Fas-ligand gene silencing in basal cell carcinoma tissue with small interfering RNA

Basal cell carcinoma (BCC) is the most frequent cancer in the Caucasian population. Cells of BCC strongly express Fas-ligand (FasL), a member of the tumor necrosis family, which induces apoptosis in Fas receptor-expressing cells. It has been suggested that by expression of FasL, BCC cells may evade...

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Veröffentlicht in:Gene therapy 2005-04, Vol.12 (8), p.678-684
Hauptverfasser: Ji, J, Wernli, M, Mielgo, A, Buechner, S A, Erb, P
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Wernli, M
Mielgo, A
Buechner, S A
Erb, P
description Basal cell carcinoma (BCC) is the most frequent cancer in the Caucasian population. Cells of BCC strongly express Fas-ligand (FasL), a member of the tumor necrosis family, which induces apoptosis in Fas receptor-expressing cells. It has been suggested that by expression of FasL, BCC cells may evade the attack of Fas-positive immune effector cells allowing the tumor to expand. Thus, downregulation of FasL should prime BCC to the assault of immune effector cells. Recently, it has been shown that RNA interference is a highly successful approach to specifically silence a gene of interest in single cells and some animal models. However, RNAi in human tissues has not been shown so far. Here, we provide evidence that small interfering RNAs (siRNAs) efficiently transfect tumor tissue ex vivo and silence the gene of interest. We demonstrate that a specific siRNA efficiently downregulates FasL not only in FasL-positive indicator cells but also in surgically excised BCC tissue at both the protein and the mRNA level. The successful transfection of tumor tissues with siRNAs now allows to test the function of the molecule under study and opens up the investigation of other target genes in the tumor.
doi_str_mv 10.1038/sj.gt.3302453
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Cells of BCC strongly express Fas-ligand (FasL), a member of the tumor necrosis family, which induces apoptosis in Fas receptor-expressing cells. It has been suggested that by expression of FasL, BCC cells may evade the attack of Fas-positive immune effector cells allowing the tumor to expand. Thus, downregulation of FasL should prime BCC to the assault of immune effector cells. Recently, it has been shown that RNA interference is a highly successful approach to specifically silence a gene of interest in single cells and some animal models. However, RNAi in human tissues has not been shown so far. Here, we provide evidence that small interfering RNAs (siRNAs) efficiently transfect tumor tissue ex vivo and silence the gene of interest. We demonstrate that a specific siRNA efficiently downregulates FasL not only in FasL-positive indicator cells but also in surgically excised BCC tissue at both the protein and the mRNA level. The successful transfection of tumor tissues with siRNAs now allows to test the function of the molecule under study and opens up the investigation of other target genes in the tumor.</description><identifier>ISSN: 0969-7128</identifier><identifier>EISSN: 1476-5462</identifier><identifier>DOI: 10.1038/sj.gt.3302453</identifier><identifier>PMID: 15660112</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animal models ; Apoptosis ; Applied cell therapy and gene therapy ; Basal cell carcinoma ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Biotechnology ; Carcinoma, Basal Cell - immunology ; Carcinoma, Basal Cell - therapy ; Cell Biology ; Cell culture ; Cell Line, Tumor ; Dermatology ; Effector cells ; fas Receptor - analysis ; fas Receptor - genetics ; FasL protein ; Flow Cytometry ; Fundamental and applied biological sciences. Psychology ; Gene Expression ; Gene Silencing ; Gene Therapy ; Genetic Therapy - methods ; Green Fluorescent Proteins ; Health. Pharmaceutical industry ; Human Genetics ; Humans ; Immunohistochemistry - methods ; In Situ Hybridization - methods ; Industrial applications and implications. Economical aspects ; Ligands ; Medical sciences ; Microscopy, Confocal ; mRNA ; Nanotechnology ; research-article ; Reverse Transcriptase Polymerase Chain Reaction ; Rhodamines ; RNA, Small Interfering - administration &amp; dosage ; RNA-mediated interference ; siRNA ; Skin cancer ; Transfection ; Transfection - methods ; Transfusions. Complications. Transfusion reactions. Cell and gene therapy ; Tumors of the skin and soft tissue. 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Cells of BCC strongly express Fas-ligand (FasL), a member of the tumor necrosis family, which induces apoptosis in Fas receptor-expressing cells. It has been suggested that by expression of FasL, BCC cells may evade the attack of Fas-positive immune effector cells allowing the tumor to expand. Thus, downregulation of FasL should prime BCC to the assault of immune effector cells. Recently, it has been shown that RNA interference is a highly successful approach to specifically silence a gene of interest in single cells and some animal models. However, RNAi in human tissues has not been shown so far. Here, we provide evidence that small interfering RNAs (siRNAs) efficiently transfect tumor tissue ex vivo and silence the gene of interest. We demonstrate that a specific siRNA efficiently downregulates FasL not only in FasL-positive indicator cells but also in surgically excised BCC tissue at both the protein and the mRNA level. The successful transfection of tumor tissues with siRNAs now allows to test the function of the molecule under study and opens up the investigation of other target genes in the tumor.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animal models</subject><subject>Apoptosis</subject><subject>Applied cell therapy and gene therapy</subject><subject>Basal cell carcinoma</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Carcinoma, Basal Cell - immunology</subject><subject>Carcinoma, Basal Cell - therapy</subject><subject>Cell Biology</subject><subject>Cell culture</subject><subject>Cell Line, Tumor</subject><subject>Dermatology</subject><subject>Effector cells</subject><subject>fas Receptor - analysis</subject><subject>fas Receptor - genetics</subject><subject>FasL protein</subject><subject>Flow Cytometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression</subject><subject>Gene Silencing</subject><subject>Gene Therapy</subject><subject>Genetic Therapy - methods</subject><subject>Green Fluorescent Proteins</subject><subject>Health. Pharmaceutical industry</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Immunohistochemistry - methods</subject><subject>In Situ Hybridization - methods</subject><subject>Industrial applications and implications. Economical aspects</subject><subject>Ligands</subject><subject>Medical sciences</subject><subject>Microscopy, Confocal</subject><subject>mRNA</subject><subject>Nanotechnology</subject><subject>research-article</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Rhodamines</subject><subject>RNA, Small Interfering - administration &amp; dosage</subject><subject>RNA-mediated interference</subject><subject>siRNA</subject><subject>Skin cancer</subject><subject>Transfection</subject><subject>Transfection - methods</subject><subject>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><subject>Tumors of the skin and soft tissue. 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Cells of BCC strongly express Fas-ligand (FasL), a member of the tumor necrosis family, which induces apoptosis in Fas receptor-expressing cells. It has been suggested that by expression of FasL, BCC cells may evade the attack of Fas-positive immune effector cells allowing the tumor to expand. Thus, downregulation of FasL should prime BCC to the assault of immune effector cells. Recently, it has been shown that RNA interference is a highly successful approach to specifically silence a gene of interest in single cells and some animal models. However, RNAi in human tissues has not been shown so far. Here, we provide evidence that small interfering RNAs (siRNAs) efficiently transfect tumor tissue ex vivo and silence the gene of interest. We demonstrate that a specific siRNA efficiently downregulates FasL not only in FasL-positive indicator cells but also in surgically excised BCC tissue at both the protein and the mRNA level. The successful transfection of tumor tissues with siRNAs now allows to test the function of the molecule under study and opens up the investigation of other target genes in the tumor.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>15660112</pmid><doi>10.1038/sj.gt.3302453</doi><tpages>7</tpages></addata></record>
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subjects Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Animal models
Apoptosis
Applied cell therapy and gene therapy
Basal cell carcinoma
Biological and medical sciences
Biomedical and Life Sciences
Biomedicine
Biotechnology
Carcinoma, Basal Cell - immunology
Carcinoma, Basal Cell - therapy
Cell Biology
Cell culture
Cell Line, Tumor
Dermatology
Effector cells
fas Receptor - analysis
fas Receptor - genetics
FasL protein
Flow Cytometry
Fundamental and applied biological sciences. Psychology
Gene Expression
Gene Silencing
Gene Therapy
Genetic Therapy - methods
Green Fluorescent Proteins
Health. Pharmaceutical industry
Human Genetics
Humans
Immunohistochemistry - methods
In Situ Hybridization - methods
Industrial applications and implications. Economical aspects
Ligands
Medical sciences
Microscopy, Confocal
mRNA
Nanotechnology
research-article
Reverse Transcriptase Polymerase Chain Reaction
Rhodamines
RNA, Small Interfering - administration & dosage
RNA-mediated interference
siRNA
Skin cancer
Transfection
Transfection - methods
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
Tumors of the skin and soft tissue. Premalignant lesions
title Fas-ligand gene silencing in basal cell carcinoma tissue with small interfering RNA
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