Please use this identifier to cite or link to this item:http://hdl.handle.net/20.500.12105/7015
Title
Systems analysis identifies melanoma-enriched pro-oncogenic networks controlled by the RNA binding protein CELF1
Author(s)
Cifdaloz, Metehan | Osterloh, Lisa | Graña Castro, Osvaldo CNIO | Riveiro-Falkenbach, Erica | Ximenez-Embun, Pilar CNIO | Muoz Peralta, Javier CNIO | Tejedo, Cristina | Calvo, Tonantzin G | Karras, Panagiotis | Olmeda, David CNIO | Miñana, Belén | Gómez-López, Gonzalo | Cañón, Estela | Eyras, Eduardo | Guo, Haihong | Kappes, Ferdinand | Ortiz-Romero, Pablo L | Rodríguez-Peralto, Jose L | Megias Vazquez, Diego CNIO | Valcárcel, Juan | Soengas, MS CNIO
Date issued
2017
Citation
Nat Commun. 2017; 8(1):2249.
Language
Inglés
Abstract
Melanomas are well-known for their altered mRNA expression profiles. Yet, the specific contribution of mRNA binding proteins (mRBPs) to melanoma development remains unclear. Here we identify a cluster of melanoma-enriched genes under the control of CUGBP Elav-like family member 1 (CELF1). CELF1 was discovered with a distinct prognostic value in melanoma after mining the genomic landscape of the 692 known mRBPs across different cancer types. Genome-wide transcriptomic, proteomic, and RNA-immunoprecipitation studies, together with loss-of-function analyses in cell lines, and histopathological evaluation in clinical biopsies, revealed an intricate repertoire of CELF1-RNA interactors with minimal overlap with other malignancies. This systems approach uncovered the oncogene DEK as an unexpected target and downstream effector of CELF1. Importantly, CELF1 and DEK were found to represent early-induced melanoma genes and adverse indicators of overall patient survival. These results underscore novel roles of CELF1 in melanoma, illustrating tumor type-restricted functions of RBPs in cancer.
MESH
3' Untranslated Regions | Biopsy | CELF1 Protein | Cell Line, Tumor | Cell Proliferation | Chromosomal Proteins, Non-Histone | Humans | Immunoprecipitation | Melanoma | Oncogene Proteins | Poly-ADP-Ribose Binding Proteins | Prognosis | Proteomics | RNA, Neoplasm | Survival Analysis | Transcriptome | Oncogenes | Systems Biology
Online version
DOI
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