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British Journal of Cancer logoLink to British Journal of Cancer
. 1987 Jun;55(6):661–664. doi: 10.1038/bjc.1987.135

An assessment of the usefulness of electrophoretic variants of esterase-D in the antenatal diagnosis of retinoblastoma in the United Kingdom.

J K Cowell, M Jay, P Rutland, J Hungerford
PMCID: PMC2002033  PMID: 3620311

Abstract

Fifty retinoblastoma families have been studied. In 41 it has been possible to determine the esterase-D phenotypes in all family members. Seven families were informative for the enzyme polymorphism and in all cases cosegregation of the retinoblastoma gene and esterase-D alleles was demonstrated, giving a lod score of 2.61. When combined with other published reports the cumulative lod score is 13.69 with no recombination in 45 meioses. In 10-15% of retinoblastoma families therefore, it is possible to offer prenatal diagnosis using the ESD protein polymorphism. The application of this test to the retinoblastoma population in the UK is limited by the low frequency of the rarer allele (0.116) and, as a result of genetic counseling, the smaller families generally associated with retinoblastoma.

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Selected References

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  1. Cavenee W. K., Murphree A. L., Shull M. M., Benedict W. F., Sparkes R. S., Kock E., Nordenskjold M. Prediction of familial predisposition to retinoblastoma. N Engl J Med. 1986 May 8;314(19):1201–1207. doi: 10.1056/NEJM198605083141901. [DOI] [PubMed] [Google Scholar]
  2. Connolly M. J., Payne R. H., Johnson G., Gallie B. L., Allderdice P. W., Marshall W. H., Lawton R. D. Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity. Hum Genet. 1983;65(2):122–124. doi: 10.1007/BF00286647. [DOI] [PubMed] [Google Scholar]
  3. Cowell J. K., Rutland P., Jay M., Hungerford J. Deletions of the esterase D locus from a survey of 200 retinoblastoma patients. Hum Genet. 1986 Feb;72(2):164–167. doi: 10.1007/BF00283938. [DOI] [PubMed] [Google Scholar]
  4. Cowell J. K., Rutland P., Jay M., Hungerford J. Effect of the esterase-D phenotype on its in vitro enzyme activity. Hum Genet. 1986 Nov;74(3):298–301. doi: 10.1007/BF00282552. [DOI] [PubMed] [Google Scholar]
  5. Cowell J. K., Thompson E., Rutland P. The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions. Arch Dis Child. 1987 Jan;62(1):8–11. doi: 10.1136/adc.62.1.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Friend S. H., Bernards R., Rogelj S., Weinberg R. A., Rapaport J. M., Albert D. M., Dryja T. P. A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma. Nature. 1986 Oct 16;323(6089):643–646. doi: 10.1038/323643a0. [DOI] [PubMed] [Google Scholar]
  7. Gallie B. L., Ellsworth R. M., Abramson D. H., Phillips R. A. Retinoma: spontaneous regression of retinoblastoma or benign manifestation of the mutation? Br J Cancer. 1982 Apr;45(4):513–521. doi: 10.1038/bjc.1982.87. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Halloran S. L., Boughman J. A., Dryja T. P., Mukai S., Long D., Roberts D. F., Craft A. W. Accuracy of detection of the retinoblastoma gene by esterase D linkage. Arch Ophthalmol. 1985 Sep;103(9):1329–1331. doi: 10.1001/archopht.1985.01050090081036. [DOI] [PubMed] [Google Scholar]
  9. Harris H., Hopkinson D. A., Robson E. B. The incidence of rare alleles determining electrophoretic variants: data on 43 enzyme loci in man. Ann Hum Genet. 1974 Jan;37(3):237–253. doi: 10.1111/j.1469-1809.1974.tb01832.x. [DOI] [PubMed] [Google Scholar]
  10. Hopkinson D. A., Mestriner M. A., Cortner J., Harris H. Esterase D: a new human polymorphism. Ann Hum Genet. 1973 Oct;37(2):119–137. doi: 10.1111/j.1469-1809.1973.tb01820.x. [DOI] [PubMed] [Google Scholar]
  11. Horai S., Matsunaga E. Differential enzyme activities in human esterase D phenotypes. Hum Genet. 1984;66(2-3):168–170. doi: 10.1007/BF00286594. [DOI] [PubMed] [Google Scholar]
  12. Mukai S., Rapaport J. M., Shields J. A., Augsburger J. J., Dryja T. P. Linkage of genes for human esterase D and hereditary retinoblastoma. Am J Ophthalmol. 1984 Jun;97(6):681–685. doi: 10.1016/0002-9394(84)90497-5. [DOI] [PubMed] [Google Scholar]
  13. Old J. M., Fitches A., Heath C., Thein S. L., Weatherall D. J., Warren R., McKenzie C., Rodeck C. H., Modell B., Petrou M. First-trimester fetal diagnosis for haemoglobinopathies: report on 200 cases. Lancet. 1986 Oct 4;2(8510):763–767. doi: 10.1016/s0140-6736(86)90296-5. [DOI] [PubMed] [Google Scholar]
  14. Rodeck C. H., Morsman J. M., Nicolaides K. H., McKenzie C., Gosden C. M., Gosden J. R. A single-operator technique for first-trimester chorion biopsy. Lancet. 1983 Dec 10;2(8363):1340–1341. doi: 10.1016/s0140-6736(83)91095-4. [DOI] [PubMed] [Google Scholar]
  15. Sparkes R. S., Murphree A. L., Lingua R. W., Sparkes M. C., Field L. L., Funderburk S. J., Benedict W. F. Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D. Science. 1983 Feb 25;219(4587):971–973. doi: 10.1126/science.6823558. [DOI] [PubMed] [Google Scholar]
  16. Sparkes R. S., Sparkes M. C., Kalina R. E., Pagon R. A., Salk D. J., Disteche C. M. Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3). Hum Genet. 1984;68(3):258–259. doi: 10.1007/BF00418397. [DOI] [PubMed] [Google Scholar]
  17. Sparkes R. S., Sparkes M. C., Wilson M. G., Towner J. W., Benedict W., Murphree A. L., Yunis J. J. Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14. Science. 1980 May 30;208(4447):1042–1044. doi: 10.1126/science.7375916. [DOI] [PubMed] [Google Scholar]
  18. Squire J., Dryja T. P., Dunn J., Goddard A., Hofmann T., Musarella M., Willard H. F., Becker A. J., Gallie B. L., Phillips R. A. Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13. Proc Natl Acad Sci U S A. 1986 Sep;83(17):6573–6577. doi: 10.1073/pnas.83.17.6573. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Ward R. H., Modell B., Petrou M., Karagözlu F., Douratsos E. Method of sampling chorionic villi in first trimester of pregnancy under guidance of real time ultrasound. Br Med J (Clin Res Ed) 1983 May 14;286(6377):1542–1544. doi: 10.1136/bmj.286.6377.1542. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Yunis J. J., Ramsay N. Retinoblastoma and subband deletion of chromosome 13. Am J Dis Child. 1978 Feb;132(2):161–163. doi: 10.1001/archpedi.1978.02120270059012. [DOI] [PubMed] [Google Scholar]

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