Bioengineering,
Год журнала:
2022,
Номер
9(11), С. 691 - 691
Опубликована: Ноя. 15, 2022
Calcium
carbonate
nanoparticles
have
been
widely
used
in
biomedicine
due
to
their
biocompatibility
and
biodegradability.
Recently,
calcium
are
largely
integrated
with
imaging
contrast
therapeutic
agents
for
various
approaches.
In
this
review,
we
first
described
the
advantages
preparation
methods
of
nanoparticles,
then
state-of-the-art
progress
diagnosis,
treatment
theranostics
was
summarized.
Finally,
discussed
challenges
recommendations
future
studies
nanoparticles.
Theranostics,
Год журнала:
2023,
Номер
13(15), С. 5386 - 5417
Опубликована: Янв. 1, 2023
Stimuli-activatable
strategies
prevail
in
the
design
of
nanomedicine
for
cancer
theranostics.Upon
exposure
to
endogenous/exogenous
stimuli,
stimuli-activatable
could
be
self-assembled,
disassembled,
or
functionally
activated
improve
its
biosafety
and
diagnostic/therapeutic
potency.A
myriad
tumor-specific
features,
including
a
low
pH,
high
redox
level,
overexpressed
enzymes,
along
with
exogenous
physical
stimulation
sources
(light,
ultrasound,
magnet,
radiation)
have
been
considered
nano-medicinal
products.Recently,
novel
stimuli
explored
elegant
designs
emerged
nanomedicine.In
addition,
multi-functional
theranostic
has
employed
imaging-guided
image-assisted
antitumor
therapy.In
this
review,
we
rationalize
development
clinical
pressing
needs.Stimuli-activatable
self-assembly,
disassembly
functional
activation
approaches
developing
realize
better
efficacy
are
elaborated
state-of-the-art
advances
their
structural
detailed.A
reflection,
status,
future
perspectives
provided.
Theranostics,
Год журнала:
2023,
Номер
13(6), С. 1774 - 1808
Опубликована: Янв. 1, 2023
Metabolic
reprogramming
is
one
of
the
most
important
hallmarks
malignant
tumors.Specifically,
lipid
metabolic
has
marked
impacts
on
cancer
progression
and
therapeutic
response
by
remodeling
tumor
microenvironment
(TME).In
past
few
decades,
immunotherapy
revolutionized
treatment
landscape
for
advanced
cancers.Lipid
plays
pivotal
role
in
regulating
immune
to
immunotherapy.Here,
we
systematically
reviewed
characteristics,
mechanism,
cells
TME,
appraised
effects
various
cell
death
modes
(specifically
ferroptosis)
metabolism,
summarized
antitumor
therapies
targeting
metabolism.Overall,
profound
microenvironment;
therefore,
may
lead
development
innovative
clinical
applications
including
sensitizing
immunotherapy.
Nature Communications,
Год журнала:
2023,
Номер
14(1)
Опубликована: Авг. 23, 2023
The
exogenous
excitation
requirement
and
electron-hole
recombination
are
the
key
elements
limiting
application
of
catalytic
therapies.
Here
a
tumor
microenvironment
(TME)-specific
self-triggered
thermoelectric
nanoheterojunction
(Bi0.5Sb1.5Te3/CaO2
nanosheets,
BST/CaO2
NSs)
with
self-built-in
electric
field
facilitated
charge
separation
is
fabricated.
Upon
exposure
to
TME,
CaO2
coating
undergoes
rapid
hydrolysis,
releasing
Ca2+,
H2O2,
heat.
resulting
temperature
difference
on
BST
NSs
initiates
effect,
driving
reactive
oxygen
species
production.
H2O2
not
only
serves
as
substrate
supplement
for
ROS
generation
but
also
dysregulates
Ca2+
channels,
preventing
efflux.
This
further
exacerbates
calcium
overload-mediated
therapy.
Additionally,
promotes
DC
maturation
antigen
presentation,
facilitating
immunotherapy.
It
worth
noting
that
NP
hydrolyzes
very
slowly
in
normal
cells,
O2
without
causing
any
adverse
effects.
Tumor-specific
combined
therapy,
ion
interference
immunotherapy
exhibit
excellent
antitumor
performance
female
mice.
Advanced Materials,
Год журнала:
2023,
Номер
35(21)
Опубликована: Март 13, 2023
Abstract
The
acidic
microenvironment
of
tumors
significantly
reduces
the
anti‐tumor
effect
immunotherapy.
Herein,
a
hierarchically
structured
fiber
device
is
developed
as
local
drug
delivery
system
for
remodeling
tumor
(TME)
to
improve
therapeutic
Proton
pump
inhibitors
in
matrix
can
be
sustainedly
released
inhibit
efflux
intracellular
H
+
from
cells,
resulting
TME.
targeted
micelles
and
M1
macrophage
membrane‐coated
nanoparticles
internal
cavities
induce
immunogenic
cell
death
(ICD)
cells
phenotypic
transformation
tumor‐associated
macrophages
(TAMs),
respectively.
relief
acidity
TME
further
promotes
ICD
polarization
TAMs,
alleviating
immunosuppressive
synergistically
enhancing
antitumor
immune
response.
In
vivo
results
reveal
this
restores
pH
value
6.8
7.2
exhibit
an
excellent
immunotherapeutic
effect.
Advanced Functional Materials,
Год журнала:
2024,
Номер
34(19)
Опубликована: Янв. 18, 2024
Abstract
Hydrogen
sulfide
(H
2
S)
is
being
progressively
integrated
as
an
emerging
inhibitor
of
the
electron
transport
chain
in
energy
interference‐based
tumor
therapy.
However,
metabolic
reprogramming
cancer
cells
causes
both
oxidative
phosphorylation
(OXPHOS)
and
glycolysis
to
occur
simultaneously,
which
contributes
ineffective
therapeutic
effect
blocking
a
single
pathway.
To
achieve
complete
suppression
production,
inorganic
H
S
donor
ZnS@ZIF‐8@CaP
nanoparticle
(ZSZC
NP)
carrying
Ca
Zn
constructed
for
achieving
simultaneous
interference
OXPHOS
glycolysis.
The
core–shell
ZSZC
nanoparticles
can
break
down
microenvironment.
This
leads
sustained
release
calcium
overload
disrupt
normal
functioning
mitochondria
by
inhibiting
expression
cytochrome
c
causing
damage
mitochondrial
membrane
potential.
Meanwhile,
presence
2+
hinders
typical
process
impeding
lactate
dehydrogenase
glyceraldehyde‐3‐phosphate
dehydrogenase.
synchronous
hampers
supply
cells.
Additionally,
expedite
necrosis
vivo
inducing
cellular
acidification
calcification.
Therefore,
this
energy‐blocking
strategy
will
completely
deplete
reserves
provide
new
insights
exploring
bioenergetic
inhibition
treatment
approach.
ACS Nano,
Год журнала:
2024,
Номер
18(9), С. 6975 - 6989
Опубликована: Фев. 20, 2024
Regarded
as
one
of
the
hallmarks
tumorigenesis
and
tumor
progression,
evasion
apoptotic
cell
death
would
also
account
for
treatment
resistance
or
failure
during
cancer
therapy.
In
this
study,
a
Ca2+/Cu2+
dual-ion
"nano
trap"
to
effectively
avoid
apoptosis
by
synchronously
inducing
paraptosis
together
with
was
successfully
designed
fabricated
breast
treatment.
brief,
disulfiram
(DSF)-loaded
amorphous
calcium
carbonate
nanoparticles
(NPs)
were
via
gas
diffusion
method.
Further
on,
Cu2+-tannic
acid
metal
phenolic
network
embedded
onto
NPs
surface
self-assembling,
followed
mDSPE-PEG/lipid
capping
form
DSF-loaded
dual-ions
trap".
The
as-prepared
nanotrap
undergo
acid-triggered
biodegradation
upon
being
endocytosed
cells
within
lysosome
Ca2+,
Cu2+,
DSF
releasing
simultaneously.
released
Ca2+
could
cause
mitochondrial
overload
lead
hydrogen
peroxide
(H2O2)
overexpression.
Meanwhile,
Ca2+/reactive
oxygen
species-associated
dysfunction
death.
Most
importantly,
be
further
induced
strengthened
toxic
dithiocarbamate
(DTC)–copper
complexes
formed
Cu2+
combined
DTC,
metabolic
products
DSF.
Additionally,
will
reduced
intracellular
glutathione
generate
Cu+,
which
can
catalyze
H2O2
produce
hydroxyl
radical
Cu+-mediated
Fenton-like
reaction
apoptosis.
Both
in
vitro
cellular
assays
vivo
antitumor
evaluations
confirmed
therapeutic
efficiency
dual
ion
nano
trap.
This
study
broaden
cognition
scope
dual-ion-mediated
multifunctional
nanoplatform.
Advanced Materials,
Год журнала:
2024,
Номер
36(24)
Опубликована: Март 19, 2024
Abstract
The
introduction
of
glucose
oxidase,
exhibiting
characteristics
consumption
and
H
2
O
production,
represents
an
emerging
antineoplastic
therapeutic
approach
that
disrupts
nutrient
supply
promotes
efficient
generation
reactive
oxygen
species
(ROS).
However,
the
instability
natural
enzymes
their
low
efficacy
significantly
impede
broader
application.
In
this
context,
2D
Ca
Mn
8
16
nanosheets
(CMO
NSs)
designed
engineered
to
serve
as
a
high‐performance
nanozyme,
enhancing
enzyodynamic
effect
for
ferroptosis–apoptosis
synergistic
tumor
therapy,
are
presented.
addition
mimicking
activities
glutathione
peroxidase,
catalase,
CMO
NSs
exhibit
oxidase‐mimicking
activities.
This
feature
contributes
antitumor
performance
through
cascade
catalytic
reactions,
involving
disruption
supply,
self‐supply
,
subsequent
ROS
generation.
exogenous
2+
released
from
NSs,
along
with
endogenous
enrichment
induced
by
peroxidase‐
collectively
mediate
overload,
leading
apoptosis.
Importantly,
ferroptosis
process
is
triggered
synchronously
output
consumption.
application
ultrasound
stimulation
further
enhances
efficiency
treatment.
work
underscores
crucial
role
in
therapy
against
tumors.
Abstract
Although
immunogenic
cell
death
(ICD)
inducers
evidently
enhance
the
effectiveness
of
immunotherapy,
their
potential
is
increasingly
restricted
by
development
apoptosis
resistance
in
tumor
cells,
poor
immunogenicity,
and
low
T‐cell
immune
responsiveness.
In
this
study,
for
first
time,
piezoelectrically
catalyzed
Mg
2+
‐doped
hydroxyapatite
(Mg‐HAP)
nanoparticles,
which
are
coated
with
a
mesoporous
silica
layer
loaded
ONC201
as
an
agonist
to
specifically
target
receptor
DR5
on
ultimately
developing
Mg‐HAP@MS/ONC201
nanoparticle
(MHMO
NP)
system,
engineered.
Owing
its
excellent
piezoelectric
properties,
MHMO
facilitates
release
significant
amount
reactive
oxygen
species
Ca
within
effectively
promoting
upregulation
expression
inducing
necroptosis
overcome
resistance.
Concurrently,
released
microenvironment
promotes
CD8
+
T
activation
response
antitumor
reaction
induced
ICD.
Using
RNA‐seq
analysis,
it
elucidated
that
can
activate
NF‐κB
pathway
under
catalysis,
thus
M1‐type
macrophage
polarization.
summary,
dual‐targeting
therapy
system
targets
both
cells
catalysis
designed.
This
holds
substantial
advancements
immunotherapy.