Progress and challenges in glypican-3 targeting for hepatocellular carcinoma therapy
Arnaud Couzinet,
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Toshihiro Suzuki,
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Tetsuya Nakatsura
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et al.
Expert Opinion on Therapeutic Targets,
Journal Year:
2024,
Volume and Issue:
28(10), P. 895 - 909
Published: Oct. 2, 2024
Introduction
Glypican-3
(GPC3)
is
a
cell
membrane-anchored
heparan
sulfate
proteoglycan
that
has
recently
garnered
attention
as
cancer
antigen
owing
to
its
high
expression
in
numerous
cancers,
particularly
hepatocellular
carcinoma
(HCC),
and
limited
adult
normal
tissue.
Language: Английский
The Role of NK Cells in Cancer Immunotherapy: Mechanisms, Evasion Strategies, and Therapeutic Advances
Paula Morcillo-Martín-Romo,
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Javier Valverde-Pozo,
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María Ortiz-Bueno
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et al.
Biomedicines,
Journal Year:
2025,
Volume and Issue:
13(4), P. 857 - 857
Published: April 2, 2025
Background/Objectives:
Natural
killer
(NK)
cells
play
a
crucial
role
in
tumor
surveillance
by
exerting
cytotoxic
activity
and
modulating
immune
responses.
However,
tumors
employ
diverse
evasion
strategies
that
limit
NK
cell
effectiveness.
This
review
aims
to
explore
the
molecular
mechanisms
of
activation
inhibition
cancer,
influence
microenvironment,
latest
advancements
cell-based
immunotherapies,
including
adoptive
transfer
Chimeric
Antigen
Receptor-Natural
Killer
(CAR-NK)
therapies.
Methods:
A
comprehensive
literature
was
conducted,
prioritizing
peer-reviewed
studies
from
last
decade
on
biology,
evasion,
immunotherapeutic
applications.
The
analysis
includes
data
preclinical
models
clinical
trials
evaluating
expansion
strategies,
cytokine-based
stimulation,
CAR-NK
therapy
developments.
Results:
eliminate
through
granule
release,
death
receptor
pathways,
cytokine
secretion.
evade
NK-mediated
immunity
downregulating
activating
ligands,
secreting
immunosuppressive
molecules,
altering
microenvironment.
Novel
therapies,
such
as
combination
approaches
with
checkpoint
inhibitors,
enhance
persistence
therapeutic
efficacy
against
both
hematologic
solid
malignancies.
Clinical
suggest
improved
safety
profiles
compared
CAR-T
reduced
release
syndrome
graft-versus-host
disease.
Conclusions:
While
immunotherapies
hold
great
promise,
challenges
remain,
limited
tumor-induced
immunosuppression.
Addressing
these
hurdles
will
be
critical
for
optimizing
therapies
advancing
next-generation,
off-the-shelf
immunotherapeutics
broader
Language: Английский
Breaking barriers: CAR-NK cell therapy breakthroughs in female-related cancers
G. Ahmad,
No information about this author
Samaneh Nouri,
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Amirhossein Mohammad Gholian
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et al.
Biomedicine & Pharmacotherapy,
Journal Year:
2025,
Volume and Issue:
187, P. 118071 - 118071
Published: April 19, 2025
Language: Английский
Comprehensive single-cell and bulk transcriptomic analyses to develop an NK cell-derived gene signature for prognostic assessment and precision medicine in breast cancer
Qianshan Hou,
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Chunzhen Li,
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Y.M. Chong
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et al.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Oct. 23, 2024
Background
Natural
killer
(NK)
cells
play
crucial
roles
in
mediating
anti-cancer
activity
breast
cancer
(BRCA).
However,
the
potential
of
NK
cell-related
molecules
predicting
BRCA
outcomes
and
guiding
personalized
therapy
remains
largely
unexplored.
This
study
focused
on
developing
a
prognostic
therapeutic
prediction
model
for
by
incorporating
genes.
Methods
The
data
analyzed
primarily
originated
from
TCGA
GEO
databases.
role
was
evaluated,
marker
genes
were
identified
via
single-cell
analysis.
Module
closely
associated
with
immunotherapy
resistance
bulk
transcriptome-based
weighted
correlation
network
analysis
(WGCNA).
Following
taking
intersection
LASSO
regression,
NK-related
(NKRGs)
relevant
to
prognosis
screened,
signature
subsequently
constructed.
Analyses
further
expanded
clinicopathological
relevance,
GSEA,
tumor
microenvironment
(TME)
analysis,
immune
function,
responsiveness,
chemotherapeutics.
Key
NKRGs
screened
machine
learning
validated
spatial
transcriptomics
(ST)
immunohistochemistry
(IHC).
Results
Tumor-infiltrating
are
favorable
factor
BRCA.
By
combining
scRNA-seq
transcriptomic
analyses,
we
7
(CCL5,
EFHD2,
KLRB1,
C1S,
SOCS3,
IRF1,
CCND2)
developed
an
risk
scoring
(NKRS)
system.
reliability
NKRS
verified
through
survival
clinical
relevance
analyses
across
multiple
cohorts.
also
demonstrated
robust
predictive
power
various
aspects,
including
TME
landscape,
functions,
responses,
chemotherapeutic
sensitivity.
Additionally,
KLRB1
CCND2
emerged
as
key
external
validation,
their
expression
confirmed
specimens
ST
IHC.
Conclusions
We
novel
gene
that
has
proven
valuable
evaluating
treatment
response
BRCA,
expecting
advance
precision
medicine
Language: Английский
Advances in cellular therapies for children and young adults with solid tumors
Current Opinion in Pediatrics,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 21, 2024
Adoptive
immunotherapy
brings
hope
to
children
and
young
adults
diagnosed
with
high-risk
solid
tumors.
Cellular
(cell)
therapies
such
as
chimeric
antigen
receptor
(CAR)
T
cell,
CAR
natural
killer
(NK)
cell
(TCR)
therapy
are
potential
avenues
of
targeted
limited
long-term
toxicities.
However,
development
for
tumors
is
in
its
nascent
stages.
Here,
we
will
review
the
current
clinical
experience,
barriers
efficacy,
strategies
improve
response
patient
access.
Language: Английский