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CREB-induced inflammation is important for malignant mesothelioma growth.
[severe combined immunodeficiency]
Malignant
mesothelioma
(
MM
)
is
an
aggressive
tumor
with
no
treatment
regimen
.
Previously
we
have
demonstrated
that
cyclic
AMP
response
element
binding
protein
(
CREB
)
is
constitutively
activated
in
MM
tumor
cells
and
tissues
and
plays
an
important
role
in
MM
pathogenesis
.
To
understand
the
role
of
CREB
in
MM
tumor
growth
,
we
generated
CREB-inhibited
MM
cell
lines
and
performed
in
Â
vitro
and
in
Â
vivo
experiments
.
In
Â
vitro
experiments
demonstrated
that
CREB
inhibition
results
in
significant
attenuation
of
proliferation
and
drug
resistance
of
MM
cells
.
CREB-silenced
MM
cells
were
then
injected
into
severe
combined
immunodeficiency
mice
,
and
tumor
growth
in
s
.
c
.
and
i
.
p
.
models
of
MM
was
followed
.
We
observed
significant
inhibition
in
MM
tumor
growth
in
both
s
.
c
.
and
i
.
p
.
models
and
the
presence
of
a
chemotherapeutic
drug
,
doxorubicin
,
further
inhibited
MM
tumor
growth
in
the
i
.
p
.
model
.
Peritoneal
lavage
fluids
from
CREB-inhibited
tumor
-bearing
mice
showed
a
significantly
reduced
total
cell
number
,
differential
cell
counts
,
and
pro-
inflammatory
cytokines
and
chemokines
(
IL
-
6
,
IL
-
8
,
regulated
on
activation
normal
T
cell
expressed
and
secreted
,
monocyte
chemotactic
protein-
1
,
and
vascular
endothelial
growth
factor
)
.
In
Â
vitro
studies
showed
that
asbestos-induced
inflammasome
/
inflammation
activation
in
mesothelial
cells
was
CREB
dependent
,
further
supporting
the
role
of
CREB
in
inflammation
-induced
MM
pathogenesis
.
In
conclusion
,
our
data
demonstrate
the
involvement
of
CREB
in
the
regulation
of
MM
pathogenesis
by
regulation
of
inflammation
.
Diseases
Validation
Diseases presenting
"severe combined immunodeficiency"
symptom
achondroplasia
alpha-thalassemia
child syndrome
cholangiocarcinoma
junctional epidermolysis bullosa
krabbe disease
omenn syndrome
severe combined immunodeficiency
wiskott-aldrich syndrome
This symptom has already been validated