Mesenchymal differentiation of glioblastoma stem cells
Glioblastoma multiforme is a severe form of cancer most likely arising from the transformation of stem or progenitor cells resident in the brain. Although the tumorigenic population in glioblastoma is defined as composed by cancer stem cells (CSCs), the cellular target of the transformation hit rema...
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Veröffentlicht in: | Cell death and differentiation 2008-09, Vol.15 (9), p.1491-1498 |
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description | Glioblastoma multiforme is a severe form of cancer most likely arising from the transformation of stem or progenitor cells resident in the brain. Although the tumorigenic population in glioblastoma is defined as composed by cancer stem cells (CSCs), the cellular target of the transformation hit remains to be identified. Glioma stem cells (SCs) are thought to have a differentiation potential restricted to the neural lineage. However, using orthotopic
versus
heterotopic xenograft models and
in vitro
differentiation assays, we found that a subset of glioblastomas contained CSCs with both neural and mesenchymal potential. Subcutaneous injection of CSCs or single CSC clones from two of seven patients produced tumor xenografts containing osteo-chondrogenic areas in the context of glioblastoma-like tumor lesions. Moreover, CSC clones from four of seven cases generated both neural and chondrogenic cells
in vitro
. Interestingly, mesenchymal differentiation of the tumor xenografts was associated with reduction of both growth rate and mitotic index. These findings suggest that in a subclass of glioblastomas the tumorigenic hit occurs on a multipotent stem cell, which may reveal its plasticity under specific environmental stimuli. The discovery of such biological properties might provide considerable information to the development of new therapeutic strategies aimed at forcing glioblastoma stem cell differentiation. |
doi_str_mv | 10.1038/cdd.2008.72 |
format | Article |
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versus
heterotopic xenograft models and
in vitro
differentiation assays, we found that a subset of glioblastomas contained CSCs with both neural and mesenchymal potential. Subcutaneous injection of CSCs or single CSC clones from two of seven patients produced tumor xenografts containing osteo-chondrogenic areas in the context of glioblastoma-like tumor lesions. Moreover, CSC clones from four of seven cases generated both neural and chondrogenic cells
in vitro
. Interestingly, mesenchymal differentiation of the tumor xenografts was associated with reduction of both growth rate and mitotic index. These findings suggest that in a subclass of glioblastomas the tumorigenic hit occurs on a multipotent stem cell, which may reveal its plasticity under specific environmental stimuli. The discovery of such biological properties might provide considerable information to the development of new therapeutic strategies aimed at forcing glioblastoma stem cell differentiation.</description><identifier>ISSN: 1350-9047</identifier><identifier>EISSN: 1476-5403</identifier><identifier>DOI: 10.1038/cdd.2008.72</identifier><identifier>PMID: 18497759</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Adult ; Aged ; Animals ; Apoptosis ; Biochemistry ; Biomedical and Life Sciences ; Brain cancer ; Brain Neoplasms - pathology ; Cell Biology ; Cell Cycle Analysis ; Cell death ; Cell Differentiation ; Clone Cells ; Cloning ; Epidermal growth factor ; Female ; Genotype & phenotype ; Glioblastoma - pathology ; Hematology ; Humans ; Life Sciences ; Male ; Mesoderm - cytology ; Mice ; Mice, SCID ; Middle Aged ; Mutation ; Neoplastic Stem Cells - chemistry ; Neoplastic Stem Cells - cytology ; Neoplastic Stem Cells - pathology ; Neurons - cytology ; Oncology ; original-paper ; Stem Cells ; Tumors ; Xenograft Model Antitumor Assays</subject><ispartof>Cell death and differentiation, 2008-09, Vol.15 (9), p.1491-1498</ispartof><rights>Springer Nature Limited 2008</rights><rights>Copyright Nature Publishing Group Sep 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-8b6d03d9838625ba06f1912e854bcb3a97f163b386a1a10dafed6d14cf22cc1d3</citedby><cites>FETCH-LOGICAL-c443t-8b6d03d9838625ba06f1912e854bcb3a97f163b386a1a10dafed6d14cf22cc1d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/cdd.2008.72$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/cdd.2008.72$$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/18497759$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ricci-Vitiani, L</creatorcontrib><creatorcontrib>Pallini, R</creatorcontrib><creatorcontrib>Larocca, L M</creatorcontrib><creatorcontrib>Lombardi, D G</creatorcontrib><creatorcontrib>Signore, M</creatorcontrib><creatorcontrib>Pierconti, F</creatorcontrib><creatorcontrib>Petrucci, G</creatorcontrib><creatorcontrib>Montano, N</creatorcontrib><creatorcontrib>Maira, G</creatorcontrib><creatorcontrib>De Maria, R</creatorcontrib><title>Mesenchymal differentiation of glioblastoma stem cells</title><title>Cell death and differentiation</title><addtitle>Cell Death Differ</addtitle><addtitle>Cell Death Differ</addtitle><description>Glioblastoma multiforme is a severe form of cancer most likely arising from the transformation of stem or progenitor cells resident in the brain. Although the tumorigenic population in glioblastoma is defined as composed by cancer stem cells (CSCs), the cellular target of the transformation hit remains to be identified. Glioma stem cells (SCs) are thought to have a differentiation potential restricted to the neural lineage. However, using orthotopic
versus
heterotopic xenograft models and
in vitro
differentiation assays, we found that a subset of glioblastomas contained CSCs with both neural and mesenchymal potential. Subcutaneous injection of CSCs or single CSC clones from two of seven patients produced tumor xenografts containing osteo-chondrogenic areas in the context of glioblastoma-like tumor lesions. Moreover, CSC clones from four of seven cases generated both neural and chondrogenic cells
in vitro
. Interestingly, mesenchymal differentiation of the tumor xenografts was associated with reduction of both growth rate and mitotic index. These findings suggest that in a subclass of glioblastomas the tumorigenic hit occurs on a multipotent stem cell, which may reveal its plasticity under specific environmental stimuli. The discovery of such biological properties might provide considerable information to the development of new therapeutic strategies aimed at forcing glioblastoma stem cell differentiation.</description><subject>Adult</subject><subject>Aged</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Brain cancer</subject><subject>Brain Neoplasms - pathology</subject><subject>Cell Biology</subject><subject>Cell Cycle Analysis</subject><subject>Cell death</subject><subject>Cell Differentiation</subject><subject>Clone Cells</subject><subject>Cloning</subject><subject>Epidermal growth factor</subject><subject>Female</subject><subject>Genotype & phenotype</subject><subject>Glioblastoma - pathology</subject><subject>Hematology</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Mesoderm - cytology</subject><subject>Mice</subject><subject>Mice, SCID</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Neoplastic Stem Cells - chemistry</subject><subject>Neoplastic Stem Cells - cytology</subject><subject>Neoplastic Stem Cells - pathology</subject><subject>Neurons - cytology</subject><subject>Oncology</subject><subject>original-paper</subject><subject>Stem Cells</subject><subject>Tumors</subject><subject>Xenograft Model Antitumor Assays</subject><issn>1350-9047</issn><issn>1476-5403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqF0M1LwzAYBvAgipvTk3ctHrxoZ9Kk-TjK8AsmXvQc0nzMjn7MpD3svzelw4EInhJ4fzzJ-wBwjuAcQczvtDHzDEI-Z9kBmCLCaJoTiA_jHecwFZCwCTgJYQ0hpEzQYzBBnAjGcjEF9NUG2-jPba2qxJTOWW-brlRd2TZJ65JVVbZFpULX1ioJna0TbasqnIIjp6pgz3bnDHw8PrwvntPl29PL4n6ZakJwl_KCGoiN4JjTLC8UpA4JlFmek0IXWAnmEMVFnCqkEDTKWUMNItplmdbI4Bm4HnM3vv3qbehkXYbhB6qxbR8kFQRzjrJ_IRKEw5wP8OoXXLe9b-ISMkOM4dioiOhmRNq3IXjr5MaXtfJbiaAcSpexdDmULtkQebGL7Ivamr3dtRzB7QhCHDUr6_dv_p13OfJGdb23P3nRDCSKb7oolUE</recordid><startdate>20080901</startdate><enddate>20080901</enddate><creator>Ricci-Vitiani, L</creator><creator>Pallini, R</creator><creator>Larocca, L M</creator><creator>Lombardi, D G</creator><creator>Signore, M</creator><creator>Pierconti, F</creator><creator>Petrucci, G</creator><creator>Montano, N</creator><creator>Maira, G</creator><creator>De Maria, R</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</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>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>20080901</creationdate><title>Mesenchymal differentiation of glioblastoma stem cells</title><author>Ricci-Vitiani, L ; Pallini, R ; Larocca, L M ; Lombardi, D G ; Signore, M ; Pierconti, F ; Petrucci, G ; Montano, N ; Maira, G ; De Maria, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-8b6d03d9838625ba06f1912e854bcb3a97f163b386a1a10dafed6d14cf22cc1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Brain cancer</topic><topic>Brain Neoplasms - 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Academic</collection><jtitle>Cell death and differentiation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ricci-Vitiani, L</au><au>Pallini, R</au><au>Larocca, L M</au><au>Lombardi, D G</au><au>Signore, M</au><au>Pierconti, F</au><au>Petrucci, G</au><au>Montano, N</au><au>Maira, G</au><au>De Maria, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mesenchymal differentiation of glioblastoma stem cells</atitle><jtitle>Cell death and differentiation</jtitle><stitle>Cell Death Differ</stitle><addtitle>Cell Death Differ</addtitle><date>2008-09-01</date><risdate>2008</risdate><volume>15</volume><issue>9</issue><spage>1491</spage><epage>1498</epage><pages>1491-1498</pages><issn>1350-9047</issn><eissn>1476-5403</eissn><abstract>Glioblastoma multiforme is a severe form of cancer most likely arising from the transformation of stem or progenitor cells resident in the brain. Although the tumorigenic population in glioblastoma is defined as composed by cancer stem cells (CSCs), the cellular target of the transformation hit remains to be identified. Glioma stem cells (SCs) are thought to have a differentiation potential restricted to the neural lineage. However, using orthotopic
versus
heterotopic xenograft models and
in vitro
differentiation assays, we found that a subset of glioblastomas contained CSCs with both neural and mesenchymal potential. Subcutaneous injection of CSCs or single CSC clones from two of seven patients produced tumor xenografts containing osteo-chondrogenic areas in the context of glioblastoma-like tumor lesions. Moreover, CSC clones from four of seven cases generated both neural and chondrogenic cells
in vitro
. Interestingly, mesenchymal differentiation of the tumor xenografts was associated with reduction of both growth rate and mitotic index. These findings suggest that in a subclass of glioblastomas the tumorigenic hit occurs on a multipotent stem cell, which may reveal its plasticity under specific environmental stimuli. The discovery of such biological properties might provide considerable information to the development of new therapeutic strategies aimed at forcing glioblastoma stem cell differentiation.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>18497759</pmid><doi>10.1038/cdd.2008.72</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Animals Apoptosis Biochemistry Biomedical and Life Sciences Brain cancer Brain Neoplasms - pathology Cell Biology Cell Cycle Analysis Cell death Cell Differentiation Clone Cells Cloning Epidermal growth factor Female Genotype & phenotype Glioblastoma - pathology Hematology Humans Life Sciences Male Mesoderm - cytology Mice Mice, SCID Middle Aged Mutation Neoplastic Stem Cells - chemistry Neoplastic Stem Cells - cytology Neoplastic Stem Cells - pathology Neurons - cytology Oncology original-paper Stem Cells Tumors Xenograft Model Antitumor Assays |
title | Mesenchymal differentiation of glioblastoma stem cells |
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