Pharmacological Research,
Journal Year:
2023,
Volume and Issue:
189, P. 106674 - 106674
Published: Jan. 23, 2023
Liver
cancer
is
one
of
the
most
common
malignancies,
with
severe
morbidity
and
mortality.
While
considerable
progress
has
been
made
in
liver
treatment,
5-year
overall
survival
(OS)
patients
not
improved
significantly.
Reasons
include
inadequate
capability
early
screening
diagnosis,
a
high
incidence
recurrence
metastasis,
degree
tumor
heterogeneity,
an
immunosuppressive
microenvironment.
Therefore,
identification
validation
specific
robust
biomarkers
are
major
importance
for
screening,
timely
accurate
prognosis,
prevention
progression.
In
this
review,
we
highlight
some
latest
research
potential
applications
biomarkers,
describing
hotspots
prospective
directions
biomarker
discovery.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: Sept. 26, 2023
Toll-like
receptors
(TLRs)
serve
as
the
body’s
first
line
of
defense,
recognizing
both
pathogen-expressed
molecules
and
host-derived
released
from
damaged
or
dying
cells.
The
wide
distribution
different
cell
types,
ranging
epithelial
to
immune
cells,
highlights
crucial
roles
TLRs
in
linking
innate
adaptive
immunity.
Upon
stimulation,
binding
mediates
expression
several
adapter
proteins
downstream
kinases,
that
lead
induction
other
signaling
such
key
pro-inflammatory
mediators.
Indeed,
extraordinary
progress
immunobiological
research
has
suggested
could
represent
promising
targets
for
therapeutic
intervention
inflammation-associated
diseases,
autoimmune
microbial
infections
well
human
cancers.
So
far,
prevention
possible
treatment
inflammatory
various
TLR
antagonists/inhibitors
have
shown
be
efficacious
at
stages
pre-clinical
evaluation
clinical
trials.
Therefore,
fascinating
role
modulating
responses
levels
directed
scientists
opt
these
sensor
suitable
developing
chemotherapeutics
immunotherapeutics
against
cancer.
Hitherto,
TLR-targeting
small
(e.g.,
Pam3CSK4,
Poly
(I:C),
(A:U)),
chemical
compounds,
phytocompounds
Curcumin),
peptides,
antibodies
been
found
confer
protection
types
However,
administration
inappropriate
doses
TLR-modulating
therapeutics
a
wrong
infusion
is
reported
induce
detrimental
outcomes.
This
review
summarizes
current
findings
on
molecular
structural
biology
gives
an
overview
potency
promises
TLR-directed
strategies
cancers
by
discussing
established
pipeline
discoveries.
Cancer Gene Therapy,
Journal Year:
2024,
Volume and Issue:
31(8), P. 1105 - 1112
Published: March 18, 2024
Abstract
Hepatocellular
Carcinoma
(HCC)
is
one
of
the
most
common
types
primary
liver
cancer.
Current
treatment
options
have
limited
efficacy
against
this
malignancy,
primarily
owing
to
difficulties
in
early
detection
and
inherent
resistance
existing
drugs.
Tumor
heterogeneity
a
pivotal
factor
contributing
significantly
recurrent
manifestations
HCC.
Intratumoral
an
important
aspect
spectrum
complex
tumor
contributes
late
diagnosis
failure.
Therefore,
it
crucial
thoroughly
understand
molecular
mechanisms
how
develops.
This
review
aims
summarize
possible
dimensions
with
emphasis
on
intratumoral
heterogeneity,
evaluate
its
profound
impact
therapeutic
strategies
for
HCC,
explore
suitability
appropriate
pre-clinical
models
that
can
be
used
best
study
heterogeneity;
thus,
opening
new
avenues
cancer
treatment.
Cell Division,
Journal Year:
2025,
Volume and Issue:
20(1)
Published: Jan. 17, 2025
Dysregulation
of
SF3A3
has
been
related
to
the
development
many
cancers.
Here,
we
investigated
functional
role
in
hepatocellular
carcinoma
(HCC).
expression
HCC
tissues
and
cell
lines
was
examined
using
RT-qPCR.
Changes
malignant
behavior
cells
after
downregulation
were
assessed
by
EdU,
colony
formation,
flow
cytometry,
wound
healing,
Transwell
invasion
assays.
Multiple
datasets
combined
identify
upstream
modifiers
SF3A3.
The
binding
relationship
between
STIL
FOXM1
explored
co-IP
assay,
effect
on
at
promoter
detected
ChIP-qPCR
assay.
A
xenograft
tumor
model
established
explore
changes
tumors
vivo,
Ki67,
GPC3,
p53
immunohistochemistry.
overexpressed
cells,
or
inhibited
promoting
p53.
An
interaction
regulated
cells.
Knockdown
further
enhanced
anti-tumor
effects
loss
vitro
whereas
overexpression
overturned
impact
vivo.
Our
findings
indicate
that
STIL/FOXM1
expedites
activating
SF3A3,
which
highlights
importance
as
a
promising
prognostic
marker
therapeutic
target
for
HCC.
Analytical Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 23, 2025
The
detection
of
disease-related
protein
biomarkers
plays
a
crucial
role
in
the
early
diagnosis,
treatment,
and
monitoring
diseases.
concentrations
can
vary
significantly
different
diseases
or
stages
same
disease.
However,
most
existing
analytical
methods
cannot
simultaneously
meet
requirements
high
sensitivity
wide
dynamic
range.
Herein,
we
developed
digital
analog
immunoassay
method
based
on
submicron
magnetic
beads
fluorescent
microspheres.
analysis
achieves
limit
as
low
46
fg/mL
(1.8
fM)
for
IL-6,
has
range
spanning
from
0.2
pg/mL
to
10
ng/mL.
Furthermore,
be
used
quickly
roughly
assess
higher
concentration
proteins
via
visual
detection,
practical
application
potential
this
was
verified
by
alpha-fetoprotein
serum
samples
12
healthy
individuals
hepatocellular
carcinoma
patients.
established
does
not
involve
use
enzymes
costly
instruments,
which
greatly
simplifies
experimental
steps,
shortens
time,
reduces
cost.
In
view
those
advantages,
proposed
great
prospects
point-of-care
applications.
Frontiers in Genetics,
Journal Year:
2022,
Volume and Issue:
13
Published: March 21, 2022
Background:
Hepatocellular
carcinoma
(HCC)
accounts
for
the
majority
of
liver
cancer,
with
incidence
and
mortality
rates
increasing
every
year.
Despite
improvement
clinical
management,
substantial
challenges
remain
due
to
its
high
recurrence
short
survival
period.
This
study
aimed
identify
potential
diagnostic
prognostic
biomarkers
in
HCC
through
bioinformatic
analysis.
Methods:
Datasets
from
GEO
TCGA
databases
were
used
Gene
Ontology
(GO)
Kyoto
Encyclopedia
Genes
Genomes
(KEGG)
enrichment
analyses
carried
out
by
WebGestalt
website
clusterProfiler
package
R.
The
STRING
database
Cytoscape
software
establish
protein-protein
interaction
(PPI)
network.
GEPIA
was
perform
expression
genes.
miRDB,
miRWalk,
TargetScan
employed
predict
miRNAs
levels
predicted
explored
via
OncomiR
database.
LncRNAs
StarBase
LncBase
while
circRNA
prediction
performed
circBank.
ROC
curve
analysis
Kaplan-Meier
(KM)
evaluate
value
gene
expression,
respectively.
Results:
A
total
327
upregulated
422
downregulated
overlapping
DEGs
identified
between
tissues
noncancerous
tissues.
PPI
network
constructed
89
nodes
178
edges
eight
hub
genes
selected
upstream
ceRNAs.
lncRNA/circRNA-miRNA-mRNA
successfully
based
on
ceRNA
hypothesis,
including
five
lncRNAs
(DLGAP1-AS1,
GAS5,
LINC00665,
TYMSOS,
ZFAS1),
six
circRNAs
(hsa_circ_0003209,
hsa_circ_0008128,
hsa_circ_0020396,
hsa_circ_0030051,
hsa_circ_0034049,
hsa_circ_0082333),
(hsa-miR-150-5p,
hsa-miR-19b-3p,
hsa-miR-23b-3p,
hsa-miR-26a-5p,
hsa-miR-651-5p,
hsa-miR-10a-5p,
hsa-miR-214-5p
hsa-miR-486-5p),
mRNAs
(CDC6,
GINS1,
MCM4,
MCM6,
MCM7).
can
promote
progression
cell
cycle,
DNA
replication,
other
pathways.
Clinical
demonstrated
that
ZFAS1/hsa-miR-150-5p/GINS1
regulatory
axis
had
a
value.
Conclusion:
These
results
revealed
cycle
replication
pathway
could
be
pathways
participate
development.
is
expected
provide
therapeutic
targets
especially
axis.
The Tohoku Journal of Experimental Medicine,
Journal Year:
2022,
Volume and Issue:
258(4), P. 265 - 276
Published: Jan. 1, 2022
Hepatocellular
carcinoma
(HCC)
is
one
of
the
most
common
and
lethal
types
cancer.
This
study
aimed
to
identify
expression
regulatory
network
a
prognostic
signature
HCC.
RNA-seq
data
from
The
Cancer
Genome
Atlas
were
used
differentially
expressed
genes
(DEGs)
between
HCC
normal
liver
tissues.
DEGs
subjected
construction
protein-protein
interaction
(PPI)
enrichment
analysis
Gene
Ontology
terms
Kyoto
Encyclopedia
Genes
Genomes
pathways.
results
showed
that
enriched
in
cell
cycle
pathway,
top
10
hub
PPI
belong
pathway.
A
ceRNA
was
constructed
using
starBase
database,
including
lncRNA
(SNHG1),
seven
miRNAs
(miR-195-5p,
miR-199a-3p,
miR-199a-5p,
miR-199b-3p,
miR-383-5p,
miR-424-5p
miR-654-3p)
six
(BUB1,
CCNA2,
CCNB1,
KIF11,
NCAPG,
TOP2A).
In
vitro
experiments
knockdown
SNHG1
lines
(Huh7
HepG2)
decreased
viability,
leading
arrest
at
G1
phase.
These
findings
indicate
promotes
proliferation
by
regulating
cycle-related
as
ceRNA.
Additionally,
Kaplan-Meier's
survival
multivariate
Cox
regression
identified
(including
SNHG1-regulated
genes)
for
overall
patients.
conclusion,
this
novel
potential
independent
factor