Wilson’s Disease—Crossroads of Genetics, Inflammation and Immunity/Autoimmunity: Clinical and Molecular Issues
Grażyna Gromadzka,
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Julia Czerwińska,
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Elżbieta Krzemińska
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et al.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(16), P. 9034 - 9034
Published: Aug. 20, 2024
Wilson's
disease
(WD)
is
a
rare,
autosomal
recessive
disorder
of
copper
metabolism
caused
by
pathogenic
mutations
in
the
Language: Английский
Exploring the Anti-PANoptosis Mechanism of Dachaihu Decoction Against Sepsis-Induced Acute Lung Injury: Network Pharmacology, Bioinformatics, and Experimental Validation
Zhen Yang,
No information about this author
Xingyu Kao,
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Lin Zhang
No information about this author
et al.
Drug Design Development and Therapy,
Journal Year:
2025,
Volume and Issue:
Volume 19, P. 349 - 368
Published: Jan. 1, 2025
Dachaihu
decoction
(DCHD)
is
a
common
Chinese
medicine
formula
against
sepsis-induced
acute
lung
injury
(SALI).
PANoptosis
novel
type
of
programmed
cell
death.
Nevertheless,
The
mechanisms
DCHD
SALI
via
anti-PANoptosis
remains
unknown.
First,
we
identified
the
intersecting
targets
among
DCHD,
SALI,
and
using
relevant
databases
published
literature.
Then,
protein-protein
interaction
(PPI)
network,
molecular
docking,
functional
enrichment
analysis
were
conducted.
In
vivo,
cecal
ligation
puncture
(CLP)
was
used
to
construct
sepsis
mouse
model,
therapeutic
effects
on
evaluated
hematoxylin
eosin
(H&E)
staining,
quantitative
real-time
PCR
(qRT-PCR),
ELISA.
Finally,
qRT-PCR,
immunofluorescence
Western
blotting
verify
effect
DCHD-containing
serum
(DCHD-DS)
LPS-induced
RAW
264.7
macrophages
in
vitro.
82
by
mapping
PANoptosis.
Enrichment
showed
that
modulating
tumor
necrosis
factor
(TNF),
AGE-RAGE,
phosphoinositide
3-kinase
(PI3K)-AKT,
Toll-like
receptor
signaling
pathways
targeting
Casp3,
cellular
antigen
p53
(TP53),
B-cell
lymphoma
2
(Bcl2),
toll-like
receptor-4
(TLR4),
STAT3,
STAT1,
RELA,
NF-κB1,
myeloid
leukemia-1
(MCL1),
JUN,
IL-1β,
HSP90AA1,
Casp9,
Casp8,
Bcl2l1.
Molecular
docking
revealed
key
components
have
high
binding
affinity
core
targets.
improved
histopathological
injury,
reduced
inflammatory
expression,
alleviated
oxidative
stress
tissues.
vitro,
DCHD-DS
morphology
changes,
release
pro-inflammatory
factors,
p65
nucleus
aggregation.
Furthermore,
verified
inhibited
downregulating
PI3K/AKT/NF-κB
signalling
pathway.
attenuates
inhibiting
control
Our
study
provides
solid
foundation
for
investigating
its
clinical
application
treatment
SALI.
Language: Английский
Potential relationship between cuproptosis and sepsis-acquired weakness: an intermediate role for mitochondria
Luying Yang,
No information about this author
Leiyu Xie,
No information about this author
Min Li
No information about this author
et al.
Frontiers in Physiology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 20, 2025
Sepsis
is
defined
as
a
life-threatening
organ
dysfunction
caused
by
dysregulated
host
response
to
infection.
Skeletal
muscle
atrophy
due
critical
illness
common
phenomenon
in
the
intensive
care
unit
(ICU)
and
referred
ICU-acquired
weakness
(ICU-AW).
The
occurrence
of
ICU-AW
patients
with
sepsis
known
sepsis-acquired
(SAW).
Furthermore,
it
well
that
maintaining
normal
function
closely
relates
mitochondrial
homeostasis.
Once
impaired,
both
quality
are
affected.
Copper
plays
key
role
homeostasis
transition
metal
regulates
stability
various
enzymes.
also
involved
oxidation-reduction
reactions,
intracellular
copper
overload
causes
oxidative
stress
induces
cell
death.
Previous
studies
have
shown
excess
death
targeting
lipid-acylated
proteins
regulate
tricarboxylic
acid
(TCA)
cycle,
which
differs
from
canonical
mechanisms
regulated
inhibitors
death,
such
apoptosis,
necroptosis,
pyroptosis
ferroptosis,
not
effective
preventing
copper-induced
This
new
form
has
been
termed
“Cuproptosis”;
however,
mechanism
SAW
remains
unclear.
In
this
paper,
we
review
possible
relationship
between
cuproptosis
SAW.
Cuproptosis
may
be
regulating
pathological
through
mitochondria-related
signaling
pathways,
ferroptosis
mechanisms,
genes,
provide
ideas
for
further
investigations
into
Language: Английский
Integrating cuproptosis and immunosenescence: A novel therapeutic strategy in cancer treatment
Biochemistry and Biophysics Reports,
Journal Year:
2025,
Volume and Issue:
42, P. 101983 - 101983
Published: March 29, 2025
Language: Английский
Exosomes derived from FN14-overexpressing BMSCs activate the NF-κB signaling pathway to induce PANoptosis in osteosarcoma
APOPTOSIS,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 20, 2025
Language: Английский
Unravelling the Role of PANoptosis in Liver Diseases: Mechanisms and Therapeutic Implications
Liver International,
Journal Year:
2025,
Volume and Issue:
45(4)
Published: March 21, 2025
PANoptosis
is
a
multimodal
form
of
cell
death
that
involves
inflammatory,
apoptotic,
and
necroptotic
pathways,
playing
key
role
in
the
development
liver
diseases.
This
article
first
outlines
definition
characteristics
PANoptosis,
then
explores
its
mechanisms
action
different
types
diseases,
including
acute
injury,
failure,
metabolic
dysfunction-associated
fatty
disease,
hepatocellular
carcinoma.
Furthermore,
this
analyses
molecular
regulatory
network
potential
therapeutic
targets.
Finally,
summarises
current
research
on
diseases
future
directions,
it
reviews
emerging
mechanism
Language: Английский
Interplay of Ferroptosis, Cuproptosis, Autophagy and Pyroptosis in Male Infertility: Molecular Crossroads and Therapeutic Opportunities
Dong-Zhen Cai,
No information about this author
Junda Li,
No information about this author
Peng Zhang
No information about this author
et al.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(8), P. 3496 - 3496
Published: April 8, 2025
Male
infertility
is
intricately
linked
to
dysregulated
cell
death
pathways,
including
ferroptosis,
cuproptosis,
pyroptosis,
and
autophagy.
Ferroptosis,
driven
by
iron-dependent
lipid
peroxidation
through
the
Fenton
reaction
inactivation
of
GPX4/Nrf2/SLC7A11
axis,
disrupts
spermatogenesis
under
conditions
oxidative
stress,
environmental
toxin
exposure,
or
metabolic
disorders.
Similarly,
cuproptosis-characterized
mitochondrial
dysfunction
disulfide
stress
due
copper
overload-exacerbates
germ
apoptosis
via
FDX1
activation
NADPH
depletion.
Pyroptosis,
mediated
NLRP3
inflammasome
gasdermin
D,
amplifies
testicular
inflammation
loss
IL-1β/IL-18
release,
particularly
in
response
insults.
Autophagy
maintains
homeostasis
clearing
damaged
organelles
proteins;
however,
its
dysregulation
impairs
sperm
maturation
compromises
blood-testis
barrier
integrity.
These
pathways
intersect
shared
regulators;
reactive
oxygen
species
mTOR
modulate
autophagy-pyroptosis
balance,
while
Nrf2
bridge
ferroptosis-cuproptosis
crosstalk.
Therapeutic
interventions
targeting
these
mechanisms
have
shown
promise
preclinical
models.
However,
challenges
persist,
tissue-specific
roles
isoforms,
off-target
effects
pharmacological
inhibitors,
transgenerational
epigenetic
impacts
toxins.
This
review
synthesizes
current
molecular
insights
into
implicated
male
infertility,
emphasizing
their
interplay
translational
potential
for
restoring
spermatogenic
function.
Language: Английский
Associations between serum trace elements and biological age acceleration in the Chinese elderly: A community-based study investigating the mediating role of inflammatory markers and the moderating effect of physical activity
Yan Wang,
No information about this author
Wenyuan Zhu,
No information about this author
Tao� Zhang
No information about this author
et al.
Journal of Hazardous Materials,
Journal Year:
2025,
Volume and Issue:
unknown, P. 138273 - 138273
Published: April 1, 2025
Language: Английский
The molecular mechanism and therapeutic landscape of copper and cuproptosis in cancer
Ziyu Guo,
No information about this author
Danyao Chen,
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Lei Yao
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et al.
Signal Transduction and Targeted Therapy,
Journal Year:
2025,
Volume and Issue:
10(1)
Published: May 8, 2025
Abstract
Copper,
an
essential
micronutrient,
plays
significant
roles
in
numerous
biological
functions.
Recent
studies
have
identified
imbalances
copper
homeostasis
across
various
cancers,
along
with
the
emergence
of
cuproptosis,
a
novel
copper-dependent
form
cell
death
that
is
crucial
for
tumor
suppression
and
therapeutic
resistance.
As
result,
manipulating
levels
has
garnered
increasing
interest
as
innovative
approach
to
cancer
therapy.
In
this
review,
we
first
delineate
at
both
cellular
systemic
levels,
clarifying
copper’s
protumorigenic
antitumorigenic
functions
cancer.
We
then
outline
key
milestones
molecular
mechanisms
including
mitochondria-dependent
independent
pathways.
Next,
explore
cuproptosis
biology,
well
interactions
mediated
by
between
cells
immune
system.
also
summarize
emerging
opportunities
targeting
discuss
clinical
associations
cuproptosis-related
genes.
Finally,
examine
potential
biomarkers
put
forward
existing
challenges
future
prospects
leveraging
Overall,
review
enhances
our
understanding
landscape
cancer,
highlighting
copper-
or
cuproptosis-based
therapies
treatment.
Language: Английский
The Effect of Cuproptosis-Related Proteins on Macrophage Polarization in Mesothelioma is Revealed by scRNA-seq
Jiaxin Xu,
No information about this author
Lijing Ma,
No information about this author
Li-Ying Tu
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et al.
Biological Trace Element Research,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 23, 2024
High
invasiveness
mesothelioma
is
a
malignant
tumor
of
the
peritoneum
or
pleura.
The
effect
cuproptosis
on
(MESO)
still
unknown,
though.
Cancer
Genome
Atlas
(TCGA)
and
Gene
Expression
Omnibus
(GEO)
datasets
were
used
to
identify
differential
genes
linked
in
mesothelioma.
Multigene
features
then
created
assess
course
disease.
Use
single-cell
data
vitro
validation
uncover
crucial
gene
regulation
mechanisms.
In
MESO,
we
found
nine
differentially
expressed
cuproptosis.
Using
univariate
Cox
LASSO
regression
techniques,
3-gene
feature
(P
<
0.05)
was
created,
showing
good
predictive
potential
for
survival
time.
According
risk
score,
patients
low-risk
subset
had
considerably
greater
rate
than
those
high-risk
=
0).
similar
pattern
prediction
performance
are
also
seen
queue.
findings
drug
sensitivity
research
indicate
that
patients,
vinblastine,
paclitaxel,
gefitinib,
erlotinib
sensitive
medications
0.05).
Classical
monocytes
identified
as
core
cells
connected
by
CellChat
results.
SLC31A1
implicated
positive
M2
macrophage
polarization,
according
cell
subtype
analysis
confirmation.
Genes
have
major
influence
immunity
can
predict
how
MESO
will
progress.
Language: Английский