Transcriptome profiling revealed multiple circadian rhythm-related genes associated with common gynecological cancers

BackgroundStudies have shown that more than half of the human genome expression is affected by circadian rhythms, which includes genes involved in cell cycle control, DNA repair and apoptosis that are critical in cancer biology. However, the roles of circadian rhythm-related genes (CRRGs) in cervica...

Full description

Saved in:
Bibliographic Details
Main Authors: Lan Peng, Meiping Jiang, Kangming Li, Shuhui Yu, Chunfang Zhao, Lan Zhang, Lan Li
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2025.1422122/full
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832582952898265088
author Lan Peng
Meiping Jiang
Kangming Li
Shuhui Yu
Chunfang Zhao
Lan Zhang
Lan Li
author_facet Lan Peng
Meiping Jiang
Kangming Li
Shuhui Yu
Chunfang Zhao
Lan Zhang
Lan Li
author_sort Lan Peng
collection DOAJ
description BackgroundStudies have shown that more than half of the human genome expression is affected by circadian rhythms, which includes genes involved in cell cycle control, DNA repair and apoptosis that are critical in cancer biology. However, the roles of circadian rhythm-related genes (CRRGs) in cervical cancer (CC) and other common gynecologic cancers remain unclear.MethodsThe transcriptome data and clinical information related to CC and other common gynecologic cancers were extracted from the UCSC Xena and Gene Expression Omnibus (GEO) databases. In this study, the differentially expressed CRRGs of CC (target genes) were obtained, and the functional enrichment analysis of these target genes was performed by “clusterProfiler”. Then, the biomarkers of CC were screened out to construct the survival risk model (risk score). Moreover, function and tumor micro-environment (TME) analyses in different risk groups were performed for further study of the potential mechanism of CC. Furthermore, the prognostic value and function analyses of biomarkers in three common gynecologic cancers were performed to reveal the potential agreement or heterogeneity regulations.ResultsA total of 19 target genes were associated with pyrimidine metabolism. The survival risk model was constructed with six biomarkers, including APOBEC3B, CDA, HELLS, RHOB, SLC15A3, and UPP1. Among these, APOBEC3B, HELLS, and SLC15A3 were identified as positive factors, while CDA, RHOB, and UPP1 were identified as negative factors in CC. It is notable that multiple immune-related signaling pathways were associated with the clinical risk of CC, and the immunotherapy sensitivity was worse in the high-risk group. In addition, we found that most of biomarkers had the prognostic values in other common gynecologic cancers. It was notable that the mechanisms by which these biomarkers influence gynecologic cancers were associated with extracellular matrix (ECM) receptor interaction, focal adhesion, etc.ConclusionThis study identified six circadian rhythm-related biomarkers, including APOBEC3B, CDA, HELLS, RHOB, SLC15A3, and UPP1, which were associated with the prognosis of CC. The mechanisms by which these biomarkers influence gynecologic cancers were associated with ECM receptor interaction, focal adhesion, and other functions. These findings might help to deepen the understanding of the agreement or heterogeneity of CRRGs in the pathological processes of common gynecologic cancers.
format Article
id doaj-art-75818c5e38e841a58a52ac1f73b30a9a
institution Kabale University
issn 2234-943X
language English
publishDate 2025-01-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Oncology
spelling doaj-art-75818c5e38e841a58a52ac1f73b30a9a2025-01-29T05:21:08ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2025-01-011510.3389/fonc.2025.14221221422122Transcriptome profiling revealed multiple circadian rhythm-related genes associated with common gynecological cancersLan PengMeiping JiangKangming LiShuhui YuChunfang ZhaoLan ZhangLan LiBackgroundStudies have shown that more than half of the human genome expression is affected by circadian rhythms, which includes genes involved in cell cycle control, DNA repair and apoptosis that are critical in cancer biology. However, the roles of circadian rhythm-related genes (CRRGs) in cervical cancer (CC) and other common gynecologic cancers remain unclear.MethodsThe transcriptome data and clinical information related to CC and other common gynecologic cancers were extracted from the UCSC Xena and Gene Expression Omnibus (GEO) databases. In this study, the differentially expressed CRRGs of CC (target genes) were obtained, and the functional enrichment analysis of these target genes was performed by “clusterProfiler”. Then, the biomarkers of CC were screened out to construct the survival risk model (risk score). Moreover, function and tumor micro-environment (TME) analyses in different risk groups were performed for further study of the potential mechanism of CC. Furthermore, the prognostic value and function analyses of biomarkers in three common gynecologic cancers were performed to reveal the potential agreement or heterogeneity regulations.ResultsA total of 19 target genes were associated with pyrimidine metabolism. The survival risk model was constructed with six biomarkers, including APOBEC3B, CDA, HELLS, RHOB, SLC15A3, and UPP1. Among these, APOBEC3B, HELLS, and SLC15A3 were identified as positive factors, while CDA, RHOB, and UPP1 were identified as negative factors in CC. It is notable that multiple immune-related signaling pathways were associated with the clinical risk of CC, and the immunotherapy sensitivity was worse in the high-risk group. In addition, we found that most of biomarkers had the prognostic values in other common gynecologic cancers. It was notable that the mechanisms by which these biomarkers influence gynecologic cancers were associated with extracellular matrix (ECM) receptor interaction, focal adhesion, etc.ConclusionThis study identified six circadian rhythm-related biomarkers, including APOBEC3B, CDA, HELLS, RHOB, SLC15A3, and UPP1, which were associated with the prognosis of CC. The mechanisms by which these biomarkers influence gynecologic cancers were associated with ECM receptor interaction, focal adhesion, and other functions. These findings might help to deepen the understanding of the agreement or heterogeneity of CRRGs in the pathological processes of common gynecologic cancers.https://www.frontiersin.org/articles/10.3389/fonc.2025.1422122/fullgynecological cancerscircadian rhythmsprognosisbiomarkersfunctionregulatory mechanism
spellingShingle Lan Peng
Meiping Jiang
Kangming Li
Shuhui Yu
Chunfang Zhao
Lan Zhang
Lan Li
Transcriptome profiling revealed multiple circadian rhythm-related genes associated with common gynecological cancers
Frontiers in Oncology
gynecological cancers
circadian rhythms
prognosis
biomarkers
function
regulatory mechanism
title Transcriptome profiling revealed multiple circadian rhythm-related genes associated with common gynecological cancers
title_full Transcriptome profiling revealed multiple circadian rhythm-related genes associated with common gynecological cancers
title_fullStr Transcriptome profiling revealed multiple circadian rhythm-related genes associated with common gynecological cancers
title_full_unstemmed Transcriptome profiling revealed multiple circadian rhythm-related genes associated with common gynecological cancers
title_short Transcriptome profiling revealed multiple circadian rhythm-related genes associated with common gynecological cancers
title_sort transcriptome profiling revealed multiple circadian rhythm related genes associated with common gynecological cancers
topic gynecological cancers
circadian rhythms
prognosis
biomarkers
function
regulatory mechanism
url https://www.frontiersin.org/articles/10.3389/fonc.2025.1422122/full
work_keys_str_mv AT lanpeng transcriptomeprofilingrevealedmultiplecircadianrhythmrelatedgenesassociatedwithcommongynecologicalcancers
AT meipingjiang transcriptomeprofilingrevealedmultiplecircadianrhythmrelatedgenesassociatedwithcommongynecologicalcancers
AT kangmingli transcriptomeprofilingrevealedmultiplecircadianrhythmrelatedgenesassociatedwithcommongynecologicalcancers
AT shuhuiyu transcriptomeprofilingrevealedmultiplecircadianrhythmrelatedgenesassociatedwithcommongynecologicalcancers
AT chunfangzhao transcriptomeprofilingrevealedmultiplecircadianrhythmrelatedgenesassociatedwithcommongynecologicalcancers
AT lanzhang transcriptomeprofilingrevealedmultiplecircadianrhythmrelatedgenesassociatedwithcommongynecologicalcancers
AT lanli transcriptomeprofilingrevealedmultiplecircadianrhythmrelatedgenesassociatedwithcommongynecologicalcancers