Developmental defects and tumor predisposition in Rb mutant mice
Open Access
- 20 September 1999
- journal article
- review article
- Published by Springer Nature in Oncogene
- Vol. 18 (38) , 5293-5303
- https://doi.org/10.1038/sj.onc.1202999
Abstract
Targeted gene disruption in the mouse germline permits the introduction of gene mutations similar to those found in inherited human diseases. New advances in gene targeting that enable cell type specific gene disruption in mice further increases the utility of mouse models to study genetic defects as found in cancer. Here we review the phenotypes observed in mice carrying germline mutated copies of the retinoblastoma tumor suppressor gene. We will illustrate how methods that permit tissue-specific Rb inactivation in mice provide new and more versatile tools to gain insight into the etiology of sporadic cancer.Keywords
This publication has 120 references indexed in Scilit:
- Retention of wild-type p53 in tumors from p53 heterozygous mice: reduction of p53 dosage can promote cancer formationThe EMBO Journal, 1998
- Loss of Heterozygosity in Normal Tissue Adjacent to Breast CarcinomasScience, 1996
- Cancer Cell CyclesScience, 1996
- Tumour-derived p16 alleles encoding proteins defective in cell-cycle inhibitionNature, 1995
- Expression of a retinoblastoma transgene results in dwarf mice.Genes & Development, 1993
- Generation of normal lymphocyte populations by Rb-deficient embryonic stem cellsCurrent Biology, 1993
- Mice deficient for Rb are nonviable and show defects in neurogenesis and haematopoiesisNature, 1992
- Effects of an Rb mutation in the mouseNature, 1992
- Retinoblastoma in transgenic miceNature, 1990
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971