Cancers,
Journal Year:
2024,
Volume and Issue:
16(17), P. 3100 - 3100
Published: Sept. 6, 2024
Spatial
transcriptomics
(ST)
examines
gene
expression
within
its
spatial
context
on
tissue,
linking
morphology
and
function.
Advances
in
ST
resolution
throughput
have
led
to
an
increase
scientific
interest,
notably
cancer
research.
This
scoping
study
reviews
the
challenges
practical
applications
of
ST,
summarizing
current
methods,
trends,
data
analysis
techniques
for
neoplasm
We
analyzed
41
articles
published
by
end
2023
alongside
public
repositories.
The
findings
indicate
biology
is
important
focus
research,
with
a
rising
number
studies
each
year.
Visium
(10x
Genomics,
Pleasanton,
CA,
USA)
leading
platform,
SCTransform
from
Seurat
R
library
preferred
method
normalization
integration.
Many
incorporate
additional
types
like
single-cell
sequencing
immunohistochemistry.
Common
include
discovering
composition
function
tumor
tissues
their
heterogeneity,
characterizing
microenvironment,
or
identifying
interactions
between
cells,
including
patterns
co-occurrence.
However,
nearly
half
lacked
comprehensive
processing
protocols,
hindering
reproducibility.
By
recommending
greater
transparency
sharing
methods
adapting
caution,
this
review
aims
improve
reproducibility
reliability
future
Journal of Dental Research,
Journal Year:
2024,
Volume and Issue:
103(13), P. 1331 - 1339
Published: Oct. 9, 2024
Spatial
transcriptomics
(ST)
is
a
cutting-edge
methodology
that
enables
the
simultaneous
profiling
of
global
gene
expression
and
spatial
information
within
histological
tissue
sections.
Traditional
transcriptomic
methods
lack
resolution
required
to
sufficiently
examine
complex
interrelationships
between
cellular
regions
in
diseased
healthy
states.
We
review
general
workflows
for
ST,
from
specimen
processing
ST
data
analysis
interpretations
dataset
using
visualizations
cell
deconvolution
approaches.
show
how
recent
studies
used
explore
development
or
pathogenesis
specific
craniofacial
regions,
including
cranium,
palate,
salivary
glands,
tongue,
floor
mouth,
oropharynx,
periodontium.
Analyses
cranial
suture
patency
palatal
fusion
during
identified
patterns
bone
morphogenetic
protein
sutures
osteogenic
differentiation
pathways
addition
discovery
several
genes
expressed
at
critical
locations
development.
glands
patients
with
Sjögren's
disease
revealed
co-localization
autoimmune
antigens
ductal
cells
subpopulation
acinar
was
specifically
depleted
by
dysregulated
response.
head
neck
lesions,
such
as
premalignant
leukoplakia
progressing
established
oral
squamous
carcinomas,
cancers
perineural
invasions,
oropharyngeal
lesions
associated
HPV
infection
spatially
profiled
tumor
microenvironment,
showing
functionally
important
signatures
differentiation,
invasion,
nontumor
dysregulation
patient
biopsies.
also
enabled
localization
periodontal
disease-associated
gingival
tissues,
involved
inflammation,
fibroblast
subtype
mediating
transition
innate
adaptive
immune
responses
periodontitis.
The
increased
use
especially
conjunction
single-cell
analyses,
promises
improve
our
understandings
unprecedented
tissue-level
both
space
time.
Small Methods,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 11, 2025
Advances
in
spatially-resolved
transcriptomics
(SRT)
technologies
have
propelled
the
development
of
new
computational
analysis
methods
to
unlock
biological
insights.
The
lowering
cost
SRT
data
generation
presents
an
unprecedented
opportunity
create
large-scale
spatial
atlases
and
enable
population-level
investigation,
integrating
across
multiple
tissues,
individuals,
species,
or
phenotypes.
Here,
unique
challenges
are
described
integration,
where
analytic
impact
varying
resolutions
is
characterized
explored.
A
succinct
review
spatially-aware
integration
strategies
provided.
Exciting
opportunities
advance
algorithms
amenable
atlas-scale
datasets
along
with
standardized
preprocessing
methods,
leading
improved
sensitivity
reproducibility
future
further
highlighted.
Biomarkers in Medicine,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 16
Published: Feb. 27, 2025
Hematological
malignancies
present
substantial
challenges
in
clinical
practice
due
to
their
heterogeneity
and
complex
biological
profiles.
In
these
diseases,
biomarkers
–
measurable
indicators
of
states
are
indispensable
for
diagnosis,
prognosis,
therapeutic
decision-making.
Emerging
significantly
improving
outcomes
hematological
cancers
by
enhancing
early
detection,
refining
prognostic
assessments,
enabling
personalized
treatment
approaches,
optimizing
overall
patient
management.
This
progress
translates
into
better
more
effective
strategies
treat
manage
malignancies.
The
field
biomarker
discovery
has
developed
from
basic
morphological
cytogenetic
markers
advanced
molecular
techniques,
including
polymerase
chain
reaction
(PCR)
next-generation
sequencing
(NGS),
which
have
enhanced
diagnostic
accuracy
led
the
development
targeted
therapies.
Additionally,
recent
advent
technologies
like
mass
spectrometry
single-cell
RNA
enables
comprehensive
profiling
reveals
novel
that
were
previously
undetectable.
Our
aim
this
manuscript
is
provide
a
overview
immunohematological
biomarkers,
applications,
future
directions
field.
International Journal of Genomics,
Journal Year:
2025,
Volume and Issue:
2025(1)
Published: Jan. 1, 2025
Rotator
cuff
injuries
are
a
common
cause
of
shoulder
pain
and
dysfunction,
with
chronic
inflammation
complicating
recovery.
Recent
advances
in
single‐cell
RNA
sequencing
(scRNA‐seq)
have
provided
new
insights
into
the
immune
cell
interactions
within
rotator
microenvironment
during
injury
healing.
This
review
focuses
on
application
scRNA‐seq
to
explore
roles
nonimmune
cells,
including
macrophages,
T‐cells,
fibroblasts,
myofibroblasts,
driving
inflammation,
tissue
repair,
fibrosis.
We
discuss
how
crosstalk
extracellular
matrix
influence
progression
healing
or
pathology.
Single‐cell
analyses
identified
distinct
molecular
signatures
associated
which
may
contribute
persistent
damage.
Additionally,
we
highlight
therapeutic
potential
targeting
emphasizing
personalized
medicine
approaches.
Overall,
integration
studying
enhances
our
understanding
cellular
mechanisms
involved
offers
perspectives
for
developing
targeted
treatments
regenerative
medicine.
Cell Genomics,
Journal Year:
2025,
Volume and Issue:
5(2), P. 100771 - 100771
Published: Feb. 1, 2025
Highlights•Spot-based
methods
struggle
to
handle
the
complexity
of
tumor
samples•STMiner
avoids
background
bias
by
optimal
transport
theory•STMiner
retains
both
high-
and
low-expression
genes
based
on
spatial
distribution•STMiner
identifies
overlapping
regions
from
a
gene-based
perspectiveSummaryAnalyzing
transcriptomics
data
tissues
poses
several
challenges
beyond
those
healthy
samples,
including
unclear
boundaries
between
different
regions,
uneven
cell
densities,
relatively
higher
cellular
heterogeneity.
Collectively,
these
against
which
spatially
variable
are
identified,
can
result
in
misidentification
structures
hinder
potential
insight
into
complex
pathologies.
To
overcome
this
problem,
STMiner
leverages
2D
Gaussian
mixture
models
theory
directly
characterize
distribution
rather
than
capture
locations
cells
expressing
them
(spots).
By
effectively
mitigating
impacts
sparsity,
reveals
key
gene
sets
overlooked
spot-based
analytic
tools,
facilitating
novel
biological
discoveries.
The
core
concept
analyzing
overall
expression
patterns
also
allows
for
broader
application
transcriptomics,
positioning
continuous
expansion
as
omics
technologies
evolve.Graphical
abstract
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 20, 2025
Diabetes
mellitus
(DM)
is
a
global
health
crisis
affecting
millions,
with
islet
transplantation
emerging
as
promising
treatment
strategy
to
restore
insulin
production.
This
review
synthesizes
the
current
research
on
single-cell
and
spatial
transcriptomics
in
context
of
transplantation,
highlighting
their
potential
revolutionize
DM
management.
Single-cell
RNA
sequencing,
offers
detailed
look
into
diversity
functionality
within
grafts,
identifying
specific
cell
types
states
that
influence
graft
acceptance
function.
Spatial
complements
this
by
mapping
gene
expression
tissue's
context,
crucial
for
understanding
microenvironment
surrounding
transplanted
islets
interactions
host
tissues.
The
integration
these
technologies
comprehensive
view
cellular
microenvironments,
elucidating
mechanisms
underlying
function,
survival,
rejection.
instrumental
developing
targeted
therapies
enhance
performance
patient
outcomes.
emphasizes
significance
avenues
informing
clinical
practices
improving
outcomes
patients
through
more
effective
strategies.
Future
directions
include
application
personalized
medicine,
developmental
biology,
regenerative
predict
disease
progression
responses.
Addressing
ethical
technical
challenges
will
be
successful
implementation
integrated
approaches
practice,
ultimately
enhancing
our
ability
manage
improve
quality
life.
Frontiers in Cell and Developmental Biology,
Journal Year:
2024,
Volume and Issue:
12
Published: April 22, 2024
Mammalian
stem
cell-based
embryo
models
have
emerged
as
innovative
tools
for
investigating
early
embryogenesis
in
both
mice
and
primates.
They
not
only
reduce
the
need
sacrificing
but
also
overcome
ethical
limitations
associated
with
human
research.
Furthermore,
they
provide
a
platform
to
address
scientific
questions
that
are
otherwise
challenging
explore
vivo
.
The
usefulness
of
model
depends
on
its
fidelity
replicating
development,
efficiency
reproducibility;
all
essential
addressing
biological
queries
quantitative
manner,
enabling
statistical
analysis.
Achieving
such
requires
robust
systems
demand
extensive
optimization
efforts.
A
profound
understanding
pre-
post-implantation
cellular
plasticity,
lineage
specification,
existing
is
imperative
making
informed
decisions
constructing
these
models.
This
review
aims
highlight
differences
development
cell
biology
between
humans,
assess
how
variances
influence
formation
partially
fully
integrated
models,
identify
critical
challenges
field.
Japanese Journal of Clinical Oncology,
Journal Year:
2024,
Volume and Issue:
54(6), P. 620 - 629
Published: March 23, 2024
Abstract
Tumor-infiltrating
lymphocytes
are
a
general
term
for
or
immune
cells
infiltrating
the
tumor
microenvironment.
Numerous
studies
have
demonstrated
tumor-infiltrating
to
be
robust
prognostic
and
predictive
biomarkers
in
breast
cancer.
Recently,
checkpoint
inhibitors,
which
directly
target
lymphocytes,
become
part
of
standard
care
treatment
triple-negative
Surprisingly,
quantified
by
conventional
methods
do
not
predict
response
highlights
heterogeneity
complexity
network
composed
diverse
cell
populations,
including
cytotoxic
CD8-positive
T
B
myeloid
cells.
Traditionally,
stroma
been
evaluated
histology.
However,
standardization
this
approach
is
limited,
necessitating
use
various
novel
technologies
elucidate
This
review
outlines
evaluation
from
pathological
approaches
that
evaluate
intratumoral
stromal
such
as
immunohistochemistry,
more
recent
advancements
computer
tissue
imaging
using
artificial
intelligence,
flow
cytometry
sorting
multi-omics
analyses
high-throughput
assays
estimate
bulk
signatures
deconvolution
tools.
We
also
discuss
higher
resolution
enable
analysis
single-cell
spatial
transcriptomics.
As
we
era
personalized
medicine,
it
important
clinicians
understand
these
technologies.