Research Square (Research Square),
Год журнала:
2024,
Номер
unknown
Опубликована: Март 15, 2024
Abstract
Background
Diabetic
nephropathy
(DN)
is
a
prominent
etiological
factor
that
contributes
to
the
development
of
end-stage
renal
disease
(ESRD).
PANoptosis
an
inflammatory
programmed
cell
death
pathway,
and
its
involvement
in
pathogenesis
DN
has
been
demonstrated.
The
objective
this
research
was
examine
potential
role
key
PANoptosis-related
genes
occurrence
assess
clinical
utility
these
predicting
DN.
Methods
This
study
employed
bioinformatics
analysis
acquire
dataset
gene
expression
data
for
patients
with
from
Gene
Expression
Omnibus
(GEO)
database.
Furthermore,
we
identified
functionally
annotated
differentially
expressed
(DEGs)
performed
immune
infiltration
analysis.
Consensus
clustering
identify
molecular
subtypes
associated
PANoptosis.
least
absolute
shrinkage
selection
operator
(LASSO)
technique
utilized
screen
crucial
genes,
leading
prediction
model
Additionally,
nomogram
constructed
validate
correlation
between
core
Finally,
Mendelian
randomization
(MR)
conducted
using
genome-wide
association
studies
ascertain
causal
impact
ITM2C
on
Results
A
total
eight
(PROM1,
MAFF,
CLEC2B,
CX3CR1,
CXCL6,
EVI2B,
ITM2C,
VIM)
incidence
were
identified.
Conclusions
We
successfully
utilizing
purpose
novel
holds
as
valuable
instrument
evaluating
imperative
need
timely
medical
intervention
mitigate
onset
EBioMedicine,
Год журнала:
2024,
Номер
100, С. 104949 - 104949
Опубликована: Янв. 9, 2024
Attention-deficit/hyperactivity
disorder
(ADHD)
and
autism
spectrum
(ASD)
are
neurodevelopmental
conditions
with
early
life
origins.
Alterations
in
blood
lipids
have
been
linked
to
ADHD
ASD;
however,
prospective
data
limited.
This
study
examined
(i)
associations
between
the
cord
lipidome
ADHD/ASD
symptoms
at
2
years
of
age,
(ii)
prenatal
perinatal
predictors
lipidome,
(iii)
mediation
by
lipidome.
Symmetry,
Год журнала:
2024,
Номер
16(4), С. 462 - 462
Опубликована: Апрель 10, 2024
Biological
systems,
characterized
by
their
complex
interplay
of
symmetry
and
asymmetry,
operate
through
intricate
networks
interacting
molecules,
weaving
the
elaborate
tapestry
life.
The
exploration
these
networks,
aptly
termed
“molecular
terrain”,
is
pivotal
for
unlocking
mysteries
biological
processes
spearheading
development
innovative
therapeutic
strategies.
This
review
embarks
on
a
comprehensive
survey
analytical
methods
employed
in
network
analysis,
focusing
elucidating
roles
asymmetry
within
networks.
By
highlighting
strengths,
limitations,
potential
applications,
we
delve
into
reconstruction,
topological
analysis
with
an
emphasis
detection,
examination
dynamics,
which
together
reveal
nuanced
balance
between
stable,
symmetrical
configurations
dynamic,
asymmetrical
shifts
that
underpin
functionality.
equips
researchers
multifaceted
toolbox
designed
to
navigate
decipher
networks’
intricate,
balanced
landscape,
thereby
advancing
our
understanding
manipulation
systems.
Through
this
detailed
exploration,
aim
foster
significant
advancements
paving
way
novel
interventions
deeper
comprehension
molecular
underpinnings
Skin Research and Technology,
Год журнала:
2024,
Номер
30(2)
Опубликована: Фев. 1, 2024
Abstract
Background
Mounting
evidence
suggest
that
there
are
an
association
between
psoriasis
and
ulcerative
colitis
(UC),
although
the
common
pathogeneses
not
fully
understood.
Our
study
aimed
to
find
potential
crucial
genes
in
UC
through
machine
learning
integrated
bioinformatics.
Methods
The
overlapping
differentially
expressed
(DEGs)
of
datasets
GSE13355
GSE87466
were
identified.
Then
functional
enrichment
analysis
was
performed.
LASSO,
SVM‐RFE
key
module
WGCNA
considered
as
genes.
receiver
operator
characteristic
(ROC)
curve
used
estimate
their
diagnostic
confidence.
CIBERSORT
conducted
evaluate
immune
cell
infiltration.
Finally,
GSE30999
GSE107499
retrieved
validate.
Results
112
DEGs
identified
revealed
they
closely
related
inflammatory
response.
Eight
genes,
including
S100A9,
PI3,
KYNU,
WNT5A,
SERPINB3,
CHI3L2,
ARNTL2,
SLAMF7,
ultimately
ROC
curves
showed
all
had
high
confidence
test
validation
datasets.
indicated
a
correlation
infiltrating
cells
Conclusion
In
our
study,
we
focused
on
comprehensive
understanding
UC.
identification
eight
may
contribute
only
mechanism,
but
also
identifying
occult
patients,
even
serving
therapeutic
targets
future.
ABSTRACT
Limosilactobacillus
reuteri
,
a
probiotic
microbe
instrumental
to
human
health
and
sustainable
food
production,
adapts
diverse
environmental
shifts
via
dynamic
gene
expression.
We
applied
the
independent
component
analysis
(ICA)
117
RNA-seq
data
sets
decode
its
transcriptional
regulatory
network
(TRN),
identifying
35
distinct
signals
that
modulate
specific
sets.
Our
findings
indicate
ICA
provides
qualitative
advancement
captures
nuanced
relationships
within
clusters
other
methods
may
miss.
This
study
uncovers
fundamental
properties
of
L.
’s
TRN
deepens
our
understanding
arginine
metabolism
co-regulation
riboflavin
fatty
acid
conversion.
It
also
sheds
light
on
conditions
regulate
genes
biosynthetic
cluster
allows
for
speculation
potential
role
isoprenoid
biosynthesis
in
adaptive
response
changes.
By
integrating
transcriptomics
machine
learning,
we
provide
system-level
mechanism
fluctuations,
thus
setting
stage
modeling
transcriptome
applications
microbial
production.
IMPORTANCE
have
studied
beneficial
plays
significant
production
foods,
type
foods
are
nutritionally
dense
healthier
low-carbon
emissions
compared
traditional
foods.
Similar
how
humans
adapt
their
lifestyles
different
environments,
this
adjusts
behavior
by
modulating
expression
genes.
learning
analyze
large-scale
these
behave
across
conditions.
From
this,
identified
unique
patterns
demonstrating
based
50
(such
as
various
sugars,
salts,
cocultures,
milk,
fruit
juice).
research
helps
us
understand
better
functions,
especially
processes
like
breaking
down
certain
nutrients
adapting
stressful
More
importantly,
with
findings,
become
closer
using
knowledge
improve
produce
more
help
microbes.
Frontiers in Genetics,
Год журнала:
2025,
Номер
16
Опубликована: Апрель 4, 2025
Background
With
the
rapid
advancement
of
gene
sequencing
technologies,
Traditional
weighted
co-expression
network
analysis
(WGCNA),
which
relies
on
pairwise
relationships,
struggles
to
capture
higher-order
interactions
and
exhibits
low
computational
efficiency
when
handling
large,
complex
datasets.
Methods
To
overcome
these
challenges,
we
propose
a
novel
Weighted
Gene
Co-expression
Hypernetwork
Analysis
(WGCHNA)
based
hypergraph,
where
genes
are
modeled
as
nodes
samples
hyperedges.
By
calculating
hypergraph
Laplacian
matrix,
WGCHNA
generates
topological
overlap
matrix
for
module
identification
through
hierarchical
clustering.
Results
four
expression
datasets
show
that
outperforms
WGCNA
in
functional
enrichment.
identifies
biologically
relevant
modules
with
greater
complexity,
particularly
processes
like
neuronal
energy
metabolism
linked
Alzheimer’s
disease.
Additionally,
enrichment
uncovers
more
comprehensive
pathway
hierarchies,
revealing
potential
regulatory
relationships
targets.
Conclusion
effectively
addresses
WGCNA’s
limitations,
providing
superior
accuracy
detecting
deeper
insights
disease
research,
making
it
powerful
tool
analyzing
biological
systems.
Frontiers in Genetics,
Год журнала:
2024,
Номер
15
Опубликована: Июнь 14, 2024
Wool
plays
an
irreplaceable
role
in
the
lives
of
livestock
and
textile
industry.
The
variety
hair
quality
shape
leads
to
diversity
its
functions
applications,
finer
wool
has
a
higher
economic
value.
In
this
study,
10
coarse
fine
ordos
sheep
skin
samples
were
collected
for
RNA-seq,
skin/hair
follicle
RNA-seq
datasets
other
five
animal
breeds
obtained
from
NCBI.
Weighted
gene
co-expression
network
analysis
showed
that
common
genes
clustered
into
eight
modules.
Similar
expression
patterns
rabbits
with
same
types,
different
species
brown
modules
significantly
correlated
breeds.
GO
KEGG
enrichment
analyses
that,
most
module
associated
development.
Hence,
tissues
may
determine
morphology
animal.
differentially
expressed
revealed
32
highly
candidate
fineness
Ordos
sheep.
Among
them,
KAZALD1
(grey
module),
MYOC
(brown
C1QTNF6
FOS
(tan
ITGAM,
MX2,
MX1,
IFI6
have
been
reported
be
involved
regulation
cycle
or
loss.
Additionally,
12
genes,
including
KAZALD1,
MYOC,
C1QTNF6,
FOS,
are
across
various
species.
above
results
suggest
share
similar
molecular
regulatory
basis
fineness.
Finally,
study
provides
theoretical
reference
breeding
as
well
investigation
origin
evolution
hair.
International Journal of Molecular Sciences,
Год журнала:
2025,
Номер
26(7), С. 3230 - 3230
Опубликована: Март 31, 2025
Neutrophil
extracellular
traps
(NETs)
play
a
key
role
in
the
development
of
bronchopulmonary
dysplasia
(BPD),
yet
their
molecular
mechanisms
contributing
to
BPD
remain
unexplored.
Using
GSE32472
dataset,
which
includes
100
blood
samples
from
postnatal
day
28,
we
conducted
comprehensive
bioinformatics
analyses
identify
differentially
expressed
genes
(DEGs)
and
construct
gene
modules.
We
identified
86
DEGs,
were
enriched
immune
inflammatory
pathways,
including
NET
formation.
Weighted
co-expression
network
analysis
(WGCNA)
revealed
module
associated
with
BPD.
By
intersecting
69
NET-related
(NRGs),
149
genes,
12
(DENRGs).
Immune
infiltration
an
increase
neutrophils,
dendritic
cells,
macrophages
patients.
Machine
learning
models
(LASSO,
SVM-RFE,
RF)
5
upregulated
biomarkers—MMP9,
Siglec-5,
DYSF,
MGAM,
S100A12—showing
potential
as
diagnostic
biomarkers
for
Validation
using
nomogram,
ROC
curves,
qRT-PCR
confirmed
accuracy
these
biomarkers.
Clinical
data
showed
that
Siglec-5
was
most
strongly
correlated
severity,
while
DYSF
grade
retinopathy
prematurity
(ROP)
its
laser
treatment.
Clustering
two
distinct
subtypes
different
microenvironment
profiles.
Drug–gene
interaction
inhibitors
targeting
MGAM
MMP9.
In
conclusion,
study
identifies
five
reliable
tools
BPD,
upregulation
association
disease
severity
complications,
such
ROP,
highlighting
clinical
relevance
advancing
diagnostics
Applied Sciences,
Год журнала:
2023,
Номер
13(12), С. 7342 - 7342
Опубликована: Июнь 20, 2023
The
process
of
aging
is
a
complex
phenomenon
that
involves
progressive
decline
in
physiological
functions
required
for
survival
and
fertility.
To
better
understand
the
mechanisms
underlying
this
process,
scientific
community
has
utilized
several
tools.
Among
them,
mitochondrial
DNA
emerged
as
crucial
factor
biological
aging,
given
dysfunction
thought
to
significantly
contribute
phenomenon.
Additionally,
Drosophila
melanogaster
proven
be
valuable
model
organism
studying
due
its
low
cost,
capacity
generate
large
populations,
ease
genetic
manipulation
tissue
dissection.
Moreover,
graph
theory
been
employed
dynamic
changes
gene
expression
patterns
associated
with
investigate
interactions
between
aging-related
diseases.
In
study,
we
have
integrated
these
approaches
examine
co-expression
at
various
stages
development.
By
applying
graph-theory
techniques,
identified
modules
co-expressing
genes,
highlighting
those
contain
high
number
genes.
We
found
important
genes
involved
age-related
diseases
melanogaster,
including
UQCR-C1,
ND-B17.2,
ND-20,
Pdhb.
Our
findings
shed
light
on
role
demonstrate
utility
research.