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Regulation of Circular RNA CircNFATC3 in Cancer Cells Alters Proliferation, Migration, and Oxidative Phosphorylation
Circular RNAs were once considered artifacts of transcriptome sequencing but have recently been identified as functionally relevant in different types of cancer. Although there is still no clear main function of circRNAs, several studies have revealed that circRNAs are expressed in various eukaryoti...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017239/ https://www.ncbi.nlm.nih.gov/pubmed/33816459 http://dx.doi.org/10.3389/fcell.2021.595156 |
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author | Karedath, Thasni Al-Dasim, Fatima M. Ahmed, Ikhlak Al-Qurashi, Albandary Raza, Afsheen Andrews, Simeon Scott Ahmed, Ayeda Abdulsalam Ali Mohamoud, Yasmin Dermime, Said Malek, Joel A. |
author_facet | Karedath, Thasni Al-Dasim, Fatima M. Ahmed, Ikhlak Al-Qurashi, Albandary Raza, Afsheen Andrews, Simeon Scott Ahmed, Ayeda Abdulsalam Ali Mohamoud, Yasmin Dermime, Said Malek, Joel A. |
author_sort | Karedath, Thasni |
collection | PubMed |
description | Circular RNAs were once considered artifacts of transcriptome sequencing but have recently been identified as functionally relevant in different types of cancer. Although there is still no clear main function of circRNAs, several studies have revealed that circRNAs are expressed in various eukaryotic organisms in a regulated manner often independent of their parental linear isoforms demonstrating conservation across species. circNFATC3, an abundant and uncharacterized circular RNA of exon 2 and 3 from NFATC3, was identified in transcriptomic data of solid tumors. Here we show that circNFATC3 gain- and loss-of-function experiments using RNAi-mediated circRNA silencing and circular mini vector-mediated overexpression of circularized constructs in breast and ovarian cancer cell lines affect molecular phenotypes. The knockdown of circNFATC3 induces a reduction in cell proliferation, invasion, migration, and oxidative phosphorylation. Gain-of-function of circNFATC3 in MDA-MB-231 and SK-OV-3 cells show a significant increase in cell proliferation, migration, and respiration. The above results suggest that circNFATC3 is a functionally relevant circular RNA in breast and ovarian cancer. |
format | Online Article Text |
id | pubmed-8017239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80172392021-04-03 Regulation of Circular RNA CircNFATC3 in Cancer Cells Alters Proliferation, Migration, and Oxidative Phosphorylation Karedath, Thasni Al-Dasim, Fatima M. Ahmed, Ikhlak Al-Qurashi, Albandary Raza, Afsheen Andrews, Simeon Scott Ahmed, Ayeda Abdulsalam Ali Mohamoud, Yasmin Dermime, Said Malek, Joel A. Front Cell Dev Biol Cell and Developmental Biology Circular RNAs were once considered artifacts of transcriptome sequencing but have recently been identified as functionally relevant in different types of cancer. Although there is still no clear main function of circRNAs, several studies have revealed that circRNAs are expressed in various eukaryotic organisms in a regulated manner often independent of their parental linear isoforms demonstrating conservation across species. circNFATC3, an abundant and uncharacterized circular RNA of exon 2 and 3 from NFATC3, was identified in transcriptomic data of solid tumors. Here we show that circNFATC3 gain- and loss-of-function experiments using RNAi-mediated circRNA silencing and circular mini vector-mediated overexpression of circularized constructs in breast and ovarian cancer cell lines affect molecular phenotypes. The knockdown of circNFATC3 induces a reduction in cell proliferation, invasion, migration, and oxidative phosphorylation. Gain-of-function of circNFATC3 in MDA-MB-231 and SK-OV-3 cells show a significant increase in cell proliferation, migration, and respiration. The above results suggest that circNFATC3 is a functionally relevant circular RNA in breast and ovarian cancer. Frontiers Media S.A. 2021-03-19 /pmc/articles/PMC8017239/ /pubmed/33816459 http://dx.doi.org/10.3389/fcell.2021.595156 Text en Copyright © 2021 Karedath, Al-Dasim, Ahmed, Al-Qurashi, Raza, Andrews, Ahmed, Ali Mohamoud, Dermime and Malek. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Karedath, Thasni Al-Dasim, Fatima M. Ahmed, Ikhlak Al-Qurashi, Albandary Raza, Afsheen Andrews, Simeon Scott Ahmed, Ayeda Abdulsalam Ali Mohamoud, Yasmin Dermime, Said Malek, Joel A. Regulation of Circular RNA CircNFATC3 in Cancer Cells Alters Proliferation, Migration, and Oxidative Phosphorylation |
title | Regulation of Circular RNA CircNFATC3 in Cancer Cells Alters Proliferation, Migration, and Oxidative Phosphorylation |
title_full | Regulation of Circular RNA CircNFATC3 in Cancer Cells Alters Proliferation, Migration, and Oxidative Phosphorylation |
title_fullStr | Regulation of Circular RNA CircNFATC3 in Cancer Cells Alters Proliferation, Migration, and Oxidative Phosphorylation |
title_full_unstemmed | Regulation of Circular RNA CircNFATC3 in Cancer Cells Alters Proliferation, Migration, and Oxidative Phosphorylation |
title_short | Regulation of Circular RNA CircNFATC3 in Cancer Cells Alters Proliferation, Migration, and Oxidative Phosphorylation |
title_sort | regulation of circular rna circnfatc3 in cancer cells alters proliferation, migration, and oxidative phosphorylation |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017239/ https://www.ncbi.nlm.nih.gov/pubmed/33816459 http://dx.doi.org/10.3389/fcell.2021.595156 |
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