Evidence map›Paper›PMID 41398877›Full record

ArticleMedicine2025

Identification and experimental validation of copper metabolism-related genes in cervical cancer.

Yusheng Ye, Yuanyi Wang, Dacai Gong, Yunya Zhao, Xing Wei

Abstract read
In one paragraph

Article in Medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yusheng YeDepartment of Clinical Laboratory, Pidu District People's Hospital, Third Affiliated Hospital of Chengdu Medical College, Chengdu, Sichuan, China.
Yuanyi Wang
Dacai Gong
Yunya Zhao

Funding

Chengdu Health Commission 2023242Sichuan Medical Association Q21094the Joint research fund for popularizing applied research projects of Pidu District People's Hospital-Chengdu Medical College 2021LHPT-07
6 · The paper itself

Abstract

Cervical cancer is a common malignancy which is very harmful to women's health worldwide. Copper metabolism has become research highlight and is expected to be new therapeutic target of cancers, but the copper metabolism related genes connect with cervical cancer remain unclear. This study identified and experimentally verified the copper metabolism-related genes in cervical cancer. First, the gene expression profile of cervical cancer was downloaded from the Gene Expression Omnibus database to identify significantly differentially expressed genes of cervical cancer, and these genes were intersected to copper metabolism data set to screened out copper metabolism related genes in cervical cancer. Then gene ontology and Kyoto Encyclopedia of Gene and Genomes enrichment analysis were conducted, the protein-protein interactions were analyzed using the online database STRING11.0. The Cancer Genome Atlas database was used to validate the screening genes and analyze their diagnostic value. Cervical tissue samples from 8 patients with cervical cancer as the experimental group and 10 patients with benign uterine fibroids as the control group were collected, mRNAs was extracted and quantitative real time polymerase chain reaction was used to verify the selected genes. The Human Protein Atlas database was used to verify the expression of the selected genes, and their immune infiltration was studied based on the The Cancer Genome Atlas database. MiRNA-hub gene network, transcription factor-hub gene network and chemical-hub gene network were constructed by us to accurately investigate the molecular mechanism and potential drugs underlying copper metabolism related genes we screened out in cervical cancer. Aquaporin1 and cyclin-dependent kinases1 were the copper metabolism-related genes in cervical cancer we screened out by bioinformatics methods and then validated by clinical samples. Aquaporin1 and cyclin-dependent kinases1 could play an important role in the mechanism of cervical cancer and could be targets of cervical cancer concerning copper metabolism.

Indexed as

CopperUterine Cervical NeoplasmsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansMicroRNAsProtein Interaction MapsCopperMicroRNAsAQP1CDK1cervical cancercopper metabolism

Identifiers

PMID41398877
PMCPMC12708092

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.