Seminars in Cancer Biology,
Год журнала:
2023,
Номер
97, С. 50 - 67
Опубликована: Ноя. 11, 2023
Pancreatic
ductal
adenocarcinoma
(PDAC)
is
an
extremely
deadly
form
of
cancer,
with
limited
progress
in
5-year
survival
rates
despite
significant
research
efforts.
The
main
challenges
treating
PDAC
include
difficulties
early
detection,
and
resistance
to
current
therapeutic
approaches
due
aggressive
molecular
microenvironment
features.
These
emphasize
the
importance
identifying
clinically
validated
biomarkers
for
detection
clinical
management.
Extracellular
vesicles
(EVs),
particularly
exosomes,
have
emerged
as
crucial
mediators
intercellular
communication
by
transporting
cargo.
Recent
has
unveiled
their
role
initiation,
metastasis,
chemoresistance
PDAC.
Consequently,
utilizing
EVs
liquid
biopsies
holds
promise
identification
prognosis,
monitoring
drug
efficacy.
However,
numerous
limitations,
including
isolation
characterization
homogeneous
populations,
well
absence
standardized
protocols,
can
affect
reliability
studies
involving
biomarkers,
underscoring
necessity
a
prudent
approach.
also
garnered
considerable
attention
promising
delivery
system
novel
therapy
tumors.
loading
biomolecules
or
chemical
drugs
into
exosomes
subsequent
target
cells
effectively
impede
tumor
progression.
Nevertheless,
there
are
obstacles
that
must
be
overcome
ensure
accuracy
efficacy
therapies
relying
on
treatment
In
this
review,
we
examine
both
recent
advancements
remaining
obstacles,
exploring
potential
biomarker
discovery
development
vehicles.
Frontiers in Immunology,
Год журнала:
2023,
Номер
13
Опубликована: Янв. 12, 2023
Three-dimensional
cancer
organoids
derived
from
self-organizing
stems
are
ex
vivo
miniatures
of
tumors
that
faithfully
recapitulate
their
structure,
distinctive
features,
and
genetic
signatures.
As
novel
tools,
current
have
been
well
established
rapidly
applied
in
drug
testing,
genome
editing,
transplantation,
with
the
ultimate
aim
entering
clinical
practice
for
guiding
personalized
therapy.
However,
given
lack
a
tumor
microenvironment,
including
immune
cells
fibrous
cells,
is
major
limitation
this
emerging
methodology,
co-culture
models
inspire
high
hope
further
application
technology
research.
Co-culture
or
fibroblasts
available
to
investigate
molecular
interactions,
chimeric
antigen
receptor-engineered
lymphocytes
treatment.
In
light
recent
progress
organoid
models,
it
only
possible
recognize
advantages
drawbacks
model
exploit
its
full
potential.
review,
we
summarize
advances
how
they
could
be
improved
future
benefit
research,
especially
precision
medicine.
Biological Research,
Год журнала:
2022,
Номер
55(1)
Опубликована: Ноя. 26, 2022
Abstract
Extracellular
vesicles
(EVs)
are
naturally
released
membrane
that
act
as
carriers
of
proteins
and
RNAs
for
intercellular
communication.
With
various
biomolecules
specific
ligands,
EV
has
represented
a
novel
form
information
transfer,
which
possesses
extremely
outstanding
efficiency
specificity
compared
to
the
classical
signal
transduction.
In
addition,
extended
concept
transduction
aspect
by
working
collection
extracellular
information.
Therefore,
functions
EVs
have
been
extensively
characterized
exhibit
an
exciting
prospect
clinical
applications.
However,
biogenesis
and,
in
particular,
regulation
this
process
signals,
essential
conduct
further
studies
support
optimal
utility,
remain
unclear.
Here,
we
review
current
understanding
EVs,
focus
on
signals
discuss
their
therapeutic
value.
Cancers,
Год журнала:
2023,
Номер
15(11), С. 2923 - 2923
Опубликована: Май 26, 2023
Pancreatic
ductal
adenocarcinoma
(PDAC)
is
among
the
leading
causes
of
death
by
cancer
in
world.
What
makes
this
pathological
condition
particularly
lethal
a
combination
clinical
and
molecular
heterogeneity,
lack
early
diagnostic
indexes,
underwhelming
results
from
current
therapeutic
protocols.
A
major
cause
PDAC
chemoresistance
seems
to
lie
ability
cells
spread
out
fill
pancreatic
parenchyma,
exchanging
nutrients,
substrates,
even
genetic
material
with
surrounding
tumor
microenvironment
(TME).
Several
components
can
be
found
TME
ultrastructure,
including
collagen
fibers,
cancer-associated
fibroblasts,
macrophages,
neutrophils,
mast
cells,
lymphocytes.
Cross-talk
between
latter
being
converted
into
cancer-favoring
phenotypes;
behavior
could
compared
an
influencer
guiding
followers
supporting
his
activity.
Moreover,
potential
target
for
some
newest
strategies;
these
include
use
pegvorhyaluronidase-α
CAR-T
lymphocytes
against
HER2,
FAP,
CEA,
MLSN,
PSCA,
CD133.
Other
experimental
therapy
options
are
currently
studied,
aiming
interfere
KRAS
pathway,
DNA-repairing
proteins,
apoptosis
resistance
cells.
Hopefully
new
approaches
will
grant
better
outcomes
future
patients.
Pharmacological Research,
Год журнала:
2023,
Номер
188, С. 106669 - 106669
Опубликована: Янв. 18, 2023
There
are
a
number
of
malignant
tumors
that
metastasize
into
the
lung
as
one
their
most
common
sites
dissemination.
The
successful
infiltration
tumor
cells
distant
organs
is
result
cooperation
between
and
host
cells.
When
have
not
yet
reached
organs,
in
situ
secrete
extracellular
vesicles
(EVs)
carrying
important
biological
information.
In
recent
years,
scholars
found
cells-derived
EVs
act
bridge
orthotopic
secondary
metastases
by
promoting
formation
pre-metastatic
niche
(PMN),
which
plays
key
role
awakening
dormant
circulating
cell
colonization.
This
review
provides
an
overview
multiple
routes
mechanisms
underlying
PMN
induced
summaries
study
findings
underline
potential
intervention
PMN,
both
target
or
carrier
for
drug
design.
this
review,
highlighted
well
applications
to
metastasis
diagnosis
treatment.
Scientific Reports,
Год журнала:
2024,
Номер
14(1)
Опубликована: Апрель 23, 2024
Abstract
Poor
treatment
responses
of
pancreatic
ductal
adenocarcinoma
(PDAC)
are
in
large
part
due
to
tumor
heterogeneity
and
an
immunosuppressive
desmoplastic
stroma
that
impacts
interactions
with
cells
the
microenvironment
(TME).
Thus,
there
is
a
pressing
need
for
models
probe
contributions
cellular
noncellular
crosstalk.
Organoids
promising
model
systems
potential
generate
plethora
data
including
phenotypic,
transcriptomic
genomic
characterization
but
still
require
improvements
culture
conditions
mimicking
TME.
Here,
we
describe
INTERaction
Organoid-in-MatriX
("InterOMaX")
system,
presents
3D
co-culture-based
platform
investigating
matrix-dependent
We
its
uncover
new
molecular
mechanisms
T
cell
murine
KPC
(
LSL-
Kras
G12D
/+27
/Trp53
tm1Tyj/J
/p48
Cre/
+
)
PDAC
as
well
patient-derived
organoids
(PDOs).
For
this,
customizable
matrix
homogenously
sized
organoid-in-matrix
positioning
cancer
were
designed
based
on
standardized
agarose
microwell
chip
array
system
established
co-culture
inclusion
stromal
cells.
detection
orthogonal
analysis
human
populations
distinct
sensitivity
killing
corroborated
vivo
.
By
enabling
both
identification
validation
gene
candidates
resistance,
this
sets
stage
better
mechanistic
understanding
cell-intrinsic
resistance
phenotypes
PDAC.