Nanoparticle troopers: Infiltrating cancer cells for targeted therapies
Nano-Structures & Nano-Objects,
Год журнала:
2025,
Номер
41, С. 101453 - 101453
Опубликована: Фев. 1, 2025
Язык: Английский
IL-6 underlies microenvironment immunosuppression and resistance to therapy in glioblastoma
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2025,
Номер
unknown
Опубликована: Март 14, 2025
The
glioblastoma
tumor
immune
microenvironment
(TIME)
is
an
immunosuppressive
barrier
to
therapy
that
encumbers
responses
checkpoint
inhibition
(ICI).
Immunosuppressive
cytokines,
pro-tumor
myeloid
cells,
and
exhausted
T-cells
are
hallmarks
of
the
TIME.
Here
we
integrate
spatial
single-cell
analyses
patient-matched
human
samples
before
after
ICI
with
genetic,
immunologic,
single-cell,
pharmacologic
studies
in
preclinical
models
reveal
interleukin-6
(IL-6)
reprograms
TIME
sensitize
mouse
radiotherapy.
Rare
patients
who
achieve
clinical
have
lower
pre-treatment
IL-6
levels
compared
glioblastomas
do
not
respond
ICI.
Immune
stimulatory
gene
suppresses
murine
glioblastoma.
Furthermore,
survival
was
longer
Il-6
knockout
mice
orthotopic
SB28
relative
wild-type
mice.
blockade
a
neutralizing
antibody
transiently
sensitizes
anti-PD-1
by
increasing
MHCII+
monocytes,
CD103+
migratory
dendritic
cells
(DCs),
CD11b+
conventional
DCs,
effector
CD8+
T
decreasing
Tregs.
To
translate
these
findings
combination
treatment
strategy
for
recurrent
patients,
show
plus
durably
high-dose
Язык: Английский
Limitations of nomogram models in predicting survival outcomes for glioma patients
Frontiers in Immunology,
Год журнала:
2025,
Номер
16
Опубликована: Март 18, 2025
Glioma
represents
a
prevalent
and
malignant
tumor
of
the
central
nervous
system
(CNS),
it
is
essential
to
accurately
predict
survival
glioma
patients
optimize
their
subsequent
treatment
plans.
This
review
outlines
most
recent
advancements
viewpoints
regarding
application
nomograms
in
prognosis
research.
With
an
emphasis
on
precision
external
applicability
predictive
models,
we
carried
out
comprehensive
literature
provided
step-by-step
guide
for
developing
evaluating
nomograms.
A
summary
thirty-nine
articles
was
produced.
The
majority
nomogram-building
research
has
used
limited
patient
samples,
disregarded
proportional
hazards
(PH)
assumption
Cox
regression
some
them
have
failed
incorporate
validation.
Furthermore,
capability
influenced
by
selection
incorporated
risk
factors.
Overall,
current
accuracy
moderately
credible.
development
validation
nomogram
models
ought
adhere
standardized
set
criteria,
thereby
augmenting
worth
clinical
decision-making
clinician-patient
communication.
Prior
nomogram,
imperative
thoroughly
scrutinize
its
statistical
foundation,
rigorously
evaluate
accuracy,
and,
whenever
feasible,
assess
utilizing
multicenter
databases.
Язык: Английский
Exploration of the multiomics-based mechanisms of Gancao Nourishing-Yin decoction in regulating mitochondrial metabolic genes CYB5R3 and PICK1 to influence glioma progression
Discover Oncology,
Год журнала:
2025,
Номер
16(1)
Опубликована: Апрель 8, 2025
Glioma
is
the
most
common
malignancy
of
central
nervous
system,
characterised
by
its
high
invasiveness
and
recurrence,
which
significantly
limit
therapeutic
outcomes.
Energy
metabolism
reprogramming,
especially
mitochondrial
dysfunction,
plays
a
pivotal
role
in
tumour
growth,
survival,
progression.
Mitochondria
serve
as
hub
for
energy
production
biosynthesis,
adapting
through
alterations
oxidative
phosphorylation,
lipid
metabolism,
tricarboxylic
acid
cycle
to
meet
metabolic
demands
gliomas.
Gancao
Nourishing-Yin
(GCNY)
decoction,
traditional
herbal
compound,
has
demonstrated
potential
antitumour
effects,
particularly
modulating
pathways
stress,
are
critical
cell
adaptation.
Genomic
data
from
glioma
GWAS
dataset
Finnish
R11
database
eQTL
13
distinct
brain
regions
were
analysed
using
Summary-data-based
Mendelian
Randomization(SMR)
identify
glioma-associated
genes.
MitoCarta3.0,
genes,
was
used
pinpoint
mitochondrial-related
Differentially
expressed
genes
(DEGs)
human
microglial
cells
treated
with
GCNY
extracted
GEO
GSE210945
cross-referenced
SMR
results
key
Colocalisation
analysis,
validation
TCGA
database,
survival
functional
annotations
performed
explore
mechanisms
action.
Integration
MitoCarta3.0
identified
19
linked
gliomas,
primarily
involved
amino
fatty
metabolism.
Among
these,
CYB5R3
PICK1
emerged
strong
genetic
links
signals
(PPH4
=
1).
CYB5R3,
upregulated
associated
enhanced
elevated
reactive
oxygen
species
(ROS)
production,
poor
outcomes
(HR
2.23,
P
<
0.001).
PICK1,
despite
being
downregulated,
showed
context-dependent
roles
progression,
expression
worse
prognosis
2.86,
moderate
predictive
capacity
one-year
(AUC
0.695).
This
study
highlights
identifying
regulators
influenced
GCNY.
By
pathways,
including
ROS
phosphorylation
activity,
offers
novel
multitarget
strategy
therapy.
These
findings
underscore
importance
target
gliomas
provide
new
insights
into
integrated
management.
Язык: Английский