Exosomes
are
a
subpopulation
of
the
tumour
microenvironment
(TME)
that
transmit
various
biological
molecules
to
promote
intercellular
communication.
derived
from
nearly
all
types
cells
and
exist
in
body
fluids.
Noncoding
RNAs
(ncRNAs)
among
most
abundant
contents
exosomes,
some
ncRNAs
with
functions
specifically
packaged
into
exosomes.
Recent
studies
have
revealed
exosome-derived
play
crucial
roles
tumorigenesis,
progression
drug
resistance
gastric
cancer
(GC).
In
addition,
regulating
expression
levels
exosomal
can
or
suppress
GC
progression.
Moreover,
membrane
structures
exosomes
protect
degradation
by
enzymes
other
chemical
substances,
significantly
increasing
stability
ncRNAs.
Specific
hallmarks
within
be
used
for
exosome
identification,
specific
determine
their
origin.
Therefore,
suitable
use
as
diagnostic
prognostic
biomarkers
therapeutic
targets.
Regulating
biogenesis
may
represent
new
way
block
eradicate
GC.
this
review,
we
summarized
origins
characteristics
analysed
association
between
development.
Cells,
Год журнала:
2019,
Номер
8(4), С. 307 - 307
Опубликована: Апрель 3, 2019
Exosomes
are
extracellular
vesicles
that
contain
a
specific
composition
of
proteins,
lipids,
RNA,
and
DNA.
They
derived
from
endocytic
membranes
can
transfer
signals
to
recipient
cells,
thus
mediating
novel
mechanism
cell-to-cell
communication.
also
thought
be
involved
in
cellular
waste
disposal.
play
significant
roles
various
biological
functions,
including
the
biomolecules
such
as
enzymes,
lipids
regulation
numerous
physiological
pathological
processes
diseases.
Because
these
properties,
they
considered
promising
biomarkers
for
diagnosis
prognosis
diseases
may
contribute
development
minimally
invasive
diagnostics
next
generation
therapies.
The
biocompatible
nature
exosomes
could
enhance
stability
efficacy
imaging
probes
therapeutics.
Due
their
potential
use
clinical
applications,
have
attracted
much
research
attention
on
health
disease.
To
explore
biomedical
arena,
it
is
essential
basic
molecular
mechanisms
behind
transport
function
well-understood.
Herein,
we
discuss
history,
biogenesis,
release,
isolation,
characterization,
functions
exosomes,
well
factors
influencing
biogenesis
technical
challenges.
We
conclude
this
review
with
discussion
future
perspectives
exosomes.
Frontiers in Immunology,
Год журнала:
2020,
Номер
11
Опубликована: Май 15, 2020
The
success
of
cancer
immunotherapy
relies
on
the
knowledge
tumor
microenvironment
and
immune
evasion
mechanisms
in
which
tumor,
stroma
infiltrating
cells
function
a
complex
network.
potential
barriers
that
profoundly
challenge
overall
clinical
outcome
promising
therapies
need
to
be
fully
identified
counteracted.
Although
has
increasingly
been
applied,
we
are
far
from
understanding
how
utilize
different
strategies
best
way
combine
therapeutic
options
optimize
benefit.
This
review
intends
give
contemporary
detailed
overview
roles
cells,
exosomes
molecules
acting
they
relate
activation
escape.
Further,
current
novel
immunotherapeutic
will
discussed.
Frontiers in Cell and Developmental Biology,
Год журнала:
2018,
Номер
6
Опубликована: Фев. 20, 2018
Tumors
are
not
isolated
entities,
but
complex
systemic
networks
involving
cell-cell
communication
between
transformed
and
non-transformed
cells.
The
milieu
created
by
tumor-associated
cells
may
either
support
or
halt
tumor
progression.
In
addition
to
contact,
communicate
through
secreted
factors
via
a
highly
system
characteristics
such
as
ligand
concentration,
receptor
expression
integration
of
diverse
signaling
pathways.
Of
these,
extracellular
vesicles,
exosomes,
emerging
novel
mediators
in
physiological
pathological
scenarios.
Exosomes,
membrane
vesicles
endocytic
origin
released
all
(both
healthy
diseased),
ranging
size
from
30
150nm,
transport
the
main
biomolecules,
including
lipids,
proteins,
DNAs,
messenger
RNAs
microRNA,
perform
intercellular
transfer
components,
locally
systemically.
By
acting
only
cells,
also
fibroblasts,
endothelium,
leukocytes
progenitor
tumor-
non-tumor
cells-derived
exosomes
have
emerged
new
players
growth
invasion,
angiogenesis,
tissue
inflammation
immunologic
remodeling.
addition,
due
their
property
carrying
molecules
cell
peripheral
circulation,
been
increasingly
studied
sources
biomarkers
liquid
biopsies.
Here
we
review
current
literature
on
participation
highlighting
role
this
process
setup
microenvironments
that
modulate
initiation
metastasis.
Exosomes
are
emerging
as
a
new
type
of
cancer
biomarkers.
Exosome
is
bilayered
nano-sized
vesicle
secreted
by
various
living
cells
in
all
body
fluids.
Based
on
the
expanding
albeit
incomplete
knowledge
their
biogenesis,
secretion
and
cell-specific
molecular
genetic
contents,
exosomes
viewed
promising,
clinically-relevant
surrogates
progression
response
to
therapy.
Preliminary
proteomic,
functional
profiling
cell-derived
or
plasma-derived
confirms
unique
characteristics.
Alterations
protein
nucleic
acid
profiles
plasma
correlate
with
pathological
processes
many
diseases
including
cancer.
However,
previous
studies
exosome
application
diagnosis
treatment
mainly
focussed
miRNAs.
With
development
rapid
large-scale
production,
purification,
extraction
screening
exosomal
can
be
explored
for
early
stage
diagnosis,
monitoring
prognosis
evaluation.
Here,
we
summarized
recent
developments
proteins
diagnosis.
Journal of Hematology & Oncology,
Год журнала:
2022,
Номер
15(1)
Опубликована: Июнь 28, 2022
Abstract
Cancer
is
one
of
the
leading
causes
death
worldwide,
and
factors
responsible
for
its
progression
need
to
be
elucidated.
Exosomes
are
structures
with
an
average
size
100
nm
that
can
transport
proteins,
lipids,
nucleic
acids.
This
review
focuses
on
role
exosomes
in
cancer
therapy.
We
discuss
how
able
modulate
components
tumor
microenvironment
influence
proliferation
migration
rates
cells.
also
highlight
that,
depending
their
cargo,
suppress
or
promote
cell
enhance
reduce
response
radio-
chemo-therapies.
In
addition,
we
describe
trigger
chronic
inflammation
lead
immune
evasion
by
focusing
ability
transfer
non-coding
RNAs
between
cells
other
molecular
signaling
pathways
such
as
PTEN
PI3K/Akt
cancer.
Subsequently,
use
carriers
anti-tumor
agents
genetic
tools
control
progression.
then
tumor-derived
carcinogenesis.
Finally,
devote
a
section
study
diagnostic
prognostic
clinical
courses
important
treatment
patients.
provides
comprehensive
understanding
therapy,
therapeutic
value
remodeling
microenvironment.
Graphical
Polymorphonuclear
neutrophils
(PMNs)
play
an
important
role
in
sepsis-related
acute
lung
injury
(ALI).
Accumulating
evidence
suggests
PMN-derived
exosomes
as
a
new
subcellular
entity
acting
fundamental
link
between
PMN-driven
inflammation
and
tissue
damage.
However,
the
of
ALI
underlying
mechanisms
remains
unclear.
Tumor
necrosis
factor-α
(TNF-α),
key
regulator
innate
immunity
ALI,
was
used
to
stimulate
PMNs
from
healthy
C57BL/6J
mice
vitro.
Exosomes
isolated
supernatant
were
injected
wild-type
intraperitoneally
(i.p.)
then
examined
for
inflammation,
macrophage
(Mϕ)
polarization
pyroptosis.
In
vitro
co-culture
system
applied
where
mouse
Raw264.7
macrophages
or
bone
marrow-derived
(BMDMs)
co-cultured
with
further
confirm
results
vivo
animal
study
explore
potential
involved.
released
by
TNF-α-stimulated
(TNF-Exo)
promoted
M1
activation
after
i.p.
injection
co-culture.
addition,
TNF-Exo
primed
pyroptosis
upregulating
NOD-like
receptor
3
(NLRP3)
inflammasome
expression
through
nuclear
factor
κB
(NF-κB)
signaling
pathway.
Mechanistic
studies
demonstrated
that
miR-30d-5p
mediated
function
targeting
suppressor
cytokine
(SOCS-1)
sirtuin
1
(SIRT1)
macrophages.
Furthermore,
intravenous
administration
inhibitors
significantly
decreased
cecal
ligation
puncture
(CLP)-induced
death
lung,
well
histological
lesions.
The
present
exosomal
contributed
inducing
priming
activating
NF-κB
signaling.
These
findings
suggest
novel
mechanism
PMN-Mϕ
interaction
which
may
provide
therapeutic
strategies
sepsis
patients.
NanoImpact,
Год журнала:
2020,
Номер
20, С. 100261 - 100261
Опубликована: Окт. 1, 2020
Exosomes,
a
class
of
small
bilayer
vesicles
derived
from
virtually
all
eukaryotic
cells,
have
been
exploited
as
promising
natural
delivery
platform
due
to
their
low
toxicity,
excellent
structural
stability,
nanoscale
size,
cargo
loading
ability,
and
editable
surface
structure.
To
load
therapeutic
or
diagnostic
cargos
(drugs,
nucleic
acids,
proteins,
peptides,
nanomaterials)
into
exosomes,
multiple
techniques
developed,
such
incubating
with
exosomes
exosome-secreting
transfection,
physical
treatments
(sonication,
electroporation,
extrusion,
freeze-thaw,
surfactant
treatment,
dialysis),
in
situ
synthesis.
Moreover,
homing-molecules
high
receptor
binding
affinity,
acidic
milieu
responsiveness,
magnetic
properties
assembled
on
exosomal
by
transfection
chemical
modification,
conferring
the
targeting
capacity
exosomes.
In
this
review,
we
summarize
biogenesis,
contents
functions
provide
comprehensive
discussion
for
strategies
membrane
modification
targeted
delivery.
Exosomes
are
extracellular
vesicles
that
mediate
cellular
communication
in
health
and
diseases.
Neutrophils
could
be
polarized
to
a
pro-tumor
phenotype
by
tumor.
The
function
of
tumor-derived
exosomes
neutrophil
regulation
remains
unclear.
We
investigated
the
effects
gastric
cancer
cell-derived
(GC-Ex)
on
activation
neutrophils
elucidated
underlying
mechanisms.
GC-Ex
prolonged
survival
induced
expression
inflammatory
factors
neutrophils.
GC-Ex-activated
neutrophils,
turn,
promoted
cell
migration.
transported
high
mobility
group
box-1
(HMGB1)
activated
NF-κB
pathway
through
interaction
with
TLR4,
resulting
an
increased
autophagic
response
Blocking
HMGB1/TLR4
interaction,
pathway,
autophagy
reversed
GC-Ex-induced
activation.
Silencing
HMGB1
cells
confirmed
as
key
factor
for
GC-Ex-mediated
Furthermore,
was
upregulated
tissues.
Increased
associated
poor
prognosis
patients
cancer.
Finally,
tissue-derived
acted
similarly
derived
from
lines
demonstrate
induce
via
HMGB1/TLR4/NF-κB
signaling,
which
provides
new
insights
into
mechanisms
sheds
lights
multifaceted
role
reshaping
tumor
microenvironment.