Cancer Research Donn Young  Genetics and Biology of Brain Cancer
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 58, 421-425, February 1, 1998]
© 1998 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Deininger, M. W. N.
Right arrow Articles by Melo, J. V.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Deininger, M. W. N.
Right arrow Articles by Melo, J. V.

Selective Induction of Leukemia-associated Fusion Genes by High-Dose Ionizing Radiation1

Michael W. N. Deininger, Shikha Bose, Joanna Gora-Tybor, Xiu-Hua Yan, John M. Goldman and Junia V. Melo2

Leukaemia Research Fund Centre for Adult Leukaemia, Department of Haematology, Royal Postgraduate Medical School, Ducane Road, London W12 0NN, United Kingdom

There is strong clinical and epidemiological evidence that ionizing radiation can cause leukemia by inducing DNA damage. This crucial initiation event is believed to be the result of random DNA breakage and misrepair, whereas the subsequent steps, promotion and progression, must rely on mechanisms of selective pressure to provide the expanding leukemic population with its proliferative/renewal advantage. To investigate the susceptibility of human cells to external agents at the genetic recombination stage of leukemogenesis, we subjected two hematopoletic cell lines, KG1 and HL60, to high doses of {gamma}-irradiation. The irradiation induced the formation of fusion genes characteristic of leukemia in both cell lines, but at a much higher frequency in KG1 than in HL60. In KG1 cells, the AML1-ETO hybrid gene [associated with the t(8;21) translocation of acute myeloid leukemia] occurred significantly more often than the BCR-ABL [associated with t(9;22) chronic myeloid leukemia] or the DEK-CAN [associated with t(6;9) acute myeloid leukemia] fusion genes. These findings support the notion that ionizing radiation can directly generate leukemia-specific fusion genes but emphasize the differing susceptibility of different cell populations and the differing frequency with which the various fusion genes are formed. The selectivity observed at the primary level of gene fusion formation may explain at least in part the differential risk for development of some but not other forms of leukemia after high-dose radiation exposure.

1 Supported in part by grants from the Leukaemia Research Fund (United Kingdom) and the Dr. Mildred Scheel-Stiftung fur Krebsforschung (Germany).

2 To whom requests for reprints should be addressed, at LRF Centre for Adult Leukaemia, Department of Haematology, Royal Postgraduate Medical School, Hammersmith Hospital, Ducane Road, London W12 0NN, United Kingdom. Phone: 44-181-383-2167; Fax: 44-181-742-9335; E-mail: jmelo@rpms.ac.uk.

Received 10/ 7/97. Accepted 11/25/97.




This article has been cited by other articles:


Home page
MutagenesisHome page
M. S. Brassesco, A. P. Montaldi, D. E. Gras, M. L. Camparoto, N. M. Martinez-Rossi, C. A. Scrideli, L. G. Tone, and E. T. Sakamoto-Hojo
Cytogenetic and molecular analysis of MLL rearrangements in acute lymphoblastic leukaemia survivors
Mutagenesis, March 1, 2009; 24(2): 153 - 160.
[Abstract] [Full Text] [PDF]


Home page
The OncologistHome page
M. A. Lichtman
Is There an Entity of Chemically Induced BCR-ABL-Positive Chronic Myelogenous Leukemia?
Oncologist, June 1, 2008; 13(6): 645 - 654.
[Abstract] [Full Text] [PDF]


Home page
NEJMHome page
J. M. Goldman and J. V. Melo
Chronic Myeloid Leukemia -- Advances in Biology and New Approaches to Treatment
N. Engl. J. Med., October 9, 2003; 349(15): 1451 - 1464.
[Full Text] [PDF]


Home page
Pharmacol. Rev.Home page
M. W. N. Deininger and B. J. Druker
Specific Targeted Therapy of Chronic Myelogenous Leukemia with Imatinib
Pharmacol. Rev., September 1, 2003; 55(3): 401 - 423.
[Abstract] [Full Text] [PDF]


Home page
ANN INTERN MEDHome page
R. Kurzrock, H. M. Kantarjian, B. J. Druker, and M. Talpaz
Philadelphia Chromosome-Positive Leukemias: From Basic Mechanisms to Molecular Therapeutics
Ann Intern Med, May 20, 2003; 138(10): 819 - 830.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
M. V. Relling, J. M. Boyett, J. G. Blanco, S. Raimondi, F. G. Behm, J. T. Sandlund, G. K. Rivera, L. E. Kun, W. E. Evans, and C.-H. Pui
Granulocyte colony-stimulating factor and the risk of secondary myeloid malignancy after etoposide treatment
Blood, May 15, 2003; 101(10): 3862 - 3867.
[Abstract] [Full Text] [PDF]


Home page
Arch. Dis. Child. Fetal Neonatal Ed.Home page
P F Ravetto, R Agarwal, M L Chiswick, S W D'Souza, O B Eden, and G M Taylor
Absence of leukaemic fusion gene transcripts in preterm infants exposed to diagnostic x rays
Arch. Dis. Child. Fetal Neonatal Ed., May 1, 2003; 88(3): F237 - F244.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
H. Harada, Y. Harada, H. Tanaka, A. Kimura, and T. Inaba
Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia
Blood, January 15, 2003; 101(2): 673 - 680.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
J. Basecke, L. Cepek, C. Mannhalter, J. Krauter, S. Hildenhagen, G. Brittinger, L. Trumper, and F. Griesinger
Transcription of AML1/ETO in bone marrow and cord blood of individuals without acute myelogenous leukemia
Blood, August 28, 2002; 100(6): 2267 - 2267.
[Full Text] [PDF]


Home page
BloodHome page
L. Dolken, F. Schuler, and G. Dolken
Frequency of BCL-2/JH translocation in healthy males exposed to low-level radiation in comparison to age-matched healthy controls
Blood, July 30, 2002; 100(4): 1513 - 1514.
[Full Text] [PDF]


Home page
BloodHome page
S. C. Finch, R. Hromas, R. Shopnick, H. G. Jumean, C. Bowers, M. Varella-Garcia, and K. Richkind
Radiation-induced leukemia
Blood, March 15, 2001; 97(6): 1897 - 1898.
[Full Text] [PDF]


Home page
BloodHome page
M. W. N. Deininger, J. M. Goldman, and J. V. Melo
The molecular biology of chronic myeloid leukemia
Blood, November 15, 2000; 96(10): 3343 - 3356.
[Full Text] [PDF]


Home page
BloodHome page
R. Hromas, R. Shopnick, H. G. Jumean, C. Bowers, M. Varella-Garcia, and K. Richkind
A novel syndrome of radiation-associated acute myeloid leukemia involving AML1 gene translocations
Blood, June 15, 2000; 95(12): 4011 - 4013.
[Abstract] [Full Text] [PDF]


Home page
ASH Education BookHome page
H. Kantarjian, J. V. Melo, S. Tura, S. Giralt, and M. Talpaz
Chronic Myelogenous Leukemia: Disease Biology and Current and Future Therapeutic Strategies
Hematology, January 1, 2000; 2000(1): 90 - 109.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
S. Bose, M. Deininger, J. Gora-Tybor, J. M. Goldman, and J. V. Melo
The Presence of Typical and Atypical BCR-ABL Fusion Genes in Leukocytes of Normal Individuals: Biologic Significance and Implications for the Assessment of Minimal Residual Disease
Blood, November 1, 1998; 92(9): 3362 - 3367.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1998 by the American Association for Cancer Research.