Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(12), P. 2834 - 2834
Published: Dec. 13, 2024
Background:
Glioblastoma
(GB)
is
a
highly
aggressive
tumor,
whose
progression
mediated
by
secretion
of
extracellular
vesicles
(EVs),
which
can
pass
the
brain–blood
barrier
and
be
found
in
plasma.
Here,
we
performed
comparative
analysis
effects
EVs
from
plasma
healthy
donors
(hEVs)
GB
patients
before
(bEVs)
after
(aEVs)
tumor
surgical
resection
on
invasion
normal
astrocytes
cells.
Methods:
We
transwell
assay,
analyzed
MAP
kinases
activation
Western
blotting,
studied
SNAI1/SNAI2
cellular
localization
confocal
microscopy,
measured
cadherins
expression
flow
cytometry,
cytokines,
regulate
migration
inflammation,
immunoassay.
Results:
hEVs
did
not
affect
cells,
there
was
down-regulated
astrocytes,
while
increased
E-
N-cadherin
inflammation
adhesion
regulators
both
bEVs
enhanced
cells
but
via
AKT,
JNK1/2/3,
p38
activation,
stimulated
clasterization
SNAI1
cell
nucleus,
promoted
an
E/N
cadherin
switch,
caused
aEVs
exhibited
most
pro-oncogenic
(stimulation
invasion,
nuclear
localization,
JNK1/2/3
cells).
However,
were
less
pronounced
than
those
bEVs.
Conclusions:
In
our
study,
revealed
common
different
plasma-derived
hEVs,
aEVs,
stimulate
some
Being
tumorigenic
then
bEVs,
are
still
able
to
promote
probably
remaining
resection.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(6), P. 3415 - 3415
Published: March 18, 2024
Glioblastoma
multiforme
(GBM)
is
a
malignancy
of
bad
prognosis,
and
advances
in
early
detection
treatment
are
needed.
GBM
heterogenous,
with
varieties
differing
within
tumor
patient
between
patients.
Means
needed
to
distinguish
these
GMB
forms,
so
that
specific
strategies
can
be
deployed
for
management.
We
study
the
participation
chaperone
system
(CS)
carcinogenesis.
The
CS
dynamic,
its
members
moving
around
body
extracellular
vesicles
(EVs)
interacting
components
other
physiological
systems
health
disease,
including
GBM.
Here,
we
describe
finding
high
amounts
Hsp70
(HSPA1A)
calcitonin
receptor
protein
(CTR)
EVs
patients
present
standardized
protocol
collecting,
purifying,
characterizing
carrying
CTR
plasma-derived
from
were
obtained
just
before
ablative
surgery
(T0)
7
days
afterwards
(T1);
was
highly
elevated
at
T0
less
T1,
greatly
increased
reduced
below
normal
values
T1.
Our
results
encourage
further
research
assess
as
biomarkers
differentiating
forms
determine
their
roles
Journal of Nanobiotechnology,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: June 18, 2024
Abstract
Recently,
the
significant
benefits
of
cancer
immunotherapy
for
most
cancers
have
been
demonstrated
in
clinical
and
preclinical
studies.
However,
efficacy
these
immunotherapies
gliomas
is
limited,
owing
to
restricted
drug
delivery
insufficient
immune
activation.
As
carriers,
exosomes
offer
advantages
low
toxicity,
good
biocompatibility,
intrinsic
cell
targeting,
which
could
enhance
glioma
efficacy.
a
review
exosome-based
systems
has
not
presented.
This
introduces
current
problems
role
addressing
issues.
Meanwhile,
preparation
application
strategies
are
discussed,
especially
enhancing
immunogenicity
reversing
immunosuppressive
tumor
microenvironment.
Finally,
we
briefly
describe
challenges
translation.
We
anticipate
that
this
will
guide
use
as
carriers
immunotherapy.
Graphical
Biomaterials Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
This
review
summarizes
naïve
extracellular
vesicles
(EVs)
in
clinical
trials
for
central
nervous
system
(CNS)
diseases
and
updates
recent
translational
preclinical
research
on
EV-loaded
drugs
or
genes
CNS
treatments.
Therapeutic Delivery,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 12
Published: Feb. 16, 2025
Gliomas
are
prominent
and
frequent
primary
malignant
brain
tumors,
with
a
generally
poor
prognosis.
Current
treatment
involves
radiation,
surgery
chemotherapy.
Exosomes
nanoscale
extracellular
vesicles
released
by
cells
that
enable
biological
molecule
movement
encourage
intercellular
communication
in
the
tumor
microenvironment.
This
contributes
to
glioma
development,
radiation
resistance,
overcomes
Exosome
functional
structural
properties
essential
for
understanding
cancer
molecular
mechanisms.
They
can
also
treat
invasive
tumors
like
glioblastomas
serve
as
diagnostic
markers.
Recent
research
depicted
exosomes'
role
cell
maintenance,
signaling,
microenvironment
modification.
hold
nucleic
acids,
proteins,
lipids,
mRNAs,
lncRNAs,
miRNAs,
immunological
regulatory
molecules
depending
on
origin
of
cell.
paper
reviews
exosomes,
their
etiology,
perspective
therapeutic
uses.
Biology,
Journal Year:
2024,
Volume and Issue:
13(8), P. 586 - 586
Published: Aug. 2, 2024
Brain
tumors,
and,
in
particular,
glioblastoma
(GBM),
are
among
the
most
aggressive
forms
of
cancer.
In
spite
advancement
available
therapies,
both
diagnosis
and
treatments
still
unable
to
ensure
pathology-free
survival
GBM
patients
for
more
than
12–15
months.
At
basis
poor
ability
cope
with
brain
we
can
consider:
(i)
intra-tumor
heterogeneity;
(ii)
heterogeneity
tumor
properties
when
compare
different
patients;
(iii)
blood–brain
barrier
(BBB),
which
makes
difficult
isolation
tumor-specific
biomarkers
delivering
therapeutic
drugs
brain.
Recently,
it
is
becoming
increasingly
clear
that
cancer
cells
release
large
amounts
extracellular
vesicles
(EVs)
transport
metabolites,
proteins,
classes
RNAs,
DNA,
lipids.
These
structures
involved
pathological
process
characterize
any
particular
form
Moreover,
EVs
able
cross
BBB
directions.
Starting
from
these
observations,
researchers
now
evaluating
possibility
use
purified
organic
fluids
(first
all,
blood
saliva),
order
obtain,
through
non-invasive
methods
(liquid
biopsy),
biomarkers,
perhaps,
also
obtaining
nanocarriers
targeted
drugs.
Cancer Medicine,
Journal Year:
2025,
Volume and Issue:
14(9)
Published: May 1, 2025
ABSTRACT
Background
Exosomes
are
extracellular
vesicles
ranging
from
40
to
100
nm
in
diameter
that
mediate
intercellular
communication
by
transferring
proteins,
lipids,
nucleic
acids,
and
other
metabolites.
In
the
context
of
cancer,
exosomes
influence
tumor
microenvironment
carrying
regulatory
RNAs
such
as
miRNA,
circRNA,
lncRNA.
They
originate
various
cells,
including
adipocytes,
fibroblasts,
hepatocellular
carcinoma
(HCC)
can
either
promote
or
inhibit
cancer
progression
through
pathways
like
MAPK
PI3K‐Akt.
Aim
This
review
aims
explore
role
solid
cancers,
emphasizing
their
self‐induced
activation
mechanisms
how
they
modulate
behavior.
Methodology
A
comprehensive
recent
literature
was
conducted,
focusing
on
studies
investigated
biological
functions
progression,
molecular
cargo,
cellular
origin,
involvement
signaling
pathways.
Results
Findings
multiple
indicate
cancer‐derived
contribute
proliferation,
metastasis,
therapy
resistance
enhancing
within
microenvironment.
These
activate
oncogenic
serve
biomarkers
therapeutic
targets
due
disease
modulation.
Conclusion
play
a
pivotal
offer
significant
potential
advancing
our
understanding
biology.
Their
capacity
key
facilitate
makes
them
promising
candidates
for
novel
diagnostic
strategies.
Extracellular Vesicle,
Journal Year:
2024,
Volume and Issue:
3, P. 100038 - 100038
Published: April 21, 2024
Brain
cancers,
a
global
menace
with
high
mortality
rates,
remain
profound
challenge,
particularly
in
treating
the
most
lethal
type
of
malignant
tumors
like
glioblastoma
multiforme
(GBM).
The
crucial
need
for
prompt
identification
and
precise
prognosis
drives
exploration
exosomes
as
non-invasive
tools.
Exosomes
are
generated
by
various
cells,
especially
facilitating
intercellular
communication
tumor
microenvironment,
fostering
glioma
progression
conveying
molecular
modifiers,
offering
insights.
These
attributes
hold
promise
enhancing
diagnosis
prognosis.
nanosized
messengers
influence
cancer
dynamics,
aiding
tailored
treatment
strategies
improved
patient
outcomes.
This
article
outlines
significance
progression,
highlighting
recent
advancements
diagnostic
therapeutic
utilizing
bioactive
molecules
biomarkers
miRNAs,
circ-RNAs,
genes,
proteins
variety
brain
tumors,
supported
advanced
isolation
techniques.
relevance
circulating
to
malignancies
glioblastoma,
astrocytoma,
craniopharyngiomas,
meningioma,
more,
has
been
discussed.
It
elucidates
immune
cross-talk
underscores
diagnostic-worthy
exosomal
proteins.
Additionally,
it
delineates
promising
avenues
forthcoming
investigations.