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The Barrett-associated variants at GDF7 and TBX5 also increase esophageal adenocarcinoma risk.

Authors :
Becker J
May A
Gerges C
Anders M
Schmidt C
Veits L
Noder T
Mayershofer R
Kreuser N
Manner H
Venerito M
Hofer JH
Lyros O
Ahlbrand CJ
Arras M
Hofer S
Heinrichs SK
Weise K
Hess T
Böhmer AC
Kosiol N
Kiesslich R
Izbicki JR
Hölscher AH
Bollschweiler E
Malfertheiner P
Lang H
Moehler M
Lorenz D
Ott K
Schmidt T
Nöthen MM
Hackelsberger A
Schumacher B
Pech O
Vashist Y
Vieth M
Weismüller J
Knapp M
Neuhaus H
Rösch T
Ell C
Gockel I
Schumacher J
Source :
Cancer medicine [Cancer Med] 2016 May; Vol. 5 (5), pp. 888-91. Date of Electronic Publication: 2016 Jan 18.
Publication Year :
2016

Abstract

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 GDF7 (rs3072), TBX5 (rs2701108), and ALDH1A2 (rs3784262) separately in BE and EAC samples in order to determine their risk effects during BE/EAC sequence. Our data show that rs3072 at GDF7 and rs2701108 at TBX5 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 ALDH1A2 was highly significantly associated with BE, but showed no association with EAC. Our data do not provide evidence that the ALDH1A2 locus confers equal risk in early and late stages of BE/EAC sequence.<br /> (© 2016 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
2045-7634
Volume :
5
Issue :
5
Database :
MEDLINE
Journal :
Cancer medicine
Publication Type :
Academic Journal
Accession number :
26783083
Full Text :
https://doi.org/10.1002/cam4.641