Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1984 Feb;21(1):4–12. doi: 10.1136/jmg.21.1.4

The origin of ovarian teratomas.

J M Parrington, L F West, S Povey
PMCID: PMC1049199  PMID: 6363699

Abstract

Chromosome and enzyme markers have been studied in 21 benign ovarian teratomas from 14 patients. Markers heterozygous in the patient were completely homozygous in 52% of the teratomas and completely heterozygous in 19%. The remainder showed a mixture of the two, 10% having homozygous centromeres with some heterozygous enzyme markers and 19% having heterozygous centromeres and some homozygous enzyme markers. These results suggest that benign ovarian teratomas in the present series arise from germ cells in a number of different ways. Those with heterozygous centromeres probably arise by failure of meiosis I. Some tumours with homozygous centromeres must arise by failure of meiosis II, but because of the low level of heterozygous enzyme markers in this group a substantial number are thought to arise by duplication of a mature ovum to give an entirely homozygous genotype, genetically the female equivalent of the complete hydatidiform mole.

Full text

PDF
4

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. CORFMAN P. A., RICHART R. M. CHROMOSOME NUMBER AND MORPHOLOGY OF BENIGN OVARIAN CYSTIC TERATOMAS. N Engl J Med. 1964 Dec 10;271:1241–1244. doi: 10.1056/NEJM196412102712405. [DOI] [PubMed] [Google Scholar]
  2. Carritt B., Parrington J. M., Welch H. M., Povey S. Diverse origins of multiple ovarian teratomas in a single individual. Proc Natl Acad Sci U S A. 1982 Dec;79(23):7400–7404. doi: 10.1073/pnas.79.23.7400. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cook P. J., Noades J. E., Lomas C. G., Buckton K. E., Robson E. B. Exclusion mapping illustrated by the MNSs blood group. Ann Hum Genet. 1980 Jul;44(Pt 1):61–73. doi: 10.1111/j.1469-1809.1980.tb00946.x. [DOI] [PubMed] [Google Scholar]
  4. Eppig J. J., Kozak L. P., Eicher E. M., Stevens L. C. Ovarian teratomas in mice are derived from oocytes that have completed the first meiotic division. Nature. 1977 Oct 6;269(5628):517–518. doi: 10.1038/269517a0. [DOI] [PubMed] [Google Scholar]
  5. Eppig J. T., Eicher E. M. Application of the ovarian teratoma mapping method in the mouse. Genetics. 1983 Apr;103(4):797–812. doi: 10.1093/genetics/103.4.797. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Ganner E., Evans H. J. The relationship between patterns of DNA replication and of quinacrine fluorescence in the human chromosome complement. Chromosoma. 1971;35(3):326–341. doi: 10.1007/BF00326282. [DOI] [PubMed] [Google Scholar]
  7. Jacobs P. A., Wilson C. M., Sprenkle J. A., Rosenshein N. B., Migeon B. R. Mechanism of origin of complete hydatidiform moles. Nature. 1980 Aug 14;286(5774):714–716. doi: 10.1038/286714a0. [DOI] [PubMed] [Google Scholar]
  8. Jeremiah S. J., Povey S., Burley M. W., Kielty C., Lee M., Spowart G., Corney G., Cook P. J. Mapping studies on human mitochondrial glutamate oxaloacetate transaminase. Ann Hum Genet. 1982 May;46(Pt 2):145–152. doi: 10.1111/j.1469-1809.1982.tb00705.x. [DOI] [PubMed] [Google Scholar]
  9. Kielty C. M., Povey S., Hopkinson D. A. Regulation of expression of liver-specific enzymes. I. Detection in mammalian tissues and cultured cells. Ann Hum Genet. 1981 Oct;45(Pt 4):341–356. doi: 10.1111/j.1469-1809.1981.tb00348.x. [DOI] [PubMed] [Google Scholar]
  10. King J., Cook P. J. Glucose dehydrogenase polymorphism in man. Ann Hum Genet. 1981 May;45(Pt 2):129–134. doi: 10.1111/j.1469-1809.1981.tb00314.x. [DOI] [PubMed] [Google Scholar]
  11. Lawler S. D., Pickthall V. J., Fisher R. A., Povey S., Evans M. W., Szulman A. E. Genetic studies of complete and partial hydatidiform moles. Lancet. 1979 Sep 15;2(8142):580–580. doi: 10.1016/s0140-6736(79)91632-5. [DOI] [PubMed] [Google Scholar]
  12. Linder D. Gene loss in human teratomas. Proc Natl Acad Sci U S A. 1969 Jul;63(3):699–704. doi: 10.1073/pnas.63.3.699. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Linder D., McCaw B. K., Hecht F. Parthenogenic origin of benign ovarian teratomas. N Engl J Med. 1975 Jan 9;292(2):63–66. doi: 10.1056/NEJM197501092920202. [DOI] [PubMed] [Google Scholar]
  14. Linder D., Power J. Further evidence for post-meiotic origin of teratomas in the human female. Ann Hum Genet. 1970 Jul;34(1):21–30. doi: 10.1111/j.1469-1809.1970.tb00216.x. [DOI] [PubMed] [Google Scholar]
  15. McCaw B. K., Hecht F., Linder D., Lovrien E. W., Wyandt H., Bacon D., Clark B., Lea N. Ovarian teratomas: cytologic data. Cytogenet Cell Genet. 1976;16(1-5):391–395. doi: 10.1159/000130640. [DOI] [PubMed] [Google Scholar]
  16. Ott J., Linder D., McCaw B. K., Lovrien E. W., Hecht F. Estimating distances from the centromere by means of benign ovarian teratomas in man. Ann Hum Genet. 1976 Nov;40(2):191–196. doi: 10.1111/j.1469-1809.1976.tb00179.x. [DOI] [PubMed] [Google Scholar]
  17. Patil S. R., Kaiser-McCaw B., Hecht F., Linder D., Lovrien E. W. Human benign ovarian teratomas: chromosomal and electrophoretic enzyme studies. Birth Defects Orig Artic Ser. 1978;14(6B):297–301. [PubMed] [Google Scholar]
  18. Riley P. A., Sutton P. M. Why are ovarian teratomas benign whilst teratomas of the testis are malignant? Lancet. 1975 Jun 21;1(7921):1360–1362. doi: 10.1016/s0140-6736(75)92265-5. [DOI] [PubMed] [Google Scholar]
  19. Sturt E. A mapping function for human chromosomes. Ann Hum Genet. 1976 Nov;40(2):147–163. doi: 10.1111/j.1469-1809.1976.tb00175.x. [DOI] [PubMed] [Google Scholar]
  20. Sumner A. T. A simple technique for demonstrating centromeric heterochromatin. Exp Cell Res. 1972 Nov;75(1):304–306. doi: 10.1016/0014-4827(72)90558-7. [DOI] [PubMed] [Google Scholar]
  21. Sutton J. G., Burgess R. Genetic evidence for four common alleles at the phosphoglucomutase-1 locus (PGM1) detectable by isoelectric focusing. Vox Sang. 1978;34(2):97–103. doi: 10.1111/j.1423-0410.1978.tb03730.x. [DOI] [PubMed] [Google Scholar]
  22. Turner B. M., Turner V. S., Beratis N. G., Hirschhorn K. Polymorphism of human alpha fucosidase. Am J Hum Genet. 1975 Sep;27(5):651–661. [PMC free article] [PubMed] [Google Scholar]
  23. Wang N., Perkins K. L., Bronson D. L., Fraley E. E. Cytogenetic evidence for premeiotic transformation of human testicular cancers. Cancer Res. 1981 Jun;41(6):2135–2140. [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES