Molecules,
Год журнала:
2024,
Номер
29(23), С. 5764 - 5764
Опубликована: Дек. 6, 2024
In
this
study,
homoisoflavone
methylophiopogonanone
A
(MOA)
was
investigated
for
its
inhibitory
effect
on
ferroptosis
of
H9c2
cells
using
a
set
cellular
assays,
such
as
BODIPY-probed
and
H
Journal of Functional Foods,
Год журнала:
2024,
Номер
121, С. 106437 - 106437
Опубликована: Сен. 1, 2024
Hepatotoxicity
is
an
significant
side
effect
of
doxorubicin
(DOX),
while
astaxanthin
(ASX)
has
the
anti-liver
injury
biological
functions.
In
this
study,
we
utilized
in
vivo
and
vitro
methods
to
investigate
protective
ASX
against
DOX-induced
hepatotoxicity
elucidate
its
potential
mechanism.
Our
researchers
measured
liver
indicators
expression
ferroptosis-related
protein
(transferrin
receptor
1
(TFRC),
ferroportin
(FPN1),
ferritin
light
chain
(FTL),
heavy
chain-1
(FTH1),
glutathione
peroxidase
4
(GPX4),
solute
carrier
family
7
member
11
(SLC7A11))
rats
HepG2
cells.
We
found
that
could
effectively
reduce
ferroptosis
level
relieve
a
range
DOX-caused
manifestations
injury,
including
inflammation
oxidative
damage.
may
play
same
role
as
inhibitor,
Fer-1
DFP,
process.
The
findings
demonstrated
intervention
with
ameliorated
by
mitigating
through
inhibiting
iron
accumulation.
Biology,
Год журнала:
2024,
Номер
13(9), С. 689 - 689
Опубликована: Сен. 3, 2024
Anthracyclines
represent
a
highly
efficacious
class
of
chemotherapeutic
agents
employed
extensively
in
antitumor
therapy.
They
are
universally
recognized
for
their
potency
treating
diverse
malignancies,
encompassing
breast
cancer,
gastrointestinal
tumors,
and
lymphomas.
Nevertheless,
the
accumulation
anthracyclines
within
body
can
lead
to
significant
cardiac
toxicity,
adversely
impacting
both
survival
rates
quality
life
tumor
patients.
This
limitation
somewhat
restricts
clinical
utilization.
Determining
how
monitor
mitigate
cardiotoxicity
at
an
early
stage
has
become
urgent
problem
be
solved.
Therefore,
this
paper
reviews
mechanism
action,
monitoring,
strategies
prevention
anthracycline-induced
reference.
Journal of Applied Toxicology,
Год журнала:
2024,
Номер
unknown
Опубликована: Июль 18, 2024
Abstract
Doxorubicin
(DOX)
is
a
chemotherapy
drug
widely
used
in
clinical
settings,
acting
as
first‐line
treatment
for
various
malignant
tumors.
However,
its
use
greatly
limited
by
the
cardiotoxicity
it
induces,
including
doxorubicin‐induced
cardiomyopathy
(DIC).
The
mechanisms
behind
DIC
are
not
fully
understood,
but
potential
biological
thought
to
include
oxidative
stress,
inflammation,
energy
metabolism
disorders,
mitochondrial
damage,
autophagy,
apoptosis,
and
ferroptosis.
Recent
studies
have
shown
that
cardiac
injury
induced
DOX
closely
related
Due
their
high
efficacy,
availability,
low
side
effects,
natural
medicine
treatments
hold
strong
potential.
Currently,
medicines
been
mitigate
DOX‐induced
ferroptosis
ease
through
functions
such
antioxidation,
iron
ion
homeostasis
correction,
lipid
regulation,
function
improvement.
Therefore,
this
review
summarizes
of
regulation
plant
products,
with
expectation
providing
reference
future
research
development
inhibitors
targeting
DIC.
This
explores
(DIC)
how
products
can
alleviate
inhibiting
reducing
correcting
homeostasis,
regulating
metabolism,
improving
function.
Biomolecules,
Год журнала:
2024,
Номер
14(12), С. 1614 - 1614
Опубликована: Дек. 17, 2024
Doxorubicin
is
a
chemotherapeutic
drug
utilized
for
solid
tumors
and
hematologic
malignancies,
but
its
clinical
application
hampered
by
life-threatening
cardiotoxicity,
including
cardiac
dilation
heart
failure.
Mitophagy,
cargo-specific
form
of
autophagy,
specifically
used
to
eliminate
damaged
mitochondria
in
autophagosomes
through
hydrolytic
degradation
following
fusion
with
lysosomes.
Recent
advances
have
unveiled
major
role
defective
mitophagy
the
etiology
DOX-induced
cardiotoxicity.
Moreover,
specific
interventions
targeting
this
mechanism
preserve
mitochondrial
function
emerged
as
potential
therapeutic
strategies
attenuate
However,
translation
challenging
because
unclear
mechanisms
action
pharmacological
adverse
effects.
This
review
aims
offer
fresh
perspectives
on
development
cardiotoxicity
investigate
that
focus
improve
management.
Frontiers in Immunology,
Год журнала:
2024,
Номер
15
Опубликована: Окт. 4, 2024
Ferroptosis,
a
form
of
regulated
cell
death
distinct
from
apoptosis,
necrosis,
and
autophagy,
is
increasingly
recognized
for
its
role
in
skin
disease
pathology.
Characterized
by
iron
accumulation
lipid
peroxidation,
ferroptosis
has
been
implicated
the
progression
various
conditions,
including
psoriasis,
photosensitive
dermatitis,
melanoma.
This
review
provides
an
in-depth
analysis
molecular
mechanisms
underlying
compares
cellular
effects
with
other
forms
context
health
disease.
We
systematically
examine
five
specific
diseases,
ichthyosis,
polymorphous
light
eruption
(PMLE),
vitiligo,
melanoma,
detailing
influence
on
pathogenesis
progression.
Moreover,
we
explore
current
clinical
landscape
ferroptosis-targeted
therapies,
discussing
their
potential
managing
treating
diseases.
Our
aim
to
shed
therapeutic
modulating
research
practice.
Molecules,
Год журнала:
2024,
Номер
29(23), С. 5764 - 5764
Опубликована: Дек. 6, 2024
In
this
study,
homoisoflavone
methylophiopogonanone
A
(MOA)
was
investigated
for
its
inhibitory
effect
on
ferroptosis
of
H9c2
cells
using
a
set
cellular
assays,
such
as
BODIPY-probed
and
H