Somatic Copy-Number Alterations across Human Cancers from LncRNA Perspective

The genome of a tumor cell presents thousands of genomic alterations including base-substitutions and somatic copy number alterations (SCNAs). SCNAs comprise amplifications and deletions of big chromosomal regions usually containing hundreds of genes. Some of these regions harbor well-studied cancer...

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Main Authors: Athie-Cuervo, A. (Alejandro), Huarte-Martínez, M. (Maite)
Format: info:eu-repo/semantics/doctoralThesis
Language:eng
Published: 2017
Subjects:
Online Access:https://hdl.handle.net/10171/45008
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author Athie-Cuervo, A. (Alejandro)
Huarte-Martínez, M. (Maite)
author_facet Athie-Cuervo, A. (Alejandro)
Huarte-Martínez, M. (Maite)
author_sort Athie-Cuervo, A. (Alejandro)
collection DSpace
description The genome of a tumor cell presents thousands of genomic alterations including base-substitutions and somatic copy number alterations (SCNAs). SCNAs comprise amplifications and deletions of big chromosomal regions usually containing hundreds of genes. Some of these regions harbor well-studied cancer drivers; however many others do not contain a known driver. The analysis of SCNA focusing on the non-coding genome helped us pinpoint a list of copy number altered long noncoding RNAs (lncRNAs). In order to validate our findings we experimentally characterized functionally and mechanistically a lncRNA amplified in lung cancer which we named LUAD-amp-1. LUAD-amp-1 acts as an oncogenic lncRNA, and its expression is induced by the transcription factor NF-B upon TNF treatment. Moreover, LUAD-amp-1 is implicated in the inhibition of a set of NF-B regulated genes including TNF itself. LUAD-amp-1 molecular mechanism relies on its association with SART3, altering its localization and modulating the nuclear translocation of its associated protein USP4.
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spelling oai:dadun.unav.edu:10171-450082024-02-08T10:52:19Z Somatic Copy-Number Alterations across Human Cancers from LncRNA Perspective Athie-Cuervo, A. (Alejandro) Huarte-Martínez, M. (Maite) Materias Investigacion::Ciencias de la Salud::Oncología The genome of a tumor cell presents thousands of genomic alterations including base-substitutions and somatic copy number alterations (SCNAs). SCNAs comprise amplifications and deletions of big chromosomal regions usually containing hundreds of genes. Some of these regions harbor well-studied cancer drivers; however many others do not contain a known driver. The analysis of SCNA focusing on the non-coding genome helped us pinpoint a list of copy number altered long noncoding RNAs (lncRNAs). In order to validate our findings we experimentally characterized functionally and mechanistically a lncRNA amplified in lung cancer which we named LUAD-amp-1. LUAD-amp-1 acts as an oncogenic lncRNA, and its expression is induced by the transcription factor NF-B upon TNF treatment. Moreover, LUAD-amp-1 is implicated in the inhibition of a set of NF-B regulated genes including TNF itself. LUAD-amp-1 molecular mechanism relies on its association with SART3, altering its localization and modulating the nuclear translocation of its associated protein USP4. 2017-12-07T07:59:56Z 2017-12-07T07:59:56Z 2017-12-05 2017-09-28 info:eu-repo/semantics/doctoralThesis https://hdl.handle.net/10171/45008 eng info:eu-repo/semantics/openAccess application/pdf
spellingShingle Materias Investigacion::Ciencias de la Salud::Oncología
Athie-Cuervo, A. (Alejandro)
Huarte-Martínez, M. (Maite)
Somatic Copy-Number Alterations across Human Cancers from LncRNA Perspective
title Somatic Copy-Number Alterations across Human Cancers from LncRNA Perspective
title_full Somatic Copy-Number Alterations across Human Cancers from LncRNA Perspective
title_fullStr Somatic Copy-Number Alterations across Human Cancers from LncRNA Perspective
title_full_unstemmed Somatic Copy-Number Alterations across Human Cancers from LncRNA Perspective
title_short Somatic Copy-Number Alterations across Human Cancers from LncRNA Perspective
title_sort somatic copy-number alterations across human cancers from lncrna perspective
topic Materias Investigacion::Ciencias de la Salud::Oncología
url https://hdl.handle.net/10171/45008
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