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      A MiRNA Signature for Defining Aggressive Phenotype and Prognosis in Gliomas

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          Abstract

          Gliomas represent a disparate group of tumours for which there are to date no cure. Thus, there is a recognized need for new diagnostic and therapeutic approaches based on increased understanding of their molecular nature. We performed the comparison of the microRNA (miRNA) profile of 8 WHO grade II gliomas and 24 higher grade tumours (2 WHO grade III and 22 glioblastomas) by using the Affymetrix GeneChip miRNA Array v. 1.0. A relative quantification method (RT-qPCR) with standard curve was used to confirm the 22 miRNA signature resulted by array analysis. The prognostic performances of the confirmed miRNAs were estimated on the Tumor Cancer Genome Atlas (TCGA) datasets. We identified 22 miRNAs distinguishing grade II gliomas from higher grade tumours. RT-qPCR confirmed the differential expression in the two patients' groups for 13 out of the 22 miRNAs. The analysis of the Glioblastoma Multiforme (GBM) and Lower Grade Glioma (LGG) datasets from TCGA demonstrated the association with prognosis for 6 of those miRNAs. Moreover, in the GBM dataset miR-21 and miR-210 were predictors of worse prognosis in both univariable and multivariable Cox regression analyses (HR 1.19, p = 0.04, and HR 1.18, p = 0.029 respectively). Our results support a direct contribution of miRNAs to glioma cancerogenesis and suggest that miR-21 and miR-210 may play a role in the aggressive clinical behaviour of glioblastomas.

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          Most cited references14

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          An integrated approach for experimental target identification of hypoxia-induced miR-210.

          miR-210 is a key player of cell response to hypoxia, modulating cell survival, VEGF-driven endothelial cell migration, and the ability of endothelial cells to form capillary-like structures. A crucial step in understanding microRNA (miRNA) function is the identification of their targets. However, only few miR-210 targets have been identified to date. Here, we describe an integrated strategy for large-scale identification of new miR-210 targets by combining transcriptomics and proteomics with bioinformatic approaches. To experimentally validate candidate targets, the RNA-induced silencing complex (RISC) loaded with miR-210 was purified by immunoprecipitation along with its mRNA targets. The complex was significantly enriched in mRNAs of 31 candidate targets, such as BDNF, GPD1L, ISCU, NCAM, and the non-coding RNA Xist. A subset of the newly identified targets was further confirmed by 3'-untranslated region (UTR) reporter assays, and hypoxia induced down-modulation of their expression was rescued blocking miR-210, providing support for the approach validity. In the case of 9 targets, such as PTPN1 and P4HB, miR-210 seed-pairing sequences localized in the coding sequence or in the 5'-UTR, in line with recent data extending miRNA targeting beyond the "classic" 3'-UTR recognition. Finally, Gene Ontology analysis of the targets highlights known miR-210 impact on cell cycle regulation and differentiation, and predicts a new role of this miRNA in RNA processing, DNA binding, development, membrane trafficking, and amino acid catabolism. Given the complexity of miRNA actions, we view such a multiprong approach as useful to adequately describe the multiple pathways regulated by miR-210 during physiopathological processes.
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            MicroRNA miR-210 modulates cellular response to hypoxia through the MYC antagonist MNT.

            The hypoxia-inducible factor (HIF) pathway is essential for cell survival under low oxygen and plays an important role in tumor cell homeostasis. We investigated the function of miR-210, the most prominent microRNA upregulated by hypoxia and a direct transcriptional target of HIFs. miR-210 expression was elevated in multiple cancer types and correlated with metastasis of breast and melanoma tumors. miR-210 overexpression in cancer cell lines bypassed hypoxia-induced cell cycle arrest and partially reversed the hypoxic gene expression signature. We identified MNT, a known MYC antagonist, as a miR-210 target. MNT mRNA contains multiple miR-210 binding sites in the 3' UTR and its knockdown phenocopied miR-210 overexpression. Furthermore, loss of MYC abolished miR-210-mediated override of hypoxia-induced cell cycle arrest. Comparison of miR-210 and MYC overexpression with MNT knockdown signatures also indicated that miR-210 triggered a "MYC-like" transcriptional response. Thus, miR-210 influences the hypoxia response in tumor cells through targeting a key transcriptional repressor of the MYC-MAX network.
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              hsa-mir-210 is a marker of tumor hypoxia and a prognostic factor in head and neck cancer.

              Hypoxia is an important mechanism of treatment resistance in head and neck squamous cell carcinoma (HNSCC). MicroRNAs are short noncoding RNAs that regulate multiple mRNAs and are frequently dysregulated in cancer. The authors have investigated the role of 3 microRNAs, including the hypoxia-induced hsa-miR-210, as potential markers of hypoxia or prognosis. Three hypoxia-related microRNAs, hsa-miR-210, hsa-miR-21, and hsa-miR-10b, were measured in 46 samples from patients with HNSCC. Expression levels were correlated with clinicopathological variables and other markers of hypoxia: a published 99-gene hypoxia metagene, individual hypoxia-related genes such as TWIST1, and immunohistochemical expression of hypoxia-inducible factor 1 and its target gene carbonic anhydrase 9. We then performed survival analyses to investigate the prognostic significance of these microRNAs. Only the level of hsa-miR-210 was significantly correlated with other markers of hypoxia, including the 99-gene hypoxia metagene (rho = 0.67, P < .001). We found no association between hsa-miR-210, hsa-miR-21, or hsa-miR-10b and clinicopathological variables such as tumor size, differentiation, and stage. However, high levels of hsa-miR-210 were associated with locoregional disease recurrence (P = .001) and short overall survival (P = .008). hsa-miR-21 and hsa-miR-10b had no prognostic significance. Expression of hsa-miR-210 in head and neck cancer correlates with other approaches for assessing hypoxia and is associated with prognosis. This warrants further study as a classification marker of patients for therapies involving modulation of hypoxia. (c) 2010 American Cancer Society.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                3 October 2014
                : 9
                : 10
                : e108950
                Affiliations
                [1 ]Laboratory of Oncology, “IRCCS Casa Sollievo della Sofferenza”, San Giovanni Rotondo, FG, Italy
                [2 ]Laboratory of Genetics, “IRCCS Casa Sollievo della Sofferenza”, San Giovanni Rotondo, FG, Italy
                [3 ]Department of Biosciences, Biotechnology and Biopharmaceutics, University of Bari “Aldo Moro”, Bari, Italy
                [4 ]LTTA, Department of Morphology, Surgery and Experimental Medicine, Human Anatomy Branch, University of Ferrara, Ferrara, Italy
                [5 ]Department of Neurosurgery, “IRCCS Casa Sollievo della Sofferenza”, San Giovanni Rotondo, FG, Italy
                [6 ]Laboratory of Oncology, “IRCCS Casa Sollievo della Sofferenza”, San Giovanni Rotondo, FG, Italy
                [7 ]Department of Pathology, “IRCCS Casa Sollievo della Sofferenza”, San Giovanni Rotondo, FG, Italy
                [8 ]Unit of Biostatistics, “IRCCS Casa Sollievo della Sofferenza”, San Giovanni Rotondo, FG, Italy
                [9 ]Department of Oncology, “IRCCS Casa Sollievo della Sofferenza”, San Giovanni Rotondo, FG, Italy
                [10 ]Laboratory of Genetics, “IRCCS Casa Sollievo della Sofferenza”, San Giovanni Rotondo, FG, Italy
                [11 ]CIR Laboratory for Molecular Medicine and Biotechnology, University Campus Biomedico, Rome, Italy
                Johns Hopkins University, United States of America
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: PP M. Carella VMF. Performed the experiments: RB OP BP M. Coco. Analyzed the data: RB BP OP MG SV M. Copetti M. Carella. Contributed reagents/materials/analysis tools: VD NI LD MG SV M. Copetti LD PG VMV EM. Wrote the paper: PP RB OP BP SV PG EM M. Carella VMF.

                Article
                PONE-D-14-31103
                10.1371/journal.pone.0108950
                4184816
                25279461
                3dbc5124-8e7c-42c5-9781-2892eebcfb8e
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 11 July 2014
                : 26 August 2014
                Page count
                Pages: 9
                Funding
                Ricerca Corrente 2013 funding was granted by the Italian Ministry of Health. This work was also supported by “5×1000” voluntary contributions, “Progetto Operativo Nazionale,” PON 2011-2014 VIRTUALAB (PON01_01297). S.V. is supported by Associazione Italiana per la Ricerca sul Cancro (AIRC – IG13585) and Ministero dell'Istruzione, dell'Università e della Ricerca Progetti di Ricerca di Interesse Nazionale (PRIN 2010) and The National Council of Research of Italy CNR EPIGEN grants. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Biotechnology
                Molecular Biology
                Neuroscience
                Medicine and Health Sciences
                Oncology
                Cancer Detection and Diagnosis
                Custom metadata
                The authors confirm that all data underlying the findings are fully available without restriction. The array data have been deposited at the ArrayExpress archive, accession number E-MTAB-1840.

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