Skip to main content
Log in

Chromosome abnormalities in peripheral blood lymphocytes from untreated Hodgkin's patients

A possible evidence for chromosome instability

  • Original Investigations
  • Published:
Human Genetics Aims and scope Submit manuscript

Summary

We describe the presence of a high frequency of spontaneous chromosome aberrations in lymphocytes from six untreated patients with Hodgkin's disease. The characteristics of the chromosome abnormalities observed suggest the existence of a certain degree of chromosome instability in these cases, that could be a predisposing factor for the development of malignancies.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Berger R, Bloomfield CD, Sutherland GR (1985) Report of the committee on chromosome rearrangements in neoplasia an on fragile sites. (8th International Workshop on Human Gene Mapping) Cytogenet Cell Genet 40: 490–535

    Google Scholar 

  • Brinker M, Buys CHCM, Poppema S (1986) Ig gene and T-cell receptor gene analysis in Hodgkin's disease. Satellite Meeting of the International Congress of Human Genetics on Molecular Genetics and Cytogenetics of Human Neoplasia, Berlin, 1986, p 28 (abstr)

  • Brown T, Dawson AA, McDonald IA, Bullock I, Watt JL (1985) Chromosome damage and sister chromatid exchanges in lymphocyte cultures from patients with two primary cancers. Cancer Genet Cytogenet 17: 35–42

    Google Scholar 

  • Czeizel A, Crosz L, Gardonyi J, Remenar K, Ruziscka P (1974) Chromosome studies in twelve patients with retinoblastoma. Humangenetik 22: 159–166

    Google Scholar 

  • Delhanty JDA, Davis MB, Wood J (1983) Chromosomal instability in lymphocytes, fibroblasts and colon epithelial-like cells from patients with familial polyposis coli. Cancer Genet Cytogenet 8: 27–50

    Google Scholar 

  • Dutrillaux B, Croquette MF, Viegas-Pequignot E, Aurias A, Coget J, Couturier J, Lejeune J (1978) Human somatic chromosome chains and rings. A preliminary note on end to end fusions. Cytogenet Cell Genet 20: 70–77

    Google Scholar 

  • Emerit I (1976) Chromosomal breakage in systemic sclerosis and related disorders. Dermatologica 153: 145–156

    Google Scholar 

  • Fonatsch C, Diehl V, Schaadt M, Burrichter H, Kirchner HH (1986) Cytogenetic investigations in Hodgkin's disease. I. Involvement of specific chromosomes in marker formation. Cancer Genet Cytogenet 20: 39–52

    Google Scholar 

  • Fukuhara S, Shirakawa S, Uchino H (1976) Specific marker chromosome 14 in malignant lymphomas. Nature 259: 210–211

    Google Scholar 

  • Griesser H, Feller AC, Lennert K, Tweedale M, Messner HA, Zalcberg J, Minden MD, Mak TW (1986) The structure of the T-cell gamma chain gene in lymphoproliferative disorders and lymphoma cell lines. Blood 68: 592–594

    Google Scholar 

  • Hafez M, El-Tahan H, El-Morsi Z, El-Ziny M, Al-Tonbary Y, Shamaa S, El-Serafi M, El-Kholi N (1985) Genetic susceptibility in Hodgkin's lymphoma. In: Müller H, Weber W (eds) Familial cancer. 1st International Research Conferences, Basel, 1985. Karger, Basel New York, pp 175–179

    Google Scholar 

  • Hansmann ML, Gödde-Salz E, Hui PK, Müller-Hermelink HK, Lennert K (1986) Cytogenetic findings in nodular paragranuloma (Hodgkin's disease with lymphocytic predominance; nodular) and in progressively transformed germinal center. Cancer Genet Cytogenet 21: 319–325

    Google Scholar 

  • Hossfeld DK (1977) Chromosome findings in effusions from patients with Hodgkin's disease. In: Chapelle A de la, Sorsa M (eds) Chromosomes today, vol 6. Elsevier/North Holland Biomedical Press, Amsterdam New York, pp 373–382

    Google Scholar 

  • Hsu TC (1983) Genetic instability in the human population: a working hypothesis. Hereditas 98: 1–9

    Google Scholar 

  • Hsu TC, Pathak S, Samaan N, Hickey RC (1981) Chromosome instability in patients with medullary carcinoma of the thyroid. JAMA 246: 2046–2048

    Google Scholar 

  • Ikeuchi T, Kawasaki T (1973) Spontaneous chromosome breakages in leukocytes from patients with hereditary spinocerebellar ataxia. Chromosome Inf Serv 14: 9–11

    Google Scholar 

  • Kadam PR, Advani SH, Bhisey AN (1986) Studies on sister chromatid exchanges in patients with Hodgkin's disease. Cancer Genet Cytogenet 22: 265–274

    Google Scholar 

  • Kasukawa T, Watanabe T, Endo A (1985) Cytogenetic and cytokinetic analysis of lymphocytes from patients with hereditary adenomatosis of the colon and rectum. Cancer Genet Cytogenet 16: 73–79

    Google Scholar 

  • Koziner B, Filipa DA, Mertelsmann R, Gupta S, Clarkson B, Good RA, Suegel FP (1977) Characterization of malignant lymphomas in leukemic phase by multiple differentiation markers of mononuclear cells. Am J Med 63: 556–567

    Google Scholar 

  • Kurvink K, Bloomfield CD, Keenan KM, Levitt S, Cervenka J (1978) Sister chromatid exchange in lymphocytes from patients with malignancy lymphoma. Hum Genet 44: 137–144

    Google Scholar 

  • Maldonado JE, Taswell HF, Kiely JM (1972) Familial Hodgkin's disease. Lancet II: 1259–1263

    Google Scholar 

  • McMahon B (1977) Is Hodgkin's disease contagious? N Engl J Med 289: 532–533

    Google Scholar 

  • Murty VVVS, Mitra AB, Luthra UK (1985) Spontaneous chromosomal aberrations in patients with precancerous and cancerous lesions of the cervix uteri. Cancer Genet Cytogenet 17: 347–354

    Google Scholar 

  • Nordenson I, Beckman K, Liden S, Stjernberg N (1984) Chromosomal aberrations and cancer risk. Hum Hered 34: 76–81

    Google Scholar 

  • Nuñez M de, Penchaszaden UB, Pimentel E (1984) Chromosome fragility in patients with sporadic unilateral retinoblastoma. Cancer Genet Cytogenet 11: 139–141

    Google Scholar 

  • O'Connor NTJ, Crick JA, Gatter KC, Mason DY, Falini B, Stern HS (1987) Cell lineage in Hodgkin's disease. Lancet I: 158

    Google Scholar 

  • Reeves BR (1973) Cytogenetics of malignant lymphomas. Studies utilising a giemsa-banding technique. Humangenetik 20: 231–250

    Google Scholar 

  • Reeves BR, Pickup VL (1980) The chromosome changes in Non-Burkitt lymphomas. Hum Genet 53: 349–355

    Google Scholar 

  • Rowley JD (1982) Chromosomes in Hodgkin's disease. Cancer Treat Rep 66: 639–643

    Google Scholar 

  • Shabtai F, Hart J, Klar D, Halbrecht I (1986) Familial fragile site found at the cancer breakpoint 1q32. Inducibility by Distamycin A, concomitance with fragile 16q22. Hum Genet 73: 232–234

    Google Scholar 

  • Slavutsky I, Vinuesa ML de, Estevez ME, Sen K, Salum SB de (1984) Cytogenetic and immunologic phenotype findings in Hodgkin's disease. Cancer Genet Cytogenet 16: 123–130

    Google Scholar 

  • Takabayashi T, Lin MS, Wilson MG (1983) Sister chromatid exchanges and chromosome aberrations in fibroblasts from patients with retinoblastoma. Hum Genet 63: 317–319

    Google Scholar 

  • Vermaelen K, Barbieri D, Van Den Berghe H (1984) Indirect stimulation of B-cell proliferation in vitro by T cells, as evidenced by cytogenetic analysis of PHA-stimulated cell cultures of B-cell lymphomas. Cancer Genet Cytogenet 11: 425–428

    Google Scholar 

  • Wang N, Kantor A, Soldat K, Linluist K, Strand R, McLaughlin H, Schuman L (1982) Higher frequency of chromosomal aberrations and polymorphism in patients with renal carcinoma. Am J Hum Genet 34: 78A

  • Weiss LM, Strickler JG, Hu E, Warnke RA, Sklar J (1986) Immunoglobulin gene rearrangements in Hodgkin's disease. Hum Pathol 17: 1009–1014

    Google Scholar 

  • Wurster-Hill DH, Cornwell GG, McIntyre OR (1974) Chromosomal aberrations and neoplasm — a family study. Cancer 33: 72–81

    Google Scholar 

  • Wurster-Hill DH, Cornwell GG, McIntyre OR (1979) Chromosome aberrations of myeloid and lymphoid cells in cancer patients and family members without evidence of cancer. Cancer Detect Prev 2: 125–126

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Barrios, L., Caballín, M.R., Mirò, R. et al. Chromosome abnormalities in peripheral blood lymphocytes from untreated Hodgkin's patients. Hum Genet 78, 320–324 (1988). https://doi.org/10.1007/BF00291727

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00291727

Keywords

Navigation