Cell Communication and Signaling,
Год журнала:
2022,
Номер
20(1)
Опубликована: Март 19, 2022
Abstract
Background
Integrin
β4
(ITGB4)
participates
in
tumorigenesis
and
progression
of
several
malignancies,
but
its
role
related
mechanisms
clear
cell
renal
carcinoma
(ccRCC)
remain
unclear.
Methods
Quantitative
real-time
PCR
(qRT-PCR),
western
blot
immunohistochemistry
were
used
to
detect
mRNA
protein
levels
relevant
genes.
Biological
functions
ITGB4
methyltransferase-like
14
(METTL14)
determined
by
vitro
vivo
experiments.
The
N6-methyladenosine
(m6A)
ccRCC
tissues
adjacent
normal
calculated
via
total
RNA
m6A
quantification
assay.
modification
was
demonstrated
immunoprecipitation
(MeRIP),
RIP
luciferase
reporter
assays.
Results
significantly
overexpressed
high
level
predicted
poor
prognosis
as
well
metastasis.
Functionally,
stimulated
migration
invasion
metastasis
with
epithelial–mesenchymal
transition
(EMT)
strengthened.
Mechanically,
the
reduced
tissues.
METTL14,
a
favorable
factor
for
patients’
prognosis,
facilitated
on
3′UTR
subsequently
accelerated
degradation,
leading
declined
expression.
Furthermore,
METTL14-mediated
inhibition
expression
dependent
YTH
domain
family
2
(YTHDF2),
which
acted
an
reader
bind
promote
decay.
In
addition,
we
that
knockdown
METTL14
promoted
migration,
invasiveness
stimulating
EMT
process
PI3K/AKT
signal
overexpressing
ITGB4.
Conclusion
Our
study
reveals
inhibits
attenuate
cells,
suggesting
METTL14/ITGB4
axis
potential
prognostic
biomarker
therapeutic
target
ccRCC.
Signal Transduction and Targeted Therapy,
Год журнала:
2023,
Номер
8(1)
Опубликована: Май 11, 2023
Abstract
Angiogenesis,
the
formation
of
new
blood
vessels,
is
a
complex
and
dynamic
process
regulated
by
various
pro-
anti-angiogenic
molecules,
which
plays
crucial
role
in
tumor
growth,
invasion,
metastasis.
With
advances
molecular
cellular
biology,
biomolecules
such
as
growth
factors,
chemokines,
adhesion
factors
involved
angiogenesis
has
gradually
been
elucidated.
Targeted
therapeutic
research
based
on
these
molecules
driven
treatment
to
become
promising
strategy
anti-tumor
therapy.
The
most
widely
used
agents
include
monoclonal
antibodies
tyrosine
kinase
inhibitors
(TKIs)
targeting
vascular
endothelial
factor
(VEGF)
pathway.
However,
clinical
benefit
this
modality
still
limited
due
several
defects
adverse
events,
acquired
drug
resistance,
recurrence,
lack
validated
biomarkers,
impel
further
mechanisms
angiogenesis,
development
multiple
drugs
combination
therapy
figure
out
how
improve
efficacy.
Here,
we
broadly
summarize
signaling
pathways
discuss
current
challenges
We
also
propose
approaches
efficacy
provide
perspective
for
Journal of Hematology & Oncology,
Год журнала:
2022,
Номер
15(1)
Опубликована: Сен. 8, 2022
Abstract
Epithelial–mesenchymal
transition
(EMT)
is
an
essential
process
in
normal
embryonic
development
and
tissue
regeneration.
However,
aberrant
reactivation
of
EMT
associated
with
malignant
properties
tumor
cells
during
cancer
progression
metastasis,
including
promoted
migration
invasiveness,
increased
stemness,
enhanced
resistance
to
chemotherapy
immunotherapy.
tightly
regulated
by
a
complex
network
which
orchestrated
several
intrinsic
extrinsic
factors,
multiple
transcription
post-translational
control,
epigenetic
modifications,
noncoding
RNA-mediated
regulation.
In
this
review,
we
described
the
molecular
mechanisms,
signaling
pathways,
stages
tumorigenesis
involved
discussed
dynamic
non-binary
its
role
metastasis.
Finally,
summarized
challenges
immunotherapy
proposed
strategies
for
therapy
targeting
EMT.
Signal Transduction and Targeted Therapy,
Год журнала:
2023,
Номер
8(1)
Опубликована: Янв. 16, 2023
Abstract
Clustered
regularly
interspaced
short
palindromic
repeats
(CRISPR)/CRISPR-associated
protein
9
(Cas9)
gene-editing
technology
is
the
ideal
tool
of
future
for
treating
diseases
by
permanently
correcting
deleterious
base
mutations
or
disrupting
disease-causing
genes
with
great
precision
and
efficiency.
A
variety
efficient
Cas9
variants
derivatives
have
been
developed
to
cope
complex
genomic
changes
that
occur
during
diseases.
However,
strategies
effectively
deliver
CRISPR
system
diseased
cells
in
vivo
are
currently
lacking,
nonviral
vectors
target
recognition
functions
may
be
focus
research.
Pathological
physiological
resulting
from
disease
onset
expected
serve
as
identifying
factors
targeted
delivery
targets
gene
editing.
Diseases
both
varied
complex,
choice
appropriate
methods
different
important.
Meanwhile,
there
still
many
potential
challenges
identified
when
targeting
CRISPR/Cas9
treatment.
This
paper
reviews
current
developments
three
aspects,
namely,
type,
vector,
characteristics.
Additionally,
this
summarizes
successful
examples
clinical
trials
finally
describes
possible
problems
associated
applications.
Signal Transduction and Targeted Therapy,
Год журнала:
2023,
Номер
8(1)
Опубликована: Июль 31, 2023
Abstract
Cellular
mechanotransduction,
a
critical
regulator
of
numerous
biological
processes,
is
the
conversion
from
mechanical
signals
to
biochemical
regarding
cell
activities
and
metabolism.
Typical
cues
in
organisms
include
hydrostatic
pressure,
fluid
shear
stress,
tensile
force,
extracellular
matrix
stiffness
or
tissue
elasticity,
viscosity.
Mechanotransduction
has
been
expected
trigger
multiple
such
as
embryonic
development,
repair
regeneration.
However,
prolonged
excessive
stimulation
can
result
pathological
multi-organ
fibrosis,
tumorigenesis,
cancer
immunotherapy
resistance.
Although
associations
between
normal
homeostasis
diseases
have
identified,
regulatory
mechanisms
among
different
are
not
yet
comprehensively
illustrated,
no
effective
therapies
currently
available
targeting
cue-related
signaling.
This
review
systematically
summarizes
characteristics
typical
conditions
with
updated
evidence.
The
key
effectors
responding
stimulations
listed,
Piezo
channels,
integrins,
Yes-associated
protein
(YAP)
/transcriptional
coactivator
PDZ-binding
motif
(TAZ),
transient
receptor
potential
vanilloid
4
(TRPV4).
We
also
reviewed
signaling
pathways,
therapeutic
targets
cutting-edge
clinical
applications
related
cues.
Frontiers in Cell and Developmental Biology,
Год журнала:
2022,
Номер
10
Опубликована: Март 9, 2022
Integrins
mediate
adhesive
interactions
between
cells
and
their
environment,
including
neighboring
extracellular
matrix
(ECM).
These
heterodimeric
transmembrane
receptors
bind
ligands
with
globular
head
domains
connect
to
the
cytoskeleton
through
multi-protein
at
cytoplasmic
tails.
Integrin
containing
cell–matrix
adhesions
are
dynamic
force-responsive
protein
complexes
that
allow
bidirectional
mechanical
coupling
of
environment.
This
allows
sense
modulate
tissue
mechanics
regulates
intracellular
signaling
impacting
on
cell
faith,
survival,
proliferation,
differentiation
programs.
Dysregulation
these
functions
has
been
extensively
reported
in
cancer
associated
tumor
growth,
invasion,
angiogenesis,
metastasis,
therapy
resistance.
central
role
multiple
hallmarks
localization
surface
makes
integrins
attractive
targets
for
therapy.
However,
despite
a
wealth
highly
encouraging
preclinical
data,
targeting
integrin
adhesion
clinical
trials
thus
far
failed
meet
expectations.
Contributing
factors
therapeutic
failure
1)
variable
expression,
2)
redundancy
function,
3)
distinct
roles
various
disease
stages,
4)
sequestering
therapeutics
by
integrin-containing
tumor-derived
vesicles.
Despite
disappointing
results,
new
promising
approaches
being
investigated
highlight
potential
as
or
prognostic
biomarkers.
Improvement
delivery
site
via
binding
is
emerging
another
successful
approach
may
enhance
both
efficacy
safety
conventional
therapeutics.
In
this
review
we
provide
an
overview
recent
findings,
discuss
apparent
disagreement
consider
opportunities
exploit
Pharmacological Research,
Год журнала:
2023,
Номер
191, С. 106777 - 106777
Опубликована: Апрель 19, 2023
Oxidative
stress
(OS)
is
a
chemical
imbalance
between
an
oxidant
and
antioxidant,
causing
damage
to
redox
signaling
control
or
molecular
damage.
Unbalanced
oxidative
metabolism
can
produce
excessive
reactive
oxygen
species
(ROS).
These
excess
ROS
cause
drastic
changes
in
platelet
further
affect
function.
It
will
also
lead
increase
procoagulant
phenotype
cell
apoptosis,
which
the
risk
of
thrombosis.
The
creation
subsequent
activation,
adhesion,
recruitment
are
then
encouraged
auto-amplifying
loop
by
produced
from
platelets.
Meanwhile,
cancer
cells
higher
concentration
due
their
fast
high
proliferation
rate.
However,
result
modification
cellular
macromolecules.
formation
its
progression
strongly
associated
with
resulting
In
addition,
platelets
important
part
tumor
microenvironment,
there
significant
cross-communication
cells.
Cancer
alter
activation
status
platelets,
RNA
spectrum,
proteome,
other
properties.
"cloaking"
providing
physical
protection,avoiding
destruction
shear
attack
immune
cells,
promoting
invasion.We
explored
vicious
circle
interaction
ROS,
this
review,
we
believe
that
play
stimulative
role
growth
metastasis
through
Journal of Experimental & Clinical Cancer Research,
Год журнала:
2025,
Номер
44(1)
Опубликована: Янв. 30, 2025
Abstract
Background
Colorectal
cancer
(CRC)
has
high
incidence
and
mortality
rates,
with
severe
prognoses
during
invasion
metastasis
stages.
Despite
advancements
in
diagnostic
therapeutic
technologies,
the
impact
of
tumour
microenvironment,
particularly
extracellular
matrix
(ECM)
stiffness,
on
CRC
progression
is
not
fully
understood.
Methods
This
study
included
107
patients.
Tumour
stiffness
was
assessed
using
magnetic
resonance
elastography
(MRE),
collagen
ratio
analysed
Masson
staining.
cell
lines
were
cultured
matrices
varying
followed
by
transcriptome
sequencing
to
identify
stiffness-related
genes.
An
HSF4
knockout
model
different
ECM
evaluate
effects
proliferation,
migration,
vitro
vivo.
Results
significantly
higher
than
normal
tissue
positively
correlated
content
TNM
staging.
High-stiffness
regulated
functions
signalling
pathways.
High
(heat
shock
transcriptional
factor
4)
expression
strongly
associated
poor
prognosis.
increased
stages,
its
inhibited
invasion,
especially
high-stiffness
matrices.
In
vivo
experiments
confirmed
that
promoted
growth
metastasis,
independent
protein
increase.
Conclusions
reveals
promotes
proliferation
regulating
EMT-related
pathways
through
HSF4.
could
be
valuable
targets
for
prognostic
assessment
intervention
CRC.
Nature Communications,
Год журнала:
2025,
Номер
16(1)
Опубликована: Фев. 6, 2025
The
lysosome-targeting
chimera
(LYTAC)
strategy
provided
a
very
powerful
tool
for
the
degradation
of
membrane
proteins.
However,
synthesis
LYTACs,
antibody-small
molecule
conjugates,
is
challenging.
ability
antibody-based
LYTACs
to
penetrate
solid
tumor
limited
as
well,
especially
cross
blood-brain
barrier
(BBB).
Here,
we
propose
covalent
chimeric
peptide-based
targeted
platform
(Pep-TACs)
by
introducing
long
flexible
aryl
sulfonyl
fluoride
group,
which
allows
proximity-enabled
cross-linking
upon
binding
with
protein
interest.
Pep-TACs
facilitates
target
proteins
through
mechanism
recycling
transferrin
receptor
(TFRC)-mediated
lysosomal
endocytosis.
Biological
experiments
demonstrate
that
can
significantly
degrade
expression
PD-L1
on
cells,
dendritic
cells
and
macrophages,
under
acidic
conditions,
markedly
enhance
function
T
phagocytosis
macrophages.
Furthermore,
both
in
anti-PD-1-responsive
-resistant
models,
exert
significant
anti-tumor
immune
response.
It
noteworthy
BBB
prolong
survival
mice
situ
brain
tumor.
As
proof-of-concept,
this
study
introduces
modular
TFRC-based
peptide
protein,
immunotherapy
tumors.
LYTAC
strategies
often
face
challenges
penetration
synthesis.
authors
introduce
Pep-TACs,
effectively
degrades
PD-L1.
This
approach
suppresses
growth,
particularly
Frontiers in Oncology,
Год журнала:
2025,
Номер
15
Опубликована: Янв. 30, 2025
Homoharringtonine
is
a
natural
alkaloid
with
significant
pharmacological
potential
that
has
demonstrated
promising
efficacy
in
the
treatment
of
hematological
malignancies
recent
years.
This
article
systematically
reviews
mechanisms
Homoharringtonine,
focusing
on
its
key
roles
inducing
apoptosis,
inhibiting
cell
cycle
progression,
and
reducing
migration
invasion.
Additionally,
HHT
exhibits
multiple
biological
activities,
including
immunomodulation,
antiviral
effects,
anti-fibrotic
properties,
studies
also
revealing
neuroprotective
functions.
In
clinical
trials,
malignancies,
particularly
various
types
such
as
acute
myeloid
leukemia
chronic
leukemia.
Despite
antitumor
effects
observed
applications,
low
bioavailability
side
remain
major
challenges
limit
widespread
use.
details
latest
research
advancements
aimed
at
enhancing
drug
delivery
systems
nanoparticles
liposomes,
well
chemical
modification
strategies.
These
approaches
not
only
improve
HHT’s
vivo
but
enhance
targeting
ability
while
toxicity
to
normal
cells.
Furthermore,
combination
other
drugs
presents
broader
prospects
for
treatment.
By
exploring
diverse
activities
depth,
this
aims
provide
foundation
developing
novel
therapeutic
based
products,
thereby
advancing
application
cancer
fields.