| Literature DB >> 30648438 |
Yasmina Kermezli1,2,3, Wiam Saadi1,2,3, Mohamed Belhocine1,2,4, Eve-Lyne Mathieu1,2, Marc-Antoine Garibal1,5, Vahid Asnafi6, Mourad Aribi3, Salvatore Spicuglia1,2, Denis Puthier1,2.
Abstract
Several studies have demonstrated that LncRNAs can play major roles in cancer development. The creation of a catalog of LncRNAs expressed in T cell acute lymphoblastic leukemia (T-ALL) is thus of particular importance. However, this task is challenging as LncRNA expression is highly restricted in time and space manner and thus may greatly differ between samples. We performed a systematic transcript discovery in RNA-Seq data obtained from T-ALL primary cells and cell lines. This led to the identification of 2560 novel LncRNAs. After the integration of these transcripts into a large compendium of LncRNAs (n = 30478) containing both known LncRNAs and those previously described in T-ALLs, we then performed a systematic genomic and epigenetic characterization of these transcript models demonstrating that these novel LncRNAs share properties with known LncRNAs. Finally, we provide evidence that these novel transcripts could be enriched in LncRNAs with potential oncogenic effects and identified a subset of LncRNAs coregulated with T-ALL oncogenes. Overall, our study represents a comprehensive resource of LncRNAs expressed in T-ALL and might provide new cues on the role of lncRNAs in this type of leukemia.Entities:
Keywords: Large non-coding RNA; LncRNA; T-ALL; T-cell acute leukemia; oncogenes
Year: 2019 PMID: 30648438 DOI: 10.1080/10428194.2018.1551534
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022