» Articles » PMID: 33867825

Extrachromosomal Circular DNAs: Origin, Formation and Emerging Function in Cancer

Overview
Journal Int J Biol Sci
Specialty Biology
Date 2021 Apr 19
PMID 33867825
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

The majority of cellular DNAs in eukaryotes are organized into linear chromosomes. In addition to chromosome DNAs, genes also reside on extrachromosomal elements. The extrachromosomal DNAs are commonly found to be circular, and they are referred to as extrachromosomal circular DNAs (eccDNAs). Recent technological advances have enriched our knowledge of eccDNA biology. There is currently increasing concern about the connection between eccDNA and cancer. Gene amplification on eccDNAs is prevalent in cancer. Moreover, eccDNAs commonly harbor oncogenes or drug resistance genes, hence providing a growth or survival advantage to cancer cells. eccDNAs play an important role in tumor heterogeneity and evolution, facilitating tumor adaptation to challenging circumstances. In addition, eccDNAs have recently been identified as cell-free DNAs in circulating system. The altered level of eccDNAs is observed in cancer patients relative to healthy controls. Particularly, eccDNAs are associated with cancer progression and poor outcomes. Thus, eccDNAs could be useful as novel biomarkers for the diagnosis and prognosis of cancer. In this review, we summarize current knowledge regarding the formation, characteristics and biological importance of eccDNAs, with a focus on the molecular mechanisms associated with their roles in cancer progression. We also discuss their potential applications in the detection and treatment of cancer. A better understanding of the functional role of eccDNAs in cancer would facilitate the comprehensive analysis of molecular mechanisms involved in cancer pathogenesis.

Citing Articles

Global characterization of extrachromosomal circular DNAs in four body fluids.

Jiang L, Song M, Song F, Wang S, Zhou Y, Wang Z Int J Legal Med. 2025; .

PMID: 39945904 DOI: 10.1007/s00414-025-03442-0.


Diverse Genome Structures among Eukaryotes May Have Arisen in Response to Genetic Conflict.

Sterner E, Cote-LHeureux A, Maurer-Alcala X, Katz L Genome Biol Evol. 2024; 16(11).

PMID: 39506510 PMC: 11606643. DOI: 10.1093/gbe/evae239.


Characterization, biogenesis model, and current bioinformatics of human extrachromosomal circular DNA.

Zhou L, Tang W, Ye B, Zou L Front Genet. 2024; 15:1385150.

PMID: 38746056 PMC: 11092383. DOI: 10.3389/fgene.2024.1385150.


Extrachromosomal Circular DNA: An Emerging Potential Biomarker for Inflammatory Bowel Diseases?.

Petito V, Di Vincenzo F, Putignani L, Abreu M, Regenberg B, Gasbarrini A Genes (Basel). 2024; 15(4).

PMID: 38674347 PMC: 11049804. DOI: 10.3390/genes15040414.


Categorizing Extrachromosomal Circular DNA as Biomarkers in Serum of Cancer.

Deng E, Fan X Biomolecules. 2024; 14(4).

PMID: 38672504 PMC: 11048305. DOI: 10.3390/biom14040488.


References
1.
Libuda D, Winston F . Amplification of histone genes by circular chromosome formation in Saccharomyces cerevisiae. Nature. 2006; 443(7114):1003-7. PMC: 3365550. DOI: 10.1038/nature05205. View

2.
Weerts M, Sieuwerts A, Smid M, Look M, Foekens J, Sleijfer S . Mitochondrial DNA content in breast cancer: Impact on in vitro and in vivo phenotype and patient prognosis. Oncotarget. 2016; 7(20):29166-76. PMC: 5045386. DOI: 10.18632/oncotarget.8688. View

3.
Marques P, Amaral S, Pires D, Nogueira L, Soriani F, Lima B . Chemokines and mitochondrial products activate neutrophils to amplify organ injury during mouse acute liver failure. Hepatology. 2012; 56(5):1971-82. DOI: 10.1002/hep.25801. View

4.
Korbel J, Campbell P . Criteria for inference of chromothripsis in cancer genomes. Cell. 2013; 152(6):1226-36. DOI: 10.1016/j.cell.2013.02.023. View

5.
Sen S, Rani S, Freireich E, Hewitt R, Stass S . Detection of extrachromosomal circular DNA sequences from tumor cells by an alkaline lysis, Alu-polymerase chain reaction technique. Mol Carcinog. 1992; 5(2):107-10. DOI: 10.1002/mc.2940050205. View