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pmid:37565919

Investigation of target genes and potential mechanisms related to compound Xiao-ai-fei honey ointment based on network pharmacology and bioinformatics analysis.

Kayisaier Abudurousuli · Ziruo Talihati · Sendaer Hailati · Meng Yuan Han · Muhadaisi Nuer · Nawaz Khan · Nulibiya Maihemuti · Dilihuma Dilimulati · Nuerbiye Nueraihemaiti · Jimilihan Simayi · Wenting Zhou

Medicine · 2023 doi:10.1097/MD.0000000000034629

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Investigation of target genes and potential mechanisms related to compound Xiao-ai-fei honey ointment based on network pharmacology and bioinformatics analysis.
doi
10.1097/MD.0000000000034629
pmid
37565919
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[0]
Kayisaier Abudurousuli
[1]
Ziruo Talihati
[2]
Sendaer Hailati
[3]
Meng Yuan Han
[4]
Muhadaisi Nuer
[5]
Nawaz Khan
[6]
Nulibiya Maihemuti
[7]
Dilihuma Dilimulati
[8]
Nuerbiye Nueraihemaiti
[9]
Jimilihan Simayi
[10]
Wenting Zhou
journal
Medicine
year
2023
abstract
BACKGROUND: Compound Xiao-ai-fei honey ointment (CXHO) is an anticancer preparation with a long history in Uyghur folk medicine in China and has been used for the treatment of gastric cancer (GC) in Xinjiang, China. Nevertheless, the mechanism of its anticancer effect remains to be investigated. METHODS: Bioactive ingredients of CXHO were retrieved from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform database. Target genes of ingredients were acquired via the PubChem and Swiss target prediction database. Gene expression profiling of GC was obtained from GSE54129 in the GEO database and analyzed using the limma package in R. The hub genes associated with CXHO in GC were validated using the TIMER2.0 database, GEPIA2 database and Auto Dock tools. The effect of CXHO on migration of GC cells was detected by Transwell chamber assay and Wound healing assay. The effect of CXHO on expression levels of MMP2/MMP9 and NF-κb, PI3K/AKT signaling pathway was detected by Western blot assay. RESULTS: Forty-five bioactive ingredients and their 819 related genes were found. A total of 462 differentially expressed genes were identified between GC patients and healthy controls. Seventeen common target genes were identified as hub genes CXHO against GC. Among them, MMP2 and MMP9 were significantly associated with tumor immune infiltrates and had good binding affinity with effective ingredients. Moreover, we validated the mRNA and protein expression levels and prognostic value of MMP2 and MMP9 by different databases. In addition, Kyoto encyclopedia of genes and genomes and gene ontology analyses showed that the 17 common target genes were mainly involved in steroid hormone biosynthesis and cancer-related pathways. Experimental results showed that CXHO inhibited migration of GC cells and down regulated the expression levels of MMP2/MMP9, NF-κb. In addition, CXHO can inhibited PI3K/AKT signaling pathway. CONCLUSION: We identified and experimental validated 2 pivotal target genes of CXHO against GC and preliminarily analyzed the potential mechanisms by which CXHO inhibits the development of GC. All these findings support CXHO as a promising drug for the treatment of GC.
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Differentially expressed genes (DEGs) between GC tissue and normal control tissue were analyzed using the limma package in R.
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A total of 462 differentially expressed genes were identified between GC patients and healthy controls.
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sections[21] "3.3. Identification of differentially expressed genes between GC and control tissue" paragraph 2
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To identify candidate pivotal genes related to the progression of GC, we performed differential expression analysis between GC and control samples and obtained 462 DEGs, including 227 upregulated genes and 235 downregulated genes (P < .05 and |log2 FC| > 2; Fig. 3A).
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, PI3K/AKT signaling pathway was detected by Western blot assay. RESULTS: Forty-five bioactive ingredi
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37565919", "kind": "science-record", "revision": 4, "content_hash": "sha256:fad1a5ad29207e6c2e957975668752bc7abb7767e85165ca9b27d712601e2722", "created_at": "2026-11-01T19:02:21Z", "updated_at": "2026-11-01T22:52:29Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Investigation of target genes and potential mechanisms related to compound Xiao-ai-fei honey ointment based on network pharmacology and bioinformatics analysis.", "doi": "10.1097/MD.0000000000034629", "pmid": "37565919", "authors": ["Kayisaier Abudurousuli", "Ziruo Talihati", "Sendaer Hailati", "Meng Yuan Han", "Muhadaisi Nuer", "Nawaz Khan", "Nulibiya Maihemuti", "Dilihuma Dilimulati", "Nuerbiye Nueraihemaiti", "Jimilihan Simayi", "Wenting Zhou"], "journal": "Medicine", "year": 2023, "abstract": "BACKGROUND: Compound Xiao-ai-fei honey ointment (CXHO) is an anticancer preparation with a long history in Uyghur folk medicine in China and has been used for the treatment of gastric cancer (GC) in Xinjiang, China. Nevertheless, the mechanism of its anticancer effect remains to be investigated.\nMETHODS: Bioactive ingredients of CXHO were retrieved from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform database. Target genes of ingredients were acquired via the PubChem and Swiss target prediction database. Gene expression profiling of GC was obtained from GSE54129 in the GEO database and analyzed using the limma package in R. The hub genes associated with CXHO in GC were validated using the TIMER2.0 database, GEPIA2 database and Auto Dock tools. The effect of CXHO on migration of GC cells was detected by Transwell chamber assay and Wound healing assay. The effect of CXHO on expression levels of MMP2/MMP9 and NF-κb, PI3K/AKT signaling pathway was detected by Western blot assay.\nRESULTS: Forty-five bioactive ingredients and their 819 related genes were found. A total of 462 differentially expressed genes were identified between GC patients and healthy controls. Seventeen common target genes were identified as hub genes CXHO against GC. Among them, MMP2 and MMP9 were significantly associated with tumor immune infiltrates and had good binding affinity with effective ingredients. Moreover, we validated the mRNA and protein expression levels and prognostic value of MMP2 and MMP9 by different databases. In addition, Kyoto encyclopedia of genes and genomes and gene ontology analyses showed that the 17 common target genes were mainly involved in steroid hormone biosynthesis and cancer-related pathways. Experimental results showed that CXHO inhibited migration of GC cells and down regulated the expression levels of MMP2/MMP9, NF-κb. In addition, CXHO can inhibited PI3K/AKT signaling pathway.\nCONCLUSION: We identified and experimental validated 2 pivotal target genes of CXHO against GC and preliminarily analyzed the potential mechanisms by which CXHO inhibits the development of GC. All these findings support CXHO as a promising drug for the treatment of GC.", "claims": [{"id": "claim-method", "statement": "Differentially expressed genes (DEGs) between GC tissue and normal control tissue were analyzed using the limma package in R.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37565919", "locator": "sections[7] \"2.5. Identification of differentially expressed genes\" paragraph 2", "quote": "Differentially expressed genes (DEGs) between GC tissue and normal control tissue were analyzed using the limma package in R."}], "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:37565919", "locator": "sections[35] \"(untitled)\" paragraph 1", "quote": "The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "A total of 462 differentially expressed genes were identified between GC patients and healthy controls.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37565919", "locator": "sections[21] \"3.3. Identification of differentially expressed genes between GC and control tissue\" paragraph 2", "quote": "To identify candidate pivotal genes related to the progression of GC, we performed differential expression analysis between GC and control samples and obtained 462 DEGs, including 227 upregulated genes and 235 downregulated genes (P < .05 and |log2 FC| > 2; Fig. 3A)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "A total of 462 differentially expressed genes were identified between GC patients and healthy controls.", "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:37565919"], "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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