Delivery systems intended for in vivo gene therapy of cancer: targeting and replication competent viral vectors (Q34258563)

31 July 2017

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title

Delivery systems intended for in vivo gene therapy of cancer: targeting and replication competent viral vectors (English)

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31 July 2017

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Galanis E

1

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PubMed ID

11369253

31 July 2017

Vile R

series ordinal

2

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PubMed ID

11369253

31 July 2017

Russell SJ

series ordinal

3

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31 July 2017

1 June 2001

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Critical Reviews in Oncology Hematology

31 July 2017

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31 July 2017

38

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31 July 2017

3

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31 July 2017

177-192

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31 July 2017

Gene therapy for cancer

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Gene therapy for cancer

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Gene therapy for cancer: what have we done and where are we going?

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Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells

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Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles

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Tissue-specific targeting of retroviral vectors through ligand-receptor interactions

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Ligand-directed retroviral targeting of human breast cancer cells

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Targeted infection of a retrovirus bearing a CD4-Env chimera into human cells expressing human immunodeficiency virus type 1.

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Retroviral retargeting by envelopes expressing an N-terminal binding domain.

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Towards efficient cell targeting by recombinant retroviruses

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Retroviral vectors displaying functional antibody fragments

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Generation of targeted retroviral vectors by using single-chain variable fragment: an approach to in vivo gene delivery

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Targeted infection of human cells via major histocompatibility complex class I molecules by Moloney murine leukemia virus-derived viruses displaying single-chain antibody fragment-envelope fusion proteins.

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Retroviral display of antibody fragments; interdomain spacing strongly influences vector infectivity.

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Selective transduction of protease-rich tumors by matrix-metalloproteinase-targeted retroviral vectors

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The efficiency of cell targeting by recombinant retroviruses depends on the nature of the receptor and the composition of the artificial cell-virus linker

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Cell-specific viral targeting mediated by a soluble retroviral receptor-ligand fusion protein

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In vivo selection of protease cleavage sites from retrovirus display libraries

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Virus-Receptor Interaction in an Adenovirus System

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Integrins alpha v beta 3 and alpha v beta 5 promote adenovirus internalization but not virus attachment

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Characterization of the knob domain of the adenovirus type 5 fiber protein expressed in Escherichia coli

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Infectious entry pathway of adenovirus type 2.

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Stepwise dismantling of adenovirus 2 during entry into cells

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Targeted gene delivery by tropism-modified adenoviral vectors

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Expression of fibroblast growth factors and their receptors in acquired immunodeficiency syndrome-associated Kaposi sarcoma tissue and derived cells

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The 'adenobody' approach to viral targeting: specific and enhanced adenoviral gene delivery

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Adenovirus targeted to heparan-containing receptors increases its gene delivery efficiency to multiple cell types

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An adenovirus vector with genetically modified fibers demonstrates expanded tropism via utilization of a coxsackievirus and adenovirus receptor-independent cell entry mechanism

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Targeted adenoviral vectors for cancer gene therapy.

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Toward cell-targeting gene therapy vectors: selection of cell-binding peptides from random peptide-presenting phage libraries

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Organ targeting in vivo using phage display peptide libraries

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Targeted integration of adeno-associated virus-derived plasmids in transfected human cells.

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Development of novel cell surface CD34-targeted recombinant adenoassociated virus vectors for gene therapy

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Targeted adeno-associated virus vector transduction of nonpermissive cells mediated by a bispecific F(ab'gamma)2 antibody

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Cell-specific targeting of Sindbis virus vectors displaying IgG-binding domains of protein A.

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Cell-specific targeting of a thymidine kinase/ganciclovir gene therapy system using a recombinant Sindbis virus vector

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Heritable formation of pancreatic beta-cell tumours in transgenic mice expressing recombinant insulin/simian virus 40 oncogenes

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GFAP promoter directs astrocyte-specific expression in transgenic mice.

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Retroviral-mediated gene therapy for the treatment of hepatocellular carcinoma: an innovative approach for cancer therapy

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Cellular promoters incorporated into the adenovirus genome: cell specificity of albumin and immunoglobulin expression

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Potential for H-DNA in the human MUC1 mucin gene promoter

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Replicating vectors for gene therapy of cancer: risks, limitations and prospects.

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Treatment of human cancer with mumps virus

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p53 status does not determine outcome of E1B 55-kilodalton mutant adenovirus lytic infection

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The use of herpes simplex virus-based vectors for gene delivery to the nervous system.

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Experimental Therapy of Human Glioma by Means of a Genetically Engineered Virus Mutant

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Thymidine kinase-negative herpes simplex virus mutants establish latency in mouse trigeminal ganglia but do not reactivate.

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Reovirus therapy of tumors with activated Ras pathway

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An effective strategy of human tumor vaccine modification by coupling bispecific costimulatory molecules

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Gene therapy death prompts review of adenovirus vector

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A novel tumor-specific replication-restricted adenoviral vector for gene therapy of hepatocellular carcinoma

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Selectivity of a replication-competent adenovirus for human breast carcinoma cells expressing the MUC1 antigen.

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Identifiers

DOI

1 reference

31 July 2017

1 reference

PubMed ID

11369253