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SRC kinase is a novel therapeutic target in lymphangioleiomyomatosis.
[lymphangioleiomyomatosis]
Lymphangioleiomyomatosis
(
LAM
)
is
a
progressive
cystic
lung
disease
affecting
some
women
with
tuberous
sclerosis
complex
(
TSC
)
.
Sporadic
LAM
can
develop
in
women
without
TSC
,
owing
to
somatic
mutations
in
the
TSC
2
gene
.
Accumulating
evidence
supports
the
view
of
LAM
as
a
low
-grade
,
destructive
,
metastasizing
neoplasm
.
The
mechanisms
underlying
the
metastatic
capability
of
LAM
cells
remain
poorly
understood
.
The
observed
behavior
of
LAM
cells
with
respect
to
their
infiltrative
growth
pattern
,
metastatic
potential
,
and
altered
cell
differentiation
bears
similarity
to
cells
undergoing
epithelial-mesenchymal
transition
.
Here
,
we
report
increased
levels
of
active
Src
kinase
in
LAM
lungs
and
in
TSC
2
(
-
/
-
)
cells
,
caused
by
a
reduction
of
autophagy
.
Furthermore
,
increased
Src
kinase
activation
promoted
migration
,
invasion
,
and
inhibition
of
E
-
cadherin
expression
in
TSC
2
(
-
/
-
)
cells
by
upregulating
the
transcription
factor
Snail
.
Notably
,
Src
kinase
inhibitors
reduced
migration
and
invasion
properties
of
TSC
2
(
-
/
-
)
cells
and
attenuated
lung
colonization
of
intravenously
injected
TSC
2
(
-
/
-
)
cells
in
vivo
to
a
greater
extent
than
control
TSC
2
(
+
/
+
)
cells
.
Our
results
reveal
mechanistic
basis
for
the
pathogenicity
of
LAM
cells
and
they
rationalize
Src
kinase
as
a
novel
therapeutic
target
for
treatment
of
LAM
and
TSC
.
Diseases
Validation
Diseases presenting
"neoplasm"
symptom
adrenal incidentaloma
alexander disease
aromatase deficiency
carcinoma of the gallbladder
cholangiocarcinoma
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
erdheim-chester disease
esophageal adenocarcinoma
esophageal carcinoma
familial hypocalciuric hypercalcemia
focal myositis
hodgkin lymphoma, classical
hydrocephalus with stenosis of the aqueduct of sylvius
junctional epidermolysis bullosa
kabuki syndrome
liposarcoma
lymphangioleiomyomatosis
pleomorphic liposarcoma
primary effusion lymphoma
proteus syndrome
pyomyositis
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wolf-hirschhorn syndrome
This symptom has already been validated