CPLX1 is a novel prognostic biomarker in CRC correlating with immunotherapy resistance and ferroptosis

BackgroundColorectal cancer (CRC) remains a predominant contributor to cancer-related mortality globally, with its resistance to immunotherapeutic strategies presenting a formidable challenge in patient management. Recent investigations have illuminated the prospective involvement of ferroptosis, a...

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Main Authors: Canyu Liu, Qiujun Liu, Yuanhao Lv, Tingmin Chang, Shiyi Song, Yuang Ding, Jiateng Zhong, Yanxuan Liu
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-07-01
Series:Frontiers in Immunology
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Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2025.1589423/full
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author Canyu Liu
Qiujun Liu
Yuanhao Lv
Tingmin Chang
Shiyi Song
Yuang Ding
Jiateng Zhong
Jiateng Zhong
Jiateng Zhong
Jiateng Zhong
Jiateng Zhong
Yanxuan Liu
author_facet Canyu Liu
Qiujun Liu
Yuanhao Lv
Tingmin Chang
Shiyi Song
Yuang Ding
Jiateng Zhong
Jiateng Zhong
Jiateng Zhong
Jiateng Zhong
Jiateng Zhong
Yanxuan Liu
author_sort Canyu Liu
collection DOAJ
description BackgroundColorectal cancer (CRC) remains a predominant contributor to cancer-related mortality globally, with its resistance to immunotherapeutic strategies presenting a formidable challenge in patient management. Recent investigations have illuminated the prospective involvement of ferroptosis, a regulated form of cell death, in both cancer progression and the development of resistance to therapeutic interventions.ObjectiveThis study aims to elucidate the prognostic significance of CPLX1 in CRC, specifically its correlation with immunotherapy resistance and its association with ferroptosis, thereby contributing to a deeper understanding of tumor biology and therapeutic vulnerability.MethodsWe conducted an integrative analysis of RNA-seq datasets from the TCGA-COAD and TCGA-READ projects, along with the GEO GSE156451 dataset, to discern differentially expressed genes. Expression levels of CPLX1 were evaluated utilizing the TIMER 2.0 database, and survival analyses were performed via Kaplan-Meier plots and Cox regression modeling to assess prognostic implications. Additionally, mutational analyses through cBioPortal and COSMIC datasets were employed to identify CPLX1 mutations in COAD. Co-expression and functional enrichment analyses, alongside Gene Set Enrichment Analysis (GSEA), were also conducted to delineate pathways impacted by CPLX1.ResultsOur findings indicate that high expression levels of CPLX1 are significantly correlated with poor prognostic outcomes in CRC patients. Through immune infiltration analyses employing ssGSEA, we observed notable associations between CPLX1 expression and specific immune cell populations. Furthermore, the interaction between CPLX1 and ferroptosis-related genes suggests a potential mechanistic linkage that could underpin therapeutic resistance.ConclusionCPLX1 is identified as a novel prognostic biomarker in CRC, exhibiting clear correlations with both immunotherapy resistance and ferroptosis. These findings indicate that targeting CPLX1 may provide novel therapeutic strategies to ameliorate treatment resistance in CRC.
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spelling doaj-art-7573db957f744a2e95e9c88dc9e528472025-08-20T02:41:32ZengFrontiers Media S.A.Frontiers in Immunology1664-32242025-07-011610.3389/fimmu.2025.15894231589423CPLX1 is a novel prognostic biomarker in CRC correlating with immunotherapy resistance and ferroptosisCanyu Liu0Qiujun Liu1Yuanhao Lv2Tingmin Chang3Shiyi Song4Yuang Ding5Jiateng Zhong6Jiateng Zhong7Jiateng Zhong8Jiateng Zhong9Jiateng Zhong10Yanxuan Liu11Department of Digestive Endoscopy Center, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, ChinaDepartment of Endocrinology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, ChinaDepartment of Pathology, Xinxiang Medical University, Xinxiang, ChinaDepartment of Digestive Endoscopy Center, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, ChinaDepartment of Digestive Endoscopy Center, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, ChinaDepartment of Pathology, Xinxiang Medical University, Xinxiang, ChinaDepartment of Pathology, Xinxiang Medical University, Xinxiang, ChinaDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, ChinaXinxiang Key Laboratory of Precision Diagnosis and Treatment for Colorectal Cancer, Xinxiang First People’s Hospital, Xinxiang, ChinaXinxiang Engineering Technology Research Center of Digestive Tumor Molecular Diagnosis, Xinxiang Medical University, Xinxiang, ChinaHenan Province Engineering Technology Research Center of Tumor Diagnostic Biomarkers and RNA Interference Drugs, The Third Affiliated Hospital of Xinxiang Medical University, Xinxiang, ChinaDepartment of Medical Genetics, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, ChinaBackgroundColorectal cancer (CRC) remains a predominant contributor to cancer-related mortality globally, with its resistance to immunotherapeutic strategies presenting a formidable challenge in patient management. Recent investigations have illuminated the prospective involvement of ferroptosis, a regulated form of cell death, in both cancer progression and the development of resistance to therapeutic interventions.ObjectiveThis study aims to elucidate the prognostic significance of CPLX1 in CRC, specifically its correlation with immunotherapy resistance and its association with ferroptosis, thereby contributing to a deeper understanding of tumor biology and therapeutic vulnerability.MethodsWe conducted an integrative analysis of RNA-seq datasets from the TCGA-COAD and TCGA-READ projects, along with the GEO GSE156451 dataset, to discern differentially expressed genes. Expression levels of CPLX1 were evaluated utilizing the TIMER 2.0 database, and survival analyses were performed via Kaplan-Meier plots and Cox regression modeling to assess prognostic implications. Additionally, mutational analyses through cBioPortal and COSMIC datasets were employed to identify CPLX1 mutations in COAD. Co-expression and functional enrichment analyses, alongside Gene Set Enrichment Analysis (GSEA), were also conducted to delineate pathways impacted by CPLX1.ResultsOur findings indicate that high expression levels of CPLX1 are significantly correlated with poor prognostic outcomes in CRC patients. Through immune infiltration analyses employing ssGSEA, we observed notable associations between CPLX1 expression and specific immune cell populations. Furthermore, the interaction between CPLX1 and ferroptosis-related genes suggests a potential mechanistic linkage that could underpin therapeutic resistance.ConclusionCPLX1 is identified as a novel prognostic biomarker in CRC, exhibiting clear correlations with both immunotherapy resistance and ferroptosis. These findings indicate that targeting CPLX1 may provide novel therapeutic strategies to ameliorate treatment resistance in CRC.https://www.frontiersin.org/articles/10.3389/fimmu.2025.1589423/fullCPLX1biomarkerCRCtumor-immune infiltrationferroptosis
spellingShingle Canyu Liu
Qiujun Liu
Yuanhao Lv
Tingmin Chang
Shiyi Song
Yuang Ding
Jiateng Zhong
Jiateng Zhong
Jiateng Zhong
Jiateng Zhong
Jiateng Zhong
Yanxuan Liu
CPLX1 is a novel prognostic biomarker in CRC correlating with immunotherapy resistance and ferroptosis
Frontiers in Immunology
CPLX1
biomarker
CRC
tumor-immune infiltration
ferroptosis
title CPLX1 is a novel prognostic biomarker in CRC correlating with immunotherapy resistance and ferroptosis
title_full CPLX1 is a novel prognostic biomarker in CRC correlating with immunotherapy resistance and ferroptosis
title_fullStr CPLX1 is a novel prognostic biomarker in CRC correlating with immunotherapy resistance and ferroptosis
title_full_unstemmed CPLX1 is a novel prognostic biomarker in CRC correlating with immunotherapy resistance and ferroptosis
title_short CPLX1 is a novel prognostic biomarker in CRC correlating with immunotherapy resistance and ferroptosis
title_sort cplx1 is a novel prognostic biomarker in crc correlating with immunotherapy resistance and ferroptosis
topic CPLX1
biomarker
CRC
tumor-immune infiltration
ferroptosis
url https://www.frontiersin.org/articles/10.3389/fimmu.2025.1589423/full
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