Cell Division,
Journal Year:
2024,
Volume and Issue:
19(1)
Published: Nov. 28, 2024
Cervical
carcinoma
poses
a
significant
health
threat,
with
traditional
treatments
proving
inadequate
in
advanced
stages.
Curcumin,
bioactive
compound
derived
from
turmeric,
exhibits
notable
anti-inflammatory,
antioxidant,
and
antineoplastic
properties,
potentially
modulating
autophagy,
metastasis
cancer
cells.
This
study
examines
curcumin's
impact
on
autophagy
cervical
carcinoma,
focusing
its
interaction
autophagy-related
gene
3
(ATG3).
SiHa
HeLa
cell
lines
were
treated
curcumin,
ATG3
knockdown
(shATG3),
their
combination.
Cell
migration
was
evaluated
via
wound
healing
assays,
while
proliferation
CCK-8
assays.
LC3
expression
assessed
using
immunofluorescence
western
blotting.
Molecular
docking
simulations
identified
binding
interactions
key
proteins.
Curcumin
shATG3
significantly
inhibited
both
proliferation,
synergistic
effect
observed
when
combined.
enhanced,
indicating
increased
autophagy.
Docking
studies
revealed
potential
to
MMP2,
MMP9,
TGF-β,
ATG3,
LC3,
p62,
suggesting
modulation
of
these
pathways.
The
combination
curcumin
also
enhancing
supporting
the
as
therapeutic
agent
for
carcinoma.
Further
clinical
research
is
needed
validate
findings.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 7, 2025
Oral
cancer
is
a
highly
malignant
disease
characterized
by
recurrence,
metastasis,
and
poor
prognosis.
Autophagy,
catabolic
process
induced
under
stress
conditions,
has
been
shown
to
play
dual
role
in
oral
development
therapy.
Recent
studies
have
identified
that
autophagy
activation
epithelial
cells
suppresses
cell
survival
inhibiting
key
pathways
such
as
the
mammalian
target
of
rapamycin
(mTOR)
mitogen-activated
protein
kinase
(MAPK),
while
activating
adenosine
monophosphate-activated
(AMPK)
pathway.
Inducing
promotes
degradation
eukaryotic
initiation
factor
4E,
thus
reducing
metastasis
enhancing
efficacy
chemotherapy,
radiotherapy,
immunotherapy.
Furthermore,
induction
can
modulate
tumor
immune
microenvironment
enhance
antitumor
immunity.
This
review
comprehensively
summarizes
relationship
between
cancer,
focusing
on
its
mechanisms
therapeutic
potential
when
combined
with
conventional
treatments.
While
promising,
precise
clinical
applications
inducers
therapy
remain
be
elucidated,
offering
new
directions
for
future
research
improve
treatment
outcomes
reduce
recurrence.
Cancers,
Journal Year:
2025,
Volume and Issue:
17(3), P. 382 - 382
Published: Jan. 24, 2025
Cancer
stem
cells
(CSCs)
play
a
central
role
in
tumor
progression,
recurrence,
and
resistance
to
conventional
therapies,
making
them
critical
focus
oncology
research.
This
review
provides
comprehensive
analysis
of
CSC
biology,
emphasizing
their
self-renewal,
differentiation,
dynamic
interactions
with
the
microenvironment
(TME).
Key
signaling
pathways,
including
Wnt,
Notch,
Hedgehog,
are
discussed
detail
highlight
potential
as
therapeutic
targets.
Current
methodologies
for
isolating
CSCs
critically
examined,
addressing
advantages
limitations
advancing
precision
medicine.
Emerging
technologies,
such
CRISPR/Cas9
single-cell
sequencing,
explored
transformative
unraveling
heterogeneity
informing
strategies.
The
also
underscores
pivotal
TME
supporting
survival,
promoting
metastasis,
contributing
resistance.
Challenges
arising
from
CSC-driven
dormancy
analyzed,
along
strategies
mitigate
these
barriers,
novel
therapeutics
targeted
approaches.
Ethical
considerations
integration
artificial
intelligence
designing
CSC-specific
therapies
essential
elements
future
manuscript
advocates
multi-disciplinary
approach
that
combines
innovative
advanced
therapeutics,
collaborative
research
address
complexities
CSCs.
By
bridging
existing
gaps
knowledge
fostering
advancements
personalized
medicine,
this
aims
guide
development
more
effective
cancer
treatment
strategies,
ultimately
improving
patient
outcomes.
Rheumatology International,
Journal Year:
2024,
Volume and Issue:
44(9), P. 1701 - 1713
Published: June 8, 2024
Systemic
lupus
erythematosus
(SLE)
is
a
chronic
autoimmune
disease
with
variable
clinical
manifestation,
potentially
leading
to
death.
Importantly,
patients
SLE
have
an
increased
risk
of
neoplastic
disorders.
Thus,
this
study
aimed
comprehensively
evaluate
the
and
laboratory
characteristics
or
without
malignancy.
Antioxidants and Redox Signaling,
Journal Year:
2024,
Volume and Issue:
41(10-12), P. 616 - 636
Published: July 3, 2024
This
study
innovates
by
systematically
integrating
the
molecular
mechanisms
of
iron
death
and
its
application
in
cancer
therapy.
By
deeply
analyzing
interaction
between
tumor
microenvironment,
provides
a
new
theoretical
basis
for
treatment
directions
developing
more
effective
strategies.
In
addition,
points
to
critical
issues
barriers
that
need
be
addressed
future
research,
providing
valuable
insights
into
use
clinical
translation.
Cells,
Journal Year:
2024,
Volume and Issue:
13(11), P. 958 - 958
Published: June 1, 2024
Autophagy
is
a
globally
conserved
cellular
activity
that
plays
critical
role
in
maintaining
homeostasis
through
the
breakdown
and
recycling
of
constituents.
In
recent
years,
there
has
been
much
emphasis
given
to
its
complex
cancer
stem
cells
(CSCs)
cell
treatment.
This
study
examines
molecular
processes
support
autophagy
how
it
regulated
context
CSCs
Although
dual
management
CSCs,
affecting
their
removal
as
well
maintenance,
intricate
interaction
between
several
signaling
channels
control
survival
death
part
mechanism
not
elucidated.
Given
have
development,
progression,
resistance
treatment
tumors,
imperative
comprehend
biological
activities.
are
important
for
biology
because
they
also
show
tissue
regeneration
model
helps
with
organoid
regeneration.
other
words,
manipulation
viable
therapeutic
approach
therapy.
Both
synthetic
natural
substances
target
pathways
demonstrated
promise
improving
cell-based
therapies
eliminating
CSCs.
Nevertheless,
difficulties
associated
limitations
CSC
regulation,
including
mechanisms
off-target
effects.
Thus,
regulation
offers
versatile
strategy
focusing
on
enhancing
results
Therefore,
understanding
interactions
would
be
essential
creating
treatments
work
both
regenerative
medicine
Cell Communication and Signaling,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: Nov. 13, 2024
Despite
the
tremendous
advancements
in
knowledge
of
pathophysiology
and
clinical
aspects
SARS-CoV-2
infection,
still
many
issues
remain
unanswered,
especially
long-term
effects.
Mounting
evidence
suggests
that
pulmonary
fibrosis
(PF)
is
one
most
severe
complications
associated
with
COVID-19.
Therefore,
understanding
molecular
mechanisms
behind
its
development
helpful
to
develop
successful
therapeutic
strategies.
Epithelial
mesenchymal
transition
(EMT)
cell
specific
variants
endothelial
(EndMT)
mesothelial
(MMT)
are
physio-pathologic
cellular
reprogramming
processes
induced
by
several
infectious,
inflammatory
biomechanical
stimuli.
Cells
undergoing
EMT
acquire
invasive,
profibrogenic
proinflammatory
activities
secreting
extracellular
mediators.
Their
activity
has
been
implicated
pathogenesis
PF
a
variety
lung
disorders,
including
idiopathic
(IPF)
Aim
this
article
provide
an
updated
survey
mechanisms,
emphasis
on
EMT-related
processes,
genesis
IFP
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: July 30, 2024
Pancreatic
cancer
is
a
leading
cause
of
cancer-related
mortality
worldwide
with
increasing
global
incidence.
We
previously
reported
the
anticancer
effect
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 25, 2024
Abstract
Cervical
carcinoma
poses
a
significant
health
threat,
with
traditional
treatments
proving
inadequate
in
advanced
stages.
Curcumin,
bioactive
compound
derived
from
turmeric,
exhibits
notable
anti-inflammatory,
antioxidant,
and
antineoplastic
properties,
potentially
modulating
autophagy,
metastasis
cancer
cells.
This
study
examines
curcumin's
impact
on
autophagy
cervical
carcinoma,
focusing
its
interaction
autophagy-related
gene
3
(ATG3).
SiHa
HeLa
cell
lines
were
treated
curcumin,
ATG3
knockdown
(shATG3),
their
combination.
Cell
migration
was
evaluated
via
wound
healing
assays,
LC3
expression
assessed
using
immunofluorescence
western
blotting.
Molecular
docking
simulations
identified
binding
interactions
key
proteins.
Curcumin
shATG3
significantly
inhibited
migration,
synergistic
effect
observed
when
combined.
enhanced,
indicating
increased
autophagy.
Docking
studies
revealed
potential
to
MMP2,
MMP9,
TGF-β,
ATG3,
LC3,
p62,
suggesting
modulation
of
these
pathways.
The
combination
curcumin
demonstrates
inhibition
enhancement
supporting
as
therapeutic
agent
for
carcinoma.
Further
clinical
research
is
warranted
confirm
findings.