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MicroRNA expression in benign breast tissue and risk of subsequent invasive breast cancer

MicroRNAs are endogenous, small non-coding RNAs that control gene expression by directing their target mRNAs for degradation and/or posttranscriptional repression. Abnormal expression of microRNAs is thought to contribute to the development and progression of cancer. A history of benign breast disea...

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Autores principales: Rohan, Thomas, Ye, Kenny, Wang, Yihong, Glass, Andrew G., Ginsberg, Mindy, Loudig, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809016/
https://www.ncbi.nlm.nih.gov/pubmed/29432432
http://dx.doi.org/10.1371/journal.pone.0191814
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author Rohan, Thomas
Ye, Kenny
Wang, Yihong
Glass, Andrew G.
Ginsberg, Mindy
Loudig, Olivier
author_facet Rohan, Thomas
Ye, Kenny
Wang, Yihong
Glass, Andrew G.
Ginsberg, Mindy
Loudig, Olivier
author_sort Rohan, Thomas
collection PubMed
description MicroRNAs are endogenous, small non-coding RNAs that control gene expression by directing their target mRNAs for degradation and/or posttranscriptional repression. Abnormal expression of microRNAs is thought to contribute to the development and progression of cancer. A history of benign breast disease (BBD) is associated with increased risk of subsequent breast cancer. However, no large-scale study has examined the association between microRNA expression in BBD tissue and risk of subsequent invasive breast cancer (IBC). We conducted discovery and validation case-control studies nested in a cohort of 15,395 women diagnosed with BBD in a large health plan between 1971 and 2006 and followed to mid-2015. Cases were women with BBD who developed subsequent IBC; controls were matched 1:1 to cases on age, age at diagnosis of BBD, and duration of plan membership. The discovery stage (316 case-control pairs) entailed use of the Illumina MicroRNA Expression Profiling Assay (in duplicate) to identify breast cancer-associated microRNAs. MicroRNAs identified at this stage were ranked by the strength of the correlation between Illumina array and quantitative PCR results for 15 case-control pairs. The top ranked 14 microRNAs entered the validation stage (165 case-control pairs) which was conducted using quantitative PCR (in triplicate). In both stages, linear regression was used to evaluate the association between the mean expression level of each microRNA (response variable) and case-control status (independent variable); paired t-tests were also used in the validation stage. None of the 14 validation stage microRNAs was associated with breast cancer risk. The results of this study suggest that microRNA expression in benign breast tissue does not influence the risk of subsequent IBC.
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spelling pubmed-58090162018-02-28 MicroRNA expression in benign breast tissue and risk of subsequent invasive breast cancer Rohan, Thomas Ye, Kenny Wang, Yihong Glass, Andrew G. Ginsberg, Mindy Loudig, Olivier PLoS One Research Article MicroRNAs are endogenous, small non-coding RNAs that control gene expression by directing their target mRNAs for degradation and/or posttranscriptional repression. Abnormal expression of microRNAs is thought to contribute to the development and progression of cancer. A history of benign breast disease (BBD) is associated with increased risk of subsequent breast cancer. However, no large-scale study has examined the association between microRNA expression in BBD tissue and risk of subsequent invasive breast cancer (IBC). We conducted discovery and validation case-control studies nested in a cohort of 15,395 women diagnosed with BBD in a large health plan between 1971 and 2006 and followed to mid-2015. Cases were women with BBD who developed subsequent IBC; controls were matched 1:1 to cases on age, age at diagnosis of BBD, and duration of plan membership. The discovery stage (316 case-control pairs) entailed use of the Illumina MicroRNA Expression Profiling Assay (in duplicate) to identify breast cancer-associated microRNAs. MicroRNAs identified at this stage were ranked by the strength of the correlation between Illumina array and quantitative PCR results for 15 case-control pairs. The top ranked 14 microRNAs entered the validation stage (165 case-control pairs) which was conducted using quantitative PCR (in triplicate). In both stages, linear regression was used to evaluate the association between the mean expression level of each microRNA (response variable) and case-control status (independent variable); paired t-tests were also used in the validation stage. None of the 14 validation stage microRNAs was associated with breast cancer risk. The results of this study suggest that microRNA expression in benign breast tissue does not influence the risk of subsequent IBC. Public Library of Science 2018-02-12 /pmc/articles/PMC5809016/ /pubmed/29432432 http://dx.doi.org/10.1371/journal.pone.0191814 Text en © 2018 Rohan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Rohan, Thomas
Ye, Kenny
Wang, Yihong
Glass, Andrew G.
Ginsberg, Mindy
Loudig, Olivier
MicroRNA expression in benign breast tissue and risk of subsequent invasive breast cancer
title MicroRNA expression in benign breast tissue and risk of subsequent invasive breast cancer
title_full MicroRNA expression in benign breast tissue and risk of subsequent invasive breast cancer
title_fullStr MicroRNA expression in benign breast tissue and risk of subsequent invasive breast cancer
title_full_unstemmed MicroRNA expression in benign breast tissue and risk of subsequent invasive breast cancer
title_short MicroRNA expression in benign breast tissue and risk of subsequent invasive breast cancer
title_sort microrna expression in benign breast tissue and risk of subsequent invasive breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809016/
https://www.ncbi.nlm.nih.gov/pubmed/29432432
http://dx.doi.org/10.1371/journal.pone.0191814
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