SNPs in lncRNA Regions and Breast Cancer Risk

Long non-coding RNAs (lncRNAs) play crucial roles in human physiology, and have been found to be associated with various cancers. Transcribed ultraconserved regions (T-UCRs) are a subgroup of lncRNAs conserved in several species, and are often located in cancer-related regions. Breast cancer is the...

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Published in:Frontiers in genetics Vol. 11; p. 550
Main Authors: Suvanto, Maija, Beesley, Jonathan, Blomqvist, Carl, Chenevix-Trench, Georgia, Khan, Sofia, Nevanlinna, Heli
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 30-06-2020
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Summary:Long non-coding RNAs (lncRNAs) play crucial roles in human physiology, and have been found to be associated with various cancers. Transcribed ultraconserved regions (T-UCRs) are a subgroup of lncRNAs conserved in several species, and are often located in cancer-related regions. Breast cancer is the most common cancer in women worldwide and the leading cause of female cancer deaths. We investigated the association of genetic variants in lncRNA and T-UCR regions with breast cancer risk to uncover candidate loci for further analysis. Our focus was on low-penetrance variants that can be discovered in a large dataset. We selected 565 regions of lncRNAs and T-UCRs that are expressed in breast or breast cancer tissue, or show expression correlation to major breast cancer associated genes. We studied the association of single nucleotide polymorphisms (SNPs) in these regions with breast cancer risk in the 122970 case samples and 105974 controls of the Breast Cancer Association Consortium's genome-wide data, and also by functional analyses using Integrated Expression Quantitative trait and prediction of GWAS targets (INQUISIT) and expression quantitative trait loci (eQTL) analysis. The eQTL analysis was carried out using the METABRIC dataset and analyses from GTEx and ncRNA eQTL databases. We found putative breast cancer risk variants ( < 1 × 10 ) targeting the lncRNA in INQUISIT and eQTL analysis. In addition, putative breast cancer risk associated SNPs ( < 1 × 10 ) in the region of two T-UCRs, uc.184 and uc.313, located in protein coding genes and , respectively, targeted these genes in INQUISIT and in eQTL analysis. Other non-coding regions containing SNPs with the defined p-value and highly significant false discovery rate (FDR) for breast cancer risk association were discovered that may warrant further studies. These results suggest candidate lncRNA loci for further research on breast cancer risk and the molecular mechanisms.
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Edited by: Ashok Sharma, Augusta University, United States
Reviewed by: Francesco Nicassio, Italian Institute of Technology (IIT), Italy; Simranjeet Kaur, Steno Diabetes Center Copenhagen (SDCC), Denmark
This article was submitted to RNA, a section of the journal Frontiers in Genetics
ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2020.00550