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Extrachromosomal circular DNAs: an extra piece of evidence to depict tumor heterogeneity

The tumor microenvironment (TME) comprises a heterogeneous number and type of cellular and noncellular components that vary in the context of molecular, genomic and epigenomic levels. The genotypic diversity and plasticity within cancer cells are known to be affected by genomic instability and genom...

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Autores principales: Tandon, Ishita, Pal, Roshni, Pal, Jayanta K, Sharma, Nilesh K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609892/
https://www.ncbi.nlm.nih.gov/pubmed/31285839
http://dx.doi.org/10.2144/fsoa-2019-0024
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author Tandon, Ishita
Pal, Roshni
Pal, Jayanta K
Sharma, Nilesh K
author_facet Tandon, Ishita
Pal, Roshni
Pal, Jayanta K
Sharma, Nilesh K
author_sort Tandon, Ishita
collection PubMed
description The tumor microenvironment (TME) comprises a heterogeneous number and type of cellular and noncellular components that vary in the context of molecular, genomic and epigenomic levels. The genotypic diversity and plasticity within cancer cells are known to be affected by genomic instability and genome alterations. Besides genomic instability within the chromosomal linear DNA, an extra factor appears in the form of extrachromosomal circular DNAs (eccDNAs; 2–20 kbp) and microDNAs (200–400 bp). This extra heterogeneity within cancer cells in the form of an abundance of eccDNAs adds another dimension to the expression of procancer players, such as oncoproteins, acting as a driver for cancer cell survival and proliferation. This article reviews research into eccDNAs centering around cancer plasticity and hallmarks, and discusses these facts in light of therapeutics and biomarker development.
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spelling pubmed-66098922019-07-08 Extrachromosomal circular DNAs: an extra piece of evidence to depict tumor heterogeneity Tandon, Ishita Pal, Roshni Pal, Jayanta K Sharma, Nilesh K Future Sci OA Review The tumor microenvironment (TME) comprises a heterogeneous number and type of cellular and noncellular components that vary in the context of molecular, genomic and epigenomic levels. The genotypic diversity and plasticity within cancer cells are known to be affected by genomic instability and genome alterations. Besides genomic instability within the chromosomal linear DNA, an extra factor appears in the form of extrachromosomal circular DNAs (eccDNAs; 2–20 kbp) and microDNAs (200–400 bp). This extra heterogeneity within cancer cells in the form of an abundance of eccDNAs adds another dimension to the expression of procancer players, such as oncoproteins, acting as a driver for cancer cell survival and proliferation. This article reviews research into eccDNAs centering around cancer plasticity and hallmarks, and discusses these facts in light of therapeutics and biomarker development. Future Science Ltd 2019-05-31 /pmc/articles/PMC6609892/ /pubmed/31285839 http://dx.doi.org/10.2144/fsoa-2019-0024 Text en © 2019 Nilesh Kumar Sharma This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Review
Tandon, Ishita
Pal, Roshni
Pal, Jayanta K
Sharma, Nilesh K
Extrachromosomal circular DNAs: an extra piece of evidence to depict tumor heterogeneity
title Extrachromosomal circular DNAs: an extra piece of evidence to depict tumor heterogeneity
title_full Extrachromosomal circular DNAs: an extra piece of evidence to depict tumor heterogeneity
title_fullStr Extrachromosomal circular DNAs: an extra piece of evidence to depict tumor heterogeneity
title_full_unstemmed Extrachromosomal circular DNAs: an extra piece of evidence to depict tumor heterogeneity
title_short Extrachromosomal circular DNAs: an extra piece of evidence to depict tumor heterogeneity
title_sort extrachromosomal circular dnas: an extra piece of evidence to depict tumor heterogeneity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609892/
https://www.ncbi.nlm.nih.gov/pubmed/31285839
http://dx.doi.org/10.2144/fsoa-2019-0024
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