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Carboxypeptidase M in apoptosis, adipogenesis and cancer.
[well-differentiated liposarcoma]
This
review
covers
carboxypeptidase
M
(
CPM
)
research
that
appeared
in
the
literature
since
2009
.
The
focus
is
on
aspects
that
are
new
or
interesting
from
a
clinical
perspective
.
Available
research
tools
are
discussed
as
well
as
their
pitfalls
and
limitations
.
Evidence
is
provided
to
suggest
the
potential
involvement
of
CPM
in
apoptosis
,
adipogenesis
and
cancer
.
This
evidence
derives
from
the
expression
pattern
of
CPM
and
its
putative
substrates
in
cells
and
tissues
.
In
recent
years
CPM
emerged
as
a
potential
cancer
biomarker
,
in
well
differentiated
liposarcoma
where
the
CPM
gene
is
co
-amplified
with
the
oncogene
MDM
2
;
and
in
lung
adenocarcinoma
where
coexpression
with
EGFR
correlates
with
poor
prognosis
.
The
available
data
call
for
extended
investigation
of
the
function
of
CPM
in
tumor
cells
,
tumor
-associated
macrophages
,
stromal
cells
and
tumor
neovascularisation
.
Such
experiments
could
be
instrumental
to
validate
CPM
as
a
therapeutic
target
.
Diseases
Validation
Diseases presenting
"tumor cells"
symptom
alpha-thalassemia
carcinoma of the gallbladder
cholangiocarcinoma
cushing syndrome
dedifferentiated liposarcoma
dentin dysplasia
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
hodgkin lymphoma, classical
junctional epidermolysis bullosa
kindler syndrome
liposarcoma
lymphangioleiomyomatosis
pleomorphic liposarcoma
primary effusion lymphoma
severe combined immunodeficiency
triple a syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
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