Understanding transformation mechanisms other than genetic aberrations has recently captured the attention of cancer researchers. To date, the role of transposable elements (TEs) in tumor development remains largely undefined. However, an increasing number of studies have reported that loss of epigenetic control causes TE reactivation and consequent oncogenic transcription. Here, we discuss principal examples of TEs-driven oncogenesis. Available data suggest that long terminal repeats and long interspersed nuclear elements play a pivotal role as alternative promoters. These findings provide definitive experimental evidence that repetitive elements are a powerful underestimated force toward oncogenesis and open the possibility to new therapeutic treatments.

Transposable elements: The enemies within

Pellegrino, Elisa;Mereu, Elisabetta;Inghirami, Giorgio;Piva, Roberto
Last
2016-01-01

Abstract

Understanding transformation mechanisms other than genetic aberrations has recently captured the attention of cancer researchers. To date, the role of transposable elements (TEs) in tumor development remains largely undefined. However, an increasing number of studies have reported that loss of epigenetic control causes TE reactivation and consequent oncogenic transcription. Here, we discuss principal examples of TEs-driven oncogenesis. Available data suggest that long terminal repeats and long interspersed nuclear elements play a pivotal role as alternative promoters. These findings provide definitive experimental evidence that repetitive elements are a powerful underestimated force toward oncogenesis and open the possibility to new therapeutic treatments.
2016
44
10
913
916
www.elsevier.com/locate/exphem
Animals; Cell Transformation, Neoplastic; Epigenesis, Genetic; Humans; Long Interspersed Nucleotide Elements; Neoplasms; Promoter Regions, Genetic; Terminal Repeat Sequences; DNA Transposable Elements; Hematology; Molecular Biology; Genetics; Cell Biology; Cancer Research
Scarfã², Irene; Pellegrino, Elisa; Mereu, Elisabetta; Inghirami, Giorgio; Piva, Roberto
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1657814
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