Pharmacological Research,
Год журнала:
2024,
Номер
210, С. 107502 - 107502
Опубликована: Ноя. 7, 2024
Cancer
continues
to
be
a
leading
cause
of
death
worldwide,
highlighting
the
urgent
need
for
development
new
therapeutic
strategies.
Chrysophanol,
naturally
occurring
anthraquinone
compound,
has
demonstrated
significant
potential
in
cancer
treatment
due
its
diverse
biological
activities.
This
review
delves
into
mechanisms
through
which
chrysophanol
exerts
anti-cancer
effects,
including
induction
cell
cycle
arrest,
promotion
apoptosis,
regulation
autophagy,
and
initiation
necrosis
across
various
lines.
Additionally,
discusses
chrysophanol's
impact
on
inhibiting
invasion
metastasis
role
modulating
chemotherapy
sensitivity.
Despite
promising
chrysophanol,
challenges
such
as
poor
water
solubility,
low
bioavailability,
safety
concerns
remain.
Comprehensive
clinical
trials
are
essential
validate
efficacy
safety.
emphasizes
candidate
therapy
underscores
necessity
further
research
fully
harness
potential.
Cells,
Год журнала:
2024,
Номер
13(10), С. 844 - 844
Опубликована: Май 16, 2024
Immune
cell
migration
is
required
for
the
development
of
an
effective
and
robust
immune
response.
This
elegant
process
regulated
by
both
cellular
environmental
factors,
with
variables
such
as
state,
anatomical
location,
disease
state
that
govern
differences
in
patterns.
In
all
cases,
a
major
factor
expression
surface
receptors
their
cognate
ligands.
Rapid
adaptation
to
conditions
partly
depends
on
intrinsic
factors
affect
cell’s
ability
adjust
new
environment.
this
review,
we
discuss
myeloid
lymphoid
cells
outline
key
determinants
migration,
including
molecules
adhesion,
modes
chemotaxis,
specific
chemokine
signaling.
Furthermore,
summarize
tumor-specific
elements
contribute
trafficking
cancer,
while
also
exploring
microenvironment
can
alter
these
dynamics
within
tumor
pro
antitumor
fashion.
Specifically,
highlight
importance
secretome
later
aspects.
review
considers
myriad
impact
trajectory
cancer.
We
aim
immunotherapeutic
targets
be
harnessed
achieve
controlled
tumors.
Nature Communications,
Год журнала:
2025,
Номер
16(1)
Опубликована: Янв. 29, 2025
Abstract
P-cadherin,
a
crucial
cell-cell
adhesion
protein
which
is
overexpressed
in
numerous
malignant
cancers,
popular
target
for
drug
delivery
antibodies.
However,
molecular
guidelines
engineering
antibodies
that
can
be
internalized
upon
binding
to
P-cadherin
are
unknown.
Here,
we
use
combination
of
biophysical,
biochemical,
and
cell
biological
methods
demonstrate
trapping
the
extracellular
region
an
X-dimer
adhesive
conformation
triggers
cadherin
endocytosis
via
outside-in
signaling
mechanism.
We
show
anti-cancer
monoclonal
antibody
CQY684,
traps
strengthens
this
structure.
Formation
stable
X-dimers
results
phosphorylation
p120-catenin,
suppressor
endocytosis.
This
dissociation
p120-catenin
from
cytoplasmic
region,
increases
turnover
targets
cadherin-antibody
complex
lysosome.
Our
establish
mechanism
provides
fundamental
insights
into
how
cells
regulate
exploited
by
anti-cadherin
intracellular
delivery.
Journal of Complementary and Integrative Medicine,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 27, 2025
Abstract
Fisetin,
a
flavonol
belonging
to
the
flavonoid
subclass,
is
ubiquitous
dietary
present
in
fruits
and
vegetables,
including
fruit
peels,
has
proven
potential
for
anticancer
activity,
especially
lung
cancer
–
leading
cause
of
cancer-related
deaths
globally.
The
current
paper
provides
most
detailed
elaborate
list
various
roles
fisetin
experimentally
induced
cells,
these
include
promotion
apoptosis,
inhibition
cell
proliferation,
migration,
invasion,
as
well
regulation
autophagy.
Among
molecular
targets,
some
identified
pathways,
such
PI3K/Akt,
MAPK,
NF-κB,
that
affects
are
crucial
tumor
formation,
so
it
can
be
considered
chemopreventive
agent.
Moreover,
improves
effectiveness
conventional
treatments
chemo-
radiosensitizer
minimizes
side
effects.
However,
overall
utility
clinical
use
now
somewhat
restricted
by
its
poor
solubility
short
half-life.
It
predicted
future
development
nanotechnologies
drug
delivery,
nanoparticle
encapsulation,
might
help
solve
difficulties.
Further
Preclinical
investigations
required
uniformly
determine
safety,
efficacy,
standard
dosage
consumption
therapy.
Frontiers in Oncology,
Год журнала:
2025,
Номер
15
Опубликована: Март 5, 2025
from
the
primary
tumor
site
to
distant
organs,
where
they
form
secondary
foci.The
occurrence
of
metastasis
involves
complex
cellular
signaling
pathways
and
changes
in
microenvironment
(1).
Tumor
resistance,
especially
chemotherapy,
targeted
therapy,
immunotherapy,
significantly
impacts
treatment
efficacy,
resulting
recurrence
cancer
progression.
To
improve
survival
quality
life
patients,
it
is
urgent
understand
molecular
mechanisms
drug
resistance
identify
new
therapeutic
targets.Tumor
a
multi-step
process,
involving
detachment
cells,
invasion,
dissemination
through
blood
or
lymphatic
systems,
growth
organs.
Epithelial-Mesenchymal
Transition
(EMT)
critical
process
which
cells
acquire
invasive
metastatic
potential
(2,3).
The
(e.g.
cancer-associated
fibroblasts,
etc.)
immune
tumor-associated
macrophages,
also
participate
(4).Additionally,
angiogenesis
an
important
condition
for
metastasis.
Deregulation
Cuproptosis
has
been
linked
metastasis,
recent
review
by
Wang
et
al.,
unbalanced
levels
copper
promote
angiogenesis,
enabling
cell
spread
(Frontiers
oncology.
2023;13:1288504.).
Moreover,
could
degrade
extracellular
matrix
secretion
metalloproteinases
other
enzymes,
creating
conditions
crossing
tissue
barriers
(5).
Some
molecules
are
involved
cells.
Adhesion
integrins,
cadherins,
etc.),
factors
cytokines
epidermal
factor,
platelet-derived
Wnt/βcatenin
pathway,
PI3K/Akt/mTOR
pathway
play
key
roles
(6,7).
Min
al.
recently
reviewed
impact
adhesion-associated
molecule
Desmoglein-2
(DSG2)
on
adhesion,
migration,
vasculogenic
mimicry.
More
importantly,
proposed
that
pro-tumorigenic
anti-tumorigenic
function
DSG2
context
dependent
2023;13:1327478.).Tumor
significant
challenge
treatment,
as
employ
various
render
drugs
ineffective
reduce
their
efficacy.
P-glycoprotein,
multidrug
resistance-associated
proteins
family,
breast
protein
examples
efflux
pumps
expel
chemotherapy
(8).
Gene
mutations
including
PIK3CA,
KRAS,
EGFR,
p53
OCT4
have
related
phenotype
(9).
undergo
metabolic
reprogramming
increasing
antioxidant
enhance
(10,11).
DNA
methylation,
histone
modification
noncoding
RNAs
regulation
alter
gene
expression
leading
escaping
drug-induced
death
(12).
repair
capabilities
resist
damage
induced
drugs.
Kaljunen
found
inactivation
Fanconi
anemia
reverse
prostate
during
DNA-damaging
line-specific
manner
2023;13:1260826.).
apoptotic
would
ability
lead
(13).
stem
small
population
within
possess
self-renewal
multi-lineage
differentiation
capabilities,
(14).
High
heterogeneity
makes
vary
sensitivity
with
some
potentially
harboring
genetic
phenotypic
features
(15).
Immune
checkpoint
inhibitors
PD-1/PD-L1
nivolumab,
pembrolizumab,
system
attack
tumors,
intensively
investigated
several
cancers
(17).
Immunotherapy
targeting
specific
antigens
(e.g.,
HPV
vaccines)
boosts
memory
prevent
(18).
Taking
into
consideration,
combining
multiple
approaches
(such
immunotherapy
chemotherapy)
become
strategy.
target
different
provide
comprehensive
against
strategy.Tumor
two
major
challenges
treatment.
Currently,
progress
made
research
targets
resistance.
In
future,
further
needed
discover
more
effective
develop
precise,
efficient,
low-toxicity
strategies
outcomes
rates
patients.
Combination
therapies,
such
therapies
radiotherapy,
may
be
direction
overcome
deserve
in-depth
exploration.
Additionally,
continuous
development
technologies
CRISPR
editing,
single-cell
sequencing),
we
expect
obtain
precise
strategies.
By
continuously
delving
open
up
avenues,
improving
Open Life Sciences,
Год журнала:
2025,
Номер
20(1)
Опубликована: Янв. 1, 2025
Abstract
The
aim
of
this
study
is
to
investigate
the
mechanism
action
and
correlation
between
transforming
growth
factor
beta
1
(TGF-β1)
β-catenin
in
pelvic
organ
prolapse
(POP).
compared
vaginal
wall
tissues
from
two
groups:
20
patients
with
POP
(POP
group)
who
had
hysterectomies
for
benign
conditions
(control
group).
Hematoxylin
Eosin
Masson
staining
visualized
collagen,
while
TUNEL
detected
apoptosis.
Protein
mRNA
expression
levels
TGF-β1,
β-catenin,
matrix
metallopeptidase
2
(MMP2),
tissue
inhibitor
metalloproteinases
(TIMP2),
type
I,
alpha
(COL1A1)
were
assessed
using
immunohistochemistry,
quantitative
real-time
polymerase
chain
reaction,
western
blot
techniques.
Relationships
protein
expressions
TGF-β1
COL1A1,
COL1A1
analyzed.
In
group,
collagen
fibers
sparse,
disorganized,
fragmented,
fewer
more
apoptotic
cells
control
group.
TIMP2,
significantly
lower,
MMP2
was
higher
(
p
<
0.05).
Positive
correlations
found
COL1A1.
Reduced
may
trigger
by
affecting
floor
metabolism.
Biomolecules,
Год журнала:
2025,
Номер
15(4), С. 457 - 457
Опубликована: Март 21, 2025
In
the
presence
of
cellular
mutations
and
impaired
mechanisms
energy
transmission
to
attached
cells
tissues,
excess
is
available
upregulate
some
mechanotransduction
pathways
that
maintain
cell
tissue
structure
function.
The
ability
transfer
applied
through
integrin-mediated
pathways,
ion
channels,
membrane,
cytoskeleton–nucleoskeleton
connections,
junctions,
cell–extracellular
matrix
attachments
provides
an
equilibrium
for
storage,
transmission,
dissipation
in
tissues.
Disruption
or
via
genetic
blocks
mechanical
communication
between
tissues
impairs
exists
This
results
local
structural
changes
altered
regulatory
which
produce
clustering,
collagen
encapsulation,
epithelial–mesenchymal
transition
(EMT),
leading
increased
motility
along
newly
reorganized
fibers
(fibrosis).
goal
this
review
postulate
how
extracellular
may
alter
pathways.
with
lead
ECM
reported
cancer,
postulated
modify
equilibria
their
ECM.
leads
uncontrolled
cancer
proliferation
remodeling.