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Mesenchymal stem cell therapy in type 2 diabetes mellitus
Type 2 diabetes mellitus (T2DM), which is characterized by the combination of relative insulin deficiency and insulin resistance, cannot be reversed with existing therapeutic strategies. Transplantation of insulin-producing cells (IPCs) was once thought to be the most promising strategy for treating...
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Published in: | Diabetology and metabolic syndrome 2017-05, Vol.9 (1), p.36-36, Article 36 |
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creator | Zang, Li Hao, Haojie Liu, Jiejie Li, Yijun Han, Weidong Mu, Yiming |
description | Type 2 diabetes mellitus (T2DM), which is characterized by the combination of relative insulin deficiency and insulin resistance, cannot be reversed with existing therapeutic strategies. Transplantation of insulin-producing cells (IPCs) was once thought to be the most promising strategy for treating diabetes, but the pace from the laboratory to clinical application has been obstructed due to its drawbacks. Mesenchymal stem cells (MSCs) harbor differentiation potential, immunosuppressive properties, and anti-inflammatory effects, and they are considered an ideal candidate cell type for treatment of DM. MSC-related research has demonstrated exciting therapeutic effects in glycemic control both in vivo and in vitro, and these results now have been translated into clinical practice. However, some critical potential problems have emerged from current clinical trials. Multi-center, large-scale, double-blind, and placebo-controlled studies with strict supervision are required before MSC transplantation can become a routine therapeutic approach for T2DM. We briefly review the molecular mechanism of MSC treatment for T2DM as well as the merits and drawbacks identified in current clinical trials. |
doi_str_mv | 10.1186/s13098-017-0233-1 |
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Transplantation of insulin-producing cells (IPCs) was once thought to be the most promising strategy for treating diabetes, but the pace from the laboratory to clinical application has been obstructed due to its drawbacks. Mesenchymal stem cells (MSCs) harbor differentiation potential, immunosuppressive properties, and anti-inflammatory effects, and they are considered an ideal candidate cell type for treatment of DM. MSC-related research has demonstrated exciting therapeutic effects in glycemic control both in vivo and in vitro, and these results now have been translated into clinical practice. However, some critical potential problems have emerged from current clinical trials. Multi-center, large-scale, double-blind, and placebo-controlled studies with strict supervision are required before MSC transplantation can become a routine therapeutic approach for T2DM. We briefly review the molecular mechanism of MSC treatment for T2DM as well as the merits and drawbacks identified in current clinical trials.</description><identifier>ISSN: 1758-5996</identifier><identifier>EISSN: 1758-5996</identifier><identifier>DOI: 10.1186/s13098-017-0233-1</identifier><identifier>PMID: 28515792</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Adults ; Bone marrow ; Clinical trials ; Diabetes ; Diabetes mellitus ; Glucose ; Glucose monitoring ; Hyperglycemia ; Immunosuppression ; Inflammation ; Insulin ; Insulin resistance ; Mesenchymal stem cells ; Mesenchyme ; Review ; Stem cells ; Transplantation ; Transplants & implants ; Type 2 diabetes mellitus ; Umbilical cord</subject><ispartof>Diabetology and metabolic syndrome, 2017-05, Vol.9 (1), p.36-36, Article 36</ispartof><rights>Copyright BioMed Central 2017</rights><rights>The Author(s) 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-9adecb4aeb30419836ff13d90e050810c215184ae26f223ebdcef206599a74b73</citedby><cites>FETCH-LOGICAL-c493t-9adecb4aeb30419836ff13d90e050810c215184ae26f223ebdcef206599a74b73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433043/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1905423001?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28515792$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zang, Li</creatorcontrib><creatorcontrib>Hao, Haojie</creatorcontrib><creatorcontrib>Liu, Jiejie</creatorcontrib><creatorcontrib>Li, Yijun</creatorcontrib><creatorcontrib>Han, Weidong</creatorcontrib><creatorcontrib>Mu, Yiming</creatorcontrib><title>Mesenchymal stem cell therapy in type 2 diabetes mellitus</title><title>Diabetology and metabolic syndrome</title><addtitle>Diabetol Metab Syndr</addtitle><description>Type 2 diabetes mellitus (T2DM), which is characterized by the combination of relative insulin deficiency and insulin resistance, cannot be reversed with existing therapeutic strategies. Transplantation of insulin-producing cells (IPCs) was once thought to be the most promising strategy for treating diabetes, but the pace from the laboratory to clinical application has been obstructed due to its drawbacks. Mesenchymal stem cells (MSCs) harbor differentiation potential, immunosuppressive properties, and anti-inflammatory effects, and they are considered an ideal candidate cell type for treatment of DM. MSC-related research has demonstrated exciting therapeutic effects in glycemic control both in vivo and in vitro, and these results now have been translated into clinical practice. However, some critical potential problems have emerged from current clinical trials. Multi-center, large-scale, double-blind, and placebo-controlled studies with strict supervision are required before MSC transplantation can become a routine therapeutic approach for T2DM. We briefly review the molecular mechanism of MSC treatment for T2DM as well as the merits and drawbacks identified in current clinical trials.</description><subject>Adults</subject><subject>Bone marrow</subject><subject>Clinical trials</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Glucose</subject><subject>Glucose monitoring</subject><subject>Hyperglycemia</subject><subject>Immunosuppression</subject><subject>Inflammation</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Mesenchymal stem cells</subject><subject>Mesenchyme</subject><subject>Review</subject><subject>Stem cells</subject><subject>Transplantation</subject><subject>Transplants & implants</subject><subject>Type 2 diabetes mellitus</subject><subject>Umbilical cord</subject><issn>1758-5996</issn><issn>1758-5996</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkUtv1TAQhS0EoqXwA9igSGzYBGb89gYJVTwqFbGBteU4k95c5XGxk0r33-NwS9WysuVz5pvxHMZeI7xHtPpDRgHO1oCmBi5EjU_YORpla-WcfvrgfsZe5LwH0EYZ-ZydcatQGcfPmftOmaa4O45hqPJCYxVpGKplRykcjlU_VcvxQBWv2j40tFCuxqL3y5pfsmddGDK9ujsv2K8vn39efquvf3y9uvx0XUfpxFK70FJsZKBGgERnhe46FK0DAgUWIXJUaIvOdce5oKaN1HHQZexgZGPEBbs6cds57P0h9WNIRz-H3v99mNOND2np40C-tSCV5RqFVlJp6VpDLXcCI3YAxhXWxxPrsDYjlU7TksLwCPpYmfqdv5lvvZKijC8K4N0dIM2_V8qLH_u8bSxMNK_ZowNA7jTYYn37n3U_r2kqq9pcSnJRrMWFJ1dMc86JuvthEPwWsj-F7EvIfgvZbzVvHv7ivuJfquIP2L2gJQ</recordid><startdate>20170515</startdate><enddate>20170515</enddate><creator>Zang, Li</creator><creator>Hao, Haojie</creator><creator>Liu, Jiejie</creator><creator>Li, Yijun</creator><creator>Han, Weidong</creator><creator>Mu, Yiming</creator><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20170515</creationdate><title>Mesenchymal stem cell therapy in type 2 diabetes mellitus</title><author>Zang, Li ; Hao, Haojie ; Liu, Jiejie ; Li, Yijun ; Han, Weidong ; Mu, Yiming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-9adecb4aeb30419836ff13d90e050810c215184ae26f223ebdcef206599a74b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adults</topic><topic>Bone marrow</topic><topic>Clinical trials</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Glucose</topic><topic>Glucose monitoring</topic><topic>Hyperglycemia</topic><topic>Immunosuppression</topic><topic>Inflammation</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Mesenchymal stem cells</topic><topic>Mesenchyme</topic><topic>Review</topic><topic>Stem cells</topic><topic>Transplantation</topic><topic>Transplants & implants</topic><topic>Type 2 diabetes mellitus</topic><topic>Umbilical cord</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zang, Li</creatorcontrib><creatorcontrib>Hao, Haojie</creatorcontrib><creatorcontrib>Liu, Jiejie</creatorcontrib><creatorcontrib>Li, Yijun</creatorcontrib><creatorcontrib>Han, Weidong</creatorcontrib><creatorcontrib>Mu, Yiming</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Diabetology and metabolic syndrome</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zang, Li</au><au>Hao, Haojie</au><au>Liu, Jiejie</au><au>Li, Yijun</au><au>Han, Weidong</au><au>Mu, Yiming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mesenchymal stem cell therapy in type 2 diabetes mellitus</atitle><jtitle>Diabetology and metabolic syndrome</jtitle><addtitle>Diabetol Metab Syndr</addtitle><date>2017-05-15</date><risdate>2017</risdate><volume>9</volume><issue>1</issue><spage>36</spage><epage>36</epage><pages>36-36</pages><artnum>36</artnum><issn>1758-5996</issn><eissn>1758-5996</eissn><abstract>Type 2 diabetes mellitus (T2DM), which is characterized by the combination of relative insulin deficiency and insulin resistance, cannot be reversed with existing therapeutic strategies. 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subjects | Adults Bone marrow Clinical trials Diabetes Diabetes mellitus Glucose Glucose monitoring Hyperglycemia Immunosuppression Inflammation Insulin Insulin resistance Mesenchymal stem cells Mesenchyme Review Stem cells Transplantation Transplants & implants Type 2 diabetes mellitus Umbilical cord |
title | Mesenchymal stem cell therapy in type 2 diabetes mellitus |
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