International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(17), P. 9341 - 9341
Published: Aug. 28, 2024
This
study
aimed
to
identify
hub
genes
involved
in
regulatory
T
cell
(Treg)
function
and
migration,
offering
insights
into
potential
therapeutic
targets
for
cancer
immunotherapy.
We
performed
a
comprehensive
bioinformatics
analysis
using
three
gene
expression
microarray
datasets
from
the
GEO
database.
Differentially
expressed
(DEGs)
were
identified
pathway
enrichment
explore
their
functional
roles
pathways.
A
protein-protein
interaction
network
was
constructed
critical
Treg
activity.
further
evaluated
co-expression
of
these
with
immune
checkpoint
proteins
(PD-1,
PD-L1,
CTLA4)
assessed
prognostic
significance.
Through
this
analysis,
we
CCR8
as
key
player
migration
explored
its
synergistic
effects
ICIs.
Our
findings
suggest
that
CCR8-targeted
therapies
could
enhance
immunotherapy
outcomes,
breast
invasive
carcinoma
(BRCA)
emerging
promising
indication
combination
therapy.
highlights
biomarker
target,
contributing
development
targeted
treatment
strategies.
Immunopharmacology and Immunotoxicology,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 9
Published: Feb. 26, 2025
Objective
Chemoresistance
in
gastric
cancer
poses
a
major
challenge
treatment,
necessitating
the
development
of
novel
therapeutic
strategies.
This
study
evaluates
efficacy
ruxolitinib,
JAK1/2
inhibitor,
both
sensitive
and
resistant
cell
lines.
BMC Musculoskeletal Disorders,
Journal Year:
2025,
Volume and Issue:
26(1)
Published: Jan. 17, 2025
The
case
of
Lumbar
spinal
stenosis
(LSS)
combined
with
tophi
due
to
gout
is
rarely
reported.
In
the
course
our
clinic
work,
we
encountered
a
young
male
patient
who
was
diagnosed
history
for
5
years
and
targeted
as
LSS
gouty
tophi,
would
like
share
this
case.
addition,
in
order
further
investigate
deep
mechanism
associated
gout,
obtained
intersecting
genes
two
diseases
based
on
machine
learning
approach
by
obtaining
dataset
GSE113212
related
from
Gene
Expression
Omnibus
(GEO)
database,
human
gene
database.
We
found
that
TGFB1,
PPARG,
SAMRCC1
may
be
important
biomarkers
treating
both
diseases.
From
clinical
perspective,
clinicians
should
vigilant
about
possibility
lumbar
patients
presenting
back
pain,
hyperuricemia,
elevated
inflammatory
markers.
A
surgical
pharmacological
treatment
plan
has
favorable
prognosis.
Investigating
mechanisms
action
core
provide
new
insights
treatment,
ultimately
leading
development
comprehensive
personalized
diagnostic
therapeutic
strategies.
Biomedicines,
Journal Year:
2025,
Volume and Issue:
13(4), P. 840 - 840
Published: April 1, 2025
Background:
The
global
prevalence
of
type
2
diabetes
mellitus
(T2DM)
with
liver
fibrosis
is
rising,
T2DM
identified
as
an
independent
risk
factor
and
key
prognostic
for
fibrosis.
However,
the
underlying
mechanisms
remain
unclear.
Methods:
To
explore
shared
pathogenesis
T2DM,
we
analyzed
gene
expression
profiles
from
GEO
database.
co-differentially
expressed
genes
(co-DEGs)
were
subsequently
through
functional
enrichment,
protein–protein
interaction
(PPI)
network
construction,
transcription
prediction,
drug
prediction.
Machine
learning
algorithms
then
applied
to
identify
genes.
Results:
A
total
175
co-DEGs
identified.
Functional
enrichment
analysis
indicated
their
involvement
in
extracellular
matrix
(ECM)
remodeling,
inflammation,
PI3K/Akt
signaling
pathway.
Through
PPI
four
algorithms,
eight
hub
identified,
including
SPARC,
COL4A2,
THBS1,
LUM,
TIMP3,
COL3A1,
IGFBP7,
FSTL1,
THBS1
being
recognized
a
by
machine
learning.
upregulation
was
observed
both
diseases,
it
closely
related
progression
T2DM.
Transcription
detected
29
regulators
these
Drug
prediction
suggested
that
retinoic
acid
may
serve
potential
therapeutic
agent.
Conclusions:
This
study
provides
novel
insights
into
offer
targets
clinical
intervention.
Cancer Medicine,
Journal Year:
2025,
Volume and Issue:
14(7)
Published: April 1, 2025
ABSTRACT
Background
Type
2
diabetes
mellitus
(T2DM)
constitutes
a
significant
risk
factor
for
breast
cancer
(BC),
with
affected
women
exhibiting
two‐
to
three‐fold
increased
likelihood
of
developing
BC.
Furthermore,
diagnosed
both
BC
and
T2DM
tend
experience
poorer
prognoses
exhibit
greater
resistance
various
treatments
compared
their
non‐diabetic
counterparts.
Consequently,
elucidating
the
comorbidities
associated
is
instrumental
in
enhancing
diagnostic
therapeutic
strategies
Methods
A
series
bioinformatics
methods
including
weighted
gene
co‐expression
network
analysis
(WGCNA),
differentially
expressed
(DEG)
analysis,
machine
learning,
single‐cell
sequencing
were
used
identify
pathogenetic
molecules
Biological
experiments
CCK‐8,
colony
formation,
wound
healing,
transwell
assay,
immunohistochemistry,
immunofluorescence
performed
determine
molecule
effect.
Results
By
conducting
WGCNA
DEG
on
profiles
(GSE25724
GSE20966)
TCGA
cohort
BC,
we
identified
total
27
common
hub
genes
shared
between
These
significantly
enriched
pathways
related
cell
differentiation,
cellular
developmental
processes,
focal
adhesion,
MAPK
signaling
pathway.
Notably,
among
these
genes,
CCNB2
,
XRCC2
CENPI
poor
prognosis
Moreover,
RNA
revealed
that
are
cells
within
tissues.
Additionally,
observed
CCNB2,
XRCC2,
elevated
tissues
provided
by
patients
history
KI67
expression.
Hyperglycemia
treatment
expression
levels
cells,
which
correlated
proliferation
mobility.
Conversely,
knockdown
partially
mitigated
pro‐proliferative
pro‐migratory
effects
induced
hyperglycemia
cells.
Conclusion
Our
findings
suggested
may
serve
as
key
pathogenic
mediators
linking
Targeting
could
potentially
attenuate
adverse
impacts
progression.
Journal of Personalized Medicine,
Journal Year:
2025,
Volume and Issue:
15(5), P. 166 - 166
Published: April 24, 2025
Gastric
cancer
(GC)
remains
one
of
the
leading
causes
cancer-related
mortality
worldwide,
with
most
cases
diagnosed
at
advanced
stages.
Traditional
biomarkers
provide
only
partial
insights
into
GC’s
heterogeneity.
Recent
advances
in
machine
learning
(ML)-driven
multiomics
technologies,
including
genomics,
epigenomics,
transcriptomics,
proteomics,
metabolomics,
pathomics,
and
radiomics,
have
facilitated
a
deeper
understanding
GC
by
integrating
molecular
imaging
data.
In
this
review,
we
summarize
current
landscape
ML-based
integration
for
GC,
highlighting
its
role
precision
diagnosis,
prognosis
prediction,
biomarker
discovery
achieving
personalized
medicine.
BMC Gastroenterology,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: April 29, 2025
Gastric
precancerous
lesions
(GPL)
represent
a
heterogeneous,
multi-stage
process
that
involves
transition
from
benign
to
malignant
state.
To
optimize
prevention
and
intervention
strategies,
accurate
methods
must
clearly
distinguish
between
stages
predict
progression
risks
at
early
stages.
The
metabolomic
profiles
of
188
GPL
tissues
matched
normal
were
characterized
using
ultra-high-performance
liquid
chromatography-tandem
mass
spectrometry.
Both
multivariate
univariate
statistical
analyses
used
identify
features
differentiating
normal,
atrophic,
intestinal
metaplasia
states
in
the
stomach,
followed
by
preliminary
functional
validation.
From
experiments
conducted
on
two
cohorts,
we
established
reliable
clinical
gastric
tissue
map,
which
distinguished
intestinalized
tissues.
We
then
identified
metabolic
biomarkers
differentiated
various
Furthermore,
key
metabolites
validated
vitro
studies.
Relative
acyl
group
glycerophospholipid
abundance
was
higher
when
compared
GPL,
whereas
organic
acids
more
prevalent
than
A
combination
glycerophosphocholine,
tiglylcarnitine,
malate,
sphingosine,
γ-glutamylglutamic
acid
may
serve
as
powerful
GPL.
chromatography
with
tandem
spectrometry
effectively
characterize
samples.
Key
targeted
metabolomics.
This
study
atrophy
mucosa,
uncovering
preliminarily
validating
be
assess
high-risk
populations
diagnose
potentially
advancing
cancer
treatment
efforts.
Circulation Research,
Journal Year:
2025,
Volume and Issue:
136(10), P. 1147 - 1165
Published: May 8, 2025
Angiogenesis,
the
formation
of
new
blood
vessels,
is
a
fundamental
biological
process
with
implications
for
both
physiological
functions
and
pathological
conditions.
While
transcriptional
regulation
angiogenesis,
mediated
by
factors
such
as
HIF-1α
(hypoxia-inducible
factor
1-alpha)
VEGF
(vascular
endothelial
growth
factor),
well-characterized,
translational
this
remains
underexplored.
Bioinformatics
has
emerged
an
indispensable
tool
advancing
our
understanding
regulation,
offering
predictive
models
that
leverage
large
data
sets
to
guide
research
optimize
experimental
approaches.
However,
significant
gap
persists
between
bioinformatics
experts
other
researchers,
limiting
accessibility
utility
these
tools
in
broader
scientific
community.
To
address
divide,
user-friendly
platforms
are
being
developed
democratize
access
analytics
empower
researchers
across
disciplines.
Translational
control,
compared
offers
more
energy-efficient
mechanism
facilitates
rapid
cellular
responses
environmental
changes.
Furthermore,
regulators
themselves
often
subject
emphasizing
interconnected
nature
regulatory
layers.
Investigating
requires
advanced,
accessible
analyze
RNA
structures,
interacting
micro-RNAs,
long
noncoding
RNAs,
RBPs
(RNA-binding
proteins).
Predictive
structure,
human
internal
ribosome
entry
site
Atlas,
RBPSuite
enable
study
motifs
RNA-protein
interactions,
shedding
light
on
critical
mechanisms.
This
review
highlights
transformative
role
using
widely
Web-browser
interface
elucidate
angiogenesis.
The
discussed
extend
beyond
applications
diverse
fields,
including
clinical
care.
By
integrating
insights,
can
streamline
hypothesis
generation,
reduce
costs,
find
novel
regulators.
bridging
knowledge
gap,
aims
worldwide
adopt
their
work,
fostering
innovation
accelerating
discovery.
Biomolecules,
Journal Year:
2024,
Volume and Issue:
14(8), P. 954 - 954
Published: Aug. 6, 2024
Cardiac
mesoderm
enhancer-associated
non-coding
RNA
(CARMN),
an
evolutionarily
conserved
long
(lncRNA),
serves
as
the
host
gene
for
miR143/145
cluster.
It
plays
a
crucial
role
in
cardiovascular
cell
differentiation
and
maintenance
of
vascular
smooth
muscle
(VSMC)
homeostasis,
which
are
vital
normal
physiological
processes.
Specifically,
CARMN
is
associated
with
pathological
progression
diseases
such
atherosclerosis,
abdominal
aortic
aneurysm,
chronic
heart
failure.
Moreover,
it
acts
tumor
suppressor
various
cancers,
including
hepatocellular
carcinoma,
bladder
cancer,
breast
highlighting
its
potential
beneficial
biomarker
therapeutic
target.
This
review
provides
detailed
examination
roles
CARMN,
evolutionary
conservation,
expression
patterns,
regulatory
mechanisms.
also
outlines
significant
implications
diagnosis,
prognosis,
treatment
these
diseases,
underscoring
need
further
translational
research
to
exploit
clinical
potential.