Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:2.7.10.1 (
ERK
)
95,504
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Achondroplasia (ACH) is one of the most common skeletal dysplasias with short stature caused by gain-of-function mutations in
FGFR3
encoding the fibroblast growth factor receptor 3. We used the drug repositioning strategy to identify an FDA-approved drug that suppresses abnormally activated
FGFR3
signaling in ACH. We found that meclozine, an anti-histamine drug that has long been used for motion sickness, facilitates chondrocyte proliferation and mitigates loss of extracellular matrix in FGF2-treated rat chondrosarcoma (RCS) cells. Meclozine also ameliorated abnormally suppressed proliferation of human chondrosarcoma (
HCS
-2/8) cells that were infected with lentivirus expressing constitutively active mutants of
FGFR3
-K650E causing thanatophoric dysplasia,
FGFR3
-K650M causing SADDAN, and
FGFR3
-G380R causing ACH. Similarly, meclozine alleviated abnormally suppressed differentiation of ATDC5 chondrogenic cells expressing
FGFR3
-K650E and -G380R in micromass culture. We also confirmed that meclozine alleviates FGF2-mediated longitudinal growth inhibition of embryonic tibia in bone explant culture. Interestingly, meclozine enhanced growth of embryonic tibia in explant culture even in the absence of FGF2 treatment. Analyses of intracellular
FGFR3
signaling disclosed that meclozine downregulates phosphorylation of
ERK
but not of MEK in FGF2-treated RCS cells. Similarly, meclozine enhanced proliferation of RCS cells expressing constitutively active mutants of MEK and RAF but not of
ERK
, which suggests that meclozine downregulates the
FGFR3
signaling by possibly attenuating
ERK
phosphorylation. We used the C-natriuretic peptide (CNP) as a potent inhibitor of the
FGFR3
signaling throughout our experiments, and found that meclozine was as efficient as CNP in attenuating the abnormal
FGFR3
signaling. We propose that meclozine is a potential therapeutic agent for treating ACH and other
FGFR3
-related skeletal dysplasias.
...
PMID:Meclozine facilitates proliferation and differentiation of chondrocytes by attenuating abnormally activated FGFR3 signaling in achondroplasia. 2432 5
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