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Department of Tumor Biology, Karolinska Institutet, S 104 01 Stockholm, Sweden [J. S., M. B., F. W., Z. W., G. K.]; Cancer Research Institute, Kanazawa University, 13-1, Takara-Michi, Kanazawa, Japan [S. O.]; and The Weizmann Institute of Science, Department of Chemical Immunology, Rehovot, Israel [N. H-G.]
Leukemias were induced by 7,12-dimethylbenzanthracene feeding of intact, thymectomized, or Freund's adjuvant-pretreated SJL mice. Four of six Thy-1-positive thymomas that arose in intact mice had a pseudodiploid stemline with one morphologically similar or identical marker. Banding analysis showed that the marker had arisen by the translocation of the distal part of one chromosome 15 to one X chromosome [t(X;ter 15)]. Two normal No. 15 chromosomes were also present in the same metaphase plates. These four Thy-1-positive lymphomas were thus trisomic for the distal part of chromosome 15. All 8 Thy-1-negative lymphomas, originating in the spleen or lymph nodes of thymectomized or adjuvant-pretreated mice, had a trisomy of chromosome 12 and also a trisomy of either chromosome 3 or chromosome 18. These results further stress the importance of gene dosage effects, related to the distal part of chromosome 15, in Thy-1-positive T-cell leukemogenesis. The cytogenetic difference between the Thy-1-positive and -negative leukemias supports our hypothesis that nonrandom chromosomal changes in murine leukemias are dependent on the target cell type, rather than the inducing agent.
1 This investigation was supported by Grant 3 R01 CA 14054-0651, awarded by the National Cancer Institute, Department of Health, Education, and Welfare, and the Swedish Cancer Society and Syskonen Svenssons fond.
2 To whom requests for reprints should be addressed.
Received 12/26/79. Accepted 4/15/80.
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C. Kozak, J. Sears, and M. Hoggan Genetic mapping of the mouse proto-oncogene c-sis to chromosome 15 Science, August 26, 1983; 221(4613): 867 - 869. [Abstract] [PDF] |
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