Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(10), P. 2236 - 2236
Published: Oct. 1, 2024
The
intrinsic
molecular
heterogeneity
of
glioblastoma
(GBM)
is
one
the
main
reasons
for
its
resistance
to
conventional
treatment.
Mesenchymal
GBM
niches
are
associated
with
hypoxic
signatures
and
a
negative
influence
on
patients'
prognosis.
To
date,
competing
endogenous
RNA
(ceRNA)
networks
have
been
shown
broad
impact
progression
various
cancers.
In
this
study,
we
decided
construct
hypoxia-specific
microRNA/
messengerRNA
(miRNA/mRNA)
putative
circular
(circRNA)
regulatory
component
using
available
bioinformatics
tools.
Cancers,
Journal Year:
2025,
Volume and Issue:
17(3), P. 530 - 530
Published: Feb. 5, 2025
Background:
Despite
advances
in
the
management
of
head
and
neck
squamous
cell
carcinoma
(HNSCC),
prognostic
models
treatment
strategies
remain
inadequate,
particularly
for
HPV-positive
oropharyngeal
(OPSCC).
The
rising
incidence
OPSCC
highlights
an
urgent
need
innovative
therapeutic
approaches.
Ferroptosis,
a
regulated
form
non-apoptotic
death,
has
gained
attention
its
role
cancer
progression,
but
potential
as
target
remains
largely
unexplored.
This
study
investigates
ferroptosis
OPSCC,
aiming
to
identify
markers
provide
insights
into
that
could
improve
patient
outcomes.
Methods:
Thirteen
gene
expression
signatures
were
retrieved
from
literature,
their
performance
association
immune
microenvironment
validated
on
meta-analysis
267
cases
(Metanalysis-HPV267)
286
samples
BD2Decide
project
(BD2-HPV286).
Results:
Our
analysis
revealed
specific
ferroptosis-related
signatures,
FER3,
FER4,
FER6,
FER12,
are
significantly
associated
(p-value
<
0.05)
with
high-risk
groups
adverse
tumor
features,
including
suppressed
activity
enhanced
stromal
involvement.
Elevated
CAV1,
suppressor,
further
delineates
profiles.
Conclusions:
These
findings
highlight
significance
stratifying
patients
identifying
those
poorer
clinical
Targeting
pathways
represents
novel
promising
approach
addressing
unmet
effective
OPSCC.
Future
research
should
focus
translating
these
applications
advance
precision
oncology
outcomes
this
growing
population.
Molecular Biomedicine,
Journal Year:
2024,
Volume and Issue:
5(1)
Published: Oct. 17, 2024
It
has
long
been
widely
acknowledged
that
ultraviolet
(UV)
light
is
an
environment
risk
factor
can
lead
to
cancer,
particularly
skin
cancer.
However,
it
worth
noting
UV
radiation
holds
potential
for
cancer
treatment
as
a
relatively
high-energy
electromagnetic
wave.
With
the
help
of
nanomaterials,
role
caught
increasing
attention
in
treatment.
In
this
review,
we
briefly
summarized
types
UV-induced
cancers,
including
malignant
melanoma,
squamous
cell
carcinoma,
basal
Merkel
carcinoma.
Importantly,
discussed
primary
mechanisms
underlying
carcinogenesis,
mutations
by
DNA
damage,
immunosuppression,
inflammation
and
epigenetic
alterations.
Historically
limited
its
shallow
penetration
depth,
introduction
nanomaterials
dramatically
transformed
utilization
The
direct
effect
itself
generally
leads
suppression
growth
initiation
apoptosis
ferroptosis.
also
be
utilized
activate
photosensitizers
reactive
oxygen
species
(ROS)
production,
sensitize
radiotherapy
achieve
controlled
drug
release.
Finally,
comprehensively
weigh
significant
risks
limitations
associated
with
therapeutic
use
radiation.
And
contradictory
exposure
promoting
inhibiting
tumor
discussed.
This
review
provides
clues
clinical
therapy
well
future
study
directions
field.
precise
delivery
control
or
wavelength
dose
effects
are
needed
thorough
understanding
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(8), P. 4559 - 4559
Published: April 22, 2024
Oxidative
stress
and
lipid
peroxidation
play
important
roles
in
numerous
physiological
pathological
processes,
while
the
bioactive
products
of
peroxidation,
hydroperoxides
reactive
aldehydes,
act
as
mediators
redox
signaling
normal
malignant
cells.
Many
types
cancer,
including
osteosarcoma,
express
altered
pathways.
Such
pathways
protect
cancer
cells
from
cytotoxic
effects
oxidative
stress,
thus
supporting
transformation,
eventually
anticancer
therapies
associated
with
stress.
In
this
review,
we
aim
to
explore
status
osteosarcoma
highlight
involvement
pathways,
therapies.
Clinical
investigations
have
demonstrated
that
the
progression
of
acute
myeloid
leukemia
(AML)
is
particularly
susceptible
to
iron
overload
and
dysregulation
homeostasis,
which
can
trigger
ferroptosis.
Consequently,
regulating
homeostasis
may
positively
impact
AML
treatment.
This
study
aimed
investigate
anticancer
properties
potential
mechanisms
realgar
transforming
solution
(RTS)
in
inducing
ferroptosis
disrupting
NB4
cells.
Cell
viability
was
assessed
using
Counting
Kit-8
(CCK-8)
assay.
Transcriptomic
analysis
conducted
identify
differentially
expressed
genes
(DEGs)
predict
pathways
through
RTS
exerts
its
antitumor
effects.
Ferroptosis
evaluated
BODIPY
C11
lipid
ROS
probe,
T-SOD,
MDA,
GSH
assay
kits,
along
with
JC-1
fluorescent
probe
Western
blot
analysis.
Iron
Fe2+
kits
metabolism.
Transcriptome
sequencing
revealed
819
DEGs,
HO-1
PML-RARα
Regulated
Adaptor
Molecule
1
(PRAM1)
being
most
prominent.
KEGG
indicated
significant
enrichment
pathway.
In
vitro
studies
treatment
resulted
increased
levels
depletion
SLC7A11
GPX4
expression
Additionally,
TFR1
NCOA4
increased,
while
FPN1
(SLC40A1),
FTH1,
IREB2
decreased
under
led
intracellular
accumulation,
ultimately
Pretreatment
inhibitors,
such
as
Ferrostatin-1
(Fer-1)
or
Deferoxamine
mesylate
(DFOM),
attenuated
RTS-induced
The
demonstrates
induce
cells
by
via
regulation
SLC7A11/GPX4
axis.
These
findings
suggest
a
therapeutic
agent
for
AML.
Advanced Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 11, 2025
Rapid
development
of
resistance
to
sorafenib
and
subsequent
hyperprogression
in
patients
with
advanced
hepatocellular
carcinoma
(HCC)
pose
significant
challenges,
the
underlying
mechanisms
still
largely
unknown.
Herein,
sorafenib-induced
TRIB3
is
identified
as
a
liver-specific
determinant
driving
secondary
by
facilitating
accumulation
protumorigenic
neutrophils
within
tumors.
Mechanistically,
TRIB3,
triggered
sorafenib-elicited
ROS-ER
stress
axis,
operates
an
NF-κB-dependent
manner
upregulate
CXCR1/2
ligands,
subsequently
promoting
neutrophil
recruitment
into
These
enriched
enhance
epithelial-mesenchymal
transition
processes
malignant
cells
through
oncostatin
M-STAT3
pathway,
thereby
repurposing
therapeutic
efficacy
away
from
anti-angiogenesis
toward
lung
metastasis.
Clinically,
elevated
expression
indicates
inferior
survival
unfavorable
clinical
HCC
patients.
Correspondingly,
strategies
that
either
inhibiting
upregulation
or
blocking
its
downstream
signaling
successfully
augment
prevent
vivo.
The
study
thus
identifies
pivotal
mechanism
HCC,
centered
on
TRIB3-mediated
disease
hyperprogression.
Antioxidants,
Journal Year:
2025,
Volume and Issue:
14(3), P. 265 - 265
Published: Feb. 25, 2025
Bee
pollen
(BP)
is
one
of
the
richest
known
natural
resources
micronutrients
and
bioactive
phytochemicals.
Some
captivating
bioactivities
BP
compounds,
although
being
largely
investigated
for
latter
as
individual
molecules,
remain
very
scarcely
or
completely
uninvestigated
in
bee
a
whole
product.
Among
most
intriguing
these
bioactivities,
we
identified
ferroptosis
major
one.
Ferroptosis,
recently
discovered
form
cell
death
(connecting
oxidative
stress
inflammation),
complex
pathophysiological
process
crucial
perplexing
events
current
challenging
human
diseases
such
cancer,
neurodegeneration,
general
aging
diseases.
Many
compounds
were
found
to
intricately
modulate
depending
on
cellular
context
by
inducing
this
mechanism
malignant
cells
preventing
it
non-malignant
cells.
Since
research
both
fields,
i.e.,
ferroptosis,
still
recent,
deemed
necessary
undertake
review
figure
out
extent
potential
modulating
mechanisms.
Our
proved
that
wide
range
(polyphenols,
phenolamides,
carotenoids,
vitamins,
minerals,
others)
substantially
diverse
Accordingly,
phytochemicals
nutrients
showed
interesting
preclinical
studies
lead
ferroptosis-mediated
outcomes
important
processes,
including
many
aging-related
disorders.
One
paramount
challenges
be
resolved
determine
how
different
act
biological
contexts,
either
through
synergistic
antagonistic
behaviors.
We
hope
our
work
constitutes
valuable
incentive
future
investigations
promising
relevant
avenue.