Biomolecules,
Journal Year:
2024,
Volume and Issue:
14(7), P. 743 - 743
Published: June 23, 2024
The
anterior
gradient
protein
2
(AGR2)
plays
a
crucial
role
in
facilitating
the
formation
of
disulfide
bonds
within
endoplasmic
reticulum
(ER).
Research
suggests
that
AGR2
can
function
as
an
oncogene,
with
its
heightened
expression
linked
to
advancement
hepatobiliary
and
pancreatic
cancers
through
invasion
metastasis.
Notably,
not
only
serves
pro-oncogenic
agent
but
also
downstream
targeting
protein,
indirectly
fostering
cancer
progression.
This
comprehensive
review
delves
into
established
functions
patterns
AGR2,
emphasizing
pivotal
progression,
particularly
malignancies.
Furthermore,
emerges
potential
prognostic
marker
promising
target
for
immunotherapy,
offering
novel
avenues
treatment
enhancing
patient
outcomes.
American Journal of Cancer Research,
Journal Year:
2024,
Volume and Issue:
14(8), P. 3935 - 3961
Published: Jan. 1, 2024
The
nuclear
factor-erythroid
2-related
factor
2
(Nrf2)
is
able
to
control
the
redox
balance
in
cells
responding
oxidative
damage
and
other
stress
signals.
Nrf2
upregulation
can
elevate
levels
of
antioxidant
enzymes
support
against
death.
In
spite
protective
function
physiological
conditions,
stimulation
cancer
has
been
favour
tumorigenesis.
Since
dysregulation
molecular
pathways
mutations/deletions
are
common
tumors,
be
a
promising
therapeutic
target.
overexpression
prevent
cell
death
tumor
by
increasing
survival
rate
cells,
ensures
carcinogenesis.
Moreover,
induction
promote
invasion
metastasis
cells.
stimulates
EMT
increase
metastasis.
Furthermore,
regarding
Nrf2,
its
triggers
chemoresistance.
natural
products
regulate
therapy
reverse
drug
resistance.
nanostructures
specifically
target
signaling
therapy.
current
review
discusses
potential
proliferation,
Then,
capacity
for
suppressing
Nrf2-mediated
progression
discussed.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: Nov. 12, 2024
Despite
public
health
measures,
type
2
diabetes
(T2D)
is
still
a
significant
concern
worldwide,
given
its
associated
complications,
including
hepatic
alterations.
The
role
of
epithelial-to-mesenchymal
transition
(EMT)
in
liver
fibrosis
well
established.
However,
effects
on
the
progression
diabetic
diseases
are
not
understood.
Therefore,
this
study
aims
to
investigate
mRNA/miRNA
axes
involved
process.
Bioinformatic
analysis
revealed
new
EMT-associated
genes
(CDH2,
ITGB1,
COL4A1,
COL1A1,
TNC,
CCN2,
and
JUN),
which
showed
higher
expression
obese
T2D
hepatocellular
carcinoma
(HCC)
patients.
In
addition,
six
miRNAs
(miR-21-5p,
miR-26a-5p,
miR-34a-5p,
miR-106a-5p,
miR-320a-3p
miR-424-5p)
have
been
found
as
potential
targets.
Among
them,
miR-26a-5p
miR-424-5p
were
significantly
downregulated
nonalcoholic
steatohepatitis
(NASH)
HCC
(p
<
0.05),
being
considered
negative
regulators
EMT
our
mesenchymal
culture
model,
negatively
regulated
cadherin
(also
known
N-cadherin,
CDH2)
promoted
1
E-cadherin,
CDH1)
expression.
Our
results
reveal
molecules
tumor
development.
Moreover,
we
observe
that
impairs
initial
stages
disease
by
inhibiting
CDH2
could
be
valuable
target
pathology.
Frontiers in Pharmacology,
Journal Year:
2023,
Volume and Issue:
14
Published: Nov. 17, 2023
Background:
Hepatocellular
carcinoma
(HCC)
originates
from
Epithelial
cells,
and
epithelial
lineage
plasticity
has
become
a
promising
research
direction
for
advancing
HCC
treatment.
This
study
aims
to
focus
on
cells
provide
target
insights
detecting
prognosis
response
drug
therapy.
Methods:
Single-cell
RNA
sequencing
(scRNA-seq)
data
GSE149614
were
clustered
using
Seurat,
the
differentiation
evolution
of
analyzed
by
Monocle
2.
Scissor+
Scissor-
associated
with
prognostic
phenotypes
bulk
RNA-seq
screened
Scissor
algorithm
differential
analysis
screen
candidate
genes.
Candidate
genes
overlapped
related
univariate
Cox
regression,
Least
Absolute
Shrinkage
Selection
Operator
(LASSO)
sparse
penalty
was
imposed
intersection
construct
risk
assessment
system.
Results:
Eight
major
cell
subpopulations
identified,
among
which
proportion
in
non-tumor
liver
tissues
significantly
different,
its
increased
advanced
clinical
stage.
During
progression
HCC,
whole
trajectory
towards
enhanced
proliferation.
Differential
between
1,265
upregulated
191
downregulated
Wherein,
enriched
Cell
processes,
Genetic
information
processing,
Metabolism
Human
disease
Infection.
Nevertheless,
immune
system
pathways
took
main
proportions
pathways.
There
17
common
genes,
CDC20,
G6PD
PLOD2
selected
as
components
constructing
Risk
score
showed
significant
correlation
tumor
stage,
epithelial-mesenchymal
transition
(EMT)
22
therapeutic
drugs,
an
independent
factor
HCC.
Conclusion:
revealed
cellular
composition
functional
landscape
further
deterioration
established
3-gene
model,
closely
features,
EMT,
sensitivity
prediction.
These
findings
provided
patient
therapy
detection
Biomedicines,
Journal Year:
2023,
Volume and Issue:
12(1), P. 87 - 87
Published: Dec. 30, 2023
Aggressive
hepatocellular
carcinoma
(HCC)
overexpressing
Angiopoietin-2
(ANG-2)
(a
protein
linked
with
angiogenesis,
proliferation,
and
epithelial–mesenchymal
transition
(EMT)),
shares
95%
of
up-regulated
genes
a
similar
poor
prognosis
the
proliferative
subgroup
intrahepatic
cholangiocarcinoma
(iCCA).
We
analyzed
pro-invasive
effect
ANG-2
its
regulator
vascular
endothelial
growth
factor
(VEGF)
on
HCC
CCA
spheroids
to
uncover
posUsible
common
ways
response.
Four
cell
lines
were
used:
Hep3B
HepG2
(HCC),
HuCC-T1
(iCCA),
EGI-1
(extrahepatic
CCA).
treated
recombinant
human
(rh)
and/or
VEGF
then
observed
changes
at
baseline,
after
24
h,
again
48
h.
Proangiogenic
stimuli
increased
migration
invasion
capability
in
HCC-
iCCA-derived
associated
modification
EMT
phenotypic
markers
decrease
E-cadherin
an
increase
N-cadherin
Vimentin),
especially
front.
Inhibitors
targeting
(Trebananib)
(Bevacizumab)
effectively
blocked
ability
that
had
been
stimulated
rh-ANG-2
rh-VEGF.
Overall,
our
findings
highlight
critical
role
played
by
enhancing
migrate
invade,
which
are
key
processes
cancer
progression.