Iron homeostasis and ferroptosis in human diseases: mechanisms and therapeutic prospects
Qin Ru,
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Yusheng Li,
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Lin Chen
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et al.
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
Language: Английский
Iron metabolism in rheumatic diseases
Aliakbar Givian,
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Amin Azizan,
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Ahmadreza Jamshidi
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et al.
Journal of Translational Autoimmunity,
Journal Year:
2025,
Volume and Issue:
10, P. 100267 - 100267
Published: Jan. 5, 2025
Iron
is
a
crucial
element
for
living
organism
in
terms
of
oxygen
transport,
hematopoiesis,
enzymatic
activity,
mitochondrial
respiratory
chain
function
and
also
immune
system
function.
The
human
being
has
evolved
mechanism
to
regulate
body
iron.
In
some
rheumatic
diseases
such
as
rheumatoid
arthritis
(RA),
systemic
lupus
erythematous
(SLE),
sclerosis
(SSc),
ankylosing
spondylitis
(AS),
gout,
this
balanced
iron
regulation
impaired.
Altered
homeostasis
can
contribute
disease
progression
through
ROS
production,
fibrosis,
inflammation,
abnormal
bone
homeostasis,
NETosis
cell
senescence.
review,
we
have
focused
on
the
metabolism
its
role
progression.
Language: Английский
Exploring the Potential of Mitochondria‐Targeted Drug Delivery for Enhanced Breast Cancer Therapy
International Journal of Breast Cancer,
Journal Year:
2025,
Volume and Issue:
2025(1)
Published: Jan. 1, 2025
Breast
cancer
stands
as
the
utmost
prevalent
malignancy
in
women,
impacting
epithelial
tissue
of
breast
and
often
displaying
resistance
to
effective
treatment
due
its
diverse
molecular
histological
features.
Current
modalities
may
exhibit
decreasing
efficacy
over
time
can
lead
disease
progression.
The
mitochondria,
a
crucial
organelle
responsible
for
cellular
metabolism
energy
supply,
stand
highly
sensitive
both
heat
reactive
oxygen
species,
presenting
an
assuring
target
photodynamic
photothermal
therapies
(PTTs)
cure.
employment
nanodrug
carriers
combination
deliveries
holds
promise
addressing
challenges
related
drug
degradation
off-target
toxicity.
By
circumventing
reticuloendothelial
system,
nanocarriers
bolster
drug's
bioavailability
at
intended
site
ensure
controlled
codelivery
multiple
drugs,
thereby
maintaining
normal
pharmacokinetic
features
regular
pharmacodynamic
characteristics
different
therapeutic
mechanisms.
precision
this
innovative
technology
have
revolutionized
delivery,
substantially
enhancing
effectiveness.
In
pursuit
targeting
mitochondrial
modifications
cells,
various
such
therapy
(PDT),
PTT,
chemodynamic
(CDT)
been
explored.
These
improved
efficiency
mitochondria-targeted
their
advantageous
properties
minimal
toxicity,
noninvasiveness,
reduced
resistance,
safer
profile.
Our
review
article
provides
exhaustive
overview
alterations
environment
BC,
impact
on
BC
development,
potential
targets
treatment,
nanotherapeutic
approaches
limitations
these
approaches.
Language: Английский
FSP1 regulates ferroptosis and mitochondrial function during mouse oocyte maturation
Hongzhen Ruan,
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Huifen Xiang,
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Yajing Liu
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et al.
Experimental Cell Research,
Journal Year:
2025,
Volume and Issue:
unknown, P. 114524 - 114524
Published: March 1, 2025
Language: Английский
Identification of key regulatory factors for m6A in myasthenia gravis and characteristics of the immune characteristics
Yaoqi Wu,
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Xiaoqing Cai,
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Yingying Jiao
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et al.
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 20, 2024
Abstract
Myasthenia
gravis
(MG),
a
rare
autoimmune
disorder,
presents
complex
pathogenesis
involving
various
immune
molecules.
The
modification
of
N6-methyladenosine
(m6A)
regulates
diverse
metabolic
and
immunopathological
processes;
however,
its
role
in
MG
remains
unclear.
We
downloaded
dataset
GSE85452
from
the
GEO
database
to
identify
differentially
expressed
genes
regulated
by
m6A.
Random
Forest
(RF)
method
was
utilized
pivotal
regulatory
associated
with
m6A
modification.
Subsequently,
prognostic
model
crafted
confirmed
using
this
gene
set.
Patients
were
stratified
according
expression
levels
these
key
genes.
Additionally,
MG-specific
signatures
delineated
examining
cell
infiltration
patterns
their
correlations.
Further
functional
annotation,
protein-protein
interaction
mapping,
molecular
docking
analyses
performed
on
biomarkers,
leading
discovery
three
that
exhibited
significant
differential
within
dataset:
RBM15,
CBLL1,
YTHDF1.The
random
forest
algorithm
as
MG,
validated
constructing
clinical
prediction
model.
Based
expression,
we
divided
patients
into
two
groups,
revealing
distinct
varying
abundances.
also
discovered
61
phenotype
conducted
an
in-depth
exploration
biological
roles.
YTHDF1
found
positively
correlated
CD56dim
natural
killer
cells,
T
type
1
helper
cells.
These
stable
diagnostic
m6A-related
markers
both
validation
cohorts.
Our
findings
suggest
for
MG.
analysis
may
elucidate
roles
microenvironment
Language: Английский
Immune imbalance in Lupus Nephritis: The intersection of T-Cell and ferroptosis
Yunhe Fan,
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Kuai Ma,
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Yumeng Lin
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Dec. 12, 2024
Ferroptosis
is
a
novel
form
of
cell
death
characterized
by
unlimited
accumulation
iron-dependent
lipid
peroxides.
It
often
accompanied
disease,
and
the
relationship
between
ferroptosis
immune
cells
regulation
has
been
attracting
increasing
attention.
Initially,
it
was
found
in
cancer
research
that
inhibition
regulatory
T
(Treg)
promotion
CD8+
jointly
promoted
formation
an
immune-tolerant
environment
tumors.
T-cell
subsequently
to
have
immunoregulatory
effects
other
diseases.
As
autoimmune
disease
imbalance,
attracted
attention
for
its
potential
regulating
balance
lupus
nephritis.
This
article
reviews
metabolic
processes
within
different
subsets
nephritis
(LN),
including
follicular
helper
(TFH)
cells,
(Th)17
Th1
Th2
Treg
reveals
these
cellular
metabolisms
not
only
facilitate
imbalance
but
are
also
closely
associated
with
occurrence
ferroptosis.
Consequently,
we
hypothesize
targeting
pathways
could
become
direction
effectively
treating
altering
differentiation
incidence
Language: Английский