| Literature DB >> 35366170 |
Andrea Martins-da-Silva1, Mirella Baroni2, Karina Bezerra Salomão2, Pablo Ferreira das Chagas3, Ricardo Bonfim-Silva4, Lenisa Geron3, Gustavo Alencastro Veiga Cruzeiro2,5, Wilson Araújo da Silva3, Carolina Alves Pereira Corrêa2, Carlos Gilberto Carlotti4, Rosane Gomes de Paula Queiroz2, Suely Kazue Nagahashi Marie6, Silvia Regina Brandalise7, José Andrés Yunes7, Carlos Alberto Scrideli2,3, Elvis Terci Valera2, Luiz Gonzaga Tone2,3.
Abstract
Medulloblastoma is the most common type of pediatric malignant primary brain tumor, and about one-third of patients die due to disease recurrence and most survivors suffer from long-term side effects. MB is clinically, genetically, and epigenetically heterogeneous and subdivided into at least four molecular subgroups: WNT, SHH, Group 3, and Group 4. We evaluated common differentially expressed genes between a Brazilian RNA-seq GSE181293 dataset and microarray GSE85217 dataset cohort of pediatric MB samples using bioinformatics methodology in order to identify hub genes of the molecular subgroups based on PPI network construction, survival and functional analysis. The main finding was the identification of five hub genes from the WNT subgroup that are tumor suppressors, and whose lower expression is related to a worse prognosis for MB patients. Furthermore, the common genes correlated with the five tumor suppressors participate in important pathways and processes for tumor initiation and progression, as well as development and differentiation, and some of them control cell stemness and pluripotency. These genes have not yet been studied within the context of MB, representing new important elements for investigation in the search for therapeutic targets, prognostic markers or for understanding of MB biology.Entities:
Keywords: Bioinformatics tools; Biomarkers; Hub genes; Molecular Subgroups; Therapeutic targets
Year: 2022 PMID: 35366170 DOI: 10.1007/s10571-022-01217-4
Source DB: PubMed Journal: Cell Mol Neurobiol ISSN: 0272-4340 Impact factor: 5.046