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Gene Amplification and the Extrachromosomal Circular DNA

Oncogene amplification is closely linked to the pathogenesis of a broad spectrum of human malignant tumors. The amplified genes localize either to the extrachromosomal circular DNA, which has been referred to as cytogenetically visible double minutes (DMs), or submicroscopic episome, or to the chrom...

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Detalles Bibliográficos
Autor principal: Shimizu, Noriaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535887/
https://www.ncbi.nlm.nih.gov/pubmed/34680928
http://dx.doi.org/10.3390/genes12101533
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author Shimizu, Noriaki
author_facet Shimizu, Noriaki
author_sort Shimizu, Noriaki
collection PubMed
description Oncogene amplification is closely linked to the pathogenesis of a broad spectrum of human malignant tumors. The amplified genes localize either to the extrachromosomal circular DNA, which has been referred to as cytogenetically visible double minutes (DMs), or submicroscopic episome, or to the chromosomal homogeneously staining region (HSR). The extrachromosomal circle from a chromosome arm can initiate gene amplification, resulting in the formation of DMs or HSR, if it had a sequence element required for replication initiation (the replication initiation region/matrix attachment region; the IR/MAR), under a genetic background that permits gene amplification. In this article, the nature, intracellular behavior, generation, and contribution to cancer genome plasticity of such extrachromosomal circles are summarized and discussed by reviewing recent articles on these topics. Such studies are critical in the understanding and treating human cancer, and also for the production of recombinant proteins such as biopharmaceuticals by increasing the recombinant genes in the cells.
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spelling pubmed-85358872021-10-23 Gene Amplification and the Extrachromosomal Circular DNA Shimizu, Noriaki Genes (Basel) Review Oncogene amplification is closely linked to the pathogenesis of a broad spectrum of human malignant tumors. The amplified genes localize either to the extrachromosomal circular DNA, which has been referred to as cytogenetically visible double minutes (DMs), or submicroscopic episome, or to the chromosomal homogeneously staining region (HSR). The extrachromosomal circle from a chromosome arm can initiate gene amplification, resulting in the formation of DMs or HSR, if it had a sequence element required for replication initiation (the replication initiation region/matrix attachment region; the IR/MAR), under a genetic background that permits gene amplification. In this article, the nature, intracellular behavior, generation, and contribution to cancer genome plasticity of such extrachromosomal circles are summarized and discussed by reviewing recent articles on these topics. Such studies are critical in the understanding and treating human cancer, and also for the production of recombinant proteins such as biopharmaceuticals by increasing the recombinant genes in the cells. MDPI 2021-09-28 /pmc/articles/PMC8535887/ /pubmed/34680928 http://dx.doi.org/10.3390/genes12101533 Text en © 2021 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Shimizu, Noriaki
Gene Amplification and the Extrachromosomal Circular DNA
title Gene Amplification and the Extrachromosomal Circular DNA
title_full Gene Amplification and the Extrachromosomal Circular DNA
title_fullStr Gene Amplification and the Extrachromosomal Circular DNA
title_full_unstemmed Gene Amplification and the Extrachromosomal Circular DNA
title_short Gene Amplification and the Extrachromosomal Circular DNA
title_sort gene amplification and the extrachromosomal circular dna
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535887/
https://www.ncbi.nlm.nih.gov/pubmed/34680928
http://dx.doi.org/10.3390/genes12101533
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