in the onset and progression of numerous malignancies, with colorectal cancer (CRC) ranking among the leading causes of cancer-related mortality worldwide. However, the relationship between necroptosisrelated genes (NRGs) and CRC remains contentious. Hence, this study aims to develop a novel NRG-based signature to predict the prognosis of CRC patients and explore its potential role.Methods: Transcriptome data from the Gene Expression Omnibus (GEO) databases and the Cancer Genome Atlas (TCGA) were employed to identify cancer hallmarks associated with outcomes in CRC. A novel NRG signature was formulated and validated using least absolute shrinkage and selection operator (LASSO) regression analysis and COX regression analysis. Subsequently, univariate and multivariate Cox regression analyses, Kaplan-Meier (K-M) survival analysis, receiver operating characteristic (ROC) curves, and nomograms were utilized to assess the predictive capability of our signature. Furthermore, a variety of bioinformatics analysis algorithms were leveraged to uncover potential mechanisms, tumor immune status, and differences in drug sensitivity between the two-risk groups. The expression of signature NRGs in CRC was evaluated through quantitative reverse transcription polymerase chain reaction (qRT-PCR).
Keywords: Results: A novel signature consisting of eighteen NRGs (CTSB, PAEP, ARL4C, TAP2, WFS1, BATF2, DUSP27, CXCL9
Received: 28 Apr 2025; Accepted: 05 Aug 2025.
Copyright: © 2025 Tan, Wang, Chang, Zhang, Deng, Yan, Zhu, Wang, Cai, Liu, Tan and Cui. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Zhibo Liu, First Affiliated Hospital of Zhengzhou University, Zhengzhou, China
Yuyan Tan, China Three Gorges University, Yichang, China
Jinyuan Cui, First Affiliated Hospital of Zhengzhou University, Zhengzhou, China
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