Enhanced antitumor effects by combination gene therapy usingMDR1gene shRNA and HSV1-tkin a xenograft mouse model
The use of a novel therapeutic vector containing HSV1-thymidine kinase (HSV1-tk) and a short hairpin RNA for theMDR1gene (shMDR) was proposed previously. We investigated the antitumor effects in anin vivomouse model of colon cancer and assessed treatment response by serial non-invasive imaging. shMD...
Gespeichert in:
Veröffentlicht in: | Cancer letters 2010-05, Vol.291 (1), p.83 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 1 |
container_start_page | 83 |
container_title | Cancer letters |
container_volume | 291 |
creator | Lee, Sang-Woo Lee, You La Lee, Yong Jin Park, Seung-Yoon Kim, In-San Choi, Tae Hyun Ha, Jeoung-Hee Ahn, Byeong-Cheol Lee, Jaetae |
description | The use of a novel therapeutic vector containing HSV1-thymidine kinase (HSV1-tk) and a short hairpin RNA for theMDR1gene (shMDR) was proposed previously. We investigated the antitumor effects in anin vivomouse model of colon cancer and assessed treatment response by serial non-invasive imaging. shMDR-TK expressing (MTKG) tumors for the dual therapy group mice with ganciclovir and doxorubicin showed a decrease in size, while tumors in the single therapy group mice showed a moderate increase (p |
doi_str_mv | 10.1016/j.canlet.2009.10.002 |
format | Article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_1550186012</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3389892261</sourcerecordid><originalsourceid>FETCH-proquest_journals_15501860123</originalsourceid><addsrcrecordid>eNqNjM1Og0AUhSdGE_HnDVzcxDV4B0qhS6M13eiibdw2U7jAINzB-Uns20saH8DNOcn3nRwhHiQmEuXyqU8qxQP5JEVczShBTC9EJMsijYtViZciwgwXcVZm-bW4ca5HxHxR5JGY1twprqgGxV77MBoL1DRUeQfHE1RmPGpWXhuGlpjAd2TVdILgNLfvr1t5pq7bfjzPDzVsdp8y9l-aQcEPsWmtajyMJjias6bhTlw1anB0_9e34vFtvX_ZxJM134GcP_QmWJ7VQeY5ynKJMs3-t_oF1E5SSg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1550186012</pqid></control><display><type>article</type><title>Enhanced antitumor effects by combination gene therapy usingMDR1gene shRNA and HSV1-tkin a xenograft mouse model</title><source>ScienceDirect Journals (5 years ago - present)</source><creator>Lee, Sang-Woo ; Lee, You La ; Lee, Yong Jin ; Park, Seung-Yoon ; Kim, In-San ; Choi, Tae Hyun ; Ha, Jeoung-Hee ; Ahn, Byeong-Cheol ; Lee, Jaetae</creator><creatorcontrib>Lee, Sang-Woo ; Lee, You La ; Lee, Yong Jin ; Park, Seung-Yoon ; Kim, In-San ; Choi, Tae Hyun ; Ha, Jeoung-Hee ; Ahn, Byeong-Cheol ; Lee, Jaetae</creatorcontrib><description>The use of a novel therapeutic vector containing HSV1-thymidine kinase (HSV1-tk) and a short hairpin RNA for theMDR1gene (shMDR) was proposed previously. We investigated the antitumor effects in anin vivomouse model of colon cancer and assessed treatment response by serial non-invasive imaging. shMDR-TK expressing (MTKG) tumors for the dual therapy group mice with ganciclovir and doxorubicin showed a decrease in size, while tumors in the single therapy group mice showed a moderate increase (p<0.05). The131I-5-iodo-2'-fluoro-2'deoxy-1-β-d-arabinofuranosyluracil (FIAU) uptake ratio of MTKG-to-parent HCT-15 tumors decreased as treatment progressed for single or dual therapy group mice, while that of the control group mice increased gradually. This study demonstrates the enhanced antitumor effects with combination gene therapy compared with a single therapeutic approach, and provides the potential of therapeutic response monitoring.</description><identifier>ISSN: 0304-3835</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2009.10.002</identifier><language>eng</language><publisher>Clare: Elsevier Limited</publisher><subject>Cameras ; Cancer therapies ; Colorectal cancer ; Experiments ; Gene expression ; Gene therapy ; Kinases ; Medical research ; Proteins ; Reporters ; Technological change ; Tumors</subject><ispartof>Cancer letters, 2010-05, Vol.291 (1), p.83</ispartof><rights>Copyright Elsevier Limited May 1, 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Lee, Sang-Woo</creatorcontrib><creatorcontrib>Lee, You La</creatorcontrib><creatorcontrib>Lee, Yong Jin</creatorcontrib><creatorcontrib>Park, Seung-Yoon</creatorcontrib><creatorcontrib>Kim, In-San</creatorcontrib><creatorcontrib>Choi, Tae Hyun</creatorcontrib><creatorcontrib>Ha, Jeoung-Hee</creatorcontrib><creatorcontrib>Ahn, Byeong-Cheol</creatorcontrib><creatorcontrib>Lee, Jaetae</creatorcontrib><title>Enhanced antitumor effects by combination gene therapy usingMDR1gene shRNA and HSV1-tkin a xenograft mouse model</title><title>Cancer letters</title><description>The use of a novel therapeutic vector containing HSV1-thymidine kinase (HSV1-tk) and a short hairpin RNA for theMDR1gene (shMDR) was proposed previously. We investigated the antitumor effects in anin vivomouse model of colon cancer and assessed treatment response by serial non-invasive imaging. shMDR-TK expressing (MTKG) tumors for the dual therapy group mice with ganciclovir and doxorubicin showed a decrease in size, while tumors in the single therapy group mice showed a moderate increase (p<0.05). The131I-5-iodo-2'-fluoro-2'deoxy-1-β-d-arabinofuranosyluracil (FIAU) uptake ratio of MTKG-to-parent HCT-15 tumors decreased as treatment progressed for single or dual therapy group mice, while that of the control group mice increased gradually. This study demonstrates the enhanced antitumor effects with combination gene therapy compared with a single therapeutic approach, and provides the potential of therapeutic response monitoring.</description><subject>Cameras</subject><subject>Cancer therapies</subject><subject>Colorectal cancer</subject><subject>Experiments</subject><subject>Gene expression</subject><subject>Gene therapy</subject><subject>Kinases</subject><subject>Medical research</subject><subject>Proteins</subject><subject>Reporters</subject><subject>Technological change</subject><subject>Tumors</subject><issn>0304-3835</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqNjM1Og0AUhSdGE_HnDVzcxDV4B0qhS6M13eiibdw2U7jAINzB-Uns20saH8DNOcn3nRwhHiQmEuXyqU8qxQP5JEVczShBTC9EJMsijYtViZciwgwXcVZm-bW4ca5HxHxR5JGY1twprqgGxV77MBoL1DRUeQfHE1RmPGpWXhuGlpjAd2TVdILgNLfvr1t5pq7bfjzPDzVsdp8y9l-aQcEPsWmtajyMJjias6bhTlw1anB0_9e34vFtvX_ZxJM134GcP_QmWJ7VQeY5ynKJMs3-t_oF1E5SSg</recordid><startdate>20100501</startdate><enddate>20100501</enddate><creator>Lee, Sang-Woo</creator><creator>Lee, You La</creator><creator>Lee, Yong Jin</creator><creator>Park, Seung-Yoon</creator><creator>Kim, In-San</creator><creator>Choi, Tae Hyun</creator><creator>Ha, Jeoung-Hee</creator><creator>Ahn, Byeong-Cheol</creator><creator>Lee, Jaetae</creator><general>Elsevier Limited</general><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope></search><sort><creationdate>20100501</creationdate><title>Enhanced antitumor effects by combination gene therapy usingMDR1gene shRNA and HSV1-tkin a xenograft mouse model</title><author>Lee, Sang-Woo ; Lee, You La ; Lee, Yong Jin ; Park, Seung-Yoon ; Kim, In-San ; Choi, Tae Hyun ; Ha, Jeoung-Hee ; Ahn, Byeong-Cheol ; Lee, Jaetae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_15501860123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Cameras</topic><topic>Cancer therapies</topic><topic>Colorectal cancer</topic><topic>Experiments</topic><topic>Gene expression</topic><topic>Gene therapy</topic><topic>Kinases</topic><topic>Medical research</topic><topic>Proteins</topic><topic>Reporters</topic><topic>Technological change</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Sang-Woo</creatorcontrib><creatorcontrib>Lee, You La</creatorcontrib><creatorcontrib>Lee, Yong Jin</creatorcontrib><creatorcontrib>Park, Seung-Yoon</creatorcontrib><creatorcontrib>Kim, In-San</creatorcontrib><creatorcontrib>Choi, Tae Hyun</creatorcontrib><creatorcontrib>Ha, Jeoung-Hee</creatorcontrib><creatorcontrib>Ahn, Byeong-Cheol</creatorcontrib><creatorcontrib>Lee, Jaetae</creatorcontrib><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><jtitle>Cancer letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Sang-Woo</au><au>Lee, You La</au><au>Lee, Yong Jin</au><au>Park, Seung-Yoon</au><au>Kim, In-San</au><au>Choi, Tae Hyun</au><au>Ha, Jeoung-Hee</au><au>Ahn, Byeong-Cheol</au><au>Lee, Jaetae</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhanced antitumor effects by combination gene therapy usingMDR1gene shRNA and HSV1-tkin a xenograft mouse model</atitle><jtitle>Cancer letters</jtitle><date>2010-05-01</date><risdate>2010</risdate><volume>291</volume><issue>1</issue><spage>83</spage><pages>83-</pages><issn>0304-3835</issn><eissn>1872-7980</eissn><abstract>The use of a novel therapeutic vector containing HSV1-thymidine kinase (HSV1-tk) and a short hairpin RNA for theMDR1gene (shMDR) was proposed previously. We investigated the antitumor effects in anin vivomouse model of colon cancer and assessed treatment response by serial non-invasive imaging. shMDR-TK expressing (MTKG) tumors for the dual therapy group mice with ganciclovir and doxorubicin showed a decrease in size, while tumors in the single therapy group mice showed a moderate increase (p<0.05). The131I-5-iodo-2'-fluoro-2'deoxy-1-β-d-arabinofuranosyluracil (FIAU) uptake ratio of MTKG-to-parent HCT-15 tumors decreased as treatment progressed for single or dual therapy group mice, while that of the control group mice increased gradually. This study demonstrates the enhanced antitumor effects with combination gene therapy compared with a single therapeutic approach, and provides the potential of therapeutic response monitoring.</abstract><cop>Clare</cop><pub>Elsevier Limited</pub><doi>10.1016/j.canlet.2009.10.002</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0304-3835 |
ispartof | Cancer letters, 2010-05, Vol.291 (1), p.83 |
issn | 0304-3835 1872-7980 |
language | eng |
recordid | cdi_proquest_journals_1550186012 |
source | ScienceDirect Journals (5 years ago - present) |
subjects | Cameras Cancer therapies Colorectal cancer Experiments Gene expression Gene therapy Kinases Medical research Proteins Reporters Technological change Tumors |
title | Enhanced antitumor effects by combination gene therapy usingMDR1gene shRNA and HSV1-tkin a xenograft mouse model |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T19%3A23%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Enhanced%20antitumor%20effects%20by%20combination%20gene%20therapy%20usingMDR1gene%20shRNA%20and%20HSV1-tkin%20a%20xenograft%20mouse%20model&rft.jtitle=Cancer%20letters&rft.au=Lee,%20Sang-Woo&rft.date=2010-05-01&rft.volume=291&rft.issue=1&rft.spage=83&rft.pages=83-&rft.issn=0304-3835&rft.eissn=1872-7980&rft_id=info:doi/10.1016/j.canlet.2009.10.002&rft_dat=%3Cproquest%3E3389892261%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1550186012&rft_id=info:pmid/&rfr_iscdi=true |