Drug Delivery Systems Based on Metal–Organic Frameworks for Tumor Immunotherapy
Ning Yang,
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Zongyan He,
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Tianqun Lang
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et al.
Pharmaceutics,
Journal Year:
2025,
Volume and Issue:
17(2), P. 225 - 225
Published: Feb. 10, 2025
Metal–organic
frameworks
(MOFs)
are
a
class
of
inorganic-organic
hybrid
nanoparticles
formed
by
the
coordination
metal
ions/clusters
and
organic
ligands.
Due
to
their
high
porosities,
large
surface
areas,
adjustable
structures,
responsiveness
light/sound,
etc.,
MOFs
have
shown
great
clinical
potential
in
field
tumor
therapy.
Tumor
immunotherapy
exerts
antitumor
effects
through
reshaping
immune
microenvironment,
showing
significant
preclinical
advantages.
Based
on
mechanisms
immunity
activation,
agents
can
be
divided
into
chemotherapeutic
agents,
immunomodulators,
enzymes,
vaccines
oligonucleotide
drugs,
etc.
Herein,
we
review
MOFs-based
drug
delivery
systems
for
immunotherapy.
The
classification
MOFs,
followed
activation
mechanisms,
first
introduced.
Drug
based
with
different
also
summarized,
especially
synergetic
triggered
loadings.
Furthermore,
merits
drawbacks
strategies
promote
applications
discussed.
Language: Английский
Nanoscale Mixed-Ligand Metal–Organic Framework for X-ray Stimulated Cancer Therapy
Wenyao Zhen,
No information about this author
Ziwan Xu,
No information about this author
Y.Z. Mao
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et al.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 20, 2024
Concurrent
localized
radiotherapy
and
systemic
chemotherapy
are
standards
of
care
for
many
cancers,
but
these
treatment
regimens
cause
severe
adverse
effects
in
patients.
Herein,
we
report
the
design
a
mixed-ligand
nanoscale
metal–organic
framework
(nMOF)
with
ability
to
simultaneously
enhance
radiotherapeutic
trigger
release
potent
chemotherapeutic
under
X-ray
irradiation.
We
synthesized
new
functional
quaterphenyl
dicarboxylate
ligand
conjugated
SN38
(H2QP-SN)
via
hydroxyl
radical-responsive
covalent
linkage.
Because
similar
length
QP-SN
bis(p-benzoato)porphyrin
(DBP)
ligands,
was
incorporated
into
Hf-DBP
nMOF
afford
novel
multifunctional
Hf-DBP-QP-SN
good
biocompatibility.
not
only
enhances
radiation
damage
tumors
unique
radiotherapy-radiodynamic
therapy
(RT-RDT)
process
also
increases
·OH
generation
from
radiolysis
electron-dense
Hf12
secondary
building
units
(SBUs)
chemotherapy.
Elevated
levels
hydrogen
peroxide
tumor
microenvironment
further
stimulate
by
enhancing
With
low
doses
irradiation,
suppressed
growth
CT26
colon
4T1
breast
93.5%
95.2%,
respectively,
without
any
sign
general
toxicity.
Our
study
highlights
potential
using
ionizing
radiation-mediated
chemistry
on-demand
activation
nanotherapeutics
synergistic
causing
effects.
Language: Английский
Nanocarrier-mediated modulation of cGAS-STING signaling pathway to disrupt tumor microenvironment
Naunyn-Schmiedeberg s Archives of Pharmacology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 5, 2025
Language: Английский
Unleashing the Potential of Metal Ions in cGAS-STING Activation: Advancing Nanomaterial-Based Tumor Immunotherapy
Xingyin Li,
No information about this author
Shaojie Xu,
No information about this author
Ziliang Su
No information about this author
et al.
ACS Omega,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 17, 2025
Immunotherapy
is
a
critical
modality
in
cancer
treatment
with
diverse
activation
pathways.
In
recent
years,
the
stimulator
of
interferon
genes
(STING)
signaling
pathway
has
exhibited
significant
potential
tumor
immunotherapy.
This
exerts
notable
antitumor
effects
by
activating
innate
and
adaptive
immunity
regulating
immune
microenvironment.
Various
metal
ions
have
been
identified
as
effective
activators
STING
and,
through
design
synthesis
nanodelivery
platforms,
applied
immunotherapy
well
combination
therapies,
such
chemotherapy,
chemodynamic
therapy,
photodynamic
vaccines.
Metal
nanomaterials
showcase
unique
advantages
immunotherapy;
however,
there
are
still
aspects
that
require
optimization.
review
systematically
examines
existing
metal-based
nanomaterials,
elaborates
on
mechanisms
which
different
activate
pathway,
discusses
their
application
models
therapies.
We
also
provide
comparative
analysis
over
other
methods.
Our
exploration
highlights
broad
prospects
treatment,
offering
new
insights
directions
for
advancement
Language: Английский
Radiotherapy-induced alterations in tumor microenvironment: metabolism and immunity
Jinpeng Chen,
No information about this author
Sheng Wang,
No information about this author
Yue Ding
No information about this author
et al.
Frontiers in Cell and Developmental Biology,
Journal Year:
2025,
Volume and Issue:
13
Published: April 28, 2025
Tumor
metabolism
plays
a
pivotal
role
in
shaping
immune
responses
within
the
tumor
microenvironment
influencing
progression,
evasion,
and
efficacy
of
cancer
therapies.
Radiotherapy
has
been
shown
to
impact
both
modulation,
often
inducing
activation
through
damage-associated
molecular
patterns
STING
pathway.
In
this
study,
we
analyse
particular
characteristics
tumour
metabolic
its
effect
on
microenvironment.
We
also
review
changes
that
are
induced
by
radiotherapy,
with
focus
sensitisation
effects
radiotherapy.
Our
aim
is
contribute
development
research
ideas
field
radiotherapy
metabolic-immunological
studies.
Language: Английский
Multipath Synergistic Immune Activation of Hydrogels Delivering STING Agonist and siXkr8 for Long‐Lasting Colorectal Cancer Therapy
Ning Yang,
No information about this author
Xiaolong Feng,
No information about this author
Lixuan Yin
No information about this author
et al.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 24, 2025
Abstract
Colorectal
cancer
(CRC)
poses
a
significant
threat
to
global
public
health,
and
immunotherapy
has
emerged
as
promising
alternative
its
treatment.
Nevertheless,
owing
the
tumor
immunosuppressive
microenvironment
(TIME),
efficacy
of
single‐agent
remains
limited.
Herein,
CSZ@Gel
is
designed
by
co‐loading
cyclic
diguanosine
(CDG)
siXkr8
in
zeolitic
imidazolate
framework‐8
(ZIF‐8)
nanoparticles
subsequently
integrating
them
into
α‐tocopherol
polyethylene
glycol
succinate
(TPGS)
hydrogels.
ZIF‐8
found
undergo
degradation
under
acidic
conditions
releasing
cargo
Zn
2+
induce
cell
pyroptosis.
CDG
triggers
activation
stimulator
interferon
genes
(STING)
pathway,
leading
enhanced
release
proinflammatory
cytokines
release,
dendritic
(DC)
maturation
CD8
+
T
infiltration.
inhibits
expression
scramblase
mXkr8
decreases
phosphatidylserine
translocation
surface,
thus
decreasing
immature
DCs
regulatory
cells
(Tregs)
reversing
TIME.
In
murine
CRC
model,
exhibits
growth
suppression
effects,
extends
median
survival
time
mice
more
than
60
days,
significantly
recurrence
after
resection
long‐term
synergistic
anti‐tumor
immune
activation.
These
findings
suggest
that
provides
an
innovative
drug
delivery
platform
with
clinical
translation
potential
through
comprehensive
strategies
for
sustained
immunotherapy.
Language: Английский
Antimony Component Schottky Nanoheterojunctions as Ultrasound‐Heightened Pyroptosis Initiators for Sonocatalytic Immunotherapy
Jihu Nie,
No information about this author
Nailin Yang,
No information about this author
Shumin Sun
No information about this author
et al.
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 21, 2024
Abstract
Pyroptosis,
an
inflammatory
modality
of
programmed
cell
death
associated
with
the
immune
response,
can
be
initiated
by
bioactive
ions
and
reactive
oxygen
species
(ROS).
However,
ion‐induced
pyroptosis
lacks
specificity,
further
exploration
other
that
induce
in
cancer
cells
is
needed.
Sonocatalytic
therapy
(SCT)
holds
promise
due
to
its
exceptional
penetration
depth;
however,
rapid
recombination
electron‐hole
(e
−
‐h
+
)
pairs
complex
tumor
microenvironment
(TME)
impede
broader
application.
Herein,
we
discovered
antimony
(Sb)‐based
nanomaterials
induced
cells.
Therefore,
Schottky
heterojunctions
containing
Sb
component
(Sb
2
Se
3
@Pt)
were
effectively
designed
constructed
via
situ
growth
platinum
(Pt)
nanoparticles
(NPs)
on
semiconductor
narrow
band
gaps,
which
utilized
as
US‐heightened
initiators
highly
effective
boost
SCT‐immunotherapy.
Under
US
irradiation,
excited
electrons
transferred
from
nanorods
(NRs)
co‐catalyst
Pt
junctions,
bending
prevented
electron
backflow
achieved
efficient
ROS
generation.
Moreover,
pores
oxidized
depleted
overexpressed
GSH
TME,
potentially
amplifying
The
biological
effects
@Pt
nanoheterojunction
itself
combined
sonocatalytic
amplification
oxidative
stress
significantly
Caspase‐1/GSDMD‐dependent
SCT
treatment
not
only
restrained
proliferation
but
also
potent
memory
responses
suppressed
recurrence.
Furthermore,
integration
this
innovative
strategy
checkpoint
blockade
(ICB)
elicited
a
systemic
augmenting
therapeutic
impeding
abscopal
tumors.
Overall,
study
provides
opportunities
explore
pyroptosis‐mediated
Language: Английский
Bifunctional Metal‐Organic Framework Synergistically Enhances Radiotherapy and Activates STING for Potent Cancer Radio‐Immunotherapy
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 8, 2024
Abstract
The
activation
of
the
stimulator
interferon
genes
(STING)
protein
by
cyclic
dinucleotide
metabolites
plays
a
critical
role
in
antitumor
immunity.
However,
synthetic
STING
agonists
like
4‐(5,6‐dimethoxybenzo[b]thiophen‐2‐yl)‐4‐oxobutanoic
acid
(MSA‐2)
exhibit
suboptimal
pharmacokinetics
and
fail
to
sustain
tumors
for
effective
responses.
Here,
we
report
design
MOF/MSA‐2,
bifunctional
MSA‐2
conjugated
nanoscale
metal–organic
framework
(MOF)
based
on
Hf
6
secondary
building
units
(SBUs)
hexakis(4′‐carboxy[1,1′‐biphenyl]‐4‐yl)benzene
bridging
ligands,
potent
cancer
radio‐immunotherapy.
By
leveraging
high‐Z
properties
SBUs,
MOF
enhances
therapeutic
effect
X‐ray
radiation
elicits
immune
stimulation
tumor
microenvironment.
MOF/MSA‐2
further
radiotherapeutic
effects
X‐rays
enabling
sustained
promoting
infiltration
cells
tumors.
plus
low‐dose
irradiation
strong
regression,
when
combined
with
an
checkpoint
inhibitor,
effectively
suppresses
both
primary
distant
through
systemic
activation.
Language: Английский
Bifunctional Metal‐Organic Framework Synergistically Enhances Radiotherapy and Activates STING for Potent Cancer Radio‐Immunotherapy
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 8, 2024
Abstract
The
activation
of
the
stimulator
interferon
genes
(STING)
protein
by
cyclic
dinucleotide
metabolites
plays
a
critical
role
in
antitumor
immunity.
However,
synthetic
STING
agonists
like
4‐(5,6‐dimethoxybenzo[b]thiophen‐2‐yl)‐4‐oxobutanoic
acid
(MSA‐2)
exhibit
suboptimal
pharmacokinetics
and
fail
to
sustain
tumors
for
effective
responses.
Here,
we
report
design
MOF/MSA‐2,
bifunctional
MSA‐2
conjugated
nanoscale
metal–organic
framework
(MOF)
based
on
Hf
6
secondary
building
units
(SBUs)
hexakis(4′‐carboxy[1,1′‐biphenyl]‐4‐yl)benzene
bridging
ligands,
potent
cancer
radio‐immunotherapy.
By
leveraging
high‐Z
properties
SBUs,
MOF
enhances
therapeutic
effect
X‐ray
radiation
elicits
immune
stimulation
tumor
microenvironment.
MOF/MSA‐2
further
radiotherapeutic
effects
X‐rays
enabling
sustained
promoting
infiltration
cells
tumors.
plus
low‐dose
irradiation
strong
regression,
when
combined
with
an
checkpoint
inhibitor,
effectively
suppresses
both
primary
distant
through
systemic
activation.
Language: Английский
Radiation-induced aerobic oxidation via solvent-derived peroxyl radicals
Yang Xu,
No information about this author
Bo‐Shuai Mu,
No information about this author
Zhiyu Tu
No information about this author
et al.
Chemical Science,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 23, 2024
Solvent-derived
peroxyl
radicals
(R
sol
OO·),
a
new
group
of
reactive
oxygen
species
(ROS),
enable
the
radiation-induced
aerobic
oxidation
strategy.
Language: Английский