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The Barrett‐associated variants at GDF 7 and TBX 5 also increase esophageal adenocarcinoma risk
Barrett's esophagus ( BE ) and esophageal adenocarcinoma ( EAC ) represent two stages within the esophagitis‐metaplasia‐dysplasia‐adenocarcinoma sequence. Previously genetic risk factors have been identified that confer risk to BE and EAC development. However, to which extent the genetic varian...
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Published in: | Cancer medicine (Malden, MA) MA), 2016-05, Vol.5 (5), p.888-891 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Barrett's esophagus (
BE
) and esophageal adenocarcinoma (
EAC
) represent two stages within the esophagitis‐metaplasia‐dysplasia‐adenocarcinoma sequence. Previously genetic risk factors have been identified that confer risk to
BE
and
EAC
development. However, to which extent the genetic variants confer risk to different stages of the
BE
/
EAC
sequence remains mainly unknown. In this study we analyzed three most recently identified
BE
variants at the genes
GDF
7
(rs3072),
TBX
5
(rs2701108), and
ALDH
1A2
(rs3784262) separately in
BE
and
EAC
samples in order to determine their risk effects during
BE
/
EAC
sequence. Our data show that rs3072 at
GDF
7
and rs2701108 at
TBX
5
are also associated with
EAC
and conclude that both loci confer disease risk also at later stages of the
BE
/
EAC
sequence. In contrast, rs3784262 at
ALDH
1A2
was highly significantly associated with
BE
, but showed no association with
EAC
. Our data do not provide evidence that the
ALDH
1A2
locus confers equal risk in early and late stages of
BE
/
EAC
sequence. |
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ISSN: | 2045-7634 2045-7634 |
DOI: | 10.1002/cam4.641 |