Innovative insights into extrachromosomal circular DNAs in gynecologic tumors and reproduction
Received date: 20 Mar 2023
Accepted date: 03 May 2023
Copyright
Originating but free from chromosomal DNA, extrachromosomal circular DNAs (eccDNAs) are organized in circular form and have long been found in unicellular and multicellular eukaryotes. Their biogenesis and function are poorly understood as they are characterized by sequence homology with linear DNA, for which few detection methods are available. Recent advances in high-throughput sequencing technologies have revealed that eccDNAs play crucial roles in tumor formation, evolution, and drug resistance as well as aging, genomic diversity, and other biological processes, bringing it back to the research hotspot. Several mechanisms of eccDNA formation have been proposed, including the breakage-fusion-bridge (BFB) and translocation–deletion–amplification models. Gynecologic tumors and disorders of embryonic and fetal development are major threats to human reproductive health. The roles of eccDNAs in these pathological processes have been partially elucidated since the first discovery of eccDNA in pig sperm and the double minutes in ovarian cancer ascites. The present review summarized the research history, biogenesis, and currently available detection and analytical methods for eccDNAs and clarified their functions in gynecologic tumors and reproduction. We also proposed the application of eccDNAs as drug targets and liquid biopsy markers for prenatal diagnosis and the early detection, prognosis, and treatment of gynecologic tumors. This review lays theoretical foundations for future investigations into the complex regulatory networks of eccDNAs in vital physiological and pathological processes.
Ning Wu , Ling Wei , Zhipeng Zhu , Qiang Liu , Kailong Li , Fengbiao Mao , Jie Qiao , Xiaolu Zhao . Innovative insights into extrachromosomal circular DNAs in gynecologic tumors and reproduction[J]. Protein & Cell, 2024 , 15(1) : 6 -20 . DOI: 10.1093/procel/pwad032
1 |
Andor N, Graham TA, Jansen M et al. Pan-cancer analysis of the extent and consequences of intratumor heterogeneity. Nat Med 2016;22:105–113.
|
2 |
Atkin NB, Baker MC, Ferti-Passantonopoulou A. Chromosome changes in early gynecologic malignancies. Acta Cytol 1983;27:450–453.
|
3 |
Bergstrom EN, Luebeck J, Petljak M et al. Mapping clustered mutations in cancer reveals APOBEC3 mutagenesis of ecDNA. Nature 2022;602:510–517.
|
4 |
Cao X, Wang S, Ge L et al. Extrachromosomal circular DNA: category, biogenesis, recognition, and functions. Front Vet Sci 2021;8:693641.
|
5 |
Carroll SM, DeRose ML, Gaudray P et al. Double minute chromosomes can be produced from precursors derived from a chromosomal deletion. Mol Cell Biol 1988;8:1525–1533.
|
6 |
deCarvalho AC, Kim H, Poisson LM et al. Discordant inheritance of chromosomal and extrachromosomal DNA elements contributes to dynamic disease evolution in glioblastoma. Nat Genet 2018;50:708–717.
|
7 |
Cen Y, Fang Y, Ren Y et al. Global characterization of extrachromosomal circular DNAs in advanced high grade serous ovarian cancer. Cell Death Dis 2022;13:342.
|
8 |
Cernat A, De Freitas C, Majid U et al. Facilitating informed choice about non-invasive prenatal testing (NIPT): a systematic review and qualitative meta-synthesis of women’s experiences. BMC Pregnancy Childbirth 2019;19:27.
|
9 |
Chen X, Shen Y, Draper W et al. ATAC-see reveals the accessible genome by transposase-mediated imaging and sequencing. Nat Methods 2016;13:1013–1020.
|
10 |
Chen Z, Li J, Salas-Leiva DE et al. Group-specific functional patterns of mitochondrion-related organelles shed light on their multiple transitions from mitochondria in ciliated protists. Mar Life Sci Technol 2022;4:609–623.
|
11 |
Cohen S, Lavi S. Induction of circles of heterogeneous sizes in carcinogen-treated cells: two-dimensional gel analysis of circular DNA molecules. Mol Cell Biol 1996;16:2002–2014.
|
12 |
Cohen Z, Lavi S. Replication independent formation of extrachromosomal circular DNA in mammalian cell-free system. PLoS One 2009;4:e6126.
|
13 |
Cohen S, Mechali M. A novel cell-free system reveals a mechanism of circular DNA formation from tandem repeats. Nucleic Acids Res 2001;29:2542–2548.
|
14 |
Cohen S, Mechali M. Formation of extrachromosomal circles from telomeric DNA in Xenopus laevis. EMBO Rep 2002;3:1168–1174.
|
15 |
Cohen S, Regev A, Lavi S. Small polydispersed circular DNA (spcDNA) in human cells: association with genomic instability. Oncogene 1997;14:977–985.
|
16 |
Cohen S, Segal D. Extrachromosomal circular DNA in eukaryotes: possible involvement in the plasticity of tandem repeats. Cytogenet Genome Res 2009;124:327–338.
|
17 |
Cohen Z, Bacharach E, Lavi S. Mouse major satellite DNA is prone to eccDNA formation via DNA Ligase IV-dependent pathway. Oncogene 2006;25:4515–4524.
|
18 |
Cox D, Yuncken C, Spriggs AI. Minute chromatin bodies in malignant tumours of childhood. Lancet 1965;1:55–58.
|
19 |
Deshpande V, Luebeck J, Nguyen ND et al. Exploring the landscape of focal amplifications in cancer using AmpliconArchitect. Nat Commun 2019;10:392.
|
20 |
Dillon LW, Kumar P, Shibata Y et al. Production of extra-chromosomal microDNAs is linked to mismatch repair pathways and transcriptional activity. Cell Rep 2015;11:1749–1759.
|
21 |
Fan X, Yang C, Li W et al. SMOOTH-seq: single-cell genome sequencing of human cells on a third-generation sequencing platform. Genome Biol 2021;22:195.
|
22 |
Gao Y, Solberg T, Wang C et al. Small RNA-mediated genome rearrangement pathways in ciliates. Trends Genet 2023;39:94–97.
|
23 |
Graux C, Cools J, Melotte C et al. Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia. Nat Genet 2004;36:1084–1089.
|
24 |
Gu X, Yu J, Chai P et al. Novel insights into extrachromosomal DNA: redefining the onco-drivers of tumor progression. J Exp Clin Cancer Res 2020;39:215.
|
25 |
Guan XY, Sham JS, Tang TC et al. Isolation of a novel candidate oncogene within a frequently amplified region at 3q26 in ovarian cancer. Cancer Res 2001;61:3806–3809.
|
26 |
Henriksen RA, Jenjaroenpun P, Sjostrom IB et al. Circular DNA in the human germline and its association with recombination. Mol Cell 2022;82:209–217.
|
27 |
Henssen AG. Shedding light on ecDNA behavior using CRISPR-based live-cell imaging. Cancer Discov 2022;12:293–295.
|
28 |
Hotta Y, Bassel A. Molecular size and circularity of DNA in cells of mammals and higher plants. Proc Natl Acad Sci USA 1965;53:356–362.
|
29 |
Hull RM, King M, Pizza G et al. Transcription-induced formation of extrachromosomal DNA during yeast ageing. PLoS Biol 2019;17:e3000471.
|
30 |
Hung KL, Yost KE, Xie L et al. EcDNA hubs drive cooperative intermolecular oncogene expression. Nature 2021;600:731–736.
|
31 |
Hung KL, Luebeck J, Dehkordi SR et al. Targeted profiling of human extrachromosomal DNA by CRISPR-CATCH. Nat Genet 2022;54:1746–1754.
|
32 |
Jin Y, Liu Z, Cao W et al. Novel functional MAR elements of double minute chromosomes in human ovarian cells capable of enhancing gene expression. PLoS One 2012;7:e30419.
|
33 |
Kalavska K, Minarik T, Vlkova B et al. Prognostic value of various subtypes of extracellular DNA in ovarian cancer patients. J Ovarian Res 2018;11:85.
|
34 |
Kim H, Nguyen NP, Turner K et al. Extrachromosomal DNA is associated with oncogene amplification and poor outcome across multiple cancers. Nat Genet 2020;52:891–897.
|
35 |
Kumar P, Dillon LW, Shibata Y et al. Normal and cancerous tissues release extrachromosomal circular DNA (eccDNA) into the circulation. Mol Cancer Res 2017;15:1197–1205.
|
36 |
Kumar P, Kiran S, Saha S et al. ATAC-seq identifies thousands of extrachromosomal circular DNA in cancer and cell lines. Sci Adv 2020;6:eaba2489.
|
37 |
Lange JT, Rose JC, Chen CY et al. The evolutionary dynamics of extrachromosomal DNA in human cancers. Nat Genet 2022;54:1527–1533.
|
38 |
Li Z, Wang B, Liang H et al. Pioneering insights of extrachromosomal DNA (ecDNA) generation, action and its implications for cancer therapy. Int J Biol Sci 2022;18:4006–4025.
|
39 |
Liao Z, Jiang W, Ye L et al. Classification of extrachromosomal circular DNA with a focus on the role of extrachromosomal DNA (ecDNA) in tumor heterogeneity and progression. Biochim Biophys Acta Rev Cancer 2020;1874:188392.
|
40 |
Lin C, Chen Y, Zhang F et al. Encoding gene RAB3B exists in linear chromosomal and circular extrachromosomal DNA and contributes to cisplatin resistance of hypopharyngeal squamous cell carcinoma via inducing autophagy. Cell Death Dis 2022;13:171.
|
41 |
Ling X, Han Y, Meng J et al. Small extrachromosomal circular DNA (eccDNA): major functions in evolution and cancer. Mol Cancer 2021;20:113.
|
42 |
van Loon N, Miller D, Murnane JP. Formation of extrachromosomal circular DNA in HeLa cells by nonhomologous recombination. Nucleic Acids Res 1994;22:2447–2452.
|
43 |
Luebeck J, Coruh C, Dehkordi SR et al. AmpliconReconstructor integrates NGS and optical mapping to resolve the complex structures of focal amplifications. Nat Commun 2020;11:4374.
|
44 |
Lv W, Pan X, Han P et al. Circle-Seq reveals genomic and disease-specific hallmarks in urinary cell-free extrachromosomal circular DNAs. Clin Transl Med 2022;12:e817.
|
45 |
Mann L, Seibt KM, Weber B et al. ECCsplorer: a pipeline to detect extrachromosomal circular DNA (eccDNA) from next-generation sequencing data. BMC Bioinf 2022;23:40.
|
46 |
Mansoori B, Mohammadi A, Davudian S et al. The different mechanisms of cancer drug resistance: a brief review. Adv Pharm Bull 2017;7:339–348.
|
47 |
McGill JR, Beitzel BF, Nielsen JL et al. Double minutes are frequently found in ovarian carcinomas. Cancer Genet Cytogenet 1993;71:125–131.
|
48 |
Mehanna P, Gagne V, Lajoie M et al. Characterization of the microDNA through the response to chemotherapeutics in lymphoblastoid cell lines. PLoS One 2017;12:e0184365.
|
49 |
Molin WT, Yaguchi A, Blenner M et al. The eccDNA replicon: a heritable, extranuclear vehicle that enables gene amplification and glyphosate resistance in amaranthus palmeri. Plant Cell 2020;32:2132–2140.
|
50 |
Moller HD. Circle-Seq: isolation and sequencing of chromosome-derived circular DNA elements in cells. Methods Mol Biol 2020;2119:165–181.
|
51 |
Moller HD, Parsons L, Jorgensen TS et al. Extrachromosomal circular DNA is common in yeast. Proc Natl Acad Sci USA 2015;112:E3114–E3122.
|
52 |
Moller HD, Lin L, Xiang X et al. CRISPR-C: circularization of genes and chromosome by CRISPR in human cells. Nucleic Acids Res 2018a;46:e131.
|
53 |
Moller HD, Mohiyuddin M, Prada-Luengo I et al. Circular DNA elements of chromosomal origin are common in healthy human somatic tissue. Nat Commun 2018b;9:1069.
|
54 |
Morton AR, Dogan-Artun N, Faber ZJ et al. Functional enhancers shape extrachromosomal oncogene amplifications. Cell 2019;179:1330–1341.
|
55 |
Mouakkad-Montoya L, Murata MM, Sulovari A et al. Quantitative assessment reveals the dominance of duplicated sequences in germline-derived extrachromosomal circular DNA. Proc Natl Acad Sci USA 2021;118:e2102842118.
|
56 |
Murnane JP. Telomere dysfunction and chromosome instability. Mutat Res 2012;730:28–36.
|
57 |
Murnane JP, Sabatier L. Chromosome rearrangements resulting from telomere dysfunction and their role in cancer. Bioessays 2004;26:1164–1174.
|
58 |
Nathanson DA, Gini B, Mottahedeh J et al. Targeted therapy resistance mediated by dynamic regulation of extra-chromosomal mutant EGFR DNA. Science 2014;343:72–76.
|
59 |
Noer JB, Horsdal OK, Xiang X et al. Extrachromosomal circular DNA in cancer: history, current knowledge, and methods. Trends Genet 2022;38:766–781.
|
60 |
Olinici CD. Double minute chromatin bodies in a case of ovarian ascitic carcinoma. Br J Cancer 1971;25:350–353.
|
61 |
Pan M, Chen P, Lu J et al. The fragmentation patterns of maternal plasma cell-free DNA and its applications in non-invasive prenatal testing. Prenat Diagn 2020;40:911–917.
|
62 |
Pauletti G, Lai E, Attardi G. Early appearance and long-term persistence of the submicroscopic extrachromosomal elements (amplisomes) containing the amplified DHFR genes in human cell lines. Proc Natl Acad Sci USA 1990;87:2955–2959.
|
63 |
Paulsen T, Shibata Y, Kumar P et al. Small extrachromosomal circular DNAs, microDNA, produce short regulatory RNAs that suppress gene expression independent of canonical promoters. Nucleic Acids Res 2019;47:4586–4596.
|
64 |
Paulsen T, Malapati P, Shibata Y et al. MicroDNA levels are dependent on MMEJ, repressed by c-NHEJ pathway, and stimulated by DNA damage. Nucleic Acids Res 2021;49:11787–11799.
|
65 |
Peng L, Zhou N, Zhang CY et al. eccDNAdb: a database of extrachromosomal circular DNA profiles in human cancers. Oncogene 2022;41:2696–2705.
|
66 |
Prada-Luengo I, Krogh A, Maretty L et al. Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads. BMC Bioinf 2019;20:663.
|
67 |
Radloff R, Bauer W, Vinograd J. A dye-buoyant-density method for the detection and isolation of closed circular duplex DNA: the closed circular DNA in HeLa cells. Proc Natl Acad Sci USA 1967;57:1514–1521.
|
68 |
Rajkumar U, Turner K, Luebeck J et al. EcSeg: semantic segmentation of metaphase images containing extrachromosomal DNA. iScience 2019;21:428–435.
|
69 |
Raymond E, Faivre S, Weiss G et al. Effects of hydroxyurea on extrachromosomal DNA in patients with advanced ovarian carcinomas. Clin Cancer Res 2001;7:1171–1180.
|
70 |
Regev A, Cohen S, Cohen E et al. Telomeric repeats on small polydisperse circular DNA (spcDNA) and genomic instability. Oncogene 1998;17:3455–3461.
|
71 |
Schwartz CL, Christiansen S, Vinggaard AM et al. Anogenital distance as a toxicological or clinical marker for fetal androgen action and risk for reproductive disorders. Arch Toxicol 2019;93:253–272.
|
72 |
Schwarzenbach H, Hoon DS, Pantel K. Cell-free nucleic acids as biomarkers in cancer patients. Nat Rev Cancer 2011;11:426–437.
|
73 |
Shibata Y, Kumar P, Layer R et al. Extrachromosomal microDNAs and chromosomal microdeletions in normal tissues. Science 2012;336:82–86.
|
74 |
Shimizu N, Nakamura H, Kadota T et al. Loss of amplified c-myc genes in the spontaneously differentiated HL-60 cells. Cancer Res 1994;54:3561–3567.
|
75 |
Shimizu N, Miura Y, Sakamoto Y et al. Plasmids with a mammalian replication origin and a matrix attachment region initiate the event similar to gene amplification. Cancer Res 2001;61:6987–6990.
|
76 |
Shoshani O, Brunner SF, Yaeger R et al. Chromothripsis drives the evolution of gene amplification in cancer. Nature 2021;591:137–141.
|
77 |
Shoura MJ, Gabdank I, Hansen L et al. Intricate and cell type-specific populations of endogenous circular DNA (eccDNA) in Caenorhabditis elegans and Homo sapiens. G3 (Bethesda) 2017;7:3295–3303.
|
78 |
Sin STK, Jiang P, Deng J et al. Identification and characterization of extrachromosomal circular DNA in maternal plasma. Proc Natl Acad Sci USA 2020;117:1658–1665.
|
79 |
Sin STK, Ji L, Deng J et al. Characteristics of fetal extrachromosomal circular DNA in maternal plasma: methylation status and clearance. Clin Chem 2021;67:788–796.
|
80 |
Sin ST, Deng J, Ji L et al. Effects of nucleases on cell-free extrachromosomal circular DNA. JCI Insight 2022;7:e156070.
|
81 |
Singer MJ, Mesner LD, Friedman CL et al. Amplification of the human dihydrofolate reductase gene via double minutes is initiated by chromosome breaks. Proc Natl Acad Sci USA 2000;97:7921–7926.
|
82 |
Sirugo G, Williams SM, Tishkoff SA. The missing diversity in human genetic studies. Cell 2019;177:1080.
|
83 |
Stanfield SW, Helinski DR. Cloning and characterization of small circular DNA from Chinese hamster ovary cells. Mol Cell Biol 1984;4:173–180.
|
84 |
Stanfield SW, Lengyel JA. Small circular DNA of Drosophila melanogaster: chromosomal homology and kinetic complexity. Proc Natl Acad Sci USA 1979;76:6142–6146.
|
85 |
Stephens PJ, Greenman CD, Fu B et al. Massive genomic rear-rangement acquired in a single catastrophic event during cancer development. Cell 2011;144:27–40.
|
86 |
Storlazzi CT, Lonoce A, Guastadisegni MC et al. Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure. Genome Res 2010;20:1198–1206.
|
87 |
Su Z, Saha S, Paulsen T et al. ATAC-Seq-based identification of extrachromosomal circular DNA in mammalian cells and its validation using inverse PCR and FISH. Bio Protoc 2021;11:e4003.
|
88 |
Sun W, Quan C, Huang Y et al. Constitutive ERK1/2 activation contributes to production of double minute chromosomes in tumour cells. J Pathol 2015;235:14–24.
|
89 |
Surico D, Bordino V, Cantaluppi V et al. Preeclampsia and intrauterine growth restriction: role of human umbilical cord mesenchymal stem cells-trophoblast cross-talk. PLoS One 2019;14:e0218437.
|
90 |
Tomaska L, Nosek J, Kramara J et al. Telomeric circles: universal players in telomere maintenance? Nat Struct Mol Biol 2009;16:1010–1015.
|
91 |
Turner KM, Deshpande V, Beyter D et al. Extrachromosomal oncogene amplification drives tumour evolution and genetic heterogeneity. Nature 2017;543:122–125.
|
92 |
Umbreit NT, Zhang CZ, Lynch LD et al. Mechanisms generating cancer genome complexity from a single cell division error. Science 2020;368:eaba0712.
|
93 |
Van Roy N, Vandesompele J, Menten B et al. Translocation-excision-deletion-amplification mechanism leading to nonsyntenic coamplification of MYC and ATBF1. Genes Chromosomes Cancer 2006;45:107–117.
|
94 |
Verhaak RGW, Bafna V, Mischel PS. Extrachromosomal oncogene amplification in tumour pathogenesis and evolution. Nat Rev Cancer 2019;19:283–288.
|
95 |
Vogt N, Lefevre SH, Apiou F et al. Molecular structure of double- minute chromosomes bearing amplified copies of the epidermal growth factor receptor gene in gliomas. Proc Natl Acad Sci USA 2004;101:11368–11373.
|
96 |
Von Hoff DD, Waddelow T, Forseth B et al. Hydroxyurea accelerates loss of extrachromosomally amplified genes from tumor cells. Cancer Res 1991;51:6273–6279.
|
97 |
Von Hoff DD, McGill JR, Forseth BJ et al. Elimination of extra-chromosomally amplified MYC genes from human tumor cells reduces their tumorigenicity. Proc Natl Acad Sci USA 1992;89:8165–8169.
|
98 |
Wang K, Tian H, Wang L et al. Deciphering extrachromosomal circular DNA in Arabidopsis. Comput Struct Biotechnol J 2021a;19:1176–1183.
|
99 |
Wang T, Zhang H, Zhou Y et al. Extrachromosomal circular DNA: a new potential role in cancer progression. J Transl Med 2021b;19:257.
|
100 |
Wang Y, Huang R, Zheng G et al. Small ring has big potential: insights into extrachromosomal DNA in cancer. Cancer Cell Int 2021c;21:236.
|
101 |
Wang Y, Wang M, Djekidel MN et al. EccDNAs are apoptotic products with high innate immunostimulatory activity. Nature 2021d;599:308–314.
|
102 |
Wang Y, Wang M, Zhang Y. Purification, full-length sequencing and genomic origin mapping of eccDNA. Nat Protoc 2023;18:683–699.
|
103 |
Wright CF, Burton H. The use of cell-free fetal nucleic acids in maternal blood for non-invasive prenatal diagnosis. Hum Reprod Update 2009;15:139–151.
|
104 |
Wu S, Turner KM, Nguyen N et al. Circular ecDNA promotes accessible chromatin and high oncogene expression. Nature 2019;575:699–703.
|
105 |
Yan Y, Guo G, Huang J et al. Current understanding of extrachromosomal circular DNA in cancer pathogenesis and therapeutic resistance. J Hematol Oncol 2020;13:124.
|
106 |
Yang W, Fan WS, Ye MX et al. Establishment of the PDTX model of gynecological tumors. Am J Transl Res 2019;11:3779–3789.
|
107 |
Yang H, He J, Huang S et al. Identification and characterization of extrachromosomal circular DNA in human placentas with fetal growth restriction. Front Immunol 2021;12:780779.
|
108 |
Yi E, Chamorro Gonzalez R, Henssen AG et al. Extrachromosomal DNA amplifications in cancer. Nat Rev Genet 2022a;23:760–771.
|
109 |
Yi E, Gujar AD, Guthrie M et al. Live-cell imaging shows uneven segregation of extrachromosomal DNA elements and transcriptionally active extrachromosomal DNA hubs in cancer. Cancer Discov 2022b;12:468–483.
|
110 |
Yu L, Zhao Y, Quan C et al. Gemcitabine eliminates double minute chromosomes from human ovarian cancer cells. PLoS One 2013;8:e71988.
|
111 |
Zhang P, Peng H, Llauro C et al. ecc_finder: a robust and accurate tool for detecting extrachromosomal circular DNA from sequencing data. Front Plant Sci 2021;12:743742.
|
112 |
Zhao Z, Tavoosidana G, Sjolinder M et al. Circular chromosome conformation capture (4C) uncovers extensive networks of epigenetically regulated intra- and inter-chromosomal interactions. Nat Genet 2006;38: 1341–1347.
|
113 |
Zhao X, Shi L, Ruan S et al. CircleBase: an integrated resource and analysis platform for human eccDNAs. Nucleic Acids Res 2022;50:D72–D82.
|
114 |
Zhong T, Wang W, Liu H et al. eccDNA Atlas: a comprehensive resource of eccDNA catalog. Brief Bioinform 2023;24:bbad037.
|
115 |
Zhu Y, Gujar AD, Wong CH et al. Oncogenic extrachromosomal DNA functions as mobile enhancers to globally amplify chromosomal transcription. Cancer Cell 2021;39:694–707.
|
116 |
Zuo S, Yi Y, Wang C et al. Extrachromosomal circular DNA (eccDNA): from chaos to function. Front Cell Dev Biol 2021;9:792555.
|
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