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Cartilage-protective effects of lopinavir/ritonavir: in vitro and in silico exploration of the HIF-1α/SOX9/IL-1β pathway
by
Pehlivanoglu, Suray
, Sirin, Duygu Yasar
, Yilmaz, Ibrahim
, Yilmaz, Omer Faruk
, Albayrak, Mehmet
, Akyuz, Aslı
, Ozbek, Hanefi
in
Chondrocyte
/ HIF-1α
/ Il-1β
/ Lopinavir/ritonavir
/ Medicine
/ Medicine & Public Health
/ Orthopedics
/ SOX9
/ Surgical Orthopedics
2025
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Cartilage-protective effects of lopinavir/ritonavir: in vitro and in silico exploration of the HIF-1α/SOX9/IL-1β pathway
by
Pehlivanoglu, Suray
, Sirin, Duygu Yasar
, Yilmaz, Ibrahim
, Yilmaz, Omer Faruk
, Albayrak, Mehmet
, Akyuz, Aslı
, Ozbek, Hanefi
in
Chondrocyte
/ HIF-1α
/ Il-1β
/ Lopinavir/ritonavir
/ Medicine
/ Medicine & Public Health
/ Orthopedics
/ SOX9
/ Surgical Orthopedics
2025
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Do you wish to request the book?
Cartilage-protective effects of lopinavir/ritonavir: in vitro and in silico exploration of the HIF-1α/SOX9/IL-1β pathway
by
Pehlivanoglu, Suray
, Sirin, Duygu Yasar
, Yilmaz, Ibrahim
, Yilmaz, Omer Faruk
, Albayrak, Mehmet
, Akyuz, Aslı
, Ozbek, Hanefi
in
Chondrocyte
/ HIF-1α
/ Il-1β
/ Lopinavir/ritonavir
/ Medicine
/ Medicine & Public Health
/ Orthopedics
/ SOX9
/ Surgical Orthopedics
2025
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Cartilage-protective effects of lopinavir/ritonavir: in vitro and in silico exploration of the HIF-1α/SOX9/IL-1β pathway
Journal Article
Cartilage-protective effects of lopinavir/ritonavir: in vitro and in silico exploration of the HIF-1α/SOX9/IL-1β pathway
2025
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Overview
Background
This study aimed to investigate the effects of Lopinavir/Ritonavir (Lop/r) on chondrocyte structure and extracellular matrix (ECM) integrity, as well as its impact on key proteins involved in anabolic and catabolic pathways, using both in vitro and in silico approaches.
Methods
Drug-target interaction networks were constructed through bioinformatics analyses, and molecular docking was performed. Human primary chondrocytes were treated with Lop/r, and untreated cells served as controls. Cell viability, proliferation, and protein expression levels were assessed using standard in vitro techniques, including spectrophotometric assays and Western blotting.
Results
Molecular docking analyses revealed strong binding affinities between Lop/r and osteoarthritis-related targets such as HIF-1α, EP300, TNF, IL-6, KCNA5, and IL-1β, suggesting modulation of hypoxia, inflammatory, and epigenetic pathways. In vitro, Lop/r did not alter chondrocyte morphology or ECM structure and was not cytotoxic (
p
< 0.05). However, it significantly reduced the expression of critical proteins including HIF-1α, SOX9, and IL-1β (
p
< 0.05).
Conclusion
These findings suggest that Lop/r may exert regulatory effects on cartilage-related molecular pathways and holds promise as a repurposed therapeutic agent for osteoarthritis. Further studies are warranted to confirm its potential in clinical applications.
Publisher
BioMed Central,BMC
Subject
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