Research Square (Research Square),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Nov. 7, 2023
Abstract
Objective:
This
study
aims
to
identify
feature
genes,
pathways,
and
infiltrating
immune
cells
related
the
metabolic
mechanisms
of
cellular
disulfidptosis
in
osteoarthritis
(OA)
through
bioinformatics
analysis.
Method:
Expression
profiles
from
two
Gene
Omnibus
datasets
(GSE207881
GSE98918)
were
analyzed
OA.
The
included
63
12
OA
patients,
respectively,
alongside
control
subjects.
Differential
expression
analysis
was
performed
after
data
preprocessing
using
‘limma’
package
R.
A
co-expression
network
constructed
weighted
gene
(WGCNA),
modules
highly
correlated
with
identified.
functionality
explored
Set
Enrichment
Analysis
(GSEA)
Variation
(GSVA).
Additionally,
protein–protein
interactions
(PPI)
key
genes
GeneMANIA.
Ontology
(GO)
Kyoto
Encyclopedia
Genes
Genomes
(KEGG)
enrichment
analyses
conducted
on
genes.
Furthermore,
diagnostic
potential
selected
evaluated,
infiltration
performed.
Result:
total
522
differentially
expressed
statistical
significance
GSEA
GSVA
revealed
multiple
significantly
enriched
signaling
such
as
ribosome,
melanogenesis,
leukocyte
transendothelial
migration.
Nine
screened
by
WGCNA,
which
blue
module
(n
=
353)
showed
strongest
positive
correlation
(r
0.78,
p
<
0.05).
Intersection
further
identified
13
hub
Through
PPI
networks
GO
KEGG
analyses,
these
found
be
Notch
pathway,
this
pathway
validated.
area
under
receiver
operating
characteristic
curve
greater
than
0.6,
suggesting
their
biomarkers
for
Immune
cell
that
TUSC3
SOX5
have
a
significant
relationship
type
17
T
helper
(p
0.001).
An
RNA-binding
protein
(RBP)–mRNA
interaction
comprising
68
nodes,
61
RBPs,
7
mRNAs,
271
edges
StarBase
online
database.
Conclusion:
used
techniques
reveal
complex
networks,
unique
interactions,
thereby
providing
insights
into
These
findings
lay
groundwork
future
approaches
diagnosis
therapeutic
intervention.
Bioinformatics Advances,
Journal Year:
2024,
Volume and Issue:
5(1)
Published: Nov. 5, 2024
Abstract
Motivation
Mitochondria
are
essential
for
cellular
metabolism
and
inherently
flexible
to
allow
correct
function
in
a
wide
range
of
tissues.
Consequently,
dysregulated
mitochondrial
affects
different
tissues
ways
leading
challenges
understanding
the
pathology
diseases.
System-level
metabolic
modelling
is
useful
studying
tissue-specific
metabolism,
yet
despite
mouse
being
common
model
organism
research,
no
specific
currently
available.
Results
Building
upon
similarity
between
human
we
present
mitoMammal,
genome-scale
that
contains
gene-product
reaction
rules.
MitoMammal
able
metabolism.
To
demonstrate
this,
using
an
adapted
E-Flux
algorithm,
integrated
proteomic
data
from
mitochondria
isolated
cardiomyocytes
brown
adipocyte
tissue,
as
well
transcriptomic
vitro
differentiated
adipocytes
modelled
context
flux
balance
analysis.
In
all
three
simulations,
mitoMammal
made
mostly
accurate,
some
novel
predictions
relating
energy
adipocytes.
This
demonstrates
its
usefulness
research
cardiac
disease
diabetes
both
contexts.
Availability
implementation
The
Jupyter
Notebook
available
at:
https://gitlab.com/habermann_lab/mitomammal.
Neurology International,
Journal Year:
2024,
Volume and Issue:
16(6), P. 1691 - 1716
Published: Dec. 4, 2024
Cluster
headache
is
a
severe,
poorly
understood
disorder
for
which
there
are
as
yet
virtually
no
rationally
derived
treatments.
Here,
Lee
Kudrow’s
1983
theory,
that
cluster
an
overly
zealous
response
to
hypoxia,
updated
according
current
understandings
of
hypoxia
detection,
signaling,
and
sensitization.
It
shown
the
distinctive
clinical
characteristics
(circadian
timing
attacks
circannual
patterning
bouts,
autonomic
symptoms,
agitation),
risk
factors
(cigarette
smoking;
male
gender),
triggers
(alcohol;
nitroglycerin),
genetic
findings
(GWAS
studies),
anatomical
substrate
(paraventricular
nucleus
hypothalamus,
solitary
tract
nucleus/NTS,
trigeminal
caudalis),
neurochemical
features
(elevated
levels
galectin-3,
nitric
oxide,
tyramine,
tryptamine),
responsiveness
treatments
(verapamil,
lithium,
melatonin,
prednisone,
oxygen,
histamine
desensitization)
can
all
be
in
terms
hypoxic
signaling.
Novel
treatment
directions
hypothesized,
including
repurposing
pharmacological
antagonists
signaling
molecules
(HIF-2;
P2X3)
headache,
breath
training,
physical
exercise,
high-dose
thiamine,
carnosine,
flavonoid
kaempferol.
The
limits
knowledge
described,
program
basic
translational
research
proposed.
Research Square (Research Square),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Nov. 7, 2023
Abstract
Objective:
This
study
aims
to
identify
feature
genes,
pathways,
and
infiltrating
immune
cells
related
the
metabolic
mechanisms
of
cellular
disulfidptosis
in
osteoarthritis
(OA)
through
bioinformatics
analysis.
Method:
Expression
profiles
from
two
Gene
Omnibus
datasets
(GSE207881
GSE98918)
were
analyzed
OA.
The
included
63
12
OA
patients,
respectively,
alongside
control
subjects.
Differential
expression
analysis
was
performed
after
data
preprocessing
using
‘limma’
package
R.
A
co-expression
network
constructed
weighted
gene
(WGCNA),
modules
highly
correlated
with
identified.
functionality
explored
Set
Enrichment
Analysis
(GSEA)
Variation
(GSVA).
Additionally,
protein–protein
interactions
(PPI)
key
genes
GeneMANIA.
Ontology
(GO)
Kyoto
Encyclopedia
Genes
Genomes
(KEGG)
enrichment
analyses
conducted
on
genes.
Furthermore,
diagnostic
potential
selected
evaluated,
infiltration
performed.
Result:
total
522
differentially
expressed
statistical
significance
GSEA
GSVA
revealed
multiple
significantly
enriched
signaling
such
as
ribosome,
melanogenesis,
leukocyte
transendothelial
migration.
Nine
screened
by
WGCNA,
which
blue
module
(n
=
353)
showed
strongest
positive
correlation
(r
0.78,
p
<
0.05).
Intersection
further
identified
13
hub
Through
PPI
networks
GO
KEGG
analyses,
these
found
be
Notch
pathway,
this
pathway
validated.
area
under
receiver
operating
characteristic
curve
greater
than
0.6,
suggesting
their
biomarkers
for
Immune
cell
that
TUSC3
SOX5
have
a
significant
relationship
type
17
T
helper
(p
0.001).
An
RNA-binding
protein
(RBP)–mRNA
interaction
comprising
68
nodes,
61
RBPs,
7
mRNAs,
271
edges
StarBase
online
database.
Conclusion:
used
techniques
reveal
complex
networks,
unique
interactions,
thereby
providing
insights
into
These
findings
lay
groundwork
future
approaches
diagnosis
therapeutic
intervention.