| Literature DB >> 32123306 |
Valentina Fragliasso1, Akanksha Verma2,3, Gloria Manzotti1, Annalisa Tameni1,4, Rohan Bareja2, Tayla B Heavican5, Javeed Iqbal5, Rui Wang6, Danilo Fiore6, Valentina Mularoni1, Wing C Chan7, Priscillia Lhoumaud8, Jane Skok8, Eleonora Zanetti9, Francesco Merli10, Alessia Ciarrocchi11, Oliver Elemento12, Giorgio Inghirami13.
Abstract
The molecular mechanisms leading to the transformation of anaplastic lymphoma kinase negative (ALK-) anaplastic large cell lymphoma (ALCL) have been only in part elucidated. To identify new culprits which promote and drive ALCL, we performed a total transcriptome sequencing and discovered 1208 previously unknown intergenic long noncoding RNAs (lncRNAs), including 18 lncRNAs preferentially expressed in ALCL. We selected an unknown lncRNA, BlackMamba, with an ALK- ALCL preferential expression, for molecular and functional studies. BlackMamba is a chromatin-associated lncRNA regulated by STAT3 via a canonical transcriptional signaling pathway. Knockdown experiments demonstrated that BlackMamba contributes to the pathogenesis of ALCL regulating cell growth and cell morphology. Mechanistically, BlackMamba interacts with the DNA helicase HELLS controlling its recruitment to the promoter regions of cell-architecture-related genes, fostering their expression. Collectively, these findings provide evidence of a previously unknown tumorigenic role of STAT3 via a lncRNA-DNA helicase axis and reveal an undiscovered role for lncRNA in the maintenance of the neoplastic phenotype of ALK-ALCL.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32123306 DOI: 10.1038/s41375-020-0754-8
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528