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Weinberg, Clarice R.
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Weitzel, Jeffrey N.
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Wendt, Camilla
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Winqvist, Robert
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Yang, Xiaohong R.
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dc.contributor.author |
Yannoukakos, Drakoulis
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dc.contributor.author |
Ziogas, Argyrios
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dc.contributor.author |
Milne, Roger L.
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dc.contributor.author |
Easton., Douglas F.
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dc.contributor.author |
Chenevix-Trench, Georgia
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dc.contributor.author |
Zheng, Wei
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Kraft, Peter
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dc.contributor.author |
Jiang, Xia
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dc.date.accessioned |
2021-06-02T07:42:32Z |
|
dc.date.available |
2021-06-02T07:42:32Z |
|
dc.date.issued |
2020-07 |
|
dc.description.abstract |
Previous transcriptome-wide association studies (TWAS) have identified breast cancer risk genes
by integrating data from expression quantitative loci and genome-wide association studies
(GWAS), but analyses of breast cancer subtype-specific associations have been limited. In this
study, we conducted a TWAS using gene expression data from GTEx and summary statistics from
the hitherto largest GWAS meta-analysis conducted for breast cancer overall, and by estrogen
receptor subtypes (ER+ and ER−). We further compared associations with ER+ and ER− subtypes,
using a case-only TWAS approach. We also conducted multigene conditional analyses in regions
with multiple TWAS associations. Two genes, STXBP4 and HIST2H2BA, were specifically
associated with ER+ but not with ER− breast cancer. We further identified 30 TWAS-significant
genes associated with overall breast cancer risk, including four that were not identified in previous
studies. Conditional analyses identified single independent breast-cancer gene in three of six
regions harboring multiple TWAS-significant genes. Our study provides new information on breast
cancer genetics and biology, particularly about genomic differences between ER+ and ER− breast
cancer. |
en_ZA |
dc.description.department |
Genetics |
en_ZA |
dc.description.librarian |
pm2021 |
en_ZA |
dc.description.uri |
https://onlinelibrary.wiley.com/journal/10982272 |
en_ZA |
dc.identifier.citation |
Feng, H., Gusev, A., Pasaniuc, B. et al. Transcriptome-wide association study of breast cancer risk by estrogen-receptor status. Genetic Epidemiology 2020;44(5): 442-468. doi:10.1002/gepi.22288. |
en_ZA |
dc.identifier.issn |
0741-0395 (print) |
|
dc.identifier.issn |
1098-2272 (online) |
|
dc.identifier.other |
10.1002/gepi.22288 |
|
dc.identifier.uri |
http://hdl.handle.net/2263/80193 |
|
dc.language.iso |
en |
en_ZA |
dc.publisher |
Wiley |
en_ZA |
dc.rights |
© 2020 The Authors. Genetic Epidemiology published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution License. |
en_ZA |
dc.subject |
Breast cancer subtype |
en_ZA |
dc.subject |
Causal gene |
en_ZA |
dc.subject |
Transcriptome-wide association studies (TWAS) |
en_ZA |
dc.subject |
Genome-wide association studies (GWAS) |
en_ZA |
dc.title |
Transcriptome-wide association study of breast cancer risk by estrogen-receptor status |
en_ZA |
dc.type |
Article |
en_ZA |