Literature DB >> 8586469

Transgenic and gene disruption techniques in the study of neurocarcinogenesis.

A Aguzzi1, S Brandner, S Isenmann, J P Steinbach, U Sure.   

Abstract

Transgenic technologies have come of age, and the field of carcinogenesis has profited extensively from the availability of these methods. Both the inappropriate expression of dominant oncogenes in specific tissues and the ability to "knock out" tumor suppressor genes in mammalian organisms have enabled substantial advancements of our understanding of development and progression of the neoplastic phenotype. In the first part of this article, we review the most popular techniques for modification of the mammalian genome in vivo, i.e. microinjection of fertilized eggs, retrovirus-mediated gene transfer, and targeted gene deletion through homologous recombination. Subsequently, we attempt a critical evaluation of the available models of neurocarcinogenesis, and discuss their impact and future potential for the study of cancer in the nervous system.

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Year:  1995        PMID: 8586469     DOI: 10.1002/glia.440150314

Source DB:  PubMed          Journal:  Glia        ISSN: 0894-1491            Impact factor:   7.452


  3 in total

1.  Deletion of RB exons 24 and 25 causes low-penetrance retinoblastoma.

Authors:  R Bremner; D C Du; M J Connolly-Wilson; P Bridge; K F Ahmad; H Mostachfi; D Rushlow; J M Dunn; B L Gallie
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

Review 2.  Animal models of cell cycle dysregulation and the pathogenesis of gliomas.

Authors:  E C Holland
Journal:  J Neurooncol       Date:  2001-02       Impact factor: 4.130

3.  Of mice and men: the evolution of animal welfare guidelines for cancer research.

Authors:  N Dey; P De; B R Smith; B Leyland-Jones
Journal:  Br J Cancer       Date:  2010-05-25       Impact factor: 7.640

  3 in total

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