Cells,
Journal Year:
2021,
Volume and Issue:
10(8), P. 2117 - 2117
Published: Aug. 18, 2021
Ovarian
cancer
is
one
of
the
deadliest
malignancies
among
women.
Approximately
75%
patients
with
ovarian
are
diagnosed
advanced
disease
that
already
has
metastasis,
particularly
to
omentum.
The
omentum
constitutes
ideal
soil
for
metastasis
due
a
complex
intraperitoneal
milieu
favors
and
supports
whole
metastatic
process.
Adipose-derived
stem/stromal
cells
(ADSCs)
part
this
microenvironment
foster
tumor
progression
via
sustained
paracrine
secretion,
including
extracellular
vesicles
(EVs).
Nonetheless,
preferential
relationship
between
ADSCs,
ADSC-derived
EVs,
could
be
exploited
use
ADSCs
EVs
as
vehicle
anti-cancer
therapies.
This
review
will
analyze
strict
relations
progression,
disease,
adipose
tissue
its
staminal
components.
In
addition,
we
describe
crosstalk
biologic
cells,
role
in
intercellular
communication,
establishment
drug
resistance,
capacity,
progression.
We
new
therapeutic
opportunities
treating
offered
by
molecules
target
precisely
limit
systemic
adverse
effects.
Finally,
discuss
limitations
these
approaches.
Cell Death and Disease,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: Jan. 18, 2022
Abstract
Chemoresistance
and
metastasis
are
the
major
challenges
for
current
ovarian
cancer
treatment.
Understanding
mechanisms
of
progression
is
critically
important
developing
novel
therapies.
The
advances
in
extracellular
vesicles
(EVs)
research
recent
years
have
attracted
extensive
attention.
EVs
contain
a
variety
proteins,
RNAs,
DNAs,
metabolites.
Accumulating
evidence
indicates
that
cells
secrete
large
amount
EVs,
playing
an
role
tumor
recurrence.
In
microenvironment
tumor,
participate
information
transmission
between
stromal
immune
cells,
promoting
escape
facilitating
metastasis.
Here,
we
review
chemoresistance,
metastasis,
evasion
cancer.
Furthermore,
also
discuss
EV
future
application
as
promising
biomarker
sources
response
to
therapy
therapy-delivery
approaches
patients.
Advanced Science,
Journal Year:
2022,
Volume and Issue:
9(34)
Published: Oct. 17, 2022
Abstract
Extracellular
vesicles
(EVs)
are
cell‐derived
nanosized
that
mediate
cell‐to‐cell
communication
via
transporting
bioactive
molecules
and
thus
critically
involved
in
various
physiological
pathological
conditions.
EVs
contribute
to
different
aspects
of
cancer
progression,
such
as
growth,
angiogenesis,
metastasis,
immune
evasion,
drug
resistance.
induce
the
resistance
cells
chemotherapy,
radiotherapy,
targeted
therapy,
antiangiogenesis
immunotherapy
by
transferring
specific
cargos
affect
efflux
regulate
signaling
pathways
associated
with
epithelial‐mesenchymal
transition,
autophagy,
metabolism,
stemness.
In
addition,
modulate
reciprocal
interaction
between
noncancer
tumor
microenvironment
(TME)
develop
therapy
detectable
many
biofluids
patients,
regarded
novel
biomarkers
for
monitoring
response
predicting
prognosis.
Moreover,
suggested
promising
targets
engineered
nanovehicles
deliver
drugs
overcoming
therapy.
this
review,
biological
roles
their
mechanisms
action
summarized.
The
preclinical
studies
on
using
also
discussed.
Drug Resistance Updates,
Journal Year:
2022,
Volume and Issue:
62, P. 100833 - 100833
Published: April 5, 2022
Drug
resistance
remains
a
major
hurdle
to
successful
cancer
treatment,
being
accountable
for
approximately
90%
of
cancer-related
deaths.
In
the
past
years,
increasing
attention
has
been
given
role
extracellular
vesicles
(EVs)
in
horizontal
transfer
drug
cancer.
Indeed,
many
studies
have
described
dissemination
therapy
traits
mediated
by
EVs,
which
may
be
transferred
from
resistant
tumor
cells
their
sensitive
counterparts.
Importantly,
different
key
players
identified
cargo
those
such
as
efflux
pumps,
oncoproteins,
antiapoptotic
proteins,
or
microRNAs,
among
others.
Interestingly,
EVs-mediated
crosstalk
between
microenvironment
(TME)
and
emerged
another
important
mechanism
that
leads
resistance.
Recently,
TME-derived
EVs
responsible
also
become
focus
attention.
addition,
possible
mechanisms
involved
sequestration
likely
contribute
resistance,
are
discussed
herein.
Despite
latest
scientific
advances
field
this
is
still
challenging
area
research,
particularly
clinical
setting.
Therefore,
further
investigation
needed
assess
relevance
failure
patients
identify
biomarkers
EV's
cargo,
develop
effective
therapeutic
strategies
surmount
This
up-to-date
review
summarizes
relevant
literature
on
competences
cells,
TME
process.
Finally,
knowledge
integrated
with
discussion
future
applications
Materials Today Bio,
Journal Year:
2022,
Volume and Issue:
13, P. 100218 - 100218
Published: Jan. 1, 2022
The
grand
challenges
of
ovarian
cancer
early
diagnosis
have
led
to
an
alarmingly
high
mortality
rate
from
(OC)
in
the
past
half
century.
In
vitro
(IVD)
has
great
potential
OC
through
non-invasive
and
dynamic
analysis
biomarkers.
However,
common
IVDs
often
fail
provide
reliable
test
results
due
lack
sensitivity,
specificity,
convenience.
recent
years,
discovery
new
biomarkers
progress
nanomaterials
can
solve
shortcomings
traditional
IVD
for
OC.
These
emerging
biosensors
based
on
offer
improvements
convenience,
speed,
selectivity,
sensitivity
IVD.
this
review,
we
firstly
systematically
summarized
limits
commercial
latest
representative
optimization
strategies
six
are
discussed
with
emphasis
nanomaterial
selection
design
detection
principles.
Then,
various
adopted
by
also
introduced
detail,
including
optical,
electrochemical,
microfluidic,
surface
plasmon
sensors.
Finally,
current
proposed,
future
research
directions
promising
field
discussed.
Diagnostics,
Journal Year:
2022,
Volume and Issue:
12(2), P. 286 - 286
Published: Jan. 23, 2022
In
recent
years,
a
growing
number
of
studies
have
evaluated
the
role
exosomes
in
pancreatic
ductal
adenocarcinoma
cancer
(PDAC)
demonstrating
their
involvement
multitude
pathways,
including
induction
chemoresistance.
The
aim
this
review
is
to
present
an
overview
current
knowledge
on
resistance
gemcitabine
and
nab-paclitaxel,
which
are
two
most
commonly
used
drugs
for
treatment
PDAC
patients.
Exosomes
vesicular
cargos
that
transport
multiple
miRNAs,
mRNAs
proteins
from
one
cell
another
some
these
factors
can
influence
specific
determinants
activity,
such
as
nucleoside
transporter
hENT1,
or
multidrug
involved
paclitaxel.
Additional
mechanisms
underlying
exosome-mediated
include
modulation
apoptotic
cellular
metabolism,
oncogenic
miRNA,
miR-21
miR-155.
status
circulating
exosomal
miRNA
possible
biomarkers
also
discussed.
Finally,
we
integrated
preclinical
data
with
emerging
clinical
evidence,
showing
how
study
could
help
predict
individual
tumors,
guide
clinicians
selection
innovative
therapeutic
strategies
overcome
drug
resistance.
Cancers,
Journal Year:
2021,
Volume and Issue:
13(18), P. 4608 - 4608
Published: Sept. 14, 2021
Cancer
is
a
leading
public
health
issue
globally,
and
diagnosis
often
associated
with
poor
outcomes
reduced
patient
survival.
One
of
the
major
contributors
to
fatality
resultant
cancer
development
resistance
chemotherapy,
known
as
chemoresistance.
Furthermore,
there
are
limitations
in
our
ability
identify
patients
that
will
respond
therapy,
versus
develop
relapse,
display
limited
or
no
response
treatment.
This
leads
being
subjected
multiple
futile
treatment
cycles,
results
reduction
their
quality
life.
Therefore,
an
urgent
clinical
need
tools
at
risk
chemoresistance,
recent
literature
has
suggested
small
extracellular
vesicles,
exosomes,
may
be
vital
source
information.
Extracellular
vesicles
(EV)
membrane
bound
involved
cell-cell
communication,
through
transfer
cargo,
which
includes
proteins,
lipids,
miRNAs.
A
defined
exploration
strategy
was
performed
this
systematic
review
order
provide
compilation
key
EV
miRNAs
predictive
We
searched
PubMed,
Science
Direct,
Scopus
databases
using
following
keywords:
OR
exosomes
EVs
AND
miRNA
Chemotherapy
Chemoresistance
Recurrence
from
2010
2020.
found
31
articles
reported
EV-associated
recurrence
related
Interestingly,
studies
same
tumor
type
identified
different
microRNAs,
few
ones.
Specifically,
miR-21,
miR-222,
miR-155
displayed
roles
were
common
colorectal
cancer,
ovarian
breast
diffuse
large
B
cell
lymphoma
(DLBCL).
miR-21
miR-222
favour
whereas
exhibited
contrasting
role,
depending
on
primary
tumor.
Whilst
high
levels
correlate
chemotherapy
DLBCL,
it
effective
towards
cancer.
Thus,
further
research
regarding
these
would
beneficial
terms
designing
novel
counteract
progression
not-to-distant
future.
Cells,
Journal Year:
2022,
Volume and Issue:
11(21), P. 3383 - 3383
Published: Oct. 26, 2022
The
cancer
burden
continues
to
grow
globally,
and
drug
resistance
remains
a
substantial
challenge
in
therapy.
It
is
well
established
that
cancerous
cells
with
clonal
dysplasia
generate
the
same
carcinogenic
lesions.
Tumor
pass
on
genetic
templates
subsequent
generations
evolutionary
terms
exhibit
simply
by
accumulating
alterations.
However,
recent
evidence
has
implied
tumor
accumulate
alterations
progressively
adapting.
As
result,
intratumor
heterogeneity
(ITH)
generated
due
genetically
distinct
subclonal
populations
of
coexisting.
adaptive
mechanisms
action
ITH
include
activating
"cellular
plasticity",
through
which
create
tumor-supportive
microenvironment
they
can
proliferate
cause
increased
damage.
These
highly
plastic
are
located
(TME)
undergo
extreme
changes
resist
therapeutic
drugs.
Accordingly,
underlying
involved
have
been
re-evaluated.
Herein,
we
will
reveal
new
themes
emerging
from
initial
studies
outline
findings
regarding
perspective
TME;
exosomes,
metabolic
reprogramming,
protein
glycosylation
autophagy,
relates
aim
provide
targets
strategies
for
reversing
cancers.