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PMID: 6694706 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Homozygosity of chromosome 13 in retinoblastoma.

The New England journal of medicine ·Vol. 310 ·No. 9 ·1984-03-01 ·Pages 550-3

Dryja TP, Cavenee W, White R, Rapaport JM, Petersen R, Albert DM, Bruns GA

Abstract

We studied the frequency of chromosome 13 homozygosity in tumor tissue obtained directly from eyes harboring retinoblastomas. The data indicate that approximately half of all retinoblastomas are homozygous for large portions of 13q, that the homozygosity occurs in vivo and not as an event secondary to culture of the tumor cells, that chromosome 13 homozygosity is not correlated with the degree of histopathologic differentiation of the tumor, and that the homozygosity occurs in both sporadic and hereditary retinoblastomas. The development of chromosome 13 homozygosity may represent a fundamental event in the oncogenesis of a considerable number of retinoblastomas. This finding may have implications for the genetic counseling of patients with hereditary retinoblastoma. It may also be important in understanding the mechanism of oncogenesis of other tumors, especially hereditary tumors.

MeSH Terms
Alleles Carboxylesterase Carboxylic Ester Hydrolases/genetics Child, Preschool Chromosome Mapping Chromosomes, Human, 13-15 DNA/analysis Eye Neoplasms/genetics Female Homozygote Humans Infant Male Retinoblastoma/genetics
Chemicals
DNA Carboxylic Ester Hydrolases Carboxylesterase ESD protein, human
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Dryja T P
Cavenee W
White R
Rapaport J M
Petersen R
Albert D M
Bruns G A
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
0028-4793
Published
1984-03-01
Pages
550-3
Language
English
Region
United States
NLM ID
0255562
Subset
IM
Grants
NEI NIH HHS · EY 04543 · United States
NICHD NIH HHS · HD 04807 · United States
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