ACS Biomaterials Science & Engineering,
Journal Year:
2024,
Volume and Issue:
10(8), P. 4701 - 4715
Published: July 3, 2024
The
utilization
of
traditional
therapies
(TTS),
such
as
chemotherapy,
reactive
oxygen
species-based
therapy,
and
thermotherapy,
to
induce
immunogenic
cell
death
(ICD)
in
tumor
cells
has
emerged
a
promising
strategy
for
the
activation
antitumor
immune
response.
However,
limited
effectiveness
most
TTS
inducing
ICD
effect
tumors
hinders
their
applications
combination
with
immunotherapy.
To
address
this
challenge,
various
intelligent
strategies
have
been
proposed
strengthen
these
TTS,
then
achieve
synergistic
efficacy
These
primarily
focus
on
augmenting
or
facilitating
antigen
(released
by
cells)
presentation
process
during
they
are
systematically
summarized
review.
Finally,
existing
bottlenecks
prospects
application
regulation
also
discussed.
Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
177, P. 116951 - 116951
Published: June 19, 2024
The
emerging
strategy
of
biomimetic
nanoparticles
(NPs)
via
cellular
membrane
camouflage
holds
great
promise
in
cancer
therapy.
This
scholarly
review
explores
the
utilization
membranes
derived
from
diverse
entities;
blood
cells,
immune
stem
and
bacterial
cells
as
examples
NP
coatings.
camouflaging
endows
NPs
with
nuanced
tumor-targeting
abilities
such
self-recognition,
homotypic
targeting,
long-lasting
circulation,
thus
also
improving
tumor
therapy
efficacy
overall.
comprehensive
examination
encompasses
a
variety
cell
camouflaged
(CMCNPs),
elucidating
their
underlying
targeted
mechanisms
delineating
strategies
for
anti-cancer
applications.
Furthermore,
systematically
presents
synthesis
source
materials
methodologies
employed
order
to
construct
characterize
these
CMCNPs,
specific
emphasis
on
use
treatment.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 5, 2024
Abstract
To
advance
the
understanding
and
potential
treatment
strategies
for
triple‐negative
breast
cancer
(TNBC),
particularly
focusing
on
its
high
metastatic
propensity
uncertain
molecular
targets,
a
biomimetic
tumor
cell
membrane‐encapsulated
nanodelivery
system
is
developed
enhanced
immunotherapy.
This
assembled
with
second
near‐infrared
(NIR‐II)
photothermal
agent,
chemotherapeutic
drug,
programmed
death‐ligand
1
(PD‐L1)
inhibitors
camouflaged
by
TNBC
membranes.
An
NIR‐II
Ag
2
S
quantum
dots
(QDs)
introduced
not
only
realizing
pronounced
imaging‐guided
therapy
(PTT),
but
also
co‐activating
immunogenic
death
(ICD)
chemotherapy.
Homologous
targeting
camouflage
properties
endowed
excellent
biocompatibility
efficient
delivery
ability
to
site,
demonstrating
synergistic
therapeutic
efficacy.
The
release
of
damage‐associated
patterns
(DAMP)
marked
induction
ICD,
crucial
reshaping
immune
microenvironment.
Further
integration
α‐PD‐L1
achieved
56.5%
checkpoint
inhibition
rate,
synergistically
amplifying
response
ultimately
activate
key
cytokines,
thereby
achieving
anti‐tumor
immunotherapy
effects.
Notably,
this
approach
realized
considerable
reduction
nodules
51.2%
in
lung
metastasis
model.
proposed
extended
remission
effectively
reduced
metastasis,
paving
way
reliable
promising
Advanced Healthcare Materials,
Journal Year:
2024,
Volume and Issue:
13(20)
Published: May 1, 2024
Abstract
Venous/arterial
thrombosis
poses
significant
threats
to
human
health.
However,
drug‐enabled
thrombolysis
treatment
often
encounters
challenges
such
as
short
half‐life
and
low
bioavailability.
To
address
these
issues,
the
design
of
erythrocyte‐membrane
(EM)
camouflaged
nanocapsules
(USIO/UK@EM)
incorporating
ultra‐small
iron
oxide
(USIO)
urokinase
(UK)
drug,
which
exhibits
remarkable
photothermal/magnetothermal
effects
drug
delivery
ability
for
venous/arterial
thrombolysis,
is
reported.
USIO,
UK,
EM
are
coextruded
fabricate
USIO/UK@EM
with
average
sizes
103.7
nm.
As
possesses
wide
photoabsorption
good
magnetic
properties,
its
solution
demonstrates
a
temperature
increase
41.8–42.9
°C
within
5
min
when
exposed
an
808
nm
laser
(0.33
mW
cm
−2
)
or
alternating
field
(AMF).
Such
effect
along
UK
confers
impressive
thrombolytic
rates
82.4%
74.2%,
higher
than
that
(≈15%)
achieved
by
alone.
Further,
coating
extends
circulating
(
t
1/2
=
3.28
h).
When
administered
mice
rabbits,
tail
vein
thrombus
in
femoral
artery
rabbits
can
be
dissolved
synergetic
thermothrombolysis
UK.
Therefore,
this
study
not
only
offers
insights
into
rational
multifunctional
biomimetic
but
also
showcases
promising
strategy
utilizing
nanomedicine.
Journal of Nanobiotechnology,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: March 22, 2025
Triple-negative
breast
cancer
(TNBC)
is
a
highly
aggressive
subtype
of
characterized
by
an
extremely
poor
prognosis.
Photoimmunotherapy
has
emerged
as
promising
strategy
for
the
treatment
TNBC.
This
approach
works
selectively
destroying
tumor
cells,
releasing
tumor-associated
antigens,
activating
immune
system,
and
effectively
inhibiting
proliferation
metastasis.
However,
majority
current
phototheranostic
approaches
are
hindered
limited
tissue
penetration
in
first
near-infrared
(NIR-I)
ultraviolet–visible
(UV–Vis)
regions.
Additionally,
due
to
lack
specific
subcellular
targets,
it
may
be
difficult
treat
deep-seated
lesions
with
ambiguous
extensive
boundaries
caused
TNBC
metastases.
Consequently,
development
effective,
deep-penetrating,
organelle-targeted
phototheranostics
essential
enhancing
outcomes
work
proposes
novel
molecular
design
NIR-II
realize
planar
rigid
conjugation
alkyl
chain
functionalization.
The
di-hexaalkyl
chains
vertical
configuration
on
donor
(4H-cyclopenta[2,1-b:3,4-b']
dithiophene)
shielding
units
(fluorene)
introduced
construct
S-D-A-D-S
type
(IR-FCD).
structure
IR-FCD
exhibits
robust
intramolecular
charge
transfer
capability,
lower
band
gap,
enhanced
photon
absorption
properties,
significant
steric
hindrance
from
vertically
arranged
minimize
non-radiative
energy
loss.
By
incorporating
N-(but-3-yn-1-yl)-4-methylbenzenesulfonamide
at
terminus
elongated
chain,
followed
self-assembly
into
DSPE-S-S-PEG2000,
excitable
(IR-FCD-Ts
NPs)
endoplasmic
reticulum
(ER)
targeting
capability
were
successfully
synthesized
imaging-guided
photoimmunotherapy
IR-FCD-Ts
NPs
demonstrate
exceptional
optical
characteristics,
maximum
1068
nm
(extending
1300
nm)
emission
1273
1700
nm),
along
high
molar
coefficient
2.76*104
L/mol·c
1064
aqueous
solution.
Under
exposure
laser
irradiation,
exhibit
superior
photothermal
properties
have
potential
photodynamic
therapy.
ER,
thereby
inducing
ER
stress
significantly
immunogenic
cell
death
(ICD)
triggers
strong
antitumor
response
inhibits
metastasis
ACS Nano,
Journal Year:
2024,
Volume and Issue:
18(39), P. 26690 - 26703
Published: Sept. 20, 2024
Herein,
we
constructed
a
paclitaxel
(PTX)
prodrug
(PA)
by
conjugating
PTX
with
acrylic
acid
as
cysteine-depleting
agent.
The
as-synthesized
PA
can
assemble
diacylphosphatidylethanolamine-PEG
Journal of Experimental & Clinical Cancer Research,
Journal Year:
2025,
Volume and Issue:
44(1)
Published: Feb. 3, 2025
Glioma,
particularly
glioblastoma
(GBM),
is
a
highly
aggressive
tumor
with
limited
responsiveness
to
immunotherapy.
PANoptosis,
form
of
programmed
cell
death
merging
pyroptosis,
apoptosis,
and
necroptosis,
plays
an
important
role
in
reshaping
the
microenvironment
(TME)
enhancing
immunotherapy
effectiveness.
This
study
investigates
PANoptosis
dynamics
glioma
explores
therapeutic
potential
its
activation,
through
natural
compounds
such
as
cinobufagin.
We
comprehensively
analyzed
PANoptosis-related
genes
(PANoRGs)
multiple
cohorts,
identifying
different
patterns
constructing
enrichment
score
(PANoScore)
evaluate
relationship
patient
prognosis
immune
activity.
Cinobufagin,
identified
activator,
was
evaluated
for
ability
induce
enhance
anti-tumor
responses
both
vitro
vivo
GBM
models.
Our
findings
indicate
that
high
PANoScore
gliomas
showed
increased
infiltration,
effector
T
cells,
enhanced
sensitivity
immunotherapies.
Cinobufagin
effectively
induced
leading
immunogenic
death,
facilitated
tumor-associated
microglia/macrophages
(TAMs)
polarization
towards
M1-like
phenotype
while
augmenting
CD4+/CD8
+
infiltration
activation.
Importantly,
cinobufagin
combined
anti-PD-1
therapy
exhibited
significant
synergistic
effects
prolonged
survival
These
highlight
PANoptosis-targeting
agents,
cinobufagin,
combination
immunotherapy,
offering
promising
approach
convert
"cold"
tumors
into
"hot"
ones
improving
treatment
outcomes.
Dimethylcurcumin
(ASC-J9)
is
an
organic
active
pharmaceutical
ingredient
with
anti-inflammatory,
antioxidant,
and
antitumor
effects.
However,
its
application
has
been
significantly
hindered
by
poor
solubility
in
aqueous
solutions,
a
short
vivo
half-life,
low
bioavailability
after
oral
administration,
limited
accumulation
absorption
target
areas.
Nano-drug
delivery
systems
can
serve
as
drug
carriers
to
enhance
delivery,
addressing
these
challenges
improved
efficacy
reduced
adverse
In
this
study,
microfluidic
swirl
mixer
used
prepare
silk
fibroin
composite
nanoparticles
containing
ASC-J9
copper
sulfate
(CuS),
the
effects
of
different
process
parameters
on
(SNPs)
were
explored
optimized.
The
synthesized
ASC-J9-CuS@SNPs
exhibited
mean
particle
diameter
180
±
10
nm
PDI
0.20
0.03.
Two-dimensional/three-dimensional
(2D/3D)
cell
experiments
showed
that
nanomaterials
have
excellent
biocompatibility
activity
noticeable
cancer
specificity.
effectively
controlled
tumor
growth
without
causing
damage
blood
cells
vital
organs.
Both
vitro
demonstrated
anticancer
effect
was
enhanced
photo
thermotherapy.
current
study
provides
promising
strategy
for
using
nanocarriers
breast
therapy.