Literature DB >> 35731990

Deepening the knowledge of rare diseases dependent on angiogenesis through semantic similarity clustering and network analysis.

Raquel Pagano-Márquez1, José Córdoba-Caballero1, Beatriz Martínez-Poveda1,2,3, Ana R Quesada1,3,4, Elena Rojano1,3,4, Pedro Seoane1,3, Juan A G Ranea1,3,4, Miguel Ángel Medina1,3,4.   

Abstract

BACKGROUND: Angiogenesis is regulated by multiple genes whose variants can lead to different disorders. Among them, rare diseases are a heterogeneous group of pathologies, most of them genetic, whose information may be of interest to determine the still unknown genetic and molecular causes of other diseases. In this work, we use the information on rare diseases dependent on angiogenesis to investigate the genes that are associated with this biological process and to determine if there are interactions between the genes involved in its deregulation.
RESULTS: We propose a systemic approach supported by the use of pathological phenotypes to group diseases by semantic similarity. We grouped 158 angiogenesis-related rare diseases in 18 clusters based on their phenotypes. Of them, 16 clusters had traceable gene connections in a high-quality interaction network. These disease clusters are associated with 130 different genes. We searched for genes associated with angiogenesis througth ClinVar pathogenic variants. Of the seven retrieved genes, our system confirms six of them. Furthermore, it allowed us to identify common affected functions among these disease clusters. AVAILABILITY: https://github.com/ElenaRojano/angio_cluster. CONTACT: seoanezonjic@uma.es and elenarojano@uma.es.
© The Author(s) 2022. Published by Oxford University Press.

Entities:  

Keywords:  angiogenesis; disease clustering; rare diseases; semantic similarity; systems biology

Mesh:

Year:  2022        PMID: 35731990      PMCID: PMC9294413          DOI: 10.1093/bib/bbac220

Source DB:  PubMed          Journal:  Brief Bioinform        ISSN: 1467-5463            Impact factor:   13.994


  55 in total

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8.  SemFunSim: a new method for measuring disease similarity by integrating semantic and gene functional association.

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