Literature DB >> 1347590

Gene therapy for cancer.

A A Gutierrez1, N R Lemoine, K Sikora.   

Abstract

The molecular basis of cancer is now understood to involve activation of dominant oncogenes and inactivation of tumour suppressor genes, and these genetic events may represent novel targets for cancer therapy. This review focuses on the potential use and ethical implications of gene transfer to alter the behaviour of somatic cells in cancer patients. Antisense nucleic acids and ribozymes represent informational drugs that may be used to modulate the expression of selected genes and suppress malignant behaviour in cancer cells. Genetic immunomodulation by introducing genes for cytokines into cancer cells or lymphocytes can stimulate a cytotoxic immune response against the tumour. Gene transfer techniques can be applied to target prodrug activation specifically to tumour cells and also to protect normal tissues against toxic chemotherapy. Gene replacement therapy could even be used to restore the function of defective tumour suppressor genes.

Entities:  

Mesh:

Year:  1992        PMID: 1347590     DOI: 10.1016/0140-6736(92)90606-4

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  22 in total

1.  Cytoplasmic molecular delivery with shock waves: importance of impulse.

Authors:  T Kodama; M R Hamblin; A G Doukas
Journal:  Biophys J       Date:  2000-10       Impact factor: 4.033

Review 2.  Melanoma vaccines. Current status and future prospects.

Authors:  P Hersey
Journal:  Drugs       Date:  1994-03       Impact factor: 9.546

3.  Transcriptional targeting of herpes simplex virus for cell-specific replication.

Authors:  S Miyatake; A Iyer; R L Martuza; S D Rabkin
Journal:  J Virol       Date:  1997-07       Impact factor: 5.103

4.  Prevention of murine breast cancer by vaccination with tumor cells modified by cytokine-producing recombinant vaccinia viruses.

Authors:  G R Peplinski; K Tsung; J B Meko; J A Norton
Journal:  Ann Surg Oncol       Date:  1996-01       Impact factor: 5.344

5.  Gene-targeted inhibition of transactivation of human immunodeficiency virus type-1 (HIV-1)-LTR by antisense oligonucleotides.

Authors:  I Demirhan; O Hasselmayer; D Hofmann; A Chandra; F P Svinarchuk; V V Vlassov; J Engels; P Chandra
Journal:  Virus Genes       Date:  1995-01       Impact factor: 2.332

6.  Gene therapy begins.

Authors:  K Davies; B Williamson
Journal:  BMJ       Date:  1993-06-19

Review 7.  Human cancer and gene therapy.

Authors:  G Schmidt-Wolf; I G Schmidt-Wolf
Journal:  Ann Hematol       Date:  1994-12       Impact factor: 3.673

8.  A transfection method for short interfering RNA with the lipid-like self-assembling nanotube, A6K.

Authors:  Daizo Yoshida; K Kim; I Takumi; F Yamaguchi; K Adachi; A Teramoto
Journal:  Med Mol Morphol       Date:  2013-02-05       Impact factor: 2.309

9.  The Human Genome Project and eugenic concerns.

Authors:  K L Garver; B Garver
Journal:  Am J Hum Genet       Date:  1994-01       Impact factor: 11.025

10.  An anti-lymphocytic choriomeningitis virus ribozyme expressed in tissue culture cells diminishes viral RNA levels and leads to a reduction in infectious virus yield.

Authors:  Z Xing; J L Whitton
Journal:  J Virol       Date:  1993-04       Impact factor: 5.103

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