Journal of Translational Medicine,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: April 30, 2024
With
the
aging
global
population,
type
2
diabetes
mellitus
(T2DM)
and
osteoporosis(OP)
are
becoming
increasingly
prevalent.
Diabetic
osteoporosis
(DOP)
is
a
metabolic
bone
disorder
characterized
by
abnormal
tissue
structure
reduced
strength
in
patients
with
diabetes.
Studies
have
revealed
close
association
among
diabetes,
increased
fracture
risk,
disturbances
iron
metabolism.
This
review
explores
concept
of
ferroptosis,
non-apoptotic
cell
death
process
dependent
on
intracellular
iron,
focusing
its
role
DOP.
Iron-dependent
lipid
peroxidation,
particularly
impacting
pancreatic
β-cells,
osteoblasts
(OBs)
osteoclasts
(OCs),
contributes
to
The
intricate
interplay
between
dysregulation,
which
comprises
deficiency
overload,
DOP
has
been
discussed,
emphasizing
how
excessive
accumulation
triggers
ferroptosis
concise
overview
highlights
need
understand
complex
relationship
T2DM
OP,
ferroptosis.
aimed
elucidate
pathogenesis
provide
prospective
for
future
research
targeting
interventions
field
Redox Biology,
Journal Year:
2024,
Volume and Issue:
75, P. 103211 - 103211
Published: May 30, 2024
Ferroptosis
is
a
pervasive
non-apoptotic
form
of
cell
death
highly
relevant
in
various
degenerative
diseases
and
malignancies.
The
hallmark
ferroptosis
uncontrolled
overwhelming
peroxidation
polyunsaturated
fatty
acids
contained
membrane
phospholipids,
which
eventually
leads
to
rupture
the
plasma
membrane.
unique
that
it
essentially
spontaneous,
uncatalyzed
chemical
process
based
on
perturbed
iron
redox
homeostasis
contributing
process,
but
nonetheless
modulated
by
many
metabolic
nodes
impinge
cells'
susceptibility
ferroptosis.
Among
affecting
sensitivity,
several
have
emerged
as
promising
candidates
for
pharmacological
intervention,
rendering
ferroptosis-related
proteins
attractive
targets
treatment
numerous
currently
incurable
diseases.
Herein,
current
members
Germany-wide
research
consortium
focusing
research,
well
key
external
experts
who
made
seminal
contributions
this
rapidly
growing
exciting
field
gathered
provide
comprehensive,
state-of-the-art
review
Specific
topics
include:
basic
mechanisms,
vivo
relevance,
specialized
methodologies,
tools,
potential
contribution
disease
etiopathology
progression.
We
hope
article
will
not
only
established
scientists
newcomers
with
an
overview
multiple
facets
ferroptosis,
also
encourage
additional
efforts
characterize
further
molecular
pathways
modulating
ultimate
goal
develop
novel
pharmacotherapies
tackle
associated
-
or
caused
Advanced Science,
Journal Year:
2023,
Volume and Issue:
10(13)
Published: Feb. 25, 2023
Abstract
Ferroptosis
has
been
linked
to
the
pathogenesis
of
hepatic
injury
induced
by
ischemia/reperfusion
(I/R).
However,
mechanistic
basis
remains
unclear.
In
this
study,
using
a
mouse
model
I/R
injury,
it
is
observed
that
glutathione
(GSH)
and
cysteine
depletion
are
associated
with
deficiency
reducing
power
nicotinamide
adenine
dinucleotide
phosphate
(NADPH).
Genes
involved
in
maintaining
NADPH
homeostasis
screened,
identified
I/R‐induced
ferroptosis
significantly
reduced
expression
activity
NADP
+
‐dependent
malic
enzyme
1
(Me1).
Mice
hepatocyte‐specific
Me1
gene
deletion
exhibit
aggravated
liver
under
treatment;
while
supplementation
L‐malate,
substrate
ME1,
restores
GSH
levels
eventually
inhibits
injury.
A
study
further
reveals
downregulation
largely
mediated
phosphatase
tensin
homologue
(PTEN)‐dependent
suppression
target
rapamycin/sterol
regulatory
element‐binding
protein
(mTOR/SREBP1)
signaling
pathway
model.
Finally,
PTEN
inhibitor,
mTOR
activator,
or
SREBP1
over‐expression
all
increase
NADPH,
block
ferroptosis,
protect
against
Taken
together,
findings
suggest
targeting
ME1
may
provide
new
therapeutic
opportunities
for
other
ferroptosis‐related
conditions.
Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
174, P. 116512 - 116512
Published: April 3, 2024
GPX4
(Glutathione
peroxidase
4)
serves
as
a
crucial
intracellular
regulatory
factor,
participating
in
various
physiological
processes
and
playing
significant
role
maintaining
the
redox
homeostasis
within
body.
Ferroptosis,
form
of
iron-dependent
non-apoptotic
cell
death,
has
gained
considerable
attention
recent
years
due
to
its
involvement
multiple
pathological
processes.
is
closely
associated
with
ferroptosis
functions
primary
inhibitor
this
process.
Together,
contribute
pathophysiology
several
diseases,
including
sepsis,
nervous
system
ischemia
reperfusion
injury,
cardiovascular
cancer.
This
review
comprehensively
explores
roles
impacts
development
progression
these
aim
providing
insights
for
identifying
potential
therapeutic
strategies
future.
ACS Applied Materials & Interfaces,
Journal Year:
2023,
Volume and Issue:
15(13), P. 17317 - 17323
Published: March 24, 2023
Anionic,
acidic,
and
metal
ions
are
common
contaminants
in
water
cause
serious
concerns
for
human
aquatic
life.
With
the
goal
of
rapid
detection
analytes,
we
herein
design
a
new
array
ligand
5-(4H-1,2,4-triazol-4-yl)pyridin-3-ol-linked
silver
coordinated
metal-organic
frameworks
Ag-MOFs
as
promising
sensor
Cr2O72-,
MnO4-,
humic
acid
(HA),
Fe3+
down
to
micro
level.
Furthermore,
evidenced
by
luminescence,
excitation-emission
matrix
(EEM)
spectroscopic,
PXRD
measurements,
designed
(MOFs)
can
be
fast,
stable,
reusable
analyte
water.
Immunity,
Journal Year:
2024,
Volume and Issue:
57(5), P. 941 - 956
Published: May 1, 2024
Ferroptosis
is
a
type
of
regulated
cell
death
that
drives
the
pathophysiology
many
diseases.
Oxidative
stress
detectable
in
types
death,
but
only
ferroptosis
involves
lipid
peroxidation
and
iron
dependency.
originates
propagates
from
several
organelles,
including
mitochondria,
endoplasmic
reticulum,
Golgi,
lysosomes.
Recent
data
have
revealed
immune
cells
can
both
induce
undergo
ferroptosis.
A
mechanistic
understanding
how
regulates
immunity
critical
to
controls
responses
this
dysregulated
disease.
Translationally,
more
work
needed
produce
ferroptosis-modulating
immunotherapeutics.
This
review
focuses
on
role
immune-related
diseases,
infection,
autoimmune
cancer.
We
discuss
immunity,
regulation
contributes
disease
pathogenesis,
targeting
may
lead
novel
therapies.
Science Advances,
Journal Year:
2024,
Volume and Issue:
10(13)
Published: March 29, 2024
Ferroptosis
is
a
form
of
iron-dependent,
lipid
peroxidation–driven
regulatory
cell
death
that
has
been
implicated
in
the
pathogenesis
multiple
diseases,
including
organ
injury,
ischemia/reperfusion,
and
neurodegenerative
diseases.
However,
inhibitors
directly
specifically
target
ferroptosis
are
not
yet
available.
Here,
we
identify
compound
AS-252424
(AS)
as
potent
inhibitor
through
kinase
library
screening.
Our
results
show
AS
effectively
inhibits
peroxidation
both
human
mouse
cells.
Mechanistically,
binds
to
glutamine
464
ACSL4
inhibit
its
enzymatic
activity,
resulting
suppression
ferroptosis.
By
using
nanoparticle-based
delivery
systems,
treatment
with
AS-loaded
nanoparticles
alleviate
ferroptosis-mediated
injury
models,
kidney
ischemia/reperfusion
acute
liver
(ALI).
Thus,
our
specific
targeted
remarkable
antiferroptosis
function,
providing
potential
therapeutic
for
ferroptosis-related
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: March 12, 2024
Abstract
Recent
evidence
indicates
ferroptosis
is
implicated
in
the
pathophysiology
of
various
liver
diseases;
however,
organ-specific
regulation
mechanism
poorly
understood.
Here,
we
demonstrate
7-dehydrocholesterol
reductase
(DHCR7),
terminal
enzyme
cholesterol
biosynthesis,
as
a
regulator
hepatocytes.
Genetic
and
pharmacological
inhibition
(with
AY9944)
DHCR7
suppress
human
hepatocellular
carcinoma
Huh-7
cells.
increases
its
substrate,
(7-DHC).
Furthermore,
exogenous
7-DHC
supplementation
using
hydroxypropyl
β-cyclodextrin
suppresses
ferroptosis.
A
7-DHC-derived
oxysterol
metabolite,
3β,5α-dihydroxycholest-7-en-6-one
(DHCEO),
increased
by
ferroptosis-inducer
RSL-3
-deficient
cells,
suggesting
that
ferroptosis-suppressive
effect
associated
with
oxidation
7-DHC.
Electron
spin
resonance
analysis
reveals
functions
radical
trapping
agent,
thus
protecting
cells
from
We
further
show
AY9944
inhibits
hepatic
ischemia-reperfusion
injury,
genetic
ablation
Dhcr7
prevents
acetaminophen-induced
acute
failure
mice.
These
findings
provide
new
insights
into
regulatory
suggest
potential
therapeutic
option
for
ferroptosis-related
diseases.
Plants,
Journal Year:
2024,
Volume and Issue:
13(4), P. 523 - 523
Published: Feb. 15, 2024
Inflammation
is
the
immune
system’s
first
biological
response
to
infection,
injury,
or
irritation.
Evidence
suggests
that
anti-inflammatory
effect
mediated
by
regulation
of
various
inflammatory
cytokines,
such
as
nitric
oxide,
interleukins,
tumor
necrosis
factor
alpha-α,
interferon
gamma-γ,
well
non-cytokine
mediator,
prostaglandin
E2.
Currently,
mechanism
action
and
clinical
usefulness
phytochemicals
known;
their
on
activity
free
radicals,
oxidative
stress.
The
latter
are
great
relevance
in
development
diseases,
evidence
collected
demonstrates
beneficial
effects
maintaining
health.
Epidemiological
indicates
regular
consumption
fruits
vegetables
related
a
low
risk
developing
cancer
other
chronic
diseases.