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
Hauptverfasser: EICHER, S. A, CLAYMAN, G. L, LIU, T.-J, SHILLITOE, E. J, STORTHZ, K. A, ROTH, J. A, LOTAN, R
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container_end_page 1664
container_issue 10
container_start_page 1659
container_title Clinical cancer research
container_volume 2
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.
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A ; CLAYMAN, G. L ; LIU, T.-J ; SHILLITOE, E. J ; STORTHZ, K. A ; ROTH, J. A ; LOTAN, R</creator><creatorcontrib>EICHER, S. A ; CLAYMAN, G. L ; LIU, T.-J ; SHILLITOE, E. J ; STORTHZ, K. A ; ROTH, J. A ; LOTAN, R</creatorcontrib><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 &lt; 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. 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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 &lt; 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. 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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. 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The number of cells in p53 transduced cultures was significantly reduced in comparison to controls at all three time points (P &lt; 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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