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KSHV microRNAs mediate cellular transformation and tumorigenesis by redundantly targeting cell growth and survival pathways.
[primary effusion lymphoma]
Kaposi
's
sarcoma
-associated
herpesvirus
(
KSHV
)
is
causally
linked
to
several
human
cancers
,
including
Kaposi
's
sarcoma
,
primary
effusion
lymphoma
and
multicentric
Castleman
's
disease
,
malignancies
commonly
found
in
HIV-infected
patients
.
While
KSHV
encodes
diverse
functional
products
,
its
mechanism
of
oncogenesis
remains
unknown
.
In
this
study
,
we
determined
the
roles
KSHV
microRNAs
(
miRs
)
in
cellular
transformation
and
tumorigenesis
using
a
recently
developed
KSHV-induced
cellular
transformation
system
of
primary
rat
mesenchymal
precursor
cells
.
A
mutant
with
a
cluster
of
10
precursor
miRs
(
pre-mi
Rs
)
deleted
failed
to
transform
primary
cells
,
and
instead
,
caused
cell
cycle
arrest
and
apoptosis
.
Remarkably
,
the
oncogenicity
of
the
mutant
virus
was
fully
restored
by
genetic
complementation
with
the
miR
cluster
or
several
individual
pre-mi
Rs
,
which
rescued
cell
cycle
progression
and
inhibited
apoptosis
in
part
by
redundantly
targeting
IκB
α
and
the
NF-κB
pathway
.
Genomic
analysis
identified
common
targets
of
KSHV
miRs
in
diverse
pathways
with
several
cancer
-related
pathways
preferentially
targeted
.
These
works
define
for
the
first
time
an
essential
viral
determinant
for
KSHV-induced
oncogenesis
and
identify
NF-κB
as
a
critical
pathway
targeted
by
the
viral
miRs
.
Our
results
illustrate
a
common
theme
of
shared
functions
with
hierarchical
order
among
the
KSHV
miRs
.
Diseases
Validation
Diseases presenting
"several human cancers"
symptom
esophageal squamous cell carcinoma
kindler syndrome
primary effusion lymphoma
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