Exploring a novel risk model based on core disulfidptosis‐related genes in periodontitis: Bioinformatics analyses and experimental validation
Yiqiang Yang,
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Qi Liu,
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Xun Lu
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et al.
The FASEB Journal,
Journal Year:
2025,
Volume and Issue:
39(3)
Published: Feb. 9, 2025
Bacteria
in
dental
plaque
invade
periodontal
tissues,
causing
chronic
inflammation
known
as
periodontitis.
Despite
advancements
understanding
periodontitis,
its
molecular
pathogenesis
remains
incompletely
elucidated.
In
this
study,
a
total
of
247
samples
were
retrieved
from
the
Gene
Expression
Omnibus
(GEO)
database,
comprising
183
individuals
with
periodontitis
and
64
healthy
controls.
Differentially
expressed
DRGs
(DE-DRGs)
identified,
their
expression
correlations
analyzed.
Immune
cell
infiltration
association
DE-DRGs
assessed.
Set
Variation
Analysis
(GSVA)
was
performed
to
determine
key
functions
pathways
related
DE-DRGs.
Characteristic
(CDE-DRGs)
identified
using
Least
Absolute
Shrinkage
Selection
Operator
(LASSO)
analysis,
risk
model
personalized
nomogram
constructed.
Model
performance
validated
through
calibration
decision
curve
analysis
(DCA).
External
experiments,
including
qRT-PCR
Western
blot,
confirmed
differential
Fourteen
identified.
revealed
strong
synergistic
correlation
between
MYH9
ACTB
(coefficient
=
0.86)
an
antagonistic
NCKAP1
FLNA
-0.52).
profiling
showed
significant
differences
proportions
22
immune
types
groups,
14
correlated
levels.
Cluster
distinct
patterns
across
two
clusters.
A
incorporating
four
CDE-DRGs
(DSTN,
SLC7A11,
SLC3A2,
RPN1)
developed,
alongside
for
predicting
risk.
blot
analyses
demonstrated
downregulation
DSTN,
IQGAP1,
CD2AP,
upregulation
RPN1,
FLNA,
MYH9,
TLN1,
ACTB,
MYH10,
CAPZB,
PDLIM1
tissues.
This
study
developed
predictive
nomogram,
detailed
profile
DRGs.
These
findings
provide
insights
into
suggest
potential
strategies
assessment,
early
diagnosis,
targeted
therapy.
Language: Английский
A Novel Disulfidptosis‐Related Diagnostic Gene Signature and Differential Expression Validation in Ischaemic Cardiomyopathy
Xin Tan,
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Shuai Xu,
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Yiyao Zeng
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et al.
Journal of Cellular and Molecular Medicine,
Journal Year:
2025,
Volume and Issue:
29(5)
Published: March 1, 2025
ABSTRACT
Ischaemic
cardiomyopathy
(IC)
predominantly
arises
from
prolonged
deprivation
of
oxygen
in
the
coronary
arteries,
resulting
compromised
cardiac
contractility
or
relaxation.
This
study
investigates
role
disulfidptosis‐associated
genes
(DiGs)
IC.
Through
analysis
datasets
GSE5406
and
GSE57338,
we
explored
association
between
DiGs
immune
characteristics
to
identify
crucial
contributing
IC
development.
The
support
vector
machine
model
emerged
as
most
effective,
identifying
key
such
MYH9,
NUBPL,
MYL6,
MYH10
NCKAP1.
Validation
with
independent
GSE57345,
GSE48166
single‐cell
GSE145154
further
supported
these
findings,
demonstrating
high
predictive
accuracy.
Experimental
validation
an
mouse
model,
using
Western
blot,
immunohistochemistry
RT‐qPCR,
confirmed
altered
expression
core
myocardial
ischaemic
regions.
research
not
only
elucidates
significance
but
also
underscores
diagnostic
potential
identified
genes.
Language: Английский
Role of Inflammatory Mediators in Chronic Obstructive Pulmonary Disease Pathogenesis: Updates and Perspectives
Pankush,
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Khushboo Bharti,
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Rohit Pandey
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et al.
Immuno,
Journal Year:
2025,
Volume and Issue:
5(2), P. 13 - 13
Published: April 15, 2025
Chronic
obstructive
pulmonary
disease
(COPD)
is
a
chronic,
debilitating
condition
that
affects
the
lungs
and
airways.
It
characterized
by
persistent
bronchitis,
exemplified
inflammation
of
bronchial
tubes,
hypersecretion
mucus,
emphysema,
destruction
airway
parenchyma.
The
combination
these
conditions
leads
to
tissue
damage,
fibrosis,
ongoing
inflammatory
response
in
COPD
complex
process
orchestrated
wide
range
immune
cells.
These
include
lung
epithelial
cells,
monocytes,
macrophages,
neutrophils,
eosinophils,
T
B
lymphocytes,
among
others.
cells
work
together
produce
biomarkers
are
involved
pathogenesis
COPD.
Some
key
have
been
identified
variety
cytokines,
C-reactive
protein/serum
albumin
ratio,
fibrinogen,
soluble
receptor
for
advanced
glycation
endproducts,
club/clara
with
molecular
weight
16
kDa,
surfactant
protein
D,
adiponectin,
reactive
oxygen
species,
proteases.
This
review
aims
provide
comprehensive
overview
role
development
progression
will
delve
into
intricacies
COPD,
exploring
various
cell
types
this
process.
By
understanding
underlying
mechanisms
drive
we
can
better
develop
targeted
treatments
help
alleviate
symptoms
Language: Английский
Exploring the diagnostic and immune infiltration roles of disulfidptosis related genes in pulmonary hypertension
Xin Tan,
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Ningning Zhang,
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Ge Zhang
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et al.
Respiratory Research,
Journal Year:
2024,
Volume and Issue:
25(1)
Published: Oct. 9, 2024
Pulmonary
hypertension
(PH)
is
marked
by
elevated
pulmonary
artery
pressures
due
to
various
causes,
impacting
right
heart
function
and
survival.
Disulfidptosis,
a
newly
recognized
cell
death
mechanism,
may
play
role
in
PH,
but
its
associated
genes
(DiGs)
are
not
well
understood
this
context.
This
study
aims
define
the
diagnostic
relevance
of
DiGs
PH.
Language: Английский