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Sangivamycin induces apoptosis by suppressing Erk signaling in primary effusion lymphoma cells.
[primary effusion lymphoma]
Sangivamycin
,
a
structural
analog
of
adenosine
and
antibiotic
exhibiting
antitumor
and
antivirus
activities
,
inhibits
protein
kinase
C
and
the
synthesis
of
both
DNA
and
RNA
.
Primary
effusion
lymphoma
(
PEL
)
is
an
aggressive
neoplasm
caused
by
Kaposi
's
sarcoma
-associated
herpesvirus
(
KSHV
)
in
immunosuppressed
patients
and
HIV-infected
homosexual
males
.
PEL
cells
are
derived
from
post-germinal
center
B
cells
,
and
are
infected
with
KSHV
.
Herein
,
we
asked
if
sangivamycin
might
be
useful
to
treat
PEL
.
We
found
that
sangivamycin
killed
PEL
cells
,
and
we
explored
the
underlying
mechanism
.
Sangivamycin
treatment
drastically
decreased
the
viability
of
PEL
cell
lines
compared
to
KSHV-uninfected
B
lymphoma
cell
lines
.
Sangivamycin
induced
the
apoptosis
of
PEL
cells
by
activating
caspase-
7
and
-
9
.
Further
,
sangivamycin
suppressed
the
phosphorylation
of
Erk
1
/
2
and
Akt
,
thus
inhibiting
activation
of
the
proteins
.
Inhibitors
of
Akt
and
MEK
suppressed
the
proliferation
of
PEL
cells
compared
to
KSHV-uninfected
cells
.
It
is
known
that
activation
of
Erk
and
Akt
signaling
inhibits
apoptosis
and
promotes
proliferation
in
PEL
cells
.
Our
data
therefore
suggest
that
sangivamycin
induces
apoptosis
by
inhibiting
Erk
and
Akt
signaling
in
such
cells
.
We
next
investigated
whether
sangivamycin
,
in
combination
with
an
HSP
90
inhibitor
geldanamycin
(
GA
)
or
valproate
(
valproic
acid
)
,
potentiated
the
cytotoxic
effects
of
the
latter
drugs
on
PEL
cells
.
Compared
to
treatment
with
GA
or
valproate
alone
,
the
addition
of
sangivamycin
enhanced
cytotoxic
activity
.
Our
data
thus
indicate
that
sangivamycin
may
find
clinical
utility
as
a
novel
anti-
cancer
agent
targeting
PEL
.
Diseases
Validation
Diseases presenting
"neoplasm"
symptom
adrenal incidentaloma
alexander disease
aromatase deficiency
carcinoma of the gallbladder
cholangiocarcinoma
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
erdheim-chester disease
esophageal adenocarcinoma
esophageal carcinoma
familial hypocalciuric hypercalcemia
focal myositis
hodgkin lymphoma, classical
hydrocephalus with stenosis of the aqueduct of sylvius
junctional epidermolysis bullosa
kabuki syndrome
liposarcoma
lymphangioleiomyomatosis
pleomorphic liposarcoma
primary effusion lymphoma
proteus syndrome
pyomyositis
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wolf-hirschhorn syndrome
This symptom has already been validated