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https://hdl.handle.net/2445/172138
Title: | The modular network structure of the mutational landscape of Acute Myeloid Leukemia |
Author: | Ibánez, Mariam Carbonell Caballero, José Such, Esperanza García Alonso, Luz Liguori, Alessandro López Pavía, María Llop, Marta Alonso, Carmen Barragán, Eva Gómez Seguí, Inés Neef, Alexander Hervás, David Montesinos, Pau Sanz, Guillermo Sanz, Miguel Angel Dopazo, Joaquín Cervera, José |
Keywords: | Leucèmia mieloide Genètica Myeloid leukemia Genetics |
Issue Date: | 10-Oct-2018 |
Publisher: | Public Library of Science (PLoS) |
Abstract: | Acute myeloid leukemia (AML) is associated with the sequential accumulation of acquired genetic alterations. Although at diagnosis cytogenetic alterations are frequent in AML, roughly 50% of patients present an apparently normal karyotype (NK), leading to a highly heterogeneous prognosis. Due to this significant heterogeneity, it has been suggested that different molecular mechanisms may trigger the disease with diverse prognostic implications. We performed whole-exome sequencing (WES) of tumor-normal matched samples of de novo AML-NK patients lacking mutations in NPM1, CEBPA or FLT3-ITD to identify new gene mutations with potential prognostic and therapeutic relevance to patients with AML. Novel candidate-genes, together with others previously described, were targeted resequenced in an independent cohort of 100 de novo AML patients classified in the cytogenetic intermediate-risk (IR) category. A mean of 4.89 mutations per sample were detected in 73 genes, 35 of which were mutated in more than one patient. After a network enrichment analysis, we defined a single in silico model and established a set of seed-genes that may trigger leukemogenesis in patients with normal karyotype. The high heterogeneity of gene mutations observed in AML patients suggested that a specific alteration could not be as essential as the interaction of deregulated pathways. |
Note: | Reproducció del document publicat a: https://doi.org/10.1371/journal.pone.0202926 |
It is part of: | PLoS One, 2018, vol. 13, num. 10, p. e0202926 |
URI: | https://hdl.handle.net/2445/172138 |
Related resource: | https://doi.org/10.1371/journal.pone.0202926 |
Appears in Collections: | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) |
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