Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT06331104 |
Other study ID # |
ChangyeZou |
Secondary ID |
|
Status |
Completed |
Phase |
|
First received |
|
Last updated |
|
Start date |
June 14, 2012 |
Est. completion date |
August 31, 2023 |
Study information
Verified date |
March 2024 |
Source |
First Affiliated Hospital, Sun Yat-Sen University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
Based on network pharmacology analysis, this study aims to explore the potential therapeutic
targets and molecular mechanisms of puerarin on giant cell tumor of bone (GCTB) genes.
Description:
The giant cell tumor of bone's pathological genes were discovered from DisGeNET and GeneCards
databases. The therapeutic genes of puerarin were gathered from Swiss Target Prediction,
CTD(Comparative Toxicogenomics Database), PharmMapper, and TCMSP databases (Traditional
Chinese Medicine Systems Pharmacology Database and Analysis Platform). Cytoscape software was
used with the MCODE algorithm to calculate key potential therapeutic targets of puerarin
against GCTB. The bulk RNA-seq datasets (GSE102193) were used to identify differential
expression of potential therapeutic genes. The sc RNA-seq (GSE168664) was utilized to
determine the expression distribution of different cell clusters. Essential targets of
puerarin against GCTB underwent function and pathway enrichment assays to elucidate
biological processes and signaling pathways. Furthermore, the investigators conducted a
comparison to determine if the primary biological processes and pathways following denosumab
treatment exhibit resemblances to the potential mechanisms of puerarin action. Molecular
docking and dynamics simulation were conducted to evaluate interactions between selected
potential therapeutic targets and puerarin. Immunohistochemical (IHC) and immunofluorescence
(IF) staining were performed to identify the expression of crucial markers in human GCTB
tissue. Expression levels of pivotal genes in primary BMSC cells and primary GCTB cells and
their alteration following puerarin treatment in primary GCTB cells were evaluated.The
significance of differences between groups was estimated by the Student t-test or Wilcoxon
test. In all the statistical analyses, data with two-tailed p < 0.05 were considered
statistically significant.