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      Integrative discovery of treatments for high-risk neuroblastoma

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          Abstract

          Despite advances in the molecular exploration of paediatric cancers, approximately 50% of children with high-risk neuroblastoma lack effective treatment. To identify therapeutic options for this group of high-risk patients, we combine predictive data mining with experimental evaluation in patient-derived xenograft cells. Our proposed algorithm, TargetTranslator, integrates data from tumour biobanks, pharmacological databases, and cellular networks to predict how targeted interventions affect mRNA signatures associated with high patient risk or disease processes. We find more than 80 targets to be associated with neuroblastoma risk and differentiation signatures. Selected targets are evaluated in cell lines derived from high-risk patients to demonstrate reversal of risk signatures and malignant phenotypes. Using neuroblastoma xenograft models, we establish CNR2 and MAPK8 as promising candidates for the treatment of high-risk neuroblastoma. We expect that our method, available as a public tool (targettranslator.org), will enhance and expedite the discovery of risk-associated targets for paediatric and adult cancers.

          Abstract

          We lack effective treatment for half of children with high-risk neuroblastoma. Here, the authors introduce an algorithm that can predict the effect of interventions on gene expression signatures associated with high disease processes and risk, and identify and validate promising drug targets.

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          Most cited references67

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          Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

          In comparative high-throughput sequencing assays, a fundamental task is the analysis of count data, such as read counts per gene in RNA-seq, for evidence of systematic changes across experimental conditions. Small replicate numbers, discreteness, large dynamic range and the presence of outliers require a suitable statistical approach. We present DESeq2, a method for differential analysis of count data, using shrinkage estimation for dispersions and fold changes to improve stability and interpretability of estimates. This enables a more quantitative analysis focused on the strength rather than the mere presence of differential expression. The DESeq2 package is available at http://www.bioconductor.org/packages/release/bioc/html/DESeq2.html. Electronic supplementary material The online version of this article (doi:10.1186/s13059-014-0550-8) contains supplementary material, which is available to authorized users.
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            Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles

            Although genomewide RNA expression analysis has become a routine tool in biomedical research, extracting biological insight from such information remains a major challenge. Here, we describe a powerful analytical method called Gene Set Enrichment Analysis (GSEA) for interpreting gene expression data. The method derives its power by focusing on gene sets, that is, groups of genes that share common biological function, chromosomal location, or regulation. We demonstrate how GSEA yields insights into several cancer-related data sets, including leukemia and lung cancer. Notably, where single-gene analysis finds little similarity between two independent studies of patient survival in lung cancer, GSEA reveals many biological pathways in common. The GSEA method is embodied in a freely available software package, together with an initial database of 1,325 biologically defined gene sets.
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              HTSeq—a Python framework to work with high-throughput sequencing data

              Motivation: A large choice of tools exists for many standard tasks in the analysis of high-throughput sequencing (HTS) data. However, once a project deviates from standard workflows, custom scripts are needed. Results: We present HTSeq, a Python library to facilitate the rapid development of such scripts. HTSeq offers parsers for many common data formats in HTS projects, as well as classes to represent data, such as genomic coordinates, sequences, sequencing reads, alignments, gene model information and variant calls, and provides data structures that allow for querying via genomic coordinates. We also present htseq-count, a tool developed with HTSeq that preprocesses RNA-Seq data for differential expression analysis by counting the overlap of reads with genes. Availability and implementation: HTSeq is released as an open-source software under the GNU General Public Licence and available from http://www-huber.embl.de/HTSeq or from the Python Package Index at https://pypi.python.org/pypi/HTSeq. Contact: sanders@fs.tum.de
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                Author and article information

                Contributors
                sven.nelander@igp.uu.se
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                3 January 2020
                3 January 2020
                2020
                : 11
                : 71
                Affiliations
                [1 ]ISNI 0000 0004 1936 9457, GRID grid.8993.b, Department of Immunology, Genetics and Pathology, , Uppsala University, ; SE-751 85 Uppsala, Sweden
                [2 ]ISNI 0000 0004 1937 0626, GRID grid.4714.6, Childhood Cancer Research Unit, Department of Women’s and Children’s Health, , Karolinska Institutet, ; SE-17176 Stockholm, Sweden
                [3 ]ISNI 0000 0004 1937 0626, GRID grid.4714.6, Department of Microbiology, Tumor and Cell Biology, , Karolinska Institutet, ; SE-171 77 Stockholm, Sweden
                [4 ]ISNI 0000 0001 0930 2361, GRID grid.4514.4, Division of Translational Cancer Research, Department of Laboratory Medicine, , Lund University, ; SE-223 81 Lund, Sweden
                [5 ]ISNI 0000 0004 1937 0626, GRID grid.4714.6, Department of Medicine, Integrated Cardio-Metabolic Centre Single Cell Facility, , Karolinska Institutet, ; SE-17177 Stockholm, Sweden
                [6 ]ISNI 0000 0001 0775 6028, GRID grid.5371.0, Mathematical Sciences, , Chalmers University of Technology, ; Gothenburg, SE-41296 Sweden
                Author information
                http://orcid.org/0000-0002-1946-9138
                http://orcid.org/0000-0002-2592-3448
                http://orcid.org/0000-0002-1664-2257
                http://orcid.org/0000-0001-5422-4243
                http://orcid.org/0000-0001-9426-9550
                http://orcid.org/0000-0002-0709-7808
                http://orcid.org/0000-0002-2202-9694
                Article
                13817
                10.1038/s41467-019-13817-8
                6941971
                31900415
                5b798bc8-ac08-45bb-9df9-0a6fa5443895
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 18 January 2019
                : 22 November 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100006313, Barncancerfonden (Swedish Childhood Cancer Foundation);
                Funded by: FundRef https://doi.org/10.13039/501100004359, Vetenskapsrådet (Swedish Research Council);
                Funded by: FundRef https://doi.org/10.13039/501100001729, Stiftelsen för Strategisk Forskning (Swedish Foundation for Strategic Research);
                Categories
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                © The Author(s) 2020

                Uncategorized
                cancer,computational biology and bioinformatics,drug discovery,systems biology,medical research

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