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Transcriptome and miRNA network analysis of familial hypercholesterolemia.
[wiskott-aldrich syndrome]
Familial
hypercholesterolemia
(
FH
)
is
a
genetic
disorder
characterized
by
a
high
serum
concentration
of
low
-density
lipoprotein
(
LDL
)
cholesterol
.
The
high
LDL
cholesterol
level
leads
to
an
excess
deposition
of
cholesterol
in
the
arterial
walls
and
accelerated
atherosclerosis
,
thereby
increasing
the
risk
of
premature
coronary
heart
disease
.
In
the
present
study
,
we
used
a
DNA
microarray
approach
to
identify
gene
expression
profiles
that
distinguish
patients
with
FH
from
healthy
control
subjects
.
Furthermore
,
transcription
factors
(
TFs
)
,
microRNAs
(
miRNAs
)
,
target
genes
and
pathways
were
analyzed
to
explore
the
potential
transcriptional
interactions
occurring
in
FH
.
Publicly
available
microarray
and
regulation
data
were
used
to
construct
a
regulatory
network
to
identify
additional
genes
related
to
FH
and
their
interactions
.
The
results
revealed
that
specificity
protein
1
(
SP
1
)
,
signal
transducer
and
activator
of
transcription
1
(
STAT
1
)
and
spleen
focus
forming
virus
(
SFFV
)
proviral
integration
oncogene
spi
1
(
SPI
1
)
play
a
central
role
in
the
FH
regulatory
network
.
In
addition
,
the
TF
,
upstream
transcription
factor
2
,
c-fos
interacting
(
USF
2
)
and
the
gene
,
Wiskott-
Aldrich
syndrome
(
WAS
)
,
were
identified
to
be
associated
with
FH
,
although
no
reports
for
these
proteins
exist
in
the
literature
.
Overall
,
transcriptional
network
analysis
proved
to
be
effective
approach
to
identify
novel
targets
for
FH
therapy
.
Diseases
Validation
Diseases presenting
"heart disease"
symptom
22q11.2 deletion syndrome
achondroplasia
acute rheumatic fever
adrenal incidentaloma
child syndrome
classical phenylketonuria
cohen syndrome
congenital diaphragmatic hernia
dentinogenesis imperfecta
esophageal adenocarcinoma
fabry disease
familial mediterranean fever
heparin-induced thrombocytopenia
hirschsprung disease
holt-oram syndrome
homocystinuria without methylmalonic aciduria
kabuki syndrome
monosomy 21
omenn syndrome
phenylketonuria
sneddon syndrome
systemic capillary leak syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
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