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Constraints on signaling network logic reveal functional subgraphs on Multiple Myeloma OMIC data.
Miannay, Bertrand; Minvielle, Stéphane; Magrangeas, Florence; Guziolowski, Carito.
Afiliación
  • Miannay B; LS2N, UMR 6004, École Centrale de Nantes, Nantes, France.
  • Minvielle S; CRCINA, INSERM, CNRS, Université d'Angers, Université de Nantes, Nantes, France.
  • Magrangeas F; CRCINA, INSERM, CNRS, Université d'Angers, Université de Nantes, Nantes, France.
  • Guziolowski C; CRCINA, INSERM, CNRS, Université d'Angers, Université de Nantes, Nantes, France.
BMC Syst Biol ; 12(Suppl 3): 32, 2018 03 21.
Article en En | MEDLINE | ID: mdl-29589566
BACKGROUND: The integration of gene expression profiles (GEPs) and large-scale biological networks derived from pathways databases is a subject which is being widely explored. Existing methods are based on network distance measures among significantly measured species. Only a small number of them include the directionality and underlying logic existing in biological networks. In this study we approach the GEP-networks integration problem by considering the network logic, however our approach does not require a prior species selection according to their gene expression level. RESULTS: We start by modeling the biological network representing its underlying logic using Logic Programming. This model points to reachable network discrete states that maximize a notion of harmony between the molecular species active or inactive possible states and the directionality of the pathways reactions according to their activator or inhibitor control role. Only then, we confront these network states with the GEP. From this confrontation independent graph components are derived, each of them related to a fixed and optimal assignment of active or inactive states. These components allow us to decompose a large-scale network into subgraphs and their molecular species state assignments have different degrees of similarity when compared to the same GEP. We apply our method to study the set of possible states derived from a subgraph from the NCI-PID Pathway Interaction Database. This graph links Multiple Myeloma (MM) genes to known receptors for this blood cancer. CONCLUSION: We discover that the NCI-PID MM graph had 15 independent components, and when confronted to 611 MM GEPs, we find 1 component as being more specific to represent the difference between cancer and healthy profiles.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Gráficos por Computador / Transducción de Señal / Biología Computacional / Redes Reguladoras de Genes / Lógica / Mieloma Múltiple Idioma: En Revista: BMC Syst Biol Asunto de la revista: BIOLOGIA / BIOTECNOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Gráficos por Computador / Transducción de Señal / Biología Computacional / Redes Reguladoras de Genes / Lógica / Mieloma Múltiple Idioma: En Revista: BMC Syst Biol Asunto de la revista: BIOLOGIA / BIOTECNOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido