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Inherited polymorphisms in hyaluronan synthase 1 predict risk of systemic B-cell malignancies but not of breast cancer.
[waldenström macroglobulinemia]
Genetic
variations
in
the
hyaluronan
synthase
1
gene
(
HAS
1
)
influence
HAS
1
aberrant
splicing
.
HAS
1
is
aberrantly
spliced
in
malignant
cells
from
multiple
myeloma
(
MM
)
and
Waldenstrom
macroglobulinemia
(
WM
)
,
but
not
in
their
counterparts
from
healthy
donors
.
The
presence
of
aberrant
HAS
1
splice
variants
predicts
for
poor
survival
in
multiple
myeloma
(
MM
)
.
We
evaluated
the
influence
of
inherited
HAS
1
single
nucleotide
polymorphisms
(
SNP
)
on
the
risk
of
having
a
systemic
B
cell
malignancy
in
1414
individuals
compromising
832
patients
and
582
healthy
controls
,
including
familial
analysis
of
an
Icelandic
kindred
.
We
sequenced
HAS
1
gene
segments
from
181
patients
with
MM
,
98
with
monoclonal
gammopathy
of
undetermined
significance
(
MGUS
)
,
72
with
Waldenstrom
macroglobulinemia
(
WM
)
,
169
with
chronic
lymphocytic
leukemia
(
CLL
)
,
as
well
as
34
members
of
a
monoclonal
gammopathy-prone
Icelandic
family
,
212
age-matched
healthy
donors
and
a
case-control
cohort
of
295
breast
cancer
patients
with
353
healthy
controls
.
Three
linked
single
nucleotide
polymorphisms
(
SNP
)
in
HAS
1
intron
3
are
significantly
associated
with
B-
cell
malignancies
(
range
p
 
=
 
0
.
007
to
p
 
=
 
10
(
-
5
)
)
,
but
not
MGUS
or
breast
cancer
,
and
predict
risk
in
a
34
member
Icelandic
family
(
p
 
=
 
0
.
005
,
Odds
Ratio
 
=
 
5
.
8
(
OR
)
)
,
a
relatively
homogeneous
cohort
.
In
contrast
,
exon
3
SNPs
were
not
significantly
different
among
the
study
groups
.
Pooled
analyses
showed
a
strong
association
between
the
linked
HAS
1
intron
3
SNPs
and
B-
cell
malignancies
(
OR
 
=
 
1
.
78
)
,
but
not
for
sporadic
MGUS
or
for
breast
cancer
(
OR
<
1
.
0
)
.
The
minor
allele
genotypes
of
HAS
1
SNPs
are
significantly
more
frequent
in
MM
,
WM
,
CLL
and
in
affected
members
of
a
monoclonal
gammopathy-prone
family
than
they
are
in
breast
cancer
,
sporadic
MGUS
or
healthy
donors
.
These
inherited
changes
may
increase
the
risk
for
systemic
B-
cell
malignancies
but
not
for
solid
tumors
.
Diseases
Validation
Diseases presenting
"malignant cells"
symptom
focal myositis
hodgkin lymphoma, classical
oral submucous fibrosis
pleomorphic liposarcoma
severe combined immunodeficiency
systemic capillary leak syndrome
waldenström macroglobulinemia
werner syndrome
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