Chromosome band 1p36 contains a putative tumor suppressor gene important in the evolution of chronic myelocytic leukemia

Blood

Volumn 92, Issue 9, 1998, Pages 3405-3409

  Mori, Naoki ^a   Morosetti, Roberta ^b   Spira, Susanne ^b   Lee, Stephen ^b   Ben Yehuda, Dina ^b   Schiller, Gary ^b   Landolfi, Raffaele ^b   Mizoguchi, Hideaki ^b   Koeffler, H Phillip ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ALLELE; ARTICLE; BLAST CELL CRISIS; BLAST TRANSFORMATION; BONE MARROW CELL; CHROMOSOME 1P; CHROMOSOME BAND; CHRONIC MYELOID LEUKEMIA; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; FEMALE; GENE LOCUS; GENE LOSS; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; MALE; MONONUCLEAR CELL; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0032211176     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v92.9.3405.421k44_3405_3409     Document Type: Article

References (27)

1. Weinberg RA: Tumor suppressor genes. Science 254:1138, 1991
2. Knudson AG: Mutation and cancer: Statistical study of retinoblastoma. Proc Natl Acad Sci USA 68:820, 1971
3. Kantarjian HM, Deisseroth A, Kurzrock R, Estrov Z, Talpaz M: Chronic myelogenous leukemia: A concise update. Blood 82:691, 1993
4. Kurzrock R, Gutterman JU, Talpaz M: The molecular genetics of Philadelphia-chromosome positive leukemias. N Engl J Med 319:990, 1988
5. Ahuja H, Bar-Eli M, Arlin Z, Advani SH, Allen SL, Goldman J, Snyder D, Foti A, Cline MJ: The spectrum of molecular alterations in the evolution of chronic myelocytic leukemia. J Clin Invest 87:2042, 1991
6. Sill H, Goldman JM, Cross NCP: Homozygous deletions of the p16 tumor-suppressor gene are associated with lymphoid transformation of chronic myeloid leukemia. Blood 85:2013, 1995
7. Towatari M, Adachi K, Kato H, Saito H: Absence of the human retinoblastoma gene product in the megakaryoblastic crisis of chronic myelogenous leukemia. Blood 78:2178, 1991
8. Melo JV: The molecular biology of chronic myeloid leukaemia. Leukemia 10:751, 1996
9. Vogelstein B, Fearon ER, Kern S, Hamilton SR, Preisinger AC, Nakamura Y, White R: Allelotype of colorectal carcinomas. Science 244:207, 1989
10. Tsuchiya E, Nakamura Y, Weng S-Y, Nakagawa K, Tsuchiya S, Sugano H, Kitagawa T: Allelotype of non-small cell lung carcinoma- comparison between loss of heterozygosity in squamous cell carcinoma and adenocarcinoma. Cancer Res 52:2478, 1992
11. Takeuchi S, Bartram CR, Wada M, Reiter A, Hatta Y, Seriu T, Lee E, Miller CW, Miyoshi I, Koeffler HP: Allelotype analysis of childhood acute lymphoblastic leukemia. Cancer Res 55:5377, 1995
12. Mori N, Morosetti R, Lee S, Spira S, Ben-Yehuda D, Schiller G, Landolfi R, Mizoguchi H, Koeffler HP: Allelotype analysis in the evolution of chronic myelocytic leukemia. Blood 90:2010, 1997
13. Sambrook J, Fritsch EF, Maniatis T: Molecular cloning: A Laboratory Manual. Plainview, NW, Cold Spring Harbor Lab Press, 1989
14. Litt M, Luty JA: A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene. Am J Hum Genet 44:397, 1989
15. Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, Lathrop M: A second-generation linkage map of the human genome. Nature 359:794, 1992
16. White PS, Maris JM, Beltinger C, Sulman E, Marshall HN, Fujimori M, Kaufman BA, Biegel JA, Allen C, Hilliard C, Valentine MB, Look AT, Enomoto H, Sakiyama S, Brodeur GM: A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3. Proc Natl Acad Sci USA 92:5520, 1995
17. Praml C, Finke LH, Herfarth C, Schlag P, Schwab M, Amier L: Deletion mapping defines different regions in 1p34.2-pter that may harbor genetic information related to human colorectal cancer. Oncogene 11:1357, 1995
18. Nagai H, Negrini M, Garter SL, Gillum DR, Rosenberg AL, Schwartz GF, Croce CM: Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer. Cancer Res 55:1752, 1995
19. Yeh S-H, Chen P-J, Chen H-L, Lai M-Y, Wang C-C, Chen D-S: Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas. Cancer Res 54:4188, 1994
20. Cryns VL, Yi SM, Tahara H, Gaz RD, Arnold A: Frequent loss of chromosome arm 1p DNA in parathyroid adenomas. Genes Chromosom Cancer 13:9, 1995
21. Dracopoli NC, Hamett P, Bale SJ, Stanger BZ, Tucker MA, Housman DE, Kefford RF: Loss of alleles from the diatal short arm of chromosome 1 occurs late in melanoma tumor progression. Proc Natl Acad Sci USA 86:4614, 1989
22. Caron H, van Sluis P, de Kraker J, Bokkerink J, Egeler M, Laureys G, Slater R, Westerveld A, Voute PA, Versteeg R: Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. N Engl J Med 334:225, 1996
23. Schwab M, Praml C, Amler LC: Genomic instability in 1p and human malignancies. Genes Chromosom Cancer 16:211, 1996
24. INK4B/MTS2-related CDK6 inhibitor, correlates with wild-type pRb function. Genes Dev 8:2939, 1994
25. Kaghad M, Bonnet H, Yang A, Creancier L, Biscan J-C, Valent A, Minty A, Chalon P, Lelias J-M, Dumont X, Ferrara P, McKeon F, Caput D: Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers. Cell 90:809, 1997
26. Rowley JD: Nonrandom chromosomal abnormalities in hematologic disorders of man. Proc Natl Acad Sci USA 72:152, 1975
27. Bernstein R: Cytogenetics of chronic myelogenous leukemia. Semin Hematol 25:20, 1988