ACS Nano,
Journal Year:
2024,
Volume and Issue:
18(27), P. 18046 - 18057
Published: June 27, 2024
Tumor
metastasis
remains
a
major
challenge
in
cancer
management.
Among
various
treatment
strategies,
immune
cell-based
therapy
holds
great
potential
for
inhibiting
metastasis.
However,
its
wide
application
is
restricted
by
complex
preparations,
as
well
inadequate
homing
and
controllability.
Herein,
we
present
groundbreaking
approach
bioorthogonally
manipulating
tumor-NK
(natural
killer)
cell
assembly
to
inhibit
tumor
Multiple
dibenzocyclootyne
(DBCO)
groups
decorated
long
single-stranded
DNA
were
tail-modified
on
core–shell
upconversion
nanoparticles
(CSUCNPs)
condensed
photosensitive
chemical
linker
(PC-Linker)
shield
most
of
the
DBCO
groups.
On
one
hand,
light-triggered
scaffolds
formed
cross-linked
network
click
chemistry,
effectively
impeding
migration.
other
efficient
cellular
facilitated
effective
communication
between
cells
NK-92
cells,
leading
enhanced
response
against
tumors
further
suppression
These
features
make
our
strategy
highly
applicable
range
metastatic
cancers.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 24, 2024
The
low
immunogenicity
of
tumors,
along
with
the
abnormal
structural
and
biochemical
barriers
tumor-associated
vasculature,
impedes
infiltration
function
effector
T
cells
at
tumor
site,
severely
inhibiting
efficacy
antitumor
immunotherapy.
In
this
study,
a
cobaloxime
catalyst
STING
agonist
(MSA-2)-coloaded
Wurster-type
covalent
organic
framework
(Co-TB
COF-M)
internal
electron
transfer-enhanced
catalytic
capacity
was
developed
as
COF-based
immune
activator.
covalently
anchored
adjusts
energy
band
structure
TB
COF
provides
it
good
substrate
adsorption
sites,
enabling
to
act
an
transmission
bridge
between
in
proton
reduction
reactions.
This
property
significantly
enhances
sonodynamic
performance.
Under
sono-irradiation,
Co-TB
COF-M
can
produce
substantial
amount
reactive
oxygen
species
(ROS)
induce
Gasdermin
D-mediated
pro-inflammatory
pyroptosis,
thereby
effectively
enhancing
tumors.
Furthermore,
MSA-2
is
specifically
released
response
ROS
minimizing
off-target
side
effects.
More
importantly,
COF-induced
activation
normalizes
vasculature
increases
expression
endothelial
cell
adhesion
molecules,
which
greatly
enhance
cells.
Thus,
activator
could
remold
microenvironment,
leading
increased
improved
for
Journal of drug targeting,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 47
Published: March 13, 2025
Hepatocellular
carcinoma
(HCC)
is
one
of
the
most
lethal
malignancies
worldwide,
characterized
by
its
complex
pathogenesis
and
poor
therapeutic
outcomes.
Despite
recent
advances
in
targeted
molecular
therapies,
immune
checkpoint
inhibitors
(ICIs),
radiotherapy,
conventional
chemotherapy,
five-year
survival
rate
for
this
neoplasm
remains
dismally
low.
The
progress
nanotechnology
has
revolutionized
cancer
treatment
years.
These
provide
unprecedented
opportunities
to
overcome
current
limitations
different
modalities.
This
review
provides
a
comprehensive
analysis
how
interfaces
with
tumor
microenvironment
(TIME)
HCC
can
present
new
frontier
interventions
HCC.
We
critically
overview
latest
developments
nanoparticle-based
delivery
systems
various
drugs
also
other
antitumor
agents
like
thermal
therapy
radiotherapy.
highlight
unique
ability
nanoparticles
modulate
immunosuppressive
(TME)
enhance
efficacy.
Furthermore,
we
analyze
emerging
strategies
that
exploit
nanoformulations
biological
barriers
drug
bioavailability
treatment.
Bioconjugate Chemistry,
Journal Year:
2023,
Volume and Issue:
34(10), P. 1789 - 1801
Published: Sept. 20, 2023
Natural
killer
(NK)
cells
exhibit
a
good
therapeutic
efficacy
against
various
malignant
cancer
cells.
However,
the
of
plain
NK
is
relatively
low
due
to
inadequate
selectivity
for
Therefore,
enhance
targeting
and
anticancer
cells,
we
have
rationally
designed
biomaterial-mediated
ex
vivo
surface
engineering
technique
membrane
decoration
recognition
ligands
onto
Our
lipid
conjugate
biomaterial
contains
three
major
functional
moieties:
(1)
1,2-distearoyl-sn-glycero-3-phosphoethanolamine
(DSPE)
cell
anchoring,
(2)
polyethylene
glycol
intracellular
penetration
blocker,
(3)
lactobionic
acid
(LBA)
recognition.
The
was
successfully
applied
surfaces
(LBA-NK)
functionalities,
especially
toward
asialoglycoprotein
receptor
(ASGPR)-overexpressing
hepatocellular
carcinoma.
Highly
efficient
homogeneous
editing
achieved
with
simple
coating
process
while
maintaining
intrinsic
properties
LBA-NK
showed
potential
ASGPR-mediated
tumor
binding
(through
LBA-ASGPR
interaction)
thereby
significantly
augmented
efficacies
HepG2
liver
Thus,
can
be
novel
strategy
treatment
cancers
via
facilitated
immune
synapse
interactions
in
comparison
currently
available
therapies.
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
136(13)
Published: Jan. 12, 2024
Abstract
Immunotherapy
has
brought
a
new
dawn
for
human
being
to
defeat
cancer.
Although
existing
immunotherapy
regimens
(CAR‐T,
etc.)
have
made
breakthroughs
in
the
treatments
of
hematological
cancer
and
few
solid
tumors
such
as
melanoma,
therapeutic
efficacy
on
most
is
still
far
from
satisfactory.
In
recent
years,
researches
tumor
based
nanocatalytic
materials
are
under
rapid
development,
significant
progresses
been
made.
Nanocatalytic
medicine
demonstrated
be
capable
overcoming
limitations
current
clinicnal
by
using
toxic
chemodrugs,
exhibits
highly
attractive
advantages
over
traditional
therapies,
enhanced
sustained
durable
catalytic
activity,
remarkably
reduced
harmful
side‐effects
without
so
on.
Most
recently,
introduced
immune‐regulation
disease
treatments,
especially,
immunoactivation
therapies.
This
article
presents
immune‐response
activations
medicine‐initiated
chemical
reactions
immunotherapy,
elucidates
mechanism
medicines
regulating
anti‐tumor
immunity.
By
reviewing
research
progress
emerging
field,
this
review
will
further
highlight
great
potential
broad
prospects
nanocatalysis‐based
immune‐therapeutics.