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WHSC1 Promotes Oncogenesis through Regulation of NIMA-related-kinase-7 in Squamous Cell Carcinoma of the Head and Neck.
[wolf-hirschhorn syndrome]
Squamous
cell
carcinoma
of
the
head
and
neck
(
SCCHN
)
is
a
relatively
common
malignancy
with
suboptimal
long
-term
prognosis
,
thus
new
treatment
strategies
are
urgently
needed
.
Over
the
last
decade
,
histone
methyltransferases
(
HMTs
)
have
been
recognized
as
promising
targets
for
cancer
therapy
,
but
their
mechanism
of
action
in
most
solid
tumors
,
including
SCCHN
,
remains
to
be
elucidated
.
This
study
investigated
the
role
of
Wolf-
Hirschhorn
syndrome
candidate
1
(
WHSC
1
)
,
a
NSD-family
histone
methyltransferase
,
in
SCCHN
.
Immunohistochemical
(
IHC
)
analysis
of
locoregionally
advanced
SCCHN
,
dysplastic
and
normal
epithelial
tissue
specimens
revealed
that
WHSC
1
expression
and
dimethylation
of
histone
H
3
lysine
36
(
H
3
K
36
me
2
)
were
significantly
higher
in
SCCHN
tissues
compared
with
normal
epithelium
.
Both
WHSC
1
expression
and
H
3
K
36
me
2
levels
were
significantly
correlated
with
histological
grade
.
WHSC
1
knockdown
in
multiple
SCCHN
cell
lines
resulted
in
significant
growth
suppression
,
induction
of
apoptosis
and
delay
of
the
cell
cycle
progression
.
Immunoblot
and
immunocytochemical
analyses
in
SCCHN
cells
demonstrated
that
WHSC
1
induced
H
3
K
36
me
2
and
H
3
K
36
me
3
.
Microarray
expression
profile
analysis
revealed
NIMA
-related-kinase-
7
(
NEK
7
)
to
be
a
downstream
target
gene
of
WHSC
1
,
and
chromatin
immunoprecipitation
(
ChIP
)
assays
showed
that
NEK
7
was
directly
regulated
by
WHSC
1
through
H
3
K
36
me
2
.
Furthermore
,
similar
to
WHSC
1
,
NEK
7
knockdown
significantly
reduced
cell
cycle
progression
,
indicating
that
NEK
7
is
a
key
player
in
the
molecular
pathway
regulated
by
WHSC
1
.
Implications
:
WHSC
1
possesses
oncogenic
functions
in
SCCHN
and
represents
a
potential
molecular
target
for
the
treatment
of
SCCHN
.
Diseases
Validation
Diseases presenting
"relatively common malignancy"
symptom
wolf-hirschhorn syndrome
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