Cancer Control,
Journal Year:
2024,
Volume and Issue:
31
Published: Jan. 1, 2024
This
study
aimed
to
investigate
the
role
of
discoidin
domain
receptor
tyrosine
kinase
1
(DDR1)
in
liver
hepatocellular
carcinoma
(LIHC)
and
evaluate
its
prognostic
value
on
patient
response
combination
therapy.
Communications Biology,
Journal Year:
2024,
Volume and Issue:
7(1)
Published: Jan. 19, 2024
Abstract
Hepatic
stellate
cell
(HSC)
activation
is
considered
as
a
central
driver
of
liver
fibrosis
and
effective
suppression
HSC
contributes
to
the
treatment
fibrosis.
Circular
RNAs
(circRNAs)
have
been
reported
be
important
in
tumor
progression.
However,
contributions
circRNAs
remain
largely
unclear.
The
fibrosis-specific
circRNA
was
explored
by
microarray
cVIM
(a
derived
from
exons
4
8
vimentin
gene
mmu_circ_32994)
selected
research
object.
Further
studies
revealed
that
cVIM,
mainly
expressed
cytoplasm,
may
act
sponge
for
miR-122-5p
miR-9-5p
enhance
expression
type
I
TGF-β
receptor
(TGFBR1)
TGFBR2
promotes
TGF-β/Smad
pathway,
thereby
accelerating
progression
Our
results
demonstrate
vital
role
promoting
provide
fresh
perspective
on
International Journal of Genomics,
Journal Year:
2025,
Volume and Issue:
2025(1)
Published: Jan. 1, 2025
Background:Helicobacter
pylori
(HP)
is
associated
with
the
development
of
various
stomach
diseases,
one
major
risk
factors
for
adenocarcinoma
(STAD).
Methods:
The
HP
infection
score
between
tumor
and
normal
groups
was
compared
by
single-sample
gene
set
enrichment
analysis
(ssGSEA).
key
modules
related
to
were
identified
weighted
coexpression
network
(WGCNA),
functional
conducted
on
these
module
genes.
Further,
limma
package
used
screen
differentially
expressed
genes
(DEGs)
HP-positive
HP-negative
STAD.
prognostic
obtained
construct
riskscore
model,
performance
model
validated.
correlation
immune
microenvironment
(TIME)
analyzed
Spearman's
method.
single-cell
atlas
STAD
delineated.
mRNA
expression
levels
verified
using
cells,
migration
invasion
capacities
cells
evaluated
wound
healing
assay
transwell
assay.
Results:
in
group
significantly
higher
than
that
group.
purple
royal
blue
showed
STAD,
enriched
immune-related
pathway.
five
(CTLA4,
CPVL,
EMB,
CXCR4,
FAM241A)
screened
from
infection-related
DEGs,
which
utilized
establishing
good
robustness.
Riskscore
exhibited
strong
TIME
Single-cell
revealed
CXCR4
highly
Epithelial
Cell
1,
2,
parietal
CTLA4,
FAM241A,
high
silencing
CPVL
could
suppress
cells.
Conclusion:
This
study
established
a
based
genes,
provide
reference
prediction
treatment
targets
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: April 13, 2025
Transcatheter
arterial
chemoembolization
(TACE)
is
a
standard
treatment
for
unresectable,
intermediate,
or
advanced-stage
hepatocellular
carcinoma
(HCC),
especially
in
elderly
patients.
The
modified
5-item
frailty
index
(mFI-5)
concise,
comorbidity-based
risk
stratification
tool
proven
to
effectively
predict
adverse
outcomes.
However,
the
prognostic
capacity
of
mFI-5
HCC
patients
after
TACE
unclear.
As
such,
we
retrospectively
analyzed
clinical
data
from
(age
≥
65
years)
who
received
their
first
between
November
2018
and
2020
at
Department
Interventional
Radiology,
Affiliated
Hospital
Xuzhou
Medical
University.
was
calculated
based
on
presence
five
co-morbidities:
congestive
heart
failure
within
30
days
prior
surgery;
insulin-dependent
noninsulin-dependent
diabetes
mellitus;
chronic
obstructive
pulmonary
disease
(COPD)
pneumonia;
partially
dependent
totally
functional
health
status
time
hypertension
requiring
medication.
Patients
were
divided
into
two
groups
scores:
2
('frail')
<
('non-frail').
primary
outcomes
overall
survival
(OS)
progression-free
(PFS).Among
143
patients,
97
group
46
group.
median
OS
40.0
months
(95%
confidence
interval
[CI]:
35.0-47.0)
non-frail
vs.
24.0
CI:
22-NA)
frail
(hazard
ratio
[HR]
=
3.343,
95%
1.802-6.201,
p
.001).
PFS
7.0
4.0-11.0)
3.0
2.0-9.0)
(HR
1.507,
0.996-2.280,
.053).
Cox
regression
identified
mFI-5,
alpha-fetoprotein
(AFP)
as
independent
predictors
OS.
useful
predictor
long-term
treated
with
TACE,
suggesting
that
incorporating
assessments
can
optimize
strategies
improve
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(13), P. e33682 - e33682
Published: June 26, 2024
AimsThis
study
explored
the
molecular
and
biologic
mechanisms
underlying
association
between
circadian
rhythm
disorders
(CRD)
increased
risk
for
hepatocellular
carcinoma
(HCC).BackgroundCRD
are
linked
to
HCC,
but
this
limited.ObjectiveThe
constructed
validated
a
CRD
related
gene
model
as
an
independent
prognostic
factor
providing
insight
into
linking
HCC
identifying
potential
indicators
efficacy
of
immunotherapy
anticancer
drugs.
This
helps
provide
important
clues
personalized
treatment
strategies
patients.MethodsGene
sets
correlated
with
were
obtained
from
Molecular
Signatures
Database
(MSigDB)
intersect
differentially
expressed
genes
(DEGs)
tumor
samples
control
in
The
Cancer
Genome
Atlas
(TCGA)
HCCDB18
Hepatocellular
Carcinoma
Cell
DataBase
(HCCDB).
was
developed
by
univariate
Cox
stepwise
multivariate
analysis.
Immune
checkpoint
blockade
(ICB)
therapy
drugs
analyzed
using
immune
dysfunction
exclusion
(TIDE)
pRRophetic,
respectively.
Seurat
determined
cell
type
analyzing
single-cell
data,
malignant
cells
identified
Copykat.
To
detect
mRNA
levels
model,
quantitative
real-time
polymerase
chain
reaction
(qRT-PCR)
carried
out.ResultsThe
activity
tissue
significantly
lower
than
that
tissue.
Subsequently,
EZH2,
IMPDH2,
TYMS
SERPINE1
selected
construct
which
prognosis.
Notably,
low-risk
patients
had
infiltration
TIDE
scores
compared
high-risk
indicating
low
may
derive
more
benefit
immunotherapy.
higher
benign
epithelial
cells.ConclusionsThis
presents
reveal
perspective
dependent
mechanism
cancer,
provides
indicator
understanding
preclinical
ICB
Frontiers in Oncology,
Journal Year:
2024,
Volume and Issue:
14
Published: July 5, 2024
Background
This
study
aimed
to
assess
the
effectiveness
and
safety
of
vascular
intervention
combined
with
lenvatinib
versus
alone
in
treatment
advanced
hepatocellular
carcinoma
(HCC)
portal
vein
tumor
thrombus
(PVTT),
identify
prognostic
factors
associated
outcomes.
Methods
We
conducted
a
retrospective
analysis
data
from
92
patients
HCC
PVTT
who
were
treated
between
February
2016
2023.
Among
them,
56
underwent
(transarterial
chemoembolization,
TACE),
while
36
received
(TACE
or
hepatic
arterial
infusion
chemotherapy
[HAIC])
lenvatinib.
The
primary
outcomes
included
progression-free
survival
(PFS),
overall
(OS),
objective
response
rate
(ORR).
Survival
rates
estimated
by
Kaplan-Meier
method,
confounders
adjusted
using
inverse
probability
weighting
(IPTW).
Prognostic
determined
through
Cox
regression
model.
Results
median
follow-up
duration
was
20.07
months
(interquartile
range:
6.41–25.36).
combination
therapy
group
had
significantly
longer
PFS
(11.00
vs.
5.00
months,
P<0.05)
OS
(12.91
6.83
comparison
monotherapy
group,
these
findings
remained
consistent
after
IPTW
matching.
Moreover,
showed
higher
ORR
(55.56%
26.79%,
based
on
mRECIST
criteria.
multivariate
identified
extrahepatic
metastasis
maximum
diameter
as
risk
for
PFS,
age,
number,
influenced
OS.
Combined
emerged
protective
factor
In
hypertension
most
frequent
adverse
event,
grade
3
4
events
occurring
rarely.
Conclusion
has
demonstrated
improved
PVTT,
its
profile
appears
be
acceptable.
Adoption
this
strategy
at
an
earlier
stage
may
enhance
patient
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(14), P. e34438 - e34438
Published: July 1, 2024
AimsTo
analyze
the
expression
of
mitochondrial
translational
initiation
factor
2
(MTIF2)
and
biological
functions
gene
in
hepatocellular
carcinoma
(HCC).BackgroundThe
treatment
HCC
its
prognostic
prediction
are
limited
by
a
lack
comprehensive
understanding
molecular
mechanisms
HCC.
OBJECTIVE:
To
determine
cells
expressing
MTIF2
function
MTIF2+
cell
subpopulation.MethodsGene
analysis
on
TIMER
2.0,
UALCAN,
GEPIA
databases
was
performed
to
measure
tissues.
Cell
clustering
subgroups
annotation
were
conducted
based
single-cell
sequencing
data
paracancerous
tissues
Gene
Expression
Omnibus
(GEO)
database.
different
types
analyzed.
Further,
pathways
potentially
regulated
each
type
identified.
In
addition,
protein-protein
interaction
(PPI)
networks
with
genes
developed.
The
assay
verify
effects
superoxide
dismutase-2
(SOD2)
cells.
Finally,
we
screened
virtual
drugs
targeting
SOD2
employing
database
screening,
docking
dynamics.ResultsMTIF2
showed
remarkably
high
We
identified
total
10
between
upregulated
epithelial
cells,
macrophages,
hepatocytes.
More
importantly,
high-expressed
mainly
derived
from
hepatocytes,
which
reactive
oxygen
species
(ROS)
pathway
significantly
positively
correlated
MTIF2.
PPI
network,
there
unique
pair
ROS
pathway.
experiments
that
overexpression
enhanced
proliferative
invasive
capacities
HCC,
could
synergize
co-promote
development
dynamics
simulations
DB00183
maintained
structural
stability
proteins
during
simulation
process.ConclusionOur
study
confirmed
might
act
regulate
pathway,
thereby
affective
progression
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(14), P. e34704 - e34704
Published: July 1, 2024
The
prognosis
and
therapeutic
response
of
patients
with
liver
hepatocellular
carcinoma
(LIHC)
can
be
predicted
based
on
programmed
cell
death
(PCD)
as
PCD
plays
a
crucial
role
during
tumor
progression.
We
developed
PCD-related
gene
signature
to
evaluate
the
for
LIHC.
Aging,
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 4, 2024
Background:
Complex
cellular
signaling
network
in
the
tumor
microenvironment
(TME)
could
serve
as
an
indicator
for
prognostic
classification
of
hepatocellular
carcinoma
(HCC)
patients.
Methods:
Univariate
Cox
regression
analysis
was
performed
to
screen
prognosis-related
TME-related
genes
(TRGs),
based
on
which
HCC
samples
were
clustered
by
running
non-negative
matrix
factorization
(NMF)
algorithm.
Furthermore,
correlation
between
different
molecular
subtypes
and
immune
cell
infiltration
level
analyzed.
Finally,
a
risk
score
(RS)
model
established
LASSO
analyses
(CRA)
using
these
TRGs.
Functional
enrichment
gene
set
(GSEA).
Results:
patients
divided
into
three
(C1,
C2,
C3)
704
subtype
C1
had
significantly
better
OS
than
C2
C3.
We
selected
13
TRGs
construct
RS
model.
multivariate
CRA
showed
that
independently
predict
patients'
prognosis.
A
nomogram
integrating
clinicopathologic
features
further
created.
also
validated
reliability
according
area
under
receiver
operating
characteristic
(ROC)
curve
value,
concordance
index
(C-index),
decision
analysis.
The
current
findings
demonstrated
correlated
with
CD8+
T
cells,
monocytic
lineage,
myeloid
dendritic
cells.
Conclusion:
This
study
provided
help
classify
their
prognoses,
contributing
personalized
treatments
HCC.
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(10), P. e30439 - e30439
Published: May 1, 2024
Hepatocellular
carcinoma
(HCC)
is
the
main
type
of
primary
liver
cancer.
This
study
aimed
to
developed
a
basement
membrane
(BM)
related
lncRNAs
risk
signature
evaluate
prognosis
HCC
patients.
We
screened
differentially
expressed
BM-related
(DE-BMRlncRNAs)
for
evaluation,
and
identified
six
DE-BMRlncRNAs
(AC072054.1,
NUP50-DT,
AC026412.3,
AC109322.2,
POLH-AS1
LINC00595)
prognostic
signature.
patients
were
divided
high
or
low
according
median
score.
Our
model
predicted
that
with
higher
score
had
worse
prognosis.
also
created
nomogram
assist
clinical
decision-making
clinicopathological
features.
Meanwhile,
we
confirmed
expression
in
tissue
cells.
knockdown
inhibited
migration
invasion
In
conclusion,
established
predictive
based
on
BMRlncRNAs
predict
HCC.
findings
offer
rationale
further
explore
biomarkers