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SUN-748 Functional Characterization of Estrogen-Regulated LncRNA16 in ER+ Breast Cancer
Long noncoding RNAs (lncRNAs) have been demonstrated to be involved in diverse cellular processes as important regulators, such as in cancer. However, their roles in breast cancer biology are greatly unknown so far. In our study, integrated analysis of subcellular fractionation RNA-seq with gene exp...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368367/ http://dx.doi.org/10.1210/jendso/bvaa046.1434 |
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author | Yang, Barbara Ramos, Enrique Ivan Choudhari, Ramesh Zilaie, Mina Sanchez-Michael, Laura A Sedano, Melina Gadad, Shrikanth |
author_facet | Yang, Barbara Ramos, Enrique Ivan Choudhari, Ramesh Zilaie, Mina Sanchez-Michael, Laura A Sedano, Melina Gadad, Shrikanth |
author_sort | Yang, Barbara |
collection | PubMed |
description | Long noncoding RNAs (lncRNAs) have been demonstrated to be involved in diverse cellular processes as important regulators, such as in cancer. However, their roles in breast cancer biology are greatly unknown so far. In our study, integrated analysis of subcellular fractionation RNA-seq with gene expression profile from human reproductive tissues yielded a comprehensive catalog of estrogen-regulated reproductive tissue-specific lncRNAs. We selected long intergenic noncoding RNA 16 (LINC16) for further study as it was the top upregulated lncRNA by estrogen and associates with clinical outcome. Analysis of RNA-seq data from different human tissues, we found that LINC16 is highly expressed in testis and followed by other reproductive organs, cervix and uterus. Interestingly, interrogation of expression data from human cancer tissues showed LINC16 is highly expressed in breast cancer compared to other cancers. We have determined the 5’ and 3’ ends of LINC16 and its exon/intron structure, and cloned LINC16 to study its function in molecular and cell-based assays. Our preliminary results suggest that LINC16 plays a critical role in ERα-dependent pathways. |
format | Online Article Text |
id | pubmed-7368367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-73683672020-07-22 SUN-748 Functional Characterization of Estrogen-Regulated LncRNA16 in ER+ Breast Cancer Yang, Barbara Ramos, Enrique Ivan Choudhari, Ramesh Zilaie, Mina Sanchez-Michael, Laura A Sedano, Melina Gadad, Shrikanth J Endocr Soc Steroid Hormones and Receptors Long noncoding RNAs (lncRNAs) have been demonstrated to be involved in diverse cellular processes as important regulators, such as in cancer. However, their roles in breast cancer biology are greatly unknown so far. In our study, integrated analysis of subcellular fractionation RNA-seq with gene expression profile from human reproductive tissues yielded a comprehensive catalog of estrogen-regulated reproductive tissue-specific lncRNAs. We selected long intergenic noncoding RNA 16 (LINC16) for further study as it was the top upregulated lncRNA by estrogen and associates with clinical outcome. Analysis of RNA-seq data from different human tissues, we found that LINC16 is highly expressed in testis and followed by other reproductive organs, cervix and uterus. Interestingly, interrogation of expression data from human cancer tissues showed LINC16 is highly expressed in breast cancer compared to other cancers. We have determined the 5’ and 3’ ends of LINC16 and its exon/intron structure, and cloned LINC16 to study its function in molecular and cell-based assays. Our preliminary results suggest that LINC16 plays a critical role in ERα-dependent pathways. Oxford University Press 2020-05-08 /pmc/articles/PMC7368367/ http://dx.doi.org/10.1210/jendso/bvaa046.1434 Text en © Endocrine Society 2020. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Steroid Hormones and Receptors Yang, Barbara Ramos, Enrique Ivan Choudhari, Ramesh Zilaie, Mina Sanchez-Michael, Laura A Sedano, Melina Gadad, Shrikanth SUN-748 Functional Characterization of Estrogen-Regulated LncRNA16 in ER+ Breast Cancer |
title | SUN-748 Functional Characterization of Estrogen-Regulated LncRNA16 in ER+ Breast Cancer |
title_full | SUN-748 Functional Characterization of Estrogen-Regulated LncRNA16 in ER+ Breast Cancer |
title_fullStr | SUN-748 Functional Characterization of Estrogen-Regulated LncRNA16 in ER+ Breast Cancer |
title_full_unstemmed | SUN-748 Functional Characterization of Estrogen-Regulated LncRNA16 in ER+ Breast Cancer |
title_short | SUN-748 Functional Characterization of Estrogen-Regulated LncRNA16 in ER+ Breast Cancer |
title_sort | sun-748 functional characterization of estrogen-regulated lncrna16 in er+ breast cancer |
topic | Steroid Hormones and Receptors |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368367/ http://dx.doi.org/10.1210/jendso/bvaa046.1434 |
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