BMC Women s Health,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: Jan. 24, 2025
Cuproptosis
is
a
novel
form
of
cell
death,
acting
on
the
tricarboxylic
acid
cycle
in
mitochondrial
respiration
and
mediated
by
protein
lipoylation.
Other
cancer
death
processes,
such
as
necroptosis,
pyroptosis,
ferroptosis,
have
been
shown
to
play
crucial
roles
therapy
prognosis
ovarian
cancer.
However,
role
cuproptosis
remains
unclear.
The
expression
profiles
10
cuproptosis-related
genes
were
extracted
from
GSE140082.
Kaplan-Meier
survival
Cox
proportional
hazards
regression
used
identify
prognostic
for
constructing
risk
models.
Following
this,
Least
Absolute
Shrinkage
Selection
Operator
was
employed
construct
score
model.
Next,
nomogram
constructed
predict
overall
Ultimately,
our
analysis
compared
two
groups
across
various
dimensions,
including
clinical
characteristics,
tumor
progression,
metabolism-related
pathways,
immune
landscape,
drug
sensitivity.
MTF1
LIAS
identified
protective
factors
cancer,
with
patients
higher
group
being
significantly
associated
poorer
survival.
Furthermore,
integrating
characteristics
demonstrated
high
specificity
sensitivity
predicting
A
propotion
M2
macrophages,
follicular
helper
T
cells,
resting
mast
cells
observed
high-risk
group.
Additionally,
IC50
values
Dasatinib,
Bortezomib,
Parthenolide,
Imatinib
lower
study
highlights
significance
provides
new
insights
into
developing
pharmacological
therapeutic
strategies
targeting
prevention
treatment
Cell Communication and Signaling,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: Feb. 12, 2024
Abstract
Cancer
treatment
faces
many
hurdles
and
resistance
is
one
among
them.
Anti-cancer
strategies
are
evolving
due
to
innate
acquired
capacity,
governed
by
genetic,
epigenetic,
proteomic,
metabolic,
or
microenvironmental
cues
that
ultimately
enable
selected
cancer
cells
survive
progress
under
unfavorable
conditions.
Although
the
mechanism
of
drug
being
widely
studied
generate
new
target-based
drugs
with
better
potency
than
existing
ones.
However,
broader
flexibility
in
resistance,
advanced
therapeutic
options
efficacy
need
be
explored.
Combination
therapy
an
alternative
a
success
rate
though
risk
amplified
side
effects
commonplace.
Moreover,
recent
groundbreaking
precision
immune
ways
overcome
has
revolutionized
anticancer
greater
extent
only
limitation
individual-specific
needs
further
attention.
This
review
will
focus
on
challenges
opted
withstand
current
therapies
at
molecular
level
also
highlights
emerging
-like
immunological,
stem
cell-based
may
prove
have
potential
challenge
problem
resistance.
Journal of Hematology & Oncology,
Journal Year:
2024,
Volume and Issue:
17(1)
Published: April 23, 2024
Abstract
Tumor
is
a
local
tissue
hyperplasia
resulted
from
cancerous
transformation
of
normal
cells
under
the
action
various
physical,
chemical
and
biological
factors.
The
exploration
tumorigenesis
mechanism
crucial
for
early
prevention
treatment
tumors.
Epigenetic
modification
common
important
in
cells,
including
DNA
methylation,
histone
modification,
non-coding
RNA
m6A
modification.
mode
cell
death
programmed
by
death-related
genes;
however,
recent
researches
have
revealed
some
new
modes
death,
pyroptosis,
ferroptosis,
cuproptosis
disulfidptosis.
regulation
deaths
mainly
involved
key
proteins
affects
up-regulating
or
down-regulating
expression
levels
proteins.
This
study
aims
to
investigate
epigenetic
modifications
regulating
disulfidptosis
tumor
explore
possible
triggering
factors
development
microscopic
point
view,
provide
potential
targets
therapy
perspective
antitumor
drugs
combination
therapies.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: May 7, 2024
Abstract
Sleep
disorders
increase
the
risk
and
mortality
of
heart
disease,
but
brain-heart
interaction
has
not
yet
been
fully
elucidated.
Cuproptosis
is
a
copper-dependent
type
cell
death
activated
by
excessive
accumulation
intracellular
copper.
Here,
we
showed
that
16
weeks
sleep
fragmentation
(SF)
resulted
in
elevated
copper
levels
male
mouse
exacerbated
myocardial
ischemia–reperfusion
injury
with
increased
cuproptosis
apoptosis.
Mechanistically,
found
SF
promotes
sympathetic
overactivity,
increases
germination
nerve
terminals,
level
norepinephrine
cardiac
tissue,
thereby
inhibits
VPS35
expression
leads
to
impaired
ATP7A
related
transport
overload
cardiomyocytes.
Copper
further
apoptosis,
these
effects
can
be
rescued
excision
or
administration
chelating
agent.
Our
study
elucidates
one
molecular
mechanisms
which
aggravate
suggests
possible
targets
for
intervention.
Clinical and Translational Medicine,
Journal Year:
2024,
Volume and Issue:
14(6)
Published: May 28, 2024
Abstract
Copper,
a
trace
element
and
vital
cofactor,
plays
crucial
role
in
the
maintenance
of
biological
functions.
Recent
evidence
has
established
significant
correlations
between
copper
levels,
cancer
development
metastasis.
The
strong
redox‐active
properties
offer
both
benefits
disadvantages
to
cells.
intestinal
tract,
which
is
primarily
responsible
for
uptake
regulation,
may
suffer
from
an
imbalance
homeostasis.
Colorectal
(CRC)
most
prevalent
primary
tract
aggressive
malignant
disease
with
limited
therapeutic
options.
Current
research
focused
on
relationship
CRC.
Innovative
concepts,
such
as
cuproplasia
cuproptosis,
are
being
explored
understand
copper‐related
cellular
proliferation
death.
Cuproplasia
regulation
cell
that
mediated
by
enzymatic
nonenzymatic
copper‐modulated
activities.
Whereas,
cuproptosis
refers
death
induced
excess
via
promoting
abnormal
oligomerisation
lipoylated
proteins
within
tricarboxylic
acid
cycle,
well
diminishing
levels
iron‐sulphur
cluster
proteins.
A
comprehensive
understanding
mechanisms
offers
new
avenues
CRC
treatment.
In
this
review,
we
summarise
evolving
molecular
mechanisms,
ranging
intracellular
concentrations
discovered,
discuss
pathogenesis,
progression
potential
therapies
Understanding
will
help
provide
theoretical
foundation
innovative
treatment
strategies
management.
Oxidative Medicine and Cellular Longevity,
Journal Year:
2021,
Volume and Issue:
2021(1)
Published: Jan. 1, 2021
Increasing
evidence
suggests
that
traditional
Chinese
medicine
strategies
are
obviously
beneficial
for
cancer
treatment,
but
scientific
research
on
the
underlying
molecular
mechanisms
is
lacking.
We
report
ursolic
acid,
a
bioactive
ingredient
isolated
from
Radix
Actinidiae
chinensis,
has
strong
antitumour
effects
osteosarcoma
cells.
Functional
studies
showed
acid
inhibited
tumour
cell
proliferation
and
promoted
apoptosis
of
variety
Ursolic
had
synergistic
cytotoxic
effect
with
cisplatin
In
mouse
xenograft
model,
low-dose
combined
significantly
reduced
growth.
Notably,
reversed
weight
loss
in
mice
treated
cisplatin.
Mechanistic
degraded
ferritin
by
activating
autophagy
induced
intracellular
overload
ferrous
ions,
leading
to
ferroptosis.
addition,
enhanced
DNA-damaging
Taken
together,
these
findings
suggest
nontoxic
adjuvant
may
enhance
effectiveness
chemotherapy
osteosarcoma.
Cells,
Journal Year:
2022,
Volume and Issue:
11(2), P. 289 - 289
Published: Jan. 15, 2022
The
Golgi
apparatus
is
a
membrane
organelle
located
in
the
center
of
protein
processing
and
trafficking
pathway.
It
consists
sub-compartments
with
distinct
biochemical
compositions
functions.
Main
functions
Golgi,
including
trafficking,
glycosylation,
sorting,
require
well-maintained
stable
microenvironment
along
metal
ion
homeostasis.
Metal
ions,
such
as
Ca2+,
Mn2+,
Zn2+,
Cu2+,
are
important
cofactors
many
resident
glycosylation
enzymes.
homeostasis
ions
secretory
pathway,
which
required
for
proper
function
stress
response
tightly
regulated
maintained
by
transporters.
Mutations
transporters
cause
human
diseases.
Here
we
provide
review
specifically
focusing
on
that
maintain
under
physiological
conditions
their
alterations
Cell Reports,
Journal Year:
2023,
Volume and Issue:
42(5), P. 112417 - 112417
Published: April 18, 2023
The
P-type
ATPase
ATP7B
exports
cytosolic
copper
and
plays
an
essential
role
in
the
regulation
of
cellular
homeostasis.
Mutants
cause
Wilson
disease
(WD),
autosomal
recessive
disorder
metabolism.
Here,
we
present
cryoelectron
microscopy
(cryo-EM)
structures
human
E1
state
apo,
putative
copper-bound,
cisplatin-bound
forms.
In
ATP7B,
N-terminal
sixth
metal-binding
domain
(MBD6)
binds
at
entry
site
transmembrane
(TMD),
facilitating
delivery
from
MBD6
to
TMD.
sulfur-containing
residues
TMD
mark
transport
pathway.
By
comparing
E2-Pi
frog
propose
ATP-driving
model
ATP7B.
These
not
only
advance
our
understanding
mechanisms
ATP7B-mediated
export
but
can
also
guide
development
therapeutics
for
treatment
WD.