Literature DB >> 8607030

In situ use of suicide genes for cancer therapy.

S M Freeman1, K A Whartenby, J L Freeman, C N Abboud, A J Marrogi.   

Abstract

Gene therapy has now become a standard experimental approach for treating cancers that have failed conventional therapies. As the understanding of the molecular nature of carcinogenesis develops, new approaches are being taken to directly target tumor cells, thus bypassing the difficulties of killing cells that are resistant to chemotherapy and radiation. One emerging gene therapy approach has been through the genetic modification of tumor cells with a suicide gene such as the herpes simplex virus thymidine kinase gene (HSV-TK) and ganciclovir (GCV) therapy. Death of tumor cells modified with the HSV-TK gene leads to killing of unmodified in situ tumor cells in a phenomenon termed the "bystander effect." The basis both for this effect and other gene therapy trials underway for the treatment of cancer will be discussed.

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Year:  1996        PMID: 8607030

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  19 in total

Review 1.  Defining the success of cardiac gene therapy: how can nuclear imaging contribute?

Authors:  Norbert Avril; Frank M Bengel
Journal:  Eur J Nucl Med Mol Imaging       Date:  2003-01-23       Impact factor: 9.236

2.  Gene doping: Olympic genes for Olympic dreams.

Authors:  Lucy Battery; Andrew Solomon; David Gould
Journal:  J R Soc Med       Date:  2011-12       Impact factor: 5.344

Review 3.  Advances in preclinical investigation of prostate cancer gene therapy.

Authors:  Marxa L Figueiredo; Chinghai Kao; Lily Wu
Journal:  Mol Ther       Date:  2007-04-24       Impact factor: 11.454

4.  Genetically engineered vesicular stomatitis virus in gene therapy: application for treatment of malignant disease.

Authors:  Marilyn Fernandez; Mercedes Porosnicu; Dubravka Markovic; Glen N Barber
Journal:  J Virol       Date:  2002-01       Impact factor: 5.103

5.  Combination gene delivery of the cell cycle inhibitor p27 with thymidine kinase enhances prodrug cytotoxicity.

Authors:  X Danthinne; K Aoki; A L Kurachi; G J Nabel; E G Nabel
Journal:  J Virol       Date:  1998-11       Impact factor: 5.103

6.  Combined suicide and cytokine gene therapy for peritoneal carcinomatosis.

Authors:  C Lechanteur; P Delvenne; F Princen; M Lopez; G Fillet; J Gielen; M P Merville; V Bours
Journal:  Gut       Date:  2000-09       Impact factor: 23.059

Review 7.  Local delivery for gene therapy.

Authors:  G L Clayman; L Dreiling
Journal:  Curr Oncol Rep       Date:  1999       Impact factor: 5.075

8.  Therapeutic efficacy of human hepatocyte transplantation in a SCID/uPA mouse model with inducible liver disease.

Authors:  Donna N Douglas; Toshiyasu Kawahara; Banu Sis; David Bond; Karl P Fischer; D Lorne J Tyrrell; Jamie T Lewis; Norman M Kneteman
Journal:  PLoS One       Date:  2010-02-18       Impact factor: 3.240

9.  Increased anti-tumor effect by a combination of HSV thymidine kinase suicide gene therapy and interferon-gamma/GM-CSF cytokine gene therapy in CT26 tumor model.

Authors:  Sung Hyun Yang; Tae Keun Oh; Seung Taik Kim
Journal:  J Korean Med Sci       Date:  2005-12       Impact factor: 2.153

10.  Bovine herpesvirus tegument protein VP22 enhances thymidine kinase/ganciclovir suicide gene therapy for neuroblastomas compared to herpes simplex virus VP22.

Authors:  Zhaohua Qiu; Jerome S Harms; Jun Zhu; Gary A Splitter
Journal:  J Virol       Date:  2004-04       Impact factor: 5.103

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