Skip to main content
The British Journal of Ophthalmology logoLink to The British Journal of Ophthalmology
. 1990 Jul;74(7):427–430. doi: 10.1136/bjo.74.7.427

Electrophoretic assessment of aqueous and serum neurone-specific enolase in retinoblastoma and ocular malignant melanoma.

B S Shine 1, J Hungerford 1, B Vaghela 1, G A Sheraidah 1
PMCID: PMC1042154  PMID: 2378858

Abstract

The isoenzyme pattern of enolase was examined in the aqueous humour and serum of patients with retinoblastoma (10 aqueous, 8 sera), malignant melanoma (4 aqueous, 25 sera), and normal subjects undergoing cataract surgery (25 aqueous, 30 sera). The assay we used allowed assessment of all three major isoenzymes, including the gamma gamma isoenzyme (neurone-specific enolase). No enolase was detectable in normal aqueous; alpha alpha isoenzyme was present in the aqueous of one patient with malignant melanoma, while aqueous from all patients with retinoblastoma contained both alpha alpha and gamma gamma. Normal serum contained only an alpha alpha band, while serum from patients with retinoblastoma contained alpha alpha, alpha gamma, and gamma gamma bands (7 sera, 87.5%), or alpha alpha only (1 patient, 12.5%). All sera from patients with malignant melanoma contained the alpha alpha band, with low levels of gamma gamma in 16 (60%). In a single patient with Coats's disease alpha alpha was present in the serum, but no enolase was detected in aqueous. Increased amounts of gamma-containing isoenzymes of enolase are found in both serum and aqueous from patients with retinoblastoma. In malignant melanoma there is often an increase in serum gamma gamma enolase. The assessment of aqueous and serum enolase patterns may be of value in the diagnosis of retinoblastoma and malignant melanoma.

Full text

PDF
427

Selected References

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

  1. Abramson D. H. Retinoma, retinocytoma, and the retinoblastoma gene. Arch Ophthalmol. 1983 Oct;101(10):1517–1518. doi: 10.1001/archopht.1983.01040020519002. [DOI] [PubMed] [Google Scholar]
  2. Akoun G. M., Scarna H. M., Milleron B. J., Bénichou M. P., Herman D. P. Serum neuron-specific enolase. A marker for disease extent and response to therapy for small-cell lung cancer. Chest. 1985 Jan;87(1):39–43. doi: 10.1378/chest.87.1.39. [DOI] [PubMed] [Google Scholar]
  3. Albert D. M. Historic review of retinoblastoma. Ophthalmology. 1987 Jun;94(6):654–662. doi: 10.1016/s0161-6420(87)33407-4. [DOI] [PubMed] [Google Scholar]
  4. Beemer F. A., Vlug A. M., van Veelen C. W., Rijksen G., Staal G. E. Isozyme pattern of enolase of childhood tumors. Cancer. 1984 Jul 15;54(2):293–296. doi: 10.1002/1097-0142(19840715)54:2<293::aid-cncr2820540218>3.0.co;2-u. [DOI] [PubMed] [Google Scholar]
  5. Das A., Roy I. S., Maitra T. K. Lactate dehydrogenase level and protein pattern in the aqueous humour of patients with retinoblastoma. Can J Ophthalmol. 1983 Dec;18(7):337–339. [PubMed] [Google Scholar]
  6. Dayal Y., Goyal J. L., Jaffery N. F., Agarwal H. C. Lactate dehydrogenase levels in aqueous humor and serum in retinoblastoma. Jpn J Ophthalmol. 1985;29(4):417–422. [PubMed] [Google Scholar]
  7. Gotoh Y., Hashimoto K., Tada K. Urine neuron-specific enolase and its clinical implication in patients with neuroblastoma. Tohoku J Exp Med. 1986 May;149(1):67–72. doi: 10.1620/tjem.149.67. [DOI] [PubMed] [Google Scholar]
  8. Hullin D. A., Brown K., Kynoch P. A., Smith C., Thompson R. J. Purification, radioimmunoassay, and distribution of human brain 14-3-2 protein (nervous-system specific enolase) in human tissues. Biochim Biophys Acta. 1980 Feb 21;628(1):98–108. doi: 10.1016/0304-4165(80)90355-4. [DOI] [PubMed] [Google Scholar]
  9. Ishiguro Y., Kato K., Shimizu A., Ito T., Nagaya M. High levels of immunoreactive nervous system-specific enolase in sera of patients with neuroblastoma. Clin Chim Acta. 1982 May 20;121(2):173–180. doi: 10.1016/0009-8981(82)90056-0. [DOI] [PubMed] [Google Scholar]
  10. Jakobiec F. A., Abramson D., Scher R. Increased aqueous lactate dehydrogenase in Coats' disease. Am J Ophthalmol. 1978 May;85(5 Pt 1):686–689. doi: 10.1016/s0002-9394(14)77106-5. [DOI] [PubMed] [Google Scholar]
  11. Kato K., Asai R., Shimizu A., Suzuki F., Ariyoshi Y. Immunoassay of three enolase isozymes in human serum and in blood cells. Clin Chim Acta. 1983 Feb 7;127(3):353–363. doi: 10.1016/0009-8981(83)90162-6. [DOI] [PubMed] [Google Scholar]
  12. Kato K., Asai R., Shimizu A., Suzuki F., Ariyoshi Y. Immunoassay of three enolase isozymes in human serum and in blood cells. Clin Chim Acta. 1983 Feb 7;127(3):353–363. doi: 10.1016/0009-8981(83)90162-6. [DOI] [PubMed] [Google Scholar]
  13. Kato K., Suzuki F., Umeda Y. Highly sensitive immunoassays for three forms of rat brain enolase. J Neurochem. 1981 Mar;36(3):793–797. doi: 10.1111/j.1471-4159.1981.tb01663.x. [DOI] [PubMed] [Google Scholar]
  14. Kivelä T. Neuron-specific enolase in retinoblastoma. An immunohistochemical study. Acta Ophthalmol (Copenh) 1986 Feb;64(1):19–25. doi: 10.1111/j.1755-3768.1986.tb06866.x. [DOI] [PubMed] [Google Scholar]
  15. Lifshitz T., Tessler Z., Maor E., Yassur Y. Increased aqueous lactic dehydrogenase in Coat's disease. Ann Ophthalmol. 1987 Mar;19(3):116–119. [PubMed] [Google Scholar]
  16. MIDDLETON W. H. Diagnosis of metastatic tumors of the anterior ocular segment. Am J Ophthalmol. 1952 Sep;35(9):1329–1334. doi: 10.1016/0002-9394(52)91151-3. [DOI] [PubMed] [Google Scholar]
  17. Margo C. E., Zimmerman L. E. Retinoblastoma: the accuracy of clinical diagnosis in children treated by enucleation. J Pediatr Ophthalmol Strabismus. 1983 Nov-Dec;20(6):227–229. doi: 10.3928/0191-3913-19831101-02. [DOI] [PubMed] [Google Scholar]
  18. Molnar M. L., Stefansson K., Marton L. S., Tripathi R. S., Molnar G. K. Immunohistochemistry of retinoblastomas in humans. Am J Ophthalmol. 1984 Mar;97(3):301–307. doi: 10.1016/0002-9394(84)90627-5. [DOI] [PubMed] [Google Scholar]
  19. Nakajima T., Kato K., Kaneko A., Tsumuraya M., Morinaga S., Shimosato Y. High concentrations of enolase, alpha- and gamma-subunits, in the aqueous humor in cases of retinoblastoma. Am J Ophthalmol. 1986 Jan 15;101(1):102–106. doi: 10.1016/0002-9394(86)90471-x. [DOI] [PubMed] [Google Scholar]
  20. Nielsen H. E., Koch C. Genetic control of the in vitro responses of rat blood lymphocytes. I. Comparison of in vitro and in vivo responses. Scand J Immunol. 1975;4(1):31–36. doi: 10.1111/j.1365-3083.1975.tb02597.x. [DOI] [PubMed] [Google Scholar]
  21. Parma A. M., Marangos P. J., Goodwin F. K. A more sensitive radioimmunoassay for neuron-specific enolase suitable for cerebrospinal fluid determinations. J Neurochem. 1981 Mar;36(3):1093–1096. doi: 10.1111/j.1471-4159.1981.tb01704.x. [DOI] [PubMed] [Google Scholar]
  22. Rider C. C., Taylor C. B. Enolase isoenzymes in rat tissues. Electrophoretic, chromatographic, immunological and kinetic properties. Biochim Biophys Acta. 1974 Sep 13;365(1):285–300. doi: 10.1016/0005-2795(74)90273-6. [DOI] [PubMed] [Google Scholar]
  23. Rodrigues M. M., Wiggert B., Shields J., Donoso L., Bardenstein D., Katz N., Friendly D., Chader G. Retinoblastoma. Immunohistochemistry and cell differentiation. Ophthalmology. 1987 Apr;94(4):378–387. doi: 10.1016/s0161-6420(87)33448-7. [DOI] [PubMed] [Google Scholar]
  24. Royds J. A., Rennie I. G., Parsons M. A., Timperley W. R., Taylor C. B. Enolase isoenzymes in uveal melanomas--a possible parameter of malignancy. Br J Ophthalmol. 1983 Apr;67(4):244–248. doi: 10.1136/bjo.67.4.244. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Scholz R., Green W. R., Baranano E. C., Erozan Y. S., Montgomery B. J. Metastatic carcinoma to the iris. Diagnosis by aqueous paracentesis and response to irradiation and chemotherapy. Ophthalmology. 1983 Dec;90(12):1524–1527. doi: 10.1016/s0161-6420(83)34375-x. [DOI] [PubMed] [Google Scholar]
  26. Swartz M., Herbst R. W., Goldberg M. F. Aqueous humor lactic acid dehydrogenase in retinoblastoma. Am J Ophthalmol. 1974 Oct;78(4):612–617. doi: 10.1016/s0002-9394(14)76298-1. [DOI] [PubMed] [Google Scholar]
  27. Terenghi G., Polak J. M., Ballesta J., Cocchia D., Michetti F., Dahl D., Marangos P. J., Garner A. Immunocytochemistry of neuronal and glial markers in retinoblastoma. Virchows Arch A Pathol Anat Histopathol. 1984;404(1):61–73. doi: 10.1007/BF00704251. [DOI] [PubMed] [Google Scholar]
  28. Viallard J. L., Caillaud D., Kantelip B., Molina C., Dastugue B. Enzymatic determination of serum neuron-specific enolase in small cell lung cancers. Utility of the serum neuron-specific enolase/serum nonneuronal enolase ratio. Chest. 1988 Jun;93(6):1225–1233. doi: 10.1378/chest.93.6.1225. [DOI] [PubMed] [Google Scholar]
  29. Viallard J. L., Murthy M. R., Dastugue B. An ultramicro bioluminescence assay of enolase: application to human cerebrospinal fluid. Neurochem Res. 1985 Dec;10(12):1555–1566. doi: 10.1007/BF00988598. [DOI] [PubMed] [Google Scholar]
  30. Viallard J. L., Ven Murthy M. R., Dastugue B. Rapid electrophoretic determination of neuron-specific enolase isoenzymes in serum. Clin Chem. 1986 Apr;32(4):593–597. [PubMed] [Google Scholar]
  31. Wevers R. A., Jacobs A. A., Hommes O. R. A bioluminescent assay for enolase (EC 4.2.1.11) activity in human serum and cerebrospinal fluid. Clin Chim Acta. 1983 Dec 15;135(2):159–168. doi: 10.1016/0009-8981(83)90131-6. [DOI] [PubMed] [Google Scholar]
  32. Woog J. J., Chess J., Albert D. M., Dueker D. K., Berson F. G., Craft J. Metastatic carcinoma of the iris simulating iridocyclitis. Br J Ophthalmol. 1984 Mar;68(3):167–173. doi: 10.1136/bjo.68.3.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Zeltzer P. M., Marangos P. J., Evans A. E., Schneider S. L. Serum neuron-specific enolase in children with neuroblastoma. Relationship to stage and disease course. Cancer. 1986 Mar 15;57(6):1230–1234. doi: 10.1002/1097-0142(19860315)57:6<1230::aid-cncr2820570628>3.0.co;2-#. [DOI] [PubMed] [Google Scholar]

Articles from The British Journal of Ophthalmology are provided here courtesy of BMJ Publishing Group

RESOURCES