EBioMedicine,
Год журнала:
2024,
Номер
107, С. 105301 - 105301
Опубликована: Авг. 23, 2024
Increasing
evidence
indicates
that
immunotherapy
is
hindered
by
a
hostile
tumor
microenvironment
(TME)
featured
with
deprivation
of
critical
nutrients
and
pooling
immunosuppressive
metabolites.
Tumor
cells
outcompete
immune
effector
for
essential
nutrients.
Meanwhile,
wide
range
cell-derived
toxic
metabolites
exerts
negative
impacts
on
anti-tumor
response,
diminishing
the
efficacy
immunotherapy.
Nanomedicine
excellent
targetability
offers
novel
approach
to
improving
cancer
via
metabolically
reprogramming
TME.
Herein,
we
review
recent
strategies
enhancing
immunotherapeutic
effects
through
rewiring
metabolism
nanomedicine.
Attention
drawn
immunometabolic
tactics
stromal
in
TME
Additionally,
discuss
future
directions
developing
metabolism-regulating
nanomedicine
precise
efficacious
Chemical Society Reviews,
Год журнала:
2021,
Номер
50(16), С. 9152 - 9201
Опубликована: Янв. 1, 2021
Photodynamic
therapy
(PDT)
has
been
extensively
investigated
for
decades
tumor
treatment
because
of
its
non-invasiveness,
spatiotemporal
selectivity,
lower
side-effects,
and
immune
activation
ability.
ACS Nano,
Год журнала:
2021,
Номер
15(3), С. 5735 - 5751
Опубликована: Март 11, 2021
As
next-generation
artificial
enzymes,
nanozymes
have
shown
great
promise
for
tumor
catalytic
therapy.
In
particular,
their
peroxidase-like
activity
has
been
employed
to
catalyze
hydrogen
peroxide
(H2O2)
produce
highly
toxic
hydroxyl
radicals
(•OH)
kill
cells.
However,
limited
by
the
low
affinity
between
with
H2O2
and
level
of
in
microenvironment,
peroxidase
usually
produced
insufficient
•OH
cells
therapeutic
purposes.
Herein,
we
present
a
pyrite
nanozyme
ultrahigh
affinity,
resulting
4144-
3086-fold
increase
compared
that
classical
Fe3O4
natural
horseradish
peroxidase,
respectively.
We
found
also
possesses
intrinsic
glutathione
oxidase-like
activity,
which
catalyzes
oxidation
reduced
accompanied
generation.
Thus,
dual-activity
constitutes
self-cascade
platform
generate
abundant
deplete
glutathione,
induces
apoptosis
as
well
ferroptosis
Consequently,
it
killed
apoptosis-resistant
harboring
KRAS
mutation
inducing
ferroptosis.
The
exhibited
favorable
tumor-specific
cytotoxicity
biodegradability
ensure
its
biosafety.
These
results
indicate
high-performance
is
an
effective
reagent
may
aid
development
nanozyme-based
Angewandte Chemie International Edition,
Год журнала:
2021,
Номер
60(25), С. 14051 - 14059
Опубликована: Апрель 2, 2021
Abstract
Despite
the
promise
of
sonodynamic
processes
in
cancer
therapy,
existing
sonosensitizers
often
fail
to
regulate
generation
reactive
oxygen
species
(ROS)
against
tumors,
potentially
leading
off‐target
toxicity
normal
tissues.
We
report
a
transformable
core‐shell
nanosonosensitizer
(TiO
2
@CaP)
that
reinvigorates
ROS
and
dissolves
its
CaP
shell
release
Ca
2+
an
acidic
tumor
microenvironment
(TME)
under
ultrasound
activation.
Thus,
TiO
@CaP
acts
as
smart
specifically
induces
mitochondrial
dysfunction
via
overloading
intracellular
ions
synergize
with
process
TME.
substantially
enhances
immunogenic
cell
death,
resulting
enhanced
T‐cell
recruitment
infiltration
into
cold
(4T1).
In
conjunction
checkpoint
blockade
therapy
(anti‐PD
1),
@CaP‐mediated
elicits
systemic
antitumor
immunity,
regression
non‐treated
distant
tumors
inhibition
lung
metastasis.
This
work
paves
way
development
“smart”
TME‐activatable
temporospatial
control
over
responses.
Advanced Materials,
Год журнала:
2021,
Номер
33(14)
Опубликована: Фев. 26, 2021
Abstract
Cell‐membrane‐coated
nanoparticles
(CCNPs)
that
integrate
the
biophysiological
advantages
of
cell
membranes
with
multifunctionalities
synthetic
materials
hold
great
promise
in
cancer
immunotherapy.
However,
strategies
have
yet
to
be
revealed
further
improve
their
immunotherapeutic
efficacy.
Herein,
a
polymer
multicellular
nanoengager
(SPNE)
for
synergistic
second‐near‐infrared‐window
(NIR‐II)
photothermal
immunotherapy
is
reported.
The
consists
an
NIR‐II
absorbing
as
core,
which
camouflaged
fused
derived
from
immunologically
engineered
tumor
cells
and
dendritic
(DCs)
vaccine
shell.
In
association
high
accumulation
lymph
nodes
tumors,
engagement
ability
SPNE
enables
effective
cross‐interactions
among
cells,
DCs,
T
leading
augmented
activation
relative
bare
or
tumor‐cell‐coated
nanoparticles.
Upon
deep‐tissue
penetrating
photoirradiation,
eradicates
induces
immunogenic
death,
eliciting
anti‐tumor
immunity.
Such
effect
eventually
inhibits
growth,
prevents
metastasis
procures
immunological
memory.
Thus,
this
study
presents
general
cell‐membrane‐coating
approach
develop
photo‐immunotherapeutic
agents
therapy.
ACS Nano,
Год журнала:
2022,
Номер
16(2), С. 2381 - 2398
Опубликована: Янв. 18, 2022
Ferroptosis
is
a
recently
discovered
route
of
regulated
cell
death
that
offers
the
opportunities
for
treatment
chemotherapy-resistant
tumor
indications,
but
its
efficacy
can
be
affected
by
glutathione
peroxidase
4
(GPX4)
and
ferroptosis
suppressor
protein
1
(FSP1)
antioxidant
mechanisms,
posing
significant
challenges
clinical
translation.
In
this
study,
we
report
Cu-tetra(4-carboxyphenyl)porphyrin
chloride(Fe(III))
(Cu-TCPP(Fe))
metal
organic
framework
(MOF)-based
nanosystem
efficient
incorporation
Au
nanoparticles
(NPs)
RSL3,
which
demonstrate
enzyme-like
activities
to
universally
suppress
antiferroptotic
pathways
in
cells
amplifying
ferroptotic
damage.
Herein,
Cu-TCPP(Fe)
MOF
nanosheets
were
integrated
with
NPs
via
situ
nucleation
loaded
RSL3
π–π
stacking,
eventually
modified
polyethylene
glycol
(PEG)
iRGD
tumor-targeted
drug
delivery.
Specifically,
glucose
oxidase-like
depletion,
thus
disrupting
pentose
phosphate
pathway
impede
reduced
(GSH)
biosynthesis
prevent
recycling
coenzyme
Q10
(CoQ10)
CoQ10H2,
while
Cu
species
oxidize
GSH
into
oxidized
(GSSG).
These
nanocatalytic
lead
simultaneous
inhibition
GPX4/GSH
FSP1/CoQ10H2
cooperate
GPX4-deactivating
function
cause
pronounced
damage,
thereby
providing
strong
rationale
application
therapy
clinic.
Photodynamic
therapy
(PDT)
has
long
been
recognized
to
be
a
promising
approach
for
cancer
treatment.
However,
the
high
oxygen
dependency
of
conventional
PDT
dramatically
impairs
its
overall
therapeutic
efficacy,
especially
in
hypoxic
solid
tumors.
Exploration
distinctive
strategy
involving
both
high-performance
less-oxygen-dependent
photosensitizers
(PSs)
and
prominent
drug
delivery
system
is
an
appealing
yet
significantly
challenging
task.
Herein,
precise
nuclear
targeting
protocol
based
on
type-I
PSs
with
aggregation-induced
emission
(AIE)
characteristics
fabricated
first
time.
Of
two
synthesized
AIE
PSs,
TTFMN
demonstrated
exhibit
superior
property
stronger
reactive
species
(ROS)
generation
efficiency
owing
introduction
tetraphenylethylene
smaller
singlet-triplet
energy
gap,
respectively.
With
aid
lysosomal
acid-activated
TAT-peptide-modified
amphiphilic
polymer
poly(lactic
acid)12k-poly(ethylene
glycol)5k-succinic
anhydride-modified
TAT,
corresponding
TTFMN-loaded
nanoparticles
accompanied
acid-triggered
peculiarity
can
quickly
accumulate
tumor
site,
effectively
generate
ROS
region
suppress
growth
under
white
light
irradiation
minimized
systematic
toxicity.
This
delicate
"Good
Steel
Used
Blade"
tactic
maximizes
efficacy
offers
conceptual
while
practical
paradigm
optimized
treatment
further
translational
medicine.
Chemical Society Reviews,
Год журнала:
2022,
Номер
51(13), С. 5330 - 5350
Опубликована: Янв. 1, 2022
This
tutorial
review
discusses
the
convergence
of
drug
delivery
systems
and
PROTACs,
surveys
burgeoning
PROTAC
strategies,
summarizes
their
design
principles,
clarifies
challenges,
outlooks
future
translational
opportunities.
Advanced Functional Materials,
Год журнала:
2022,
Номер
32(13)
Опубликована: Фев. 1, 2022
Abstract
The
immunosuppression
and
immune
escape
of
current
immunotherapy
result
in
low
efficacy,
ferroptosis
is
greatly
restricted
by
the
reactive
oxygen
species
(ROS)
production
efficiency.
Here,
for
first
time
a
“closed‐loop”
therapy
based
on
photothermal
enhancement
stimulated
each
other
multifunctional
nanoplatform
reported.
This
platform
composed
copper
silicate
iron
mesoporous
hollow
nanospheres,
followed
situ
growth
Au
nanoparticles
loading
an
adjuvant
resiquimod
R848.
laser
irradiation‐mediated
heat
introduction
ions
significantly
enhance
ROS
generation,
leading
to
simultaneous
depletion
glutathione
peroxidase
4
(GPX4)
(GSH).
onset
tumor
cells
thus
enhanced
response
with
immunogenic
cell
death
(ICD)
triggered,
promoting
dendritic
(DCs)
maturation
T
infiltration.
Interferon
γ
(IFN‐γ)
released
from
CD8
+
downregulates
expression
SLC7A11
GPX4,
which
turn
enhances
expression,
constituting
“closed‐Loop”
therapy.
Importantly,
this
system
effective
both
killing
primary
inhibiting
metastasis.
proposed
therapeutic
strategy
may
provide
guidance
design
future
antitumor
nanoplatforms.
Advanced Materials,
Год журнала:
2021,
Номер
33(36)
Опубликована: Июль 23, 2021
Immunometabolic
modulation
offers
new
opportunities
to
treat
cancers
as
it
is
highly
associated
with
cancer
progression
and
immunosuppressive
microenvironment.
However,
traditional
regimens
using
nonselective
small-molecule
immunomodulators
lead
the
off-target
adverse
effects
insufficient
therapeutic
outcomes.
Herein
a
second
near-infrared
(NIR-II)
photothermally
activatable
semiconducting
polymeric
nanoantagonist
(ASPA)
for
synergistic
photothermal
immunometabolic
therapy
of
reported.
ASPA
backbone
obtained
by
conjugating
vipadenant,
an
antagonist
adenosine
A2A
receptor,
onto
NIR-II
light-absorbing
polymer
via
azo-based
thermolabile
linker.
Under
deep-penetrating
photoirradiation,
induces
tumor
thermal
ablation
subsequently
immunogenic
cell
death,
triggers
cleavage
linker,
releases
block
adenosinergic
pathway.
Such
remotely
controlled
regulation
potentiates
cytotoxic
T
functions
while
suppresses
regulatory
activities,
leading
efficient
primary
inhibition,
pulmonary
metastasis
prevention,
long-term
immunological
memory.
Thereby,
this
work
provides
generic
approach
precise
spatiotemporal
immunometabolism.
Advanced Materials,
Год журнала:
2023,
Номер
35(25)
Опубликована: Март 15, 2023
Overcoming
the
resistance
to
apoptosis
and
immunosuppression
of
tumor
cells
is
a
significant
challenge
in
augmenting
effect
cancer
immunotherapy.
Pyroptosis,
lytic
programmed
cell-death
pathway
unlike
apoptosis,
considered
type
immunogenic
cell
death
(ICD)
that
can
intensify
ICD
process
cells,
releasing
dramatically
increased
tumor-associated
antigens
damage-associated
molecular
patterns
promote
Herein,
membrane-targeted
aggregation-induced
emission
photosensitive
dimer
found
be
able
achieve
highly
efficient
under
synergistic
photodynamic
photothermal
therapy.
The
efficiently
produce
type-I
reactive
oxygen
species
(ROS)
by
therapy
hypoxic
tissue,
leading
pyroptosis
direct
membrane
damage,
which
further
reinforced
its
effect.
Furthermore,
enhanced
based
on
completely
eliminate
primary
seventh
day
treatment
also
boost
systemic
antitumor
immunity
generating
immune
memory,
demonstrated
superior
therapeutic
effects
both
solid
tumors
metastatic
when
healing
4T1
mouse
models
with
poor
immunogenicity.