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Retinoblastoma, chromosome abnormalities and oncogene expression
- Source :
- Ophthalmic Paediatrics and Genetics. 8:3-10
- Publication Year :
- 1987
- Publisher :
- Informa UK Limited, 1987.
-
Abstract
- Recurrent chromosomal abnormalities in retinoblastomas involve numbers 13, 1, and 6, as well as homogeneously staining regions (HSR) and double minutes (DMS). Evidence suggesting that chromosome 13 contains a gene responsible for tumorigenesis has already been presented. We postulate that the genetic changes resulting from abnormalities of chromosomes 1 and 6 and the HSR/DMS provide a selective growth advantage to cells in which they occur. Support for this hypothesis, as it relates to the HSR/DMS and oncogene amplification, is discussed.
- Subjects :
- Chromosome Disorders
Biology
medicine.disease_cause
medicine
Humans
Gene
Genetics (clinical)
Oncogene amplification
Chromosome 13
Chromosome Aberrations
Chromosomes, Human, Pair 13
Oncogene
Retinoblastoma
Eye Neoplasms
fungi
Chromosome
Oncogenes
medicine.disease
Molecular biology
Ophthalmology
Chromosomes, Human, Pair 1
Pediatrics, Perinatology and Child Health
Chromosomes, Human, Pair 6
Chromosome Deletion
Carcinogenesis
Subjects
Details
- ISSN :
- 01676784
- Volume :
- 8
- Database :
- OpenAIRE
- Journal :
- Ophthalmic Paediatrics and Genetics
- Accession number :
- edsair.doi.dedup.....1fc7f657620fab0f0d68ec60a7eb3bca
- Full Text :
- https://doi.org/10.3109/13816818709028508