ACS Nano,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 25, 2024
The
tumor
microenvironment
(TME)
plays
a
crucial
role
in
cancer
progression
and
immune
evasion,
partially
mediated
by
the
activity
of
TME-derived
exosomes.
These
extracellular
vesicles
are
pivotal
shaping
responses
through
transfer
proteins,
lipids,
nucleic
acids
between
cells,
facilitating
complex
interplay
that
promotes
growth
metastasis.
This
review
delves
into
dual
roles
exosomes
TME,
highlighting
both
their
immunosuppressive
functions
emerging
therapeutic
potential.
Exosomes
can
inhibit
T
cell
function
promote
escape
carrying
immune-modulatory
molecules,
such
as
PD-L1,
yet
they
also
hold
promise
for
therapy
vehicles
delivering
antigens
costimulatory
signals.
Additionally,
discusses
intricate
crosstalk
among
various
types
within
influencing
to
immunotherapies.
Moreover,
this
highlights
current
challenges
future
directions.
Collectively,
elucidating
detailed
mechanisms
which
mediate
offers
promising
avenue
revolutionizing
treatment.
Understanding
these
interactions
allows
development
targeted
therapies
manipulate
exosomal
pathways
enhance
system's
response
tumors.
ACS Nano,
Journal Year:
2024,
Volume and Issue:
18(19), P. 12049 - 12095
Published: May 2, 2024
Cancer,
as
one
of
the
leading
causes
death
worldwide,
drives
advancement
cutting-edge
technologies
for
cancer
treatment.
Transition-metal-based
nanozymes
emerge
promising
therapeutic
nanodrugs
that
provide
a
reference
therapy.
In
this
review,
we
present
recent
breakthrough
First,
comprehensively
outline
preparation
strategies
involved
in
creating
transition-metal-based
nanozymes,
including
hydrothermal
method,
solvothermal
chemical
reduction
biomimetic
mineralization
and
sol–gel
method.
Subsequently,
elucidate
catalytic
mechanisms
(catalase
(CAT)-like
activities),
peroxidase
(POD)-like
oxidase
(OXD)-like
activities)
superoxide
dismutase
(SOD)-like
along
with
their
activity
regulation
such
morphology
control,
size
manipulation,
modulation,
composition
adjustment
surface
modification
under
environmental
stimulation.
Furthermore,
elaborate
on
diverse
applications
anticancer
therapies
encompassing
radiotherapy
(RT),
chemodynamic
therapy
(CDT),
photodynamic
(PDT),
photothermal
(PTT),
sonodynamic
(SDT),
immunotherapy,
synergistic
Finally,
challenges
faced
by
are
discussed
alongside
future
research
directions.
The
purpose
review
is
to
offer
scientific
guidance
will
enhance
clinical
based
transition
metals.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(11), P. 5632 - 5632
Published: May 22, 2024
Photothermal
therapy
(PTT)
is
a
promising
cancer
modality
with
significant
advantages
such
as
precise
targeting,
convenient
drug
delivery,
better
efficacy,
and
minimal
adverse
effects.
effectively
absorbs
the
photothermal
transducers
in
near-infrared
region
(NIR),
which
induces
effect
to
work.
Although
PTT
has
role
tumor
therapy,
it
also
suffers
from
low
conversion
efficiency,
biosafety,
incomplete
elimination.
Therefore,
use
of
nanomaterials
themselves
photosensitizers,
targeted
modification
improve
targeting
or
combined
other
therapies
can
therapeutic
effects
reduce
side
Notably,
noble
metal
have
attracted
much
attention
because
they
strong
surface
plasmon
resonance
an
effective
absorbance
light
at
specific
wavelengths.
be
used
excellent
photosensitizers
mediate
its
efficiency.
This
paper
provides
comprehensive
review
key
played
by
therapy.
It
describes
major
challenges
encountered
during
implementation
Cell Death Discovery,
Journal Year:
2024,
Volume and Issue:
10(1)
Published: Aug. 26, 2024
Abstract
CAFs
(cancer-associated
fibroblasts)
are
highly
flexible
cells
of
the
cancer
microenvironment.
They
produce
extracellular
matrix
(ECM)
constituents
that
form
structure
tumor
stroma
but
also
a
source
metabolites,
growth
factors,
chemokines,
and
exosomes
impact
every
aspect
tumor,
including
its
response
to
treatment.
It
is
believed
exosomal
miRNAs
facilitate
intercellular
signaling,
which
essential
for
development
cancer.
The
role
in
microenvironment
(TME)
carcinogenesis
reviewed
this
paper.
preferred
reporting
items
systematic
reviews
meta-analyses
(PRISMA)
2020
guidelines
were
used
perform
review.
Several
databases,
Web
Science,
Medline,
Embase,
Cochrane
Library,
Scopus,
searched
using
following
keywords:
CAFs,
CAF,
cancer-associated
fibroblasts,
stromal
miRNA,
miRNAs,
exosome
similar
terms.
We
identified
studies
investigating
TME
their
carcinogenesis.
A
total
12,572
papers
identified.
After
removing
duplicates
(
n
=
3803),
8774
articles
screened
by
title
abstract.
Of
these,
421
excluded
from
further
analysis.
has
been
reported
if
not
functioning
correctly,
may
influence
secretory
phenotype
tip
contribute
increased
invasiveness,
spread,
decreased
treatment
efficacy,
poorer
prognosis.
Under
influence,
normal
fibroblasts
(NFs)
transformed
into
CAFs.
Furthermore,
they
participate
metabolic
reprogramming,
allows
fast
proliferation
cell
population,
adaptation
growing
energy
demands,
capacity
avoid
immune
system
identification.
International Journal of Nanomedicine,
Journal Year:
2025,
Volume and Issue:
Volume 20, P. 2371 - 2394
Published: Feb. 1, 2025
Lung
cancer
is
the
leading
cause
of
cancer-related
mortality
globally,
with
non-small
cell
lung
(NSCLC)
constituting
85%
cases.
Immune
checkpoint
inhibitors
(ICIs)
represented
by
anti-programmed
death
protein
1
(PD-1)/
programmed
ligand
(PD-L1)
have
emerged
as
a
promising
frontier
in
treatment,
effectively
extending
survival
patients
NSCLC.
However,
efficacy
ICIs
exhibits
significant
variability
across
diverse
patient
populations,
substantial
proportion
showing
poor
responsiveness
and
acquired
resistance
those
initially
responsive
to
treatments.
With
advancement
nanotechnology,
nanoparticles
offer
unique
advantages
tumor
immunotherapy,
including
high
permeability
prolonged
retention(EPR)
effects,
enhanced
drug
delivery
stability,
modulation
inflammatory
microenvironment(TME).
This
review
summarizes
mechanisms
NSCLC,
focusing
on
antigens
loss
defective
antigen
processing
presentation,
failure
T
priming,
impaired
migration
infiltration,
immunosuppressive
TME,
genetic
mutations.
Furthermore,
we
discuss
how
nanoparticles,
through
their
intrinsic
properties
such
EPR
effect,
active
targeting
shielding
self-regulatory
synergistic
can
potentiate
reverse
resistance.
In
conclusion,
serve
robust
platform
for
ICIs-based
NSCLC
therapy,
aiding
overcoming
challenges.
Acta Pharmaceutica Sinica B,
Journal Year:
2023,
Volume and Issue:
14(4), P. 1742 - 1758
Published: Dec. 16, 2023
Mitochondrial
membrane
remodeling
can
trigger
the
release
of
mitochondrial
DNA
(mtDNA),
leading
to
activation
cellular
oxidative
stress
and
immune
responses.
While
role
in
promoting
inflammation
hepatocytes
is
well-established,
its
effects
on
tumors
have
remained
unclear.
In
this
study,
we
designed
a
novel
Pt(IV)
complex,
OAP2,
which
composed
oxaliplatin
(Oxa)
acetaminophen
(APAP),
enhance
anti-tumor
amplify
response.
Our
findings
demonstrate
that
OAP2
induces
nuclear
damage,
resulting
production
DNA.
Additionally,
downregulates
expression
Sam50,
promote
mtDNA
secretion,
double-stranded
accumulation
ultimately
synergistically
activating
intracellular
cGAS-STING
pathway.
The
induced
by
overcomes
limitations
Oxa
STING
pathway
simultaneously
promotes
gasdermin-D-mediated
cell
pyroptosis.
also
dendritic
maturation
enhances
quantity
efficacy
cytotoxic
T
cells,
thereby
inhibiting
cancer
proliferation
metastasis.
Briefly,
our
study
introduces
first
small-molecule
inhibitor
regulates
for
active
immunotherapy
research,
may
provide
creative
idea
targeting
organelle
therapy.
npj Vaccines,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: Jan. 18, 2024
Abstract
Recently,
chemically
synthesized
minimal
mRNA
(CmRNA)
has
emerged
as
a
promising
alternative
to
in
vitro
transcribed
(IVT-mRNA)
for
cancer
therapy
and
immunotherapy.
CmRNA
lacking
the
untranslated
regions
polyadenylation
exhibits
enhanced
stability
efficiency.
Encapsulation
of
within
lipid-polymer
hybrid
nanoparticles
(LPPs)
offers
an
effective
approach
personalized
neoantigen
vaccines
with
improved
control
over
tumor
growth.
LPP-based
delivery
systems
provide
superior
pharmacokinetics,
stability,
lower
toxicity
compared
viral
vectors,
naked
mRNA,
or
lipid
that
are
commonly
used
delivery.
Precise
customization
LPPs
terms
size,
surface
charge,
composition
allows
optimized
cellular
uptake,
target
specificity,
immune
stimulation.
CmRNA-encoded
neo-antigens
demonstrate
high
translational
efficiency,
enabling
recognition
by
CD8
+
T
cells
upon
processing
presentation.
This
perspective
highlights
potential
benefits,
challenges,
future
directions
Circular
RNAs
IVT-mRNA.
Further
research
is
needed
optimize
vaccine
design,
delivery,
safety
assessment
clinical
trials.
Nevertheless,
LPP-CmRNA
hold
great
advancing
immunotherapy,
paving
way
medicine.
Pharmaceuticals,
Journal Year:
2024,
Volume and Issue:
17(7), P. 932 - 932
Published: July 11, 2024
Photodynamic
therapy
(PDT)
is
a
promising
cancer
treatment
method
that
uses
photosensitizing
(PS)
compounds
to
selectively
destroy
tumor
cells
using
laser
light.
This
review
discusses
the
main
advantages
of
PDT,
such
as
its
low
invasiveness,
minimal
systemic
toxicity
and
risk
complications.
Special
attention
paid
photosensitizers
obtained
by
chemical
synthesis.
Three
generations
are
presented,
starting
with
first,
based
on
porphyrins,
through
second
generation,
including
modified
chlorins,
5-aminolevulinic
acid
(ALA)
derivative
hexyl
aminolevulinate
(HAL),
third
which
use
nanotechnology
increase
selectivity
therapy.
In
addition,
current
research
trends
highlighted,
search
for
new
can
overcome
limitations
existing
therapies,
heavy-atom-free
nonporphyrinoid
photosensitizers,
antibody–drug
conjugates
(ADCs)
or
near-infrared
(NIR)
absorption
peak.
Finally,
prospects
development
PDTs
taking
into
account
advances
in
biomedical
engineering.
The
references
include
both
older
newer
works.
many
cases,
when
writing
about
given
group
first-
second-generation
publications
used
because
properties
described
therein
have
not
changed
over
years.
Moreover,
articles
provide
information
serves
an
introduction
drugs.
International Journal of Nanomedicine,
Journal Year:
2024,
Volume and Issue:
Volume 19, P. 2755 - 2772
Published: March 1, 2024
Purpose:
The
drug
resistance
and
low
response
rates
of
immunotherapy
limit
its
application.
This
study
aimed
to
construct
a
new
nanoparticle
(CaCO
3
-polydopamine-polyethylenimine,
CPP)
effectively
deliver
interleukin-12
(IL-12)
suppress
cancer
progress
through
immunotherapy.
Methods:
size
distribution
CPP
zeta
potential
were
measured
using
Malvern
Zetasizer
Nano-ZS90.
morphology
electrophoresis
tentative
delay
analyzed
JEM-1400
transmission
electron
microscope
an
ultraviolet
spectrophotometer,
respectively.
Cell
proliferation
was
by
MTT
assay.
Proteins
Western
blot.
IL-12
HMGB1
levels
estimated
ELISA
kits.
Live/dead
staining
assay
performed
Calcein-AM/PI
kit.
ATP
production
detected
xenografts
in
vivo
C57BL/6
mice.
CD80
+
/CD86
,
CD3
/CD4
/CD8
flow
cytometry.
Results:
could
express
EGFP
or
increase
ROS
levels.
Laser
treatment
promoted
CPP-IL-12
induced
the
number
dead
apoptotic
cell.
laser
further
enhance
CALR
extracellular
decrease
intracellular
levels,
indicating
that
it
may
induce
immunogenic
cell
death
(ICD).
tumors
weights
laser-treated
mice
significantly
reduced
than
controls.
expression,
expression
DC
from
lymph
glands,
T
cells
spleen
increased
CPP-IL-12-treated
compared
with
granzyme
B,
IFN-γ,
TNF-α
serum
increased.
Interestingly,
local
back
inhibit
growth
distant
untreated
tumor.
Conclusion:
novel
overexpress
melanoma
achieve
inducing
ICD,
activating
CD4
cell,
enhancing
function
tumor-reactive
CD8
cells.
Keywords:
immunotherapy,
CaCO
nanoparticle,
interleukin-12,
death,
tumor
therapy
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(12)
Published: Jan. 15, 2024
Abstract
The
scar
repair
inevitably
causes
damage
of
skin
function
and
loss
appendages
such
as
hair
follicles
(HF).
It
is
great
challenge
in
wound
that
how
to
intervene
formation
while
simultaneously
remodeling
HF
niche
inducing
situ
regeneration.
Here,
chemical
reprogramming
techniques
are
used
identify
a
clinically
cocktail
(Tideglusib
Tamibarotene)
can
drive
fibroblasts
toward
dermal
papilla
cell
(DPC)
fate.
Considering
the
advantage
biomaterials
tissue
their
regulation
behavior
may
contributes
cellular
reprogramming,
artificial
seeding
(AHFS)
hydrogel
microspheres,
inspired
by
natural
processes
“seeding
harvest”,
constructed
via
using
combination
liposome
nanoparticle
drug
delivery
system,
photoresponsive
shell,
positively
charged
polyamide
modification,
microfluidic
photocrosslinking
techniques.
identified
core
nucleus
AHFS.
In
vitro
vivo
studies
show
AHFS
regulate
fibroblast
fate,
induce
fibroblast‐to‐DPC
activating
PI3K/AKT
pathway,
finally
promoting
healing
regeneration
inhibiting
two‐pronged
translational
approach.
conclusion,
provides
new
effective
strategy
for
functional
wounds.