Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: Sept. 23, 2024
Lung
cancer
remains
one
of
the
leading
causes
cancer-related
mortality
worldwide,
necessitating
innovative
research
methodologies
to
improve
treatment
outcomes
and
develop
novel
strategies.
The
advent
three-dimensional
(3D)
cell
cultures
has
marked
a
significant
advancement
in
lung
research,
offering
more
physiologically
relevant
model
compared
traditional
two-dimensional
(2D)
cultures.
This
review
elucidates
various
types
3D
culture
models
currently
used
pharmacology,
including
spheroids,
organoids
engineered
tissue
models,
having
pivotal
roles
enhancing
our
understanding
biology,
facilitating
drug
development,
advancing
precision
medicine.
systems
mimic
complex
spatial
architecture
microenvironment
tumours,
providing
critical
insights
into
cellular
molecular
mechanisms
tumour
progression,
metastasis
responses.
Spheroids,
derived
from
commercialized
lines,
effectively
(TME),
formation
hypoxic
nutrient
gradients,
crucial
for
evaluating
penetration
efficacy
anti-cancer
therapeutics.
Organoids
tumouroids,
primary
tissues,
recapitulate
heterogeneity
cancers
are
instrumental
personalized
medicine
approaches,
supporting
simulation
vivo
pharmacological
responses
patient-specific
context.
Moreover,
these
have
been
co-cultured
with
biomimicry
extracellular
matrix
(ECM)
components
further
heterotypic
cell-cell
cell-ECM
interactions
present
within
TME.
significantly
contributing
identification
therapeutic
targets
resistance
against
conventional
therapies.
Therefore,
this
summarizes
latest
findings
involving
together
common
laboratory-based
assays
study
effects.
Additionally,
integration
development
workflows
is
discussed.
accelerating
translation
laboratory
clinical
applications,
thereby
landscape
treatment.
By
closely
mirroring
human
not
only
enhance
disease
but
also
pave
way
effective
Journal of Cancer Research and Clinical Oncology,
Journal Year:
2024,
Volume and Issue:
150(5)
Published: May 7, 2024
Abstract
Background
Tumor
growth
is
closely
linked
to
the
activities
of
various
cells
in
tumor
microenvironment
(TME),
particularly
immune
cells.
During
progression,
circulating
monocytes
and
macrophages
are
recruited,
altering
TME
accelerating
growth.
These
adjust
their
functions
response
signals
from
stromal
Tumor-associated
(TAMs),
similar
M2
macrophages,
key
regulators
TME.
Methods
We
review
origins,
characteristics,
TAMs
within
This
analysis
includes
mechanisms
through
which
facilitate
evasion
promote
metastasis.
Additionally,
we
explore
potential
therapeutic
strategies
that
target
TAMs.
Results
instrumental
mediating
malignant
behaviors.
They
release
cytokines
inhibit
effector
attract
additional
immunosuppressive
primarily
T
cells,
inducing
exhaustion
directly,
influencing
activity
indirectly
cellular
interactions,
or
suppressing
checkpoints.
directly
involved
proliferation,
angiogenesis,
invasion,
Summary
Developing
innovative
tumor-targeted
therapies
immunotherapeutic
currently
a
promising
focus
oncology.
Given
pivotal
role
evasion,
several
approaches
have
been
devised
them.
include
leveraging
epigenetics,
metabolic
reprogramming,
engineering
repolarize
TAMs,
inhibiting
recruitment
activity,
using
as
drug
delivery
vehicles.
Although
some
these
remain
distant
clinical
application,
believe
future
targeting
will
offer
significant
benefits
cancer
patients.
APL Bioengineering,
Journal Year:
2024,
Volume and Issue:
8(1)
Published: Feb. 21, 2024
Within
the
complex
tumor
microenvironment,
cells
experience
mechanical
cues-such
as
extracellular
matrix
stiffening
and
elevation
of
solid
stress,
interstitial
fluid
pressure,
shear
stress-that
significantly
impact
cancer
cell
behavior
immune
responses.
Recognizing
significance
these
cues
not
only
sheds
light
on
progression
but
also
holds
promise
for
identifying
potential
biomarkers
that
would
predict
therapeutic
outcomes.
However,
standardizing
methods
studying
how
affect
is
challenging.
This
challenge
stems
from
limitations
traditional
Pharmacological Research,
Journal Year:
2022,
Volume and Issue:
187, P. 106564 - 106564
Published: Nov. 21, 2022
Tumor-associated
macrophages
(TAMs)
play
a
dual
role
in
tumors.
However,
the
factors
which
drive
function
of
TAMs
cholangiocarcinoma
remain
largely
undefined.SHH
signaling
pathway
and
endoplasmic
reticulum
stress
(ERS)
indicators
were
detected
clinical
tissues
cell
lines.
co-cultured
with
cells
under
conditions
hypoxia/normoxia.
Polarized
counted
by
flow
cytometry,
TGF-β1
levels
supernatants
ELISA.
The
effects
glioma-associated
oncogene
GLI2
on
themselves
examined
conducting
interference
overexpression
assays.The
SHH
ERS
both
activated
tumor
or
lines
hypoxia.
In
co-culture
experiments,
presence
increased
proportion
M2-polarized
secretion
TAMs,
while
knockdown
expression
reversed
those
increases.
Overexpression
TAMS
stimulation
Hh-Ag1.5
their
expression.
Furthermore,
conditions,
reduced
migration,
invasion,
ER
homeostasis
induced
Hh-Ag1.5-pretreated
TAMs.
Under
hypoxia,
promoted
Tams,
turn,
inhibited
apoptosis
migration
invasion
cells.
vivo,
an
injection
plus
contributed
to
growth,
EMT,
tissue,
had
opposite
effects.Cholangiocarcinoma
regulated
TAM
polarization
via
paracrine
pathway,
TGF-β1.
Frontiers in Cell and Developmental Biology,
Journal Year:
2024,
Volume and Issue:
12
Published: Oct. 3, 2024
Chimeric
Antigen
Receptor
(CAR)
technology
has
revolutionized
cellular
immunotherapy,
particularly
with
the
success
of
CAR-T
cells
in
treating
hematologic
malignancies.
However,
have
limited
efficacy
against
solid
tumors.
To
address
these
limitations,
CAR-macrophages
(CAR-Ms)
leverage
innate
properties
macrophages
specificity
and
potency
CAR
technology,
offering
a
novel
promising
approach
to
cancer
immunotherapy.
Preclinical
studies
shown
that
CAR-Ms
can
effectively
target
destroy
tumor
cells,
even
within
challenging
microenvironments,
by
exhibiting
direct
cytotoxicity
enhancing
recruitment
activation
other
immune
cells.
Additionally,
favorable
safety
profile
their
persistence
tumors
position
as
potentially
safer
more
durable
therapeutic
options
compared
This
review
explores
recent
advancements
including
engineering
strategies
optimize
anti-tumor
preclinical
evidence
supporting
use.
We
also
discuss
challenges
future
directions
developing
therapies,
emphasizing
potential
revolutionize
By
harnessing
unique
macrophages,
offer
groundbreaking
overcoming
current
limitations
cell
paving
way
for
effective
sustainable
treatments.