Cardiometry,
Journal Year:
2022,
Volume and Issue:
24, P. 115 - 120
Published: Nov. 30, 2022
Abstract
Regenerative
medicine
is
a
vital
area
that
advances
methods
addressing
the
process
of
liver
regeneration.
The
has
unique
ability
to
return
standard
size
within
short
period
time
after
its
injury
or
partial
hepatectomy.
Hepatocytes
are
highly
active
metabolic
cells,
which
have
large
number
mitochondria,
suggesting
biologically
significant
role
for
mitochondrial
dynamics
in
hepatocyte
damage
and
repair.
aim
hereof
develop
method
accelerating
regeneration
rats
based
on
transplantation
mitochondria
isolated
from
intact
rats.
Materials
methods.
Experimental
animals
(n
=
30)
used
by
us
were
white
outbred
divided
into
groups
as
follows:
1)
comparison
group
include
10);
2)
reference
with
resection
+
use
saline
solution
3)
main
therapy
(MCT)
10).
In
groups,
under
xylazoletil
anesthesia,
median
laparotomy
was
performed
maximum
allowable
left
lobe
executed.
Mitochondria
diluted
0.9%
NaCl
protein
concentration
11.6
g/l
injected
post-surgery
(group
No.
3).
above
procedure
carried
out
14
days.
Animals
intraperitoneally
0.5
ml
according
similar
scheme.
Statistical
analysis
Statistica
10.0
Software.
Results.
According
weight
indices
MCT,
mass
organ
increased
factor
1.7
р˂0.05)
relative
without
MCT.
At
same
time,
compared
indicators
(intact
animals),
exceeded
1.6
times
(p˂0.05),
stump
itself
during
MCT
3.2
Conclusion.
As
result
experiment
liver,
it
can
be
concluded
subsequent
processes
tissue
against
background
acquire
pronounced
features
physiological
regeneration,
restoration
stromal
parenchymal
components.
Therapeutic Advances in Medical Oncology,
Journal Year:
2019,
Volume and Issue:
11
Published: Jan. 1, 2019
The
gut
microbiota
is
involved
in
the
maintenance
of
homeostasis
human
body
and
its
alterations
are
associated
with
development
different
pathological
conditions.
liver
organ
most
exposed
to
influence
microbiota,
recently
important
connections
between
intestinal
flora
hepatocellular
carcinoma
(HCC)
have
been
described.
In
fact,
HCC
commonly
cirrhosis
develops
a
microenvironment
where
inflammation,
immunological
alterations,
cellular
aberrations
dramatically
evident.
Prevention
diagnosis
earliest
stages
still
effective
weapons
fighting
this
tumor.
Animal
models
show
that
can
be
promotion
progression
directly
or
through
pathogenic
mechanisms.
Recent
data
humans
confirmed
these
preclinical
findings,
shedding
new
light
on
pathogenesis.
Limitations
due
experimental
design,
ethnic
hepatological
setting
make
it
difficult
compare
results
draw
definitive
conclusions,
but
studies
lay
foundations
for
pathogenetic
redefinition
HCC.
Therefore,
evident
characterization
modulation
an
enormous
diagnostic,
preventive,
therapeutic
potential,
especially
patients
early
stage
Biomolecules,
Journal Year:
2023,
Volume and Issue:
13(5), P. 857 - 857
Published: May 18, 2023
Forkhead
box
(FOX)
proteins
are
a
wing-like
helix
family
of
transcription
factors
in
the
DNA-binding
region.
By
mediating
activation
and
inhibition
interactions
with
all
kinds
transcriptional
co-regulators
(MuvB
complexes,
STAT3,
β-catenin,
etc.),
they
play
significant
roles
carbohydrate
fat
metabolism,
biological
aging
immune
regulation,
development,
diseases
mammals.
Recent
studies
have
focused
on
translating
these
essential
findings
into
clinical
applications
order
to
improve
quality
life,
investigating
areas
such
as
diabetes,
inflammation,
pulmonary
fibrosis,
increase
human
lifespan.
Early
shown
that
forkhead
M1
(FOXM1)
functions
key
gene
pathological
processes
multiple
by
regulating
genes
related
proliferation,
cell
cycle,
migration,
apoptosis
diagnosis,
therapy,
injury
repair.
Although
FOXM1
has
long
been
studied
relation
diseases,
its
role
needs
be
elaborated
on.
expression
is
involved
development
or
repair
including
pneumonia,
liver
repair,
adrenal
lesions,
vascular
brain
arthritis,
myasthenia
gravis,
psoriasis.
The
complex
mechanisms
involve
signaling
pathways,
WNT/β-catenin,
STAT3/FOXM1/GLUT1,
c-Myc/FOXM1,
FOXM1/SIRT4/NF-κB,
FOXM1/SEMA3C/NRP2/Hedgehog.
This
paper
reviews
kidney,
vascular,
lung,
brain,
bone,
heart,
skin,
blood
vessel
elucidate
progression
non-malignant
makes
suggestions
for
further
research.
Artificial Cells Nanomedicine and Biotechnology,
Journal Year:
2019,
Volume and Issue:
47(1), P. 1908 - 1916
Published: May 10, 2019
Introduction
Hepatocellular
carcinoma
(HCC)
ranks
fourth
in
global
cancer
mortality,
accounting
for
8.2%
of
all
deaths.
Early
detection
HCC
has
a
significant
impact
on
clinical
outcomes.
The
aim
this
study
was
to
identify
blood-based
biomarkers
which
are
HCC-specific.Methods
Comprehensive
gene
expression
raw
data
purified
RNA
peripheral
blood
mononuclear
cells
(PBMC)
downloaded
from
GEO
and
then
analyzed.
Differentially
expressed
genes
(DEGs)
were
screened
the
method
weighted
co-expression
network
analysis
applied
candidate
associated
with
HCC.Results
Three
modules
closely
related
using
WGCNA.
Nuclear
localization
signal
(NLS)-bearing
protein
import
into
nucleus
biological
process
most
enriched
physiological
identified
by
MCODE,
3
(DICER1,
GMPS
NCOR1)
selected
as
biomarkers.Conclusion
In
our
study,
three
novel
HCC-specific
diagnostic
human
hepatocellular
identified.
These
findings
may
contribute
non-invasive
early
patients.
Scientific Reports,
Journal Year:
2020,
Volume and Issue:
10(1)
Published: March 23, 2020
Abstract
The
liver
is
a
unique
organ
that
has
phenomenal
capacity
to
regenerate
after
injury.
Different
surgical
procedures,
including
partial
hepatectomy
(PH),
intraoperative
portal
vein
ligation
(PVL),
and
associated
partition
for
staged
(ALPPS)
show
clinically
distinct
recovery
patterns
regeneration.
observable
clinical
differences
likely
mirror
some
underlying
variations
in
the
of
gene
activation
regeneration
pathways.
In
this
study,
we
provided
comprehensive
comparative
transcriptomic
analysis
regulation
regenerating
rat
livers
temporally
spaced
at
24
h
96
PH,
PVL,
ALPPS.
time-dependent
factors
appear
be
most
important
determinant
post-injury
alterations
expression
Gene
profile
ALPPS
showed
more
similar
pattern
PH
than
PVL
early
phase
Early
changes
predicted
upstream
regulators
were
found
all
three
procedures
included
cell
cycle
genes
(
E2F1,
CCND1,
FOXM1,
TP53
,
RB1
),
transcription
Myc,
TBX2,
FOXM1
DNA
replication
CDKN1A,
EZH2,
RRM2
G1/S-transition
CCNB1,
RABL6
cytokines
growth
CSF2,
IL-6,
TNF,
HGF,
VEGF
EGF
ATM
p53
signaling
functional
pathway,
upstream,
network
analyses
revealed
both
overlapping
molecular
mechanisms
pathways
each
procedure.
Identification
signatures
regenerative
procedure
further
our
understanding
key
as
well
patient
populations
are
benefit
from
International Journal of Molecular Sciences,
Journal Year:
2020,
Volume and Issue:
21(22), P. 8823 - 8823
Published: Nov. 21, 2020
Kinase
drug
discovery
represents
an
active
area
of
therapeutic
research,
with
previous
pharmaceutical
success
improving
patient
outcomes
across
a
wide
variety
human
diseases.
In
pancreatic
ductal
adenocarcinoma
(PDAC),
innovative
strategies
such
as
kinase
targeting
have
been
unable
to
appreciably
increase
survival.
This
may
be
due,
in
part,
unchecked
desmoplastic
reactions
tumors.
Desmoplastic
stroma
enhances
tumor
development
and
progression
while
simultaneously
restricting
delivery
the
cells
it
protects.
Emerging
evidence
indicates
that
many
pathologic
fibrotic
processes
directly
or
indirectly
supporting
desmoplasia
driven
by
targetable
protein
tyrosine
kinases
Fyn-related
(FRK);
B
lymphoid
(BLK);
hemopoietic
cell
(HCK);
ABL
proto-oncogene
2
(ABL2);
discoidin
domain
receptor
1
(DDR1);
Lck/Yes-related
novel
(LYN);
ephrin
A8
(EPHA8);
FYN
(FYN);
lymphocyte
cell-specific
(LCK);
tec
(TEC).
Herein,
we
review
literature
related
these
posit
signaling
networks,
mechanisms,
biochemical
relationships
which
this
group
contribute
PDAC
growth
desmoplasia.
Bioscience Reports,
Journal Year:
2019,
Volume and Issue:
39(8)
Published: Aug. 1, 2019
Abstract
Aims:
A
large
number
of
studies
have
suggested
that
exportins
(XPOs)
play
a
pivotal
role
in
human
cancers.
In
the
present
study,
we
analyzed
XPO
mRNA
expression
cancer
tissues
and
explored
their
prognostic
value
hepatocellular
carcinoma
(HCC).
Methods:
Transcriptional
survival
data
related
to
HCC
patients
were
obtained
through
ONCOMINE
UALCAN
databases.
Survival
analysis
plots
drawn
with
Gene
Expression
Profiling
Interactive
Analysis
(GEPIA).
Sequence
alteration
for
XPOs
from
The
Cancer
Genome
Atlas
(TCGA)
database
c-BioPortal.
functional
enrichment
analyses
performed
Database
Annotation,
Visualization
Integrated
Discovery
(DAVID).
Results:
Compared
normal
liver
tissues,
significant
overexpression
was
observed
tissues.
There
trend
higher
more
advanced
clinical
stages
lower
differentiated
pathological
grades
HCC.
patients,
high
XPO1,
CSE1L,
XPOT,
XPO4/5/6
poor
overall
(OS),
CSE1L
XPO5/6
correlated
disease-free
(DFS).
main
genetic
alterations
involved
up-regulation,
DNA
amplification
deletion.
General
mutations
remarkably
associated
worse
OS
mostly
affected
pathways
RNA
transport
oocyte
meiosis.
Conclusion:
High
prognosis
patients.
may
be
exploited
as
good
biomarkers
Cold Spring Harbor Perspectives in Biology,
Journal Year:
2021,
Volume and Issue:
14(9), P. a040832 - a040832
Published: Nov. 8, 2021
Roger
Liang1,
Yu-Hsuan
Lin1
and
Hao
Zhu
Children's
Research
Institute,
Departments
of
Pediatrics
Internal
Medicine,
Center
for
Regenerative
Science
University
Texas
Southwestern
Medical
Center,
Dallas,
75390,
USA
Correspondence:
Hao.Zhu{at}utsouthwestern.edu
↵1
These
authors
contributed
equally
to
this
work.