International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(24), P. 13706 - 13706
Published: Dec. 22, 2024
Single-cell
sequencing
technology
provides
apparent
advantages
in
cell
population
heterogeneity,
allowing
individuals
to
better
comprehend
tissues
and
organs.
Sequencing
is
currently
moving
beyond
the
standard
transcriptome
single-cell
level,
which
likely
bring
new
insights
into
function
of
breast
cells.
In
this
study,
we
examine
primary
types
involved
development,
as
well
achievements
study
scRNA-seq
microenvironment,
stressing
finding
novel
subsets
using
approaches
analyzing
problems
solutions
scRNA-seq.
Furthermore,
are
excited
about
field’s
promising
future.
Journal of Hematology & Oncology,
Journal Year:
2024,
Volume and Issue:
17(1)
Published: Aug. 24, 2024
The
emergence
of
spatial
multi-omics
has
helped
address
the
limitations
single-cell
sequencing,
which
often
leads
to
loss
context
among
cell
populations.
Integrated
analysis
genome,
transcriptome,
proteome,
metabolome,
and
epigenome
enhanced
our
understanding
biology
molecular
basis
human
diseases.
Moreover,
this
approach
offers
profound
insights
into
interactions
between
intracellular
intercellular
mechanisms
involved
in
development,
physiology,
pathogenesis
In
comprehensive
review,
we
examine
current
advancements
technologies,
focusing
on
their
evolution
refinement
over
past
decade,
including
improvements
throughput
resolution,
modality
integration,
accuracy.
We
also
discuss
pivotal
contributions
revealing
heterogeneity,
constructing
detailed
atlases,
deciphering
crosstalk
tumor
immunology,
advancing
translational
research
cancer
therapy
through
precise
mapping.
Allergy,
Journal Year:
2024,
Volume and Issue:
79(10), P. 2662 - 2679
Published: Oct. 1, 2024
Abstract
Interleukin
(IL)‐5
is
the
key
cytokine
in
maturation,
activation,
proliferation,
migration
and
survival
of
eosinophils,
which
are
effector
cells
many
upper
lower
airway
diseases.
Through
its
effects
on
IL‐5
indirectly
contributes
to
various
pathophysiological
processes
including
tissue
damage,
repair
remodelling.
Understanding
importance
eosinophil‐associated
diseases
led
development
anti‐IL‐5
therapies,
provide
clinical
benefits
across
a
range
conditions.
However,
recent
evidence
suggests
that
eosinophil‐depletion
alone
may
not
account
for
all
therapeutic
therapy
also
contribute
disease
independently
eosinophils.
Indeed,
from
ex
vivo
studies
targeted
demonstrates
inhibition
affects
much
broader
beyond
epithelial
cells,
plasma
mast
basophils,
neutrophils,
type
2
innate
lymphoid
T
regulatory
fibroblasts.
This
review
will
an
update
supporting
breadth
biology
relevant
pathogenesis
inflammation,
where
there
need
additional
insight,
implications
more
central
role
inflammation.
Journal of Translational Medicine,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: Jan. 13, 2025
Diabetic
retinopathy
is
a
major
ocular
complication
of
diabetes,
characterized
by
progressive
retinal
microvascular
damage
and
significant
visual
impairment
in
working-age
adults.
Traditional
bulk
RNA
sequencing
offers
overall
gene
expression
profiles
but
does
not
account
for
cellular
heterogeneity.
Single-cell
overcomes
this
limitation
providing
transcriptomic
data
at
the
individual
cell
level
distinguishing
novel
subtypes,
developmental
trajectories,
intercellular
communications.
Researchers
can
use
single-cell
to
draw
atlases
identify
features
cells,
enhancing
our
understanding
pathogenesis
pathological
changes
diabetic
retinopathy.
Additionally,
widely
employed
analyze
organoids
single
extracellular
vesicles.
multi-omics
integrates
omics
information,
whereas
stereo-sequencing
analyzes
spatiotemporal
simultaneously.
This
review
discusses
protocols
obtaining
cells
from
retina
accurate
data.
It
highlights
applications
advancements
study
normal
retinas
associated
with
underscores
potential
these
technologies
deepen
that
may
lead
introduction
new
therapeutic
strategies.
Journal of Inflammation Research,
Journal Year:
2025,
Volume and Issue:
Volume 18, P. 549 - 563
Published: Jan. 1, 2025
Autophagy
and
immunity
play
important
regulatory
roles
in
lung
developmental
disorders.
However,
there
is
currently
a
lack
of
bioinformatics
analysis
on
autophagy-related
genes
(ARGs)
immune
infiltration
bronchopulmonary
dysplasia
(BPD).
We
aim
to
screen
validate
the
signature
BPD
by
vivo
experiment.
GSE8586
was
obtained
from
Gene
Expression
Omnibus
(GEO)
database.
The
differentially
expressed
(DEGs)
were
identified
using
R
program.
Using
cell-type
identification
with
CIBERSORT
analyze
inflammatory
status
BPD.
Subsequently,
hub
Lasso
Cytoscape
three
machine-learning
algorithms
(MCC,
Degree
MCODE).
In
addition,
validated
ROC,
single-cell
sequence
IHC
hyperoxia
rats.
Finally,
we
searched
drug
targets
these
genes,
established
nomogram
model
for
predicting
risk
There
73
(DE-ARGs)
overlapping
DEGs
ARGs.
Five
BRIX1,
JUN,
PES1,
NR4A1
RRP9,
lowly
group
had
high
diagnostic
value
model.
All
are
mainly
located
B
cell,
epithelial
fibroblast,
endothelial
smooth
muscle
cell
pneumocyte
sequencing.
Moreover,
showed
cells
higher
closely
associated
genes.
also
predict
result
rats
that
expression
BRX1,
lower
compared
normoxia
group.
NR4A1,
may
be
promising
therapeutic
Our
findings
provided
researchers
clinicians
more
evidence
regarding
immunotherapeutic
strategies
treatment.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 28, 2025
Abstract
Bladder
cancer
(BC)
is
a
malignancy
that
originates
from
the
cells
lining
bladder
and
one
of
most
common
cancers
urinary
system,
capable
occurring
in
any
part
bladder.
However,
molecular
mechanisms
underlying
malignant
transformation
BC
have
not
been
systematically
studied.
This
study
integrated
cutting-edge
techniques
spatial
transcriptomics
(ST)
metabolomics
(SM)
to
capture
transcriptomic
metabolomic
landscapes
both
adjacent
normal
tissues.
ST
results
revealed
significant
upregulation
genes
associated
with
choline
metabolism
glucose
metabolism,
while
related
sphingolipid
tryptophan
were
significantly
downregulated.
Additionally,
metabolic
reprogramming
was
observed
tissues,
including
as
well
downregulation
metabolism.
These
alterations
may
play
crucial
role
promoting
tumorigenesis
immune
evasion
BC.
The
interpretation
SM
data
this
offers
new
insights
into
progression
provides
valuable
clues
for
prevention
treatment
Burns & Trauma,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 17, 2025
Diabetic
foot
ulcer
(DFU)
is
one
of
the
most
common
and
complex
complications
diabetes,
but
underlying
pathophysiology
remains
unclear.
Single-cell
RNA
sequencing
(scRNA-seq)
has
been
conducted
to
explore
novel
cell
types
or
molecular
profiles
DFU
from
various
perspectives.
This
study
aimed
comprehensively
analyze
potential
mechanisms
impaired
re-epithelization
in
a
single-cell
perspective.
We
scRNA-seq
on
tissues
human
normal
skin,
acute
wound,
investigate
epidermal
differentiation
pathological
microenvironment.
Pseudo-time
lineage
inference
analyses
revealed
distinct
states
transition
trajectories
cells
under
different
conditions.
Transcription
factor
analysis
regulatory
mechanism
key
subtypes
keratinocytes.
Cell-cell
interaction
network
between
proinflammatory
microenvironment
cells.
Laser-capture
microscopy
coupled
with
(LCM-seq)
multiplex
immunohistochemistry
were
used
validate
expression
location
Our
research
provided
comprehensive
map
phenotypic
dynamic
changes
that
occur
during
differentiation,
alongside
corresponding
networks
DFU.
Importantly,
we
identified
two
keratinocytes:
basal
(BC-2)
diabetes-associated
keratinocytes
(DAK)
might
play
crucial
roles
impairment
homeostasis.
BC-2
DAK
showed
marked
increase
DFU,
an
inactive
state
insufficient
motivation
for
differentiation.
was
involved
cellular
response
apoptosis
processes,
high
TXNIP,
IFITM1,
IL1R2.
Additionally,
pro-differentiation
transcription
factors
downregulated
indicating
process
be
inhibited
associated
glucose
Furthermore,
increased
CCL2
+
CXCL2+
fibroblasts,
VWA1+
vascular
endothelial
cells,
GZMA+CD8+
T
detected
These
wound
could
regulate
fate
through
TNFSF12-TNFRSF12A,
IFNG-IFNGR1/2,
IL-1B-IL1R2
pathways,
which
result
persistent
inflammation
findings
offer
insights
into
present
therapeutic
targets
improve
care
treatment
outcomes
patients.
Inflammation and Regeneration,
Journal Year:
2025,
Volume and Issue:
45(1)
Published: Feb. 20, 2025
Spatial
transcriptomics
is
a
cutting-edge
technology
that
analyzes
gene
expression
at
the
cellular
level
within
tissues
while
integrating
spatial
location
information.
This
concept,
which
combines
high-plex
RNA
sequencing
with
data,
emerged
in
early
2010s.
has
rapidly
expanded
development
of
technologies
such
as
situ
hybridization,
sequencing,
barcoding,
and
microdissection-based
methods.
Each
technique
offers
advanced
mapping
resolution
precise
assessments
single-cell
level.
Over
past
decade,
use
on
clinical
samples
enabled
researchers
to
identify
expressions
specific
diseased
foci,
significantly
enhancing
our
understanding
interactions
disease
processes.
In
field
rheumatology,
complex
elusive
pathophysiology
diseases
rheumatoid
arthritis,
systemic
lupus
erythematosus,
Sjögren's
syndrome
remains
challenge
for
personalized
treatment.
provides
insights
into
how
different
cell
populations
interact
synovial
tissue,
kidneys,
salivary
glands.
review
summarizes
current
autoimmune
rheumatic
diseases,
focusing
immune
distribution
tissues.
We
also
explore
potential
from
perspective
discuss
possibilities
translating
this
bedside.
Exploration of Immunology,
Journal Year:
2025,
Volume and Issue:
5
Published: April 8, 2025
Neoantigen
vaccines
are
a
promising
strategy
in
cancer
immunotherapy
that
leverage
tumor-specific
mutations
to
elicit
targeted
immune
responses.
Although
they
have
considerable
potential,
development
challenges
related
antigen
prediction
accuracy,
manufacturing
complexity,
and
scalability
remain
key
obstacles
their
widespread
clinical
use.
This
literature
review
was
conducted
using
PubMed,
Scopus,
Web
of
Science,
Google
Scholar
databases
identify
relevant
studies.
Keywords
included
“neoantigen
vaccines,”
“personalized
immunotherapy,”
“tumor
heterogeneity,”
“bioinformatics
pipelines,”
“prediction
algorithms”.
Clinical
trial
data
were
sourced
from
ClinicalTrials.gov,
Trialtrove,
other
publicly
available
registries.
Eligible
studies
peer-reviewed
research
articles,
systematic
reviews,
trials
focusing
on
neoantigen
vaccine
development,
bioinformatic
strategies,
immunotherapy.
Tumor
heterogeneity
clonal
evolution
significantly
impact
efficacy,
necessitating
multi-epitope
targeting
adaptive
design.
Current
algorithms
suffer
high
false-positive
false-negative
rates,
requiring
further
integration
with
multi-omics
machine
learning
enhance
accuracy.
Manufacturing
remains
complex,
time-intensive,
costly,
advancements
standardization
automation.
Combination
therapies,
such
as
checkpoint
inhibitors
adoptive
cell
counteract
the
immunosuppressive
tumor
microenvironment,
improving
treatment
outcomes.
hold
great
potential
for
personalized
therapy
but
require
bioinformatics,
scalability,
immunomodulatory
strategies
efficacy.
Continued
interdisciplinary
collaboration
essential
refining
applications.