
doi: 10.2741/4666
pmid: 29293456
LINE-1 retrotransposons are ubiquitous genetic elements interspersed within the primary nuclear genome of modern day humans. Although shorter LINE-1-derived sequences occupy nearly one-in-five nucleotides of our genome, we are just beginning to appreciate the link between these important genetic elements and cancer, perhaps the most well-studied major degenerative disorder affecting humanity today. Herein, I summarize empirical observations linking LINE-1 to tumorigenesis. The work is organized into three major parts. First, I provide an overview of LINE-1 activity in cancer; highlighting major features of LINE-1 life-cycle such as: promoter methylation, transcription, translation, and retrotransposition. Second, I discuss three genetic pathways - epigenetic regulation, interferon signaling, and genome integrity - as they relate to LINE-1 regulation in cancer. Finally, I review most recent body of work linking LINE-1 as not only a diagnostic cancer biomarker, but also a potential therapeutic target.
Gene Expression Regulation, Neoplastic, Mutagenesis, Insertional, Long Interspersed Nucleotide Elements, Neoplasms, Biomarkers, Tumor, Humans, Genomic Instability, Epigenesis, Genetic, Signal Transduction
Gene Expression Regulation, Neoplastic, Mutagenesis, Insertional, Long Interspersed Nucleotide Elements, Neoplasms, Biomarkers, Tumor, Humans, Genomic Instability, Epigenesis, Genetic, Signal Transduction
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