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miR-17-92 cluster promotes cholangiocarcinoma growth: evidence for PTEN as downstream target and IL-6/Stat3 as upstream activator.
[severe combined immunodeficiency]
miR-
17
-
92
is
an
oncogenic
miRNA
cluster
implicated
in
the
development
of
several
cancers
;
however
,
it
remains
unknown
whether
the
miR-
17
-
92
cluster
is
able
to
regulate
cholangiocarcinogenesis
.
This
study
was
designed
to
investigate
the
biological
functions
and
molecular
mechanisms
of
the
miR-
17
-
92
cluster
in
cholangiocarcinoma
.
In
situ
hybridization
and
quantitative
RT-PCR
analysis
showed
that
the
miR-
17
-
92
cluster
is
highly
expressed
in
human
cholangiocarcinoma
cells
compared
with
the
nonneoplastic
biliary
epithelial
cells
.
Forced
overexpression
of
the
miR-
17
-
92
cluster
or
its
members
,
miR-
92
a
and
miR-
19
a
,
in
cultured
human
cholangiocarcinoma
cells
enhanced
tumor
cell
proliferation
,
colony
formation
,
and
invasiveness
,
in
Â
vitro
.
Overexpression
of
the
miR-
17
-
92
cluster
or
miR-
92
a
also
enhanced
cholangiocarcinoma
growth
in
Â
vivo
in
hairless
outbred
mice
with
severe
combined
immunodeficiency
(
SHO-Prkdc
(
scid
)
Hr
(
hr
)
)
.
The
tumor
-suppressor
,
phosphatase
and
tensin
homolog
deleted
on
chromosome
10
(
PTEN
)
,
was
identified
as
a
bona
fide
target
of
both
miR-
92
a
and
miR-
19
a
in
cholangiocarcinoma
cells
via
sequence
prediction
,
3
'
untranslated
region
luciferase
activity
assay
,
and
Western
blot
analysis
.
Accordingly
,
overexpression
of
the
PTEN
open
reading
frame
protein
(
devoid
of
3
'
untranslated
region
)
prevented
miR-
92
a-
or
miR-
19
a-induced
cholangiocarcinoma
cell
growth
.
Microarray
analysis
revealed
additional
targets
of
the
miR-
17
-
92
cluster
in
human
cholangiocarcinoma
cells
,
including
APAF-
1
and
PRDM
2
.
Moreover
,
we
observed
that
the
expression
of
the
miR-
17
-
92
cluster
is
regulated
by
IL
-
6
/
Stat
3
,
a
key
oncogenic
signaling
pathway
pivotal
in
cholangiocarcinogenesis
.
Taken
together
,
our
findings
disclose
a
novel
IL
-
6
/
Stat
3
-
miR-
17
-
92
cluster-
PTEN
signaling
axis
that
is
crucial
for
cholangiocarcinogenesis
and
tumor
progression
.
Diseases
Validation
Diseases presenting
"tumor progression"
symptom
carcinoma of the gallbladder
cholangiocarcinoma
dedifferentiated liposarcoma
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
hodgkin lymphoma, classical
liposarcoma
pleomorphic liposarcoma
severe combined immunodeficiency
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
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