Abstract
The relationship between chromosome abnormalities and neoplasia has been the subject of investigation and speculation for many years. It was noted very early that mitotic irregularities were common in routine sections prepared from many human tumors, and these observations were extended by workers such as von Hansemann (1890) and Boveri (1914) near the turn of the century, to suggest a causal relationship between chromosome alterations and cancer. With the development of modern techniques of mammalian cytogenetics in the late 1950s, interest in chromosome studies of tumors was reawakened, and subsequently a wide variety of human and animal neoplasms were studied. This work has received additional impetus recently from the introduction of “banding” methods which permit the identification of individual chromosomes and of alterations in smaller segments of chromosomes than was possible by previous methods. These newest techniques have not yet been fully exploited, but it must also be recognized that even with the “banding” procedures there may still remain significant genetic alterations in neoplastic cells which are below the level of visual detection.
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References
Al-Saadi, A. A., and Beierwaltes, W. H., 1967, Sequential cytogenetic changes in the evolution of transplanted thyroid tumors to metastatic carcinoma in the Fischer rat, Cancer Res. 27: 1831.
Atkin, N. B., 1970, Cytogenetic studies on human tumors and premalignant lesions, in: Genetic concepts and Neoplasia (M. D. Anderson Hospital Symposium), pp. 36–56, Williams and Wilkins, Baltimore.
Atkin, N. B., 1971, Modal DNA value and chromosome number in ovarian neoplasia. Cancer 27: 1064.
Atkin, N. B., and Baker, M. C., 1966, Chromosome abnormalities as primary events in human malignant disease; evidence from marker chromosomes, J. Natl. Cancer Inst. 36: 539.
Auersperg, N., Corey, M. J., and Worth, A., 1967, Chromosomes in preinvasive lesions of the human uterine cervix. Cancer Res. 27: 1394.
Benedict, W. F., Porter, I. H., Brown, C. D., and Florentin, R. A., 1970, Cytogenetic diagnosis of malignancy in recurrent meningioma, Lancet 1: 971.
Bottura, C., Ferrari, I., and Veiga, A. A., 1961, Chromosome abnormalities in Waldenström’s macroglobulinemia, Lancet 1: 1170.
Boveri, T., 1914, Zur Frage der Entstehung maligner Tumoren, Vol. 1, Gustav Fischer Verlag, Jena.
Braun, A. C., 1969, The Cancer Problem, Columbia University Press, New York.
DiBerardino, M. A., and King, T. J., 1965, Transplantation of nuclei from the frog renal adenocarcinoma. II. Chromosomal and histologic analysis of tumor nuclear-transplant embryos. Develop. Biol. 11: 217.
Enterline, H. T., and Aryan, D. A., 1967, Chromosome constitution of adenoma and adenocarcinoma of the colon, Cancer 20: 1746.
Fialkow, P. J., 1970, Genetic marker studies in neoplasia, in: Genetic Concepts and Neoplasia (M. D. Anderson Hospital Symposium), pp. 112–137, Williams and Wilkins, Baltimore.
Finney, R., McDonald, G. A., Baikie, A. G., and Douglas, A. S., 1972, Chronic granulocytic leukemia with Ph negative cells in bone marrow and a ten year remission after Busulphan hypoplasia, Brit. J. Haematol. 23: 283.
Fitzgerald, P. H., 1965, Abnormal length of the small acrocentric chromosomes in chronic lymphocytic leukemia. Cancer Res. 25: 1094
Fitzgerald, P. H., Crossen, P. E., Adams, A. C., Sharman, C. V., and Gunz, F. W., 1966, Chromosome studies in familial leukemia, J. Med. Genet. 3: 96.
Fitzgerald, P. H., Crossen, P. E., and Hamer, J. W., 1973, Abnormal karyotypic clones in human acute leukemia: Their nature and significance. Cancer 31: 1069.
Ford, C. E., 1966, The use of chromosome markers, in: Tissue Grafting and Radiation ( H. Micklem and J. Loutit, eds.), pp. 197–206, Academic Press, New York and London.
Forni, A., and Moreo, L., 1967, Cytogenetic studies in a case of benzene leukemia, Europ. J. Cancer 3: 251.
Freed, J. J., and Schatz, S. A., 1969, Chromosome aberrations in cultured cells deprived of single, Exp. Cell Res. 55: 393.
Freeman, A. E., and Huebner, R. J., 1973, Problems in interpretation of experimental evidence of cell transformation, J. Natl. Cancer Inst. 50: 303.
Gellhorn, A., 1973, The background and promise of tumor virology, immunology, and chemotherapy and a challenge to radiotherapy. Am. J. Roentgenol. Radium Ther. Nucl. Med. 117: 489.
German, J., 1972, Genes which increase chromosomal instability in somatic cells and predispose to cancer. Prog. Med. Genet. 8: 61.
Harris, H., Miller, O. J., Klein, G., Worst, P., and Tachibana, T., 1969, Suppression of malignancy by cell fusion. Nature (Lond.) 223: 363.
Hauschka, T. S., 1961, The chromosome in ontogeny and oncogeny, Cancer Res. 21: 957.
Hecht, F., McCaw, B. K., and Koler, R. D., 1973, Ataxia-telangiectasia—Clonal growth of translocation lymphocytes, New Engl. J. Med. 289: 286.
Hitotsumachi, S., Rabinowitz, Z., and Sachs, L., 1971, Chromosomal control of reversion in transformed cells, Nature (Lond.) 231: 511.
Hsu, T. C., 1961, Chromosomal evolution in cell populations. Int. Rev. Cytol. 12: 69.
Huang, C. C., Minowada, J., Smith, R. T., and Osunkoya, B. O., 1970, Revaluation of relationship between C chromosome marker and Epstein-Barr virus, J. Natl. Cancer Inst. 45: 815.
Jacobs, P., Tough, I. M., and Wright, D. H., 1963, Cytogenetic studies in Burkitt’s lymphoma, Lancet 2: 1144.
Jensen, M. K., and Philip, P., 1970, Cytogenetic studies in potentially leukemic myeloid disorders, in: Proceedings of the XIII International Congress of Hematology, Munich, p. 20 (abst.).
Johnson, A. S., Friedman, R. M., and Pastan, I., 1971, Restoration of general morphological characteristics of normal fibroblasts in sarcoma cells treated with adenosine 3’:5’-cyclic monophosphate and its derivatives, Proc. Natl. Acad. Sci. 68: 425.
Knudson, A. G., Strong, L. C., and Anderson, D. E., 1973, Heredity and cancer in man. Prog. Med. Genet. 9: 113.
Kohn, G., Mellman, W. J., Moorhead, P. S., Loftus, J., and Henle, G., 1967, Involvement of C-group chromosomes in five Burkitt lymphoma cell lines, J. Natl. Cancer Inst. 38: 209.
Koller, P. C., 1972, The Role of Chromosomes in Cancer Biology, Springer, New York.
Lawler, S. D., Millard, R. E., and Kay, H. E. M., 1970, Further cytogenetical investigations in polycythemia vera, Europ. J. Cancer 6: 223.
Levan, A., and Biesele, J. J., 1958, Role of chromosomes in cancerogenesis as studied in serial tissue culture of mammal cells, Ann. N.Y. Acad. Sci. 71: 1022.
MacPherson, I., 1970, Characteristics of animal cells transformed in vitro, Advan. Cancer Res. 13: 169.
Makino, S., 1956, Further evidence favoring the concept of the stem cell in ascites tumors of rats, Ann. N.Y. Acad. Sci. 14: 818.
Makino, S., 1963, Some epidemiologic aspects of venereal tumors of dogs as revealed by chromosome and DNA studies, Ann. N.Y. Acad. Sci. 108: 1106.
Manolov, G., and Manolova, Y., 1971, A marker band in one chromosome No. 14 in biopsies and cultures from Burkitt lymphomas, Hereditas 69: 300.
Mark, J., 1969, Rous sarcoma in mice: The chromosomal progression in primary tumors, Europ. J. Cancer 5: 307.
Mark, J., Levan, G., and Mitelman, F., 1972, Identification by fluorescence of the G chromosome lost in human meningiomas, Hereditas 71: 163.
Martineau, M., 1966, A similar marker chromosome in testicular tumors. Lancet 1: 839.
McDougall, J. K., 1970, Effects of adenoviruses on the chromosomes of normal human cells and cells trisomic for an E chromosome. Nature (Lond.) 225: 456.
Miles, C. P., Geller, W., and O’Neill, F., 1966, Chromosomes in Hodgkin’s disease and other malignant lymphomas. Cancer 19: 1103.
Millard, R. E., 1968, Chromosome abnormalities in the malignant lymphomas, Europ. J. Cancer 4: 91.
Millard, R. E., Lawler, S. D., Kay, H. E. M., and Cameron, C. B., 1968, Further observations on patients with a chromosomal abnormality associated with polycythemia vera, Brit. J. Haematol. 14: 363.
Miller, O. J., Miller, D. A., and Warburton, D., 1973, Application of new staining techniques to the study of human chromosomes. Prog. Med. Genet. 9: 1.
Miller, R. W., and Todaro, G. J., 1969, Viral transformation of cells from persons at high risk of cancer, Lancet 1: 81.
Mitelman, F., 1971, The chromosomes of fifty primary Rous rat sarcomas, Hereditas 69: 155.
Moorhead, P. S., and Weinstein, D., 1966, Cytogenetic alterations during malignant transformation, in: Recent Results in Cancer Research, Vol. VI: Malignant Transformation by Viruses ( W. Kirsten, ed.), pp. 104–111, Springer, New York.
Nichols, W. W., 1963, Relationships of viruses, chromosomes, and carcinogenesis, Hereditas 50: 53.
Nichols, W. W., 1966, The role of viruses in the etiology of chromosome aberrations. Am. J. Hum. Genet. 18: 81.
Nichols, W. W., Levan, A., Coriell, L. L., Goldner, H., and Ahlström, C. G., 1964, Chromosome abnormalities in vitro in human leukocytes associated with Schmidt-Ruppin Rous sarcoma virus, Science 146: 248.
Nowell, P. C., 1965a, Unstable chromosome changes in tuberculin-stimulated leukocyte cultures from irradiated patients. Blood 26: 798.
Nowell, P. C., 19656, Chromosome changes in primary tumors, Prog. Exp. Tumor Res. 7: 83.
Nowell, P. C., 1967, Chromosome abnormalities in the childhood leukemias, in: The Clinical Pathology of Infancy (F. Sunderman and F. Sunderman Jr., eds.), pp. 447–482, Thomas, Springfield, 111.
Nowell, P. C., 1969, Biological significance of induced human chromosome aberrations. Fed. Proc. 28: 1797.
Nowell, P. C., 1971, Marrow chromosome studies in “preleukemia”: Further correlation with clinical course. Cancer 28: 513.
Nowell, P. C., and Cole, L. J., 1965, Hepatomas in mice: Incidence increased after gamma irradiation at low dose rates. Science 148: 96.
Nowell, P. C., and Hungerford, D. A., 1964, Chromosome changes in human leukemia and a tentative assessment of their significance, J. Natl. Cancer Inst. 27: 1013.
Nowell, P. C., and Morris, H. P., 1969, Chromosomes of “minimal deviation hepatomas”: A further report on diploid tumors, Cancer Res. 29: 969.
Nowell, P. C., Morris, H. P., and Potter, V. R., 1967, Chromosomes of “minimal deviation” hepatomas and some other transplantable rat tumors, Cancer Res. 27: 1565.
Ohno, S., 1971, Genetic implication of karyological instability of malignant somatic cells, Physiol. Rev. 51: 496.
O’Riordan, M.L., Berry, E., and Tough, I., 1970, Chromosome studies on bone marrow from a male control population, Brit. J. Haematol. 19: 83.
Peckham, M. J., 1972, Lymphocyte transformation in chronic lymphocytic leukemia. Lancet 1: 1127.
Pedersen, B., 1973, The blastic crisis of chronic myeloid leukemia: Acute transformation of a preleukemic condition? Brit. J. Haematol. 25: 141.
Pedersen, B., and Hayhoe, F. G. J., 1971, Cellular changes in chronic myeiiod leukemia, Brit. J. Haemetol. 21: 251.
Prasad, K. N., 1972, Morphological differentiation induced by prostaglandin in mouse neuroblastoma cells in culture. Nature (Lond.) 236: 49.
Propp, S., and Lizzi, F. A., 1970, Philadelphia chromosome in acute lymphocytic leukemia. Blood 36: 353.
Rabinowitz, Z., and Sachs, L., 1970, Control of the reversion of properties in transformed cells. Nature (Lond.) 225: 136.
Rowley, J. D., 1970, The chromosomes in the myelodysplasias, in: Myeloproliferative Disorders of Animals and Man ( W. Clark, ed.), pp. 556–569, US AEC, Washington.
Rowley, J. D., 1973, A new consistent chromosomal abnormality in chronic myelogenous leukemia identified by quinacrine fluorescence and Giemsa staining. Nature (Lond.) 243: 290.
Sandberg, A. A., 1966, The chromosomes and causation of human cancer and leukemia. Cancer Res. 26: 2064.
Sandberg, A. A., and Hossfeld, D. K., 1970, Chromosomal abnormalities in human neoplasia, Ann. Rev. Med. 21: 379.
Shaw, M. W., 1970, Human chromosome damage by chemical agents, Ann. Rev. Med. 21: 409.
Stich H. F., 1960, Chromosomes of tumor cells. I. Murine leukemias induced by one or two injections of 7,12-dimethylbenz[a]anthracene, J. Natl. Cancer Inst. 25: 649.
Stich, H. F., 1963, Chromosome and carcinogenesis, Canad. Cancer Conf. 5: 99.
Sugiyama, T., Kurita, Y., and Nishizuka, Y., 1967, Chromosome abnormality in rat leukemia induced by 7,12-dimethylbenz[a]anthracene, Science 158: 1058.
Tassoni, E. M., Durant, J. R., Becker, S., and Kravitz, B., 1967, Cytogenetic studies in multiple myeloma: A study of fourteen cases. Cancer Res. 27: 806.
Todaro, G. J., Green, H., and Swift, M. R., 1966, Human diploid fibroblasts transformed with SV40 or hybrid Adeno-7x SV40, Science 153: 1252.
Trujillo, J. M., and Ohno, S., 1963, Chromosomal alteration of erythropoietic cells in chronic myeloid leukemia. Acta Haematol. 29: 311.
von Hansemann, D., 1890 Über asymmetrische Zellteilung in Epithelkrebsen und deren biologische Bedeutung, Virchows Arch. Pathol. Anat. Physiol. 119: 298.
Wald, N., Upton, A. C., Jenkins, V. K., and Borges, W. H., 1964, Mouse post-irradiation leukemia: Consistent occurrence of an extra and a marker chromosome. Science 143: 810.
Weber, W. T., Nowell, P. C., and Hare, W. C. D., 1965, Chromosome studies of a transplanted and a primary canine venereal sarcoma, J. Natl. Cancer Inst. 35: 537.
Whang, J., Frei, E., Tjio, J. H., Carbone, P. P., and Bregher, G., 1963, The distribution of the Philadelphia chromosome in patients with chronic myelogenous leukemia. Blood 22: 664.
Whang-Peng, J., Canellos, G. P., Carbone, P. P., and Tjio, J. H., 1968, Clinical implications of cytogenetic variants in chronic myelocytic leukemia (CML), Blood 32: 755.
Wilson, M. G., Towner, J. W., and Fujimoto, A., 1973, Retinoblastoma and D-chromosome deletion. Am. J. Hum. Genet. 25: 57.
Woodlife, H. J., 1971, Leukemia Cytogenetics, Lloyd-Luke, London.
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© 1975 Plenum Press, New York
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Nowell, P.C. (1975). Cytogenetics. In: Becker, F.F. (eds) Cancer. A Comprehensive Treatise. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-4449-0_1
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