International Journal of Nanomedicine,
Journal Year:
2024,
Volume and Issue:
Volume 19, P. 13805 - 13821
Published: Dec. 1, 2024
Liver
cancer
has
become
a
major
global
health
challenge
due
to
its
high
incidence,
rate
of
late
diagnosis
and
limited
treatment
options.
Although
there
are
many
clinical
treatments
available
for
liver
cancer,
the
cure
is
still
very
low,
now
researchers
have
begun
explore
new
aspects
treatment,
nanotechnology
shown
great
potential
improving
diagnostic
accuracy
therapeutic
efficacy
therefore
promising
option.
In
diagnosis,
nanomaterials
such
as
gold
nanoparticles,
magnetic
silver
nanoparticles
can
realize
highly
sensitive
specific
detection
biomarkers,
supporting
real-time
monitoring
disease
process.
terms
nanocarriers
precise
targeted
delivery
drugs,
improve
bioavailability
drugs
reduce
systemic
toxic
side
effects.
addition,
advanced
technologies
nanoparticle-based
photothermal
therapy
photodynamic
provide
innovative
solutions
overcome
drug
resistance
local
tumor
ablation.
Therefore,
in
this
paper,
we
will
introduce
hepatocellular
carcinoma
marker
detection,
delivery,
synergistic
PDT/CDT
therapy.
APL Bioengineering,
Journal Year:
2025,
Volume and Issue:
9(1)
Published: March 1, 2025
Cancer-associated
fibroblasts
(CAFs)
play
a
crucial
role
in
the
tumor
microenvironment
by
promoting
growth,
immune
evasion,
and
metastasis.
Recently,
drug
delivery
systems
targeting
CAFs
have
emerged
as
promising
long-term
effective
approach
to
cancer
treatment.
Advances
nanotechnology,
particular,
led
development
of
nanomedicine
designed
specifically
target
CAFs,
offering
new
possibilities
for
precise
personalized
therapies.
This
article
reviews
recent
progress
using
nanocarriers
that
CAFs.
Additionally,
we
explore
potential
combining
multiple
therapies,
such
chemotherapy
immunotherapy,
with
enhance
efficacy
overcome
resistance.
Although
many
preclinical
studies
show
promise,
clinical
application
still
faces
considerable
challenges,
especially
terms
penetration
large-scale
production.
Therefore,
this
review
aims
provide
fresh
perspective
on
CAF-targeted
highlight
future
research
directions
applications.
Biology,
Journal Year:
2025,
Volume and Issue:
14(4), P. 351 - 351
Published: March 28, 2025
CCA
is
a
highly
desmoplastic
malignant
cancer
and
the
second
most
common
primary
liver
malignancy
after
hepatocellular
carcinoma
(HCC),
accounting
for
approximately
15%
of
all
tumors.
has
poor
prognosis,
with
an
average
five-year
survival
rate
9%,
which
lower
than
that
pancreatic
cancer.
Although
considerable
efforts
have
been
invested
into
genomics,
epigenetics,
risk
factors,
very
little
known
about
what
might
key
causes
high
level
CCA.
In
this
review,
we
analyze
incidence
mortality
in
different
regions
based
on
data
from
1994
to
2022
obtained
International
Agency
Research
Cancer
(IARC),
discuss
current
status
treatment
disease,
focus
be
main
factors
contributing
CCA:
alkalosis
caused
by
Fenton
reaction,
hypoxia,
TIME.
The
review
includes
studies
published
1979
2024,
aiming
provide
updated
synthesis
basic
early
classical
theoretical
knowledge
By
revealing
epidemiological
characteristics
CCA,
potential
mechanisms
malignancy,
challenges
treatment,
aims
new
directions
future
research,
promote
development
personalized
strategies,
facilitate
deeper
understanding
more
effective
management
worldwide.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 14, 2025
Heat
shock
protein
70
(HSP70)
is
a
highly
conserved
molecular
chaperone
that
plays
core
role
in
assisting
folding
and
maintaining
cellular
homeostasis.
In
recent
years,
studies
have
revealed
HSP70
has
dual
functions
immune
regulation:
on
the
one
hand,
it
enhances
responses
by
activating
non-specific
immunity
(such
as
Toll-like
receptor
2/4
(TLR2/4)
signaling
pathways)
specific
cross-presentation
of
antigens,
T
helper
1
(Th1)/T
17
(Th17)
differentiation);
other
inhibits
excessive
reactions
inducing
differentiation
regulatory
cells
(Treg)
promoting
secretion
anti-inflammatory
factors
[such
interleukin-10
(IL-10)].
cancer,
duality
also
very
prominent:
can
drive
tumor
progression
through
pathways
such
inhibiting
apoptosis,
angiogenesis,
metastasis,
inhibit
growth
immunogenic
cell
death
(ICD),
enhancing
antigen
presentation,
natural
killer
(NK)
activity.
This
review
aims
to
systematically
analyze
HSP70,
focusing
its
mechanisms
“double-edged
sword”
nature
immunotherapy
innovative
targeted
strategies,
well
providing
theoretical
basis
research
directions
for
precision
medicine
treatment
strategies
related
diseases.
Clinical and Translational Science,
Journal Year:
2025,
Volume and Issue:
18(4)
Published: April 1, 2025
ABSTRACT
TIGIT
(T
cell
immunoreceptor
with
immunoglobulin
and
tyrosine‐based
inhibitory
motif
(ITIM)
domain),
Vstm3,
VSIG9,
are
newly
recognized
immunological
checkpoints.
They
prominently
expressed
on
CD4+
CD8+
T
cells,
tumor‐infiltrating
lymphocytes
(TILs),
natural
killer
(NK)
regulatory
cells
(Tregs).
The
(TIGIT)
protein
is
crucial
for
immune
modulation
since
it
diminishes
NK
populations
hinders
activity
in
cancer
patients
experimental
models.
CD155,
the
principal
ligand
of
humans,
has
been
as
a
pivotal
target
immunotherapy
owing
to
its
interaction
TIGIT.
CD155
linked
efficacy
anti‐programmed
death
1
(PD‐1)
therapy,
even
without
expression,
underscoring
importance
checkpoint
suppression.
Anti‐TIGIT
medicines,
either
independently
or
conjunction
anti‐PD‐1
treatments,
have
demonstrated
potential
augmenting
responses
malignancies.
This
review
examines
structural
functional
characteristics
protein,
new
developments
anti‐TIGIT
drugs,
their
prospective
use
immunotherapy.
Pharmaceutics,
Journal Year:
2024,
Volume and Issue:
16(12), P. 1549 - 1549
Published: Dec. 3, 2024
Nanodrug
delivery
systems
have
revolutionized
tumor
therapy
like
never
before.
By
overcoming
the
complexity
of
microenvironment
(TME)
and
bypassing
drug
resistance
mechanisms,
nanotechnology
has
shown
great
potential
to
improve
efficacy
reduce
toxic
side
effects.
This
review
examines
impact
TME
on
recent
advances
in
nanomedicine
overcome
this
challenge.
Characteristics
such
as
hypoxia,
acidity,
high
interstitial
pressure
significantly
effectiveness
chemotherapy
radiotherapy,
leading
increased
cells.
Then,
summarizes
innovative
nanocarrier
designs
for
these
microenvironmental
features,
including
hypoxia-sensitive
nanoparticles,
pH-responsive
carriers,
multifunctional
nanosystems
that
enable
targeted
release
improved
penetration
accumulation
tumors.
combining
with
therapeutic
strategies,
offers
a
novel
perspective
by
focusing
design
nanocarriers
interact
TME,
dimension
often
overlooked
similar
reviews.
We
highlight
dual
role
modulation,
emphasize
their
resistance,
look
at
future
research
directions.
Current Pharmaceutical Design,
Journal Year:
2024,
Volume and Issue:
30(10), P. 727 - 741
Published: March 1, 2024
Abstract:
This
review
investigates
the
revolutionary
application
of
cell
membrane-coated
nanoparticles
(CMNPs)
as
a
promising
avenue
for
cancer
therapy
within
embryonic
landscape
nanotechnology.
Nanoparticles,
pivotal
in
treatment,
are
systematically
examined
their
diverse
physicochemical
structures,
categorized
organic
(lipid-based,
protein-based,
and
polymer-assisted)
inorganic
(carbon-based
metal)
varieties.
A
significant
focus
is
placed
on
CMNPs,
which
serve
an
innovative
drug
delivery
vehicle,
overcoming
limitations
associated
with
conventional
nanoparticle
therapies.
manuscript
accurately
explores
advantages
challenges
various
membranes,
including
those
derived
from
cells,
red
blood
platelets,
stem
white
cells.
Importance
roles
enhancing
precision,
immune
system
circumvention,
targeted
recognition.
Detailed
insights
into
crafting
CMNPs
provided,
elucidating
membrane
extraction
fusion
techniques,
such
sonication,
extrusion,
co-extrusion,
microfluidic
electroporation.
Maintaining
integrity
during
benefits
coating
techniques
augmenting
biocompatibility
underscored.
comprehensive
resource
consolidates
latest
advancements
delivery,
positioning
itself
at
forefront
nanotechnology
biomedicine
research.
Encapsulating
methodologies
like
electrospray,
chemical
conjugation,
this
showcases
expanding
toolbox
available
to
researchers
dynamic
field.
Focusing
unique
characteristics
multifaceted
applications
biomedical
research,
particularly
tumour
therapy.
It
provides
indepth
analysis
stability,
evasion
capabilities,
increased
payload
capacity,
retained
biological
functionality.
The
outlines
current
future
prospects
chemotherapy,
photothermal
photodynamic
therapy,
immunotherapy,
gene
therapeutic
methods.
concludes
by
highlighting
transformative
potential
reshaping
treatment.
Journal of Molecular Pathology,
Journal Year:
2024,
Volume and Issue:
5(4), P. 437 - 453
Published: Oct. 5, 2024
The
extracellular
matrix
is
an
organized
three-dimensional
network
of
protein-based
molecules
and
other
macromolecules
that
provide
structural
biochemical
support
to
tissues.
Depending
on
its
properties,
the
influences
cell
adhesion
signal
transduction
and,
in
general,
can
influence
differentiation
proliferation
through
specific
mechanisms
chemical
mechanical
sensing.
development
body
tissues
during
ontogenesis
accompanied
by
changes
not
only
cells
but
also
composition
properties
matrix.
Similarly,
tumor
carcinogenesis
a
continuous
change
cells,
called
‘oncomatrix’,
as
matures,
from
primary
focus
stage
metastasis.
In
this
paper,
characteristics
are
considered,
well
evolution
patterns
be
used
biomarkers
oncological
diseases
potential
targets
for
promising
anti-tumor
therapies.
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: March 13, 2024
Abstract
Background:
Cancer-associated
fibroblasts
(CAFs)
play
a
critical
role
in
tumor
progression.
In
this
study,
we
explored
the
influence
of
exosomal
piR-35462
(piR-35462)
derived
from
CAFs
on
oral
squamous
cell
carcinoma
(OSCC)
Methods:
and
normal
(NFs)
were
obtained
patients-derived
samples
OSCC
adjacent
tissues.
Exosomes
extracted
NFs
confirmed
piRNAs
was
identified
screened.
CCK8
assays,
EdU
Transwell
assays
performed
to
assess
proliferation
metastasis.
A
nude
mouse
model
established
impact
Results:
CAFs-derived
exosomes
showed
enhanced
expression
promoted
proliferation,
migration
invasion.
Additionally,
elevated
tissues
correlates
with
poor
prognosis.
Mechanistically,
increased
fat
mass
obesity-associated
protein
(FTO)
cells.
By
inhibiting
N6-methyladenosine
(m6A)
RNA
methylation,
overexpression
FTO
further
enhances
stability
levels
Twist1
mRNA,
thereby
contributing
epithelial-mesenchymal
transition
(EMT)
vivo
xenograft
also
same
results.
Conclusion:
The
achieved
outcomes
elucidate
that
can
deliver
containing
cells
promote
progression
via
FTO/Twist
mediated
EMT
pathways,
could
represent
promising
therapeutic
target
for
OSCC.