2018
DOI: 10.21037/ncri.2018.06.04
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circRNA meets gene amplification

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Cited by 2 publications
(2 citation statements)
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References 23 publications
(47 reference statements)
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“…In normal cells, the accumulation of nascent circRNAs contributes considerably to their detection at steady-state levels (Ashwal-Fluss et al, 2014; Zhang Y. et al, 2016), underlining the importance of circRNA biogenesis. This section is mainly focused on the effect of cancer-related genetic alterations, including single nucleotide variants (SNPs), genomic rearrangements, recurrent somatic mutations, and copy number alterations (Manguso et al, 2018), which modulate the expression of circRNAs through circRNA biogenesis. We discuss aberrant events in circRNA biogenesis in chronological order, and this section is divided into five subsections: aberrant cis -elements, aberrant chromosomes and genomes, aberrant transcription, aberrant spliceosomal machinery, and aberrant trans-acting factors.…”
Section: The Aberrant Regulation Of Circrnas In Cancermentioning
confidence: 99%
“…In normal cells, the accumulation of nascent circRNAs contributes considerably to their detection at steady-state levels (Ashwal-Fluss et al, 2014; Zhang Y. et al, 2016), underlining the importance of circRNA biogenesis. This section is mainly focused on the effect of cancer-related genetic alterations, including single nucleotide variants (SNPs), genomic rearrangements, recurrent somatic mutations, and copy number alterations (Manguso et al, 2018), which modulate the expression of circRNAs through circRNA biogenesis. We discuss aberrant events in circRNA biogenesis in chronological order, and this section is divided into five subsections: aberrant cis -elements, aberrant chromosomes and genomes, aberrant transcription, aberrant spliceosomal machinery, and aberrant trans-acting factors.…”
Section: The Aberrant Regulation Of Circrnas In Cancermentioning
confidence: 99%
“…For example, circFoxo3 can regulate p53-influenced immune responses by inducing the ubiquitination-dependent degradation of p53 through binding to MDM2 17 , 18 . Tumor cells may produce abnormal circRNAs caused by genetic mutations 19 , chromosomal translocation 20 , TGF-β signaling regulation 21 , and other aberrant events 22 . For example, PML/RARα chromosomal translocations lead to the generation of fusion circRNAs (F-circRNAs) in acute promyelocytic leukemia, which promote cellular transformation, cell viability, and resistance to therapy 23 .…”
Section: Introductionmentioning
confidence: 99%