Analysis of early initiating event(s) in radiation-induced thymic lymphomagenesis

Japanese Journal of Cancer Research

Volumn 87, Issue 3, 1996, Pages 247-257

  Muto, Masahiro ^a   Chen, Ying ^a,b   Kubo, Eiko ^a   Mita, Kazuei ^a  

^a NATIONAL INSTITUTE OF RADIOLOGICAL SCIENCES   (Japan)

^b CHINA INSTITUTE FOR RADIATION PROTECTION   (China)

Author keywords

Chromosome aberration; Clonality; Initiation; p53; T cell receptor rearrangement

Indexed keywords

LEUKEMIA ANTIGEN; PROTEIN P53; T LYMPHOCYTE RECEPTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CARCINOGENESIS; CELL DIFFERENTIATION; CHROMOSOME ABERRATION; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; FEMALE; GENE MUTATION; GENE REARRANGEMENT; IRRADIATION; MOUSE; NONHUMAN; PRECANCER; PRIORITY JOURNAL; T CELL LYMPHOMA; THYMUS LYMPHOMA; TRISOMY;

EID: 0029963868     PISSN: 09105050     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1349-7006.1996.tb00213.x     Document Type: Article

References (28)

1. Kaplan, H. S. and Brown, M. B. A quantitative dose-response study of lymphoid tumor development in irradiated C57 black mice. J. Natl. Cancer Inst., 13, 185-208 (1952).
2. Muto, M., Kubo, E. and Sado, T. Cellular events during radiation-induced thymic leukemogenesis in mice: abnormal T cell differentiation in the thymus and defect of thymocyte precursors in the bone marrow after split-dose irradiation. J. Immunol., 134, 2026-2031 (1985).
3. Muto, M., Sado, T., Hayata, L, Nagasawa, F., Kamisaku, H. and Kubo, E. Reconfirmation of indirect induction of radiogenic lymphomas using thymectomized, irradiated B10 mice grafted with neonatal thymuses from Thy 1 congenic donors. Cancer Res., 43, 3822-3827 (1983).
4. Defresne, M. P., Rongy, A. M., Greimers, R. and Boniver, J. Cellular aspects of radiation leukemogenesis in C57BL/ Ka mice: alterations to thymic microenvironment and lymphopoiesis. Leuk. Res., 10, 783-789 (1986).
5. Boniver, J., Decleve, A., Lieberman, M., Honsik, C., Travis, M. and Kaplan, H. S. Marrow-thymus interactions during radiation leukemogenesis in C57BL/Ka mice. Cancer Res., 41, 390-392 (1981).
6. Sen-Majumdar, A., Guidos, C., Kina, T., Lieberman, M. and Weissman, I. L. Characterization of preneoplastic thymocytes and of their neoplastic progression in irradiated C57BL/Ka mice. J. Immunol, 153, 1581-1592 (1994).
7. Muto, M., Kubo, E. and Sado, T. Development of prelymphoma cells committed to thymic lymphomas during radiation-induced thymic lymphomagenesis in B10 mice. Cancer Res., 47, 3469-3472 (1987).
8. Muto, M., Kubo, E., Kamisaku, H. and Sado, T. Phenotypic characterization of thymic prelymphoma cells of B10 mice treated with split-dose irradiation. J. Immunol., 144, 849-853 (1990).
9. Cowell, J. K. A photographic representation of the variability in the G-banded structure of the chromosomes in the mouse karyotype. Chromosome, 89, 294-320 (1984).
10. Committee on Standard Genetic Nomenclature for Mice. Standard karyotype of the mouse, Mus musculus. J. Hered., 63, 69 (1972).
11. Maniatis, T., Fritsch, E. F. and Sambrook, J. In "Molecular Cloning. A Laboratory Manual," pp. 324-389 (1982). Cold Spring Harbor Laboratory Press, New York.
12. Kubo, E., Muto, M., Sado, T., Takeshita, S., Shimizu, T. and Yamagishi, H. Novel TCR gene rearrangements and expression in radiation-induced thymic lymphomas. J. Radiat. Res., 33, 227-242 (1992).
13. Shimizu, T., Muto, M., Kubo, E., Sado, T. and Yamagishi, H. Multiple pre-neoplastic events and clonal selection of radiation induced mouse thymic lymphomas shown by TCR gene rearrangements. Leuk. Res., 17, 959-965 (1993).
14. Zakut-Houri, R., Oren, M., Bienz, B., Lavie, V., Hazum, S. and Givol, D. A single gene and a pseudogene for the cellular tumour antigen p53. Nature, 306, 594-597 (1983).
15. Brathwaite, O., Bayona, W. and Newcomb, E. W. p53 mutations in C57BL/6J murine thymic lymphomas induced by γ-irradiation and N-methylnitrosourea. Cancer Res., 52, 3791-3795 (1992).
16. Orita, M., Suzuki, Y., Sekiya, T. and Hayashi, K. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics, 5, 874-879 (1989).
17. Sanger, F. Determination of nucleotide sequences in DNA. Science, 214, 1205-1210 (1981).
18. Nenoi, M., Mita, K., Ichimura, S. and Cartwright, I. L. Novel structure of a Chinese hamster polyubiquitin gene. Biochim. Biophys. Acta, 1204, 271-278 (1994).
19. Pardoll, D. M., Fowlkes, B. J., Bluestone, J. A., Kruisbeek, A., Maloy, W. L., Coligan, J. E. and Schwartz, R. H. Differential expression of two distinct T-cell receptors during thymocyte development. Nature, 326, 79-81 (1987).
20. Thompson, S. D., Manzo, A. R., Pelkonen, J., Larche, M. and Hurwitz, J. L. Developmental T-cell receptor gene rearrangements: relatedness of the α/β and γ/δ T-cell precursor. Eur. J. Immunol., 21, 1939-1950 (1991).
21. Iwasato, T. and Yamagishi, H. Novel excision products of T cell receptor gamma gene rearrangements and developmental stage specificity implied by the frequency of nucleotide insertions at signal joints. Eur. J. Immunol., 22, 101-106 (1992).
22. Muto, M., Kubo, E., Sado, T., Shimizu, T. and Yamagishi, H. Characterization and clonality of prelymphoma cells of B10 mice treated with fractionated X-irradiation (FX). In "Proceedings of International Conference on Radiation Effects and Protection," pp. 198-205 (1992). JAERI Press, Tokyo.
23. Zakut-Houri, R., Givol, D., Bienz, B., Rogel, A. and Oren, M. Structure and expression of the genes encoding the murine p53 cellular tumor antigen. In "CSH Conferences on Cell Proliferation and Cancer," Vol. 11, pp. 393-401 (1984). Cold Spring Harbor Laboratory Press, New York.
24. Sasaki, M. Current status of cytogenetic studies in animal tumors with special reference to nonrandom chromosome changes. Cancer Genet. Cytogenet., 5, 153-172 (1982).
25. Miller, D. A. and Miller, O. J. Chromosomes and cancer in the mouse: studies in tumor, established cell lines, and cell hybrids. Adv. Cancer Res., 39, 153-182 (1983).
26. McMorrow, L. E., Newcomb, E. W. and Pellicer. A. Identification of a specific marker chromosome early in tumor development in γ-irradiated C57BL/6J mice. Leukemia, 2, 115-119 (1988).
27. Chan, F. P. H., Ball, J. K. and Sergovich, F. R. Trisomy #15 in murine thymomas induced by chemical carcinogens, X-irradiation, and an endogenous murine leukemia virus. J. Natl. Cancer Inst., 62, 605-610 (1975).
28. Carbonell, F., Eul, J., Anselstetter, V., Hameister, H., Seidel, H. J. and Kreja, L. Trisomy 15 as a regular finding in chemically induced murine T-cell leukemogenesis. Int. J. Cancer, 39, 534-537 (1987).