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. 1. Department of Molecular Biology and Biochemistry, University of Malaga, Andalucia Tech, Bulevar Louis Pasteur 31, E-29071, Malaga, Spain. 2. CIBER de Enfermedades Cardiovasculares, CIBERCV, Av. Monforte de Lemos, 3-5, Pabellon 11, Planta 0, 28029, Madrid, Spain. 3. Biomedical Research Institute of Malaga, IBIMA, Calle Doctor Miguel Diaz Recio 28, 29010, Malaga, Spain. 4. CIBER de Enfermedades Raras, CIBERER, Av. Monforte de Lemos, 3-5, Pabellon 11, Planta 0, 28029, Madrid, Spain.
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.
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.
Authors: L Rigoli; F Prisco; R A Caruso; D Iafusco; G Ursomanno; D Zuccarello; N Ingenito; M Rigoli; I Barberi Journal: Diabet Med Date: 2001-04 Impact factor: 4.359
Authors: Jesus V Soriano; Ningfei Liu; Yang Gao; Zhu-Jun Yao; Toshio Ishibashi; Charles Underhill; Terrence R Burke; Donald P Bottaro Journal: Mol Cancer Ther Date: 2004-10 Impact factor: 6.261
Authors: Christian von Mering; Lars J Jensen; Berend Snel; Sean D Hooper; Markus Krupp; Mathilde Foglierini; Nelly Jouffre; Martijn A Huynen; Peer Bork Journal: Nucleic Acids Res Date: 2005-01-01 Impact factor: 16.971
Authors: Aaron J Masino; Elizabeth T Dechene; Matthew C Dulik; Alisha Wilkens; Nancy B Spinner; Ian D Krantz; Jeffrey W Pennington; Peter N Robinson; Peter S White Journal: BMC Bioinformatics Date: 2014-07-21 Impact factor: 3.169
Authors: Luke T Slater; John A Williams; Andreas Karwath; Hilary Fanning; Simon Ball; Paul N Schofield; Robert Hoehndorf; Georgios V Gkoutos Journal: Comput Biol Med Date: 2021-09-27 Impact factor: 4.589