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.
Cancers,
Год журнала:
2025,
Номер
17(1), С. 146 - 146
Опубликована: Янв. 5, 2025
Glioblastoma,
the
most
common
and
aggressive
primary
brain
tumor
in
adults,
presents
a
formidable
challenge
due
to
its
rapid
progression,
treatment
resistance,
poor
survival
outcomes.
Standard
care
typically
involves
maximal
safe
surgical
resection,
followed
by
fractionated
external
beam
radiation
therapy
concurrent
temozolomide
chemotherapy.
Despite
these
interventions,
median
remains
approximately
12–15
months,
with
five-year
rate
below
10%.
Prognosis
is
influenced
factors
such
as
patient
age,
molecular
characteristics,
extent
of
resection.
Patients
IDH-mutant
tumors
or
methylated
MGMT
promoters
generally
have
improved
survival,
while
recurrent
glioblastoma
associated
only
six
therapies
cases
are
often
palliative.
Innovative
treatments,
including
TTFields,
add
incremental
benefits,
extending
around
20.9
months
for
eligible
patients.
Symptom
management—addressing
seizures,
headaches,
neurological
deficits—alongside
psychological
support
patients
caregivers
essential
enhance
quality
life.
Emerging
targeted
immunotherapies,
though
still
limited
efficacy,
show
promise
part
an
evolving
landscape.
Continued
research
clinical
trials
remain
crucial
developing
more
effective
treatments.
This
multidisciplinary
approach,
incorporating
diagnostics,
personalized
therapy,
supportive
care,
aims
improve
outcomes
provides
hopeful
foundation
advancing
management.
Cancers,
Год журнала:
2024,
Номер
16(17), С. 2975 - 2975
Опубликована: Авг. 27, 2024
Malignant
gliomas
present
great
difficulties
in
treatment,
with
little
change
over
the
past
30
years
median
survival
time
of
15
months.
Current
treatment
options
include
surgery,
radiotherapy
(RT),
and
chemotherapy.
New
therapies
aimed
at
suppressing
formation
new
vasculature
(antiangiogenic
treatments)
or
destroying
formed
tumor
(vascular
disrupting
agents)
show
promise.
This
study
summarizes
existing
knowledge
regarding
processes
by
which
glioblastoma
(GBM)
tumors
acquire
resistance
to
antiangiogenic
treatments.
The
discussion
encompasses
activation
redundant
proangiogenic
pathways,
heightened
cell
invasion
metastasis,
induced
hypoxia,
creation
vascular
mimicry
channels,
regulation
immune
microenvironment.
Subsequently,
we
explore
potential
strategies
overcome
this
resistance,
such
as
combining
other
methods,
personalizing
treatments
for
each
patient,
focusing
on
therapeutic
targets,
incorporating
immunotherapy,
utilizing
drug
delivery
systems
based
nanoparticles.
Additionally,
would
like
discuss
limitations
methods
future
directions
enhance
beneficial
effects
patients
GBM.
Therefore,
review
aims
research
outcome
GBM
provide
a
more
promising
opportunity
thoroughly
exploring
mechanisms
investigating
novel
strategies.
ACS Chemical Neuroscience,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 25, 2025
Glioblastoma
multiforme
(GBM)
is
a
highly
aggressive
brain
cancer
with
median
survival
of
15
months.
Despite
advancements
in
conventional
treatment
approaches
such
as
surgery
and
chemotherapy,
the
prognosis
remains
poor.
This
study
investigates
use
rapid
evaporative
ionization
mass
spectrometry
(REIMS)
for
real-time
overall
time
classification
GBM
samples
uses
matrix-assisted
laser
desorption
imaging
(MALDI-MSI)
to
compare
lipidomic
differences
within
tumors.
A
total
45
biopsies
were
analyzed
develop
prediction
model
IDH-wild
type
GBM.
REIMS
patterns
from
28
patients
classified
97.7%
correct
rate,
identifying
key
discriminators
between
short-term
(0–12
months)
prolonged
(>12
survivors.
Cross-validation
additional
showed
that
correctly
66.7
69.4%
accuracy,
respectively.
MALDI-MSI
was
performed
confirm
derived
data.
Results
indicated
42
33
discriminating
features
survival,
Proteomic
profiling
by
isolating
tumor
regions
via
laser-capture
microdissection
(LMD)
liquid
chromatography-tandem
(LC-MS/MS).
Subsequently,
1387
proteins
identified,
which
79
significantly
altered.
In
conclusion,
this
shows
rapidly
predicts
glioblastoma
times
based
on
profiles
during
electrosurgical
dissection.
confirmed
these
specific
region
sections.
LMD-guided
LC-MS/MS-based
proteomics
revealed
altered
pathways
survival.
research,
including
comprehensive
predictive
GBM,
could
guide
resection
surgeries
accurate
tissue
identification
well
provide
insights
into
mechanisms,
possibly
related
therapy
response.
Cancer Cell International,
Год журнала:
2024,
Номер
24(1)
Опубликована: Дек. 18, 2024
Cancer
remains
a
significant
global
challenge,
and
despite
the
numerous
strategies
developed
to
advance
cancer
therapy,
an
effective
cure
for
metastatic
elusive.
A
major
hurdle
in
treatment
success
is
ability
of
cells,
particularly
stem
cells
(CSCs),
resist
therapy.
These
CSCs
possess
unique
abilities,
including
self-renewal,
differentiation,
repair,
which
drive
tumor
progression
chemotherapy
resistance.
The
resilience
linked
certain
signaling
pathways.
Tumors
with
pathway-dependent
often
develop
genetic
resistance,
whereas
those
pathway-independent
undergo
epigenetic
changes
that
affect
gene
regulation.
can
evade
cytotoxic
drugs,
radiation,
apoptosis
by
increasing
drug
efflux
transporter
activity
activating
survival
mechanisms.
Future
research
should
prioritize
identification
new
biomarkers
molecules
better
understand
use
cutting-edge
approaches,
such
as
bioinformatics,
genomics,
proteomics,
nanotechnology,
offers
potential
solutions
this
challenge.
Key
include
developing
targeted
therapies,
employing
nanocarriers
precise
delivery,
focusing
on
CSC-targeted
pathways
Wnt,
Notch,
Hedgehog
Additionally,
investigating
multitarget
inhibitors,
immunotherapy,
nanodrug
delivery
systems
critical
overcoming
resistance
cells.
Epigenomics,
Год журнала:
2025,
Номер
17(2), С. 125 - 140
Опубликована: Янв. 19, 2025
Gliomas,
highly
aggressive
tumors
of
the
central
nervous
system,
present
overwhelming
challenges
due
to
their
heterogeneity
and
therapeutic
resistance.
Glioblastoma
multiforme
(GBM),
most
malignant
form,
underscores
this
clinical
urgency
dismal
prognosis
despite
treatment
regimens.
Recent
advances
in
cancer
research
revealed
signaling
pathways
epigenetic
mechanisms
that
intricately
govern
glioma
progression,
offering
multifaceted
targets
for
intervention.
This
review
explores
dynamic
interplay
between
events
regulation
context
glioma,
with
a
particular
focus
on
crucial
roles
played
by
non-coding
RNAs
(ncRNAs).
Through
direct
indirect
targeting,
ncRNAs
emerge
as
key
regulators
shaping
molecular
landscape
glioblastoma
across
its
various
stages.
By
dissecting
these
intricate
regulatory
networks,
novel
patient-tailored
strategies
could
be
devised
improve
patient
outcomes
devastating
disease.
Molecular Medicine Reports,
Год журнала:
2025,
Номер
31(3)
Опубликована: Янв. 24, 2025
Renowned
as
a
highly
invasive
and
lethal
tumor
derived
from
neural
stem
cells
in
the
central
nervous
system,
glioblastoma
(GBM)
exhibits
substantial
histopathological
variation
genomic
complexity,
which
drive
its
rapid
progression
therapeutic
resistance.
Alterations
mitochondrial
DNA
(mtDNA)
copy
number
(CN)
serve
crucial
role
GBM
development
progression,
affecting
various
aspects
of
biology,
including
energy
production,
oxidative
stress
regulation
cellular
adaptability.
Fluctuations
mtDNA
levels,
whether
elevated
or
diminished,
can
impair
function,
potentially
disrupting
phosphorylation
amplifying
reactive
oxygen
species
generation,
thereby
fueling
growth
influencing
treatment
responses.
Understanding
mechanisms
mtDNA‑CN
variations,
their
interplay
with
genetic
environmental
elements
microenvironment,
is
essential
for
advancing
diagnostic
strategies.
Targeting
alterations
could
strengthen
efficacy,
mitigate
resistance
ultimately
enhance
prognosis
patients
this
aggressive
brain
tumor.
The
present
review
summarizes
existing
literature
on
alterations,
specifically
emphasizing
variations
association
by
surveying
articles
published
between
1996
2024,
sourced
databases
such
Scopus,
PubMed
Google
Scholar.
In
addition,
provides
brief
overview
genome
architecture,
knowledge
regarding
integrity
CN,
how
mitochondria
significantly
impact
tumorigenesis.
This
further
presents
information
approaches
restoring
that
contribute
to
optimized
function
improved
health
outcomes.
Journal of Neuroinflammation,
Год журнала:
2025,
Номер
22(1)
Опубликована: Март 15, 2025
Clinical
studies
have
revealed
a
bidirectional
relationship
between
glioma
and
ischemic
stroke,
with
evidence
of
spatial
overlap
the
two
conditions.
This
connection
arises
from
significant
similarities
in
their
pathological
processes,
including
regulation
cellular
metabolism,
inflammation,
coagulation,
hypoxia,
angiogenesis,
neural
repair,
all
which
involve
common
biological
factors.
A
shared
feature
both
diseases
is
crucial
role
extracellular
vesicles
(EVs)
mediating
intercellular
communication.
Extracellular
vesicles,
characteristic
bilayer
structure,
encapsulate
proteins,
lipids,
nucleic
acids,
shielding
them
enzymatic
degradation
by
ribonucleases,
deoxyribonucleases,
proteases.
structural
protection
facilitates
long-distance
communication
multicellular
organisms.
In
gliomas,
EVs
are
pivotal
intracranial
signaling
shaping
tumor
microenvironment.
Importantly,
cargos
carried
glioma-derived
closely
align
factors
involved
underscoring
substantial
impact
on
stroke
pathology,
particularly
through
roles
as
key
mediators
this
interaction.
review
explores
interplay
addressing
clinical
manifestations
pathophysiological
processes
across
stages
onset,
progression,
recovery,
particular
focus
these
interactions.
Abstract
Background
Glioblastoma
(GBM)
is
a
highly
aggressive
brain
tumor
characterized
by
poor
prognosis
and
limited
therapeutic
options.
Understanding
the
molecular
mechanisms
driving
GBM
progression
essential
for
developing
more
effective
diagnostic
approaches.
Specifically,
investigating
Cell
Division
Cycle-Associated
(CDCA)
genes
offers
new
perspectives
on
cell
cycle
regulation
proliferation
of
cells,
which
are
key
factors
in
growth
resistance
to
treatment.
These
have
not
been
extensively
studied
GBM,
making
them
promising
area
targeted
research
potential
interventions.
This
project
was
launched
elucidate
pathogenic,
diagnostic,
roles
CDCA
GBM.
Methodology
Total
RNA
extracted
from
lines
followed
RT-qPCR
analyze
expression
genes.
The
validation,
prognostic
significance,
mutational
analysis
were
performed
using
various
databases.
Functional
assays,
including
gene
knockdown,
colony
formation,
proliferation,
wound
healing,
conducted
U87MG
cells
assess
role
CDCA7
CDCA8
Results
12
6
normal
revealed
significant
overexpression
these
ROC
curve
demonstrated
excellent
potential,
with
AUC
values
1
most
indicates
that
effectively
distinguishes
cells.
Validation
additional
TCGA
data
confirmed
upregulation
tumors,
association
cancer-related
pathways.
Survival
showed
higher
correlated
patients.
Mutation,
CNV,
methylation
analyses
alterations
genes,
further
supporting
their
Additionally,
linked
immune
modulation
cycle-related
functions,
suggesting
involvement
evasion
proliferation.
Knockdown
experiments
reduction
migration,
highlighting
as
targets.
Conclusion
Overall,
our
findings
suggest
could
serve
both
biomarkers
targets