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pmid:34080795
Cyclin-dependent kinase 1 shows to be a potential genetic target for chemical cystitis.
Kun Wang · Huaping Du · Qianfeng Zhuang · Hao Lu · Renfang Xu · Dong Xue
Immunity, inflammation and disease · 2021 doi:10.1002/iid3.454
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Experiment
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Complete file
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The differentially expressed genes (DEGs) were identified by using GEO2R. The DAVID 6.8 Beta and R software were used to perform Kyoto Encyclopedia of Genes and Genomes pathway analysis and Gene Ontology function analysis of DEGs. The protein-protein interaction network was constructed by STRING 11.0 to reveal the potential gene interactions. The expression of cyclin-dependent kinase 1 (Cdk1) at the messnger RNA (mRNA) and protein levels was examined by real-time polymerase chain reaction (PCR) and Western blot analysis analysis, respectively.\nRESULTS: The GEO database was searched, and the gene expression profiles of GSE55986 and GSE68539 were downloaded. A total of 262 DEGs and 356 DEGs were identified from GSE55986 and GSE68539, respectively. We found that the p53 signaling pathway might play a key role in the development of chemical cystitis, and Cdk1 acted as a crucial gene in the p53 signaling pathway. Moreover, the experimental results of real-time PCR and Western blot analysis analysis demonstrated that the expression of Cdk1 at the mRNA and protein levels in cystitis tissues was significantly increased in different animal models of chemical cystitis compared with the control group.\nCONCLUSION: Cdk1 might be a potential pathogenic genetic target for chemical cystitis.", "claims": [{"id": "claim-method", "statement": "Statistical analysis was performed by SPSS 23.0 Statistics software using Student's t test.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:34080795", "locator": "sections[11] \"Statistical analysis\" paragraph 2", "quote": "Statistical analysis was performed by SPSS 23.0 Statistics software using Student's t test."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The series matrix files of GSE55986 and GSE68539 were downloaded from the GEO database. 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RESULTS: Th", "he experimental results of real-time PCR and Western blot analysis analysis demonstrated that the expr", "expression of Cdk1 was validated by qPCR and Western blot analysis analysis. Figure 5A‐D demonstrates", "expression of Cdk1 was verified by qPCR and Western blot analysis analysis. (A) The primer sequences"], "order_basis": "paper_text_order:789", "id": "assay:1"}, {"role": "data_generation", "definition_id": "qpcr", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["thway. Moreover, the experimental results of real-time PCR and Western blot analysis analysis demonstra", "ls. Gene expression of Cdk1 was validated by qPCR and Western blot analysis analysis. Figure 5", "roup. The expression of Cdk1 was verified by qPCR and Western blot analysis analysis. (A) The", "on of Cdk1 at the mRNA level was examined by qPCR analysis in three models. (C, D) The express"], "order_basis": "paper_text_order:1245", "id": "assay:2"}, {"role": "data_generation", "definition_id": "animal_model", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["y, 24 ± 1°C and a 12‐h light/dark cycle. The mice were given free access to tap water and food. All", "idelines. In the ketamine‐induced model, the mice were administered with 30 mg/kg/day ketamine (Sig", "normal saline. In the CYP‐induced model, the mice were administered with 300 mg/kg/day CYP (Thermo", "normal saline. 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