BMC Cancer,
Journal Year:
2024,
Volume and Issue:
24(1)
Published: Nov. 29, 2024
Renal
cell
carcinoma
(RCC)
is
characterised
by
its
immunogenic
and
proangiogenic
nature
resistance
to
conventional
therapies.
The
advent
of
immune
checkpoint
inhibitors
(ICIs)
tyrosine
kinase
(TKIs)
has
significantly
improved
patient
survival,
but
these
treatments
remains
a
challenge.
B7-H3,
potential
checkpoint,
been
implicated
in
modulating
the
tumour
microenvironment
escape
mechanisms
RCC.
Immunohistochemical
analysis
B7-H3
expression
was
performed
84
metastatic
RCC
patients.
Tissue
microarrays
separate
sections
formalin-fixed
paraffin-embedded
tissue
were
used
for
immunohistochemical
staining.
Membranous
staining
tumor
cells
scored
statistical
analyses
assess
correlation
between
treatment
outcome.
absent
31%
patients,
while
33.3%
had
score
1+,
2+,
4.8%
3+.
High
correlated
with
poorer
OS
(20
months
vs.
45
months,
p
=
0.012).
In
patients
receiving
nivolumab,
those
high
shorter
PFS
(2
8
0.037)
(17
51
0.01).
only
factor
affecting
multivariate
analysis.
associated
survival
outcomes
reduced
response
nivolumab
may
serve
as
predictive
biomarker
immunotherapy
response.
Future
studies
should
explore
targeting
combination
existing
therapies
enhance
efficacy.
Cancer Urology,
Journal Year:
2025,
Volume and Issue:
20(4), P. 104 - 111
Published: Feb. 28, 2025
Sarcomatoid
variant
of
urothelial
carcinoma
is
a
rare
histological
subtype:
it
diagnosed
in
0.1–0.3
%
all
neoplasms
the
bladder.
The
standard
1
st
line
therapy
for
types
advanced
chemotherapy
which
does
not
necessarily
allow
to
achieve
best
or
complete
responses,
especially
presence
sarcomatoid
differentiation.
High
programmed
cell
death-ligand
(PD-L1)
expression
this
morphological
subtype
allows
assume
better
results
immunotherapy
compared
chemotherapy.
However,
large
number
observations
necessary
confirm
hypothesis
and
suggest
pembrolizumab
as
1st
metastatic
with
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(7), P. 2923 - 2923
Published: March 24, 2025
Understanding
the
modulation
of
specific
immune
cells
within
tumor
microenvironment
(TME)
offers
new
hope
in
cancer
treatments,
especially
immunotherapies.
In
recent
years,
and
resistance
to
immunotherapy
have
become
critical
challenges
treatments.
However,
novel
strategies
for
emerged
as
promising
approaches
oncology
due
vital
roles
immunomodulators
regulating
progression
metastasis
modulating
immunological
responses
standard
care
With
progress
immuno-oncology,
a
growing
number
mechanisms
are
being
uncovered,
offering
potential
enhanced
clinical
near
future.
Thus,
gaining
comprehensive
understanding
broader
context
is
essential.
Herein,
we
particularly
summarize
paradoxical
role
tumor-related
cells,
focusing
on
how
targeted
their
actions
modulated
by
immunotherapies
overcome
immunotherapeutic
cells.
We
also
highlight
molecular
employed
tumors
evade
long-term
effects
agents,
rendering
them
ineffective.
World Journal of Surgical Oncology,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: April 9, 2025
There
is
still
controversy
regarding
the
safety
and
efficacy
of
atezolizumab
for
treatment
urothelial
carcinoma
(UC).
This
research
aimed
to
extensively
investigate
effectiveness
as
a
therapy
UC.
A
thorough
literature
review
was
conducted
using
databases
including
PubMed,
Embase,
Cochrane
Library,
Web
Science.
The
search
included
studies
published
from
inception
each
database
until
May
24,
2024.
primary
outcomes,
progression-free
survival
(PFS)
overall
(OS),
were
calculated
hazard
ratios
(HRs)
their
corresponding
95%
confidence
intervals
(CIs).
Ten
randomized
controlled
trials
(RCTs)
totaling
4,148
participants
in
our
analysis.
Compared
UC
patients
who
received
placebo,
either
alone
or
combination
with
chemotherapy
medications,
aggregated
data
showed
that
had
significantly
longer
OS(HR
=
0.88,
CI
[0.83,
0.94],
p
<
0.0001).
Three
RCTs
also
provided
on
PFS,
showing
atezolizumab,
addition
instead
chemotherapy,
PFS
than
those
placebo
without
(HR
0.85,
[0.76,
0.95],
0.004).
Atezolizumab
has
demonstrated
significant
improvements
OS
among
UC,
offering
crucial
insights
decision-making
immunotherapy.
https://www.crd.york.ac.uk/PROSPERO/#recordDetails
,
identifier
[CRD42024556757].
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: April 12, 2025
Phosphoinositides
(PI)
and
their
metabolic
enzymes
are
known
to
be
involved
in
cellular
processes
associated
with
the
hallmarks
of
cancer.
The
impact
PI
metabolism-related
components
on
urinary
tract
(or
urological)
cancers,
however,
remains
unexplored.
Considering
this,
herein,
we
performed
a
comprehensive
bioinformatic
analysis
clear
cell
renal
carcinoma,
bladder
cancer,
adenocarcinoma
prostate
using
public
databases
investigate
relative
contribution
metabolism
these
clinical
phenotypes.
Primarily,
computed
phosphoinositide
scores
assess
biological
further
enriched
by
predicting
drug
sensitivity,
immune
profiling,
risk
stratification.
Besides,
utilized
single-cell
RNA
sequencing
datasets
identify
intercellular
communication
networks
cancer
subtypes.
Of
interest,
our
identified
PNPLA7
gene
as
potential
biomarker
urological
which
validated
immunohistochemical
evaluation
samples.
In
conclusion,
study
reveals
that
is
critical
prognostic
for
cancers
may
guide
therapies,
including
immunosuppressants.
Therefore,
could
serve
target
requires
attention.
Biomolecules,
Journal Year:
2025,
Volume and Issue:
15(5), P. 620 - 620
Published: April 25, 2025
Renal
cell
carcinoma
(RCC)
is
the
most
lethal
malignancy
of
urinary
system,
with
limited
treatment
options
due
to
drug
resistance
and
adverse
effects
associated
current
therapies.
This
review
aims
systematically
examine
therapeutic
potential
flavonoids,
which
are
natural
polyphenolic
compounds
possessing
anti-inflammatory,
antioxidant,
anticancer
properties,
in
context
RCC
treatment.
We
summarize
activities
26
classified
into
six
subclasses,
explore
their
mechanisms
action,
including
inhibition
tumor
proliferation,
migration,
invasion,
as
well
induction
apoptosis,
autophagy,
ferroptosis.
Particular
attention
paid
modulation
key
signaling
pathways
such
JAK/STAT3,
PI3K/Akt/mTOR,
miRNA-related
axes,
miR-21/YAP1
miR-324-3p/GPX4,
providing
a
molecular
basis
for
anti-RCC
activity.
also
address
several
pharmacological
challenges
that
limit
clinical
application
poor
bioavailability,
metabolic
instability,
toxicity.
Emerging
solutions
novel
flavonoid
derivatives,
advanced
delivery
systems,
rational
combination
therapy
strategies
discussed.
Current
evidence,
phase
II
trial
flavopiridol
RCC,
highlights
but
need
further
validation.
In
conclusion,
flavonoids
offer
promising
approach
improving
Future
research
should
focus
on
optimizing
efficacy
ensuring
safe
translation,
goal
achieving
personalized
minimally
invasive
cancer
Biomolecules,
Journal Year:
2024,
Volume and Issue:
14(8), P. 1043 - 1043
Published: Aug. 22, 2024
Purpose:
This
study
aims
to
explore
the
potential
mechanisms
of
esculin
in
treatment
renal
cell
carcinoma
(RCC).
Methods:
We
employed
network
pharmacology
predict
and
targets
RCC.
Molecular
docking
techniques
were
then
validate
predicted
targets.
Additionally,
a
series
vitro
experiments
conducted
verify
anticancer
effects
on
RCC
cells,
including
CCK-8
assay,
EdU
wound
healing
apoptosis
Western
blot.
Results:
Network
molecular
results
identified
GAPDH,
TNF,
GSK3B,
CCND1,
MCL1,
IL2,
CDK2
as
core
GO
KEGG
analyses
suggested
that
may
influence
apoptotic
processes
target
PI3K/Akt
pathway
Furthermore,
assay
demonstrated
inhibited
viability.
Microscopic
observations
revealed
following
treatment,
there
was
an
increase
crumpling,
reduction
density,
accumulation
floating
dead
cells.
with
increasing
concentrations,
proportion
EdU-positive
cells
decreased,
closure
ratio
PI-positive
increased,
expression
levels
BAX
cleaved-caspase-3
proteins
level
Bcl2
protein
decreased.
These
findings
inhibits
proliferation
migration
while
promoting
apoptosis.
Moreover,
found
GAPDH
inhibit
pathway.
Conclusions:
is
first
elucidate
therapeutic
The
provide
evidence
supporting
clinical
application
introduce
promising
new
candidate
for
treatment.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Nov. 25, 2024
Tumor
immune
escape
has
become
a
research
hotspot
in
the
field
of
cancer
immunotherapy.
Tumor-associated
macrophages
(TAMs)
are
key
component
tumor
microenvironment,
which
play
pivotal
role
by
regulating
immunity
checkpoints,
inhibiting
activity
T
lymphocytes
and
natural
killer
(NK)
cells,
modulating
proportion
different
cells.
Stanniocalcin-1(STC1)is
ubiquitously
expressed
human
body,
is
proven
to
involve
with
progression
clinical
prognosis.
Recently,
STC1
implicated
microenvironment
as
phagocytosis
checkpoint,
well
regulates
via
macrophages.
In
review,
we
discussed
TAMs
their
crosstalk,
hoping
provide
references
for
Cureus,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 16, 2024
Bladder
cancer
is
the
second
most
common
genitourinary
(GU)
malignancy
worldwide.
Treatment
involves
early
cystectomy
and
intravesical
Bacillus
Calmette-Guérin
(BCG),
which
effective
for
T1
high-grade
tumors
carcinoma
in
situ
(CIS)
but
can
cause
significant
side
effects,
including
chemical
bacterial
cystitis,
hematuria,
incontinence,
pneumonitis,
malaise,
fever,
sepsis.
We
present
case
of
a
47-year-old
male
with
transitional
cell
(TCC,
G3
pTa)
treated
transurethral
resection
bladder
tumor
(TURBT)
who
developed
fever
non-productive
cough
after
BCG
injections.
Initially
discharged,
he
returned
worsened
symptoms.
His
vital
signs
showed
38.2°C,
heart
rate
104
beats
per
minute
(bpm),
saturation
93%
on
room
air.
Blood
tests
indicated
inflammation
liver
dysfunction.
Imaging
revealed
lung
micronodularity,
further
CT
imaging
bilateral
miliary
nodules
indicative
pneumonitis.
MRI
ruled
out
disseminated
tuberculosis,
identifying
hepatic
cyst.
Cultures
from
blood,
urine,
sputum,
broncho-alveolar
lavage
were
negative,
granulomatous
was
confirmed
biopsy.
The
patient
oral
glucocorticoids
anti-tuberculosis
medications
(rifampicin,
isoniazid,
ethambutol),
clinical
improvement
shown.
follow-up
at
respiratory
clinic
scheduled.
severe
therapy
complication,
necessitates
diagnosis
management
to
reduce
morbidity
mortality.