Advanced Materials,
Год журнала:
2023,
Номер
35(49)
Опубликована: Сен. 25, 2023
The
increased
incidence
of
inflammatory
bowel
disease
(IBD)
has
seriously
affected
the
life
quality
patients.
IBD
develops
due
to
excessive
intestinal
epithelial
cell
(IEC)
apoptosis,
disrupting
gut
barrier,
colonizing
harmful
bacteria,
and
initiating
persistent
inflammation.
current
therapeutic
approaches
that
reduce
inflammation
are
limited.
Although
can
be
treated
significantly
by
directly
preventing
IEC
achieving
this
approach
remains
challenging.
Accordingly,
authors
first
develop
an
oral
pifithrin-α
(PFTα,
a
highly
specific
p53
inhibitor)
embedded
nanomedicine
(OPEN)
effectively
treat
inhibiting
apoptosis.
As
major
hub
for
various
stressors,
is
central
determinant
fate,
its
inhibition
tailored
OPEN
precisely
inhibit
off-target
inactivation
resulting
from
PFTα
entry
into
bloodstream.
Subsequently,
it
persistently
targets
lesions
with
high
specificity
pathological
events
caused
Eventually,
exerts
significant
curative
effect
compared
clinical
first-line
drugs
5-aminosalicylic
acid
(5-ASA)
dexamethasone
(DEX).
Consequently,
strategy
provides
new
insights
comprehensive
therapy.
Immunotherapy
is
used
to
regulate
systemic
hyperactivation
or
hypoactivation
treat
various
diseases.
Biomaterial-based
immunotherapy
systems
can
improve
therapeutic
effects
through
targeted
drug
delivery,
immunoengineering,
etc.
However,
the
immunomodulatory
of
biomaterials
themselves
cannot
be
neglected.
In
this
review,
we
outline
with
functions
discovered
in
recent
years
and
their
applications
disease
treatment.
These
inflammation,
tumors,
autoimmune
diseases
by
regulating
immune
cell
function,
exerting
enzyme-like
activity,
neutralizing
cytokines,
The
prospects
challenges
biomaterial-based
modulation
are
also
discussed.
Signal Transduction and Targeted Therapy,
Год журнала:
2023,
Номер
8(1)
Опубликована: Ноя. 24, 2023
Abstract
Mesoporous
silica
nanoparticles
(MSNs)
are
recognized
as
a
prime
example
of
nanotechnology
applied
in
the
biomedical
field,
due
to
their
easily
tunable
structure
and
composition,
diverse
surface
functionalization
properties,
excellent
biocompatibility.
Over
past
two
decades,
researchers
have
developed
wide
variety
MSNs-based
nanoplatforms
through
careful
design
controlled
preparation
techniques,
demonstrating
adaptability
various
application
scenarios.
With
continuous
breakthroughs
MSNs
fields
biosensing,
disease
diagnosis
treatment,
tissue
engineering,
etc.,
gradually
moving
from
basic
research
clinical
trials.
In
this
review,
we
provide
detailed
summary
beginning
with
comprehensive
overview
development
history.
We
then
discuss
types
nanostructured
architectures,
well
classification
nanocomposites
according
elements
existed
inorganic
functional
components.
Subsequently,
summarize
primary
purposes
surface-functionalized
modifications
MSNs.
following,
applications
MSNs,
highlight
targeted
therapeutic
modalities
currently
developed.
Given
importance
translation,
also
progress
Finally,
take
perspective
on
future
direction
remaining
challenges
field.
Advanced Materials,
Год журнала:
2023,
Номер
36(6)
Опубликована: Сен. 19, 2023
Abstract
Insufficient
activation
of
the
stimulator
interferon
genes
(STING)
signaling
pathway
and
profoundly
immunosuppressive
microenvironment
largely
limits
effect
cancer
immunotherapy.
Herein,
tumor
(TME)‐responsive
nanoparticles
(PMM
NPs)
are
exploited
that
simultaneously
harness
STING
Toll‐like
receptor
4
(TLR4)
to
augment
via
TLR4‐mediated
nuclear
factor‐kappa
B
stimulation,
leading
increased
secretion
type
I
interferons
(i.e.,
4.0‐fold
enhancement
IFN‐β)
pro‐inflammatory
cytokines
promote
a
specific
T
cell
immune
response.
Moreover,
PMM
NPs
relieve
immunosuppression
TME
by
decreasing
percentage
regulatory
cells,
polarizing
M2
macrophages
M1
type,
thus
creating
an
immune‐supportive
unleash
cascade
adaptive
Combined
with
anti‐PD‐1
antibody,
synergistic
efficacy
is
achieved
in
both
inflamed
colorectal
noninflamed
metastatic
breast
models.
rechallenging
tumor‐free
animals
homotypic
cells
induced
complete
rejection,
indicating
generation
systemic
antitumor
memory.
These
TME‐responsive
may
open
new
avenue
achieve
spatiotemporal
orchestration
activation,
providing
promising
clinical
candidate
for
next‐generation
Advanced Materials,
Год журнала:
2024,
Номер
36(35)
Опубликована: Июнь 27, 2024
Cuproptosis
is
a
novel
copper-dependent
programmed
cell
death.
The
efficacy
of
cuproptosis
highly
dependent
on
intracellular
copper
accumulation
and
counteracted
by
high
level
glutathione
(GSH)
in
tumor
cells.
Here,
this
work
develops
self-amplified
nanoparticles
(Cel-Cu
NP)
using
celastrol
(Cel),
natural
product
isolated
from
medical
plant.
In
Cel-Cu
NP,
Cel
serves
as
versatile
ionophore,
exhibiting
an
ideal
coordination
capacity
toward
ions
without
compromising
the
induction.
Notably,
can
simultaneously
scavenge
GSH
content
to
amplify
cuproptosis.
Moreover,
further
activates
immunogenic
death
(ICD)
elicit
robust
immune
response.
Combining
with
checkpoint
blockade,
NP
effectively
eradicates
metastatic
tumors
mouse
lung
metastasis
model.
This
study
provides
efficient
nanomedicine
inducing
for
immunotherapy.
ACS Nano,
Год журнала:
2023,
Номер
17(16), С. 15449 - 15465
Опубликована: Авг. 2, 2023
Ions
play
a
vital
role
in
regulating
various
biological
processes,
including
metabolic
and
immune
homeostasis,
which
involves
tumorigenesis
therapy.
Thus,
the
perturbation
of
ion
homeostasis
can
induce
tumor
cell
death
evoke
responses,
providing
specific
antitumor
effects.
However,
strategies
that
exploit
effects
multiion
are
rare.
We
herein
prepared
pH-responsive
nanomodulator
by
coloading
curcumin
(CU,
Ca
Bioactive Materials,
Год журнала:
2023,
Номер
32, С. 124 - 146
Опубликована: Окт. 4, 2023
Due
to
its
multiple
features,
including
the
ability
orchestrate
remote
communication
between
different
tissues,
exosomes
are
extracellular
vesicles
arousing
highest
interest
in
scientific
community.
Their
size,
established
as
an
average
of
30-150
nm,
allows
them
be
easily
uptaken
by
most
cells.
According
type
cells-derived
exosomes,
they
may
carry
specific
biomolecular
cargoes
used
reprogram
cells
interacting
with.
In
certain
circumstances,
stimulate
immune
response
facilitating
or
amplifying
release
foreign
antigens-killing
cells,
inflammatory
factors,
antibodies
(immune
activation).
Meanwhile,
other
cases,
efficiently
malignant
elements
such
cancer
mislead
recognition
mechanism,
carrying
and
transferring
their
cancerous
distant
healthy
thus
contributing
antigenic
invasion
suppression).
Exosome
dichotomic
patterns
upon
system
regulation
present
broad
advantages
immunotherapy.
Its
perfect
comprehension,
from
early
biogenesis
interaction
with
recipient
will
promote
a
significant
enhancement
immunotherapy
employing
molecular
biology,
nanomedicine,
nanotechnology.
Abstract
Cuproptosis,
an
emerging
form
of
programmed
cell
death,
has
received
tremendous
attention
in
cancer
therapy.
However,
the
efficacy
cuproptosis
remains
limited
by
poor
delivery
efficiency
copper
ion
carriers.
Herein,
complex
nanoparticles
(denoted
as
Cu(I)
NP)
are
developed
that
can
efficiently
deliver
into
cells
to
induce
cuproptosis.
NP
demonstrate
stimulus‐responsive
release
complexes,
which
results
mitochondrial
dysfunction
and
promotes
aggregation
lipoylated
dihydrolipoamide
S‐acetyltransferase
(DLAT),
leading
Notably,
not
only
cuproptosis,
but
also
elicit
robust
immune
responses
suppress
tumor
growth.
Overall,
this
study
provides
a
promising
strategy
for
cuproptosis‐based
Advanced Materials,
Год журнала:
2024,
Номер
36(21)
Опубликована: Фев. 14, 2024
Activation
of
the
cyclic
GMP-AMP
synthase-stimulator
interferon
genes
(cGAS-STING)
pathway
has
emerged
as
an
efficient
strategy
to
improve
therapeutic
outcomes
immunotherapy.
However,
"constantly
active"
mode
current
STING
agonist
delivery
strategies
typically
leads
off-target
toxicity
and
hyperimmunity.
To
address
this
critical
issue,
herein
a
metal-organic
frameworks-based
nanoagonist
(DZ@A7)
featuring
tumor-specific
near-infrared
(NIR)
light-enhanced
decomposition
is
constructed
for
precisely
localized
activation
photodynamic-metalloimmunotherapy.
The
engineered
enabled
generation
mitochondria-targeted
reactive
oxygen
species
under
NIR
irradiation
specifically
release
mitochondrial
DNA
(mtDNA)
inhibit
repair
nuclear
via
hypoxia-responsive
drugs.
Oxidized
tumor
mtDNA
serves
endogenous
danger-associated
molecular
pattern
that
activates
cGAS-STING
pathway.
Concurrently,
NIR-accelerated
zinc
ions
overloading
in
cancer
cells
further
enhance
cGAS
enzymatic
activity
through
metalloimmune
effects.
By
combining
synergistically
enhanced
triggered
by
irradiation,
facilitated
maturation
dendritic
infiltration
cytotoxic
T
lymphocytes
primary
eradication,
which
also
established
long-term
anti-tumor
immunity
suppress
metastasis.
Therefore,
developed
NIR-triggered,
agonist-free,
tandem-amplified
pathway,
thereby
offering
distinct
paradigm