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A novel E2F1-regulated lncRNA, LAPAS1, is required for S phase progression and cell proliferation
The transcription factor E2F1 induces both proliferation and apoptosis and is a critical downstream target of the tumor suppressor RB. Long non-coding RNAs (lncRNAs) are major regulators of many cellular processes, including cell cycle progression and cell proliferation. However, the mode of action...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169067/ https://www.ncbi.nlm.nih.gov/pubmed/34084281 http://dx.doi.org/10.18632/oncotarget.27962 |
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author | Baruch, Esther Nizri-Megnaji, Tali Berkowitz, Oron Ginsberg, Doron |
author_facet | Baruch, Esther Nizri-Megnaji, Tali Berkowitz, Oron Ginsberg, Doron |
author_sort | Baruch, Esther |
collection | PubMed |
description | The transcription factor E2F1 induces both proliferation and apoptosis and is a critical downstream target of the tumor suppressor RB. Long non-coding RNAs (lncRNAs) are major regulators of many cellular processes, including cell cycle progression and cell proliferation. However, the mode of action as well as the transcriptional regulation of most lncRNAs are only beginning to be understood. Here, we report that a novel human lncRNA, LAPAS1, is an E2F1- regulated lncRNA that affects S phase progression. Inhibition of LAPAS1 expression increases percentage of S phase cells, and its silencing in synchronized cells delays their progression through S phase. In agreement with its suggested role in cell cycle progression, prolonged inhibition of LAPAS1 attenuates proliferation of human cancer cells. Our data demonstrate that LAPAS1 predominantly functions in trans to repress expression of Sphingolipid Transporter 2 (SPNS2). Importantly, knockdown of SPNS2 rescues the effect of LAPAS1 silencing on cell cycle and cell proliferation. Notably, low levels of LAPAS1 are associated with increased survival of kidney cancer patients. Summarily, we identify LAPAS1 as a novel E2F-regulated lncRNA that has a potential role in human cancer and regulates cell-cycle progression and cell proliferation, at least in part, via regulation of SPNS2. |
format | Online Article Text |
id | pubmed-8169067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-81690672021-06-02 A novel E2F1-regulated lncRNA, LAPAS1, is required for S phase progression and cell proliferation Baruch, Esther Nizri-Megnaji, Tali Berkowitz, Oron Ginsberg, Doron Oncotarget Research Paper The transcription factor E2F1 induces both proliferation and apoptosis and is a critical downstream target of the tumor suppressor RB. Long non-coding RNAs (lncRNAs) are major regulators of many cellular processes, including cell cycle progression and cell proliferation. However, the mode of action as well as the transcriptional regulation of most lncRNAs are only beginning to be understood. Here, we report that a novel human lncRNA, LAPAS1, is an E2F1- regulated lncRNA that affects S phase progression. Inhibition of LAPAS1 expression increases percentage of S phase cells, and its silencing in synchronized cells delays their progression through S phase. In agreement with its suggested role in cell cycle progression, prolonged inhibition of LAPAS1 attenuates proliferation of human cancer cells. Our data demonstrate that LAPAS1 predominantly functions in trans to repress expression of Sphingolipid Transporter 2 (SPNS2). Importantly, knockdown of SPNS2 rescues the effect of LAPAS1 silencing on cell cycle and cell proliferation. Notably, low levels of LAPAS1 are associated with increased survival of kidney cancer patients. Summarily, we identify LAPAS1 as a novel E2F-regulated lncRNA that has a potential role in human cancer and regulates cell-cycle progression and cell proliferation, at least in part, via regulation of SPNS2. Impact Journals LLC 2021-05-25 /pmc/articles/PMC8169067/ /pubmed/34084281 http://dx.doi.org/10.18632/oncotarget.27962 Text en Copyright: © 2021 Baruch et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Baruch, Esther Nizri-Megnaji, Tali Berkowitz, Oron Ginsberg, Doron A novel E2F1-regulated lncRNA, LAPAS1, is required for S phase progression and cell proliferation |
title | A novel E2F1-regulated lncRNA, LAPAS1, is required for S phase progression and cell proliferation |
title_full | A novel E2F1-regulated lncRNA, LAPAS1, is required for S phase progression and cell proliferation |
title_fullStr | A novel E2F1-regulated lncRNA, LAPAS1, is required for S phase progression and cell proliferation |
title_full_unstemmed | A novel E2F1-regulated lncRNA, LAPAS1, is required for S phase progression and cell proliferation |
title_short | A novel E2F1-regulated lncRNA, LAPAS1, is required for S phase progression and cell proliferation |
title_sort | novel e2f1-regulated lncrna, lapas1, is required for s phase progression and cell proliferation |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169067/ https://www.ncbi.nlm.nih.gov/pubmed/34084281 http://dx.doi.org/10.18632/oncotarget.27962 |
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