Association of the chromodomain helicase DNA‐binding protein 4 (CHD4) missense variation p.D140E with cancer: Potential interaction with smoking. Issue 2 (19th November 2014)
- Record Type:
- Journal Article
- Title:
- Association of the chromodomain helicase DNA‐binding protein 4 (CHD4) missense variation p.D140E with cancer: Potential interaction with smoking. Issue 2 (19th November 2014)
- Main Title:
- Association of the chromodomain helicase DNA‐binding protein 4 (CHD4) missense variation p.D140E with cancer: Potential interaction with smoking
- Authors:
- Yamada, Miki
Sato, Noriko
Ikeda, Shinobu
Arai, Tomio
Sawabe, Motoji
Mori, Seijiro
Yamada, Yoshiji
Muramatsu, Masaaki
Tanaka, Masashi - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Chromodomain helicase DNA‐binding protein 4 (CHD4) plays a pivotal role in chromatin‐remodeling and has been implicated in the development of cancer. The aim of this study is to determine the association of <italic>CHD4</italic> gene variants with cancer. Nine missense single nucleotide variations (SNVs) in <italic>CHD4</italic> were retrieved from genotyping, by an exome‐chip, 2, 343 consecutive autopsy cases, in which the presence or absence of cancer was pathologically reviewed. The association of <italic>CHD4</italic> variants with the presence of cancer and with different types of cancer was determined. Interaction with smoking was also determined. There were 1, 446 patients with cancer and 897 patients without cancer. Of the nine SNVs, eight SNVs were monomorphic, while two nonsynonymous SNVs; rs7479004 (p.D140E) and rs1639122 (p.E139D) were further verified by direct sequencing. The p.D140E was associated with the presence of cancer (adjusted odds ratio [OR], 2.17; 95% confidence interval [CI], 1.37–3.44, <italic>P =</italic> 0.001), but not p.E139D. The effect size was larger in the smokers (adjusted OR, 4.66; 95% CI, 1.82–11.9; <italic>P =</italic>0.001), suggesting that there may be a gene environment interaction. For individual cancer types, p.D140E was associated with lung cancer (adjusted OR, 3.99; 95% CI, 2.07–7.67; <italic>P</italic> &lt; 0.001), malignant lymphoma<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Chromodomain helicase DNA‐binding protein 4 (CHD4) plays a pivotal role in chromatin‐remodeling and has been implicated in the development of cancer. The aim of this study is to determine the association of <italic>CHD4</italic> gene variants with cancer. Nine missense single nucleotide variations (SNVs) in <italic>CHD4</italic> were retrieved from genotyping, by an exome‐chip, 2, 343 consecutive autopsy cases, in which the presence or absence of cancer was pathologically reviewed. The association of <italic>CHD4</italic> variants with the presence of cancer and with different types of cancer was determined. Interaction with smoking was also determined. There were 1, 446 patients with cancer and 897 patients without cancer. Of the nine SNVs, eight SNVs were monomorphic, while two nonsynonymous SNVs; rs7479004 (p.D140E) and rs1639122 (p.E139D) were further verified by direct sequencing. The p.D140E was associated with the presence of cancer (adjusted odds ratio [OR], 2.17; 95% confidence interval [CI], 1.37–3.44, <italic>P =</italic> 0.001), but not p.E139D. The effect size was larger in the smokers (adjusted OR, 4.66; 95% CI, 1.82–11.9; <italic>P =</italic>0.001), suggesting that there may be a gene environment interaction. For individual cancer types, p.D140E was associated with lung cancer (adjusted OR, 3.99; 95% CI, 2.07–7.67; <italic>P</italic> &lt; 0.001), malignant lymphoma (adjusted OR, 3.24; 95% CI, 1.43–7.33; <italic>P =</italic> 0.005), and rectum cancer (adjusted OR, 6.23; 95% CI, 2.31–16.8; <italic>P</italic> &lt; 0.001). A nonsynonymous SNV of <italic>CHD4</italic>, p.D140E, confers a risk of cancer and may interact with smoking habit to increase the risk. © 2014 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Genes, chromosomes & cancer. Volume 54:Issue 2(2015:Feb.)
- Journal:
- Genes, chromosomes & cancer
- Issue:
- Volume 54:Issue 2(2015:Feb.)
- Issue Display:
- Volume 54, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 54
- Issue:
- 2
- Issue Sort Value:
- 2015-0054-0002-0000
- Page Start:
- 122
- Page End:
- 128
- Publication Date:
- 2014-11-19
- Subjects:
- Cancer -- Genetic aspects -- Periodicals
616.994042 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-2264 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/gcc.22227 ↗
- Languages:
- English
- ISSNs:
- 1045-2257
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4111.763000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3397.xml