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Monitoring the growth effect of xenotransplanted human medulloblastoma in an immunocompromised mouse model using in vitro and ex vivo green fluorescent protein imaging
Medulloblastoma (MB) is one of the most common malignant brain tumors in children. It is a radiosensitive tumor. At 5 years after radical surgical excision and craniospinal axis irradiation, the tumor-free survival rate is from 50 to 70% [Halperin EC, Constine LS, Tarbell NJ, Kun LE. Pediatric radia...
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Published in: | Child's nervous system 2006-05, Vol.22 (5), p.475-480 |
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container_title | Child's nervous system |
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creator | Chiou, Shih-Hwa Kao, Chung-Lan Lin, Han-Tso Tseng, Wen-Ser Liu, Ren-Shyan Chung, Chen-Fun Ku, Hung-Hai Lin, Ching-Po Wong, Tai-Tong |
description | Medulloblastoma (MB) is one of the most common malignant brain tumors in children. It is a radiosensitive tumor. At 5 years after radical surgical excision and craniospinal axis irradiation, the tumor-free survival rate is from 50 to 70% [Halperin EC, Constine LS, Tarbell NJ, Kun LE. Pediatric radiation oncology (2005)].
In this study, we established xenotransplanted human MB (hMB) cells - isochromosome 17q - in a severe combined immunodeficiency (SCID) mouse model. We further transduced green fluorescent protein (GFP) into hMB cells to evaluate these hMB cells grafted in SCID mice.
The result of an ex vivo GFP imaging system showed that a small lesion of the third-week-hMB-transplanted graft presented "green" signals with a clear tumor margin before any tumor-related symptoms were noted. We also demonstrated that the tumor progression could be monitored by GFP imaging for up to 12 weeks post-transplantation.
This novel approach of GFP imaging assessment provides more accurate information of tumor status for experimental brain tumor studies. Because MB is sensitive to radiation and also response to chemotherapy, this SCID mouse model will be helpful for preclinical studies in the future. |
doi_str_mv | 10.1007/s00381-005-0026-y |
format | article |
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In this study, we established xenotransplanted human MB (hMB) cells - isochromosome 17q - in a severe combined immunodeficiency (SCID) mouse model. We further transduced green fluorescent protein (GFP) into hMB cells to evaluate these hMB cells grafted in SCID mice.
The result of an ex vivo GFP imaging system showed that a small lesion of the third-week-hMB-transplanted graft presented "green" signals with a clear tumor margin before any tumor-related symptoms were noted. We also demonstrated that the tumor progression could be monitored by GFP imaging for up to 12 weeks post-transplantation.
This novel approach of GFP imaging assessment provides more accurate information of tumor status for experimental brain tumor studies. Because MB is sensitive to radiation and also response to chemotherapy, this SCID mouse model will be helpful for preclinical studies in the future.</description><identifier>ISSN: 0256-7040</identifier><identifier>EISSN: 1433-0350</identifier><identifier>DOI: 10.1007/s00381-005-0026-y</identifier><identifier>PMID: 16541296</identifier><language>eng</language><publisher>Germany</publisher><subject>Animals ; Cell Proliferation ; Diagnostic Imaging ; Disease Models, Animal ; Glial Fibrillary Acidic Protein - metabolism ; Green Fluorescent Proteins - biosynthesis ; Green Fluorescent Proteins - metabolism ; Humans ; In Vitro Techniques ; Medulloblastoma - metabolism ; Medulloblastoma - pathology ; Medulloblastoma - physiopathology ; Mice ; Mice, SCID ; Neoplasm Transplantation - methods ; Time Factors</subject><ispartof>Child's nervous system, 2006-05, Vol.22 (5), p.475-480</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c299t-4e8ba772cb64703dc9a0945d346f03bb12a80d85c07f3abc3302b8c82c98e3fc3</citedby><cites>FETCH-LOGICAL-c299t-4e8ba772cb64703dc9a0945d346f03bb12a80d85c07f3abc3302b8c82c98e3fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16541296$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chiou, Shih-Hwa</creatorcontrib><creatorcontrib>Kao, Chung-Lan</creatorcontrib><creatorcontrib>Lin, Han-Tso</creatorcontrib><creatorcontrib>Tseng, Wen-Ser</creatorcontrib><creatorcontrib>Liu, Ren-Shyan</creatorcontrib><creatorcontrib>Chung, Chen-Fun</creatorcontrib><creatorcontrib>Ku, Hung-Hai</creatorcontrib><creatorcontrib>Lin, Ching-Po</creatorcontrib><creatorcontrib>Wong, Tai-Tong</creatorcontrib><title>Monitoring the growth effect of xenotransplanted human medulloblastoma in an immunocompromised mouse model using in vitro and ex vivo green fluorescent protein imaging</title><title>Child's nervous system</title><addtitle>Childs Nerv Syst</addtitle><description>Medulloblastoma (MB) is one of the most common malignant brain tumors in children. It is a radiosensitive tumor. At 5 years after radical surgical excision and craniospinal axis irradiation, the tumor-free survival rate is from 50 to 70% [Halperin EC, Constine LS, Tarbell NJ, Kun LE. Pediatric radiation oncology (2005)].
In this study, we established xenotransplanted human MB (hMB) cells - isochromosome 17q - in a severe combined immunodeficiency (SCID) mouse model. We further transduced green fluorescent protein (GFP) into hMB cells to evaluate these hMB cells grafted in SCID mice.
The result of an ex vivo GFP imaging system showed that a small lesion of the third-week-hMB-transplanted graft presented "green" signals with a clear tumor margin before any tumor-related symptoms were noted. We also demonstrated that the tumor progression could be monitored by GFP imaging for up to 12 weeks post-transplantation.
This novel approach of GFP imaging assessment provides more accurate information of tumor status for experimental brain tumor studies. Because MB is sensitive to radiation and also response to chemotherapy, this SCID mouse model will be helpful for preclinical studies in the future.</description><subject>Animals</subject><subject>Cell Proliferation</subject><subject>Diagnostic Imaging</subject><subject>Disease Models, Animal</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>Green Fluorescent Proteins - biosynthesis</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Medulloblastoma - metabolism</subject><subject>Medulloblastoma - pathology</subject><subject>Medulloblastoma - physiopathology</subject><subject>Mice</subject><subject>Mice, SCID</subject><subject>Neoplasm Transplantation - methods</subject><subject>Time Factors</subject><issn>0256-7040</issn><issn>1433-0350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNpFUctu3CAURVGjZpr2A7qpWHXn5gJ-4GUV9SUlyiZZI4wvM45smAJOM1_U3-wdzUhdALroPDgcxj4K-CIAupsMoLSoABpasq0OF2wjaqUqUA28YRuQTVt1UMMVe5fzM4BotOzfsivRNrWQfbthf-9jmEpMU9jyskO-TfFP2XH0Hl3h0fNXDLEkG_J-tqHgyHfrYgNfcFznOQ6zzSUulk-B0-20LGuILi77FJcpE3qJa0baR5z5mo8uhHyZSoqEHzm-0vASyRYxcD-vMWF2GAonhYLTUdJuifaeXXo7Z_xwPq_Z0_dvj7c_q7uHH79uv95VTvZ9qWrUg-066Ya27kCNrrfQ182o6taDGgYhrYZRNw46r-zglAI5aKel6zUq79Q1-3zSJf_fK-ZiKIfDmcIjRTFt14PsdEtAcQK6FHNO6M0-0VvTwQgwx3bMqR1D7ZhjO-ZAnE9n8XWgD_zPONeh_gG6SpCZ</recordid><startdate>200605</startdate><enddate>200605</enddate><creator>Chiou, Shih-Hwa</creator><creator>Kao, Chung-Lan</creator><creator>Lin, Han-Tso</creator><creator>Tseng, Wen-Ser</creator><creator>Liu, Ren-Shyan</creator><creator>Chung, Chen-Fun</creator><creator>Ku, Hung-Hai</creator><creator>Lin, Ching-Po</creator><creator>Wong, Tai-Tong</creator><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>7X8</scope></search><sort><creationdate>200605</creationdate><title>Monitoring the growth effect of xenotransplanted human medulloblastoma in an immunocompromised mouse model using in vitro and ex vivo green fluorescent protein imaging</title><author>Chiou, Shih-Hwa ; Kao, Chung-Lan ; Lin, Han-Tso ; Tseng, Wen-Ser ; Liu, Ren-Shyan ; Chung, Chen-Fun ; Ku, Hung-Hai ; Lin, Ching-Po ; Wong, Tai-Tong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c299t-4e8ba772cb64703dc9a0945d346f03bb12a80d85c07f3abc3302b8c82c98e3fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Cell Proliferation</topic><topic>Diagnostic Imaging</topic><topic>Disease Models, Animal</topic><topic>Glial Fibrillary Acidic Protein - metabolism</topic><topic>Green Fluorescent Proteins - biosynthesis</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Medulloblastoma - metabolism</topic><topic>Medulloblastoma - pathology</topic><topic>Medulloblastoma - physiopathology</topic><topic>Mice</topic><topic>Mice, SCID</topic><topic>Neoplasm Transplantation - methods</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chiou, Shih-Hwa</creatorcontrib><creatorcontrib>Kao, Chung-Lan</creatorcontrib><creatorcontrib>Lin, Han-Tso</creatorcontrib><creatorcontrib>Tseng, Wen-Ser</creatorcontrib><creatorcontrib>Liu, Ren-Shyan</creatorcontrib><creatorcontrib>Chung, Chen-Fun</creatorcontrib><creatorcontrib>Ku, Hung-Hai</creatorcontrib><creatorcontrib>Lin, Ching-Po</creatorcontrib><creatorcontrib>Wong, Tai-Tong</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>Child's nervous system</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chiou, Shih-Hwa</au><au>Kao, Chung-Lan</au><au>Lin, Han-Tso</au><au>Tseng, Wen-Ser</au><au>Liu, Ren-Shyan</au><au>Chung, Chen-Fun</au><au>Ku, Hung-Hai</au><au>Lin, Ching-Po</au><au>Wong, Tai-Tong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monitoring the growth effect of xenotransplanted human medulloblastoma in an immunocompromised mouse model using in vitro and ex vivo green fluorescent protein imaging</atitle><jtitle>Child's nervous system</jtitle><addtitle>Childs Nerv Syst</addtitle><date>2006-05</date><risdate>2006</risdate><volume>22</volume><issue>5</issue><spage>475</spage><epage>480</epage><pages>475-480</pages><issn>0256-7040</issn><eissn>1433-0350</eissn><abstract>Medulloblastoma (MB) is one of the most common malignant brain tumors in children. It is a radiosensitive tumor. At 5 years after radical surgical excision and craniospinal axis irradiation, the tumor-free survival rate is from 50 to 70% [Halperin EC, Constine LS, Tarbell NJ, Kun LE. Pediatric radiation oncology (2005)].
In this study, we established xenotransplanted human MB (hMB) cells - isochromosome 17q - in a severe combined immunodeficiency (SCID) mouse model. We further transduced green fluorescent protein (GFP) into hMB cells to evaluate these hMB cells grafted in SCID mice.
The result of an ex vivo GFP imaging system showed that a small lesion of the third-week-hMB-transplanted graft presented "green" signals with a clear tumor margin before any tumor-related symptoms were noted. We also demonstrated that the tumor progression could be monitored by GFP imaging for up to 12 weeks post-transplantation.
This novel approach of GFP imaging assessment provides more accurate information of tumor status for experimental brain tumor studies. Because MB is sensitive to radiation and also response to chemotherapy, this SCID mouse model will be helpful for preclinical studies in the future.</abstract><cop>Germany</cop><pmid>16541296</pmid><doi>10.1007/s00381-005-0026-y</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Cell Proliferation Diagnostic Imaging Disease Models, Animal Glial Fibrillary Acidic Protein - metabolism Green Fluorescent Proteins - biosynthesis Green Fluorescent Proteins - metabolism Humans In Vitro Techniques Medulloblastoma - metabolism Medulloblastoma - pathology Medulloblastoma - physiopathology Mice Mice, SCID Neoplasm Transplantation - methods Time Factors |
title | Monitoring the growth effect of xenotransplanted human medulloblastoma in an immunocompromised mouse model using in vitro and ex vivo green fluorescent protein imaging |
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