Long noncoding RNAs (lncRNAs) are regarded as crucial regulators ofcellular processes in Eukaryotes. About 40% of currently characterizedlncRNAs are specifically expressed in central nervous system,where they are involved in critical neural functions. Consistently,lncRNA aberrant expression is associated to neurological disorders.We recently identified a novel human lncRNA, linc-NeD125,that is induced in response to neuronal differentiation stimulusboth in tumour cell lines and in embryonic stem cells. Notably,linc-Ned125 is significantly upregulated in a specific and stilllargely uncharacterized subgroup (Group 4) of Medulloblastoma(MB), the most common malignant paediatric brain tumour.Combining mechanistic and functional studies, we unveiled a novellncRNA-mediated miRNA sponge regulatory network, in which thecross-talk among linc-NeD125, microRNAs and four Group 4 MBdriver gene transcripts may significantly contribute to Group 4 MBcancerogenesis.

Linc-NeD125 establishes a ceRNA network in Group 4 Medulloblastoma

Evelina Miele;
2016-01-01

Abstract

Long noncoding RNAs (lncRNAs) are regarded as crucial regulators ofcellular processes in Eukaryotes. About 40% of currently characterizedlncRNAs are specifically expressed in central nervous system,where they are involved in critical neural functions. Consistently,lncRNA aberrant expression is associated to neurological disorders.We recently identified a novel human lncRNA, linc-NeD125,that is induced in response to neuronal differentiation stimulusboth in tumour cell lines and in embryonic stem cells. Notably,linc-Ned125 is significantly upregulated in a specific and stilllargely uncharacterized subgroup (Group 4) of Medulloblastoma(MB), the most common malignant paediatric brain tumour.Combining mechanistic and functional studies, we unveiled a novellncRNA-mediated miRNA sponge regulatory network, in which thecross-talk among linc-NeD125, microRNAs and four Group 4 MBdriver gene transcripts may significantly contribute to Group 4 MBcancerogenesis.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14245/19447
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