Inhibition of Ovarian Cancer Growth, Metastasis and Reverse the Tumor Microenvironment by Dual Drug-Loaded Polymer Micelle Targeting Tumor Microenvironment
Lu Zhang,
No information about this author
Rui-bo Guo,
No information about this author
Muhan Chen
No information about this author
et al.
International Journal of Nanomedicine,
Journal Year:
2025,
Volume and Issue:
Volume 20, P. 2969 - 2990
Published: March 1, 2025
Introduction:
Ovarian
cancer
is
a
malignant
tumor
that
arises
in
the
female
reproductive
system
and
associated
with
very
high
mortality
rate.
This
primarily
due
to
highly
invasive
nature
of
metastasis
recurrence.
Transforming
immune
environment
from
an
immunosuppressive
state
anti-tumor
through
phenotypic
transformation
tumor-associated
macrophages
crucial
for
inhibiting
growth,
metastasis,
recurrence
ovarian
cancer.
Methods:
A
polymer
micelle
(RC-PH-Ms)
containing
paclitaxel
(PTX)
honokiol
(HNK)
was
designed
based
on
expression
reactive
oxygen
species
microenvironment.
Once
micelles
are
actively
targeted
microenvironment
characterized
by
elevated
levels
species,
responsive
bond
cleaved,
thereby
exposing
secondary
targeting
ligand
C7R.
The
released
PTX
HNK
facilitate
relevant
M2
phenotype
M1
phenotype,
which
turn
inhibits
invasion
inhibit
angiogenesis
reduce
Results:
effects
RC-PH-Ms
modulating
vascularization
were
investigated
both
vivo
vitro.
Conclusion:
can
significantly
cancer,
provides
new
perspective
clinical
treatment.
Keywords:
recrudescence,
immunotherapy,
Language: Английский
From Defense to Disease: How the Immune System Fuels Epithelial–Mesenchymal Transition in Ovarian Cancer
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(9), P. 4041 - 4041
Published: April 24, 2025
Ovarian
cancer
is
one
of
the
most
deadly
gynecological
cancers,
with
over
300
thousand
new
cases
per
year,
which
are
diagnosed
in
advanced
stages.
The
limited
availability
effective
biomarkers
and
lack
characteristic
symptoms
make
early
diagnosis
difficult,
resulting
a
five-year
survival
rate
30–40%.
Mutations
BRCA1
BRCA2
genes
abnormalities
signaling
pathways
such
as
PI3K/AKT
TP53
play
key
role
progression
ovarian
cancer.
immune
system,
can
act
against
tumors,
often
supports
tumor
development
microenvironment
through
immunoevasion,
influenced
by
cytokines
IL-6,
IL-10,
TGF-β.
Epithelial-to-mesenchymal
transition
(EMT)
allows
cells
to
acquire
mesenchymal
characteristics,
increasing
their
invasiveness
metastatic
capacity.
Immunological
factors,
including
pro-inflammatory
signals
from
regulate
EMT
process.
This
review
aims
present
progression,
its
interactions
potential
therapeutic
targets.
Modulation
response
inhibition
may
constitute
basis
for
personalized
therapies,
opens
possibilities
improving
prognosis
efficacy
treatment
patients
Language: Английский
Construction of a prognostic model for ovarian cancer based on a comprehensive bioinformatics analysis of cuproptosis-associated long non-coding RNA signatures
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(15), P. e35004 - e35004
Published: July 23, 2024
Ovarian
cancer
(OCa)
is
a
common
malignancy
in
women,
and
the
role
of
cuproptosis
its
related
genes
OCa
unclear.
Using
GSE14407
dataset,
we
analyzed
expression
correlation
cuproptosis-related
(CRGs)
between
tumor
normal
groups.
From
TCGA-OV
identified
20
long
non-coding
RNAs
(CuLncs)
associated
with
patient
survival
through
univariate
Cox
analysis.
patients
were
divided
into
early-stage
late-stage
groups
to
analyze
CuLncs
expression.
Cluster
analysis
classified
two
clusters,
Cluster1
having
poorer
prognosis.
Significant
differences
"Lymphatic
Invasion"
"Cancer
status"
observed
clusters.
Seven
CRGs
showed
significant
differences,
validated
using
human
protein
atlas
(HPA)
databases.
Immune
revealed
higher
ImmuneScore
Cluster1.
GSEA
signaling
pathways.
LASSO
regression
included
11
construct
validate
prediction
model,
classifying
high-risk
low-risk
Correlations
riskScore,
phenotype,
ImmuneScore,
immune
cell
infiltration
explored.
Cell
experiments
that
knocking
down
AC023644.1
decreases
viability.
In
conclusion,
constructed
an
accurate
prognostic
model
for
based
on
CuLncs,
providing
basis
prognosis
assessment
potential
immunotherapy
targets.
Language: Английский
Research progress of immune checkpoint inhibitors in ovarian cancer
Lingli Zhao,
No information about this author
Yanhong Zhai,
No information about this author
Gaoli Niu
No information about this author
et al.
Exploration of Immunology,
Journal Year:
2024,
Volume and Issue:
unknown, P. 853 - 870
Published: Dec. 18, 2024
Ovarian
cancer
is
the
deadliest
malignant
tumor
in
female
reproductive
system.
Despite
advancements
standard
treatments
such
as
debulking
surgery
and
platinum-based
chemotherapy,
overall
survival
rate
remains
low.
The
emergence
of
targeted
therapies,
including
Poly(ADP-ribose)
polymerase
(PARP)
inhibitors
anti-angiogenic
agents,
has
provided
new
avenues
for
treatment.
However,
drug
resistance
disease
heterogeneity
continue
to
pose
significant
challenges.
Immune
checkpoint
(ICIs),
an
emerging
therapeutic
approach,
primarily
target
programmed
cell
death
protein
1
(PD-1)/programmed
ligand
(PD-L1)
cytotoxic
T-lymphocyte
antigen
4
(CTLA-4)
pathways
restore
anti-tumor
immune
responses.
Although
ICIs
have
shown
efficacy
other
malignancies,
their
effectiveness
ovarian
limited,
with
a
response
only
10–15%
monotherapy.
Recent
studies
focused
on
combining
or
PARP
enhance
outcomes.
This
article
reviews
progress
cancer,
monotherapy
combination
treatment
strategies,
explores
targets
strategies
aimed
at
improving
patient
prognosis
achieving
personalized
By
gaining
deeper
understanding
microenvironment
its
evasion
mechanisms,
there
hope
developing
more
effective
options
future,
ultimately
rates
quality
life
patients.
Language: Английский