Discover Oncology,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Dec. 5, 2024
Gastric
adenocarcinoma
(GC),
along
with
its
tumor
microenvironment
(TME),
poses
great
challenges
for
clinical
treatment
strategies.
Single-cell
sequencing
has
become
an
important
tool
analyzing
TME
heterogeneity,
cell
subpopulation,
and
gene
expression
patterns.
56
GC
single-cell
samples
were
analyzed,
focusing
on
by
delineating
cancer
cells,
cancer-associated
fibroblasts
(CAFs),
macrophages.
The
spatial
transcriptome
was
used
to
clarify
the
distribution
characteristics
of
each
cellular
component
in
tissue
slice.
Despite
widespread
genetic
mutations
observed
certain
recurrent
alterations
identified
specific
chromosomal
regions.
heterogeneity
among
cells
is
profound,
four
subpopulations
through
drug
sensitivity
profiling.
Subtype
4,
although
only
present
some
samples,
demonstrates
strongest
stemness
metabolic
activity,
possibly
indicative
early-stage
subpopulation.
Their
profiles
may
hold
promise
guiding
intervention.
In
addition,
robust
co-localization
patterns
between
CAFs,
M2
macrophages,
endothelial
cells.
CAFs
further
categorized
into
six
subgroups,
which
a
novel
subgroup
termed
metallothionein(mt)-positive
CAF
(mtCAF),
characterized
elevated
metallothionein
1X
(MT1X)
subsequent
vascular
growth
factor
A
(VEGFA)
secretion,
identified.
Immunohistochemistry
preliminary
confirmed
presence
this
unique
subgroup.
Additionally,
M2d
besides
exhibiting
high
VEGFA
expression,
also
demonstrated
various
factors
such
as
Aamphiregulin
(AREG).
M2d-mtCAF
axis
play
role
angiogenesis.
This
study
not
enhances
our
understanding
but
sheds
light
interaction
tumor-associated
macrophages
(TAMs)
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(5), P. 2670 - 2670
Published: Feb. 25, 2024
Over
the
past
century,
molecular
biology’s
focus
has
transitioned
from
proteins
to
DNA,
and
now
RNA.
Once
considered
merely
a
genetic
information
carrier,
RNA
is
recognized
as
both
vital
element
in
early
cellular
life
regulator
complex
organisms.
Long
noncoding
RNAs
(lncRNAs),
which
are
over
200
bases
long
but
do
not
code
for
proteins,
play
roles
gene
expression
regulation
signal
transduction
by
inducing
epigenetic
changes
or
interacting
with
various
RNAs.
These
interactions
exhibit
range
of
functions
cell
types,
including
macrophages.
Notably,
some
macrophage
lncRNAs
influence
activation
NF-κB,
crucial
transcription
factor
governing
immune
inflammatory
responses.
Macrophage
NF-κB
instrumental
progression
pathological
conditions
sepsis,
atherosclerosis,
cancer,
autoimmune
disorders,
hypersensitivity.
It
orchestrates
related
responses,
inflammation,
survival,
proliferation.
Consequently,
its
malfunction
key
contributor
onset
development
these
diseases.
This
review
aims
summarize
function
regulating
activity
particular
emphasis
on
their
relevance
human
diseases
potential
therapeutic
targets.
The
insights
gained
studies
lncRNAs,
discussed
this
review,
could
provide
valuable
knowledge
treatments
involving
Immunological Investigations,
Journal Year:
2024,
Volume and Issue:
53(7), P. 1030 - 1091
Published: June 24, 2024
An
event
of
increasing
interest
during
host-pathogen
interactions
is
the
polarization
patrolling/naive
monocytes
(MOs)
into
macrophage
subsets
(MФs).
Therapeutic
strategies
aimed
at
modulating
this
are
under
investigation.
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(17), P. e37192 - e37192
Published: Aug. 30, 2024
In
immunology,
the
role
of
macrophages
extends
far
beyond
their
traditional
classification
as
mere
phagocytes;
they
emerge
pivotal
architects
immune
response,
with
function
being
significantly
influenced
by
multidimensional
environmental
stimuli.
This
review
investigates
nuanced
mechanisms
which
diverse
external
signals
ranging
from
chemical
cues
to
physical
stress
orchestrate
macrophage
polarization,
a
process
that
is
crucial
for
modulation
responses.
By
transitioning
between
pro-inflammatory
(M1)
and
anti-inflammatory
(M2)
states,
exhibit
remarkable
plasticity,
enabling
them
adapt
influence
surroundings
effectively.
The
exploration
polarization
provides
compelling
narrative
on
how
these
cells
can
be
manipulated
foster
an
environment
conducive
tissue
repair
regeneration.
Highlighting
cutting-edge
research,
this
presents
innovative
strategies
leverage
dynamic
interplay
environment,
proposing
novel
therapeutic
avenues
harness
potential
in
regenerative
medicine.
Moreover,
critically
evaluates
current
challenges
future
prospects
translating
macrophage-centered
laboratory
clinical
applications.
Journal of Personalized Medicine,
Journal Year:
2024,
Volume and Issue:
14(5), P. 537 - 537
Published: May 17, 2024
Inflammation
during
the
perioperative
period
of
joint
arthroplasty
is
a
critical
aspect
patient
outcomes,
influencing
both
pathophysiology
pain
and
healing
process.
This
narrative
review
comprehensively
evaluates
roles
specific
cytokines
inflammatory
biomarkers
in
this
context
their
implications
for
management.
Inflammatory
responses
are
initiated
propagated
by
cytokines,
which
pivotal
development
acute
chronic
postoperative
pain.
Pro-inflammatory
play
essential
up-regulating
response,
which,
if
not
adequately
controlled,
leads
to
sustained
impaired
tissue
healing.
Anti-inflammatory
work
dampen
promote
resolution.
Our
discussion
extends
genetic
molecular
influences
on
cytokine
production,
influence
perception
recovery
rates
post-surgery.
Furthermore,
role
PAI-1
modulating
inflammation
through
its
impact
fibrinolytic
system
highlights
potential
as
therapeutic
target.
The
modulation
these
various
analgesic
anesthetic
techniques,
including
fascia
iliac
compartment
block,
demonstrates
significant
reduction
markers,
thus
underscoring
importance
targeted
strategies.
analysis
suggests
that
nuanced
understanding
interplay
between
pro-inflammatory
anti-inflammatory
required.
Future
research
should
focus
individualized
management
Cancer Medicine,
Journal Year:
2025,
Volume and Issue:
14(3)
Published: Feb. 1, 2025
ABSTRACT
Background
Lung
cancer
is
among
the
most
common
and
deadliest
malignant
tumors
worldwide.
It
often
detected
at
late
stages,
resulting
in
unfavorable
outcomes,
with
tumor
cell
heterogeneity
medication
resistance.
Tumor‐associated
macrophages
are
key
cells
contributing
to
progression.
They
categorized
into
two
primary
phenotypes:
Proinflammatory
(M1)
anti‐inflammatory
(M2)
which
involved
onset
progression
of
NSCLC.
The
role
cytokines
secreted
by
lung
described,
effects
various
substances
such
as
RNA
or
protein
on
differentiation
polarization
phenotypes
highlighted
characterize
impact
immune
state
therapeutic
effect
treatments
patient
prognosis.
Researchers
have
primarily
aimed
investigate
innovative
carriers
strategies
based
modify
microenvironment.
Objectives
These
approaches
integrated
other
treatments,
particularly
immunotherapy,
enhance
efficacy.
Methods
A
comprehensive
review
was
carried
out
systematically
synthesizing
existing
literature
PubMed,
using
combination
keywords
“TAMs”,
“NSCLC”,
“Drug
resistance”,
“therapy”.
available
studies
were
screened
for
selection
quality
relevance.
Conclusions
TAMs
promote
invasion,
growth,
metastasis
promoting
angiogenesis
EMT.
In
addition,
they
contribute
development
drug
resistance
immunosuppressive
microenvironment
establishment.
factors
TAM
can
weaken
activity
cells,
inhibit
their
killing
tumors,
leading
suppression
hindering
effectiveness
treatment.
Therefore,
a
target
immunotherapy.
Various
being
explored,
including
reducing
recruitment
influencing
treat
treatment
systems
achieve
precise
delivery
drugs
gene
interfering
molecules
without
causing
side
effects.
European journal of medical research,
Journal Year:
2025,
Volume and Issue:
30(1)
Published: April 17, 2025
Sepsis
is
a
highly
dangerous
and
complex
condition
that
can
result
in
death.
It
characterized
by
strong
reaction
to
an
infection,
causing
dysfunction
multiple
bodily
systems
high
risk
of
mortality.
The
transformation
macrophages
vital
stage
the
procedure
as
they
possess
capability
interchange
between
two
separate
types:
M1,
which
promotes
inflammation,
M2,
inhibits
inflammation.
choice
greatly
affects
immune
response
host.
This
analysis
underscores
rapidly
expanding
roles
exosomes
microRNAs
(miRNAs)
regulating
trajectory
macrophage
polarization
during
episodes
sepsis.
Exosomes,
extremely
small
extracellular
vesicles,
facilitate
cellular
communication
transferring
biologically
active
compounds,
including
miRNAs,
proteins,
lipids.
We
investigate
impact
changes
exosome
production
composition
caused
sepsis
on
function.
Unique
present
play
significant
role
controlling
crucial
signaling
pathways
govern
phenotype
macrophages.
Through
thorough
examination
recent
progress
this
area,
we
clarify
ways
miRNAs
derived
from
either
aggravate
or
alleviate
inflammatory
reactions
occur
revelation
not
only
deepens
our
comprehension
underlying
mechanisms
sepsis,
but
it
also
reveals
potential
new
biomarkers
targets
for
treatment.
assessment
aims
amalgamate
diverse
research
investigations
propose
avenues
future
influence
have
body's
These
entities
are
essential
host's
hold
important
functions
mechanism.