Seminars in Liver Disease,
Год журнала:
2024,
Номер
44(02), С. 159 - 179
Опубликована: Май 1, 2024
Primary
liver
cancer,
represented
mainly
by
hepatocellular
carcinoma
(HCC)
and
intrahepatic
cholangiocarcinoma
(CCA),
is
one
of
the
most
common
deadliest
tumors
worldwide.
While
surgical
resection
or
transplantation
are
best
option
in
early
disease
stages,
these
often
present
advanced
stages
systemic
treatment
required
to
improve
survival
time.
The
emergence
immune
checkpoint
inhibitor
(ICI)
therapy
has
had
a
positive
impact
especially
on
cancers,
thereby
establishing
immunotherapy
as
part
first-line
HCC
CCA.
Nevertheless,
low
response
rates
reflect
usually
cold
immunosuppressed
tumor
microenvironment
primary
cancer.
In
this
review,
we
aim
summarize
mechanisms
resistance
leading
escape
with
special
focus
composition
both
CCA,
also
reflecting
recent
important
developments
ICI
combination
therapy.
Furthermore,
discuss
how
ICIs
established
cancer
treatments
(e.g.
multikinase
inhibitors
chemotherapy)
well
more
complex
combinations
state-of-the-art
therapeutic
concepts
may
reshape
microenvironment,
higher
long-lasting
antitumor
immunity
for
patients.
Journal of Cellular Physiology,
Год журнала:
2022,
Номер
237(7), С. 2770 - 2795
Опубликована: Май 13, 2022
Metastasis
of
tumor
cells
is
a
complex
challenge
and
significantly
diminishes
the
overall
survival
prognosis
cancer
patients.
The
epithelial-to-mesenchymal
transition
(EMT)
well-known
mechanism
responsible
for
invasiveness
cells.
A
number
molecular
pathways
can
regulate
EMT
in
nuclear
factor-kappaB
(NF-κB)
one
them.
translocation
NF-κB
p65
induce
transcription
several
genes
involved
induction.
present
review
describes
interaction
their
association
progression.
Due
to
oncogenic
role
signaling,
its
activation
enhances
metastasis
via
This
has
been
confirmed
various
cancers
including
brain,
breast,
lung
gastric
cancers,
among
others.
ZEB1/2,
transforming
growth
factor-β,
Slug
as
inducers
undergo
upregulation
by
promote
After
induction
driven
NF-κB,
significant
decrease
occurs
E-cadherin
levels,
while
N-cadherin
vimentin
levels
an
increase.
noncoding
RNAs
potentially
also
function
upstream
mediators
modulate
NF-κB/EMT
axis
cancers.
Moreover,
mediating
drug
resistance
Thus,
suppressing
sensitivity
chemotherapeutic
agents.
Signal Transduction and Targeted Therapy,
Год журнала:
2023,
Номер
8(1)
Опубликована: Март 11, 2023
Abstract
Despite
the
success
of
targeted
therapies
in
cancer
treatment,
therapy-induced
resistance
remains
a
major
obstacle
to
complete
cure.
Tumor
cells
evade
treatments
and
relapse
via
phenotypic
switching
driven
by
intrinsic
or
induced
cell
plasticity.
Several
reversible
mechanisms
have
been
proposed
circumvent
tumor
plasticity,
including
epigenetic
modifications,
regulation
transcription
factors,
activation
suppression
key
signaling
pathways,
as
well
modification
environment.
Epithelial-to-mesenchymal
transition,
stem
formation
also
serve
roads
towards
Corresponding
treatment
strategies
recently
developed
that
either
target
plasticity-related
employ
combination
treatments.
In
this
review,
we
delineate
plasticity
its
manipulation
evasion
from
therapy.
We
discuss
non-genetic
drug-induced
various
types
tumors
provide
insights
into
contribution
acquired
drug
resistance.
New
therapeutic
such
inhibition
reversal
are
presented.
multitude
clinical
trials
ongoing
worldwide
with
intention
improving
outcomes.
These
advances
direction
for
developing
novel
therapy
regimens
Pharmacological Research,
Год журнала:
2022,
Номер
187, С. 106553 - 106553
Опубликована: Ноя. 16, 2022
Cancer
progression
results
from
activation
of
various
signaling
networks.
Among
these,
PI3K/Akt
contributes
to
proliferation,
invasion,
and
inhibition
apoptosis.
Hepatocellular
carcinoma
(HCC)
is
a
primary
liver
cancer
with
high
incidence
rate,
especially
in
regions
prevalence
viral
hepatitis
infection.
Autoimmune
disorders,
diabetes
mellitus,
obesity,
alcohol
consumption,
inflammation
can
also
lead
initiation
development
HCC.
The
treatment
HCC
depends
on
the
identification
oncogenic
factors
that
tumor
cells
develop
resistance
therapy.
present
review
article
focuses
role
progression.
Activation
promotes
glucose
uptake,
favors
glycolysis
increases
cell
proliferation.
It
inhibits
both
apoptosis
autophagy
while
promoting
survival.
stimulates
epithelial-to-mesenchymal
transition
(EMT)
matrix-metalloproteinase
(MMP)
expression
during
metastasis.
In
addition
increasing
colony
formation
capacity
facilitating
spread
cells,
angiogenesis.
Therefore,
silencing
prevents
aggressive
behavior.
confer
drug
resistance,
particularly
sorafenib,
decreases
radio-sensitivity
cells.
Anti-cancer
agents,
like
phytochemicals
small
molecules
suppress
by
limiting
Being
upregulated
tissues
clinical
samples,
be
used
as
biomarker
predict
patients'
response
Medicinal Research Reviews,
Год журнала:
2023,
Номер
43(5), С. 1263 - 1321
Опубликована: Март 23, 2023
Abstract
Gastrointestinal
(GI)
tumors
(cancers
of
the
esophagus,
gastric,
liver,
pancreas,
colon,
and
rectum)
contribute
to
a
large
number
deaths
worldwide.
STAT3
is
an
oncogenic
transcription
factor
that
promotes
genes
associated
with
proliferation,
antiapoptosis,
survival,
metastasis.
overactivated
in
many
human
malignancies
including
GI
which
accelerates
tumor
progression,
metastasis,
drug
resistance.
Research
recent
years
demonstrated
noncoding
RNAs
(ncRNAs)
play
major
role
regulation
signaling
pathways
pathway.
The
types
endogenous
ncRNAs
are
being
extensively
studied
oncology
microRNAs,
long
RNAs,
circular
RNAs.
These
can
either
be
tumor‐promoters
or
tumor‐suppressors
each
one
them
imparts
their
activity
via
different
mechanisms.
pathway
also
tightly
modulated
by
ncRNAs.
In
this
article,
we
have
elaborated
on
tumor‐promoting
tumors.
Subsequently,
comprehensively
discussed
as
well
suppressor
functions
mechanism
action
known
modulate
cancers.
Abstract
Hepatocellular
carcinoma
(HCC)
is
the
most
common
primary
liver
cancer
with
a
high
mortality
rate.
It
regarded
as
significant
public
health
issue
because
of
its
complicated
pathophysiology,
metastasis,
and
recurrence
rates.
There
are
no
obvious
symptoms
in
early
stage
HCC,
which
often
leads
to
delays
diagnosis.
Traditional
treatment
methods
such
surgical
resection,
radiotherapy,
chemotherapy,
interventional
therapies
have
limited
therapeutic
effects
for
HCC
patients
or
metastasis.
With
development
molecular
biology
immunology,
signaling
pathways
immune
checkpoint
were
identified
main
mechanism
progression.
Targeting
these
molecules
has
become
new
direction
HCC.
At
present,
combination
targeted
drugs
inhibitors
first
choice
advanced
patients.
In
this
review,
we
mainly
focus
on
cutting‐edge
research
corresponding
therapy
immunotherapy
great
significance
comprehensively
understand
pathogenesis
search
potential
targets,
optimize
strategies
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(2), С. 1417 - 1417
Опубликована: Янв. 11, 2023
Hepatocellular
carcinoma
(HCC)
is
one
of
the
leading
causes
cancer
death
globally.
The
stem
cells
(CSCs)
HCC
are
responsible
for
tumor
growth,
invasion,
metastasis,
recurrence,
chemoresistance,
target
therapy
resistance
and
radioresistance.
reported
main
surface
markers
used
to
identify
liver
CSCs
include
epithelial
cell
adhesion/activating
molecule
(EpCAM),
cluster
differentiation
90
(CD90),
CD44
CD133.
molecular
signaling
pathways
Wnt/β-catenin,
transforming
growth
factors-β
(TGF-β),
sonic
hedgehog
(SHH),
PI3K/Akt/mTOR
Notch.
Patients
with
EpCAM-positive
alpha-fetoprotein
(AFP)-positive
usually
young
but
have
advanced
tumor-node-metastasis
(TNM)
stages.
CD90-positive
HCCs
poorly
differentiated
worse
prognosis.
Those
CD44-positive
develop
early
metastases.
CD133
expression
a
higher
recurrence
rate
shorter
overall
survival.
Wnt/β-catenin
pathway
triggers
angiogenesis,
infiltration
metastasis
through
enhancement
angiogenic
factors.
All
CD133+
CSCs,
CD133+/EpCAM+
CD44+
contribute
sorafenib
resistance.
SHH
could
protect
against
ionizing
radiation
in
an
autocrine
manner.
Reducing
CSC
population
crucial
improvement
HCC.
However,
targeting
still
challenging.
Cell Communication and Signaling,
Год журнала:
2023,
Номер
21(1)
Опубликована: Фев. 9, 2023
Autophagy
is
an
evolutionarily
conserved
process
that
plays
a
role
in
regulating
homeostasis
under
physiological
conditions.
However,
dysregulation
of
autophagy
observed
the
development
human
diseases,
especially
cancer.
has
reciprocal
functions
cancer
and
may
be
responsible
for
either
survival
or
death.
Hepatocellular
carcinoma
(HCC)
one
most
lethal
common
malignancies
liver,
smoking,
infection,
alcohol
consumption
can
lead
to
its
development.
Genetic
mutations
alterations
molecular
processes
exacerbate
progression
HCC.
The
function
HCC
controversial
both
tumor
suppressive
promoting.
Activation
affect
apoptosis
regulator
proliferation
glucose
metabolism.
Induction
promote
metastasis
via
induction
EMT.
In
addition,
stem
cell
formation
HCC,
pro-survival
leads
resistance
chemotherapy
radiotherapy.
Targeting
impairs
growth
improves
response
therapy.
Of
note,
large
number
signaling
pathways
such
as
STAT3,
Wnt,
miRNAs,
lncRNAs,
circRNAs
regulate
Moreover,
regulation
(induction
inhibition)
by
antitumor
agents
could
suggested
effective
treatment
this
paper,
we
comprehensively
review
mechanisms
discuss
potential
benefit
targeting
Video
Abstract.
Cell Death and Disease,
Год журнала:
2023,
Номер
14(3)
Опубликована: Март 29, 2023
Abstract
N-glycosylation
is
one
of
the
most
common
types
protein
modifications
and
it
plays
a
vital
role
in
normal
physiological
processes.
However,
aberrant
N-glycan
are
closely
associated
with
pathogenesis
diverse
diseases,
including
processes
such
as
malignant
transformation
tumor
progression.
It
known
that
conformation
glycoproteins
altered
during
different
stages
hepatocarcinogenesis.
Characterizing
heterogeneity
biological
functions
glycans
liver
cancer
patients
will
facilitate
deeper
understanding
molecular
mechanisms
injury
In
this
article,
we
review
hepatocarcinogenesis,
focusing
on
epithelial-mesenchymal
transition,
extracellular
matrix
changes,
microenvironment
formation.
We
highlight
its
potential
applications
treatment
or
diagnosis
cancer.
Biomedicines,
Год журнала:
2023,
Номер
11(1), С. 190 - 190
Опубликована: Янв. 12, 2023
Lung
cancer
is
the
leading
cause
of
cancer-related
deaths
worldwide.
The
standard
care
for
advanced
non-small-cell
lung
(NSCLC)
without
driver-gene
mutations
a
combination
an
anti-PD-1/PD-L1
antibody
and
chemotherapy,
or
anti-CTLA-4
with
chemotherapy.
Although
there
were
fewer
cases
disease
progression
in
early
stages
treatment
than
antibodies
alone,
only
approximately
half
patients
had
long-term
response.
Therefore,
it
necessary
to
elucidate
mechanisms
resistance
immune
checkpoint
inhibitors.
Recent
reports
such
include
reduced
cancer-cell
immunogenicity,
loss
major
histocompatibility
complex,
dysfunctional
tumor-intrinsic
interferon-γ
signaling,
oncogenic
signaling
immunoediting.
Among
these,
Wnt/β-catenin
pathway
notable
potential
mechanism
escape
In
this
review,
we
will
summarize
findings
on
these
NSCLC
other
cancers,
focusing
signaling.
First,
review
molecular
biology
then
discuss
how
can
induce
immunoediting
We
also
describe
various
immune-checkpoint-inhibitor
resistance.
Finally,
propose
therapeutic
approaches
overcome
mechanisms.