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The expression of the long NEAT1_2 isoform is associated with human epidermal growth factor receptor 2-positive breast cancers
The long non-coding RNA NEAT1 locus is transcribed into two overlapping isoforms, NEAT1_1 and NEAT1_2, of which the latter is essential for the assembly of nuclear paraspeckles. NEAT1 is abnormally expressed in a wide variety of human cancers. Emerging evidence suggests that the two isoforms have di...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987222/ https://www.ncbi.nlm.nih.gov/pubmed/31992741 http://dx.doi.org/10.1038/s41598-020-57759-4 |
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author | Knutsen, Erik Lellahi, Seyed Mohammad Aure, Miriam Ragle Nord, Silje Fismen, Silje Larsen, Kenneth Bowitz Gabriel, Marta Tellez Hedberg, Annica Bjørklund, Sunniva Stordal Bofin, Anna Mary Mælandsmo, Gunhild Mari Sørlie, Therese Mortensen, Elin Synnøve Perander, Maria |
author_facet | Knutsen, Erik Lellahi, Seyed Mohammad Aure, Miriam Ragle Nord, Silje Fismen, Silje Larsen, Kenneth Bowitz Gabriel, Marta Tellez Hedberg, Annica Bjørklund, Sunniva Stordal Bofin, Anna Mary Mælandsmo, Gunhild Mari Sørlie, Therese Mortensen, Elin Synnøve Perander, Maria |
author_sort | Knutsen, Erik |
collection | PubMed |
description | The long non-coding RNA NEAT1 locus is transcribed into two overlapping isoforms, NEAT1_1 and NEAT1_2, of which the latter is essential for the assembly of nuclear paraspeckles. NEAT1 is abnormally expressed in a wide variety of human cancers. Emerging evidence suggests that the two isoforms have distinct functions in gene expression regulation, and recently it was shown that NEAT1_2, but not NEAT1_1, expression predicts poor clinical outcome in cancer. Here, we report that NEAT1_2 expression correlates with HER2-positive breast cancers and high-grade disease. We provide evidence that NEAT1_1 and NEAT1_2 have distinct expression pattern among different intrinsic breast cancer subtypes. Finally, we show that NEAT1_2 expression and paraspeckle formation increase upon lactation in humans, confirming what has previously been demonstrated in mice. |
format | Online Article Text |
id | pubmed-6987222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69872222020-02-03 The expression of the long NEAT1_2 isoform is associated with human epidermal growth factor receptor 2-positive breast cancers Knutsen, Erik Lellahi, Seyed Mohammad Aure, Miriam Ragle Nord, Silje Fismen, Silje Larsen, Kenneth Bowitz Gabriel, Marta Tellez Hedberg, Annica Bjørklund, Sunniva Stordal Bofin, Anna Mary Mælandsmo, Gunhild Mari Sørlie, Therese Mortensen, Elin Synnøve Perander, Maria Sci Rep Article The long non-coding RNA NEAT1 locus is transcribed into two overlapping isoforms, NEAT1_1 and NEAT1_2, of which the latter is essential for the assembly of nuclear paraspeckles. NEAT1 is abnormally expressed in a wide variety of human cancers. Emerging evidence suggests that the two isoforms have distinct functions in gene expression regulation, and recently it was shown that NEAT1_2, but not NEAT1_1, expression predicts poor clinical outcome in cancer. Here, we report that NEAT1_2 expression correlates with HER2-positive breast cancers and high-grade disease. We provide evidence that NEAT1_1 and NEAT1_2 have distinct expression pattern among different intrinsic breast cancer subtypes. Finally, we show that NEAT1_2 expression and paraspeckle formation increase upon lactation in humans, confirming what has previously been demonstrated in mice. Nature Publishing Group UK 2020-01-28 /pmc/articles/PMC6987222/ /pubmed/31992741 http://dx.doi.org/10.1038/s41598-020-57759-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Knutsen, Erik Lellahi, Seyed Mohammad Aure, Miriam Ragle Nord, Silje Fismen, Silje Larsen, Kenneth Bowitz Gabriel, Marta Tellez Hedberg, Annica Bjørklund, Sunniva Stordal Bofin, Anna Mary Mælandsmo, Gunhild Mari Sørlie, Therese Mortensen, Elin Synnøve Perander, Maria The expression of the long NEAT1_2 isoform is associated with human epidermal growth factor receptor 2-positive breast cancers |
title | The expression of the long NEAT1_2 isoform is associated with human epidermal growth factor receptor 2-positive breast cancers |
title_full | The expression of the long NEAT1_2 isoform is associated with human epidermal growth factor receptor 2-positive breast cancers |
title_fullStr | The expression of the long NEAT1_2 isoform is associated with human epidermal growth factor receptor 2-positive breast cancers |
title_full_unstemmed | The expression of the long NEAT1_2 isoform is associated with human epidermal growth factor receptor 2-positive breast cancers |
title_short | The expression of the long NEAT1_2 isoform is associated with human epidermal growth factor receptor 2-positive breast cancers |
title_sort | expression of the long neat1_2 isoform is associated with human epidermal growth factor receptor 2-positive breast cancers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987222/ https://www.ncbi.nlm.nih.gov/pubmed/31992741 http://dx.doi.org/10.1038/s41598-020-57759-4 |
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