Nano Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 13, 2024
Elevated
production
of
extracellular
matrix
(ECM)
in
tumor
stroma
is
a
critical
obstacle
for
drug
penetration.
Here
we
demonstrate
that
ATP-citrate
lyase
(ACLY)
significantly
upregulated
cancer-associated
fibroblasts
(CAFs)
to
produce
ECM.
Using
self-assembling
nanoparticle-design
approach,
carrier-free
nanoagent
(CFNA)
fabricated
by
simply
assembling
NDI-091143,
specific
ACLY
inhibitor,
and
doxorubicin
(DOX)
or
paclitaxel
(PTX),
the
first-line
chemotherapeutic
drug,
via
multiple
noncovalent
interactions.
After
arriving
at
CAFs-rich
site,
NDI-091143-mediated
inhibition
CAFs
can
block
de
novo
synthesis
fatty
acid,
thereby
dampening
acid-involved
energy
metabolic
process.
As
lack
enough
energy,
energetic
will
be
dispirited
state
unable
abundant
ECM,
improving
perfusion
tumors
enhancing
efficacy
chemotherapy.
Such
simple
strategy
aimed
CAFs'
ACLY-mediated
metabolism
pathway
presents
feasibility
stromal
reduction
potentiate
Theranostics,
Journal Year:
2024,
Volume and Issue:
15(3), P. 993 - 1016
Published: Dec. 2, 2024
Immunotherapy
has
transformed
current
cancer
management,
and
it
achieved
significant
progress
over
last
decades.
However,
an
immunosuppressive
tumor
microenvironment
(TME)
diminishes
the
effectiveness
of
immunotherapy
by
suppressing
activity
immune
cells
facilitating
immune-evasion.
Adenosine
monophosphate-activated
protein
kinase
(AMPK),
a
key
modulator
cellular
energy
metabolism
homeostasis,
gained
growing
attention
in
anti-tumor
immunity.
Metformin
is
usually
considered
as
cornerstone
diabetes
its
role
activating
AMPK
pathway
also
been
extensively
explored
therapy
although
findings
on
remain
inconsistent.
nanomedicine
formulation
found
to
hold
potential
reprogramming
TME
through
immunometabolic
modulation
both
cells.
This
review
elaborates
foundation
via
metformin-based
nanomedicines,
offering
valuable
insights
for
next
generation
therapy.
Small Methods,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 28, 2025
Abstract
Non‐small
cell
lung
cancer
(NSCLC)
has
a
strikingly
high
incidence
rate
globally.
Although
immunotherapy
brings
great
breakthrough
in
its
clinical
treatment
of
NSCLC,
significant
challenges
still
need
to
be
overcome.
The
development
novel
multi‐functional
nanomedicines
the
realm
tumor
offers
promising
opportunities
for
NSCLC
patients,
as
exhibit
advantages,
including
specific
targeting
cells,
improved
drug
bioavailability,
reduced
systemic
toxicity,
and
overcoming
immune
resistance.
In
this
review,
core
features
current
status
strategies
checkpoint
blockade,
antibody–drug
conjugates,
engagers,
adoptive
vaccines,
are
surveyed.
Particular
emphasis
is
placed
on
recent
that
boost
these
strategies.
Nanomedicine
can
provide
perspectives
immunotherapy.
International Journal of Biological Sciences,
Journal Year:
2025,
Volume and Issue:
21(6), P. 2606 - 2628
Published: March 24, 2025
Natural
killer
(NK)
cells
have
emerged
as
a
novel
and
effective
treatment
for
breast
cancer.
Nevertheless,
the
cancer
tumor
microenvironment
(TME)
manifests
multiple
immunosuppressive
mechanisms,
impeding
proper
execution
of
NK
cell
functions.
This
review
summarizes
recent
research
on
influence
TME
functionality
in
It
delves
into
effects
internal
environment
elucidates
roles
diverse
stromal
components,
immune
cells,
signaling
molecules
regulating
activity
within
TME.
also
therapeutic
strategies
based
small-molecule
inhibitors,
antibody
therapies,
natural
products,
well
progress
preclinical
clinical
trials.
By
enhancing
our
understanding
formulating
to
counteract
its
effects,
we
could
fully
harness
promise
treatment.
Molecular Pharmaceutics,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 17, 2025
Malignant
tumors
pose
a
considerable
threat
to
human
life
and
health.
Traditional
treatments,
such
as
radiotherapy
chemotherapy,
often
lack
specificity,
leading
collateral
damage
normal
tissues.
Tumor
microenvironment
(TME)
is
characterized
by
hypoxia,
acidity,
redox
imbalances,
elevated
ATP
levels
factors
that
collectively
promote
tumor
growth
metastasis.
This
review
provides
comprehensive
overview
of
the
nanoparticles
developed
in
recent
years
for
TME-responsive
strategies
or
TME-modulating
methods
therapy.
The
focus
on
designing
synthesizing
can
interact
with
achieve
precisely
controlled
drug
release.
These
activate
release
under
specific
conditions
within
environment,
thereby
enhancing
efficacy
drugs
while
reducing
toxicity
cells.
Moreover,
simply
eliminating
cells
does
not
fundamentally
solve
problem.
Only
comprehensively
regulating
TME
make
it
unsuitable
cell
survival
proliferation
we
more
thorough
therapeutic
effects
reduce
risk
recurrence.
regulation
aim
suppress
metastasis
modulating
various
components
TME.
only
improve
treatment
outcomes
but
also
have
potential
lay
foundation
future
personalized
cancer
therapies.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 2, 2025
Higher
and
richer
nutrient
requirements
are
typical
features
that
distinguish
tumor
cells
from
AU:
cells,
ensuring
adequate
substrates
energy
sources
for
cell
proliferation
migration.
Therefore,
deprivation
strategies
based
on
targeted
technologies
can
induce
impaired
viability
in
which
more
sensitive
than
normal
cells.
In
this
review,
nutrients
required
by
related
metabolic
pathways
introduced,
anti-tumor
developed
to
target
described.
addition
the
nutritional
characteristics
of
other
microenvironment
(including
macrophages,
neutrophils,
natural
killer
T
cancer-associated
fibroblasts)
new
also
summarized.
conclusion,
recent
advances
targeting
blockade
reviewed,
challenges
prospects
these
discussed,
theoretical
significance
optimizing
clinical
application
nutrition
strategies.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 17, 2025
Strategically
targeting
lymph
nodes
(LNs)
to
orchestrate
the
initiation
and
regulation
of
adaptive
immune
responses
is
one
most
pressing
challenges
in
context
vaccination.
Herein,
a
series
polymer-TLR
agonist
conjugates
(PTACs)
developed
investigate
impact
dendritic-topological
characteristics
on
their
LN
activity
vivo,
molecular
weight
(MW)
pharmacokinetics
support
homing.
Notably,
dendritic
6-arm
PTAC
with
MW
60
kDa
(6A-PTAC-60k)
rapidly
delivered
cargo
draining
LNs
after
administration
peripheral
tissues.
Specifically,
this
topologic
structure
ameliorated
behavior
within
lymphatic
vessels
LNs,
including
an
elevated
amount
TLR7/8
improved
distribution
pattern
among
barrier
cells
cells,
increased
permeability,
prolonged
retention.
Furthermore,
6A-PTAC-60k
formulation
induced
broad
antibody
T
cell
responses,
enhancing
vaccine
immunogenicity
suppressing
tumor
growth.
The
results
revealed
that
both
topology
polymers
are
crucial
factors
for
immunoadjuvant
functional
which,
turn,
enhanced
formulation.
This
study
may
provide
chemical
structural
basis
optimizing
design
delivery
systems.
Molecular Medicine,
Journal Year:
2025,
Volume and Issue:
31(1)
Published: March 7, 2025
Abstract
Background
Canopy
FGF
signaling
regulator
3
(CNPY3)
has
been
implicated
in
tumor
progression.
However,
its
specific
role
colon
cancer
(CC)
remains
unclear.
This
study
aims
to
investigate
the
function
of
CNPY3
CC
and
potential
as
a
therapeutic
target.
Methods
A
total
201
tissue
specimens
67
adjacent
non-cancerous
tissues
were
collected
for
analysis.
expression
was
assessed
using
immunohistochemistry
quantitative
real-time
PCR.
Functional
assays
conducted
cell
lines
(HT-29
SW-620)
following
knockdown
evaluate
effects
on
proliferation,
migration,
apoptosis.
Gene
profiling,
fibroblast
co-culture
experiments,
vivo
xenograft
models
also
conducted.
Results
Increased
correlated
with
advanced
stages
poorer
prognosis.
Knockdown
significantly
inhibited
induced
apoptosis
lines.
depletion
modulated
behavior,
inhibiting
their
transformation
into
cancer-associated
fibroblasts.
Pathway
analysis
revealed
that
affected
cycle
p53
pathways,
reduced
activation
MAPK
PI3K/AKT
pathways.
Additionally,
enhanced
sensitivity
5-fluorouracil.
In
studies
demonstrated
resulted
smaller
sizes
weights
than
controls.
Conclusions
is
crucial
progression,
correlating
aggressiveness
poor
patient
outcomes.
Targeting
may
offer
promising
strategy
valuable
prognostic
marker
management.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
12(2)
Published: Nov. 18, 2024
Abstract
Phosphate
and
phosphonate
drugs
are
vital
in
building
organisms,
regulating
physiological
processes,
exhibiting
diverse
biological
activities,
including
antiviral,
antibacterial,
antineoplastic,
enzyme‐inhibitory
effects.
However,
their
therapeutic
potential
is
limited
by
the
lack
of
advanced
nanoengineering
technologies.
Herein,
a
competitive
coordination
strategy
for
phosphate/phosphonate
introduced.
By
leveraging
difference
capabilities
between
polyphenols
phosphates/phosphonates
with
metal
ions,
various
phosphate/phosphonate‐based
nanodrugs
using
metal‐phenolic
networks
(MPNs)
as
templates
agents
constructed.
The
dynamic
nature
these
bonds
imparts
stimuli‐responsiveness
to
nanodrugs,
allowing
targeted
release
therapy.
As
proof
concept,
Fe
3+
galangin
used
form
MPN
template,
zoledronic
acid
cGAMP
agents,
DOX
loaded
drug
construct
DOX@Fe‐galangin@Fe‐zoledronic
acid‐cGAMP
nanodrugs.
results
demonstrate
that,
triggering
pyroptosis
activating
cGAS‐STING
pathway,
exhibit
potent
cytotoxicity
accurate
selectivity
eradicating
orthotopic
breast
tumors,
activate
an
antitumor
immune
response
against
lung
bone
metastases.
Because
applicable
variety
it
holds
significant
enhancing
clinical
efficacy
advancing
nanodrug
development
complex
applications.