CCDC58 is a potential biomarker for diagnosis, prognosis, immunity, and genomic heterogeneity in pan-cancer
Kai Yang1, Yan Ma2, Weigang Chen1
1Department of Hepatobiliary Surgery, Xi Jing Hospital, Air Force Medical University, Xi'an, 710032, China.
Scientific Reports
|April 12, 2024
Summary
Coiled-coil domain-containing 58 (CCDC58) is a promising pan-cancer biomarker. This study reveals its diagnostic and prognostic value, potential role in the tumor immune microenvironment, and links to cell cycle regulation, suggesting it as a future therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Bioinformatics
Background:
- Coiled-coil domain-containing 58 (CCDC58) is implicated in tumorigenesis across various cancers.
- A comprehensive pan-cancer analysis of CCDC58's roles in diagnosis, prognosis, and immune infiltration is lacking.
Purpose of the Study:
- To conduct a systematic pan-cancer analysis of CCDC58 expression, its correlation with clinical outcomes, and its role in the tumor immune microenvironment.
- To investigate the biological functions of CCDC58 in liver hepatocellular carcinoma (LIHC).
Main Methods:
- Utilized TCGA, GTEx, UALCAN, HPA, CancerSEA, BioGRID, GEPIA 2.0, TIMER 2.0, and TISIDB databases for expression and clinical data analysis.
- Assessed CCDC58's association with diagnosis, prognosis, genetic alterations, DNA methylation, genomic heterogeneity, and immune infiltration.
- Performed enrichment analysis and functional experiments in LIHC.
Main Results:
- CCDC58 is differentially expressed in most tumors, demonstrating significant diagnostic and prognostic value.
- CCDC58 expression correlates with genetic alterations, DNA methylation, and genomic heterogeneity in specific cancers.
- CCDC58 influences the tumor immune microenvironment and is linked to cell cycle and mitosis-related genes.
Conclusions:
- CCDC58 serves as a novel pan-cancer biomarker with potential as a therapeutic target for improving patient outcomes.
- CCDC58 plays a crucial role in tumor cell proliferation and migration, particularly in LIHC.


