Current understanding of extrachromosomal circular DNA in cancer pathogenesis and therapeutic resistance

被引:0
作者
Yuanliang Yan
Guijie Guo
Jinzhou Huang
Ming Gao
Qian Zhu
Shuangshuang Zeng
Zhicheng Gong
Zhijie Xu
机构
[1] Central South University,Department of Pharmacy, Xiangya Hospital
[2] Mayo Clinic,Department of Oncology
[3] Central South University,Department of Pathology, Xiangya Hospital
[4] Central South University,National Clinical Research Center for Geriatric Disorders, Xiangya Hospital
来源
Journal of Hematology & Oncology | / 13卷
关键词
Extrachromosomal circular DNA; Oncogene amplification; Therapeutic resistance; Cancer pathogenesis; Biomarkers; Clinical utility;
D O I
暂无
中图分类号
学科分类号
摘要
Extrachromosomal circular DNA was recently found to be particularly abundant in multiple human cancer cells, although its frequency varies among different tumor types. Elevated levels of extrachromosomal circular DNA have been considered an effective biomarker of cancer pathogenesis. Multiple reports have demonstrated that the amplification of oncogenes and therapeutic resistance genes located on extrachromosomal DNA is a frequent event that drives intratumoral genetic heterogeneity and provides a potential evolutionary advantage. This review highlights the current understanding of the extrachromosomal circular DNA present in the tissues and circulation of patients with advanced cancers and provides a detailed discussion of their substantial roles in tumor regulation. Confirming the presence of cancer-related extrachromosomal circular DNA would provide a putative testing strategy for the precision diagnosis and treatment of human malignancies in clinical practice.
引用
收藏
相关论文
共 678 条
  • [41] Lee C(2013)Chromothripsis and beyond: rapid genome evolution from complex chromosomal rearrangements Genes & development. 27 133-79
  • [42] Kohl NE(2018)Defective DNA damage repair leads to frequent catastrophic genomic events in murine and human tumors Nature communications. 9 9131-223
  • [43] Kanda N(2020)Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Nature genetics. 52 2152-985
  • [44] Schreck RR(2020)Double-strand breakage in the extrachromosomal double minutes triggers their aggregation in the nucleus, micronucleation, and morphological transformation Genes, chromosomes & cancer. 59 4275-3461
  • [45] Bruns G(2014)Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer Nucleic acids research. 42 1296-1131
  • [46] Latt SA(2018)MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequences Leukemia. 32 29-400
  • [47] Gilbert F(2019)Long non-coding RNA PVT1 interacts with MYC and its downstream molecules to synergistically promote tumorigenesis CMLS. 76 212-4524
  • [48] Vogt N(2007)Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution Genome research. 17 73-39
  • [49] Lefevre SH(1990)Tissue-specific and age-related variations in repetitive sequences of mouse extrachromosomal circular DNAs Mutation research. 237 213-932
  • [50] Apiou F(2017)Cancer genomics: ECdetect hunts extrachromosomal DNA Nature reviews Genetics. 18 977-146