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Updated: Nov 6, 2025

Tissue Collection and RNA Extraction from the Human Osteoarthritic Knee Joint
Published on: July 22, 2021
Text Mining-Based Drug Discovery in Osteoarthritis
Rong-Guo Yu1, Jia-Yu Zhang2, Zhen-Tao Liu3
1Department of Orthopedics, Fuzhou Second Hospital Affiliated to Xiamen University, Fuzhou 350007, Fujian, China.
Background:
Osteoarthritis (OA) is a chronic and degenerative joint disease, which causes stiffness, pain, and decreased function. At the early stage of OA, nonsteroidal anti-inflammatory drugs (NSAIDs) are considered the first-line treatment. However, the efficacy and utility of available drug therapies are limited. We aim to use bioinformatics to identify potential genes and drugs associated with OA.
Methods:
The genes related to OA and NSAIDs therapy were determined by text mining. Then, the common genes were performed for GO, KEGG pathway analysis, and protein-protein interaction (PPI) network analysis. Using the MCODE plugin-obtained hub genes, the expression levels of hub genes were verified using quantitative real-time polymerase chain reaction (qRT-PCR). The confirmed genes were queried in the Drug Gene Interaction Database to determine potential genes and drugs.
Results:
The qRT-PCR result showed that the expression level of 15 genes was significantly increased in OA samples. Finally, eight potential genes were targetable to a total of 53 drugs, twenty-one of which have been employed to treat OA and 32 drugs have not yet been used in OA.
Conclusions:
The 15 genes (including PTGS2, NLRP3, MMP9, IL1RN, CCL2, TNF, IL10, CD40, IL6, NGF, TP53, RELA, BCL2L1, VEGFA, and NOTCH1) and 32 drugs, which have not been used in OA but approved by the FDA for other diseases, could be potential genes and drugs, respectively, to improve OA treatment. Additionally, those methods provided tremendous opportunities to facilitate drug repositioning efforts and study novel target pharmacology in the pharmaceutical industry.
Insights
Bioinformatics identified 15 key genes and 32 potential drugs for osteoarthritis (OA) treatment. Eight genes are targeted by 53 drugs, offering new avenues for OA therapy and drug repositioning.
Area of Science:
- Bioinformatics and computational biology
- Genomics and molecular biology
- Pharmacology and drug discovery
Background:
- Osteoarthritis (OA) is a chronic joint disease causing pain and stiffness.
- Current treatments, including NSAIDs, have limited efficacy.
- Novel therapeutic targets and drugs are needed for OA management.
Purpose of the Study:
- To identify potential genes and drugs associated with osteoarthritis using bioinformatics.
- To explore new therapeutic strategies for OA through data mining and analysis.
Main Methods:
- Text mining to identify OA and NSAID-related genes.
- Gene ontology (GO), KEGG pathway, and protein-protein interaction (PPI) network analysis.
- Quantitative real-time polymerase chain reaction (qRT-PCR) for gene expression validation.
- Drug Gene Interaction Database query for drug discovery.
Main Results:
- Fifteen genes showed significantly increased expression in OA samples.
- Eight of these genes are targeted by 53 drugs.
- Twenty-one existing OA drugs and 32 novel drugs (FDA-approved for other conditions) were identified.
Conclusions:
- Identified 15 genes and 32 potential drugs for improving OA treatment.
- Highlighted opportunities for drug repositioning and novel target pharmacology in OA.
- The study provides a foundation for developing new therapeutic strategies for osteoarthritis.
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