Impact of DLK1-DIO3 imprinted cluster hypomethylation in smoker patients with lung cancer
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Sonia Molina-Pinelo1,2,3, Ana Salinas1, Nicolás Moreno-Mata4, Irene Ferrer1,2,3, Rocío Suarez1,2,3, Eduardo Andrés-León1, Manuel Rodríguez-Paredes5,6, Julian Gutekunst5, Eloisa Jantus-Lewintre7,8, Carlos Camps9,10, Amancio Carnero1,3 and Luis Paz-Ares1,2,3
1Instituto de Biomedicina de Sevilla (IBIS) (HUVR, CSIC, Universidad de Sevilla), Sevilla, Spain
2Medical Oncology Department, Hospital Universitario Doce de Octubre & Centro Nacional de Investigaciones Oncológicas (CNIO), Madrid, Spain
3CIBER de Cáncer, Madrid, Spain
4Thoracic Surgery Department, Hospital Universitario Virgen del Rocio, Sevilla, Spain
5Division of Epigenetics, DKFZ-ZMBH Alliance, German Cancer Research Center, Heidelberg, Germany
6University Tumor Center Düsseldorf, University of Düsseldorf, Düsseldorf, Germany
7Molecular Oncology Laboratory, Fundación para la Investigación del Hospital General Universitario de Valencia, Valencia, Spain
8Department of Biotechnology, Universitat Politècnica de Valencia, Valencia, Spain
9Department of Medicine, University of Valencia, Valencia, Spain
10Department of Medical Oncology, Hospital General Universitario de Valencia, Valencia, Spain
Sonia Molina-Pinelo, email: [email protected]
Luis Paz-Ares, email: [email protected]
Keywords: lung cancer, epigenetic, DLK1-DIO3 cluster, transcriptional regulation, COPD
Received: September 16, 2015 Accepted: June 02, 2016 Published: July 15, 2016
DNA methylation is important for gene expression and genome stability, and its disruption is thought to play a key role in the initiation and progression of cancer and other diseases. The DLK1-DIO3 cluster has been shown to be imprinted in humans, and some of its components are relevant to diverse pathological processes. The purpose of this study was to assess the methylation patterns of the DLK1-DIO3 cluster in patients with lung cancer to study its relevance in the pathogenesis of this disease. We found a characteristic methylation pattern of this cluster in smoking associated lung cancer, as compared to normal lung tissue. This methylation profile is not patent however in lung cancer of never smokers nor in lung tissue of COPD patients. We found 3 deregulated protein-coding genes at this locus: one was hypermethylated (DIO3) and two were hypomethylated (DLK1 and RTL1). Statistically significant differences were also detected in two different families of SNORDs, two miRNA clusters and four lncRNAs (MEG3, MEG8, MEG9 and LINC00524). These findings were validated using data from the cancer genome atlas (TCGA) database. We have then showed an inverse correlation between DNA methylation and expression levels in 5 randomly selected genes. Several targets of miRNAs included in the DLK1-DIO3 cluster have been experimentally verified as tumor suppressors. All of these results suggest that the dysmethylation of the imprinted DLK1-DIO3 cluster could have a relevant role in the pathogenesis of lung cancer in current and former smokers and may be used for diagnostic and/or therapeutic purposes.
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