Retinoblastoma, chromosome abnormalities and oncogene expression

Ophthalmic Paediatr Genet. 1987 Mar;8(1):3-10. doi: 10.3109/13816818709028508.

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.

Publication types

  • Review

MeSH terms

  • Chromosome Aberrations / genetics*
  • Chromosome Deletion
  • Chromosome Disorders
  • Chromosomes, Human, Pair 1*
  • Chromosomes, Human, Pair 13*
  • Chromosomes, Human, Pair 6*
  • Eye Neoplasms / genetics*
  • Humans
  • Oncogenes*
  • Retinoblastoma / genetics*