For and against tumor microenvironment: Nanoparticle-based strategies for active cancer therapy
Soroush Karimi,
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Roksana Bakhshali,
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Soheil Bolandi
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et al.
Materials Today Bio,
Journal Year:
2025,
Volume and Issue:
31, P. 101626 - 101626
Published: March 1, 2025
Cancer
treatment
is
challenged
by
the
tumor
microenvironment
(TME),
which
promotes
drug
resistance
and
cancer
cell
growth.
This
review
offers
a
comprehensive
innovative
perspective
on
how
nanomedicine
can
modify
TME
to
enhance
therapy.
Strategies
include
using
nanoparticles
improve
oxygenation,
adjust
acidity,
alter
extracellular
matrix,
making
treatments
more
effective.
Additionally,
immune
responses
activating
cells
reducing
suppression
within
tumors.
By
integrating
these
approaches
with
existing
therapies,
such
as
chemotherapy
radiotherapy,
show
promise
in
overcoming
traditional
barriers.
The
discusses
changes
effectiveness
of
itself,
creating
reciprocal
relationship
that
boosts
overall
efficacy.
We
also
highlight
novel
strategies
aimed
at
exploiting
TME,
leveraging
nanoparticle-based
for
targeted
therapy
through
precise
modulation.
Language: Английский
Targeting myofibroblastic cancer-associated fibroblasts (myCAFs): a promising strategy for overcoming tumor progression and immunotherapy resistance
Danting Wang,
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Zhigang Chen
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Visualized Cancer Medicine,
Journal Year:
2025,
Volume and Issue:
6, P. 4 - 4
Published: Jan. 1, 2025
Cancer-associated
fibroblasts
(CAFs),
as
the
dominant
stromal
cell
population
in
tumor
microenvironment
(TME),
exhibit
substantial
heterogeneity,
with
subtypes
such
myofibroblastic
cancer-associated
(myCAFs)
and
inflammatory
(iCAFs)
playing
distinct
roles
cancer
progression.
MyCAFs,
defined
by
elevated
ACTA2
expression,
are
particularly
significant
promoting
growth,
remodeling
stroma,
contributing
to
an
immunosuppressive
TME.
Despite
advances
understanding
CAF
precise
role
of
myCAFs
invasion,
metastasis,
resistance
therapies,
especially
immunotherapy,
remains
underexplored.
This
perspective
highlights
recent
insights
into
myCAF
functions
within
TME,
emphasizing
their
potential
therapeutic
targets.
By
disrupting
formation
or
combining
myCAF-targeting
approaches
there
is
a
promise
for
improving
treatment
outcomes
overcoming
immunotherapy
cancer.
Language: Английский