EIF4E-mediated biogenesis of circPHF14 promotes the growth and metastasis of pancreatic ductal adenocarcinoma via Wnt/β-catenin pathway
Fang Zhou,
No information about this author
Zhuo Wu,
No information about this author
Chao Yu
No information about this author
et al.
Molecular Cancer,
Journal Year:
2025,
Volume and Issue:
24(1)
Published: Feb. 26, 2025
CircRNAs
are
critically
involved
in
the
development
and
progression
of
various
cancers.
However,
their
functions
mechanisms
pancreatic
ductal
adenocarcinoma
(PDAC)
remain
largely
unknown.
CircPHF14
(hsa_circ_0079440)
was
identified
through
analysis
RNA
sequencing
data
from
PDAC
normal
adjacent
tissues.
The
biological
circPHF14
were
then
evaluated
using
CCK8,
EdU,
transwell,
colony
formation,
wound
healing
assays,
as
well
orthotopic
xenograft
liver
metastasis
models.
interaction
between
PABPC1,
which
enhance
stability
WNT7A
mRNA,
investigated
pull-down,
mass
spectrometry,
Immunoprecipitation
(RIP),
actinomycin
D
assays.
role
EIF4E
promoting
biogenesis
examined
RIP,
western
blotting.
In
this
study,
we
observed
a
significant
upregulation
both
clinical
samples
cell
lines.
Functionally,
enhanced
proliferation
vitro
vivo.
Mechanistically,
interacted
with
PABPC1
to
stabilize
thereby
activating
Wnt/β-catenin
pathway,
subsequently
upregulated
SNAI2
initiated
Epithelial-Mesenchymal
Transition
(EMT)
PDAC.
Additionally,
found
bind
PHF14
pre-mRNA,
facilitating
biogenesis.
Finally,
developed
lipid
nanoparticle
(LNP)
formulation
encapsulating
sh-circPHF14
plasmids
confirmed
its
anti-tumor
efficacy
patient-derived
(PDX)
model.
EIF4E-mediated
stabilizes
mRNA
via
activates
growth
These
findings
indicate
that
holds
promise
biomarker
therapeutic
target
for
Language: Английский
Mulberrin suppresses gastric cancer progression and enhances chemosensitivity to oxaliplatin through HSP90AA1/PI3K/AKT axis
Yongsen Li,
No information about this author
Mengyao Dong,
No information about this author
Hong Qin
No information about this author
et al.
Phytomedicine,
Journal Year:
2025,
Volume and Issue:
unknown, P. 156441 - 156441
Published: Jan. 1, 2025
Language: Английский
Cuproptosis-related gene ACAD8 inhibits the metastatic ability of colorectal cancer by inducing cuproptosis
HuiE Zhuang,
No information about this author
Yizhen Chen,
No information about this author
Sifu Huang
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 3, 2025
Background
Distant
metastasis
of
colorectal
cancer
(CRC)
significantly
impacts
patient
prognosis.
Cuproptosis
is
a
new
form
copper
ion-dependent
cell
death.
However,
whether
cuproptosis-related
genes
(CRGs)
play
role
in
the
metastatic
potential
CRC
remains
unclear.
This
study
focuses
on
CRGs-ACAD8
to
explore
its
and
mechanism
(mCRC).
Methods
Clinical
sample
data
from
TCGA,
GEO,
Fujian
Provincial
Hospital
patients
were
integrated
analyze
ACAD8
expression
association
with
diagnosis
prognosis
CRC.
Small
interfering
RNA,
immunohistochemistry,
colony
formation,
wound-healing
assays
so
used
evaluate
biological
functions
ACAD8.
Bioinformatics
was
applied
investigate
relationships
immune
infiltration,
chemotherapy
sensitivity,
signaling
pathways.
Results
reduced
mCRC
demonstrated
excellent
diagnostic
performance.
Patients
high
had
better
survival.
closely
associated
enhanced
sensitivity.
Pathway
enrichment
analysis
suggested
that
might
inhibit
by
regulating
pathways
such
as
response
metal
ions
tight
junction
organization.
Finally,
experiments
confirmed
positive
correlation
between
levels
mRNA
expression,
CuCl
2
upregulating
expression.
Knockdown
induced
cuproptosis.
inhibited
proliferation,
stemness,
migratory
abilities
cells,
while
si
attenuated
these
effects.
Moreover,
sensitivity
cells
oxaliplatin
5-fluorouracil,
whereas
diminished
this
chemosensitizing
effect.
Conclusion
As
novel
tumor
suppressor,
low
holds
prognostic
value
may
contribute
precise
treatment
infiltration
Language: Английский
High expression of HECW1 is associated with the poor prognosis and cancer progression of gastric cancer
Zhihui Yang,
No information about this author
Peng Zhou,
No information about this author
Liping Wang
No information about this author
et al.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 3, 2025
Abstract
Background
The
E3
ubiquitin
ligase
HECW1
was
found
to
be
involved
in
ubiquitination
modifications
during
malignant
progression
of
multiple
tumors.
However,
the
prognostic
role
expression
gastric
cancer
(GC)
remains
unclear.
Methods
Tumor
Immunoassay
Resource
(TIMER2.0)
system
evaluated
association
with
tumor-infiltrating
lymphocytes
carcinomas.
UALCAN
assessed
mRNA
levels
GC
tissues
and
examined
their
associations
clinicopathological
characteristics.
Kaplan
Meier-plotter
analyzed
effect
on
survival
patients.
cBioPortal
retrieved
information
about
genetic
variants
gene.
Protein‒protein
interaction
(PPI)
networks
associated
were
explored
using
STRING
database.
functional
effects
cells
through
proliferation
(Cell
Counting
Kit-8),
apoptosis
(Flow
cytometry),
migration
(Transwell
wound
healing
assays).
RNA-Seq
applied
explore
underlying
mechanisms.
Results
demonstrated
significant
overexpression
tumor
tissues,
correlating
adverse
clinical
outcomes.
Clinically,
elevated
exhibited
an
inverse
CD8
+
T
while
demonstrating
a
positive
correlation
macrophages,
DCs,
neutrophils
infiltration,
suggesting
its
potential
involvement
immune
evasion
Functional
validation
revealed
that
knockdown
markedly
suppressed
cell
migratory
capacity,
concurrently
promoting
apoptotic
death.
Mechanistic
investigations
identified
exerts
oncogenic
dysregulation
Hippo
signaling
pathway,
silencing
effectively
attenuating
via
pathway
modulation.
Conclusions
upregulation
is
significantly
poor
prognosis
infiltration
patients,
emphasizing
as
biomarker.
Language: Английский
Nanomaterials in the diagnosis and treatment of gastrointestinal tumors: New clinical choices and treatment strategies
Liping Chen,
No information about this author
Qingqing Li
No information about this author
Materials Today Bio,
Journal Year:
2025,
Volume and Issue:
unknown, P. 101782 - 101782
Published: April 1, 2025
Language: Английский
Research progress on m6A and drug resistance in gastrointestinal tumors
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 28, 2025
Gastrointestinal
(GI)
tumors
represent
a
significant
global
health
burden
and
are
among
the
leading
causes
of
cancer-related
mortality
worldwide.
their
drug
resistance
is
one
major
challenges
in
cancer
therapy.
In
recent
years,
epigenetic
modifications,
especially
N6-methyladenosine
(m6A)
RNA
have
become
hot
research
topic.
m6A
modification
plays
an
important
role
gene
expression
progression
by
regulating
splicing,
translation,
stability,
degradation,
which
regulated
“writers,”
“erasers”
“readers.”
GI
tumors,
to
chemotherapy,
targeted
therapy,
immunotherapy
closely
associated
with
modification.
Therefore,
molecular
mechanism
its
development
provide
new
therapeutic
strategies
for
overcoming
efficacy
tumors.
this
review,
biological
functions
were
explored,
specific
mechanisms
different
types
ideas
targets
future
treatment
identified,
limitations
field
highlighted.
Language: Английский
TRIM47 drives gastric cancer cell proliferation and invasion by regulating CYLD protein stability
Biology Direct,
Journal Year:
2024,
Volume and Issue:
19(1)
Published: Nov. 8, 2024
The
expression
of
TRIM47,
a
member
the
TRIM
protein
and
E3
ubiquitin
ligase
families,
is
elevated
in
various
cancers,
such
as
non-small
cell
lung
cancer
colorectal
cancer,
linked
to
poor
prognosis.
This
study
aimed
investigate
role
TRIM47
gastric
development.
Using
Cancer
Genome
Atlas-Stomach
Adenocarcinoma
(TCGA-STAD)
dataset
analysis
20
patient
samples
from
our
center,
was
found
be
significantly
up-regulated
tissues
associated
with
advanced
N-stage
We
constructed
stable
knockdown
overexpressing
lines.
CCK8,
EDU,
colony
formation,
wound
healing,
Transwell
tests
were
used
evaluate
effects
on
proliferation,
invasion,
migration.
results
showed
that
inhibited
migration
invasion
cells,
while
overexpression
promoted
these
behaviors.
These
further
confirmed
vivo.
In
mechanism
part,
we
interacts
CYLD
protein.
Moreover,
promotes
K48-linked
ubiquitination,
leading
degradation
by
proteasome,
thereby
activating
NF-κB
pathway
regulating
biological
behavior
cells.
Taken
together,
demonstrated
involved
proliferation
metastasis
through
CYLD/NF-κB
pathway.
Language: Английский