Autism Spectrum Disorder: Signaling Pathways and Prospective Therapeutic Targets
The Autism Spectrum Disorder (ASD) consists of a prevalent and heterogeneous group of neurodevelopmental diseases representing a severe burden to affected individuals and their caretakers. Despite substantial improvement towards understanding of ASD etiology and pathogenesis, as well as increased so...
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Veröffentlicht in: | Cellular and molecular neurobiology 2021-05, Vol.41 (4), p.619-649 |
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creator | Baranova, Juliana Dragunas, Guilherme Botellho, Mayara C. S. Ayub, Ana Luisa P. Bueno-Alves, Rebeca Alencar, Rebeca R. Papaiz, Debora D. Sogayar, Mari C. Ulrich, Henning Correa, Ricardo G. |
description | The Autism Spectrum Disorder (ASD) consists of a prevalent and heterogeneous group of neurodevelopmental diseases representing a severe burden to affected individuals and their caretakers. Despite substantial improvement towards understanding of ASD etiology and pathogenesis, as well as increased social awareness and more intensive research, no effective drugs have been successfully developed to resolve the main and most cumbersome ASD symptoms. Hence, finding better treatments, which may act as “disease-modifying” agents, and novel biomarkers for earlier ASD diagnosis and disease stage determination are needed. Diverse mutations of core components and consequent malfunctions of several cell signaling pathways have already been found in ASD by a series of experimental platforms, including genetic associations analyses and studies utilizing pre-clinical animal models and patient samples. These signaling cascades govern a broad range of neurological features such as neuronal development, neurotransmission, metabolism, and homeostasis, as well as immune regulation and inflammation. Here, we review the current knowledge on signaling pathways which are commonly disrupted in ASD and autism-related conditions. As such, we further propose ways to translate these findings into the development of genetic and biochemical clinical tests for early autism detection. Moreover, we highlight some putative druggable targets along these pathways, which, upon further research efforts, may evolve into novel therapeutic interventions for certain ASD conditions. Lastly, we also refer to the crosstalk among these major signaling cascades as well as their putative implications in therapeutics. Based on this collective information, we believe that a timely and accurate modulation of these prominent pathways may shape the neurodevelopment and neuro-immune regulation of homeostatic patterns and, hopefully, rescue some (if not all) ASD phenotypes. |
doi_str_mv | 10.1007/s10571-020-00882-7 |
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S. ; Ayub, Ana Luisa P. ; Bueno-Alves, Rebeca ; Alencar, Rebeca R. ; Papaiz, Debora D. ; Sogayar, Mari C. ; Ulrich, Henning ; Correa, Ricardo G.</creator><creatorcontrib>Baranova, Juliana ; Dragunas, Guilherme ; Botellho, Mayara C. S. ; Ayub, Ana Luisa P. ; Bueno-Alves, Rebeca ; Alencar, Rebeca R. ; Papaiz, Debora D. ; Sogayar, Mari C. ; Ulrich, Henning ; Correa, Ricardo G.</creatorcontrib><description>The Autism Spectrum Disorder (ASD) consists of a prevalent and heterogeneous group of neurodevelopmental diseases representing a severe burden to affected individuals and their caretakers. Despite substantial improvement towards understanding of ASD etiology and pathogenesis, as well as increased social awareness and more intensive research, no effective drugs have been successfully developed to resolve the main and most cumbersome ASD symptoms. Hence, finding better treatments, which may act as “disease-modifying” agents, and novel biomarkers for earlier ASD diagnosis and disease stage determination are needed. Diverse mutations of core components and consequent malfunctions of several cell signaling pathways have already been found in ASD by a series of experimental platforms, including genetic associations analyses and studies utilizing pre-clinical animal models and patient samples. These signaling cascades govern a broad range of neurological features such as neuronal development, neurotransmission, metabolism, and homeostasis, as well as immune regulation and inflammation. Here, we review the current knowledge on signaling pathways which are commonly disrupted in ASD and autism-related conditions. As such, we further propose ways to translate these findings into the development of genetic and biochemical clinical tests for early autism detection. Moreover, we highlight some putative druggable targets along these pathways, which, upon further research efforts, may evolve into novel therapeutic interventions for certain ASD conditions. Lastly, we also refer to the crosstalk among these major signaling cascades as well as their putative implications in therapeutics. Based on this collective information, we believe that a timely and accurate modulation of these prominent pathways may shape the neurodevelopment and neuro-immune regulation of homeostatic patterns and, hopefully, rescue some (if not all) ASD phenotypes.</description><identifier>ISSN: 0272-4340</identifier><identifier>ISSN: 1573-6830</identifier><identifier>EISSN: 1573-6830</identifier><identifier>DOI: 10.1007/s10571-020-00882-7</identifier><identifier>PMID: 32468442</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Animal models ; Animals ; Autism ; Autism Spectrum Disorder - drug therapy ; Autism Spectrum Disorder - epidemiology ; Autism Spectrum Disorder - metabolism ; Biomedical and Life Sciences ; Biomedicine ; Cell Biology ; Cell Survival ; Cytokines - metabolism ; Drug development ; Etiology ; Genetic analysis ; Homeostasis ; Humans ; Immunoregulation ; Immunosuppressive agents ; Inflammation ; Metabolic Networks and Pathways ; Molecular Targeted Therapy ; Neurobiology ; Neurodevelopment ; Neurodevelopmental disorders ; Neurosciences ; Neurotransmission ; Phenotypes ; Review Paper ; Signal Transduction ; Therapeutic applications ; Therapeutic targets</subject><ispartof>Cellular and molecular neurobiology, 2021-05, Vol.41 (4), p.619-649</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-b7d58d335a2fea972befaeb95cd8d8bf115c6dfeefe1cb9d9ec5f87fcf54467d3</citedby><cites>FETCH-LOGICAL-c375t-b7d58d335a2fea972befaeb95cd8d8bf115c6dfeefe1cb9d9ec5f87fcf54467d3</cites><orcidid>0000-0002-1848-6999 ; 0000-0002-1492-2220 ; 0000-0002-2114-3815 ; 0000-0002-4420-529X ; 0000-0003-4805-4609 ; 0000-0001-6940-7034 ; 0000-0002-1550-5824 ; 0000-0003-3091-4244 ; 0000-0002-1401-7263 ; 0000-0001-6560-8402</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10571-020-00882-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10571-020-00882-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32468442$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baranova, Juliana</creatorcontrib><creatorcontrib>Dragunas, Guilherme</creatorcontrib><creatorcontrib>Botellho, Mayara C. S.</creatorcontrib><creatorcontrib>Ayub, Ana Luisa P.</creatorcontrib><creatorcontrib>Bueno-Alves, Rebeca</creatorcontrib><creatorcontrib>Alencar, Rebeca R.</creatorcontrib><creatorcontrib>Papaiz, Debora D.</creatorcontrib><creatorcontrib>Sogayar, Mari C.</creatorcontrib><creatorcontrib>Ulrich, Henning</creatorcontrib><creatorcontrib>Correa, Ricardo G.</creatorcontrib><title>Autism Spectrum Disorder: Signaling Pathways and Prospective Therapeutic Targets</title><title>Cellular and molecular neurobiology</title><addtitle>Cell Mol Neurobiol</addtitle><addtitle>Cell Mol Neurobiol</addtitle><description>The Autism Spectrum Disorder (ASD) consists of a prevalent and heterogeneous group of neurodevelopmental diseases representing a severe burden to affected individuals and their caretakers. Despite substantial improvement towards understanding of ASD etiology and pathogenesis, as well as increased social awareness and more intensive research, no effective drugs have been successfully developed to resolve the main and most cumbersome ASD symptoms. Hence, finding better treatments, which may act as “disease-modifying” agents, and novel biomarkers for earlier ASD diagnosis and disease stage determination are needed. Diverse mutations of core components and consequent malfunctions of several cell signaling pathways have already been found in ASD by a series of experimental platforms, including genetic associations analyses and studies utilizing pre-clinical animal models and patient samples. These signaling cascades govern a broad range of neurological features such as neuronal development, neurotransmission, metabolism, and homeostasis, as well as immune regulation and inflammation. Here, we review the current knowledge on signaling pathways which are commonly disrupted in ASD and autism-related conditions. As such, we further propose ways to translate these findings into the development of genetic and biochemical clinical tests for early autism detection. Moreover, we highlight some putative druggable targets along these pathways, which, upon further research efforts, may evolve into novel therapeutic interventions for certain ASD conditions. Lastly, we also refer to the crosstalk among these major signaling cascades as well as their putative implications in therapeutics. Based on this collective information, we believe that a timely and accurate modulation of these prominent pathways may shape the neurodevelopment and neuro-immune regulation of homeostatic patterns and, hopefully, rescue some (if not all) ASD phenotypes.</description><subject>Animal models</subject><subject>Animals</subject><subject>Autism</subject><subject>Autism Spectrum Disorder - drug therapy</subject><subject>Autism Spectrum Disorder - epidemiology</subject><subject>Autism Spectrum Disorder - metabolism</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Biology</subject><subject>Cell Survival</subject><subject>Cytokines - metabolism</subject><subject>Drug development</subject><subject>Etiology</subject><subject>Genetic analysis</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Immunoregulation</subject><subject>Immunosuppressive agents</subject><subject>Inflammation</subject><subject>Metabolic Networks and Pathways</subject><subject>Molecular Targeted Therapy</subject><subject>Neurobiology</subject><subject>Neurodevelopment</subject><subject>Neurodevelopmental disorders</subject><subject>Neurosciences</subject><subject>Neurotransmission</subject><subject>Phenotypes</subject><subject>Review Paper</subject><subject>Signal Transduction</subject><subject>Therapeutic applications</subject><subject>Therapeutic targets</subject><issn>0272-4340</issn><issn>1573-6830</issn><issn>1573-6830</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1PGzEQhi1URFLgD3CoVuqlly3jr9jbW0S_kCIRiXC2vPY4bJTdTe3dVvx7HAJU4sBpDvO872geQi4ofKUA6jJRkIqWwKAE0JqV6ohMqVS8nGkOH8gUmGKl4AIm5GNKGwCoAOQJmXAmZloINiXL-Tg0qS1ud-iGOLbF9yb10WP8Vtw2685um25dLO1w_88-pMJ2vljGPu3h5i8Wq3uMdoe5whUrG9c4pDNyHOw24fnzPCV3P3-srn6Xi5tf11fzRem4kkNZKy-151xaFtBWitUYLNaVdF57XQdKpZv5gBiQurryFToZtAouSCFmyvNT8uXQu4v9nxHTYNomOdxubYf9mAwToBlITiGjn9-gm36M-bdMyb3CSgueKXagXH4wRQxmF5vWxgdDwex9m4Nvk32bJ99G5dCn5-qxbtG_Rl4EZ4AfgJRX3Rrj_9vv1D4CbmyMhQ</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Baranova, Juliana</creator><creator>Dragunas, Guilherme</creator><creator>Botellho, Mayara C. 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S.</creatorcontrib><creatorcontrib>Ayub, Ana Luisa P.</creatorcontrib><creatorcontrib>Bueno-Alves, Rebeca</creatorcontrib><creatorcontrib>Alencar, Rebeca R.</creatorcontrib><creatorcontrib>Papaiz, Debora D.</creatorcontrib><creatorcontrib>Sogayar, Mari C.</creatorcontrib><creatorcontrib>Ulrich, Henning</creatorcontrib><creatorcontrib>Correa, Ricardo G.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cellular and molecular neurobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baranova, Juliana</au><au>Dragunas, Guilherme</au><au>Botellho, Mayara C. S.</au><au>Ayub, Ana Luisa P.</au><au>Bueno-Alves, Rebeca</au><au>Alencar, Rebeca R.</au><au>Papaiz, Debora D.</au><au>Sogayar, Mari C.</au><au>Ulrich, Henning</au><au>Correa, Ricardo G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autism Spectrum Disorder: Signaling Pathways and Prospective Therapeutic Targets</atitle><jtitle>Cellular and molecular neurobiology</jtitle><stitle>Cell Mol Neurobiol</stitle><addtitle>Cell Mol Neurobiol</addtitle><date>2021-05-01</date><risdate>2021</risdate><volume>41</volume><issue>4</issue><spage>619</spage><epage>649</epage><pages>619-649</pages><issn>0272-4340</issn><issn>1573-6830</issn><eissn>1573-6830</eissn><abstract>The Autism Spectrum Disorder (ASD) consists of a prevalent and heterogeneous group of neurodevelopmental diseases representing a severe burden to affected individuals and their caretakers. Despite substantial improvement towards understanding of ASD etiology and pathogenesis, as well as increased social awareness and more intensive research, no effective drugs have been successfully developed to resolve the main and most cumbersome ASD symptoms. Hence, finding better treatments, which may act as “disease-modifying” agents, and novel biomarkers for earlier ASD diagnosis and disease stage determination are needed. Diverse mutations of core components and consequent malfunctions of several cell signaling pathways have already been found in ASD by a series of experimental platforms, including genetic associations analyses and studies utilizing pre-clinical animal models and patient samples. These signaling cascades govern a broad range of neurological features such as neuronal development, neurotransmission, metabolism, and homeostasis, as well as immune regulation and inflammation. Here, we review the current knowledge on signaling pathways which are commonly disrupted in ASD and autism-related conditions. As such, we further propose ways to translate these findings into the development of genetic and biochemical clinical tests for early autism detection. Moreover, we highlight some putative druggable targets along these pathways, which, upon further research efforts, may evolve into novel therapeutic interventions for certain ASD conditions. Lastly, we also refer to the crosstalk among these major signaling cascades as well as their putative implications in therapeutics. Based on this collective information, we believe that a timely and accurate modulation of these prominent pathways may shape the neurodevelopment and neuro-immune regulation of homeostatic patterns and, hopefully, rescue some (if not all) ASD phenotypes.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>32468442</pmid><doi>10.1007/s10571-020-00882-7</doi><tpages>31</tpages><orcidid>https://orcid.org/0000-0002-1848-6999</orcidid><orcidid>https://orcid.org/0000-0002-1492-2220</orcidid><orcidid>https://orcid.org/0000-0002-2114-3815</orcidid><orcidid>https://orcid.org/0000-0002-4420-529X</orcidid><orcidid>https://orcid.org/0000-0003-4805-4609</orcidid><orcidid>https://orcid.org/0000-0001-6940-7034</orcidid><orcidid>https://orcid.org/0000-0002-1550-5824</orcidid><orcidid>https://orcid.org/0000-0003-3091-4244</orcidid><orcidid>https://orcid.org/0000-0002-1401-7263</orcidid><orcidid>https://orcid.org/0000-0001-6560-8402</orcidid></addata></record> |
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subjects | Animal models Animals Autism Autism Spectrum Disorder - drug therapy Autism Spectrum Disorder - epidemiology Autism Spectrum Disorder - metabolism Biomedical and Life Sciences Biomedicine Cell Biology Cell Survival Cytokines - metabolism Drug development Etiology Genetic analysis Homeostasis Humans Immunoregulation Immunosuppressive agents Inflammation Metabolic Networks and Pathways Molecular Targeted Therapy Neurobiology Neurodevelopment Neurodevelopmental disorders Neurosciences Neurotransmission Phenotypes Review Paper Signal Transduction Therapeutic applications Therapeutic targets |
title | Autism Spectrum Disorder: Signaling Pathways and Prospective Therapeutic Targets |
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