Exploring CX3CR1 as a prognostic biomarker and immunotherapeutic target in sarcoma
Tengfei Li,
No information about this author
Xun Li,
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Pengcheng Kang
No information about this author
et al.
Translational Oncology,
Journal Year:
2025,
Volume and Issue:
53, P. 102283 - 102283
Published: Jan. 20, 2025
Language: Английский
Redefining bladder cancer treatment: innovations in overcoming drug resistance and immune evasion
Peng Huang,
No information about this author
Jie Wang,
No information about this author
Zongze Yu
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et al.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Jan. 22, 2025
Bladder
cancer
is
one
of
the
most
common
malignancies
urinary
system
and
has
always
presented
great
challenges
in
treatment
due
to
its
intricate
biological
features
high
recurrence
rates.
Although
developments
were
achieved
immunotherapy
targeted
therapies
within
last
decade,
therapeutic
outcomes
for
a
number
patients
remain
unsatisfactory,
particularly
as
long-term
efficacy.
Review
discusses
molecular
mechanisms
developed
during
process
bladder
progression:
genetic
epigenetic
alterations,
dynamics
tumor
microenvironment
(TME),
dysregulation
abnormal
activation
various
signaling
pathways—all
contributing
resistance.
It
mutation,
especially
both
low-
high-grade
tumors,
that,
alongside
modifications,
plays
considerable
role
aggressiveness
drug
TME,
comprising
cancer-associated
fibroblasts
(CAFs),
immunosuppressive
cells,
different
components
extracellular
matrix
(ECM),
orchestrates
setting
that
fosters
growth
immune
evasion
confers
resistance
on
any
regime
might
be
used.
The
review
also
provides
an
overview
PI3K/AKT
MAPK
pathways
progression
development
against
them.
Further,
it
immunotherapy,
including
those
involving
checkpoint
inhibitors.
Other
promising
approaches
include
new
strategies
target
not
only
but
checkpoints
combination
therapies.
This
aims
contribute
elaboration
more
effective
personalized
by
fully
understanding
underlying
involved
cancer.
Language: Английский
Endogenous protein S100A14 stabilizes glutaminase to render hepatocellular carcinoma resistant to sorafenib
Journal of Translational Medicine,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: April 11, 2025
Many
cases
of
advanced
hepatocellular
carcinoma
(HCC)
are
resistant
to
the
widely
used
drug
sorafenib,
which
worsens
prognosis.
While
many
studies
have
explored
how
acquired
resistance
emerges
during
exposure,
mechanism
underlying
primary
before
treatment
still
remain
elusive.
Single-cell
lineage
tracing
and
RNA
sequencing
were
performed
identify
sorafenib-resistant
lineages
in
HCC.
Differential
gene
expression
analysis
was
employed
biomarkers
drug-resistant
cells.
Cell
viability
colony
formation
assays
adopted
assess
involvement
S100A14
on
sorafenib
resistance.
Co-immunoprecipitation
(CO-IP)
mass
spectrometry
conducted
uncover
downstream
targets
regulatory
mechanisms
sorafenib.
In
vivo
mouse
xenograft
experiments
carried
out
effect
or
its
interacting
protein
glutaminase
(GLS)
identified
a
cluster
cells,
S100A14,
Ca2+-binding
protein,
determined
be
critical
biomarker
for
Knockdown
significantly
increases
sensitivity
HCC
Mechanistically,
binds
GLS
blocks
phosphorylation
at
residues
Y308
S314,
turn
inhibits
ubiquitination
subsequent
degradation.
By
stabilizing
GLS,
reduces
oxidative
stress
thereby
antagonizing
sorafenib-induced
apoptosis.
Inhibiting
improved
efficacy
against
tumors
vivo.
Our
results
demonstrate
that
plays
pivotal
role
promoting
by
reduce
stress,
acts
as
potential
therapeutic
target
enhance
patients.
Language: Английский
Impact of exercise on cancer: mechanistic perspectives and new insights
Feng Ye,
No information about this author
Xingting Feng,
No information about this author
Renwen Wan
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Sept. 13, 2024
This
review
critically
evaluates
the
substantial
role
of
exercise
in
enhancing
cancer
prevention,
treatment,
and
patient
quality
life.
It
conclusively
demonstrates
that
regular
physical
activity
not
only
reduces
risk
but
also
significantly
mitigates
side
effects
therapies.
The
key
findings
include
notable
improvements
fatigue
management,
reduction
cachexia
symptoms,
enhancement
cognitive
functions.
Importantly,
elucidates
profound
impact
on
tumor
behavior,
modulation
immune
responses,
optimization
metabolic
pathways,
advocating
for
integration
into
standard
oncological
care
protocols.
refined
abstract
encourages
further
exploration
application
as
a
pivotal
element
management.
Language: Английский