Medicina,
Год журнала:
2024,
Номер
60(12), С. 2091 - 2091
Опубликована: Дек. 21, 2024
Background
and
Objectives:
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
is
an
important
chronic
with
major
health
risks,
especially
in
the
presence
of
T2DM,
but
pathophysiology
this
condition
not
fully
understood.
This
study
aimed
to
investigate
platelet
hematometric
indices
patients
T2DM
MASLD.
Materials
Methods:
Demographic
medical
(including
anthropometric)
data
were
collected
from
271
participants,
whom
blood
samples
also
drawn
fasting
conditions
for
complete
count,
metabolic
panel,
ferritin,
haptoglobin,
creatinine,
fibrosis
markers.
The
correlations
main
parameters
clinical
laboratory
investigated
by
bivariate
multiple
regression
analyses.
Results:
median
platelets
number
was
235·103/μL,
thus,
population
divided
into
two
subgroups:
higher
lower
numbers
(group
1
(mean):
286.38
±
43.29·103/μL
group
2
188.12
39.77·103/μL).
Despite
similar
BMIs,
had
fatty
index
(FLI)
(84.44
18.04
vs.
79.85
17.98;
p
=
0.0088)
insulin
resistance
(HOMA-IR:
3.16
1.50
2.63
1.31;
0.0008),
direct
bilirubin,
transaminases,
uric
acid,
ferritin
concentrations.
Higher
percentages
males
subjects
HOMA-IR
values
>2.5
accounted
group.
In
analyses,
count
plateletcrit
(PTC)
correlated
independently
sex,
leucocyte
HOMA-IR,
bilirubin
concentrations
(p
<
0.0001).
distribution
width
(PDW)
positively
separate
analyses
(β
0.060;
0.0004,
β
0.052;
0.0025),
GGT,
while
mean
volume
presented
a
weak
significant
positive
association
FLI.
Patients
PDW
PTC.
Conclusions:
Male
MASLD
PTC
larger
PDW.
associated
Journal of Hepatology,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 1, 2025
Fibrosis
is
a
pathological
condition
characterized
by
excessive
accumulation
of
extracellular
matrix
(ECM)
components,
particularly
collagens,
leading
to
tissue
scarring
and
organ
dysfunction.
In
fibrosis,
an
imbalance
between
collagen
synthesis
(fibrogenesis)
degradation
(fibrolysis)
results
in
the
deposition
fibrillar
collagens
disrupting
structural
integrity
ECM
and,
consequently,
architecture.
associated
with
wide
range
chronic
diseases,
including
liver
cirrhosis,
kidney
pulmonary
autoimmune
diseases.
Recently,
concept
"hot"
"cold"
fibrosis
has
emerged,
referring
immune
status
within
fibrotic
tissues
nature
fibrogenic
signaling.
Hot
active
cell
infiltration
inflammation,
while
cold
auto-
paracrine
myofibroblast
activation,
exclusion
quiescence.
This
article
aims
explore
relationship
hot
role
various
types
their
biologically
fragments
modulating
system,
how
serological
biomarkers
can
help
understanding
disease-relevant
interactions
mesenchymal
cells
tissues.
Additionally,
we
draw
lessons
from
immuno-oncology
research
solid
tumors
shed
light
on
potential
strategies
for
treatment
highlight
advantage
having
"hot
environment"
treat
enhancing
through
modulation
system.
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(10), С. 5238 - 5238
Опубликована: Май 11, 2024
Currently,
metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
and
steatohepatitis
(MASH)
are
considered
to
be
the
main
causes
of
fibrosis.
In
turn,
fibrosis
may
lead
development
hepatocellular
carcinoma
or
advanced
cirrhosis,
i.e.,
potentially
life-threatening
conditions.
It
is
likely
that
therapy
aimed
at
reducing
risk
developing
hepatic
steatosis
inflammation
could
helpful
in
minimizing
threat/probability
organ
recent
years,
increasing
attention
has
been
paid
influence
nutraceuticals
prevention
treatment
diseases.
Therefore,
aim
this
review
was
describe
precise
role
selected
ingredients
such
as
vitamin
C,
beta-carotene,
omega-3
fatty
acids,
curcumin.
use
these
patients
with
MASLD/MASH,
along
behavioral
pharmacological
therapy,
have
a
beneficial
effect
on
combating
inflammation,
oxidative
stress,
thereby
preventing
damage.
Frontiers in Immunology,
Год журнала:
2024,
Номер
15
Опубликована: Сен. 3, 2024
Liver
cancer
is
a
major
global
health
concern,
ranking
among
the
top
causes
of
cancer-related
deaths
worldwide.
Despite
advances
in
medical
research,
prognosis
for
liver
remains
poor,
largely
due
to
inherent
limitations
current
therapies.
Traditional
treatments
like
surgery,
radiation,
and
chemotherapy
often
fail
provide
long-term
remission
are
associated
with
significant
side
effects.
Immunotherapy
has
emerged
as
promising
avenue
treatment,
leveraging
body's
immune
system
target
destroy
cells.
However,
its
application
been
limited.
One
primary
challenges
liver's
unique
microenvironment,
which
can
inhibit
effectiveness
immunotherapeutic
agents.
This
microenvironment
creates
barrier,
leading
drug
resistance
reducing
overall
efficacy
treatment.
Recent
studies
have
focused
on
understanding
immunological
landscape
develop
strategies
that
overcome
these
obstacles.
By
identifying
specific
factors
within
contribute
suppression
resistance,
researchers
aim
enhance
immunotherapy.
Prospective
include
combining
immunotherapy
other
treatments,
using
targeted
therapies
modulate
developing
new
agents
bypass
or
counteract
inhibitory
mechanisms
liver.
These
advancements
hold
promise
improving
outcomes
Cancers,
Год журнала:
2025,
Номер
17(2), С. 236 - 236
Опубликована: Янв. 13, 2025
Hepatocellular
carcinoma
(HCC)
is
a
leading
cause
of
cancer-related
mortality
worldwide,
and,
with
only
15-20%
HCC
patients
being
suitable
for
potentially
curative
treatments,
the
vast
majority
ultimately
require
systemic
therapy.
For
decades,
choice
effective
therapy
remained
sparse.
In
recent
years,
after
combination
atezolizumab
and
bevacizumab
demonstrated
superior
overall
survival
over
first-line
standard,
sorafenib,
there
has
been
major
therapeutic
paradigm
shift
to
immunotherapy-based
regimens
HCC.
While
representing
great
leap
forward
treatment
this
cancer,
reality
that
less
than
one-third
achieve
an
objective
response
immune
checkpoint
inhibitor-based
therapy,
so
remains
significant
clinical
need
further
optimization.
review,
we
provide
overview
current
landscape
immunotherapy
unresectable
delve
into
tumor
intrinsic
extrinsic
mechanisms
resistance
established
immunotherapies
focus
on
novel
targets
strong
translational
potential.
Following
this,
spotlight
emerging
approaches
notable
trials
aiming
optimize
efficacy
in
include
inhibitors,
microenvironment
modulators,
targeted
delivery
systems,
locoregional
interventions.
Journal of Clinical Medicine,
Год журнала:
2025,
Номер
14(6), С. 1856 - 1856
Опубликована: Март 10, 2025
The
extracellular
matrix
(ECM)
is
the
common
denominator
of
more
than
50
chronic
diseases.
Some
these
pathologies
lead
to
enhanced
tissue
formation
and
deposition,
whereas
others
are
associated
with
increased
degradation,
some
exhibit
a
combination
both,
leading
severe
alterations.
To
develop
effective
therapies
for
diseases
affecting
lung,
liver,
kidney,
skin,
intestine,
musculoskeletal
system,
heart,
solid
tumors,
we
need
modulate
ECM’s
composition
restore
its
organization
function.
Across
diverse
organ
diseases,
there
denominators
distinguishing
factors
in
this
fibroinflammatory
axis,
which
may
be
used
foster
new
insights
into
drug
development
across
disease
indications.
2nd
Extracellular
Matrix
Pharmacology
Congress
took
place
Copenhagen,
Denmark,
from
17
19
June
2024
was
hosted
by
International
Society
Pharmacology.
event
attended
450
participants
35
countries,
among
whom
were
prominent
scientists
who
brought
together
state-of-the-art
research
on
asked
important
questions
facilitate
development.
We
highlight
key
aspects
ECM
lungs,
tumors
advance
our
understanding
central
targets
also
advances
tools
technology
that
enable
development,
thereby
supporting
ECM.
Advanced Healthcare Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 8, 2025
Abstract
Liver
fibrosis,
characterized
by
excessive
tissue
remodeling
as
a
response
to
chronic
liver
injury,
is
accompanied
capillarization
of
sinusoidal
endothelial
cells
(LSECs)
and
activated
hepatic
stellate
(HSCs).
Simvastatin
(Sim)
can
modulate
function
increasing
nitric
oxide
synthase
(eNOS)‐dependent
(NO)
release,
thereby
reversing
attenuating
fibrosis.
However,
monotherapy
often
demonstrates
limited
therapeutic
effectiveness
given
the
complex
pathophysiology
Herein,
type
multifunctional
liposomal
microbubbles
(MBs)
carrying
both
Sim
platelet
membrane
(PM)
has
been
designed
for
drug
delivery
targeting
inflammatory
LSECs,
with
ultrasound‐targeted
microbubble
destruction
(UTMD)
mediate
efficient
release
these
agents
inside
sinusoidal.
In
rat
fibrosis
model,
MBs
reverses
through
increase
eNOS‐dependent
NO
production.
Subsequently,
adhering
LSECs
block
adhesion
activation
inherent
(PLT),
decreasing
platelet‐derived
growth
factor
β
(PDGF‐β)
inhibit
HSCs
activation.
This
study
strong
efficacy
integrating
PLT
against
which
highlights
great
potential
effectively
managing
this
intractable
disease.
Frontiers in Cell and Developmental Biology,
Год журнала:
2024,
Номер
12
Опубликована: Сен. 5, 2024
Non-alcoholic
fatty
liver
disease
(NAFLD)
and
its
more
advanced
form,
non-alcoholic
steatohepatitis
(NASH),
have
become
global
health
challenges
with
significant
morbidity
mortality
rates.
NAFLD
encompasses
several
diseases,
ranging
from
simple
steatosis
to
severe
inflammatory
fibrotic
forms.
Ultimately,
this
can
lead
cirrhosis
hepatocellular
carcinoma.
The
intricate
role
of
hepatic
macrophages,
particularly
Kupffer
cells
(KCs)
monocyte-derived
macrophages
(MoMFs),
in
the
pathogenesis
NASH,
has
received
increasing
attention.
Hepatic
interact
hepatocytes,
stellate
cells,
endothelial
playing
a
crucial
maintaining
homeostasis.
Paradoxically,
they
also
participate
some
diseases.
This
review
highlights
fundamental
emphasizing
their
plasticity
contribution
inflammation
fibrosis,
hopes
provide
ideas
for
subsequent
experimental
research
clinical
treatment.