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pmid:37747014

Mechanism of Chinese botanical drug Dizhi pill for myopia: An integrated study based on bioinformatics and network analysis.

Longkun Liu · Yoann Birling · Yan Zhao · Wenxin Ma · Yang Tang · Yuxin Sun · Xuehui Wang · Mingkun Yu · Hongsheng Bi · Jian-Ping Liu · Li Li · Zhaolan Liu

Medicine · 2023 doi:10.1097/MD.0000000000034753

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Mechanism of Chinese botanical drug Dizhi pill for myopia: An integrated study based on bioinformatics and network analysis.
doi
10.1097/MD.0000000000034753
pmid
37747014
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Longkun Liu
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Yoann Birling
[2]
Yan Zhao
[3]
Wenxin Ma
[4]
Yang Tang
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Yuxin Sun
[6]
Xuehui Wang
[7]
Mingkun Yu
[8]
Hongsheng Bi
[9]
Jian-Ping Liu
[10]
Li Li
[11]
Zhaolan Liu
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Medicine
year
2023
abstract
To identify the active constituents, core targets, immunomodulatory functions and potential mechanisms of Dizhi pill (DZP) in the treatment of myopia. The active constituents and drug targets of DZP were searched in the TCMSP, Herb databases and correlational studies. The targets of myopia were searched in the TTD, Genecards, OMIM and Drugbank databases. Gene expression profile data of GSE136701 were downloaded from the GEO database and subjected to WGCNA and DEG analysis to screen for significant modules and targets of myopia. Intersectional targets of myopia and DZP and core targets of myopia were analyzed through the String database. The GO and KEGG enrichment analyses of the interested targets were conducted. Cibersort algorithm was used for immune infiltration analysis to investigate the immunomodulatory functions of DZP on myopia. Autodock was used to dock the important targets and active constituents. Eight targets (STAT3, PIK3CA, PIK3R1, MAPK1, MAPK3, HSP90AA1, MIP, and LGSN) and 5 active constituents (Quercetin, Beta-sitosterol, Diincarvilone A, Ferulic acid methyl ester, and Naringenin) were identified from DZP. In pathways identified by the GO and KEGG enrichment analyses, "ATP metabolic process" and "AGE-RAGE diabetes complication signaling" pathways were closely related to the mechanisms of DZP in the treatment of myopia. Molecular docking showed that both the intersectional targets and core targets of myopia could bind stably and spontaneously with the active constituents of DZP. This study suggested that the mechanisms of DZP in the treatment of myopia were related to active constituents: Quercetin, Beta-sitosterol, Diincarvilone A, Ferulic acid methyl ester and Naringenin, intersectional targets: STAT3, PIK3CA, PIK3R1, MAPK1, MAPK3, and HSP90AA1, core targets of myopia: MIP and LGSN, AGE-RAGE signaling pathway, positive regulation of ATP metabolic process pathway and immunomodulatory functions.
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Complete file
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