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Volumn 29, Issue 17, 2010, Pages 2509-2516

Genomic segmental duplications on the basis of the t(9;22) rearrangement in chronic myeloid leukemia

Author keywords

Chronic myeloid leukemia; Microdeletions; Segmental duplications

Indexed keywords

ABL GENE; ARTICLE; BCR GENE; BIOINFORMATICS; CHROMOSOME 22; CHROMOSOME 9; CHROMOSOME TRANSLOCATION 22; CHROMOSOME TRANSLOCATION 9; CHRONIC MYELOID LEUKEMIA; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE DELETION; GENE DUPLICATION; HUMAN; LEUKEMOGENESIS; MAJOR CLINICAL STUDY; PRIORITY JOURNAL;

EID: 77951831501     PISSN: 09509232     EISSN: 14765594     Source Type: Journal    
DOI: 10.1038/onc.2009.524     Document Type: Article
Times cited : (31)

References (24)
  • 1
    • 34247100205 scopus 로고    scopus 로고
    • Home-brew' FISH assay shows higher efficiency than BCR-ABL dual color, dual fusion probe in detecting microdeletions and complex rearrangements associated with t(9;22) in chronic myeloid leukemia
    • Albano F, Anelli L, Zagaria A, Archidiacono N, Liso V, Specchia G et al. (2007). 'Home-brew' FISH assay shows higher efficiency than BCR-ABL dual color, dual fusion probe in detecting microdeletions and complex rearrangements associated with t(9;22) in chronic myeloid leukemia. Cancer Genet Cytogenet 174: 121-126.
    • (2007) Cancer Genet Cytogenet , vol.174 , pp. 121-126
    • Albano, F.1    Anelli, L.2    Zagaria, A.3    Archidiacono, N.4    Liso, V.5    Specchia, G.6
  • 2
    • 33745373606 scopus 로고    scopus 로고
    • Primate segmental duplications: Crucibles of evolution, diversity and disease
    • Bailey JA, Eichler EE. (2006). Primate segmental duplications: crucibles of evolution, diversity and disease. Nat Rev Genet 7: 552-564.
    • (2006) Nat Rev Genet , vol.7 , pp. 552-564
    • Bailey, J.A.1    Eichler, E.E.2
  • 3
    • 9144264835 scopus 로고    scopus 로고
    • The breakpoint region of the most commonisochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats
    • Barbouti A, Stankiewicz P, Nusbaum C, Cuomo C, Cook A, Hoglund M et al. (2004). The breakpoint region of the most commonisochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats. Am J Hum Genet 74: 1-10.
    • (2004) Am J Hum Genet , vol.74 , pp. 1-10
    • Barbouti, A.1    Stankiewicz, P.2    Nusbaum, C.3    Cuomo, C.4    Cook, A.5
  • 4
    • 40449128815 scopus 로고    scopus 로고
    • Segmental duplications and evolutionary plasticity at tumor chromosome break-prone regions
    • Darai-Ramqvist E, Sandlund A, Muller S, Klein G, Imreh S, Kost-Alimova M. (2008). Segmental duplications and evolutionary plasticity at tumor chromosome break-prone regions. Genome Res 18: 370-379.
    • (2008) Genome Res , vol.18 , pp. 370-379
    • Darai-Ramqvist, E.1    Sandlund, A.2    Muller, S.3    Klein, G.4    Imreh, S.5    Kost-Alimova, M.6
  • 5
    • 0036480427 scopus 로고    scopus 로고
    • Double-strand breaks and translocations in cancer
    • Elliott B, Jasin M. (2002). Double-strand breaks and translocations in cancer. Cell Mol Life Sci 59: 373-385.
    • (2002) Cell Mol Life Sci , vol.59 , pp. 373-385
    • Elliott, B.1    Jasin, M.2
  • 6
    • 33745765411 scopus 로고    scopus 로고
    • Size matters: The prognostic implications of large and small deletions of the derivative 9 chromosome in chronic myeloid leukemia
    • Fourouclas N, Campbell PJ, Bench AJ, Swanton S, Baxter EJ, Huntly BJ et al. (2006). Size matters: the prognostic implications of large and small deletions of the derivative 9 chromosome in chronic myeloid leukemia. Haematologica 91: 952-955.
    • (2006) Haematologica , vol.91 , pp. 952-955
    • Fourouclas, N.1    Campbell, P.J.2    Bench, A.J.3    Swanton, S.4    Baxter, E.J.5
  • 7
    • 33947187562 scopus 로고    scopus 로고
    • High-resolution mapping identifies a commonly amplified 11q13.3 region containing multiple genes flanked by segmental duplications
    • Gibcus JH, Kok K, Menkema L, Hermsen MA, Mastik M, Kluin PM et al. (2007). High-resolution mapping identifies a commonly amplified 11q13.3 region containing multiple genes flanked by segmental duplications. Hum Genet 121: 187-201.
    • (2007) Hum Genet , vol.121 , pp. 187-201
    • Gibcus, J.H.1    Kok, K.2    Menkema, L.3    Hermsen, M.A.4    Mastik, M.5
  • 8
    • 62549134411 scopus 로고    scopus 로고
    • Mechanisms for human genomic rearrangements
    • Gu W, Zhang F, Lupski JR. (2008). Mechanisms for human genomic rearrangements. Pathogenetics 1: 4.
    • (2008) Pathogenetics , vol.1 , pp. 4
    • Gu, W.1    Zhang, F.2    Lupski, J.R.3
  • 9
    • 0035885928 scopus 로고    scopus 로고
    • Deletions of the derivative chromosome 9 occur at the time of the Philadelphia translocation and provide a powerful and independent prognostic indicator in chronic myeloid leukemia
    • Huntly BJ, Reid AG, Bench AJ, Campbell LJ, Telford N, Shepherd P et al. (2001). Deletions of the derivative chromosome 9 occur at the time of the Philadelphia translocation and provide a powerful and independent prognostic indicator in chronic myeloid leukemia. Blood 98: 1732-1738.
    • (2001) Blood , vol.98 , pp. 1732-1738
    • Huntly, B.J.1    Reid, A.G.2    Bench, A.J.3    Campbell, L.J.4    Telford, N.5
  • 10
    • 57149099396 scopus 로고    scopus 로고
    • Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history
    • Kim PM, Lam HY, Urban AE, Korbel JO, Affourtit J, Grubert F et al. (2008). Analysis of copy number variants and segmental duplications in the human genome: evidence for a change in the process of formation in recent evolutionary history. Genome Res 18: 1865-1874.
    • (2008) Genome Res , vol.18 , pp. 1865-1874
    • Kim, P.M.1    Lam, H.Y.2    Urban, A.E.3    Korbel, J.O.4    Affourtit, J.5
  • 11
    • 0035383839 scopus 로고    scopus 로고
    • Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicro-scopic deletions and may lead to altered prognosis
    • Kolomietz E, Al-Maghrabi J, Brennan S, Karaskova J, Minkin S, Lipton J et al. (2001). Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicro-scopic deletions and may lead to altered prognosis. Blood 97: 3581-3588.
    • (2001) Blood , vol.97 , pp. 3581-3588
    • Kolomietz, E.1    Al-Maghrabi, J.2    Brennan, S.3    Karaskova, J.4    Minkin, S.5    Lipton, J.6
  • 12
    • 0037766264 scopus 로고    scopus 로고
    • Quantitative PCR identifies a minimal deleted region of 120kb extending from the Philadelphia chromosome ABL translo-cation breakpoint in chronic myeloid leukemia with poor outcome
    • Kolomietz E, Marrano P, Yee K, Thai B, Braude I, Kolomietz A et al. (2003). Quantitative PCR identifies a minimal deleted region of 120kb extending from the Philadelphia chromosome ABL translo-cation breakpoint in chronic myeloid leukemia with poor outcome. Leukemia 17: 1313-1323.
    • (2003) Leukemia , vol.17 , pp. 1313-1323
    • Kolomietz, E.1    Marrano, P.2    Yee, K.3    Thai, B.4    Braude, I.5    Kolomietz, A.6
  • 13
    • 34447628963 scopus 로고    scopus 로고
    • Heterogeneous prognostic impact of derivative chromosome 9 deletions in chronic myelogenous leukemia
    • Kreil S, Pfirrmann M, Haferlach C, Waghorn K, Chase A, Hehlmann R et al. (2007). Heterogeneous prognostic impact of derivative chromosome 9 deletions in chronic myelogenous leukemia. Blood 110: 1283-1290.
    • (2007) Blood , vol.110 , pp. 1283-1290
    • Kreil, S.1    Pfirrmann, M.2    Haferlach, C.3    Waghorn, K.4    Chase, A.5    Hehlmann, R.6
  • 14
    • 0025128991 scopus 로고
    • High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones
    • Lichter P, Tang CJ, Call K, Hermanson G, Evans GA, Housman D et al. (1990). High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. Science 247: 64-69.
    • (1990) Science , vol.247 , pp. 64-69
    • Lichter, P.1    Tang, C.J.2    Call, K.3    Hermanson, G.4    Evans, G.A.5    Housman, D.6
  • 15
    • 0027497958 scopus 로고
    • Duplication of small segments within the major breakpoint cluster region in chronic myelogenous leukemia
    • Litz CE, McClure JS, Copenhaver CM, Brunning RD. (1993). Duplication of small segments within the major breakpoint cluster region in chronic myelogenous leukemia. Blood 81: 1567-1572.
    • (1993) Blood , vol.81 , pp. 1567-1572
    • Litz, C.E.1    McClure, J.S.2    Copenhaver, C.M.3    Brunning, R.D.4
  • 17
    • 68649123353 scopus 로고    scopus 로고
    • Duplication hotspots, rare genomic disorders, and common disease
    • Mefford HC, Eichler EE. (2009). Duplication hotspots, rare genomic disorders, and common disease. Curr Opin Genet Dev 19: 196-204.
    • (2009) Curr Opin Genet Dev , vol.19 , pp. 196-204
    • Mefford, H.C.1    Eichler, E.E.2
  • 18
    • 0037162516 scopus 로고    scopus 로고
    • A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: Possible involvement in the genesis of the Philadelphia chromosome translocation
    • Saglio G, Storlazzi CT, Giugliano E, Surace C, Anelli L, Rege-Cambrin G et al. (2002). A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation. Proc Natl Acad Sci USA 99: 9882-9887.
    • (2002) Proc Natl Acad Sci USA , vol.99 , pp. 9882-9887
    • Saglio, G.1    Storlazzi, C.T.2    Giugliano, E.3    Surace, C.4    Anelli, L.5    Rege-Cambrin, G.6
  • 19
    • 33748333194 scopus 로고    scopus 로고
    • Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome
    • Sharp AJ, Hansen S, Selzer RR, Cheng Z, Regan R, Hurst JA et al. (2006). Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. Nat Genet 38: 1038-1042.
    • (2006) Nat Genet , vol.38 , pp. 1038-1042
    • Sharp, A.J.1    Hansen, S.2    Selzer, R.R.3    Cheng, Z.4    Regan, R.5    Hurst, J.A.6
  • 20
    • 12944295358 scopus 로고    scopus 로고
    • Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia
    • Sinclair PB, Nacheva EP, Leversha M, Telford N, Chang J, Reid A et al. (2000). Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia. Blood 95: 738-743.
    • (2000) Blood , vol.95 , pp. 738-743
    • Sinclair, P.B.1    Nacheva, E.P.2    Leversha, M.3    Telford, N.4    Chang, J.5    Reid, A.6
  • 21
    • 10744230123 scopus 로고    scopus 로고
    • Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes
    • Specchia G, Albano F, Anelli L, Storlazzi CT, Zagaria A, Liso A et al. (2004). Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes. Leuk Lymphoma 45: 689-694.
    • (2004) Leuk Lymphoma , vol.45 , pp. 689-694
    • Specchia, G.1    Albano, F.2    Anelli, L.3    Storlazzi, C.T.4    Zagaria, A.5    Liso, A.6
  • 23
    • 34548748074 scopus 로고    scopus 로고
    • Clinical implications of der(9q) deletions detected through dual-fusion fluorescence in situ hybridization in patients with chronic myeloid leukemia
    • Vaz de Campos MG, Montesano FT, Rodrigues MM, Chauffaille Mde L. (2007). Clinical implications of der(9q) deletions detected through dual-fusion fluorescence in situ hybridization in patients with chronic myeloid leukemia. Cancer Genet Cytogenet 178: 49-56.
    • (2007) Cancer Genet Cytogenet , vol.178 , pp. 49-56
    • Vaz De Campos, M.G.1    Montesano, F.T.2    Rodrigues, M.M.3    Chauffaille Mde, L.4
  • 24
    • 65549090043 scopus 로고    scopus 로고
    • Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome
    • Yatsenko SA, Brundage EK, Roney EK, Cheung SW, Chinault AC, Lupski JR. (2009). Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome. Hum Mol Genet 18: 1924-1936.
    • (2009) Hum Mol Genet , vol.18 , pp. 1924-1936
    • Yatsenko, S.A.1    Brundage, E.K.2    Roney, E.K.3    Cheung, S.W.4    Chinault, A.C.5    Lupski, J.R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.