Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: April 23, 2024
Citation:
Wu
J,
Rong
Y,
Li
T,
Wilson
CM,
He
Chen
D,
Han
J
and
Zhang
X
(2024)
Editorial:
Targeting
nucleotide
metabolism
for
enhancing
antitumor
immunity.
Front.
Immunol.
15:1412057.
doi:
10.3389/fimmu.2024.1412057
Deleted Journal,
Journal Year:
2024,
Volume and Issue:
2(2)
Published: April 1, 2024
Abstract
T
cells
engineered
to
express
chimeric
antigen
receptors
(CARs)
with
specificity
toward
tumor
have
led
promising
outcomes
in
patients
hematological
malignancies.
Nevertheless,
the
application
of
CAR‐T
cell
therapy
solid
tumors
encounters
several
obstacles.
These
include
heterogeneity
and
immune
escape,
exhaustion
restricted
infiltration
into
that
affect
therapeutic
efficacy
cells,
as
well
“on‐target,
off‐tumor”
toxicities
can
lead
severe
even
fatal
adverse
events.
In
recent
years,
clinical
trials
new
approaches
for
made
certain
progress.
Here,
we
update
related
summarize
strategies
aiming
improve
safety
based
on
experimental
studies.
Molecular Biomedicine,
Journal Year:
2024,
Volume and Issue:
5(1)
Published: Nov. 29, 2024
Abstract
Tumor
energy
metabolism
plays
a
crucial
role
in
the
occurrence,
progression,
and
drug
resistance
of
tumors.
The
study
tumor
has
gradually
become
an
emerging
field
treatment.
Recent
studies
have
shown
that
epigenetic
regulation
is
closely
linked
to
metabolism,
influencing
metabolic
remodeling
biological
traits
cells.
This
review
focuses
on
primary
pathways
explores
therapeutic
strategies
target
these
pathways.
It
covers
key
areas
such
as
glycolysis,
Warburg
effect,
mitochondrial
function,
oxidative
phosphorylation,
adaptability
Additionally,
this
article
examines
regulator
SWI/SNF
complex
specifically
its
interactions
with
glucose,
lipids,
amino
acids.
Summarizing
aimed
at
pathways,
including
inhibitors
mitochondrial-targeted
drugs,
exploitation
vulnerabilities,
recent
developments
related
complexes
potential
targets.
clinical
significance,
challenges,
future
directions
research
are
discussed,
overcome
resistance,
combination
therapy,
application
new
technologies.
Medicinal Research Reviews,
Journal Year:
2023,
Volume and Issue:
44(3), P. 1121 - 1146
Published: Dec. 26, 2023
Cancer
heterogeneity
remains
a
significant
challenge
for
effective
cancer
treatments.
Altered
energetics
is
one
of
the
hallmarks
and
influences
tumor
growth
drug
resistance.
Studies
have
shown
that
exists
within
metabolic
profile
tumors,
personalized-combination
therapy
with
relevant
interventions
could
improve
patient
response.
Metabolomic
studies
are
identifying
novel
biomarkers
therapeutic
targets
improved
treatment
The
spatial
location
elements
in
microenvironment
becoming
increasingly
important
understanding
disease
progression.
evolution
metabolomics
analysis
now
allows
scientists
to
deeply
understand
how
metabolite
distribution
contributes
biology.
Recently,
these
techniques
spatially
resolved
subcellular
level.
It
has
been
proposed
mapping
outcomes
by
improving
precision
medicine,
enabling
earlier
diagnosis
intraoperatively
margins.
This
review
will
discuss
altered
pathways
contribute
progression
resistance
explore
current
capabilities
technologies
be
integrated
into
clinical
practice
outcomes.
Cancers,
Journal Year:
2023,
Volume and Issue:
15(10), P. 2862 - 2862
Published: May 22, 2023
Approximately
a
century
ago,
Otto
Warburg
discovered
that
cancer
cells
use
fermentative
rather
than
oxidative
metabolism
even
though
the
former
is
more
inefficient
in
terms
of
energy
production
per
molecule
glucose.
Cancer
increase
this
presence
oxygen,
and
process
called
aerobic
glycolysis
or
effect.
This
alternative
mainly
characterized
by
higher
glycolytic
rates,
which
allow
to
obtain
amounts
total
ATP,
lactate,
but
there
are
also
an
activation
protumoral
signaling
pathways
generation
molecules
favor
progression.
One
these
succinate,
Krebs
cycle
intermediate
whose
concentration
increased
considered
oncometabolite.
Several
actions
have
been
associated
succinate
its
role
several
types
has
already
described.
Despite
playing
major
cancer,
so
far,
potential
as
target
prevention
treatment
remained
mostly
unexplored,
most
previous
Warburg-directed
anticancer
strategies
focused
on
other
intermediates.
In
review,
we
aim
summarize
succinate's
functions
discuss
expression
regulators
therapy
strategy.
Analytica Chimica Acta,
Journal Year:
2025,
Volume and Issue:
1349, P. 343826 - 343826
Published: Feb. 20, 2025
The
imperative
need
for
early
cancer
detection,
which
is
crucial
improved
survival
rates
in
many
severe
cancers
such
as
lung
cancer,
remains
challenging
due
to
the
lack
of
reliable
early-diagnosis
technologies
and
robust
biomarkers.
To
address
this
gap,
innovative
screening
platforms
are
essential
unveil
chemical
signatures
its
treatments.
It
established
that
oxidative
tumor
environment
induces
alterations
host
metabolic
processes
influences
endogenous
volatile
synthesis.
Despite
efforts,
consensus
on
unique
markers
detection
has
been
elusive,
partly
genetic
variation
leading
heterogeneity
humans
standardized
procedures
analytical
analyses.
In
study,
we
utilized
advanced
secondary
electrospray
ionization
(SESI)
technique
coupled
with
a
high-resolution
mass
spectrometer
(HRMS)
non-invasively
monitor
volatiles
pre-clinical
mouse
model
real
time.
Our
findings
revealed
651
dysregulated
features
upon
onset
identified
36
correlated
size.
Endogenous
tracing
glucose
metabolism
highlighted
γ-glutamyl
cycle
downstream
pathway
implicated
driven
by
an
imbalance
glutathione
reactive
oxygen
species
(ROS)
accumulation.
Notably,
our
study
unveiled
changes
associated
gemcitabine
cisplatin
treatment,
significantly
abrogated
growth
vivo.
Furthermore,
5-oxoproline
metabolite
indicative
response
treatment.
conclusion,
SESI-HRMS
based
analysis
systematically
explores
provides
novel
non-invasive
platform
possess
great
potential
real-time,
confident,
sensitive
monitoring
cancer.
Oral Diseases,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 6, 2025
This
study
aimed
to
integrate
the
available
data
published
in
literature
identify
and
elucidate
impact
of
targeted
therapy
for
oral
potentially
malignant
disorders
(OPMDs).
systematic
review
was
conducted
according
guidelines
Preferred
Reporting
Items
Systematic
Reviews
Meta-analyses
(PRISMA)
2020
statement.
An
electronic
search
across
five
databases
with
no
publication
date
restriction
January
2023
subsequently
updated
2024.
Eligibility
criteria
included
studies
focusing
on
therapies.
Interventions
that
either
did
not
align
specific
definition
or
failed
meet
precision-based
treatment
approaches
were
excluded
from
this
review.
Six
clinical
trials
identified,
all
United
States.
The
sample
size
ranged
12
150
subjects.
Celecoxib,
erlotinib,
cetuximab,
metformin,
nivolumab
employed
as
systemic
therapies
at
varying
doses.
Some
patients
experienced
disease
progression
statistically
significant
differences
histological
improvement
rates
increases.
Certain
reported
treatment-related
toxicity.
findings
do
support
use
managing
OPMDs,
highlighting
need
additional
further
evaluate
their
efficacy.
Journal of Medicinal Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
Ferroptosis
is
a
nonapoptotic
form
of
cell
death
discovered
in
2012.
Noninvasive
treatments
regulating
ferroptosis
are
important
for
wide
range
diseases.
Among
the
noninvasive
treatments,
sonodynamic
therapy
(SDT)
has
become
promising
due
to
its
strong
tissue
penetration
and
few
side
effects.
In
recent
years,
targeted
drug
delivery
platforms
constructed
on
basis
SDT
have
provided
an
efficient
mode
regulation
ferroptosis.
Based
latest
research
reports,
this
Perspective
introduces
basic
mechanism
influencing
factors
therapeutic
effects,
elucidates
significance
ferroptosis-targeted
SDT,
summarizes
studies
through
different
pathways.
We
also
present
innovative
composite
ultrasound-responsive
platforms.
Finally,
brief
summary
outlook
based
current
presented.
Translational Andrology and Urology,
Journal Year:
2023,
Volume and Issue:
12(4), P. 549 - 571
Published: April 1, 2023
Previous
studies
have
shown
that
aldolase
B
(ALDOB)
might
play
controversial
roles
in
multiple
types
of
cancer,
which
could
act
as
a
cancer-promoting
factor
or
cancer-inhibiting
depending
on
the
subtype
cancer.
However,
role
ALDOB
clear
cell
renal
carcinoma
(ccRCC)
patients
has
not
been
clearly
elucidated.
Therefore,
this
study
aimed
to
comprehensively
explore
expression
level,
prognostic
value,
functional
enrichment,
immune
infiltration,
and
N6-methyladenosine
(m6A)
modification
ccRCC
patients.A
total
1,070
tissues
409
normal
from
Gene
Expression
Omnibus
(GEO)
database,
The
Cancer
Genome
Atlas
(TCGA)
ArrayExpress
database
were
enrolled
evaluate
level
value
ccRCC.
Kaplan-Meier
survival
curves
Log-Rank
test
performed
assess
value.
univariate
multivariate
Cox
regression
analysis
used
identify
independent
predictors
patients.
In
addition,
R
version
4.2.0
with
its
suitable
packages
perform
enrichment
analysis,
infiltration
m6A
methylation
analysis.
Statistical
significance
was
set
at
P
<0.05.The
significantly
down-regulated
compared
tissue,
noticeably
correlated
T
stage,
M
histologic
grade
revealed
ALODB
predictor
overall
(OS),
disease-specific
(DSS),
progression-free
(PFS)
showed
related
genes
mainly
involved
metabolism
metabolic
pathways
substances,
including
glycolysis,
gluconeogenesis,
fatty
acid
degradation.
Finally,
suggested
closely
abundance
cells
stromal
tumor
microenvironment
several
regulators
ccRCC.As
potential
biomarker
for
ccRCC,
downregulation
associated
clinicopathological
features,
poor
prognosis,
Aging,
Journal Year:
2023,
Volume and Issue:
unknown
Published: Aug. 10, 2023
Solute
carrier
family
1
member
5
(SLC1A5)
is
a
of
the
solute
(SLC)
superfamily
transporters
and
plays
an
important
role
in
tumors
as
key
transporter
glutamine
into
cells.
However,
relationship
between
SLC1A5,
which
involved
immune
regulation,
cell
infiltration
tumor
microenvironment
has
not
been
elucidated,
SLC1A5
ferroptosis
rarely
reported.
Therefore,
we
comprehensively
analyzed
expression
level
across
cancers
compared
it
with
that
normal
tissues.
Then,
was
by
single-cell
analysis,
gene
set
enrichment
analysis
(GSEA),
Tumor
Immune
Estimation
Resource
(TIMER).
Next,
correlations
immunotherapy
response,
immunomodulator
expression,
mutation
burden
(TMB)
microsatellite
instability
(MSI)
were
evaluated.
Finally,
vitro
experiments
verified
participates
glioma
cells
to
regulate
progression.
Our
results
indicated
aberrantly
expressed
most
cancer
types
closely
associated
prognosis.
The
GSEA
showed
activation
processes
related
levels
different
types.
Upon
further
investigation,
found
suppressor
glioma,
knockdown
inhibited
proliferation
migration
vitro.
In
conclusion,
conducted
pancancer
demonstrated
its
prognostic
biomarker
patients
explored
potential
biological
functions.