Deleted Journal,
Год журнала:
2024,
Номер
unknown, С. 1 - 12
Опубликована: Дек. 31, 2024
Liver
cancer,
especially
hepatocellular
carcinoma
(HCC),
is
one
of
the
most
common
malignant
tumors
worldwide,
and
its
high
mortality
rate
treatment
difficulty
have
always
been
major
challenges
faced
by
medical
community.
With
continuous
development
biotechnology,
stem
cell
research
has
shown
great
potential
hope
in
liver
cancer
treatment.
This
review
provides
a
brief
overview
importance
cells
research,
including
identification
(LCSCs),
molecular
maintenance
mechanisms
stemness
LCSCs,
targeted
therapy
strategies,
as
well
therapy,
proposing
future
directions.
Stem Cell Research & Therapy,
Год журнала:
2025,
Номер
16(1)
Опубликована: Янв. 6, 2025
Chronic
liver
diseases,
including
cirrhosis
and
failure,
remain
formidable
challenges
due
to
their
complex
progression
limited
therapeutic
options.
Mesenchymal
stem
cell
(MSC)
therapy
has
emerged
as
a
game-changing
approach,
leveraging
its
potent
immunomodulatory,
anti-fibrotic,
regenerative
capabilities,
along
with
the
ability
transdifferentiate
into
hepatocytes.
This
review
delves
latest
advances
in
MSC-based
treatments
for
chronic
end-stage
highlighted
current
clinical
trials.
MSCs
derived
from
bone
marrow
umbilical
cord
have
shown
remarkable
promise
reversing
damage,
improving
function,
providing
hope
patients
who
do
not
respond
conventional
therapies.
When
administered
through
hepatic,
portal,
or
peripheral
veins,
significantly
improved
histology,
reduced
fibrosis,
restored
functional
capacity.
Furthermore,
MSC-derived
materials,
such
extracellular
vesicles
exosomes,
are
emerging
cutting-edge
tools
treating
failure
mitigating
post-transplant
complications.
While
autologous
hepatocytes
hold
non-fatal
cirrhosis,
allogeneic
being
applied
more
severe
conditions,
transplantation
cases.
Despite
these
promising
early
outcomes,
larger
trials
long-term
studies
essential
fully
harness
transformative,
off-the-shelf
alternative
transplantation,
heralding
new
era
Abstract
Liver
fibrosis
is
a
chronic
pathological
condition
lacking
specific
clinical
treatments.
Stem
cells,
with
notable
potential
in
regenerative
medicine,
offer
promise
treating
liver
fibrosis.
However,
stem
cell
therapy
hindered
by
immunological
rejection,
carcinogenesis
risk,
efficacy
variation,
and
high
cost.
secretome‐based
cell‐free
offers
solutions
to
address
these
challenges,
but
it
limited
low
delivery
efficiency
rapid
clearance.
Herein,
an
innovative
approach
for
situ
implantation
of
smart
microneedle
(MN)
arrays
enabling
precisely
controlled
multiple
therapeutic
agents
directly
into
fibrotic
tissues
developed.
By
integrating
platinum‐based
nanocatalytic
combination
therapy,
the
MN
can
deactivate
hepatic
stellate
cells.
Moreover,
they
promote
excessive
extracellular
matrix
degradation
more
than
75%,
approaching
normal
levels.
Additionally,
provide
hepatocyte
protection
while
reducing
inflammation
levels
≈70–90%.
They
also
exhibit
remarkable
capability
scavenging
almost
100%
reactive
oxygen
species
alleviating
hypoxia.
Ultimately,
this
treatment
strategy
effectively
restrain
progression.
The
comprehensive
vitro
vivo
experiments,
supplemented
proteome
transcriptome
analyses,
substantiate
effectiveness
fibrosis,
holding
immense
applications.
Current Stem Cell Research & Therapy,
Год журнала:
2024,
Номер
19(11), С. 1484 - 1496
Опубликована: Янв. 11, 2024
The
effectiveness
of
fucoxanthin
(Fx)
in
liver
diseases
has
been
reported
due
to
its
anti-inflammatory
and
antifibrotic
effects.
Mesenchymal
stem
cells
(MSCs)-based
therapy
also
proposed
as
a
promising
strategy
for
fibrosis
treatment.
Recent
studies
have
shown
that
the
co-administration
MSCs
drugs
demonstrates
pronounced
effect
on
fibrosis.
Liver
inflammation,
injury,
and
hepatic
cell
death
are
caused
by
external
agents
(viruses,
bacteria,
drugs,
alcohol,
etc.)
along
with
the
genetic
susceptibility
of
an
individual.
Persistent
activation
fibrogenic
response
in
cells
leads
to
liver
fibrosis
which
turn
progresses
cirrhosis
cancer.
The
dysregulation
immune
system
generates
reactive
oxygen
species
induce
necrosis
hepatocytes.
This
process
activates
stellate
myofibroblasts
produce
a
huge
quantity
collagens,
alpha-smooth
muscle
actin,
extracellular
matrix
deposition
parenchyma.
Due
multifactorial
nature
this
disease,
conventional
therapies
increasingly
attempted
combinatorial
therapy
or
polytherapy
target
multiple
mechanistic
sites
order
prevent
entry
into
further
complicated
irreversible
stages.
Despite
advancements
therapy,
several
cases
aggravate
(grade
3
4)
cirrhosis.
inconsistency
treatment
outcomes
limited
organ
donors
for
transplantation
have
led
ever-increasing
challenging
demand
alternative
therapies.
In
review,
we
analyze
mechanism
causative
factors
diseases,
mode,
therapeutic
options.
central
diseases
dysregulation,
hence
bioactive
immunomodulatory
properties
should
be
searched
exploited
meet
needs.
Mesenchymal
stem
(MSCs)
their
specialized
anti-inflammatory
could
utilized
as
effective
candidate
treating
inflammatory
diseases.
MSC-derived
exosome
provides
additional
option
that
work
tandem
MSC
synergistic
form.
series,
reviewed
preconditioned
genetically
edited
MSCs
augment
homing,
proliferation,
differentiation.
Importantly,
all
clinical
challenges
noted
addressed
before
cytotherapy
considered
safe
patients
Published
literature
indicated
has
potential
substitute
options
high-grade
Annaly khirurgicheskoy gepatologii = Annals of HPB surgery,
Год журнала:
2025,
Номер
30(1), С. 11 - 19
Опубликована: Фев. 28, 2025
Aim
.
To
justify
the
necessity
of
combined
intraportal
administration
mononuclear
stem
cells,
transjugular
intrahepatic
portosystemic
shunting,
and
partial
splenic
embolization
in
patients
with
portal
hypertension
hepatocellular
insufficiency
against
background
liver
cirrhosis,
to
develop
a
technology,
evaluate
its
safety
efficacy.
Materials
methods
The
study
involved
results
treatment
for
1631
cirrhosis
various
etiologies
from
2018
2023;
272
(16.7%)
were
included
waiting
list
cadaveric
transplantation.
During
period,
195
(71.6%)
underwent
some
method
surgical
correction
hypertension:
84
(43.1%)
endoscopic
ligation
esophageal
varices,
46
(23.6%)
had
21
(10.7%)
received
embolization,
35
(17.9%)
both
shunting
one
procedure.
In
15
cases
(5.5%),
autologous
bone
marrow
cells
was
performed.
9
(4.7%),
this
technology
minimally
invasive
correcting
6
(3.1%)
3
(1.6%)
embolization.
Results
Following
techniques
complications
hypertension,
no
or
adverse
events
observed.
average
follow-up
period
(3;15)
months,
MELD
score
during
dynamic
observation
16
(12;18)
points.
No
progression
related
noted.
Conclusion
combination
represents
promising,
effective,
safe
strategy
reducing
mortality
awaiting
transplantation
improving
outcomes
terminal
diffuse
diseases.
International Journal of Molecular Sciences,
Год журнала:
2025,
Номер
26(7), С. 3084 - 3084
Опубликована: Март 27, 2025
Mesenchymal
stem
cells
(MSCs)
have
emerged
as
a
relevant
strategy
in
regenerative
medicine
due
to
their
multipotent
differentiation
capacity,
immunomodulatory
properties,
and
therapeutic
applications
various
medical
fields.
This
review
explores
the
use
of
MSCs,
focusing
on
role
treating
autoimmune
disorders
neoplastic
diseases
tissue
regeneration.
We
discuss
mechanisms
underlying
MSC-mediated
repair,
including
paracrine
activity,
migration
injury
sites,
interaction
with
immune
system.
Advances
cellular
therapies
such
genome
engineering
MSC-derived
exosome
treatments
further
enhance
applicability.
Key
methodologies
analyzed
include
genomic
studies,
next-generation
sequencing
(NGS),
bioinformatics
approaches
optimize
MSC-based
interventions.
Additionally,
we
reviewed
preclinical
clinical
evidence
demonstrating
potential
MSCs
conditions
graft-versus-host
disease,
osteoarthritis,
liver
cirrhosis,
neurodegenerative
disorders.
While
promising,
challenges
remain
regarding
standardization,
long-term
safety,
tumorigenic
risks
associated
MSC
therapy.
Future
research
should
focus
refining
efficacy
minimize
risks.
underscores
need
for
large-scale
trials
validate
interventions
fully
harness
potential.
Frontiers in Pharmacology,
Год журнала:
2025,
Номер
16
Опубликована: Апрель 4, 2025
Objective
Our
group
aimed
to
explore
the
effect
of
different
dosages
citicoline
on
ischemic
stroke
(IS)
patients
and
determine
most
appropriate
dosage
for
these
patients.
Methods
The
databases
PubMed,
Cochrane
Library,
Medline,
Web
Science,
Embase
were
searched
from
their
establishment
15
October
2024.
We
assessed
quality
all
included
articles
by
using
evaluation
method
or
Newcastle-Ottawa
Scale
(NOS),
which
was
based
study
type.
Relative
risk
(RR)
95%
confidence
interval
(CI)
used
dichotomous
data,
mean
standardized
difference
(SD)
continuous
data.
outcome
indicators
death,
improvement
in
neurological
function
daily
living
activities,
adverse
effects.
Results
In
this
study,
a
total
13
studies
included.
Of
these,
370
treated
with
500
mg
citicoline,
502
1,000
1,891
2,000
2,582
control
(CON).
evaluated
treatment
ranking.
terms
both
demonstrated
lower
mortality
than
CON,
having
lowest
mortality.
improvement,
we
found
that
compared
rates
higher
ineffective
results
500-mg
2,000-mg
1,000-mg
groups.
MBI
scores
2000
while
score
not.
Lastly,
aspect
effects,
rate
effects
it
citicoline.
Conclusion
research
findings
revealed
significantly
affect
function,
acute
IS.
Notably,
not
only
demonstrate
activities
but
also
have
results.
However,
does
specify
best
one
two
dosages.