BMC Cardiovascular Disorders,
Год журнала:
2024,
Номер
24(1)
Опубликована: Дек. 30, 2024
To
screen
Myocardial
ischemia-reperfusion
Injury
in
mice.
adenosine
monophate-activatedprotein
kinase
(AMPK)
-related
differentially
expressed
circularRNA
(circRNA)
MIRI
model,
Ampk-related
circRNA
network
was
drawn
to
provide
possible
ideas
for
the
prevention
and
treatment
of
MIRI.
Molecular Genetics Microbiology and Virology (Russian),
Год журнала:
2025,
Номер
43(1), С. 24 - 24
Опубликована: Апрель 10, 2025
The
aim.
aim
of
this
work
is
to
evaluate
the
expression
circRNA
circLDLR,
circSPARC,
circSMARCA5
and
circTMEM181,
mediated
targets
which
are
mRNAs
genes
associated
with
atherogenesis.
This
study
may
provide
updated
information
on
involvement
atherogenesis
in
pathogenesis
coronary
heart
disease,
as
well
suggest
possible
prospects
for
their
use
biomarkers
therapeutic
treatment
cardiovascular
diseases.
Material
methods.
included
68
patients
artery
stenosis
41
control
without
atherosclerosis
confirmed
by
angiography.
Using
real-time
PCR,
we
measured
levels
circSMARCA5,
circTMEM181
RNA
preparations
isolated
from
peripheral
blood
mononuclear
cells.
Results
discussion.
An
increase
circSPARC
disease
compared
confirms
pro-atherogenic
effect.
Conclusion.
Has
been
suggested
potential
significance
diagnosis
atherosclerosis.
Current Atherosclerosis Reports,
Год журнала:
2025,
Номер
27(1)
Опубликована: Июнь 3, 2025
Circular
RNAs
(circRNAs),
a
distinct
class
of
long
noncoding
characterized
by
covalently
closed-loop
structures,
have
emerged
as
pivotal
regulators
gene
expression.
Their
stability,
abundance,
and
cell-type
specificity
make
them
increasingly
relevant
in
cardiovascular
disease
pathogenesis
clinical
management.
Atherosclerosis,
chronic
inflammatory
disorder
the
arterial
wall,
underlies
many
cerebrovascular
events,
including
myocardial
infarction
stroke.
This
review
provides
comprehensive
analysis
circRNAs'
influence
on
development
progression
atherosclerotic
plaques.
The
role
circRNAs
atherogenesis,
where
they
may
function
atheroprotective
or
atherogenic
factors
modulating
endothelial
smooth
muscle
cell
functions,
macrophage
activity,
lipid
metabolism,
signaling,
has
recently
emerged.
explores
both
experimental
vivo
findings
functions
specific
their
involvement
cellular
autophagy,
apoptosis,
oxidative
stress,
vascular
remodeling.
Additionally,
diagnostic
potential
circulating
biomarkers
for
plaque
instability
rupture
been
investigated.
Understanding
circRNA-mediated
regulatory
networks
open
new
avenues
precision
diagnostics
targeted
therapies
disease.
Biomedicines,
Год журнала:
2024,
Номер
12(5), С. 1071 - 1071
Опубликована: Май 12, 2024
Hypertension
(HT)
is
a
disease
that
poses
serious
threat
to
human
health,
mediating
organ
damage
such
as
the
cardiovascular
(CV)
system,
kidneys,
central
nervous
system
(CNS),
and
retinae,
ultimately
increasing
risk
of
death
due
entire
vascular
system.
Thus,
widespread
prevalence
hypertension
brings
enormous
health
problems
socioeconomic
burdens
worldwide.
The
goal
management
prevent
hypertension-mediated
excess
mortality
diseases.
To
achieve
this
goal,
guidelines
recommend
accurate
monitoring
blood
pressure
assessment
associated
target
damage.
Early
identification
mediated
by
therefore
crucial.
Plasma
biomarkers
non-invasive
test
can
help
identify
patients
with
who
will
benefit
from
antihypertensive
treatment
optimization
improved
prognosis.
In
review,
we
provide
an
overview
some
currently
available,
under-researched,
potential
plasma
hypertension,
looking
for
be
detected
simple
testing
hypertensive
damage,
which
great
significance
in
clinical
work.
Natriuretic
peptides
(NPs)
utilized
traditional
biomarker
detect
especially
heart
failure.
Nevertheless,
additionally
may
need
combine
two
or
more
monitor
early
stages
hypertension.
BMC Cardiovascular Disorders,
Год журнала:
2024,
Номер
24(1)
Опубликована: Июнь 17, 2024
Abstract
Background
The
role
of
circular
RNAs
(circRNAs)
as
biomarkers
coronary
artery
disease
(CAD)
remains
poorly
explored.
This
study
aimed
to
identify
and
validate
potential
circulating
circRNAs
for
the
diagnosis
CAD.
Methods
expression
profile
associated
with
CAD
was
obtained
from
Gene
Expression
Omnibus
(GEO)
database.
Differential
analysis,
weighted
gene
co-expression
network
analysis
(WGCNA)
least
absolute
shrinkage
selection
operation
(LASSO)
were
employed
CAD-related
hub
circRNAs.
levels
these
validated
using
qRT-PCR
in
blood
samples
100
patients
controls.
diagnostic
performance
evaluated
through
logistic
regression
receiver
operator
characteristic
(ROC)
integrated
discrimination
improvement
(IDI),
net
reclassification
(NRI).
Functional
enrichment
analyses
performed
predict
possible
mechanisms
Results
A
total
ten
identified
WGCNA
LASSO
analysis.
Among
them,
hsa_circ_0069972
hsa_circ_0021509
highly
expressed
patients,
they
independent
predictors
after
adjustment
relevant
confounders.
area
under
ROC
curve
0.760
0.717,
respectively.
classification
improved
incorporation
into
clinical
model
composed
conventional
cardiovascular
risk
factors,
showing
an
IDI
0.131
NRI
0.170
hsa_circ_0069972,
0.111
0.150
hsa_circ_0021509.
revealed
that
hsa_circ_0069972-miRNA-mRNA
enriched
TGF-β
、
FoxO
Hippo
signaling
pathways,
while
hsa_circ_0021509-miRNA-mRNA
PI3K/Akt
MAPK
pathways.
Conclusion
Hsa_circ_0069972
by
are
patients.
They
may
serve
novel
JACC Basic to Translational Science,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 1, 2024
Circular
RNAs
are
associated
with
cardiovascular
disease,
including
coronary
artery
but
the
mechanisms
have
not
been
completely
elucidated.
We
found
a
new
protein,
circBTBD7-420aa,
encoded
by
hsa_circ_0000563.
Our
results
suggest
that
circBTBD7-420aa
may
inhibit
abnormal
proliferation
and
migration
of
human
smooth
muscle
cells
promoting
SLC3A2
degradation
through
ubiquitin-proteasome
pathway.
In
addition,
we
constructed
engineered
exosomes
loaded
can
target
vascular
modifying
peptide
fragments
targeting
osteopontin.
This
study
suggests
progression
atherosclerosis
serve
as
for
diagnosis
treatment
disease.
Journal of Thoracic Disease,
Год журнала:
2023,
Номер
15(11), С. 5971 - 5991
Опубликована: Ноя. 1, 2023
Calcific
aortic
valve
disease
(CAVD)
is
a
common
cardiovascular
with
high
morbidity
and
mortality,
no
effective
prevention
or
treatment
available.
In
recent
years,
increasing
evidence
has
shown
that
noncoding
RNAs
(ncRNAs)
play
an
important
role
in
the
pathogenesis
prognosis
of
CAVD.
Several
associated
circular
(circRNAs)
have
been
reported
to
be
involved
CAVD,
such
as
circRIC3
TGFBR2.
However,
limited
number
circRNAs
identified
CAVD
warrants
further
in-depth
investigation,
comprehensive
elucidation
their
key
mechanisms
this
needed.The
expression
microRNAs
(miRNAs)
were
analyzed
by
RNA
sequencing.
Quantitative
real-time
polymerase
chain
reaction
(qRT-PCR)
was
conducted
analyze
circRNA
ARHGAP10
(circARHGAP10),
miR-335-3p,
RUNX2.
Luciferase
reporter
assay,
pull-down
binding
protein
immunoprecipitation
(RIP)
assay
performed
evaluate
miR-335-3p
circARHGAP10
Alizarin
red
S
staining
showed
formation
calcified
nodules
interstitial
cells
(VICs).
The
altered
through
lentivirus
infection.
Alkaline
phosphatase
(ALP)
activity
used
verify
correlation
between
miR-335-3p.
proteins
assessed
via
Western
blot.
fluorescence
situ
hybridization
(FISH)
confirm
localization
cytoplasm
VICs.
Immunofluorescence
detect
level
ApoE-/-
mice
construct
model,
short
hairpin
(shRNA)
inhibitor
intraperitoneally
injected,
scramble
normal
control
(NC)
injected
controls,
followed
hematoxylin
eosin
(HE)
staining.Through
sequencing,
we
found
(hsa_circ_0008975)
highly
expressed
calcific
valves.
CircARHGAP10
knockdown
effectively
inhibited
extent
osteogenic
differentiation
We
then
competing
endogenous
(ceRNA)
miR-355-3p
targeted
vitro
experiments
confirmed
regulated
VICs
miR-355-3p/RUNX2
pathway,
validated
vivo
using
mouse
model.These
findings
provide
foundation
for
circRNA-directed
diagnostics
therapeutics
Research Square (Research Square),
Год журнала:
2024,
Номер
unknown
Опубликована: Март 21, 2024
AbstractBackground:
The
role
of
circular
RNAs
(circRNAs)
as
biomarkers
coronary
artery
disease
(CAD)
remains
poorly
explored.
The
aim
the
current
study
was
to
identify
and
validate
potential
circulating
circRNA
for
diagnosis
CAD.
Methods:CircRNAs
expression
profile
data
CAD
acquired
from
Gene
Expression
Omnibus
(GEO)
database.
Differential
gene
analysis,
weighted
coexpression
network
analysis
(WGCNA)
least
absolute
shrinkage
selection
operation
(LASSO)
were
used
screen
CAD-related
hub
circRNAs.
levels
circRNAs
further
verified
by
qRT-PCR
in
blood
100
patients
control
individuals.
diagnostic
evaluated
using
logistic
regression
receiver
operator
characteristic
(ROC)
integrated
discrimination
improvement
(IDI),
net
reclassification
(NRI).
Functional
enrichment
performed
predict
possible
mechanisms
Results:Herein,
10
revealed
byWGCNA
Lasso
analysis.
Among
these,
hsa_circ_0069972
hsa_circ_0021509
highly
expressed
samples
patients,
they
identified
independent
predictors
after
adjusting
relevant
confounders.
area
under
ROC
curve
0.760
0.717,
respectively.
classification
improved
with
incorporation
into
clinical
model
composed
conventional
cardiovascular
risk
factors,
showing
an
IDI
0.131
NRI
0.170
hsa_circ_0069972,
0.111
0.150
hsa_circ_0021509.
showed
that
hsa_circ_0069972-miRNA-mRNA
enriched
TGF-β、FoxOHippo
signaling
pathways,
hsa_circ_0021509-miRNA-mRNA
PI3K/AktMAPK
pathways.
Conclusion:
Hsa_circ_0069972
are
patients.
They
may
serve
novel
International Journal of Molecular Medicine,
Год журнала:
2024,
Номер
55(1)
Опубликована: Окт. 31, 2024
Coronary
heart
disease
(CHD)
remains
a
leading
cause
of
morbidity
and
mortality
worldwide,
posing
substantial
public
health
burden.
Despite
advancements
in
treatment,
the
complex
etiology
CHD
necessitates
ongoing
exploration
novel
diagnostic
markers
therapeutic
targets.
Circular
RNAs
(circRNAs),
distinct
class
non‑coding
with
covalently
closed
loop
structure,
have
emerged
as
significant
regulators
various
diseases,
including
CHD.
Their
high
stability,
tissue‑specific
expression
evolutionary
conservation
underscore
their
potential
biomarkers
agents
This
review
discusses
current
knowledge
on
circRNAs
context
explores
molecular
mechanisms
by
which
influence
pathophysiology
CHD,
cardiomyocyte
death,
endothelial
injury,
vascular
dysfunction
inflammation.
It
also
summarizes
emerging
evidence
highlighting
differential
patients
utilities
non‑invasive
prognostic
targets
for
this
disease.