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Identification of Genes Related to Ribosomal Proteins in Colorectal Cancer: Exploring Their Potential As Biomarkers, Prognostic Indicators, and Therapeutic Targets Publisher Pubmed



Salehinia N1, 4 ; Mohammad Almosawi AK2, 4 ; Almoussawi DK3, 4 ; Sadeghi ES4 ; Zamani A4, 5 ; Mahdevar M4, 6
Authors
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Authors Affiliations
  1. 1. Department of Biology, Islamic Azad University, Qaemshahr, Iran
  2. 2. Department of biology, College of Sciences, University of Thi Qar, Nasiriyah, Iraq
  3. 3. General Directorate of Education in Thi-Qar, Ministry of Education, Al-Nasiriya City, Iraq
  4. 4. Genius Gene, Genetics and Biotechnology Company, Isfahan, Iran
  5. 5. Department of Biology, Faculty of Basic Sciences, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran
  6. 6. Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Molecular Biology Reports Published:2024


Abstract

Background: Colorectal cancer (CRC) ranks as the third most commonly diagnosed cancer in both females and males, underscoring the need for the identification of effective biomarkers. Methods and results: We assessed the expression levels of ribosomal proteins (RPs) at both mRNA and protein levels. Subsequently, leveraging the STRING database, we constructed a protein-protein interaction network and identified hub genes. The co-expression network of differentially expressed genes associated with CRC and their target hub RPs was constructed using the weighted gene co-expression network analysis algorithm. Gene ontology and molecular signatures database were conducted to gain insights into the biological roles of genes associated with the identified module. To confirm the results, the expression level of the candidate genes in the CRC samples compared to the adjacent healthy was evaluated by the RT-qPCR method. Our findings indicated that the genes related to RPs were predominantly enriched in biological processes associated with Myc Targets, Oxidative Phosphorylation, and cell proliferation. Also, results demonstrated that elevated levels of GRWD1, MCM5, IMP4, and RABEPK that related to RPs were associated with poor prognostic outcomes for CRC patients. Notably, IMP4 and RABEPK exhibited higher diagnostic value. Moreover, the expression of IMP4 and RABEPK showed a significant association with drug resistance using cancer cell line encyclopedia and genomics of drug sensitivity in cancer databases. Also, the results showed that the expression level of IMP4 and RABEPK in cancerous samples was significantly higher compared to the adjacent healthy ones. Conclusion: The general results of this study have shown that many genes related to RPs are increased in cancer and could be associated with the death rate of patients. We also highlighted the therapeutic and prognostic potentials of RPs genes in CRC. © The Author(s), under exclusive licence to Springer Nature B.V. 2024.
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