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Systemically circulating viral and tumor-derived microRNAs in KSHV-associated malignancies.
[primary effusion lymphoma]
MicroRNAs
(
miRNAs
)
are
stable
,
small
non-coding
RNAs
that
modulate
many
downstream
target
genes
.
Recently
,
circulating
miRNAs
have
been
detected
in
various
body
fluids
and
within
exosomes
,
prompting
their
evaluation
as
candidate
biomarkers
of
diseases
,
especially
cancer
.
Kaposi
's
sarcoma
(
KS
)
is
the
most
common
AIDS-associated
cancer
and
remains
prevalent
despite
Highly
Active
Anti-
Retroviral
Therapy
(
HAART
)
.
KS
is
caused
by
KS
-associated
herpesvirus
(
KSHV
)
,
a
gamma
herpesvirus
also
associated
with
Primary
Effusion
Lymphoma
(
PEL
)
.
We
sought
to
determine
the
host
and
viral
circulating
miRNAs
in
plasma
,
pleural
fluid
or
serum
from
patients
with
the
KSHV-associated
malignancies
KS
and
PEL
and
from
two
mouse
models
of
KS
.
Both
KSHV-encoded
miRNAs
and
host
miRNAs
,
including
members
of
the
miR-
17
-
92
cluster
,
were
detectable
within
patient
exosomes
and
circulating
miRNA
profiles
from
KSHV
mouse
models
.
Further
characterization
revealed
a
subset
of
miRNAs
that
seemed
to
be
preferentially
incorporated
into
exosomes
.
Gene
ontology
analysis
of
signature
exosomal
miRNA
targets
revealed
several
signaling
pathways
that
are
known
to
be
important
in
KSHV
pathogenesis
.
Functional
analysis
of
endothelial
cells
exposed
to
patient-derived
exosomes
demonstrated
enhanced
cell
migration
and
IL
-
6
secretion
.
This
suggests
that
exosomes
derived
from
KSHV-associated
malignancies
are
functional
and
contain
a
distinct
subset
of
miRNAs
.
These
could
represent
candidate
biomarkers
of
disease
and
may
contribute
to
the
paracrine
phenotypes
that
are
a
characteristic
of
KS
.
Diseases
Validation
Diseases presenting
"especially cancer"
symptom
primary effusion lymphoma
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