Annals of 3D Printed Medicine,
Год журнала:
2024,
Номер
15, С. 100161 - 100161
Опубликована: Июнь 22, 2024
Additive
manufacturing
techniques
capable
of
fabricating
biocompatible
scaffolds
with
a
given
submicron/micron/supramicron
structure
are
growing
interest
for
biomedical
applications,
including
tissue
engineering
and
tumor
biology
studies.
Here,
we
propose
antisolvent
3D
printing
electrospinning
to
obtain
biopolymer
different
structural,
mechanical,
surface
properties
compare
the
cultivation
patterns
glioblastoma
cells.
We
found
that
human
G01
cells,
derived
from
tissue,
were
able
colonize
in
time-dependent
manner;
cells
showed
high
viability
as
confirmed
by
colorimetric
MTT
assay,
confocal
fluorescence
microscopy,
scanning
electron
microscopy
data.
Electrospun
collagen
(low
porosity,
thin
2.75±0.22
μm
fibers,
low
Young's
modulus
0.076±0.033
MPa)
provided
monolayer-like
growth
dense
cell-cell
contacts,
while
3D-printed
PLGA
(high
thick
∼150
µm
18±2
stimulated
glioblastoma-specific
spindle-like
morphology.
All
non-toxic
maintained
cell
at
least
2
weeks.
The
developed
could
be
further
used
research
model
vitro
or
brain
injury.
Background
Canopy
FGF
signalling
regulator
3
(CNPY3)
is
involved
in
immune
regulation,
tumorigenesis
and
development,
nevertheless,
its
role
glioma
remains
largely
unexplored.
Our
study
aimed
to
explore
the
regulatory
of
CNPY3
as
a
prognostic
biomarker
human
cell
migration,
invasion
infiltration.
Methods
Bioinformatics
analysis
clinical
relevance
public
databases
was
performed.
COX
regression
performed
assess
relationship
between
prognosis.
GO
Kyoto
Encyclopedia
Genes
Genomes
analyses
were
conducted
predict
signaling
pathways
gliomas.
Tumor
infiltration
explored
using
TIMER,
CIBERSORT,
Pearson
correlation
analysis.
GSVA
single-cell
sequencing
data
employed
for
further
validation.
The
effects
on
migration
cells
investigated
through
scratch
assay
transwell
assay.
Results
positively
correlated
with
IDH
mutation
status,
1p/19q
histopathologic
grade,
MGMT
promoter
methylation
but
negatively
overall
survival
patients
(
P
<
0.05).
significantly
associated
tumor
response,
inflammatory
lipopolysaccharide-mediated
pathway.
influenced
different
types
which
affected
microenvironment
glioma.
promoted
increase
M2
macrophage
positive
regulation
macrophages
apoptotic
process.
In
vitro
suggested
promotion
U87MG
an
increased
capacity
drug
sensitivity
showed
more
towards
temozolomide,
irinotecan,
cisplatin
among
high
expression
Conclusion
Increased
impacts
enhances
recommended
patients.
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(12), С. 6810 - 6810
Опубликована: Июнь 20, 2024
Glioblastoma
is
the
most
aggressive
tumor
in
central
nervous
system,
with
a
survival
rate
of
less
than
15
months
despite
multimodal
therapy.
Tumor
recurrence
frequently
occurs
after
removal.
Tumoral
angiogenesis,
formation
neovessels,
has
positive
impact
on
progression
and
invasion,
although
there
are
controversial
results
specialized
literature
regarding
its
survival.
This
study
aims
to
correlate
immunoexpression
angiogenesis
markers
(CD34,
CD105)
proliferation
index
Ki67
p53
primary
secondary
glioblastomas.
retrospective
included
54
patients
diagnosed
glioblastoma
at
Pathology
Department
County
Emergency
Clinical
Hospital
Târgu
Mureș.
Microvascular
density
was
determined
using
CD34
CD105
antibodies,
were
correlated
p53,
IDH1,
ATRX
Ki67.
The
number
neoformed
blood
vessels
varied
among
cases,
characterized
by
different
shapes
calibers,
endothelial
cells
showing
modified
morphology
moderate
marked
pleomorphism.
Neovessels
glomeruloid
aspect,
associated
intense
positivity
for
or
cells,
observed,
characteristic
Mean
microvascular
values
higher
marker
all
though
no
statistically
significant
differences
compared
CD105.
Mutant
IDH1
glioblastomas,
wild-type
those
above
20%
showed
more
abundant
density,
statistical
correlations
not
reaching
significance.
highlighted
variety
percentage
intervals
glioblastomas
immunohistochemical
CD105,
respectively,
correlation
between
evaluated
Computer Methods in Biomechanics & Biomedical Engineering,
Год журнала:
2025,
Номер
unknown, С. 1 - 13
Опубликована: Янв. 1, 2025
The
effect
of
ferroptosis-related
long
non-coding
RNAs
(lncRNAs)
in
predicting
immunotherapy
response
to
glioblastoma
(GBM)
remains
obscure.
This
study
established
a
11-lncRNAs
prognostic
signature.
Differential
gene
expression
analysis,
univariate
and
multivariate
Cox
regression
analyses
the
least
absolute
shrinkage
selection
operator
(LASSO)
algorithm
were
used
identify
genes
establish
nomogram
model
risk
score.
Kaplan-Meier
survival
plots
receiver
operating
characteristic
(ROC)
curve
analysis
evaluate
accuracy
TCGA-GBM
cohort.
To
verify
these
signatures,
we
analyzed
levels
three
lncRNAs
(AGAP2-AS1,
OSMR-AS1,
UNC5B-AS1)
LN229
U87
cells.
ROC
showed
that
area
under
(AUC)
this
signature
is
0.814,
suggesting
it
has
promising
performance
on
GBM
prediction.
rate
patients
high-risk
group
was
significantly
lower
than
low-risk
group,
prediction
superior
conventional
clinicopathological
factors.
Further
qRT-PCR
experiment
also
confirmed
our
lncRNA
signatures.
These
might
be
therapeutic
targets
for
glioblastoma,
targeting
can
improve
efficacy
immunotherapy,
especially
immune
checkpoint
inhibitors.
Mechanistically,
findings
attribute
N6-methyladenosine
(m6A)
mRNA
modification
lncRNAs.
Biomedicines,
Год журнала:
2025,
Номер
13(1), С. 133 - 133
Опубликована: Янв. 8, 2025
Glioblastoma
is
one
of
the
most
aggressive
brain
cancers,
characterized
by
active
infiltrative
growth
and
high
resistance
to
radiotherapy
chemotherapy.
Sesquiterpene
triterpenoids
(STLs)
their
semi-synthetic
analogs
are
considered
as
a
promising
source
novel
anti-tumor
agents
due
low
systemic
toxicity
multi-target
pharmacological
effects
on
key
processes
associated
with
tumor
progression.
The
current
review
aims
systematize
knowledge
anti-glioblastoma
potential
STLs
accumulated
over
last
decade
identify
in
glioblastoma
cells
that
susceptible
action
STLs.
An
analysis
published
data
clearly
demonstrated
STLs,
which
can
successfully
cross
blood-brain
barrier,
exert
complex
inhibitory
effect
through
induction
"mitochondrial
dysfunction-oxidative
stress-apoptosis"
axis,
inhibition
glucose
metabolism
cell
cycle
phase
transition,
suppression
motility
invasion
blockade
proneural-mesenchymal
transition.
Taken
together,
this
highlights
not
only
able
induce
death,
but
also
effectively
affect
diffusive
spread,
suggests
possible
directions
for
further
investigation
context
better
understand
mechanism
action.
Cells,
Год журнала:
2025,
Номер
14(4), С. 292 - 292
Опубликована: Фев. 16, 2025
Glioblastoma
(GBM)
is
a
relatively
rare
but
highly
aggressive
form
of
brain
cancer
characterized
by
rapid
growth,
invasiveness,
and
resistance
to
standard
therapies.
Despite
significant
progress
in
understanding
its
molecular
cellular
mechanisms,
GBM
remains
one
the
most
challenging
cancers
treat
due
high
heterogeneity
complex
tumor
microenvironment.
To
address
these
obstacles,
researchers
have
employed
range
models,
including
vitro
cell
cultures
vivo
animal
often
fail
replicate
complexity
GBM.
As
result,
there
has
been
growing
focus
on
refining
models
incorporating
human-origin
cells,
along
with
advanced
genetic
techniques
stem
cell-based
bioengineering
approaches.
In
this
context,
variety
based
organoids
were
developed
confirmed
be
clinically
relevant
are
contributing
advancement
research
at
preclinical
level.
This
review
explores
preparation
use
organoid-based
deepen
our
biology
explore
novel
therapeutic
These
innovative
hold
promise
for
improving
ability
study
deadly
advancing
development
more
effective
treatments.
Current Issues in Molecular Biology,
Год журнала:
2025,
Номер
47(3), С. 180 - 180
Опубликована: Март 10, 2025
Glioblastoma
(GMB)
is
a
remarkably
aggressive
brain
malignancy
characterized
by
high
mortality
rates,
despite
continuous
advances
in
therapeutic
approaches.
Compounds
derived
from
plants
are
being
studied
for
their
potent
medicinal
properties
the
quest
more
efficient
therapies.
This
study
investigated
anti-glioma
of
Methyl
rosmarinate,
hydroxycinnamic
acid
isolated
Thymus
thracicus
Velen,
which
has
previously
demonstrated
anti-cancer
activity
various
cell
lines.
Human
glioblastoma
lines
U87
and
T98
were
treated
with
rosmarinate
to
assess
its
effect
on
viability,
cycle
distribution
migratory
capacity
using
Trypan
blue
assay,
flow
cytometry
scratch
wound
healing
respectively.
The
combinatorial
effects
temozolomide
also
analyzed
CompoSyn
software.
According
outcomes,
significantly
reduced
induced
death
interfering
checkpoints,
inhibited
migration
both
GMB
Notably,
cells,
compound
showed
synergistic
impact
temozolomide,
whereas
there
was
an
antagonistic
relationship.
These
results
suggest
that
potential
properties;
however,
vivo
research
needed.
International Journal of Nanomedicine,
Год журнала:
2025,
Номер
Volume 20, С. 3303 - 3337
Опубликована: Март 1, 2025
Traditional
drug
therapies
suffer
from
problems
such
as
easy
degradation,
side
effects,
and
treatment
resistance.
disease
diagnosis
also
suffers
high
error
rates
late
diagnosis.
Extracellular
vesicles
(EVs)
are
nanoscale
spherical
lipid
bilayer
secreted
by
cells
that
carry
various
biologically
active
components
integral
to
intercellular
communication.
EVs
can
be
found
in
different
body
fluids
may
reflect
the
state
of
parental
cells,
making
them
ideal
noninvasive
biomarkers
for
disease-specific
The
multifaceted
characteristics
render
optimal
candidates
delivery
vehicles,
with
evidence
suggesting
their
efficacy
ailments.
However,
poor
stability
degradation
natural
have
affected
applications.
To
solve
EVs,
they
engineered
modified
obtain
more
stable
multifunctional
EVs.
In
this
study,
we
review
shortcomings
traditional
methods
describe
how
modify
form
improve
utilization.
An
innovative
stimulus-responsive
system
has
been
proposed.
We
summarize
current
applications
research
status
systemic
diseases,
look
forward
future
directions,
providing
ideas
scholars.
Antioxidants,
Год журнала:
2025,
Номер
14(3), С. 351 - 351
Опубликована: Март 18, 2025
Curcumin,
a
polyphenol
found
in
turmeric,
demonstrates
multifaceted
anti-cancer
activity
against
glioblastoma.
Its
therapeutic
potential
stems
from
its
ability
to
modulate
various
molecular
pathways
implicated
glioblastoma
development
and
progression,
enhance
the
effectiveness
of
radiation
therapy,
induce
cancer
cell
death
through
diverse
mechanisms,
including
apoptosis,
autophagy,
cycle
arrest.
These
combined
actions
make
curcumin
promising
candidate
for
treatment,
warranting
further
investigation
into
clinical
application.
In
this
review,
we
summarize
latest
research
on
analogs'
therapy.