MicroRNAs as Potential Circulating Biomarkers for Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis (ALS) is a condition primarily characterized by the selective loss of upper and lower motor neurons. Motor neuron loss gives rise to muscle tissue malfunctions, including weakness, spasticity, atrophy, and ultimately paralysis, with death typically due to respiratory fa...
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Veröffentlicht in: | Journal of molecular neuroscience 2015-05, Vol.56 (1), p.102-112 |
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description | Amyotrophic lateral sclerosis (ALS) is a condition primarily characterized by the selective loss of upper and lower motor neurons. Motor neuron loss gives rise to muscle tissue malfunctions, including weakness, spasticity, atrophy, and ultimately paralysis, with death typically due to respiratory failure within 2 to 5 years of symptoms’ onset. The mean delay in time from presentation to diagnosis remains at over 1 year. Biomarkers are urgently needed to facilitate ALS diagnosis and prognosis as well as to act as indicators of therapeutic response in clinical trials. MicroRNAs (miRNAs) are small molecules that can influence posttranscriptional gene expression of a variety of transcript targets. Interestingly, miRNAs can be released into the circulation by pathologically affected tissues. This review presents therapeutic and diagnostic challenges associated with ALS, highlights the potential role of miRNAs in ALS, and discusses the diagnostic potential of these molecules in identifying ALS-specific miRNAs or in distinguishing between the various genotypic and phenotypic forms of ALS. |
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Motor neuron loss gives rise to muscle tissue malfunctions, including weakness, spasticity, atrophy, and ultimately paralysis, with death typically due to respiratory failure within 2 to 5 years of symptoms’ onset. The mean delay in time from presentation to diagnosis remains at over 1 year. Biomarkers are urgently needed to facilitate ALS diagnosis and prognosis as well as to act as indicators of therapeutic response in clinical trials. MicroRNAs (miRNAs) are small molecules that can influence posttranscriptional gene expression of a variety of transcript targets. Interestingly, miRNAs can be released into the circulation by pathologically affected tissues. This review presents therapeutic and diagnostic challenges associated with ALS, highlights the potential role of miRNAs in ALS, and discusses the diagnostic potential of these molecules in identifying ALS-specific miRNAs or in distinguishing between the various genotypic and phenotypic forms of ALS.</description><identifier>ISSN: 0895-8696</identifier><identifier>EISSN: 1559-1166</identifier><identifier>DOI: 10.1007/s12031-014-0471-8</identifier><identifier>PMID: 25433762</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Age groups ; Amyotrophic lateral sclerosis ; Amyotrophic Lateral Sclerosis - blood ; Animals ; Biomarkers ; Biomarkers - blood ; Biomedical and Life Sciences ; Biomedicine ; Cell Biology ; Dementia ; Humans ; Medical prognosis ; MicroRNAs ; MicroRNAs - blood ; Mutation ; Neurochemistry ; Neurology ; Neurons ; Neurosciences ; Proteomics ; Respiratory failure ; Risk factors ; Spinal cord</subject><ispartof>Journal of molecular neuroscience, 2015-05, Vol.56 (1), p.102-112</ispartof><rights>Springer Science+Business Media New York 2014</rights><rights>Springer Science+Business Media New York 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c541t-5895907aae38b68273e7ed07e834562c70c44ad7af26fa8e14d7d96d1e3070613</citedby><cites>FETCH-LOGICAL-c541t-5895907aae38b68273e7ed07e834562c70c44ad7af26fa8e14d7d96d1e3070613</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12031-014-0471-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12031-014-0471-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25433762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cloutier, Frank</creatorcontrib><creatorcontrib>Marrero, Alier</creatorcontrib><creatorcontrib>O’Connell, Colleen</creatorcontrib><creatorcontrib>Morin, Pier Jr</creatorcontrib><title>MicroRNAs as Potential Circulating Biomarkers for Amyotrophic Lateral Sclerosis</title><title>Journal of molecular neuroscience</title><addtitle>J Mol Neurosci</addtitle><addtitle>J Mol Neurosci</addtitle><description>Amyotrophic lateral sclerosis (ALS) is a condition primarily characterized by the selective loss of upper and lower motor neurons. Motor neuron loss gives rise to muscle tissue malfunctions, including weakness, spasticity, atrophy, and ultimately paralysis, with death typically due to respiratory failure within 2 to 5 years of symptoms’ onset. The mean delay in time from presentation to diagnosis remains at over 1 year. Biomarkers are urgently needed to facilitate ALS diagnosis and prognosis as well as to act as indicators of therapeutic response in clinical trials. MicroRNAs (miRNAs) are small molecules that can influence posttranscriptional gene expression of a variety of transcript targets. Interestingly, miRNAs can be released into the circulation by pathologically affected tissues. This review presents therapeutic and diagnostic challenges associated with ALS, highlights the potential role of miRNAs in ALS, and discusses the diagnostic potential of these molecules in identifying ALS-specific miRNAs or in distinguishing between the various genotypic and phenotypic forms of ALS.</description><subject>Age groups</subject><subject>Amyotrophic lateral sclerosis</subject><subject>Amyotrophic Lateral Sclerosis - blood</subject><subject>Animals</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Biology</subject><subject>Dementia</subject><subject>Humans</subject><subject>Medical prognosis</subject><subject>MicroRNAs</subject><subject>MicroRNAs - blood</subject><subject>Mutation</subject><subject>Neurochemistry</subject><subject>Neurology</subject><subject>Neurons</subject><subject>Neurosciences</subject><subject>Proteomics</subject><subject>Respiratory failure</subject><subject>Risk factors</subject><subject>Spinal cord</subject><issn>0895-8696</issn><issn>1559-1166</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkcFO3DAQhi0EKgvlAbigSFx6CczYju0cl1VLKy2lasvZMskEDNl4sZMDb1_TpQghIfU0B3_zz3g-xg4RThBAnybkILAElCVIjaXZYjOsqrpEVGqbzcDUVWlUrXbZXkp3ABwlmg9sl1dSCK34jF1e-CaGn9_nqXCp-BFGGkbv-mLhYzP1bvTDTXHmw8rFe4qp6EIs5qvHMMawvvVNsXQjxYz_anqKIfn0ke10rk908Fz32dWXz78XX8vl5fm3xXxZNpXEsazyZjVo50iYa2W4FqSpBU1GyErxRkMjpWu167jqnCGUrW5r1SIJ0KBQ7LNPm9x1DA8TpdGufGqo791AYUoWc6ipOQrxPyhIqaFSGT1-g96FKQ75I5lSebea_6VwQ-XLpRSps-vo84UeLYJ9EmM3YmwWY5_EWJN7jp6Tp-sVtS8d_0xkgG-AlJ-GG4qvRr-b-gdE75Zw</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Cloutier, Frank</creator><creator>Marrero, Alier</creator><creator>O’Connell, Colleen</creator><creator>Morin, Pier Jr</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7N</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20150501</creationdate><title>MicroRNAs as Potential Circulating Biomarkers for Amyotrophic Lateral Sclerosis</title><author>Cloutier, Frank ; 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subjects | Age groups Amyotrophic lateral sclerosis Amyotrophic Lateral Sclerosis - blood Animals Biomarkers Biomarkers - blood Biomedical and Life Sciences Biomedicine Cell Biology Dementia Humans Medical prognosis MicroRNAs MicroRNAs - blood Mutation Neurochemistry Neurology Neurons Neurosciences Proteomics Respiratory failure Risk factors Spinal cord |
title | MicroRNAs as Potential Circulating Biomarkers for Amyotrophic Lateral Sclerosis |
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