메뉴 건너뛰기




Volumn 79, Issue 7, 1997, Pages 1438-1446

Monosomy 7 myelodysplastic syndrome and other second malignant neoplasms in children with neurofibromatosis type 1

Author keywords

chromosome; DNA; human; human chromosome 7 monosomy; leukemia; myelodysplastic syndromes; myeloid; neoplasm; neurofibromatosis 1; neurofibromatosis 1 gene; pair 7 monosomy; ras genes; second primary; suppressor; tumor

Indexed keywords

ANTINEOPLASTIC AGENT; RAS PROTEIN;

EID: 0030982905     PISSN: 0008543X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1097-0142(19970401)79:7<1438::aid-cncr22>3.0.co;2-%23     Document Type: Article
Times cited : (87)

References (44)
  • 1
    • 0017880413 scopus 로고
    • Neurofibromatosis and childhood leukemia
    • Bader JL, Miller RW. Neurofibromatosis and childhood leukemia. J Pediatr 1978;92:925-9.
    • (1978) J Pediatr , vol.92 , pp. 925-929
    • Bader, J.L.1    Miller, R.W.2
  • 4
    • 0022599645 scopus 로고
    • Long-term follow-up of von Recklinghausen neurofibromatosis. Survival and malignant neoplasms
    • Sorensen SA, Mulvihill JJ, Nielsen A. Long-term follow-up of von Recklinghausen neurofibromatosis. Survival and malignant neoplasms. N Engl J Med 1986;314:1010-5.
    • (1986) N Engl J Med , vol.314 , pp. 1010-1015
    • Sorensen, S.A.1    Mulvihill, J.J.2    Nielsen, A.3
  • 5
    • 0028176825 scopus 로고
    • Neurofibromatosis type I and malignancy: Review of 32 pediatric cases treated at a single institution
    • Shearer P, Parham D, Kovnar E, Kun L, Rao B, Lobe T, et al. Neurofibromatosis type I and malignancy: review of 32 pediatric cases treated at a single institution. Med Pediatr Oncol 1994;22:78-83.
    • (1994) Med Pediatr Oncol , vol.22 , pp. 78-83
    • Shearer, P.1    Parham, D.2    Kovnar, E.3    Kun, L.4    Rao, B.5    Lobe, T.6
  • 7
    • 0027979146 scopus 로고
    • Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders
    • Shannon KM, O'Connell P, Martin GA, Paderanga D, Olson K, Dinndorf P, et al. Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders. N Engl J Med 1994;330:597-601.
    • (1994) N Engl J Med , vol.330 , pp. 597-601
    • Shannon, K.M.1    O'Connell, P.2    Martin, G.A.3    Paderanga, D.4    Olson, K.5    Dinndorf, P.6
  • 8
    • 0026502986 scopus 로고
    • Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: Epidemiology and molecular analysis
    • Shannon KM, Watterson J, Johnson P, O'Connell P, Lange B, Shah N, et al. Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: epidemiology and molecular analysis. Blood 1992;79:1311-8.
    • (1992) Blood , vol.79 , pp. 1311-1318
    • Shannon, K.M.1    Watterson, J.2    Johnson, P.3    O'Connell, P.4    Lange, B.5    Shah, N.6
  • 9
    • 0025369709 scopus 로고
    • Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus
    • Viskochil D, Buchberg AM, Xu G, Cawthon RM, Stevens J, Wolff RK, et al. Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus. Cell 1990;62:187-92.
    • (1990) Cell , vol.62 , pp. 187-192
    • Viskochil, D.1    Buchberg, A.M.2    Xu, G.3    Cawthon, R.M.4    Stevens, J.5    Wolff, R.K.6
  • 10
    • 0025297599 scopus 로고
    • Type 1 neurofibromatosis gene: Identification of a large transcript disrupted in three NF1 patients
    • Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, et al. Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients. Science 1990;249:181-6.
    • (1990) Science , vol.249 , pp. 181-186
    • Wallace, M.R.1    Marchuk, D.A.2    Andersen, L.B.3    Letcher, R.4    Odeh, H.M.5    Saulino, A.M.6
  • 11
    • 0025326726 scopus 로고
    • A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations
    • Cawthon RM, Weiss R, Xu G, Viskochil D, Culver M, Stevens J, et al. A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations. Cell 1990;62:193-201.
    • (1990) Cell , vol.62 , pp. 193-201
    • Cawthon, R.M.1    Weiss, R.2    Xu, G.3    Viskochil, D.4    Culver, M.5    Stevens, J.6
  • 13
    • 0024957180 scopus 로고
    • Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis: Loss of heterozygosity for chromosome 17
    • Skuse GR, Kosciolek BA, Rowley PT. Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis: loss of heterozygosity for chromosome 17. Genes Chromosom Cancer 1989;1:36-41.
    • (1989) Genes Chromosom Cancer , vol.1 , pp. 36-41
    • Skuse, G.R.1    Kosciolek, B.A.2    Rowley, P.T.3
  • 14
    • 0025108408 scopus 로고
    • Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis
    • Menon AG, Anderson KM, Riccardi VM, Chung RY, Whaley JM, Yandell DW, et al. Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis. Proc Natl Acad Sci USA 1990;87:5435-9.
    • (1990) Proc Natl Acad Sci USA , vol.87 , pp. 5435-5439
    • Menon, A.G.1    Anderson, K.M.2    Riccardi, V.M.3    Chung, R.Y.4    Whaley, J.M.5    Yandell, D.W.6
  • 17
    • 0027468594 scopus 로고
    • Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis
    • Legius E, Marchuk DA, Collins FS, Glover TW. Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis. Nat Genet 1993;3:122-6.
    • (1993) Nat Genet , vol.3 , pp. 122-126
    • Legius, E.1    Marchuk, D.A.2    Collins, F.S.3    Glover, T.W.4
  • 18
    • 0022617302 scopus 로고
    • Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: Further evidence for characteristic abnormalities of chromosomes 5 and 7
    • LeBeau M, Albain KS, Larson RA, Vardiman J, Davis E, Blough R, et al. Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes 5 and 7. J Clin Oncol 1986;3:325-45.
    • (1986) J Clin Oncol , vol.3 , pp. 325-345
    • LeBeau, M.1    Albain, K.S.2    Larson, R.A.3    Vardiman, J.4    Davis, E.5    Blough, R.6
  • 19
    • 0019445309 scopus 로고
    • Nonrandom chromosome abnormalities in acute leukemia and dysmyelopoietic syndromes in patients with previously treated malignant disease
    • Rowley JD, Golomb HM, Vardiman JW. Nonrandom chromosome abnormalities in acute leukemia and dysmyelopoietic syndromes in patients with previously treated malignant disease. Blood 1981;58:759-68.
    • (1981) Blood , vol.58 , pp. 759-768
    • Rowley, J.D.1    Golomb, H.M.2    Vardiman, J.W.3
  • 20
    • 0027185294 scopus 로고
    • Therapy-related myelodysplastic syndromes: FAB classification, bone marrow histology, and immunohistology in the prognostic assessment
    • Orazi A, Cattoretti G, Soligo D, Luksch R, Lambertenghi-Deliliers G. Therapy-related myelodysplastic syndromes: FAB classification, bone marrow histology, and immunohistology in the prognostic assessment. Leukemia 1993;7:838-847.
    • (1993) Leukemia , vol.7 , pp. 838-847
    • Orazi, A.1    Cattoretti, G.2    Soligo, D.3    Luksch, R.4    Deliliers, G.5
  • 21
    • 0025880799 scopus 로고
    • Therapy-related myelodysplastic syndrome and acute myeloid leukemia in children: Abnormalities of chromosome 5 and 7 are common
    • Rubin CM, Arthur DC, Woods WG, Lange BJ, Nowell PC, Rowley JD, et al. Therapy-related myelodysplastic syndrome and acute myeloid leukemia in children: abnormalities of chromosome 5 and 7 are common. Blood 1991;78:2982-7.
    • (1991) Blood , vol.78 , pp. 2982-2987
    • Rubin, C.M.1    Arthur, D.C.2    Woods, W.G.3    Lange, B.J.4    Nowell, P.C.5    Rowley, J.D.6
  • 22
    • 0028910402 scopus 로고
    • Childhood monosomy 7: Epidemiology, biology, and mechanistic implications
    • Luna-Fineman S, Shannon KM, Lange BJ. Childhood monosomy 7: epidemiology, biology, and mechanistic implications [review]. Blood 1995;85:1985-99.
    • (1995) Blood , vol.85 , pp. 1985-1999
    • Luna-Fineman, S.1    Shannon, K.M.2    Lange, B.J.3
  • 23
    • 0027219301 scopus 로고
    • Sequential development of Wilms tumor, T-cell acute lymphoblastic leukemia, medulloblastoma and myeloid leukemia in a child with type 1 neurofibromatosis: A clinical and cytogenetic case report
    • Perilongo G, Felix CA, Meadows AT, Nowell P, Biegel J, Lange BJ. Sequential development of Wilms tumor, T-cell acute lymphoblastic leukemia, medulloblastoma and myeloid leukemia in a child with type 1 neurofibromatosis: a clinical and cytogenetic case report. Leukemia 1993;7:912-5.
    • (1993) Leukemia , vol.7 , pp. 912-915
    • Perilongo, G.1    Felix, C.A.2    Meadows, A.T.3    Nowell, P.4    Biegel, J.5    Lange, B.J.6
  • 24
    • 0023885121 scopus 로고
    • Neurofibromatosis: Conference statement
    • NIH Consensus Development Conference. Neurofibromatosis: conference statement. Arch Neurol 1988;45:575-8.
    • (1988) Arch Neurol , vol.45 , pp. 575-578
  • 25
    • 0028090409 scopus 로고
    • Treatment of children with stages II to IV anaplastic Wilms' tumor: A report from the National Wilms' Tumor Study Group
    • Green DM, Beckwith JB, Breslow NE, Faria P, Moksness J, Finklestein JZ, et al. Treatment of children with stages II to IV anaplastic Wilms' tumor: a report from the National Wilms' Tumor Study Group. J Clin Oncol 1994;12:2126-31.
    • (1994) J Clin Oncol , vol.12 , pp. 2126-2131
    • Green, D.M.1    Beckwith, J.B.2    Breslow, N.E.3    Faria, P.4    Moksness, J.5    Finklestein, J.Z.6
  • 26
    • 0024372477 scopus 로고
    • The effectiveness of chemotherapy for treatment of high grade astrocytoma in children: Results of a randomized trial
    • Sposto R, Ertel IJ, Jenkin RDT, Boesel CP, Venes JL, Ortega JA, et al. The effectiveness of chemotherapy for treatment of high grade astrocytoma in children: results of a randomized trial. J Neurooncol 1989;7:165-77.
    • (1989) J Neurooncol , vol.7 , pp. 165-177
    • Sposto, R.1    Ertel, I.J.2    Rdt, J.3    Boesel, C.P.4    Venes, J.L.5    Ortega, J.A.6
  • 27
    • 0023765197 scopus 로고
    • Intensive therapy for children with acute lymphoblastic leukemia and unfavorable presenting features: Early conclusions of CCG 106 by the Children's Cancer Study Group
    • Gaynon PS, Steinherz PG, Bleyer WA, Ablin AR, Albo VE, Finkelstein JZ, et al. Intensive therapy for children with acute lymphoblastic leukemia and unfavorable presenting features: early conclusions of CCG 106 by the Children's Cancer Study Group. Lancet 1988;2(8617):921-4.
    • (1988) Lancet , vol.2 , Issue.8617 , pp. 921-924
    • Gaynon, P.S.1    Steinherz, P.G.2    Bleyer, W.A.3    Ablin, A.R.4    Albo, V.E.5    Finkelstein, J.Z.6
  • 28
    • 0024443745 scopus 로고
    • Familial bone marrow monosomy 7: Evidence that the predisposing locus is not on the long arm of chromosome 7
    • Shannon KM, Turhan AG, Chang SSY, Bowcock AM, Rogers PCJ, Carroll WL, et al. Familial bone marrow monosomy 7: evidence that the predisposing locus is not on the long arm of chromosome 7. J Clin Invest 1989;84:984-9.
    • (1989) J Clin Invest , vol.84 , pp. 984-989
    • Shannon, K.M.1    Turhan, A.G.2    Ssy, C.3    Bowcock, A.M.4    Rogers, P.C.J.5    Carroll, W.L.6
  • 29
    • 0025813519 scopus 로고
    • An Alu polymorphism intragenic to the neurofibromatosis type 1 gene
    • Xu G, Nelson L, O'Connell P, White R. An Alu polymorphism intragenic to the neurofibromatosis type 1 gene. Nucleic Acids Res 1991;19:3764.
    • (1991) Nucleic Acids Res , vol.19 , pp. 3764
    • Xu, G.1    Nelson, L.2    O'Connell, P.3    White, R.4
  • 30
    • 0027199643 scopus 로고
    • A highly informative compound nucleotide repeat in the neurofibromatosis (NF1) gene
    • Andersen LB, Tarle SA, Marchuk DA, Legius E, Collins FS. A highly informative compound nucleotide repeat in the neurofibromatosis (NF1) gene. Hum Mol Genet 1993; 2:1083-6.
    • (1993) Hum Mol Genet , vol.2 , pp. 1083-1086
    • Andersen, L.B.1    Tarle, S.A.2    Marchuk, D.A.3    Legius, E.4    Collins, F.S.5
  • 32
    • 0025293818 scopus 로고
    • Detection of ras gene mutations in human lung cancers by single- Strand conformation polymorphism analysis of polymerase chain reaction products
    • Suzuki Y, Orita M, Shiraishi M, Hayashi K, Sekiya T. Detection of ras gene mutations in human lung cancers by single-strand conformation polymorphism analysis of polymerase chain reaction products. Oncogene 1990;5:1037-43.
    • (1990) Oncogene , vol.5 , pp. 1037-1043
    • Suzuki, Y.1    Orita, M.2    Shiraishi, M.3    Hayashi, K.4    Sekiya, T.5
  • 33
    • 0028125213 scopus 로고
    • Genetic analysis is consistent with the hypothesis that NF1 limits myeloid cell growth through p21ras
    • Kalra R, Paderanga DC, Olson K, Shannon KM. Genetic analysis is consistent with the hypothesis that NF1 limits myeloid cell growth through p21ras. Blood 1994;84:3435-9.
    • (1994) Blood , vol.84 , pp. 3435-3439
    • Kalra, R.1    Paderanga, D.C.2    Olson, K.3    Shannon, K.M.4
  • 34
    • 0028807618 scopus 로고
    • Malignant transformation in patients with congenital neutropenia during treatment with recombinant granulocyte colony stimulating factor
    • Kalra R, Dale D, Freedman M, Bonilla MA, Weinblatt M, Ganser A, et al. Malignant transformation in patients with congenital neutropenia during treatment with recombinant granulocyte colony stimulating factor. Blood 1995;86:4579-86.
    • (1995) Blood , vol.86 , pp. 4579-4586
    • Kalra, R.1    Dale, D.2    Freedman, M.3    Ma, B.4    Weinblatt, M.5    Ganser, A.6
  • 35
    • 85080420089 scopus 로고
    • Allelic loss at the NF1 locus and hematopoietic lineage involvement in malignant bone marrows from children with neurofibromatosis type 1
    • Miles DK, Freedman MH, Stephens K, Pallavicinin M, Sievers E, Leppig K, et al. Allelic loss at the NF1 locus and hematopoietic lineage involvement in malignant bone marrows from children with neurofibromatosis type 1. Blood 1995; 86:51a.
    • (1995) Blood , vol.86
    • Miles, D.K.1    Freedman, M.H.2    Stephens, K.3    Pallavicinin, M.4    Sievers, E.5    Leppig, K.6
  • 37
    • 0026578223 scopus 로고
    • Prevalence of N-ras mutations in children with myelodysplastic syndromes and acute myeloid leukemia
    • Lubbert M, Mirro J, Kitchingman G, McCormick F, Mertelesmann R, Herrmann F, et al. Prevalence of N-ras mutations in children with myelodysplastic syndromes and acute myeloid leukemia. Oncogene 1992;7:263-8.
    • (1992) Oncogene , vol.7 , pp. 263-268
    • Lubbert, M.1    Mirro, J.2    Kitchingman, G.3    McCormick, F.4    Mertelesmann, R.5    Herrmann, F.6
  • 38
    • 0026101050 scopus 로고
    • Mutations of the ras protooncogenes in childhood monosomy 7
    • Neubauer A, Shannon K, Liu E. Mutations of the ras protooncogenes in childhood monosomy 7. Blood 1991;77:594-8.
    • (1991) Blood , vol.77 , pp. 594-598
    • Neubauer, A.1    Shannon, K.2    Liu, E.3
  • 40
    • 9044251606 scopus 로고    scopus 로고
    • Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in murine and human hematopoietic cells
    • Bollag G, Clapp DW, Shih S, Adler F, Zhang Y, Thompson P, et al. Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in murine and human hematopoietic cells. Nat Genet 1996;12:144-8.
    • (1996) Nat Genet , vol.12 , pp. 144-148
    • Bollag, G.1    Clapp, D.W.2    Shih, S.3    Adler, F.4    Zhang, Y.5    Thompson, P.6
  • 41
    • 0030045594 scopus 로고    scopus 로고
    • Nf1 deficiency causes Ras-mediated granulocyte-macrophage colony stimulating factor hypersensitivity and chronic myeloid leuekemia
    • Largaespada DA, Brannan CI, Jenkins NA, Copeland NG. Nf1 deficiency causes Ras-mediated granulocyte-macrophage colony stimulating factor hypersensitivity and chronic myeloid leuekemia. Nat Genet 1996;12:137-43.
    • (1996) Nat Genet , vol.12 , pp. 137-143
    • Largaespada, D.A.1    Brannan, C.I.2    Jenkins, N.A.3    Copeland, N.G.4
  • 42
    • 0022623369 scopus 로고
    • Second primary neoplasms in patients with retinoblastoma
    • Draper GJ, Sanders BM, Kingston JE. Second primary neoplasms in patients with retinoblastoma. Br J Cancer 1986; 53:661-71.
    • (1986) Br J Cancer , vol.53 , pp. 661-671
    • Draper, G.J.1    Sanders, B.M.2    Kingston, J.E.3
  • 43
    • 0028120348 scopus 로고
    • Molecular basis of neurofibromatosis type 1 (NF1): Mutation analysis and polymorphisms in the NF1 gene
    • Upadhyaya M, Shaw D, Harper P. Molecular basis of neurofibromatosis type 1 (NF1): mutation analysis and polymorphisms in the NF1 gene. Hum Mutat 1994;4:83-101.
    • (1994) Hum Mutat , vol.4 , pp. 83-101
    • Upadhyaya, M.1    Shaw, D.2    Harper, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.