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Targeting VEGF and interleukin-6 for controlling malignant effusion of primary effusion lymphoma.
[primary effusion lymphoma]
Primary
effusion
lymphoma
(
PEL
)
is
an
aggressive
subtype
of
non-
Hodgkin
lymphoma
that
shows
malignant
effusion
most
commonly
seen
in
advanced
AIDS
patients
.
In
this
study
,
we
clarified
the
potential
role
of
VEGF
and
IL
-
6
in
PEL
fluid
retention
and
evaluated
the
efficacy
of
humanized
anti-
VEGF
monoclonal
antibody
(
mAb
)
,
bevacizumab
,
and
humanized
anti-
IL
-
6
receptor
mAb
,
tocilizumab
,
against
PEL
.
T
he
production
of
VEGF
and
IL
-
6
,
and
the
expression
of
IL
-
6
R
α
in
PEL
cell
lines
were
examined
.
The
antiproliferative
effect
of
bevacizumab
and
tocilizumab
on
PEL
cells
was
evaluated
in
vitro
.
The
effect
of
tocilizumab
on
VEGF
was
also
examined
.
An
intraperitoneal
xenograft
mouse
model
was
used
for
in
vivo
efficacy
.
Although
we
found
the
production
of
VEGF
and
IL
-
6
,
and
the
expression
of
IL
-
6
R
α
in
PEL
cell
lines
,
bevacizumab
and
tocilizumab
did
not
inhibit
the
proliferation
of
PEL
cells
in
vitro
.
Tocilizumab
decreased
VEGF
mRNA
and
VEGF
production
by
inhibiting
Stat
3
phosphorylation
and
Stat
3
binding
to
VEGF
promoter
.
In
a
PEL
xenograft
mouse
model
that
showed
profuse
ascites
,
bevacizumab
suppressed
ascites
formation
completely
,
indicating
the
critical
role
of
VEGF
for
PEL
fluid
retention
.
Tocilizumab
also
significantly
inhibited
ascites
formation
in
vivo
.
Moreover
,
these
mAbs
improved
the
overall
survival
of
treated
mice
.
IL
-
6
-
VEGF
axis
contributed
to
fluid
retention
,
and
bevacizumab
and
tocilizumab
could
be
effective
molecular
targeting
therapies
for
PEL
.
Diseases
Validation
Diseases presenting
"the critical role of vegf for pel fluid retention"
symptom
primary effusion lymphoma
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