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WIP is necessary for matrix invasion by breast cancer cells.
[wiskott-aldrich syndrome]
Actin
filament
assembly
and
reorganisation
during
cell
migration
and
invasion
into
extracellular
matrices
is
a
well-documented
phenomenon
.
Among
actin-binding
proteins
regulating
its
polymerisation
,
the
members
of
the
WASP
(
Wiskott
Aldrich
Syndrome
Protein
)
family
are
generally
thought
to
play
the
most
significant
role
in
supporting
cell
invasiveness
.
In
situ
,
cytosolic
N-WASP
(
neural
WASP
)
is
associated
with
a
partner
protein
termed
WIP
(
WASP
Interacting
Protein
)
that
is
bound
to
the
N-
terminal
domain
of
N-WASP
.
Despite
much
effort
,
rather
little
is
known
about
the
role
of
WIP
in
regulating
N-WASP
and
consequent
actin-filament
assembly
.
Even
less
is
known
about
the
function
of
WIP
within
the
specialised
cell
adhesion
and
attachment
structures
known
as
podosomes
and
invadopodia
.
In
particular
,
whilst
the
interaction
of
WIP
with
known
participants
in
the
development
and
maturation
of
invadopodia
such
as
N-WASP
,
the
Arp
2
/
3
complex
and
cortactin
has
been
described
,
little
is
known
concerning
the
direct
contribution
of
WIP
to
invadopodia
and
its
potential
role
as
a
regulator
of
cancer
cell
invasion
.
In
this
report
,
we
use
2
D
and
3
D
culture
systems
to
describe
the
role
played
by
WIP
in
modulating
the
morphology
and
invasiveness
of
metastatic
breast
cancer
cells
in
vitro
,
as
well
as
its
effect
on
the
process
of
mesenchymal-epithelial
transition
(
MET
)
seen
in
these
cells
.
We
demonstrate
that
WIP
is
necessary
for
invadopodium
formation
and
matrix
degradation
by
basal
breast
cancer
cells
,
but
not
sufficient
to
induce
invasiveness
in
luminal
cells
.
Diseases
Validation
Diseases presenting
"breast cancer"
symptom
acute rheumatic fever
aromatase deficiency
carcinoma of the gallbladder
child syndrome
cowden syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
esophageal squamous cell carcinoma
junctional epidermolysis bullosa
kindler syndrome
liposarcoma
lymphangioleiomyomatosis
oral submucous fibrosis
proteus syndrome
severe combined immunodeficiency
systemic capillary leak syndrome
von hippel-lindau disease
waldenström macroglobulinemia
werner syndrome
wiskott-aldrich syndrome
This symptom has already been validated