International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(2), P. 1148 - 1148
Published: Jan. 17, 2024
We
have
recently
demonstrated
that
exosomal
communication
between
endothelial
progenitor
cells
(EPCs)
and
brain
is
compromised
in
hypertensive
conditions,
which
might
contribute
to
the
poor
outcomes
of
stroke
subjects
with
hypertension.
The
present
study
investigated
whether
exercise
intervention
can
regulate
EPC–exosome
(EPC-EX)
functions
conditions.
Bone
marrow
EPCs
from
sedentary
exercised
transgenic
mice
were
used
for
generating
EPC-EXs,
denoted
as
R-EPC-EXs
R-EPC-EXET.
microRNA
profile
was
analyzed,
EX
determined
a
co-culture
system
N2a
challenged
by
angiotensin
II
(Ang
II)
plus
hypoxia.
EX-uptake
efficiency,
cellular
survival
ability,
reactive
oxygen
species
(ROS)
production,
mitochondrial
membrane
potential,
expressions
cytochrome
c
superoxide-generating
enzyme
(Nox4)
assessed.
found
(1)
improves
uptake
efficiency
EPC-EXs
cells.
(2)
restores
miR-27a
levels
R-EPC-EXs.
(3)
R-EPC-EXET
improved
ability
reduced
ROS
overproduction
Ang
(4)
potential
decreased
Nox4
hypoxia-injured
All
these
effects
significantly
inhibitor.
Together,
data
exercise-intervened
function
be
ascribed
their
carried
miR-27a.
BMC Cancer,
Journal Year:
2019,
Volume and Issue:
19(1)
Published: Nov. 21, 2019
A
severe
lack
of
early
diagnosis
coupled
with
resistance
to
most
available
therapeutic
options
renders
pancreatic
cancer
as
a
major
clinical
concern.
The
limited
efficacy
current
treatments
necessitates
the
development
novel
strategies
that
are
based
on
an
understanding
molecular
mechanisms
involved
in
progression.
MicroRNAs
(miRNAs)
non-coding
small
RNAs
regulate
expression
multiple
proteins
post-translation
process
and
thus
have
promise
biomarkers,
prognostic
agents,
advanced
therapies.
Profiling
deregulated
miRNAs
can
correlate
diagnosis,
indicate
optimal
treatment
predict
response
therapy.
Furthermore,
main
effector
genes
along
downstream
pathways
identify
possible
candidates.
Additionally,
obstacles
translation
into
clinic
also
considered.
Distinct
miRNA
profiles
stages
malignant
disease,
hold
potential
markers
targets.
However,
validation
specific
role
such
stunts
application.
Target
prediction
using
algorithms
provides
wide
range
targets,
but
these
still
require
through
pre-clinical
studies
determine
knock-on
genetic
effects.
Frontiers in Oncology,
Journal Year:
2021,
Volume and Issue:
11
Published: March 11, 2021
Breast
cancer
progression
is
a
complex
process
controlled
by
genetic
and
epigenetic
factors
that
coordinate
the
crosstalk
between
tumor
cells
components
of
microenvironment
(TME).
Among
those,
immune
play
dual
role
during
onset
progression,
as
they
can
protect
from
killing
immunogenic
neoplastic
cells,
but
in
meanwhile
also
shape
immunogenicity,
contributing
to
escape.
The
interplay
TME
influences
outcome
immunotherapy
many
other
anti-cancer
therapies.
Herein,
we
present
an
updated
view
pro-
anti-tumor
activities
main
cell
populations
breast
TME,
such
T
NK
myeloid
innate
lymphoid
mast
eosinophils,
underlying
cytokine-,
cell-cell
contact-
microvesicle-based
mechanisms.
Moreover,
current
novel
therapeutic
options
revert
immunosuppressive
activity
will
be
discussed.
To
this
end,
clinical
trials
assessing
efficacy
CAR-T
CAR-NK
vaccination,
death-inducing
chemotherapy,
DNA
methyl
transferase
histone
deacetylase
inhibitors,
cytokines
or
their
inhibitors
immunotherapies
patients
reviewed.
knowledge
elapses
experimental
therapies
targeting
it,
would
help
develop
new
combination
treatments
able
overcome
evasion
mechanisms
optimize
benefit
immunotherapies.
Seminars in Cancer Biology,
Journal Year:
2019,
Volume and Issue:
60, P. 351 - 361
Published: Aug. 24, 2019
Several
lines
of
compelling
pre-clinical
evidence
identify
chemotherapy
as
a
potentially
double-edged
sword:
therapeutic
efficacy
on
the
primary
tumor
may
in
fact
be
counterbalanced
by
induction
tumor/host
reactive
responses
supportive
for
survival
and
dissemination
cancer
cell
subpopulations.
This
paradoxical
effect
can
affect
different
districts
such
tumor,
circulation
distant
organs
simultaneously
shaping
properties
composition
stromal
cells.
At
site,
has
been
reported
to
promote
selection
chemoresistant
disseminating
cells
endowed
with
stem
(CSCs)
through
activation
autocrine
paracrine
self-renewing/survival
pathways
promoted
jointly
therapy-selected
Resistant
CSCs
represent
seeds
relapse
increased
infiltration
immune
cells,
together
enhanced
vascular
permeability
induced
chemotherapy,
facilitates
intravasation,
first
step
metastatic
cascade.
As
consequence
tumor/metastasis
re-shaping
circulating
(CTCs)
detected
during
therapy
display
shift
towards
more
mesenchymal
stem-like
phenotype,
conductive
ability
survive
seed
organs.
host
activate
inflammatory
that
ultimately
facilitate
extravasation
colonization.
Finally,
cooperation
endothelial
at
perivascular
niches
favors
high
potential
metastasis
initiation
protects
them
from
chemotherapy.
review
highlights
pro-metastatic
effects
linking
treatment
formation
remodeling
generation
favorable
niche.
Journal of Hematology & Oncology,
Journal Year:
2020,
Volume and Issue:
13(1)
Published: Oct. 15, 2020
Abstract
Cancer
stem
cells
(CSCs)
represent
a
tumor
subpopulation
responsible
for
metastasis
and
resistance
to
chemo-
radiotherapy,
ultimately
leading
relapse.
As
consequence,
the
detection
eradication
of
this
cell
current
challenge
in
oncology
medicine.
CSC
phenotype
is
dependent
on
microenvironment
(TME),
which
involves
differentiated
cells,
as
well
different
types,
such
mesenchymal
endothelial
fibroblasts
immune
system,
addition
extracellular
matrix
(ECM),
composition
ECM
healthy
tissues.
CSCs
regulate
multiple
cancer
hallmarks
through
interaction
with
their
environment
by
secreting
vesicles
including
exosomes,
soluble
factors
interleukins,
cytokines,
growth
other
metabolites
TME.
Through
these
factors,
generate
activate
own
niche
recruiting
stromal
modulate
angiogenesis,
metastasis,
antitumor
treatments
maintenance
secretion
IL-6,
VEGF
TGF-ß.
Due
strong
influence
secretome
disease
development,
new
therapies
focus
targeting
communication
networks
eradicate
prevent
relapse
drug
resistance.
This
review
summarizes
first
time
main
components
how
they
mediate
processes.
Lastly,
relevance
development
more
precise
personalized
discussed.
Journal of Experimental & Clinical Cancer Research,
Journal Year:
2020,
Volume and Issue:
39(1)
Published: April 16, 2020
Tumor
microenvironment
(TME)
is
the
internal
environment
in
which
tumor
cells
survive,
consisting
of
cells,
fibroblasts,
endothelial
and
immune
as
well
non-cellular
components,
such
exosomes
cytokines.
Exosomes
are
tiny
extracellular
vesicles
(40-160nm)
containing
active
substances,
proteins,
lipids
nucleic
acids.
carry
biologically
miRNAs
to
shuttle
between
TME,
thereby
affecting
development.
Tumor-derived
exosomal
induce
matrix
reprogramming
creating
a
that
conducive
growth,
metastasis,
escape
chemotherapy
resistance.
In
this
review,
we
updated
role
process
TME
reshaping.
Molecular Cancer,
Journal Year:
2022,
Volume and Issue:
21(1)
Published: Feb. 16, 2022
Abstract
Background
Detecting
cancer
at
an
early
stage
before
clinical
manifestation
could
be
effective
strategy
to
decrease
mortality.
Thus,
identifying
liquid
biopsy
biomarkers
with
high
efficacy
a
promising
approach
for
non-invasive
diagnosis
of
cancer.
Main
text
Liquid
biopsies
are
increasingly
used
as
supplement
biopsy,
it
enables
disease
progression
detected
months
and
radiographic
confirmation.
Many
bodily
fluids
contain
exosomal
microRNAs
(miRNAs)
which
provide
new
class
minimally
invasive
due
the
stability
miRNAs
in
exosomes.
In
this
review,
we
mainly
focused
on
(liquid
biopsy)
prognosis
various
cancers.
Conclusion
Exosomal
can
diagnostic
that
unique
insights
more
dynamic
perspective
therapeutic
responses
malignancies.
Therefore,
development
novel
sensitive
technologies
exploit
should
priority
management.
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.