Elucidating prognostic significance of purine metabolism in colorectal cancer through integrating data from transcriptomic, immunohistochemical, and single-cell RNA sequencing analysis
- Sungyeon Kim 1, Myunghee Kang 2, Soyeon Jeong 3, Jisup Kim 2, Kyoung Oh Kim 3, Won-Suk Lee 4, Jeong-Heum Baek 4, Jung Ho Kim 3,5,6, Seungyoon Nam 1,6,7
- Sungyeon Kim 1, Myunghee Kang 2, Soyeon Jeong 3
- 1Department of Genome Medicine and Science, Gachon Institute of Genome Medicine and Science, Gachon University Gil Medical Center, Gachon University College of Medicine, Gachon University, Incheon, Korea.
- 2Department of Pathology, Gachon University Gil Medical Center, Gachon University College of Medicine, Gachon University, Incheon, Korea.
- 3Department of Internal Medicine, Gachon University Gil Medical Center, Gachon University College of Medicine, Gachon University, Incheon, Korea.
- 4Department of Surgery, Gachon University Gil Medical Center, Gachon University College of Medicine, Gachon University, Incheon, Korea.
- 5Gachon Medical Research Institute, Gachon Biomedical Convergence Institute, Gachon University Gil Medical Center, Incheon, Korea.
- 6Department of Translational-Clinical Medicine, Gachon Advanced Institute for Health Sciences and Technology (GAIHST), Gachon University, Incheon, Korea.
- 7Department of Health Sciences and Technology, Gachon Advanced Institute for Health Sciences and Technology (GAIHST), Gachon University, Incheon, Korea.
- 0Department of Genome Medicine and Science, Gachon Institute of Genome Medicine and Science, Gachon University Gil Medical Center, Gachon University College of Medicine, Gachon University, Incheon, Korea.
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View abstract on PubMed
Summary
This summary is machine-generated.Low expression of key purine metabolism genes indicates a worse prognosis in colorectal cancer (CRC). These findings suggest purine metabolism alterations can serve as a novel prognostic marker for CRC patients.
Area Of Science
- Oncology
- Molecular Biology
- Biochemistry
Background
- Colorectal cancer (CRC) presents high mortality rates, with purine metabolism as a potential therapeutic target.
- Purine metabolism's prognostic value in CRC lacks validation via immunohistochemical analysis.
Purpose Of The Study
- To assess the clinical relevance of purine metabolism in colorectal cancer using integrated multi-omics approaches.
- To validate purine metabolism genes as prognostic markers in CRC through immunohistochemistry.
Main Methods
- Bulk transcriptome analysis and single-cell RNA sequencing (scRNA-seq) were employed.
- Immunohistochemistry (IHC) was used to validate gene expression and prognostic significance.
- Analysis included CRC patient subgroups (TP53 wild-type/mutant, microsatellite-stable).
Main Results
- Low expression of ADSL, APRT, ADCY3, NME3, and NME6 correlated with worse prognosis in CRC subgroups.
- NME3 expression was an independent prognostic factor; ADSL and NME6 predicted prognosis based on clinical variables.
- NME3 predicted high risk in early-stage CRC, while ADSL and NME6 were predictive in late-stage CRC.
Conclusions
- Alterations in purine metabolism show consistent directional protein expression in CRC tissues.
- Five purine metabolism-related genes (ADSL, APRT, ADCY3, NME3, NME6) demonstrate prognostic potential in CRC.
- Purine metabolism alterations represent a clinically useful prognostic marker for colorectal cancer.
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