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Oncogenic Potential of Replication Factor C Subunit 4: Correlations with Tumor Progression and Assessment of
Muhammad Alaa Eldeen1, Farag Mamdouh2, Waleed K Abdulsahib3
1Cell Biology, Histology & Genetics Division, Zoology Department, Faculty of Science, Zagazig University, Zagazig 44519, Egypt.
Abstract:
Replication Factor C Subunit 4 (RFC4), an oncogene implicated in many human cancers, has yet to be extensively studied in many cancer types to determine its expression patterns and tumor tissue function. Various bioinformatics tools were used to analyze RFC4 as a potential oncogene and therapeutic target across many cancers. We first examined RFC4 expression levels in several human tumor types to determine relationships with tumor grade, stage, metastasis, and patient survival. We also examined RFC4's genetic changes, epigenetic methylation, and effect on tumor microenvironment (TME) immune cell infiltration. We also analyzed RFC4's connections with immunological checkpoints to identify potential molecular pathways involved in carcinogenesis. Our findings show that RFC4 is upregulated in several tumor types and associated with poor prognoses in many human cancers. This study shows that RFC4 significantly affects the tumor immunological microenvironment, specifically immune cell populations. Finally, we screened for RFC4-inhibiting pharmacological compounds with anti-cancer potential. This study fully elucidates RFC4's carcinogenic activities, emphasizing its potential as a prognostic biomarker and a target for anti-cancer therapy.
Insights
Replication Factor C Subunit 4 (RFC4) is upregulated in many cancers, correlating with poor patient outcomes. This oncogene impacts the tumor microenvironment and shows potential as a therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Bioinformatics
Background:
- Replication Factor C Subunit 4 (RFC4) is an oncogene implicated in human cancers.
- Its expression patterns and tumor tissue function require further investigation across diverse cancer types.
Purpose of the Study:
- To analyze RFC4 as a potential oncogene and therapeutic target using bioinformatics tools.
- To determine RFC4 expression levels and their correlation with tumor characteristics and patient survival.
- To investigate RFC4's role in the tumor microenvironment (TME) and its association with immune cell infiltration and immunological checkpoints.
Main Methods:
- Utilized various bioinformatics tools for comprehensive RFC4 analysis.
- Examined RFC4 expression, genetic alterations, and epigenetic methylation across multiple human tumor types.
- Assessed RFC4's impact on TME immune cell infiltration and immunological checkpoints.
- Screened for pharmacological compounds that inhibit RFC4.
Main Results:
- RFC4 is upregulated in several human tumor types.
- Elevated RFC4 expression is associated with poor prognoses in many cancers.
- RFC4 significantly influences the TME, affecting immune cell populations.
- RFC4 demonstrates connections with immunological checkpoints, suggesting involvement in carcinogenesis.
Conclusions:
- RFC4 plays a significant role in cancer development and progression.
- RFC4 serves as a potential prognostic biomarker in numerous cancers.
- Targeting RFC4 with pharmacological agents presents a promising anti-cancer therapeutic strategy.
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