Correction to: A systematic review on the role of MSC‑derived exosomal miRNAs in the treatment of heart failure
Background Heart failure (HF) is a deeply serious clinical problem that remains unsolved. Many reports highlight the cardioprotective properties of mesenchymal stem cells (MSCs), the factors contained in their secretome being particularly important for this function; these include the exosomal miRNA...
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Veröffentlicht in: | Molecular biology reports 2022-09, Vol.49 (9), p.8975-8975 |
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creator | Botello-Flores, Yesica Abril Yocupicio-Monroy, Martha Balderrábano-Saucedo, Norma Contreras-Ramos, Alejandra |
description | Background
Heart failure (HF) is a deeply serious clinical problem that remains unsolved. Many reports highlight the cardioprotective properties of mesenchymal stem cells (MSCs), the factors contained in their secretome being particularly important for this function; these include the exosomal miRNAs (exo-miRNAs) secreted with or without stimulus which can modulate various biological processes. In search of new paradigms in heart failure, we wondered whether MSC-derived exosomal microRNAs could play a role in the management of clinical patients.
Methods
To analyze whether there is sufficient evidence to support this hypothesis we designed a systematic review of studies on exo-miRNAs in heart diseases causing HF during the last decade.
Results
The cardioprotective functions of twenty-four exo-miRNAs derived from bone marrow MSCs (BM-MSCs) are known and the functions of exo-miRNAs from other MSC sources such as adipose tissue, trophoblasts, amniotic fluid, and endometrium were also determined. Inhibition of apoptosis is the most reported biological function and the targets for thirty exo-miRNAs are known.
Conclusions
The results from this systematic review support the initial hypothesis and encourage us to test it in future experimental research works but more importantly, we seek to encourage other researchers in the field to propose other hypotheses aimed at the possible use of exo-miRNAs in HF secondary to cardiac disease. |
doi_str_mv | 10.1007/s11033-022-07537-4 |
format | Article |
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Heart failure (HF) is a deeply serious clinical problem that remains unsolved. Many reports highlight the cardioprotective properties of mesenchymal stem cells (MSCs), the factors contained in their secretome being particularly important for this function; these include the exosomal miRNAs (exo-miRNAs) secreted with or without stimulus which can modulate various biological processes. In search of new paradigms in heart failure, we wondered whether MSC-derived exosomal microRNAs could play a role in the management of clinical patients.
Methods
To analyze whether there is sufficient evidence to support this hypothesis we designed a systematic review of studies on exo-miRNAs in heart diseases causing HF during the last decade.
Results
The cardioprotective functions of twenty-four exo-miRNAs derived from bone marrow MSCs (BM-MSCs) are known and the functions of exo-miRNAs from other MSC sources such as adipose tissue, trophoblasts, amniotic fluid, and endometrium were also determined. Inhibition of apoptosis is the most reported biological function and the targets for thirty exo-miRNAs are known.
Conclusions
The results from this systematic review support the initial hypothesis and encourage us to test it in future experimental research works but more importantly, we seek to encourage other researchers in the field to propose other hypotheses aimed at the possible use of exo-miRNAs in HF secondary to cardiac disease.</description><identifier>ISSN: 0301-4851</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-022-07537-4</identifier><identifier>PMID: 35499688</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animal Anatomy ; Animal Biochemistry ; Biomedical and Life Sciences ; Correction ; Histology ; Life Sciences ; Morphology</subject><ispartof>Molecular biology reports, 2022-09, Vol.49 (9), p.8975-8975</ispartof><rights>Springer Nature B.V. 2022</rights><rights>2022. Springer Nature B.V.</rights><rights>Springer Nature B.V. 2022.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-5173-9927</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/s11033-022-07537-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11033-022-07537-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51298</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35499688$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Botello-Flores, Yesica Abril</creatorcontrib><creatorcontrib>Yocupicio-Monroy, Martha</creatorcontrib><creatorcontrib>Balderrábano-Saucedo, Norma</creatorcontrib><creatorcontrib>Contreras-Ramos, Alejandra</creatorcontrib><title>Correction to: A systematic review on the role of MSC‑derived exosomal miRNAs in the treatment of heart failure</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><addtitle>Mol Biol Rep</addtitle><description>Background
Heart failure (HF) is a deeply serious clinical problem that remains unsolved. Many reports highlight the cardioprotective properties of mesenchymal stem cells (MSCs), the factors contained in their secretome being particularly important for this function; these include the exosomal miRNAs (exo-miRNAs) secreted with or without stimulus which can modulate various biological processes. In search of new paradigms in heart failure, we wondered whether MSC-derived exosomal microRNAs could play a role in the management of clinical patients.
Methods
To analyze whether there is sufficient evidence to support this hypothesis we designed a systematic review of studies on exo-miRNAs in heart diseases causing HF during the last decade.
Results
The cardioprotective functions of twenty-four exo-miRNAs derived from bone marrow MSCs (BM-MSCs) are known and the functions of exo-miRNAs from other MSC sources such as adipose tissue, trophoblasts, amniotic fluid, and endometrium were also determined. Inhibition of apoptosis is the most reported biological function and the targets for thirty exo-miRNAs are known.
Conclusions
The results from this systematic review support the initial hypothesis and encourage us to test it in future experimental research works but more importantly, we seek to encourage other researchers in the field to propose other hypotheses aimed at the possible use of exo-miRNAs in HF secondary to cardiac disease.</description><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Correction</subject><subject>Histology</subject><subject>Life Sciences</subject><subject>Morphology</subject><issn>0301-4851</issn><issn>1573-4978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kctu1TAURS1ERS-FH2CALDFhEurjR-wwu7oqD6mAxGNsOc4xTZXErZ0UOuMX-ov9EnxJAYkBIw_O2ts-XoQ8AfYCGNPHGYAJUTHOK6aV0JW8RzagtKhko819smGCQSWNgkPyMOdzxpgErR6QQ6Fk09TGbMjlLqaEfu7jROf4km5pvs4zjm7uPU141eM3uh-dIU1xQBoDffdpd_vjpsPUX2FH8XvMcXQDHfuP77eZ9is8J3TziNO8T5yhSzMNrh-WhI_IQXBDxsd35xH58urk8-5Ndfrh9dvd9rTyHJSsnIcauFTaMCODgWAcOh2CghahY6i1YNh50elGl118g6JtJXS8VcEz5cQReb72XqR4uWCe7dhnj8PgJoxLtrxWppZ1-ZCCPvsHPY9LmsrrLNfAAUAIXSi-Uj7FnBMGe5H60aVrC8zuhdhViC1C7C8hVpbQ07vqpR2x-xP5baAAYgVyGU1fMf29-z-1PwEn9ZaY</recordid><startdate>20220901</startdate><enddate>20220901</enddate><creator>Botello-Flores, Yesica Abril</creator><creator>Yocupicio-Monroy, Martha</creator><creator>Balderrábano-Saucedo, Norma</creator><creator>Contreras-Ramos, Alejandra</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5173-9927</orcidid></search><sort><creationdate>20220901</creationdate><title>Correction to: A systematic review on the role of MSC‑derived exosomal miRNAs in the treatment of heart failure</title><author>Botello-Flores, Yesica Abril ; Yocupicio-Monroy, Martha ; Balderrábano-Saucedo, Norma ; Contreras-Ramos, Alejandra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2154-ac16124578084f81f8aea7ff51be1d0e7730edc3d797996c9e3bb41d2b5fc05a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Correction</topic><topic>Histology</topic><topic>Life Sciences</topic><topic>Morphology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Botello-Flores, Yesica Abril</creatorcontrib><creatorcontrib>Yocupicio-Monroy, Martha</creatorcontrib><creatorcontrib>Balderrábano-Saucedo, Norma</creatorcontrib><creatorcontrib>Contreras-Ramos, Alejandra</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular biology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Botello-Flores, Yesica Abril</au><au>Yocupicio-Monroy, Martha</au><au>Balderrábano-Saucedo, Norma</au><au>Contreras-Ramos, Alejandra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correction to: A systematic review on the role of MSC‑derived exosomal miRNAs in the treatment of heart failure</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><addtitle>Mol Biol Rep</addtitle><date>2022-09-01</date><risdate>2022</risdate><volume>49</volume><issue>9</issue><spage>8975</spage><epage>8975</epage><pages>8975-8975</pages><issn>0301-4851</issn><eissn>1573-4978</eissn><abstract>Background
Heart failure (HF) is a deeply serious clinical problem that remains unsolved. Many reports highlight the cardioprotective properties of mesenchymal stem cells (MSCs), the factors contained in their secretome being particularly important for this function; these include the exosomal miRNAs (exo-miRNAs) secreted with or without stimulus which can modulate various biological processes. In search of new paradigms in heart failure, we wondered whether MSC-derived exosomal microRNAs could play a role in the management of clinical patients.
Methods
To analyze whether there is sufficient evidence to support this hypothesis we designed a systematic review of studies on exo-miRNAs in heart diseases causing HF during the last decade.
Results
The cardioprotective functions of twenty-four exo-miRNAs derived from bone marrow MSCs (BM-MSCs) are known and the functions of exo-miRNAs from other MSC sources such as adipose tissue, trophoblasts, amniotic fluid, and endometrium were also determined. Inhibition of apoptosis is the most reported biological function and the targets for thirty exo-miRNAs are known.
Conclusions
The results from this systematic review support the initial hypothesis and encourage us to test it in future experimental research works but more importantly, we seek to encourage other researchers in the field to propose other hypotheses aimed at the possible use of exo-miRNAs in HF secondary to cardiac disease.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>35499688</pmid><doi>10.1007/s11033-022-07537-4</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-5173-9927</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animal Anatomy Animal Biochemistry Biomedical and Life Sciences Correction Histology Life Sciences Morphology |
title | Correction to: A systematic review on the role of MSC‑derived exosomal miRNAs in the treatment of heart failure |
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