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pmid:38637125
Mining and exploration of rehabilitation nursing targets for colorectal cancer.
Ruipu Li · Jie He · Zhijie Ni · Jie Zhang · Xiaoqian Chi · Chunbo Kang · Zhongbo Li · Xubin Li
Aging · 2024 doi:10.18632/aging.205739
Paper
complete
Experiment
complete
Data
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Analysis
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Execution
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Complete file
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However, it is not yet clear how MYC and NCAPG2 are involved in colorectal cancer.\nMETHOD: We obtained colorectal cancer datasets GSE32323 and GSE113513 from the Gene Expression Omnibus (GEO). After downloading, we identified differentially expressed genes (DEGs) and performed Weighted Gene Co-expression Network Analysis (WGCNA). We then undertook functional enrichment assay, gene set enrichment assay (GSEA) and immune infiltration assay. Protein-protein interaction (PPI) network construction and analysis were undertaken. Survival analysis and Comparative Toxicogenomics Database (CTD) analysis were conducted. A gene expression heat map was generated. We used TargetScan to identify miRNAs that are regulators of DEGs.\nRESULTS: 1117 DEGs were identified. Their predominant enrichment in activities like the cellular phase of the cell cycle, in cell proliferation, in nuclear and cytoplasmic localisation and in binding to protein-containing complexes was revealed by Gene Ontology (GO). When the enrichment data from GSE32323 and GSE113513 colon cancer datasets were merged, the primary enriched DEGs were linked to the cell cycle, protein complex, cell cycle control, calcium signalling and P53 signalling pathways. In particular, MYC, MAD2L1, CENPF, UBE2C, NUF2 and NCAPG2 were identified as highly expressed in colorectal cancer samples. Comparative Toxicogenomics Database (CTD) demonstrated that the core genes were implicated in the following processes: colorectal neoplasia, tumour cell transformation, inflammation and necrosis.\nCONCLUSIONS: High MYC and NCAPG2 expression has been observed in colorectal cancer, and increased MYC and NCAPG2 expression correlates with worse prognosis.", "claims": [{"id": "claim-method", "statement": "When examining clinical survival data for colorectal cancer from The Cancer Genome Atlas (TCGA), we employed the R software package maxstat (version: 0.7–25) to determine the ideal RiskScore truncation value associated with core genes.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38637125", "locator": "sections[11] \"Survival analysis\" paragraph 2", "quote": "When examining clinical survival data for colorectal cancer from The Cancer Genome Atlas (TCGA), we employed the R software package maxstat (version: 0.7–25) to determine the ideal RiskScore truncation value associated with core genes."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38637125", "locator": "sections[15] \"Data availability\" paragraph 2", "quote": "The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:38637125"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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