Extrachromosomal DNA (ecDNA): an origin of tumor heterogeneity, genomic remodeling, and drug resistance.
Lauren T PecorinoRoel G W VerhaakAnton HenssenPaul S MischelPublished in: Biochemical Society transactions (2022)
The genome of cancer cells contains circular extrachromosomal DNA (ecDNA) elements not found in normal cells. Analysis of clinical samples reveal they are common in most cancers and their presence indicates poor prognosis. They often contain enhancers and driver oncogenes that are highly expressed. The circular ecDNA topology leads to an open chromatin conformation and generates new gene regulatory interactions, including with distal enhancers. The absence of centromeres leads to random distribution of ecDNAs during cell division and genes encoded on them are transmitted in a non-mendelian manner. ecDNA can integrate into and exit from chromosomal DNA. The numbers of specific ecDNAs can change in response to treatment. This dynamic ability to remodel the cancer genome challenges long-standing fundamentals, providing new insights into tumor heterogeneity, cancer genome remodeling, and drug resistance.
Keyphrases
- genome wide
- poor prognosis
- single cell
- circulating tumor
- papillary thyroid
- cell free
- copy number
- single molecule
- long non coding rna
- squamous cell
- dna methylation
- induced apoptosis
- gene expression
- dna damage
- childhood cancer
- cell cycle arrest
- transcription factor
- cell therapy
- cell death
- minimally invasive
- squamous cell carcinoma
- cell proliferation
- signaling pathway
- lymph node metastasis
- combination therapy
- endoplasmic reticulum stress
- stem cells
- mesenchymal stem cells
- pi k akt
- bioinformatics analysis