Frontiers in Genetics,
Год журнала:
2023,
Номер
14
Опубликована: Ноя. 6, 2023
Background:
Diabetic
nephropathy
(DN)
is
the
most
common
complication
of
diabetes,
and
its
pathogenesis
complex
involving
a
variety
programmed
cell
death,
inflammatory
responses,
autophagy
mechanisms.
Disulfidptosis
newly
discovered
mechanism
death.
There
are
little
studies
about
role
disulfidptosis
on
DN.
Methods:
First,
we
obtained
data
required
for
this
study
from
GeneCards
database,
Nephroseq
v5
GEO
database.
Through
differential
analysis,
disulfidptosis-related
genes.
At
same
time,
through
WGCNA
key
module
genes
in
DN
patients.
The
intersecting
were
further
screened
by
Lasso
as
well
SVM-RFE.
By
results
two,
ended
up
with
gene
diabetic
nephropathy.
diagnostic
performance
expression
verified
GSE30528,
GSE30529,
GSE96804,
datasets.
Using
clinical
information
investigated
correlation
between
estimated
glomerular
filtration
rate
(eGFR)
serum
creatinine
content.
Next,
constructed
nomogram
analyzed
immune
microenvironment
patients
identification
subtypes
facilitates
individualized
treatment
Results:
We
91
39
Taking
intersection
preliminarily
20
characteristic
found
that
these
positively
correlated
each
other.
Further
screening
SVM-RFE
algorithms
identified
CXCL6,
CD48,
C1QB,
COL6A3
Clinical
analysis
levels
closely
related
to
eGFR.
Immune
infiltration
higher
samples
than
normal
samples.
Conclusion:
validated
4
may
be
promote
onset
eGFR
infiltrated
kidney
tissue.
Drug Design Development and Therapy,
Год журнала:
2025,
Номер
Volume 19, С. 737 - 757
Опубликована: Фев. 1, 2025
Background:
Diabetic
liver
injury
(DLI)
is
a
common
complication
of
diabetes
mellitus
(DM),
which
seriously
endangers
the
health
diabetic
patients.
Puerarin,
main
active
component
Pueraria
lobata
,
has
shown
positive
effects
in
lowering
blood
glucose
and
lipids,
resisting
oxidative
stress,
protecting
liver.
However,
mechanism
protective
effect
Puerarin
on
DLI
remains
unclear.
Methods:
Various
databases
were
used
to
screen
for
targets
ferroptosis
DLI.
Protein-protein
interaction
(PPI)
network
Kyoto
Encyclopedia
Genes
Genomes
(KEGG)
enrichment
analysis
predict
key
pathways.
Molecular
docking
was
interactions
between
core
targets.
KK/Upj-Ay/J
(KKAy)
mice
high
(HG)-induced
AML12
cells
study
The
molecular
mechanisms
by
acts
further
verified
vivo
vitro
experiments.
Results:
KEGG
indicated
that
JAK/STAT
pathway
might
be
related
anti-DLI
Puerarin.
revealed
good
affinity
JAK2
STAT3.
In
vivo,
(80
mg/kg)
reduced
body
weight,
glucose,
lipids
function
KKAy
fed
high-sugar,
high-fat
diet.
also
ameliorated
hepatic
pathological
changes
inflammatory
responses,
attenuated
stress
iron
overload
mice.
Western
blotting
results
showed
could
regulate
expression
proteins
JAK2/STAT3
pathway.
vitro,
(25,
50,
100
μM)
increased
cell
viability
decreased
steatosis
indexes
induced
HG
(30
mm)
varying
degrees.
More
importantly,
AG490
blocker
experiments
regulation
process
dependent
Conclusion:
conclusion,
this
may
inhibiting
treatment
Keywords:
puerarin,
injury,
ferroptosis,
pathway,
pharmacology
International Journal of Biological Sciences,
Год журнала:
2023,
Номер
19(12), С. 3726 - 3743
Опубликована: Янв. 1, 2023
Ferroptosis
is
an
iron-dependent
programmed
cell
death
pattern
that
characterized
by
iron
overload,
reactive
oxygen
species
(ROS)
accumulation
and
lipid
peroxidation.
Growing
viewpoints
support
the
imbalance
of
homeostasis
disturbance
metabolism
contribute
to
tissue
or
organ
injury
in
various
kidney
diseases
triggering
ferroptosis.
At
present,
key
regulators
complicated
network
mechanisms
associated
with
ferroptosis
have
been
deeply
studied;
however,
its
role
initiation
progression
has
not
fully
revealed.
Herein,
we
aim
discuss
features,
ferroptosis,
explore
emerging
roles
organelles
gather
pharmacological
progress,
systematically
summarize
most
recent
discoveries
about
crosstalk
between
diseases,
including
renal
carcinoma
(RCC),
acute
(AKI),
diabetic
disease
(DKD),
autosomal
dominant
polycystic
(ADPKD),
fibrosis,
lupus
nephritis
(LN)
IgA
nephropathy.
We
further
conclude
potential
therapeutic
strategies
targeting
for
prevention
treatment
hope
this
work
will
provide
insight
study
pathogenesis
kidney-related
diseases.
Annals of Medicine,
Год журнала:
2024,
Номер
56(1)
Опубликована: Апрель 24, 2024
Diabetic
nephropathy
(DN)
is
a
severe
complication
of
diabetes
mellitus,
causing
substantive
threat
to
the
public,
which
receives
global
concern.
However,
there
are
limited
drugs
targeting
treatment
DN.
Owing
this,
it
highly
crucial
investigate
pathogenesis
and
potential
therapeutic
targets
The
process
ferroptosis
type
regulated
cell
death
(RCD)
involving
presence
iron,
distinct
from
autophagy,
apoptosis,
pyroptosis.
A
primary
mechanism
associated
with
iron
metabolism,
lipid
accumulation
ROS.
Recently,
many
studies
testified
significance
in
kidney
tissue
under
diabetic
conditions
explored
DN
therapy.
Our
review
summarized
most
current
between
DN,
along
investigating
significant
processes
different
cells,
providing
novel
target
option
for
Journal of Translational Internal Medicine,
Год журнала:
2024,
Номер
12(1), С. 22 - 34
Опубликована: Фев. 1, 2024
Abstract
Fibrosis
occurs
in
many
organs,
and
its
sustained
progress
can
lead
to
organ
destruction
malfunction.
Although
numerous
studies
on
fibrosis
have
been
carried
out,
underlying
mechanism
is
largely
unknown,
no
ideal
treatment
currently
available.
Ferroptosis
an
iron-dependent
process
of
programmed
cell
death
that
characterized
by
lipid
peroxidation.
In
the
past
decade,
a
growing
body
evidence
demonstrated
association
between
ferroptosis
fibrotic
diseases,
while
targeting
may
serve
as
potential
therapeutic
strategy.
This
review
highlights
recent
advances
crosstalk
fibrosis,
discusses
ferroptosis-targeted
approaches
against
are
being
explored.
Frontiers in Pharmacology,
Год журнала:
2024,
Номер
15
Опубликована: Июнь 19, 2024
Introduction
Diabetic
nephropathy
(DN)
is
the
leading
cause
of
end-stage
renal
disease.
Due
to
its
complex
pathogenesis,
new
therapeutic
agents
are
urgently
needed.
Orthosiphon
aristatus
(Blume)
Miq.,
commonly
known
as
kidney
tea,
widely
used
in
DN
treatment
China.
However,
mechanisms
have
not
been
fully
elucidated.
Methods
We
db/db
mice
model
and
evaluated
efficacy
tea
by
measuring
fasting
blood
glucose
(FBG),
serum
inflammatory
cytokines,
injury
indicators
histopathological
changes.
Furthermore,
16S
rDNA
gene
sequencing,
untargeted
metabolomics,
electron
microscope,
ELISA,
qRT-PCR,
Western
blotting
were
performed
explore
which
exerted
effects.
Results
Twelve
polyphenols
identified
from
extract
ameliorated
FBG,
inflammation
mice.
Moreover,
reshaped
gut
microbiota,
reduced
abundance
Muribaculaceae
,
Lachnoclostridium
Prevotellaceae_UCG-001
Corynebacterium
Akkermansia
enriched
Alloprevotella
Blautia
Lachnospiraceae_NK4A136_group
.
Kidney
altered
levels
metabolites
pathways
such
ferroptosis,
arginine
biosynthesis
mTOR
signaling
pathway.
Importantly,
improved
mitochondrial
damage,
increased
SOD
activity,
decreased
MDA
4-HNE
tissues
Meanwhile,
this
functional
upregulated
GPX4
FTH1
expression
downregulated
ACSL4
NCOA4
expression,
indicating
that
it
could
inhibit
ferroptosis
kidneys.
Conclusion
Our
findings
imply
can
attenuate
development
modulating
microbiota
presents
a
novel
scientific
rationale
for
clinical
application
tea.
Antioxidants,
Год журнала:
2024,
Номер
13(3), С. 334 - 334
Опубликована: Март 10, 2024
Ferroptosis
is
a
recently
discovered
type
of
programmed
cell
death
that
mechanistically
different
from
other
types
such
as
apoptosis,
necroptosis,
and
autophagy.
It
characterized
by
the
accumulation
intracellular
iron,
overproduction
reactive
oxygen
species,
depletion
glutathione,
extensive
lipid
peroxidation
lipids
in
membrane.
was
ferroptosis
interconnected
with
many
diseases,
neurodegenerative
ischemia/reperfusion
injury,
cancer,
chronic
kidney
disease.
Polyphenols,
plant
secondary
metabolites
known
for
bioactivities,
are
being
extensively
researched
context
their
influence
on
which
resulted
great
number
publications
showing
need
systematic
review.
In
this
review,
an
literature
search
performed.
Databases
(Scopus,
Web
Science,
PubMed,
ScienceDirect,
Springer)
were
searched
time
span
2017
to
November
2023,
using
keyword
“ferroptosis”
alone
combination
“flavonoid”,
“phenolic
acid”,
“stilbene”,
“coumarin”,
“anthraquinone”,
“chalcone”;
after
selection
studies,
we
had
311
papers
143
phenolic
compounds.
total,
53
compounds
showed
ability
induce
ferroptosis,
110
able
inhibit
out
those
compounds,
20
both
abilities
depending
model
system.
The
most
shikonin,
curcumin,
quercetin,
resveratrol,
baicalin.
common
modes
action
modulation
Nrf2/GPX4
Nrf2/HO-1
axis
iron
metabolism.
Pharmacological Research - Modern Chinese Medicine,
Год журнала:
2024,
Номер
10, С. 100377 - 100377
Опубликована: Янв. 26, 2024
Ferroptosis,
an
iron-dependent
cell
death
characterized
by
lethal
lipid
peroxidation,
has
been
involved
in
the
pathogenesis
of
various
diseases,
such
as
ischemia/reperfusion
injury,
neurodegenerative
and
inflammatory
disorders.
Pharmacological
inhibition
ferroptosis
represents
a
promising
strategy
for
treatment
above
diseases.
Flavonoids,
class
natural
products
found
medicinal
plants
functional
foods,
are
known
numerous
activities,
especially
newly
discovered
anti-ferroptotic
activity.
Our
review
aims
to
expand
our
understanding
flavonoids'
activity
on
multiple
biological
systems
highlight
importance
utilizing
flavonoids
ferroptosis-associated
A
systematic
literature
search
was
conducted
using
Google
Scholar,
PubMed,
Web
Science,
ScienceDirect,
Springer
Link.
The
following
keywords:
flavonoids,
products,
ferroptosis,
mechanism,
available
information
comprehensively
studied
compiled.
We
recent
advances
molecular
mechanisms
its
roles
diverse
further
systematically
summarize
inhibitory
underlying
suggest
that
ROS
accumulation
labile
Fe2+
availability
well
activation
Nrf2
signaling
responsible
inhibition.
also
discuss
their
clinical
applications
ferroptosis-related
Taken
together,
exhibit
prospect
This
is
expected
not
only
facilitate
design
development
flavonoid-based
inhibitors,
but
diseases
therapies.
Acta Physiologica,
Год журнала:
2024,
Номер
240(7)
Опубликована: Май 20, 2024
Ferroptosis
is
a
novel
type
of
programmed
cell
death
that
performs
critical
function
in
diabetic
nephropathy
(DN).
Augmenter
liver
regeneration
(ALR)
exists
the
inner
membrane
mitochondria,
and
inhibits
inflammation,
apoptosis,
oxidative
stress
acute
kidney
injury;
however,
its
role
DN
remains
unexplored.
Here,
we
aimed
to
identify
ALR
ferroptosis
induction
macrophage
activation
DN.