Journal of the Pakistan Medical Association,
Год журнала:
2023,
Номер
73(4), С. S184 - S190
Опубликована: Май 25, 2023
To
assess
the
serum
expression
levels
of
long
non-coding
ribonucleic
acid
growth
arrest
specific-5
and
micro-ribonucleic
acid-137,
different
genotypes
arrestspecific-5
rs2067079
(C>T)
acid-137
rs1625579
(T>G)
in
acute
ischaemic
stroke
patients.The
case-control
study
was
conducted
at
Cairo
University,
Cairo,
Egypt,
from
January
to
August
2020,
comprised
adult
patients
either
gender
selected
unit
Neurology
Department
Kasr
Alainy
Hospital
University.
Healthy
individuals
matched
for
age
were
enrolled
as
controls.
Quantitative
real-time
polymerase
chain
reaction
used
quantify
genotype
non
coding
lncRNA
using
TaqMan
allelic
discrimination.
Data
analysed
SPSS
22.Of
100
subjects,
50(50%)
patients;
34(68%)
males
16(32%)
females
with
mean
60.4±10.0
years.
The
remaining
controls;
28(56%)
22(44%)
56.9±12.2
years
(p>0.05).
had
more
smokers,
hypertensives
diabetics
than
controls
(p<0.05).
Long
significantly
increased,
while
microribonucleic
reduced
among
patients(p<0.05).
Acute
risk
higher
recessive
model
(homozygous
minor
TT
genotype),
protective
against
(G
allele),
codominant
(GT
dominant
(GT+GG),
over-dominant
genotype)
models
(p<0.05).Long
may
act
novel
genetic
markers
risk.
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(2), С. 842 - 842
Опубликована: Янв. 10, 2024
Cerebral
ischemic
stroke
(CIS)
is
a
severe
cerebral
vascular
event.
This
research
aimed
to
evaluate
the
role
of
single-nucleotide
polymorphisms
(SNPs)
lncRNAs
MIAT
rs2331291
and
H19
rs217727
epigenetic
methylation
in
expression
patterns
serum
lncRNA
CIS
Egyptian
patients.
It
included
80
cases
40
healthy
subjects.
Serum
levels
decreased,
whereas
increased
among
compared
controls.
For
rs2331291,
there
were
significant
differences
genotypic
allelic
frequencies
between
subjects
at
p
=
0.02
0.0001,
respectively.
Our
findings
illustrated
significantly
T/T
genotype
frequency
hypertensive
non-hypertensive
0.004.
However,
gene
C/C
was
not
higher
than
CIS.
The
promoter
patients
level
positively
correlated
with
Receiver
operating
characteristics
(ROC)
analysis
revealed
that
have
high
diagnostic
potential
for
distinguishing
from
ones.
In
conclusion,
MIAT-rs2331291
polymorphism
might
serve
as
novel
indicator
ACS Chemical Neuroscience,
Год журнала:
2022,
Номер
14(1), С. 180 - 194
Опубликована: Дек. 20, 2022
Repaglinide,
a
meglitinide
insulinotropic
antidiabetic,
was
unraveled
as
promising
therapeutic
agent
for
Huntington's
disease
by
targeting
the
neuronal
calcium
sensor
downstream
regulatory
element
antagonist
modulator
(DREAM).
However,
its
mechanistic
profile
in
Parkinson's
(PD)
especially
impact
on
endoplasmic
reticulum
(ER)
stress,
mitophagy,
and
their
interconnections
is
poorly
elucidated.
This
study
first
to
examine
neuroprotective
potential
of
repaglinide
rotenone-induced
PD
rats
exploring
effects
DREAM,
BiP/ATF6/CHOP
ER
stress
pathway,
apoptosis,
mitophagy/autophagy,
oxidative
astrogliosis/microgliosis,
neuroinflammation.
Male
Wistar
were
randomly
assigned
four
groups:
groups
1
2
received
vehicle
or
(0.5
mg/kg/day
p.o).
Groups
3
4
rotenone
(1.5
mg/kg/48
h
s.c)
21
days;
meanwhile,
group
additionally
p.o)
15
days
starting
from
day
11.
Interestingly,
lessened
striatal
apoptosis
evidenced
reduced
caspase-3
levels;
however,
it
augmented
DREAM
mRNA
expression.
Repaglinide
triggered
expression
mitophagy
marker
PINK1
autophagy
protein
beclin1
alleviated
through
escalating
catalase
activity.
In
addition,
halted
astrocyte/microglial
activation
neuroinflammation
striatum
expressed
reducing
glial
fibrillary
acidic
(GFAP)
ionized
calcium-binding
adaptor
(Iba1)
immunostaining
decreasing
interleukin
(IL)-6
IL-1β
levels.
restored
morphological
alterations,
intact
neuron
count,
neurobehavioral
motor
performance
examined
an
open
field,
grip
strength,
footprint
gait
analysis.
Conclusively,
modulates
DREAM-ER
cascade,
increases
inhibits
lessens
activation,
PD.
Scientific Reports,
Год журнала:
2023,
Номер
13(1)
Опубликована: Янв. 2, 2023
Abstract
The
genetic
and
epigenetic
architecture
of
clinical
subclinical
hypothyroidism
remains
unclear.
We
investigated
the
impact
long
noncoding
RNA
(LncRNA)-PAX8-AS1
LAIR-2
variants
on
susceptibility
to
hypothyroidism,
their
influence
LncRNA-PAX8-AS1
expression
potential
as
hypothyroid
biomarkers.
Hundred
patients,
110
95
healthy
controls
were
enrolled.
Gene
analysis
genotyping
performed
by
qPCR.
protein,
a
proinflammatory
mediator,
was
tested
ELISA.
Serum
downregulated,
whereas
mRNA
protein
levels
upregulated
in
patients
compared
controls.
rs4848320
rs1110839
associated
with
increased
risk
hypothyroidism.
Interestingly,
both
SNPs
differential
serum
among
.
rs2287828
elevated
Harboring
T
allele
augmented
while
patients.
rs4848320-rs1110839-rs2287828
TTT,
CTT,
CGT
haplotypes
risk.
Surprisingly,
demonstrated
superior
diagnostic
accuracy
for
turned
out
independent
predictors
multivariate
analysis.
Conclusively,
are
novel
biomarkers
that
could
alter
expression.
profiles
have
effective
prognostic
indicators
Frontiers in Immunology,
Год журнала:
2021,
Номер
12
Опубликована: Дек. 7, 2021
Multiple
sclerosis
(MS),
a
chronic
inflammatory
demyelinating
disease
of
the
central
nervous
system,
is
one
most
common
neurodegenerative
diseases
worldwide.
MS
results
in
serious
neurological
dysfunctions
and
disability.
Disturbances
coding
non-coding
genes
are
key
components
leading
to
neurodegeneration
along
with
environmental
factors.
Long
RNAs
(lncRNAs)
long
molecules
cells
that
take
part
regulation
gene
expression.
Several
studies
have
confirmed
role
lncRNAs
such
as
MS.
In
current
study,
we
performed
systematic
analysis
this
disorder.
total,
53
were
recognized
eligible
for
review.
Of
listed
lncRNAs,
52
upregulated,
37
downregulated,
11
had
no
significant
expression
difference
patients
compared
controls.
We
also
summarized
some
mechanisms
lncRNA
functions
The
emerging
suggests
their
dysregulation
could
trigger
neuronal
death
via
still
unexplored
RNA-based
regulatory
mechanisms.
Evaluation
diagnostic
significance
therapeutic
potential
help
design
novel
treatments
Therapeutic Advances in Chronic Disease,
Год журнала:
2023,
Номер
14
Опубликована: Янв. 1, 2023
Auto-immune
diseases
are
a
form
of
chronic
disorders
in
which
the
immune
system
destroys
body’s
cells
due
to
loss
tolerance
self-antigens.
Systemic
lupus
erythematosus
(SLE),
identified
by
production
autoantibodies
different
body
parts,
is
one
most
well-known
examples
these
diseases.
Although
etiology
SLE
unclear,
disease’s
progression
may
be
affected
genetic
and
environmental
factors.
As
studies
twins
provide
adequate
evidence
for
involvement
SLE,
other
phenomena
such
as
metallization,
histone
modifications,
alterations
expression
noncoding
RNAs
(ncRNAs)
also
indicate
epigenetic
factors
this
disease.
Among
all
alterations,
ncRNAs
appear
have
crucial
contribution
pathogenesis
SLE.
The
ncRNAs’
length
size
divided
into
three
main
classes:
micro
RNAs,
long
(LncRNA),
circular
(circRNAs).
Accumulating
suggests
that
dysregulations
contributed
Hence,
clarifying
function
groups
pathophysiology
provides
deeper
understanding
It
opens
up
new
opportunities
develop
targeted
therapies
Molecular Medicine,
Год журнала:
2020,
Номер
26(1)
Опубликована: Окт. 1, 2020
Current
blood-based
tests
for
rheumatoid
arthritis
(RA)
have
inherent
limitations,
necessitating
the
need
additional
new
biomarkers
its
diagnosis
and
monitoring
disease
activity
responsiveness
to
therapy.
MicroRNAs
(miRNAs)
a
proliferation-inducing
ligand
(APRIL)
are
deregulated
in
RA
were
linked
pathogenesis.
This
study
investigated
serum
levels
of
APRIL,
miR-223
miR-155
patients,
their
potential
as
diagnostic
prognostic
biomarkers,
correlation
with
clinicopathological
data.One
hundred
twenty
Egyptian
patients
130
healthy
controls
included.
Serum
miRNAs
APRIL
assayed
by
RT-qPCR
ELISA,
respectively.Serum
significantly
upregulated,
while
was
unchanged
compared
controls.
discriminated
from
AUC
=
0.85,
whereas
superiorly
distinguished
two
groups
1
(sensitivity
specificity
100%
at
cutoff>
4.19
ng/ml)
receiver-operating-characteristic
analysis.
significant
predictor
multivariate
logistic
regression
In
group,
positively
correlated
score
(DAS28-CRP).
expression
miR-155,
presence
subcutaneous
nodules.
antinuclear
antibody
titer
reverse
direction.Our
results
suggest
could
serve
RA,
risk
an
excellent
biomarker
activity.
Our
data
be
implicated
accurate
non-invasive
prognosis
RA.
Journal of Clinical Laboratory Analysis,
Год журнала:
2021,
Номер
35(10)
Опубликована: Сен. 2, 2021
Long
non-coding
RNA
growth
arrest-specific
5
(lnc-GAS5)
and
its
targets
(microRNA
[miR]-21
miR-140)
are
involved
in
the
development
progression
of
allergic
rhinitis
(AR).
However,
correlation
lnc-GAS5
with
miR-21
miR-140
their
associations
disease
risk,
symptom
severity,
Th1/Th2
cytokines
AR
remain
unclear.
Thus,
this
study
aimed
to
investigate
topic.In
total,
120
patients
60
controls
were
recruited.
Nasal-mucosa
tissues
collected
from
all
participants.
Lnc-GAS5,
(miR-21
miR-140),
interferon
(IFN)-γ,
interleukin
(IL)-2,
IL-4,
IL-10
detected
by
reverse-transcription
quantitative
polymerase
chain
reaction.Lnc-GAS5
was
elevated,
while
downregulated
than
(p
<
0.001).
In
patients,
negatively
correlated
0.001),
IFN-γ
=
0.019),
IL-2
0.039)
positively
IL-4
0.004)
individual
nasal
scores
(INSSs)
for
itching,
sneezing,
congestion
0.05),
total
score
(TNSS)
Moreover,
some
INSSs,
TNSS
score,
0.05).Lnc-GAS5
is
that
AR;
meanwhile,
lnc-GAS5,
miR-21,
imbalance
AR,
suggesting
potential
these
biomarkers
AR.
Frontiers in Genetics,
Год журнала:
2022,
Номер
13
Опубликована: Окт. 17, 2022
Slow-burning
inflammation
at
the
lesion
rim
is
connected
to
expansion
of
chronic
multiple
sclerosis
(MS)
lesions.
However,
underlying
processes
causing
are
not
clearly
realized.
In
this
context,
current
study
used
a
bioinformatics
approach
identify
expression
profiles
and
related
lncRNA-associated
ceRNA
regulatory
axes
in
periplaque
region
MS
patients.
Expression
data
(GSE52139)
from
regions
secondary
progressive
spinal
cord
controls
were
downloaded
Gene
Omnibus
database
(GEO),
which
has
details
on
mRNAs
lncRNAs.
Using
R
software’s
limma
package,
differentially
expressed
lncRNAs
(DElncRNAs)
(DEmRNAs)
found.
The
RNA
interactions
also
found
using
DIANA-LncBase,
miRTarBase,
HMDD
databases.
Pearson
correlation
coefficient
was
determine
whether
there
any
positive
correlations
between
DEmRNAs
DElncRNAs
network.
Finally,
created
based
co-expression
connections
DElncRNA,
miRNA,
DEmRNA.
We
Enrichr
tool
enrich
biological
process,
molecular
function,
pathways
for
DElncRNAs.
A
network
DEmRNAs’
protein-protein
developed,
top
five
hub
genes
Cytoscape
STRING.
indicates
that
15
DEmRNAs,
including
FOS
,
GJA1
NTRK2
CTNND1
SP3
Additionally,
four
(such
as
TUG1
ASB16-AS1
LINC01094
)
regulated
aforementioned
by
sponging
14
MS-related
miRNAs
(e.g.,
hsa-miR-145-5p
hsa-miR-200a-3p
hsa-miR-20a-5p
hsa-miR-22-3p
hsa-miR-23a-3p
hsa-miR-27a-3p
hsa-miR-29b-3p
hsa-miR-29c-3p
hsa-miR-34a-5p
addition,
analysis
pathway
enrichment
revealed
enriched
“MAPK
signaling
pathway”,
“Kaposi
sarcoma-associated
herpesvirus
infection”,
“Human
immunodeficiency
virus
one
“Lipid
atherosclerosis”,
“Amphetamine
addiction”.
Even
though
function
these
needs
be
investigated
further,
provides
research
targets
studying
ceRNA-mediated
mechanisms
demyelination
MS.
Frontiers in Genetics,
Год журнала:
2024,
Номер
15
Опубликована: Май 15, 2024
Currently,
an
increasing
body
of
research
suggests
that
blood-based
long
non-coding
RNAs
(lncRNAs)
could
serve
as
biomarkers
for
diagnosing
multiple
sclerosis
(MS).
This
meta-analysis
evaluates
the
diagnostic
capabilities
selected
lncRNAs
in
distinguishing
individuals
with
MS
from
healthy
controls
and
differentiating
between
relapsing
remitting
phases
disease.
Non-coding RNA Research,
Год журнала:
2024,
Номер
9(4), С. 995 - 1008
Опубликована: Июнь 13, 2024
To
date,
the
epigenetic
signature
of
preeclampsia
(PE)
is
not
completely
deciphered.
Oxidative
stress-responsive
long
non-coding
RNAs
(lncRNAs)
are
deregulated
in
preeclamptic
placenta;
however,
their
circulating
profiles
and
diagnostic
abilities
still
unexplored.
We
investigated
serum
redox-sensitive
lncRNAs
TUG1,
H19,
NEAT1,
target
miR-29b/cystine/neutral/dibasic
amino
acids
transporter
solute
carrier
family
3,
member
1
(SLC3A1)
as
potential
non-invasive
biomarkers
PE
risk,
onset,
severity.
recruited
82
patients
with
78
healthy
pregnant
women.
classified
into
early-onset
(EOPE)
late-onset
(LOPE)
subgroups
at
a
cut-off
34
gestational
weeks
severe
mild
by
blood
pressure
proteinuria
criteria.
Bioinformatics
analysis
was
employed
to
select
lncRNAs/microRNA/target
gene
interactions.
Serum
SLC3A1
mRNA
expression
were
reduced,
meanwhile
miR-29b
levels
elevated,
whereas
there
no
significant
difference
TUG1
between
pregnancies.
H19
lower,
higher
EOPE
versus
LOPE.
PE.
ROC
identified
miR-29b,
markers,
(AUC
=
0.818,
95%CI
0.744–0.894)
0.82,
0.755–0.885)
superior
discriminators.
Only
discriminated
cases.
In
multivariate
logistic
analysis,
associated
EOPE,
using
maternal
age
covariates,
while
PE,
covariate.
Studied
markers
correlated
clinical
ultrasound
data
overall
group.
negatively
albuminuria
LOPE,
respectively.
NEAT1
EOPE.
Likewise,
showed
correlations
Conclusively,
this
study
configures
novel
biomarker
advocates