Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Uracil-DNA glycosylase (UNG) rs246079 G/A polymorphism is associated with decreased risk of esophageal cancer in a Chinese population.
[esophageal squamous cell carcinoma]
Esophageal
cancer
is
the
sixth
leading
cause
of
cancer
-associated
death
worldwide
.
In
addition
to
environmental
risk
factors
,
genetic
factors
might
play
an
important
role
in
esophageal
cancer
carcinogenesis
.
We
conducted
a
hospital-based
case-control
study
to
evaluate
the
association
between
functional
single
nucleotide
polymorphisms
(
SNPs
)
in
uracil-
DNA
glycosylase
(
UNG
)
and
the
development
of
esophageal
cancer
.
A
total
of
380
esophageal
squamous
cell
carcinoma
(
ESCC
)
cases
and
380
controls
were
recruited
for
this
study
.
The
UNG
rs
3219218
A
/
G
and
UNG
rs
246079
G
/
A
genotypes
were
determined
using
matrix-assisted
laser
desorption
/
ionization
time-of-flight
mass
spectrometry
(
MALDI-TOF
MS
)
.
When
the
UNG
rs
246079
GG
homozygote
genotype
was
used
as
the
reference
group
,
the
GA
genotype
was
associated
with
a
significantly
decreased
risk
for
ESCC
(
GA
vs
.
GG
:
adjusted
OR
0
.
67
,
95
%
CI
0
.
49
-
0
.
91
,
P
=
0
.
011
)
;
the
AA
genotype
was
not
associated
with
the
risk
of
ESCC
.
In
stratification
analyses
,
a
significantly
decreased
risk
of
ESCC
associated
with
the
UNG
rs
246079
G
/
A
polymorphism
was
evident
among
women
,
younger
patients
and
never-smokers
and
never-drinkers
.
The
UNG
rs
3219218
A
/
G
polymorphism
was
not
associated
with
the
risk
for
ESCC
.
These
findings
indicated
that
UNG
rs
246079
G
/
A
might
contribute
to
a
decreased
risk
of
ESCC
in
specific
populations
.
Because
of
the
limited
sample
size
,
further
studies
including
a
larger
and
more
diverse
population
,
as
well
as
tissue-
specific
biological
characterization
,
are
required
to
confirm
the
current
findings
.
Diseases
Validation
Diseases presenting
"decreased risk of"
symptom
acute rheumatic fever
esophageal adenocarcinoma
esophageal squamous cell carcinoma
You can validate or delete this automatically detected symptom
Validate the Symptom
Delete the Symptom