Atherosclerosis,
Journal Year:
2023,
Volume and Issue:
374, P. 99 - 106
Published: April 5, 2023
Atherosclerosis
and
numerous
other
cardiovascular
diseases
develop
in
an
age-dependent
manner.
The
endothelial
cells
that
line
the
vessel
walls
play
important
role
development
of
atherosclerosis.
Non-coding
RNA
like
microRNAs
long
non-coding
RNAs
are
known
to
function
implicated
disease
progression.
Here,
we
summarize
several
have
altered
expression
with
aging
discuss
their
cell
senescence.
These
processes
contribute
aging-induced
atherosclerosis
by
targeting
controlling
senescence,
can
potentially
be
attenuated.
Journal of Tissue Engineering,
Journal Year:
2025,
Volume and Issue:
16
Published: Jan. 1, 2025
Endothelial
injury
is
a
key
factor
initiating
in-stent
restenosis
(ISR)
following
peripheral
artery
stent
implantation.
Genetically
modified
endothelial
progenitor
cells
(EPCs)
can
promote
reendothelialization
of
injured
arteries
and
inhibit
neointimal
hyperplasia.
However,
the
role
engineered
EPCs
overexpressing
lncRNA
H19
in
these
processes
remains
unclear.
We
constructed
investigated
their
effects
mechanisms
promoting
inhibiting
hyperplasia
both
vitro
vivo.
Compared
to
normal
control
group,
ISR
patients
exhibited
significant
reduction
circulating
EPCs.
Engineered
promoted
inhibited
arteries.
Exogenous
overexpression
significantly
upregulated
repair-related
gene
S1PR3
EPCs,
while
opposite
was
also
observed.
Additionally,
enhanced
proliferation,
migration,
tube
formation
vitro;
were
lost
with
inhibition.
Binding
sites
for
H3K27
acetylation
identified
on
promoter.
Mechanistically,
we
found
that
directly
interacted
HDAC2,
known
H3K27ac
deacetylase,
disrupting
its
binding
acetylation.
Our
findings
suggest
positively
regulates
expression
by
HDAC2
/
binding,
thereby
Frontiers in Genetics,
Journal Year:
2025,
Volume and Issue:
16
Published: April 7, 2025
Steroid-induced
osteonecrosis
of
the
femoral
head
(SONFH)
is
a
debilitating
condition
linked
to
glucocorticoid-induced
adipogenic
dysregulation
bone
marrow
mesenchymal
stem
cells
(BMSCs).
While
long
noncoding
RNA
H19
has
been
implicated
in
differentiation
disorders
across
pathologies,
its
role
SONFH
remains
undefined.
This
study
investigated
H19's
regulatory
mechanism
progression.
We
observed
significant
upregulation
both
lesions
and
BMSCs
from
patients
compared
controls.
Knockdown
SONFH-derived
suppressed
peroxisome
proliferator-activated
receptor
γ
(PPARγ)
expression,
attenuated
differentiation,
reduced
lipid
accumulation,
as
evidenced
by
decreased
Oil
Red
O
staining
FABP4
levels.
Mechanistically,
acted
competitive
endogenous
(ceRNA)
sponging
miR-130b-3p,
thereby
alleviating
miR-130b-3p-mediated
repression
PPARγ.
Luciferase
assays
confirmed
direct
binding
between
miR-130b-3p
H19/PPARγ,
while
rescue
experiments
demonstrated
that
inhibition
reversed
PPARγ
downregulation
induced
silencing.
Our
findings
reveal
novel
H19/miR-130b-3p/PPARγ
axis
driving
SONFH,
positioning
potential
therapeutic
target.
provides
critical
insights
into
epigenetic
regulation
BMSC
lineage
commitment
pathogenesis,
offering
new
avenues
for
intervention.
Cells,
Journal Year:
2025,
Volume and Issue:
14(7), P. 553 - 553
Published: April 7, 2025
Heart
failure
(HF)
is
a
leading
cause
of
morbidity
and
mortality
worldwide,
representing
complex
clinical
syndrome
in
which
the
heart’s
ability
to
pump
blood
efficiently
impaired.
HF
can
be
subclassified
into
heart
with
reduced
ejection
fraction
(HFrEF)
preserved
(HFpEF),
each
distinct
pathophysiological
mechanisms
varying
levels
severity.
The
progression
significantly
driven
by
cardiac
fibrosis,
pathological
process
extracellular
matrix
undergoes
abnormal
uncontrolled
remodelling.
Cardiac
fibrosis
characterized
excessive
protein
deposition
activation
myofibroblasts,
increasing
stiffness
heart,
thus
disrupting
its
normal
structure
function
promoting
lethal
arrythmia.
MicroRNAs,
long
non-coding
RNAs,
circular
collectively
known
as
RNAs
(ncRNAs),
have
recently
gained
significant
attention
due
growing
body
evidence
suggesting
their
involvement
remodelling
such
fibrosis.
ncRNAs
found
peripheral
blood,
indicating
potential
biomarkers
for
assessing
In
this
review,
we
critically
examine
recent
advancements
findings
related
use
discuss
implication
development.
Journal of Orthopaedic Surgery and Research,
Journal Year:
2025,
Volume and Issue:
20(1)
Published: April 11, 2025
This
study
aimed
to
investigate
the
regulatory
effect
of
linc00963
on
postmenopausal
osteoporosis
and
potential
molecular
mechanisms.
Taking
MC3T3-E1
cells
as
object,
a
cell
cycle
assay
was
used
evaluate
proliferation.
mRNA
levels
Runx2,
OCN,
collagenia-1,
OPG,
RANKL
RANK
were
detected.
Dual
luciferase
reporter
verified
targeting
relationship
between
miR-506-3p.
A
rat
model
established
after
ovariectomy
in
32
Sprague-Dawley
rats.
The
rats
divided
into
sham
group,
OVX
overexpression
blank
plasmid
group.
bone
mineral
density
(BMD)
femur
measured
by
X-ray
densitometer.
Serum
expression
detected
RT-qPCR.
protein
ALP,
BGP
serum
ELISA.
Cell
studies
have
shown
that
alleviates
down-regulating
Animal
showed
compared
with
level,
BMD,
Ca,
P,
LEP,
SOD,
OPG
group
significantly
decreased,
while
body
weight,
BGP,
IL-6,
IL-13,
RANKL,
increased.
Compared
use
can
improve
above
indexes
play
corresponding
therapeutic
menopausal
Linc00963
is
involved
pathogenesis
up-regulating
miR-506-3p
activating
OPG/RANKL/RANK
pathway.
expected
be
target
for
osteoporosis.
International Journal of Biological Macromolecules,
Journal Year:
2025,
Volume and Issue:
310, P. 143309 - 143309
Published: April 17, 2025
Long
non-coding
RNAs
(lncRNAs)
regulate
liquid-liquid
phase
separation
(LLPS),
driving
the
formation
of
biomolecular
condensates
essential
for
cellular
function.
However,
this
regulatory
mechanism
is
yet
to
be
reported
in
skeletal
muscles.
In
study,
we
comprehensively
analyzed
lncRNAs
muscle
across
multiple
pig
breeds,
developmental
stages,
and
tissues.
Our
analysis
identified
over
10,000
novel
lncRNAs.
We
found
that
lnc-regulator
growth
(lnc-RMG)
regulates
myogenesis
by
modulating
LLPS
Meis
homeobox
2
(MEIS2).
Lnc-RMG
was
specifically
expressed
muscle,
with
significantly
higher
expression
fetal
stage
than
embryonic
stage.
Notably,
lnc-RMG
highly
conserved
between
pigs
humans
exhibits
similar
biological
functions
myogenesis.
Furthermore,
knockdown
promoted
regeneration.
Mechanistically,
produces
mature
microRNA
(miR)-133a-3p,
which
targets
inhibits
MEIS2
expression,
thereby
inhibiting
LLPS.
This
inhibition
transcription
transforming
factor-β
receptor
II
(TGFβR2),
ultimately
regulating
Overall,
our
findings
revealed
a
lnc-RMG/miR-133a-3p/MEIS2/TGFβR2
axis
regulated
through
provided
new
insights
into
molecular
mechanisms
drive
development
These
highlight
potential
therapeutic
muscle-related
diseases
strategies
livestock
improvement.
Journal of Clinical Medicine,
Journal Year:
2025,
Volume and Issue:
14(8), P. 2846 - 2846
Published: April 21, 2025
Background/Objectives:
Air
pollution
is
the
highest
environmental
risk
factor
of
mortality
and
morbidity
worldwide,
leading
to
over
4
million
deaths
each
year.
Among
different
air
pollutants,
ultrafine
particles
(UFPs)
constitute
cardiovascular
diseases
(CVDs).
Epidemiological
studies
have
associated
UFPs
with
short-
long-term
imbalance
numerous
blood
markers.
Our
objective
was
systematically
review
short-term
impact
UFP
exposure
on
markers
CVDs.
Methods:
We
prepared
systematic
CVD
meta-analyses
effects
high-sensitivity
C-reactive
protein
(hsCRP)
concentration.
The
eligibility
criteria
were
established
use
Provider,
Enrollment,
Chain,
Ownership
System
(PECOS)
model,
literature
search
conducted
in
Web
Science,
PubMed,
Scopus
databases
from
1
January
2013
9
2025.
bias
(RoB)
according
a
World
Health
Organization
(WHO)
template.
Results:
results
showed
an
increase
hsCRP
as
result
both
UFPs.
Moreover,
IL-6
IL-1β
together
other
inflammatory
increased
after
exposure.
In
addition,
nucleic
acids,
among
which
miR-24-3p
let-7d-5p,
differentially
expressed
(DE)
Chronic
could
lead
persistent
Conclusions:
findings
underline
that
may
development
and/or
worsening
outcomes
fragile
populations
living
air-polluted
areas.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: April 14, 2024
Abstract
Diabetes
mellitus
(DM)
is
a
significant
risk
factor
for
peripheral
arterial
disease
(PAD),
and
PAD
an
independent
predictor
of
cardiovascular
disorders
(CVDs).
Growing
evidence
suggests
that
long
non-coding
RNAs
(lncRNAs)
significantly
contribute
to
development
underlying
complications,
particularly
affecting
smooth
muscle
cells
(SMCs).
So
far,
no
study
has
focused
on
transcriptome
analysis
lncRNAs
in
patients
with
without
DM.
Tissue
samples
were
obtained
from
our
Vascular
Biobank.
Due
the
sample’s
heterogeneity,
expression
whole
tissue
detected
only
ACTA2-AS1
4.9-fold
increase
In
contrast,
transcriptomics
SMCs
revealed
28
differentially
expressed
between
DM
(FDR
<
0.1).
Sixteen
unknown
function,
six
described
cancer,
one
connected
macrophages
polarisation,
four
associated
CVDs,
mainly
SMC
function
phenotypic
switch
(NEAT1,
MIR100HG,
HIF1A-AS3,
MRI29B2CHG).
The
enrichment
additional
H19,
CARMN,
FTX,
MEG3
linked
Our
several
diabetic
physiological
SMCs.
These
might
serve
as
potential
therapeutic
targets
improve
within
diseased
and,
thus,
clinical
outcome.
Advanced Exercise and Health Science,
Journal Year:
2024,
Volume and Issue:
1(2), P. 86 - 98
Published: May 31, 2024
MicroRNAs
(miRs)
are
pivotal
in
regulating
gene
expression
and
orchestrating
adaptive
responses
to
physical
exercise.
This
review
delves
into
the
dynamic
interplay
between
exercise
circulating
muscle-specific
miRs
(myo-miRs),
with
a
specific
focus
on
endurance
resistance
training
modalities.
Endurance
exercise,
involving
moderate
high-intensity
activities,
triggers
acute
sustained
changes
myo-miRs
levels,
mirroring
physiological
adaptations
muscle
tissue.
Conversely,
emphasizing
high-intensity,
short-duration
elicits
diverse
myo-miRs,
particularly
older
individuals.
Moreover,
interventions
exercises
yield
distinct
effects
miR
profiles,
underscoring
relationship
type,
intensity,
duration.
The
potential
of
as
biomarkers
monitor
exercise-induced
mechanisms
behind
their
release
circulation
promising
areas
for
future
research.
Understanding
role
mediating
systemic
could
pave
way
innovative
therapeutic
strategies,
enhancing
function
promoting
overall
health
well-being.