Cells,
Journal Year:
2025,
Volume and Issue:
14(2), P. 97 - 97
Published: Jan. 10, 2025
Background:
The
wide
variability
in
clinical
responses
to
anti-tumor
immunotherapy
drives
the
search
for
personalized
strategies.
One
of
promising
approaches
is
drug
screening
using
patient-derived
models
composed
tumor
and
immune
cells.
In
this
regard,
selection
an
appropriate
vitro
model
choice
cellular
response
assay
are
critical
reliable
predictions.
Fluorescence
lifetime
imaging
microscopy
(FLIM)
a
powerful,
non-destructive
tool
that
enables
direct
monitoring
metabolism
on
label-free
basis
with
potential
resolve
metabolic
rearrangements
cells
associated
their
reactivity.
Objective:
aim
study
was
develop
glioma
explant
enriched
by
autologous
peripheral
lymphocytes
explore
FLIM
redox-cofactor
NAD(P)H
living
measure
checkpoint
inhibitors.
Methods:
light
microscopy,
flow
cytometry
were
used.
Results:
results
demonstrate
responsive
displayed
significant
increase
free
fraction
α1
after
treatment,
shift
towards
glycolysis
due
lymphocyte
activation.
non-responsive
exhibited
no
alterations
or
decrease
treatment.
data
correlated
well
standard
assays
vitro,
including
morphological
changes,
T-cells
activation
marker
CD69,
cell
proliferation
index
Ki67.
Conclusions:
proposed
platform
includes
explants
co-cultured
represents
solution
patient-specific
immunotherapeutic
screening.
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 10, 2025
Abstract
Glioblastoma
(GBM),
the
most
malignant
brain
tumor
with
high
prevalence,
remains
highly
resistant
to
existing
immunotherapies
due
significant
immunosuppression
within
microenvironment
(TME),
predominantly
manipulated
by
M2‐phenotypic
tumor‐associated
macrophages
(M2‐TAMs).
Here
in
this
work,
an
M2‐TAMs
targeted
nano‐reprogrammers,
MG5‐S‐IMDQ,
is
established
decorating
mannose
molecule
as
targeting
moiety
well
toll‐like
receptor
(TLR)
7/8
agonist,
imidazoquinoline
(IMDQ)
on
dendrimeric
nanoscaffold.
MG5‐S‐IMDQ
demonstrated
excellent
capacity
of
penetrating
blood‐brain
barrier
(BBB)
selectively
GBM
microenvironment,
leading
a
phenotype
transformation
and
function
restoration
TAMs
shown
heightened
phagocytic
activity
toward
cells,
enhanced
cytotoxic
effects,
improved
antigen
cross‐presentation
capability.
In
meantime,
induction
function‐oriented
“gear
effect”,
treatment
extended
its
impact
systemically
enhancing
infiltration
type
I
conventional
dendritic
cells
(cDC1s)
into
sites
bolstering
adaptive
immune
responses.
sum,
precisely
working
unique
target
situ,
nano‐reprogrammers
successfully
robust
network
that
worked
synergistically
combat
tumors.
This
facile
nanoplatform‐based
immunomodulatory
strategy,
serving
powerful
convenient
monotherapy
or
complementary
alongside
other
therapies
like
surgery,
provided
deep
insights
for
advancing
translational
study
GBM.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 14, 2025
In
recent
years,
significant
breakthroughs
have
been
made
in
cancer
therapy,
particularly
with
the
development
of
molecular
targeted
therapies
and
immunotherapies,
owing
to
advances
tumor
biology
immunology.
High-grade
gliomas
(HGGs),
characterized
by
their
high
malignancy,
remain
challenging
treat
despite
standard
treatment
regimens,
including
surgery,
radiotherapy,
chemotherapy,
treating
fields
(TTF).
These
provide
limited
efficacy,
highlighting
need
for
novel
strategies.
Molecular
immunotherapy
emerged
as
promising
avenues
improving
outcomes
high-grade
gliomas.
This
review
explores
current
status
advancements
immunotherapeutic
approaches
Acta Pharmaceutica Sinica B,
Journal Year:
2024,
Volume and Issue:
14(9), P. 3834 - 3854
Published: June 3, 2024
Immunotherapy
is
an
important
cancer
treatment
method
that
offers
hope
for
curing
patients.
While
immunotherapy
has
achieved
initial
success,
a
major
obstacle
to
its
widespread
adoption
the
inability
benefit
majority
of
The
success
or
failure
closely
linked
tumor's
immune
microenvironment.
Recently,
there
been
significant
attention
on
strategies
regulate
tumor
microenvironment
in
order
stimulate
anti-tumor
responses
immunotherapy.
distinctive
physical
properties
and
design
flexibility
nanomedicines
have
extensively
utilized
target
cells
(including
tumor-associated
macrophages
(TAMs),
T
cells,
myeloid-derived
suppressor
(MDSCs),
fibroblasts
(TAFs)),
offering
promising
advancements
In
this
article,
we
reviewed
aimed
at
targeting
various
focus
models
are
based
nanomedicines,
with
goal
inducing
enhancing
improve
It
worth
noting
combining
other
treatments,
such
as
chemotherapy,
radiotherapy,
photodynamic
therapy,
can
maximize
therapeutic
effects.
Finally,
identified
challenges
nanotechnology-mediated
needs
overcome
more
effective
nanosystems.
MedComm – Oncology,
Journal Year:
2024,
Volume and Issue:
3(1)
Published: Feb. 1, 2024
Abstract
Glioblastoma
multiforme
(GBM),
a
WHO
grade
IV
diffuse
glioma,
is
highly
aggressive
brain
tumor
with
median
survival
of
less
than
year.
Characterized
by
robust
proliferation
and
invasion,
recent
studies
spotlight
glioma
stem
cells
(GSCs)
within
GBM
tumors,
pivotal
in
development,
progression,
treatment
resistance.
This
review
aims
to
shed
light
on
the
critical
role
GSCs
initiation
progression
GBM,
emphasizing
their
contribution
development
resistance
existing
treatments.
Unlike
normal
cells,
play
pathogenesis.
The
delves
into
unique
characteristics
GSCs,
marked
heightened
metabolic
activities
distinct
epigenetic
transcriptional
programming.
Recognizing
significance
years,
examines
how
presence
amplifies
lethal
nature
GBM.
also
critically
evaluates
advancements
diagnostic
methods
therapies,
which
include
targeting
GSCs.
Providing
concise
yet
comprehensive
overview,
contributes
insights
GBM's
intricate
dynamics,
offering
potential
directions
for
future
research
therapeutic
strategies.
Abstract
Gliomas
are
the
most
common
primary
tumors
of
central
nervous
system,
with
glioblastoma
multiforme
(GBM)
having
highest
incidence,
and
their
therapeutic
efficacy
depends
primarily
on
extent
surgical
resection
postoperative
chemotherapy.
The
role
intracranial
blood–brain
barrier
occurrence
drug‐resistant
gene
O6‐methylguanine‐DNA
methyltransferase
have
greatly
limited
chemotherapeutic
agents
in
patients
GBM
made
it
difficult
to
achieve
expected
clinical
response.
In
recent
years,
rapid
development
nanotechnology
has
brought
new
hope
for
treatment
tumors.
Nanoparticles
(NPs)
shown
great
potential
tumor
therapy
due
unique
properties
such
as
light,
heat,
electromagnetic
effects,
passive
targeting.
Furthermore,
NPs
can
effectively
load
drugs,
significantly
reduce
side
effects
improve
efficacy,
showing
chemotherapy
glioma.
this
article,
we
reviewed
mechanisms
glioma
drug
resistance,
physicochemical
NPs,
advances
resistance.
We
aimed
provide
perspectives
Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(2), P. 375 - 375
Published: Feb. 6, 2024
Research
on
the
development
of
photodynamic
therapy
for
treatment
brain
tumors
has
shown
promise
in
this
highly
aggressive
form
cancer.
Analysis
both
vivo
studies
and
clinical
shows
that
can
provide
significant
benefits,
such
as
an
improved
median
rate
survival.
The
use
is
characterized
by
relatively
few
side
effects,
which
a
advantage
compared
to
conventional
methods
often-used
tumor
surgery,
advanced
radiotherapy,
classic
chemotherapy.
Continued
research
area
could
bring
advances,
influencing
future
standards
difficult
deadly
disease.
Cancers,
Journal Year:
2024,
Volume and Issue:
16(15), P. 2752 - 2752
Published: Aug. 2, 2024
The
isocitrate
dehydrogenase
1
and
2
(IDH1
IDH2)
enzymes
are
involved
in
key
metabolic
processes
human
cells,
regulating
differentiation,
proliferation,
oxidative
damage
response.
IDH
mutations
have
been
associated
with
tumor
development
progression
various
solid
tumors
such
as
glioma,
cholangiocarcinoma,
chondrosarcoma,
other
types
become
crucial
markers
molecular
classification
prognostic
assessment.
intratumoral
serum
levels
of
D-2-hydroxyglutarate
(D-2-HG)
could
serve
diagnostic
biomarkers
for
identifying
mutant
(IDHmut)
tumors.
As
a
result,
an
increasing
number
clinical
trials
evaluating
targeted
treatments
IDH1/IDH2
mutations.
Recent
studies
shown
that
the
focus
these
new
therapeutic
strategies
is
not
only
neomorphic
activity
IDHmut
but
also
epigenetic
shift
induced
by
potential
role
combination
treatments.
Here,
we
provide
overview
current
knowledge
about
tumors,
particular
on
available
IDH-targeted
emerging
results
from
aiming
to
explore
tumor-specific
features
identify
benefit
therapies
their
strategies.
An
insight
into
future
perspectives
roles
circulating
radiomic
included.
Discover Oncology,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Feb. 7, 2025
Laminin
subunit
beta
1
(LAMB1)
has
regulatory
functions
on
the
proliferation,
attachment,
and
migration
of
tumor
cells,
with
increased
levels
linked
to
different
cancers.
This
study
aims
at
investigating
effects
mechanisms
LAMB1
in
glioma.
Glioma
cell
models
overexpression
or
downregulation
were
constructed.
Cell
viability,
invasion
evaluated.
Glucose
uptake
lactate
production
examined,
Seahorse
was
used
assess
extracellular
acidification
rate
(ECAR).
The
EC50
temozolomide
(TMZ)
glioma
cells
tested.
Western
blotting
conducted
monitor
expression
HK1,
HK2,
PDHA,
PKM.
Bioinformatic
analysis
employed
investigate
downstream
mechanism
LAMB1.
In
addition,
a
subcutaneous
model
constructed
determine
influence
GBM
growth
vivo.
enhanced
promoted
growth.
upregulation
cellular
glycolysis
repressed
sensitivity
TMZ.
activated
NF-κB
pathway.
Downregulation
mitigating
pathway
by
Bay
11-7082
inhibited
growth,
TMZ
sensitivity.
exerted
antitumor
regulating
NF-κB/HK2
axis.