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HSP70 inhibition by 2-phenylethynesulfonamide induces lysosomal cathepsin D release and immunogenic cell death in primary effusion lymphoma.
[primary effusion lymphoma]
Heat-shock
protein
(
HSP
)
70
is
aberrantly
expressed
in
different
malignancies
and
has
a
cancer
-
specific
cell-protective
effect
.
As
such
,
it
has
emerged
as
a
promising
target
for
anticancer
therapy
.
In
this
study
,
the
effect
of
the
HSP
70
-
specific
inhibitor
(
PES
)
,
also
Pifitrin-μ
,
on
primary
effusion
lymphoma
(
PEL
)
cell
viability
was
analyzed
.
PES
treatment
induced
a
dose-
and
time-dependent
cytotoxic
effect
in
BC
3
and
BCBL
1
PEL
cells
by
inducing
lysosome
membrane
permeabilization
,
relocation
of
cathepsin
D
in
the
cytosol
,
Bid
cleavage
,
mitochondrial
depolarization
with
release
and
nuclear
translocation
of
apoptosis-activating
factor
.
The
PES-induced
cell
death
in
PEL
cells
was
characterized
by
the
appearance
of
Annexin-
V
/
propidium
iodide
double
-
positive
cells
from
the
early
times
of
treatment
,
indicating
the
occurrence
of
an
additional
type
of
cell
death
other
than
apoptosis
,
which
,
accordingly
,
was
not
efficiently
prevented
by
the
pan-caspase
inhibitor
Z-VAD-fmk
.
Conversely
,
PES-induced
cell
death
was
robustly
reduced
by
pepstatin
A
,
which
inhibits
Bid
and
caspase
8
processing
.
In
addition
,
PES
was
responsible
for
a
block
of
the
autophagic
process
in
PEL
cells
.
Finally
,
we
found
that
PES-induced
cell
death
has
immunogenic
potential
being
able
to
induce
dendritic
cell
activation
.
Diseases
Validation
Diseases presenting
"cancer"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
alpha-thalassemia
benign recurrent intrahepatic cholestasis
cadasil
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
familial hypocalciuric hypercalcemia
familial mediterranean fever
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
hirschsprung disease
hodgkin lymphoma, classical
inclusion body myositis
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
primary effusion lymphoma
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
triple a syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
This symptom has already been validated