메뉴 건너뛰기




Volumn 46, Issue 1, 2006, Pages 90-97

A role for mitotic recombination in leukemogenesis

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; ARTICLE; DNA MICROARRAY; GENETIC RECOMBINATION; GENETICS; HUMAN; LEUKEMIA; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 33748063938     PISSN: 00652571     EISSN: None     Source Type: Book Series    
DOI: 10.1016/j.advenzreg.2006.01.015     Document Type: Article
Times cited : (16)

References (34)
  • 1
    • 0031056793 scopus 로고    scopus 로고
    • The commonly deleted region at 9p21-22 in lymphoblastic leukemias spans at least 400 kb and includes p16 but not p15 or the IFN gene cluster
    • Aguiar R.C., Sill H., Goldman J.M., and Cross N.C. The commonly deleted region at 9p21-22 in lymphoblastic leukemias spans at least 400 kb and includes p16 but not p15 or the IFN gene cluster. Leukemia 11 (1997) 233-238
    • (1997) Leukemia , vol.11 , pp. 233-238
    • Aguiar, R.C.1    Sill, H.2    Goldman, J.M.3    Cross, N.C.4
  • 2
    • 0030725637 scopus 로고    scopus 로고
    • Allelic loss in childhood acute lymphoblastic leukemia
    • Baccichet A., Qualman S.K., and Sinnett D. Allelic loss in childhood acute lymphoblastic leukemia. Leuk Res 21 (1997) 817-823
    • (1997) Leuk Res , vol.21 , pp. 817-823
    • Baccichet, A.1    Qualman, S.K.2    Sinnett, D.3
  • 3
    • 10744230160 scopus 로고    scopus 로고
    • High-resolution analysis of DNA copy number using oligonucleotide microarrays
    • Bignell G.R., Huang J., Greshock J., Watt S., Butler A., West S., et al. High-resolution analysis of DNA copy number using oligonucleotide microarrays. Genome Res 14 (2004) 287-295
    • (2004) Genome Res , vol.14 , pp. 287-295
    • Bignell, G.R.1    Huang, J.2    Greshock, J.3    Watt, S.4    Butler, A.5    West, S.6
  • 4
    • 3442875564 scopus 로고    scopus 로고
    • Loss of heterozygosity occurs via mitotic recombination in Trp53+/- mice and associates with mammary tumor susceptibility of the BALB/c strain
    • Blackburn A.C., McLary S.C., Naeem R., Luszcz J., Stockton D.W., Donehower L.A., et al. Loss of heterozygosity occurs via mitotic recombination in Trp53+/- mice and associates with mammary tumor susceptibility of the BALB/c strain. Cancer Res 64 (2004) 5140-5147
    • (2004) Cancer Res , vol.64 , pp. 5140-5147
    • Blackburn, A.C.1    McLary, S.C.2    Naeem, R.3    Luszcz, J.4    Stockton, D.W.5    Donehower, L.A.6
  • 5
    • 0031874333 scopus 로고    scopus 로고
    • High-resolution allelotype analysis of childhood B-lineage acute lymphoblastic leukemia
    • Chambon-Pautas C., Cave H., Gerard B., Guidal-Giroux C., Duval M., Vilmer E., et al. High-resolution allelotype analysis of childhood B-lineage acute lymphoblastic leukemia. Leukemia 12 (1998) 1107-1113
    • (1998) Leukemia , vol.12 , pp. 1107-1113
    • Chambon-Pautas, C.1    Cave, H.2    Gerard, B.3    Guidal-Giroux, C.4    Duval, M.5    Vilmer, E.6
  • 6
    • 0037732933 scopus 로고    scopus 로고
    • Genome-wide analysis of acute myeloid leukemia with normal karyotype reveals a unique pattern of homeobox gene expression distinct from those with translocation-mediated fusion events
    • Debernardi S., Lillington D.M., Chaplin T., Tomlinson S., Amess J., Rohatiner A., et al. Genome-wide analysis of acute myeloid leukemia with normal karyotype reveals a unique pattern of homeobox gene expression distinct from those with translocation-mediated fusion events. Genes Chromosomes Cancer 37 (2003) 149-158
    • (2003) Genes Chromosomes Cancer , vol.37 , pp. 149-158
    • Debernardi, S.1    Lillington, D.M.2    Chaplin, T.3    Tomlinson, S.4    Amess, J.5    Rohatiner, A.6
  • 7
    • 0026602439 scopus 로고
    • Mutations of the p53 gene in B-cell lymphoblastic acute leukemia: a report on 60 cases
    • Fenaux P., Jonveaux P., Quiquandon I., Preudhomme C., Lai J.L., Vanrumbeke M., et al. Mutations of the p53 gene in B-cell lymphoblastic acute leukemia: a report on 60 cases. Leukemia 6 (1992) 42-46
    • (1992) Leukemia , vol.6 , pp. 42-46
    • Fenaux, P.1    Jonveaux, P.2    Quiquandon, I.3    Preudhomme, C.4    Lai, J.L.5    Vanrumbeke, M.6
  • 8
    • 27144478643 scopus 로고    scopus 로고
    • An association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukaemias
    • (in press)
    • Fitzgibbon J., Smith L.L., Raghavan M., Smith M.L., Debernardi S., et al. An association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukaemias. Cancer Res (2005) (in press)
    • (2005) Cancer Res
    • Fitzgibbon, J.1    Smith, L.L.2    Raghavan, M.3    Smith, M.L.4    Debernardi, S.5
  • 10
    • 0032188805 scopus 로고    scopus 로고
    • The importance of diagnostic cytogenetics on outcome in AML: analysis of 1612 patients entered into the MRC AML 10 trial. The Medical Research Council Adult and Children's Leukaemia Working Parties
    • Grimwade D., Walker H., Oliver F., Wheatley K., Harrison C., Harrison G., et al. The importance of diagnostic cytogenetics on outcome in AML: analysis of 1612 patients entered into the MRC AML 10 trial. The Medical Research Council Adult and Children's Leukaemia Working Parties. Blood 92 (1998) 2322-2333
    • (1998) Blood , vol.92 , pp. 2322-2333
    • Grimwade, D.1    Walker, H.2    Oliver, F.3    Wheatley, K.4    Harrison, C.5    Harrison, G.6
  • 11
    • 0033020244 scopus 로고    scopus 로고
    • Mitotic recombination map of 13cen-13q14 derived from an investigation of loss of heterozygosity in retinoblastomas
    • Hagstrom S.A., and Dryja T.P. Mitotic recombination map of 13cen-13q14 derived from an investigation of loss of heterozygosity in retinoblastomas. Proc Natl Acad Sci USA 96 (1999) 2952-2957
    • (1999) Proc Natl Acad Sci USA , vol.96 , pp. 2952-2957
    • Hagstrom, S.A.1    Dryja, T.P.2
  • 12
    • 0027938776 scopus 로고
    • Candidate tumor-suppressor genes MTS1 (p16INK4A) and MTS2 (p15INK4B) display frequent homozygous deletions in primary cells from T- but not from B-cell lineage acute lymphoblastic leukemias
    • Hebert J., Cayuela J.M., Berkeley J., and Sigaux F. Candidate tumor-suppressor genes MTS1 (p16INK4A) and MTS2 (p15INK4B) display frequent homozygous deletions in primary cells from T- but not from B-cell lineage acute lymphoblastic leukemias. Blood 84 (1994) 4038-4044
    • (1994) Blood , vol.84 , pp. 4038-4044
    • Hebert, J.1    Cayuela, J.M.2    Berkeley, J.3    Sigaux, F.4
  • 15
    • 0027378164 scopus 로고
    • Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci
    • Johansson B., Mertens F., and Mitelman F. Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci. Genes Chromosomes Cancer 8 (1993) 205-218
    • (1993) Genes Chromosomes Cancer , vol.8 , pp. 205-218
    • Johansson, B.1    Mertens, F.2    Mitelman, F.3
  • 16
    • 0034640657 scopus 로고    scopus 로고
    • Complete maternal isodisomy of chromosome 8 in an individual with an early onset ileal carcinoid tumor
    • Karanjawala Z.E., Kaariainen H., Ghosh S., Tannenbaum J., Martin C., Ally D., et al. Complete maternal isodisomy of chromosome 8 in an individual with an early onset ileal carcinoid tumor. Am J Med Genet 93 (2000) 207-210
    • (2000) Am J Med Genet , vol.93 , pp. 207-210
    • Karanjawala, Z.E.1    Kaariainen, H.2    Ghosh, S.3    Tannenbaum, J.4    Martin, C.5    Ally, D.6
  • 18
    • 0036191941 scopus 로고    scopus 로고
    • Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera
    • Kralovics R., Guan Y., and Prchal J.T. Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera. Exp Hematol 30 (2002) 229-236
    • (2002) Exp Hematol , vol.30 , pp. 229-236
    • Kralovics, R.1    Guan, Y.2    Prchal, J.T.3
  • 19
    • 0035189488 scopus 로고    scopus 로고
    • Loss of heterozygosity and heterogeneity of its appearance and persisting in the course of acute myeloid leukemia and myelodysplastic syndromes
    • Krskova-Honzatkova L., Cermak J., Sajdova J., Stary J., Sedlacek P., and Sieglova Z. Loss of heterozygosity and heterogeneity of its appearance and persisting in the course of acute myeloid leukemia and myelodysplastic syndromes. Leuk Res 25 (2001) 45-53
    • (2001) Leuk Res , vol.25 , pp. 45-53
    • Krskova-Honzatkova, L.1    Cermak, J.2    Sajdova, J.3    Stary, J.4    Sedlacek, P.5    Sieglova, Z.6
  • 20
    • 0034425049 scopus 로고    scopus 로고
    • Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays
    • Lindblad-Toh K., Tanenbaum D.M., Daly M.J., Winchester E., Lui W.O., Villapakkam A., et al. Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays. Nat Biotechnol 18 (2000) 1001-1005
    • (2000) Nat Biotechnol , vol.18 , pp. 1001-1005
    • Lindblad-Toh, K.1    Tanenbaum, D.M.2    Daly, M.J.3    Winchester, E.4    Lui, W.O.5    Villapakkam, A.6
  • 22
    • 0030929119 scopus 로고    scopus 로고
    • Allelotype analysis in the evolution of chronic myelocytic leukemia
    • Mori N., Morosetti R., Lee S., Spira S., Ben-Yehuda D., Schiller G., et al. Allelotype analysis in the evolution of chronic myelocytic leukemia. Blood 90 (1997) 2010-2014
    • (1997) Blood , vol.90 , pp. 2010-2014
    • Mori, N.1    Morosetti, R.2    Lee, S.3    Spira, S.4    Ben-Yehuda, D.5    Schiller, G.6
  • 23
    • 0036903315 scopus 로고    scopus 로고
    • Loss of heterozygosity associated with uniparental disomy in breast carcinoma
    • Murthy S.K., DiFrancesco L.M., Ogilvie R.T., and Demetrick D.J. Loss of heterozygosity associated with uniparental disomy in breast carcinoma. Mod Pathol 15 (2002) 1241-1250
    • (2002) Mod Pathol , vol.15 , pp. 1241-1250
    • Murthy, S.K.1    DiFrancesco, L.M.2    Ogilvie, R.T.3    Demetrick, D.J.4
  • 24
    • 17344371740 scopus 로고    scopus 로고
    • High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
    • Pinkel D., Segraves R., Sudar D., Clark S., Poole I., Kowbel D., et al. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet 20 (1998) 207-211
    • (1998) Nat Genet , vol.20 , pp. 207-211
    • Pinkel, D.1    Segraves, R.2    Sudar, D.3    Clark, S.4    Poole, I.5    Kowbel, D.6
  • 25
    • 12544257171 scopus 로고    scopus 로고
    • Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias
    • Raghavan M., Lillington D.M., Skoulakis S., Debernardi S., Chaplin T., Foot N.J., et al. Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias. Cancer Res 65 (2005) 375-378
    • (2005) Cancer Res , vol.65 , pp. 375-378
    • Raghavan, M.1    Lillington, D.M.2    Skoulakis, S.3    Debernardi, S.4    Chaplin, T.5    Foot, N.J.6
  • 26
    • 0028805799 scopus 로고
    • Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia
    • Rogan P.K., Close P., Blouin J.L., Seip J.R., Gannutz L., Ladda R.L., et al. Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia. Am J Med Genet 59 (1995) 174-181
    • (1995) Am J Med Genet , vol.59 , pp. 174-181
    • Rogan, P.K.1    Close, P.2    Blouin, J.L.3    Seip, J.R.4    Gannutz, L.5    Ladda, R.L.6
  • 27
    • 0035865322 scopus 로고    scopus 로고
    • A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
    • Sachidanandam R., Weissman D., Schmidt S.C., Kakol J.M., Stein L.D., Marth G., et al. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 409 (2001) 928-933
    • (2001) Nature , vol.409 , pp. 928-933
    • Sachidanandam, R.1    Weissman, D.2    Schmidt, S.C.3    Kakol, J.M.4    Stein, L.D.5    Marth, G.6
  • 28
    • 0032734971 scopus 로고    scopus 로고
    • Hemizygous deletions of chromosome band 16q24 in Wilms tumor: detection by fluorescence in situ hybridization
    • Shearer P.D., Valentine M.B., Grundy P., DeCou J.M., Banavali S.D., Komuro H., et al. Hemizygous deletions of chromosome band 16q24 in Wilms tumor: detection by fluorescence in situ hybridization. Cancer Genet Cytogenet 115 (1999) 100-105
    • (1999) Cancer Genet Cytogenet , vol.115 , pp. 100-105
    • Shearer, P.D.1    Valentine, M.B.2    Grundy, P.3    DeCou, J.M.4    Banavali, S.D.5    Komuro, H.6
  • 31
    • 0030776156 scopus 로고    scopus 로고
    • Loss of heterozygosity or: how I learned to stop worrying and love mitotic recombination
    • Tischfield J.A. Loss of heterozygosity or: how I learned to stop worrying and love mitotic recombination. Am J Hum Genet 61 (1997) 995-999
    • (1997) Am J Hum Genet , vol.61 , pp. 995-999
    • Tischfield, J.A.1
  • 32
    • 0032054429 scopus 로고    scopus 로고
    • Acquired homozygosity (isodisomy) of chromosome 3 in uveal melanoma
    • White V.A., McNeil B.K., and Horsman D.E. Acquired homozygosity (isodisomy) of chromosome 3 in uveal melanoma. Cancer Genet Cytogenet 102 (1998) 40-45
    • (1998) Cancer Genet Cytogenet , vol.102 , pp. 40-45
    • White, V.A.1    McNeil, B.K.2    Horsman, D.E.3
  • 33
    • 0035476264 scopus 로고    scopus 로고
    • Absence of the wild-type allele predicts poor prognosis in adult de novo acute myeloid leukemia with normal cytogenetics and the internal tandem duplication of FLT3: a cancer and leukemia group B study
    • Whitman S.P., Archer K.J., Feng L., Baldus C., Becknell B., Carlson B.D., et al. Absence of the wild-type allele predicts poor prognosis in adult de novo acute myeloid leukemia with normal cytogenetics and the internal tandem duplication of FLT3: a cancer and leukemia group B study. Cancer Res 61 (2001) 7233-7239
    • (2001) Cancer Res , vol.61 , pp. 7233-7239
    • Whitman, S.P.1    Archer, K.J.2    Feng, L.3    Baldus, C.4    Becknell, B.5    Carlson, B.D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.