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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
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.
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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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