Evaluation of topical gene therapy for head and neck squamous cell carcinoma in an organotypic model
The organotypic (raft) culture system has been shown to be a useful model for examining the effects of biochemical manipulations on various epithelial cell types, using in vitro conditions that simulate the in vivo environment of the tissue of origin. To investigate this method as a model for topica...
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Veröffentlicht in: | Clinical cancer research 1996-10, Vol.2 (10), p.1659-1664 |
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creator | EICHER, S. A CLAYMAN, G. L LIU, T.-J SHILLITOE, E. J STORTHZ, K. A ROTH, J. A LOTAN, R |
description | The organotypic (raft) culture system has been shown to be a useful model for examining the effects of biochemical manipulations
on various epithelial cell types, using in vitro conditions that simulate the in vivo environment of the tissue of origin.
To investigate this method as a model for topical gene therapy, we cultured the oral head and neck squamous cell carcinoma
cell line TR146 on fibroblast-containing collagen gels at the air-medium interface and assessed the efficiency of transduction
of a topically applied adenoviral vector containing beta-galactosidase cDNA. Diffuse expression of -galactosidase activity
in multiple cell layers demonstrated effective penetration of the vector. Transduction efficiency and therapeutic activity
of a replication-defective recombinant adenovirus containing wild-type p53 cDNA linked to a FLAG marker (AdCMV-p53-FLAG) were
then assessed in TR146 organotypic cultures transduced by topical application. Twenty-four, 48, and 72 h after transduction,
the cultures were harvested, and residual cell number and FLAG peptide expression were determined. The number of cells in
p53 transduced cultures was significantly reduced in comparison to controls at all three time points (P < 0.001), which resulted
from the induction of apoptosis as determined by in situ DNA end labeling. In addition, the FLAG peptide was expressed diffusely
in the residual cells, further confirming effective transduction and expression of the exogenous gene products throughout
multiple layers. We conclude that the organotypic culture is an effective in vitro model for assessing the efficacy of topically
applied gene therapy on head and neck squamous carcinomas and premalignancies. |
format | Article |
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on various epithelial cell types, using in vitro conditions that simulate the in vivo environment of the tissue of origin.
To investigate this method as a model for topical gene therapy, we cultured the oral head and neck squamous cell carcinoma
cell line TR146 on fibroblast-containing collagen gels at the air-medium interface and assessed the efficiency of transduction
of a topically applied adenoviral vector containing beta-galactosidase cDNA. Diffuse expression of -galactosidase activity
in multiple cell layers demonstrated effective penetration of the vector. Transduction efficiency and therapeutic activity
of a replication-defective recombinant adenovirus containing wild-type p53 cDNA linked to a FLAG marker (AdCMV-p53-FLAG) were
then assessed in TR146 organotypic cultures transduced by topical application. Twenty-four, 48, and 72 h after transduction,
the cultures were harvested, and residual cell number and FLAG peptide expression were determined. The number of cells in
p53 transduced cultures was significantly reduced in comparison to controls at all three time points (P < 0.001), which resulted
from the induction of apoptosis as determined by in situ DNA end labeling. In addition, the FLAG peptide was expressed diffusely
in the residual cells, further confirming effective transduction and expression of the exogenous gene products throughout
multiple layers. We conclude that the organotypic culture is an effective in vitro model for assessing the efficacy of topically
applied gene therapy on head and neck squamous carcinomas and premalignancies.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>PMID: 9816113</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Adenoviridae - genetics ; Antineoplastic agents ; Apoptosis - genetics ; Apoptosis - physiology ; Biological and medical sciences ; Carcinoma, Squamous Cell - genetics ; Carcinoma, Squamous Cell - pathology ; Carcinoma, Squamous Cell - therapy ; Gene Expression Regulation, Neoplastic ; Gene Transfer Techniques ; General aspects ; Genetic Therapy ; Head and Neck Neoplasms - genetics ; Head and Neck Neoplasms - pathology ; Head and Neck Neoplasms - therapy ; Humans ; Medical sciences ; Oligopeptides ; Organ Culture Techniques ; Peptides - genetics ; Pharmacology. Drug treatments ; Recombinant Fusion Proteins - genetics ; Tumor Cells, Cultured ; Tumor Suppressor Protein p53 - genetics</subject><ispartof>Clinical cancer research, 1996-10, Vol.2 (10), p.1659-1664</ispartof><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3242708$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9816113$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>EICHER, S. A</creatorcontrib><creatorcontrib>CLAYMAN, G. L</creatorcontrib><creatorcontrib>LIU, T.-J</creatorcontrib><creatorcontrib>SHILLITOE, E. J</creatorcontrib><creatorcontrib>STORTHZ, K. A</creatorcontrib><creatorcontrib>ROTH, J. A</creatorcontrib><creatorcontrib>LOTAN, R</creatorcontrib><title>Evaluation of topical gene therapy for head and neck squamous cell carcinoma in an organotypic model</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>The organotypic (raft) culture system has been shown to be a useful model for examining the effects of biochemical manipulations
on various epithelial cell types, using in vitro conditions that simulate the in vivo environment of the tissue of origin.
To investigate this method as a model for topical gene therapy, we cultured the oral head and neck squamous cell carcinoma
cell line TR146 on fibroblast-containing collagen gels at the air-medium interface and assessed the efficiency of transduction
of a topically applied adenoviral vector containing beta-galactosidase cDNA. Diffuse expression of -galactosidase activity
in multiple cell layers demonstrated effective penetration of the vector. Transduction efficiency and therapeutic activity
of a replication-defective recombinant adenovirus containing wild-type p53 cDNA linked to a FLAG marker (AdCMV-p53-FLAG) were
then assessed in TR146 organotypic cultures transduced by topical application. Twenty-four, 48, and 72 h after transduction,
the cultures were harvested, and residual cell number and FLAG peptide expression were determined. The number of cells in
p53 transduced cultures was significantly reduced in comparison to controls at all three time points (P < 0.001), which resulted
from the induction of apoptosis as determined by in situ DNA end labeling. In addition, the FLAG peptide was expressed diffusely
in the residual cells, further confirming effective transduction and expression of the exogenous gene products throughout
multiple layers. We conclude that the organotypic culture is an effective in vitro model for assessing the efficacy of topically
applied gene therapy on head and neck squamous carcinomas and premalignancies.</description><subject>Adenoviridae - genetics</subject><subject>Antineoplastic agents</subject><subject>Apoptosis - genetics</subject><subject>Apoptosis - physiology</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Squamous Cell - therapy</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Gene Transfer Techniques</subject><subject>General aspects</subject><subject>Genetic Therapy</subject><subject>Head and Neck Neoplasms - genetics</subject><subject>Head and Neck Neoplasms - pathology</subject><subject>Head and Neck Neoplasms - therapy</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Oligopeptides</subject><subject>Organ Culture Techniques</subject><subject>Peptides - genetics</subject><subject>Pharmacology. Drug treatments</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>Tumor Cells, Cultured</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kF9LwzAUxYsoU6cfQciDiC-FpEnb9FHG_AMDX_ZebpPbNdomW9Iq-_ZmrPh0D5wfh3PPRXLD8rxMeVbkl1HTUqZU8Ow6uQ3hi1ImGBWLZFFJVjDGbxK9_oF-gtE4S1xLRrc3CnqyQ4tk7NDD_kha50mHoAlYTSyqbxIOEwxuCkRh3xMFXhnrBiDGRoY4vwPrxmOMIoPT2N8lVy30Ae_nu0y2r-vt6j3dfL59rF42aZcVcky1qBrIdVWIpiolR8bzkgksJDLaZPEljVJypQUwFA0HxVuVM95mlDXIcr5Mns6xe-8OE4axHkw4NQSLsWxdyrIQVMgIPszg1Ayo6703A_hjPa8S_cfZhxDXaD1YZcI_xjORlfQU83zGOrPrfo3HWkUQvceAcZKuzmpGa1bkFf8DKYV6Nw</recordid><startdate>19961001</startdate><enddate>19961001</enddate><creator>EICHER, S. A</creator><creator>CLAYMAN, G. L</creator><creator>LIU, T.-J</creator><creator>SHILLITOE, E. J</creator><creator>STORTHZ, K. A</creator><creator>ROTH, J. A</creator><creator>LOTAN, R</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19961001</creationdate><title>Evaluation of topical gene therapy for head and neck squamous cell carcinoma in an organotypic model</title><author>EICHER, S. A ; CLAYMAN, G. L ; LIU, T.-J ; SHILLITOE, E. J ; STORTHZ, K. A ; ROTH, J. A ; LOTAN, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h268t-d49ba5d964b9783e135714e68e10b2326de883cd4a1e4b3ac3fc513f201be153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adenoviridae - genetics</topic><topic>Antineoplastic agents</topic><topic>Apoptosis - genetics</topic><topic>Apoptosis - physiology</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Squamous Cell - therapy</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Gene Transfer Techniques</topic><topic>General aspects</topic><topic>Genetic Therapy</topic><topic>Head and Neck Neoplasms - genetics</topic><topic>Head and Neck Neoplasms - pathology</topic><topic>Head and Neck Neoplasms - therapy</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Oligopeptides</topic><topic>Organ Culture Techniques</topic><topic>Peptides - genetics</topic><topic>Pharmacology. Drug treatments</topic><topic>Recombinant Fusion Proteins - genetics</topic><topic>Tumor Cells, Cultured</topic><topic>Tumor Suppressor Protein p53 - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>EICHER, S. A</creatorcontrib><creatorcontrib>CLAYMAN, G. L</creatorcontrib><creatorcontrib>LIU, T.-J</creatorcontrib><creatorcontrib>SHILLITOE, E. J</creatorcontrib><creatorcontrib>STORTHZ, K. A</creatorcontrib><creatorcontrib>ROTH, J. A</creatorcontrib><creatorcontrib>LOTAN, R</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>EICHER, S. A</au><au>CLAYMAN, G. L</au><au>LIU, T.-J</au><au>SHILLITOE, E. J</au><au>STORTHZ, K. A</au><au>ROTH, J. A</au><au>LOTAN, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of topical gene therapy for head and neck squamous cell carcinoma in an organotypic model</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>1996-10-01</date><risdate>1996</risdate><volume>2</volume><issue>10</issue><spage>1659</spage><epage>1664</epage><pages>1659-1664</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>The organotypic (raft) culture system has been shown to be a useful model for examining the effects of biochemical manipulations
on various epithelial cell types, using in vitro conditions that simulate the in vivo environment of the tissue of origin.
To investigate this method as a model for topical gene therapy, we cultured the oral head and neck squamous cell carcinoma
cell line TR146 on fibroblast-containing collagen gels at the air-medium interface and assessed the efficiency of transduction
of a topically applied adenoviral vector containing beta-galactosidase cDNA. Diffuse expression of -galactosidase activity
in multiple cell layers demonstrated effective penetration of the vector. Transduction efficiency and therapeutic activity
of a replication-defective recombinant adenovirus containing wild-type p53 cDNA linked to a FLAG marker (AdCMV-p53-FLAG) were
then assessed in TR146 organotypic cultures transduced by topical application. Twenty-four, 48, and 72 h after transduction,
the cultures were harvested, and residual cell number and FLAG peptide expression were determined. The number of cells in
p53 transduced cultures was significantly reduced in comparison to controls at all three time points (P < 0.001), which resulted
from the induction of apoptosis as determined by in situ DNA end labeling. In addition, the FLAG peptide was expressed diffusely
in the residual cells, further confirming effective transduction and expression of the exogenous gene products throughout
multiple layers. We conclude that the organotypic culture is an effective in vitro model for assessing the efficacy of topically
applied gene therapy on head and neck squamous carcinomas and premalignancies.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>9816113</pmid><tpages>6</tpages></addata></record> |
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source | MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Adenoviridae - genetics Antineoplastic agents Apoptosis - genetics Apoptosis - physiology Biological and medical sciences Carcinoma, Squamous Cell - genetics Carcinoma, Squamous Cell - pathology Carcinoma, Squamous Cell - therapy Gene Expression Regulation, Neoplastic Gene Transfer Techniques General aspects Genetic Therapy Head and Neck Neoplasms - genetics Head and Neck Neoplasms - pathology Head and Neck Neoplasms - therapy Humans Medical sciences Oligopeptides Organ Culture Techniques Peptides - genetics Pharmacology. Drug treatments Recombinant Fusion Proteins - genetics Tumor Cells, Cultured Tumor Suppressor Protein p53 - genetics |
title | Evaluation of topical gene therapy for head and neck squamous cell carcinoma in an organotypic model |
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