Allelic loss in childhood acute lymphoblastic leukemia

Leukemia Research

Volumn 21, Issue 9, 1997, Pages 817-823

  Baccichet, Annie ^a,b   Qualman, Sarah K ^a,b   Sinnett, Daniel ^a,b  

^a Centre de Cancerologie Charles Bruneau   (Canada)

^b UNIVERSITY OF MONTREAL   (Canada)

Author keywords

Allelotype; Childhood acute lymphoblastic leukemia; Loss of heterozygosity; Microsatellite; Tumor suppressor gene

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ALLELE; ARTICLE; B CELL LEUKEMIA; CHILD; CHILDHOOD LEUKEMIA; CHROMOSOME 11; CHROMOSOME 12P; CHROMOSOME 13Q; CHROMOSOME 17; CHROMOSOME 18Q; CHROMOSOME 3P; CHROMOSOME 5Q; CHROMOSOME 6; CHROMOSOME 9; CLINICAL ARTICLE; FEMALE; GENE LOSS; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; MALE; MARKER GENE; PRIORITY JOURNAL; T CELL LEUKEMIA; TUMOR SUPPRESSOR GENE;

ADOLESCENT; ALLELES; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN; DNA, NEOPLASM; FEMALE; GENE DELETION; GENES, TUMOR SUPPRESSOR; HUMANS; LEUKEMIA, LYMPHOCYTIC, ACUTE, L1; LOSS OF HETEROZYGOSITY; MALE; MICROSATELLITE REPEATS;

EID: 0030725637     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0145-2126(97)00075-1     Document Type: Article

References (29)

1. Greaves, M., A natural history for paediatric acute leukemia. Blood, 1993, 82, 1043.
2. LoCoco, F. and Saglio, G., Single or multiple origin of hemopoietic tumors: the contribution of clonality studies. Leukemia, 1995, 9, 1586.
3. Weinberg, R. A., Oncogenes, anti-oncogenes, and the molecular basis of multistep carcinogenesis. Cancer Research, 1989, 49, 3713.
4. Vogelstein, B. and Kinzler, K. W., The multistep nature of cancer. Trends in Genetics, 1993, 9, 138.
5. Rabbitts, T. H., Chromosomal translocations in human cancer. Nature, 1994, 372, 143.
6. Prigogina, E. L., Puchkova, G. P. and Mayakova, S. A., Nonrandom chromosomal abnormalities in acute lymphoblastic leukemia of childhood. Cancer Genetics and Cytogenetics, 1988, 32, 183.
7. Johansson, B., Mertens, F. and Mitelman, F., Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci. Genes Chromosomes Cancer, 1993, 8, 205.
8. Raimondi, S. C., Current status of cytogenetic research in childhood acute lymphoblastic. Blood, 1993, 81, 2237.
9. Cayuela, J.-M., Madani, A., Sanhes, L., Stern, M.-H. and Sigaux, F., Multiple tumor-suppressor gene 1 inactivation is the most frequent genetic alteration in T-cell acute lymphoblastic leukemia. Blood, 1996, 87, 2180.
10. Kamb, A., Gruis, N. A., Weaver-Feldhaus, J., Liu, Q., Harshman, K., Tavtigian, S. V., Stockert, E., Day, R. S.III, Johnson, B. E. and Skolnick, M. H., A cell cycle regulator potentially involved in genesis of many tumor types. Science, 1994, 264, 436.
11. Nobori, T., Miura, K., Wu, D. J., Lois, A., Takabayashi, K. and Carson, D. A., Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers. Nature, 1994, 368, 753.
12. Chen, Y. C., Chen, P. J., Yeh, S. H., Tien, H.-F., Wang, C.-H., Tang, J.-L. and Hong, R.-L., Deletion of the human retinoblastoma gene in primary leukemias. Blood, 1990, 76, 2060.
13. Schottelius, A., Brennscheidt, U., Ludwig, W.-D., Mertelsmann, R. H., Herrmann, F. and Lübbert, M., Mechanisms of p53 alteration in acute leukemias. Leukemia, 1994, 8, 1673.
14. Knudson, A. G., Mutation and cancer: statistical study of retinoblastoma. PNAS, 1971, 68, 820.
15. Sinnett, D., Lavergne, L., Melançon, S. B., Dallaire, L., Potier, M. and Labuda, D., Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using HPRT cDNA probe. Human Genetics, 1988, 81, 4.
16. Richards, B., Skoletsky, J., Shuber, A. P., Balfour, R., Stern, R. C., Dorkin, H. L., Parad, R. B., Witt, D. and Klinger, K. W., Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/ swabs. Human Molecular Genetics, 1993, 2, 159.
17. Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M. and Weissenbach, J., The 1993-1994 Genethon human genetic linkage map. Nature Genetics, 1994, 7, 246.
18. Baccichet, A., Benachenhou, N., Couture, F., Leclerc, J.-M. and Sinnett, D., Microsatellite instability in childhood T-cell acute lymphoblastic leukemia. Leukemia, 1997, 11, 797.
19. Champlin, R. and Gale, R. P., Acute lymphoblastic leukemia: recent advances in biology and therapy. Blood, 1989, 73, 2051.
20. Menasce, L. P., Orphanos, V., Santibanez-Koref, M., Boyle, J. M. and Harrison, C. J., Common region of deletion on the long arm of chromosome 6 in non-Hodgkin's lymphoma and acute lymphoblastic leukaemia. Genes Chromosomes Cancer, 1994, 10, 286.
21. Raimondi, S. C., Williams, D. L., Callihan, T., Peiper, S., Rivera, G. K. and Murphy, S. B., Nonrandom involvement of 12p12 breakpoint in chromosome abnormalities of childhood acute lymphoblastic leukemia. Blood, 1986, 68, 69.
22. Mitelman, F. (ed), ISCN 1991: cancer cytogenetics, supplement to an international system for human cytogenetic nomenclature. S. Karger AG, Basel, Switzerland, 1991.
23. Kobayashi, H., Montgomery, K. T., Bohlander, S. K., Adra, C. N., Lim, B. L., Kucherlapati, R. S., Donis Keller, H., Holt, M. S., LeBeau, M. M. and Rowley, J. D., Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases. Blood, 1994, 84, 3473.
24. Baccichet, A., Leclerc, J.-M. and Sinnett, D., Deletion mapping of a candidate tumor suppressor gene in chromosome 12p12.3 involved in acute lymphoblastic leukemia. Blood, suppl., 1995, 86, 724A.
25. Sato, Y., Suto, Y., Pietenpol, J., Golub, T. R., Gilliland, D. G., Davis, E. M., Lebeau, M. M., Roberts, J. M., Vogelstien, B., Rowley, J. D. and Bohlander, S. K., TEL and KIPl define the smallest region of deletions on 12p13 in hematopoietic malignancies. Blood, 1995, 86, 1525.
26. Stegmaier, K., Pendse, S., Barker, G. F., Bray-Ward, P., Ward, D. C., Montgomery, K. T., Krauter, K. S., Reynolds, C., Sklar, J., Donnelly, M., Bohlander, S. K., Rowley, J. D., Sallan, S. E., Gilliland, D. G. and Golob, T. R., Frequent loss of heterozygosity at the TEL gene locus in acute lymphoblastic leukemia in childhood. Blood, 1995, 86, 38.
27. Takeuchi, S., Bartram, C. R., Miller, C. W., Reiter, A., Seriu, T., Zimmermann, M., Schrappe, M., Mori, N., Slater, J., Miyoshi, I. and Koeffler, H. P., Acute lymphoblastic leukemia of childhood: identification of two distinct regions of deletion on the short arm of chromosome 12 in the region of TEL and KIP1. Blood, 1996, 87, 3368.
28. Takeuchi, S., Bartram, C. R., Wada, M., Reiter, A., Hatta, Y., Seriu, T., Lee, E., Miller, C. W., Miyoshi, I. and Koeffler, H. P., Allelotype analysis of childhood acute lymphoblastic leukemia. Cancer Research, 1995, 55, 5377.
29. Cavé, H., Guidal, C., Elion, J., Vilmer, E. and Grandchamp, B., A low rate of loss of heterozygosity is found at many different loci in childhood B-lineage acute lymphocytic leukemia. Leukemia, 1996, 10, 1486.