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Glucocorticoid receptor and molecular chaperones in the pathogenesis of adrenal incidentalomas: potential role of reduced sensitivity to glucocorticoids.
[adrenal incidentaloma]
Glucocorticoid
(
GC
)
sensitivity
depends
on
glucocorticoid
receptor
(
GR
)
and
heat
shock
proteins
(
Hsps
)
.
We
investigated
whether
common
GR
genes
(
ER
22
/
23
EK
,
N
363
S
,
Bcl
I
,
and
9
β
)
and
adrenocorticotropin
receptor
promoter
polymorphisms
influence
susceptibility
for
unilateral
adrenal
incidentaloma
(
AI
)
,
plus
GR
and
Hsp
expression
in
tumorous
(
n
=
19
)
,
peritumorous
(
n
=
13
)
and
normal
adrenocortical
(
n
=
11
)
tissues
.
Patients
(
n
=
112
)
,
population-matched
controls
(
n
=
100
)
and
tumor
tissues
(
n
=
32
)
were
genotyped
for
these
polymorphisms
.
Postdexamethasone
serum
cortisol
was
higher
in
patients
(
p
<
0
.
001
)
.
GR
gene
variants
,
larger
allele
of
Bcl
I
(
odds
ratio
[
OR
]
2
.
9
;
95
%
confidence
interval
[
CI
]
1
.
7
-
5
.
1
;
p
<
0
.
001
]
and
minor
allele
of
9
β
(
OR
3
.
0
;
95
%
CI
1
.
6
-
5
.
7
;
p
<
0
.
001
)
were
independent
predictors
of
AI
.
In
patients
,
the
first
allele
is
linked
with
larger
tumors
(
p
=
0
.
002
)
and
the
latter
with
higher
postdexamethasone
cortisol
levels
(
p
=
0
.
025
)
.
Both
allele
carriers
had
lesser
waist
circumference
(
p
=
0
.
02
)
,
similar
adrenocorticotropin
and
higher
basal
(
p
=
0
.
024
)
and
postdexamethasone
cortisol
concentrations
(
p
<
0
.
001
)
.
Tumorous
and
constitutional
genotypes
were
similar
.
GR-D
is
the
major
receptor
isoform
in
normal
adrenal
cortex
by
Western
blotting
.
Loss
of
other
receptor
isoforms
,
decrease
in
immunostaining
for
GR
(
p
<
0
.
0001
)
,
underexpression
of
chaperones
(
p
≤
0
.
01
)
and
the
presence
of
inducible
Hsp
70
were
found
in
adenomas
.
In
conclusion
,
GR
gene
variants
,
C
allele
of
Bcl
I
and
minor
allele
of
9
β
,
are
associated
with
AIs
.
Their
concurrent
presence
in
patients
reduces
GC
sensitivity
.
Normal
adrenal
cortex
preferentially
expresses
GR-D
.
In
adenomas
,
the
lack
of
other
GR
isoforms
and
underexpression
of
heat
shock
proteins
perhaps
permanently
impair
GC
signaling
,
which
could
promote
dysregulated
cortisol
production
and
tumor
growth
.
The
innate
GC
sensitivity
probably
modifies
these
effects
.
Diseases
Validation
Diseases presenting
"tumor tissues"
symptom
adrenal incidentaloma
alpha-thalassemia
cholangiocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
liposarcoma
primary effusion lymphoma
von hippel-lindau disease
wiskott-aldrich syndrome
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