Angiogenesis within Atherosclerotic Plaques: Mechanical Regulation, Molecular Mechanism and Clinical Diagnosis
Hanxiao Chen,
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Chih-Yu Peng,
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Fei Fang
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et al.
Mechanobiology in Medicine,
Journal Year:
2025,
Volume and Issue:
unknown, P. 100114 - 100114
Published: Feb. 1, 2025
Language: Английский
Sirtuin 2 inhibitor AGK2 exerts antiviral effects by inducing epigenetic suppression of hepatitis B virus covalently closed circular DNA through recruitment of repressive histone lysine methyltransferases and reduction of cccDNA
Jumi Kim,
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Jiseon Ha,
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Chanho Song
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et al.
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2025,
Volume and Issue:
15
Published: April 9, 2025
Chronic
hepatitis
B
virus
(HBV)
infection
continues
to
be
a
global
health
concern
because
current
treatments
such
as
interferon-α
and
nucleos(t)ide
analogs
cannot
fully
eliminate
the
due
persistence
of
covalently
closed
circular
DNA
(cccDNA)
integrated
HBV
DNA.
Earlier
research
suggests
that
AGK2,
selective
SIRT2
inhibitor,
suppresses
replication
by
modifying
key
signaling
pathways.
This
study
aimed
further
explore
anti-HBV
effects
AKG2,
particularly
its
on
epigenetic
landscape
cccDNA.
HBV-transfected
-infected
cells
were
used
assess
impact
AGK2
viral
replication.
Changes
in
expression
α-tubulin
acetylation
(SDS-PAGE-immunoblotting),
core
particle
formation
(native
agarose
gel
electrophoresis
immunoblotting),
RNA
(northern
blotting)
(Southern
synthesis,
cccDNA
levels
measured.
Chromatin
immunoprecipitation
assays
performed
examine
deposition
transcriptionally
repressive
markers
reduced
SIRT2,
increased
acetylated
levels,
synthesis
Importantly,
also
histone
H4K20me1,
H3K27me3,
H3K9me3
cccDNA,
mediated
lysine
methyltransferases
PR-Set7,
EZH2,
SETDB1,
SUV39H1.
Additionally,
there
was
reduction
recruitment
polymerase
II
H3
indicating
enhances
transcriptional
repression.
through
direct
antiviral
actions,
modulation
using
target
associated
regulators
shows
promise
functional
cure
for
chronic
B.
Language: Английский
Spotlight on the Mechanism of Action of Semaglutide
Current Issues in Molecular Biology,
Journal Year:
2024,
Volume and Issue:
46(12), P. 14514 - 14541
Published: Dec. 23, 2024
Initially
intended
to
control
blood
glucose
levels
in
patients
with
type
2
diabetes,
semaglutide,
a
potent
glucagon-like
peptide
1
analogue,
has
been
established
as
an
effective
weight
loss
treatment
by
controlling
appetite.
Integrating
the
latest
clinical
trials,
semaglutide
or
without
diabetes
presents
significant
therapeutic
efficacy
ameliorating
cardiometabolic
risk
factors
and
physical
functioning,
independent
of
body
reduction.
Semaglutide
may
modulate
adipose
tissue
browning,
which
enhances
human
metabolism
exhibits
possible
benefits
skeletal
muscle
degeneration,
accelerated
obesity
ageing.
This
be
attributed
anti-inflammatory,
mitochondrial
biogenesis,
antioxidant
autophagy-regulating
effects.
However,
most
supporting
evidence
on
mechanistic
actions
is
preclinical,
demonstrated
rodents
not
actually
confirmed
humans,
therefore
warranting
caution
interpretation.
article
aims
explore
potential
innovative
molecular
mechanisms
action
restoring
balance
several
interlinking
aspects
metabolism,
pointing
distinct
functions
inflammation
oxidative
stress
insulin-sensitive
musculoskeletal
tissues.
Moreover,
applications
protection
from
infections
anti-aging
properties
are
discussed.
enhancement
core
involved
progress
although
mostly
provide
framework
for
future
research
diseases
overall.
Language: Английский