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Leiomyosarcoma With Alternative Lengthening of Telomeres Is Associated With Aggressive Histologic Features, Loss of ATRX Expression, and Poor Clinical Outcome.
[alpha-thalassemia]
Leiomyosarcoma
is
an
aggressive
soft
tissue
sarcoma
with
poor
patient
survival
.
Recently
,
it
was
shown
that
53
%
to
62
%
of
leiomyosarcomas
use
the
alternative
lengthening
of
telomeres
(
ALT
)
as
their
telomere
maintenance
mechanism
.
The
molecular
basis
of
this
mechanism
has
not
been
elucidated
.
Studies
of
pancreatic
neuroendocrine
tumor
have
suggested
that
the
inactivation
of
either
α-thalassemia
/
mental
retardation
syndrome
X-
linked
(
ATRX
)
or
death
domain-associated
(
DAXX
)
protein
is
associated
with
the
ALT
phenotype
.
In
this
study
,
we
sought
to
determine
the
clinicopathologic
features
of
leiomyosarcoma
with
the
ALT
phenotype
and
the
possible
relationship
between
this
phenotype
and
ATRX
/
DAXX
expression
.
Telomerase
reverse
transcriptase
gene
(
TERT
)
promoter
mutation
analysis
was
also
performed
.
Ninety
-
two
leiomyosarcomas
derived
from
the
uterus
,
retroperitoneum
/
intra-abdomen
,
and
various
other
sites
were
analyzed
.
Telomere-
specific
fluorescence
in
situ
hybridization
revealed
that
59
%
(
51
/
86
)
of
leiomyosarcomas
had
the
ALT
phenotype
.
Loss
of
ATRX
expression
was
observed
in
33
%
of
the
tumors
(
30
/
92
)
,
and
all
but
2
ATRX
-
deficient
tumors
were
ALT
positive
.
Both
the
ALT
phenotype
and
loss
of
ATRX
expression
were
associated
with
epithelioid
/
pleomorphic
cell
morphology
,
tumor
necrosis
,
and
poor
differentiation
.
None
of
the
92
cases
lost
DAXX
expression
.
No
TERT
promoter
mutation
was
detected
(
n
=
39
)
.
For
survival
analysis
,
poor
differentiation
,
high
FNCLCC
grade
,
tumor
size
,
and
ALT
phenotype
were
correlated
with
poor
overall
survival
in
univariate
analysis
.
Tumor
size
and
ALT
phenotype
remained
independent
prognostic
factors
in
multivariate
analysis
.
We
concluded
that
the
ALT
phenotype
in
the
leiomyosarcoma
is
associated
with
aggressive
histologic
features
,
loss
of
ATRX
expression
,
and
poor
clinical
outcome
.
Diseases
Validation
Diseases presenting
"poor differentiation"
symptom
alpha-thalassemia
carcinoma of the gallbladder
cholangiocarcinoma
dystrophic epidermolysis bullosa
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
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