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Restoration of C/EBPα in dedifferentiated liposarcoma induces G2/M cell cycle arrest and apoptosis.
[dedifferentiated liposarcoma]
Well-differentiated
liposarcoma
(
WDLS
)
and
dedifferentiated
liposarcoma
(
DDLS
)
represent
the
most
common
biological
group
of
liposarcoma
,
and
there
is
a
pressing
need
to
develop
targeted
therapies
for
patients
with
advanced
disease
.
To
identify
potential
therapeutic
targets
,
we
sought
to
identify
differences
in
the
adipogenic
pathways
between
DDLS
,
WDLS
,
and
normal
adipose
tissue
.
In
a
microarray
analysis
of
DDLS
(
n
=
84
)
,
WDLS
(
n
=
79
)
,
and
normal
fat
(
n
=
23
)
,
C
/
EBPα
,
a
transcription
factor
involved
in
cell
cycle
regulation
and
differentiation
,
was
underexpressed
in
DDLS
when
compared
to
both
WDLS
and
normal
fat
(
15
.
2
-
and
27
.
8
-
fold
,
respectively
)
.
In
normal
adipose-derived
stem
cells
,
C
/
EBPα
expression
was
strongly
induced
when
cells
were
cultured
in
differentiation
media
,
but
in
three
DDLS
cell
lines
,
this
induction
was
nearly
absent
.
We
restored
C
/
EBPα
expression
in
one
of
the
cell
lines
(
DDLS
8817
)
by
transfection
of
an
inducible
C
/
EBPα
expression
vector
.
Inducing
C
/
EBPα
expression
reduced
proliferation
and
caused
cells
to
accumulate
in
G
2
/
M
.
Under
differentiation
conditions
,
the
cell
proliferation
was
reduced
further
,
and
66
%
of
the
DDLS
cells
containing
the
inducible
C
/
EBPα
expression
vector
underwent
apoptosis
as
demonstrated
by
annexin
V
staining
.
These
cells
in
differentiation
conditions
expressed
early
adipocyte-
specific
mRNAs
such
as
LPL
and
FABP
4
,
but
they
failed
to
accumulate
intracellular
lipid
droplets
,
a
characteristic
of
mature
adipocytes
.
These
results
demonstrate
that
loss
of
C
/
EBP
α
is
an
important
factor
in
suppressing
apoptosis
and
maintaining
the
dedifferentiated
state
in
DDLS
.
Restoring
C
/
EBPα
may
be
a
useful
therapeutic
approach
for
DDLS
.
Diseases
Validation
Diseases presenting
"normal adipose-derived stem cells"
symptom
dedifferentiated liposarcoma
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