International Journal of Medical Sciences,
Journal Year:
2024,
Volume and Issue:
21(9), P. 1629 - 1639
Published: Jan. 1, 2024
The
complete
molecular
mechanism
underlying
doxorubicin-induced
cardiomyopathy
remains
incompletely
elucidated.
In
this
investigation,
we
engineered
mice
with
cardiomyocyte-specific
Signal Transduction and Targeted Therapy,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: Oct. 14, 2024
Iron,
an
essential
mineral
in
the
body,
is
involved
numerous
physiological
processes,
making
maintenance
of
iron
homeostasis
crucial
for
overall
health.
Both
overload
and
deficiency
can
cause
various
disorders
human
diseases.
Ferroptosis,
a
form
cell
death
dependent
on
iron,
characterized
by
extensive
peroxidation
lipids.
Unlike
other
kinds
classical
unprogrammed
death,
ferroptosis
primarily
linked
to
disruptions
metabolism,
lipid
peroxidation,
antioxidant
system
imbalance.
Ferroptosis
regulated
through
transcription,
translation,
post-translational
modifications,
which
affect
cellular
sensitivity
ferroptosis.
Over
past
decade
or
so,
diseases
have
been
as
part
their
etiology,
including
cancers,
metabolic
disorders,
autoimmune
diseases,
central
nervous
cardiovascular
musculoskeletal
Ferroptosis-related
proteins
become
attractive
targets
many
major
that
are
currently
incurable,
some
regulators
shown
therapeutic
effects
clinical
trials
although
further
validation
potential
needed.
Therefore,
in-depth
analysis
its
molecular
mechanisms
may
offer
additional
strategies
prevention
treatment.
In
this
review,
we
discuss
significance
contribution
etiology
development
along
with
evidence
supporting
targeting
approach.
Importantly,
evaluate
recent
promising
interventions,
providing
guidance
future
targeted
treatment
therapies
against
Antioxidants,
Journal Year:
2025,
Volume and Issue:
14(1), P. 70 - 70
Published: Jan. 9, 2025
Oxidative
stress
(OS)
refers
to
the
production
of
a
substantial
amount
reactive
oxygen
species
(ROS),
leading
cellular
and
organ
damage.
This
imbalance
between
oxidant
antioxidant
activity
contributes
various
diseases,
including
cancer,
cardiovascular
disease,
diabetes,
neurodegenerative
conditions.
The
body’s
system,
mediated
by
signaling
pathways,
includes
AMPK-SIRT1-FOXO
pathway.
In
oxidative
conditions,
AMPK,
an
energy
sensor,
activates
SIRT1,
which
in
turn
stimulates
FOXO
transcription
factor.
cascade
enhances
mitochondrial
function,
reduces
damage,
mitigates
OS-induced
injury.
review
provides
comprehensive
analysis
biological
roles,
regulatory
mechanisms,
functions
pathway
diseases
influenced
OS,
offering
new
insights
methods
for
understanding
OS
pathogenesis
its
therapeutic
approaches.
Circulation Research,
Journal Year:
2025,
Volume and Issue:
136(5), P. 524 - 550
Published: Feb. 27, 2025
Cardiovascular
diseases
(CVDs)
are
experiencing
a
rapid
surge
and
widely
recognized
as
the
leading
cause
of
mortality
in
current
aging
society.
Given
multifactorial
etiology
CVDs,
understanding
intricate
molecular
cellular
mechanisms
is
imperative.
Over
past
2
decades,
many
scientists
have
focused
on
Sirtuins,
family
nicotinamide
adenine
dinucleotide–dependent
deacylases.
Sirtuins
highly
conserved
across
species,
from
yeasts
to
primates,
play
crucial
role
linking
diseases.
participate
nearly
all
key
physiological
pathological
processes,
ranging
embryogenic
development
stress
response
aging.
Abnormal
expression
activity
exist
aging-related
diseases,
while
their
activation
has
shown
efficacy
mitigating
these
(eg,
CVDs).
In
terms
research,
this
field
maintained
fast,
sustained
growth
recent
years,
fundamental
studies
clinical
trials.
review,
we
present
comprehensive,
up-to-date
discussion
biological
functions
roles
regulating
cardiovascular
biology
CVDs.
Furthermore,
highlight
latest
advancements
utilizing
Sirtuin-activating
compounds
dinucleotide
boosters
potential
pharmacological
targets
for
preventing
treating
The
unresolved
issues
field—from
chemicobiological
regulation
Sirtuin-targeted
CVD
investigations—are
also
discussed.
This
timely
review
could
be
critical
updated
knowledge
Sirtuin
CVDs
facilitating
accessibility
Sirtuin-targeting
interventions.
Cardiovascular Diabetology,
Journal Year:
2025,
Volume and Issue:
24(1)
Published: Feb. 7, 2025
Cardiovascular
diseases
represent
the
principal
cause
of
death
and
comorbidity
among
people
with
diabetes.
Ferroptosis,
an
iron-dependent
non-apoptotic
regulated
cellular
characterized
by
lipid
peroxidation,
is
involved
in
pathogenesis
diabetic
cardiovascular
diseases.
The
susceptibility
to
ferroptosis
hearts
possibly
related
myocardial
iron
accumulation,
abnormal
metabolism
excess
oxidative
stress
under
hyperglycemia
conditions.
Accumulating
evidence
suggests
can
be
therapeutic
target
for
This
review
summarizes
ferroptosis-related
mechanisms
novel
choices
targeting
pathways.
Further
study
on
ferroptosis-mediated
cardiac
injury
enhance
our
understanding
pathophysiology
provide
more
potential
choices.
Redox Biology,
Journal Year:
2024,
Volume and Issue:
76, P. 103321 - 103321
Published: Aug. 19, 2024
Cell
death
constitutes
a
critical
component
of
the
pathophysiology
cardiovascular
diseases.
A
growing
array
non-apoptotic
forms
regulated
cell
(RCD)-such
as
necroptosis,
ferroptosis,
pyroptosis,
and
cuproptosis-has
been
identified
is
intimately
linked
to
various
conditions.
These
RCD
are
governed
by
genetically
programmed
mechanisms
within
cell,
with
epigenetic
modifications
being
common
crucial
regulatory
method.
Such
include
DNA
methylation,
RNA
histone
acetylation,
non-coding
RNAs.
This
review
recaps
roles
modifications,
RNAs
in
diseases,
well
which
regulate
key
proteins
involved
death.
Furthermore,
we
systematically
catalog
existing
pharmacological
agents
targeting
novel
their
action
article
aims
underscore
pivotal
role
precisely
regulating
specific
pathways
thus
offering
potential
new
therapeutic
avenues
that
may
prove
more
effective
safer
than
traditional
treatments.
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 13, 2025
The
pathogenesis
of
renal
fibrosis
is
related
to
blood
stasis,
and
the
method
promoting
circulation
removing
stasis
often
used
as
treatment
principle.
Danshen
injection
(DSI)
a
commonly
drug
for
in
clinic.
However,
whether
DSI
slows
progression
or
potential
mechanism
uncertain.
We
investigated
models
using
UUO
mice
TGF-β
stimulation
HK-2
cells.
Our
findings
revealed
that
Fer-1
alleviated
kidney
injury
by
ameliorating
morphology
pathological
vivo.
Besides,
inhibited
vivo
TGF-β-induced
Furthermore,
ferroptosis
was
lessened
under
treatment.
More
importantly,
active
ingredients
(danshensu,
salvianolic
acid
B,
protocatechuic
aldehyde,
caffeic
tanshinone
IIA)
could
bind
SIRT1.
protein
levels
SIRT1
GPX4
were
downregulated
accompanied
incremental
concentrations
Erastin,
which
repaired
intervention.
inhibition
owing
reversed
inhibitor
EX527.
Taken
together,
our
results
indicated
protect
against
attenuate
activating
SIRT1/GPX4
pathway.
It
expected
be
agent
treat
fibrosis.