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Название: Forward Genetics-Based Approaches to Understanding the Systems Biology and Molecular Mechanisms of Epilepsy
Авторы: Shevlyakov, A. D.
Kolesnikova, T. O.
de, Abreu, M. S.
Petersen, E. V.
Yenkoyan, K. B.
Demin, K. A.
Kalueff, A. V.
Дата публикации: 2023
Издатель: Multidisciplinary Digital Publishing Institute (MDPI)
Библиографическое описание: Shevlyakov, AD, Kolesnikova, TO, De abreu, MS, Petersen, EV, Yenkoyan, KB, Demin, KA & Kalueff, AV 2023, 'Forward Genetics-Based Approaches to Understanding the Systems Biology and Molecular Mechanisms of Epilepsy', International Journal of Molecular Sciences, Том. 24, № 6, 5280. https://doi.org/10.3390/ijms24065280
Shevlyakov, A. D., Kolesnikova, T. O., De abreu, M. S., Petersen, E. V., Yenkoyan, K. B., Demin, K. A., & Kalueff, A. V. (2023). Forward Genetics-Based Approaches to Understanding the Systems Biology and Molecular Mechanisms of Epilepsy. International Journal of Molecular Sciences, 24(6), [5280]. https://doi.org/10.3390/ijms24065280
Аннотация: Epilepsy is a highly prevalent, severely debilitating neurological disorder characterized by seizures and neuronal hyperactivity due to an imbalanced neurotransmission. As genetic factors play a key role in epilepsy and its treatment, various genetic and genomic technologies continue to dissect the genetic causes of this disorder. However, the exact pathogenesis of epilepsy is not fully understood, necessitating further translational studies of this condition. Here, we applied a computational in silico approach to generate a comprehensive network of molecular pathways involved in epilepsy, based on known human candidate epilepsy genes and their established molecular interactors. Clustering the resulting network identified potential key interactors that may contribute to the development of epilepsy, and revealed functional molecular pathways associated with this disorder, including those related to neuronal hyperactivity, cytoskeletal and mitochondrial function, and metabolism. While traditional antiepileptic drugs often target single mechanisms associated with epilepsy, recent studies suggest targeting downstream pathways as an alternative efficient strategy. However, many potential downstream pathways have not yet been considered as promising targets for antiepileptic treatment. Our study calls for further research into the complexity of molecular mechanisms underlying epilepsy, aiming to develop more effective treatments targeting novel putative downstream pathways of this disorder. © 2023 by the authors.
Ключевые слова: EPILEPSY
GENES
GENETIC BASES
IN SILICO MODELING
MOLECULAR NETWORK
ANTICONVULSIVE AGENT
MAMMALIAN TARGET OF RAPAMYCIN
TRANSCRIPTION FACTOR
ANTICONVULSANT THERAPY
CELL DIVISION
CHROMATIN ASSEMBLY AND DISASSEMBLY
COMPUTER MODEL
CYTOSKELETON
EPILEPSY
EPILEPTOGENESIS
GENETIC ASSOCIATION
HEREDITY
HUMAN
METABOLISM
MITOCHONDRIAL BIOGENESIS
MITOCHONDRION
MOLECULAR PATHOLOGY
MTOR SIGNALING
NONHUMAN
REVIEW
SIGNAL TRANSDUCTION
SYSTEMS BIOLOGY
EPILEPSY
GENOME
SEIZURE
ANTICONVULSANTS
EPILEPSY
GENOME
HUMANS
SEIZURES
SYSTEMS BIOLOGY
URI: http://elar.urfu.ru/handle/10995/130306
Условия доступа: info:eu-repo/semantics/openAccess
cc-by
Текст лицензии: https://creativecommons.org/licenses/by/4.0/
Идентификатор SCOPUS: 85151110646
Идентификатор WOS: 000959151300001
Идентификатор PURE: 37087834
ISSN: 1661-6596
DOI: 10.3390/ijms24065280
Сведения о поддержке: 075-15-2021-684; 857600; Saint Petersburg State University, SPbU: 93020614; Suzhou University of Science and Technology: NRB-RND-2116; State Committee of Science, SCS: 20TTCG-3A012, N10-14/I-1
The study was performed in collaboration with the YSMU COBRAIN Scientific-Educational Center for Fundamental Brain Research, supported by the Republic of Armenia State Committee of Science (20TTCG-3A012 and N10-14/I-1) and the European Union-funded H2020 COBRAIN project (857600).
The research was supported by Sirius University of Science and Technology Project ID NRB-RND-2116. K.A.D. was supported by St. Petersburg State University state budgetary funds (Project ID 93020614). The study partially used the facilities and equipment of the Resource Fund of Applied Genetics MIPT (support grant 075-15-2021-684).
Располагается в коллекциях:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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