Low incidence of deletion of the esterase D locus in retinoblastoma patients

Hum Genet. 1983;64(2):151-5. doi: 10.1007/BF00327114.

Abstract

Esterase D was quantitatively measured in the red blood cells from three patients from three separate kindreds who had abnormalities of chromosome 13. The esterase D activity was proportional to the number of copies of the q14 region of chromosome 13 present. These findings confirm published data localizing the esterase D gene to chromosome band 13q14, a region which is important in the etiology of retinoblastoma. Fifty-one additional retinoblastoma patients not known to have any chromosomal defect also underwent esterase D determination. In none of these patients did the esterase D measurement detect a 13q14 deletion. The normal esterase D levels in this series of 51 retinoblastoma patients suggest that deletion of an esterase D locus is infrequent in retinoblastoma patients. It must be noted that patients who are mosaics, with a 13q14 deletion in only a fraction of all somatic cells, could possibly have normal red blood cell esterase D levels. Further study is necessary to determine if esterase D determination of all retinoblastoma patients is a worthwhile clinical tool.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Carboxylesterase*
  • Carboxylic Ester Hydrolases / blood
  • Carboxylic Ester Hydrolases / genetics*
  • Child
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, 13-15 / ultrastructure*
  • Eye Neoplasms / enzymology
  • Eye Neoplasms / genetics*
  • Female
  • Humans
  • Infant
  • Isoenzymes / blood
  • Isoenzymes / genetics
  • Male
  • Middle Aged
  • Retinoblastoma / enzymology
  • Retinoblastoma / genetics*
  • Trisomy

Substances

  • Isoenzymes
  • Carboxylic Ester Hydrolases
  • Carboxylesterase
  • ESD protein, human