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Volumn 340, Issue 25, 1999, Pages 1954-1961

Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 17Q; CLINICAL TRIAL; CYTOGENETICS; GENE DELETION; GENETIC ANALYSIS; HUMAN; HUMAN CELL; HUMAN TISSUE; MAJOR CLINICAL STUDY; MULTICENTER STUDY; NEUROBLASTOMA; PREDICTION; PRIORITY JOURNAL; PROGNOSIS; SURVIVAL RATE;

EID: 0033600283     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJM199906243402504     Document Type: Article
Times cited : (463)

References (28)
  • 2
    • 0029977194 scopus 로고    scopus 로고
    • Role of ploidy, chromosome 1p, and Schwann cells in the maturation of neuroblastoma
    • Ambros IM, Zellner A, Roald B, et al. Role of ploidy, chromosome 1p, and Schwann cells in the maturation of neuroblastoma. N Engl J Med 1996;334:1505-11.
    • (1996) N Engl J Med , vol.334 , pp. 1505-1511
    • Ambros, I.M.1    Zellner, A.2    Roald, B.3
  • 3
    • 0022388606 scopus 로고
    • Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas
    • Seeger RC, Brodeur GM, Sather H, et al. Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas. N Engl J Med 1985;313:1111-6.
    • (1985) N Engl J Med , vol.313 , pp. 1111-1116
    • Seeger, R.C.1    Brodeur, G.M.2    Sather, H.3
  • 5
    • 0002947534 scopus 로고
    • Human neuroblastoma cytogenetics: Search for significance of homogeneously staining regions and double minute chromosomes
    • Evan AE, ed. New York: Raven Press
    • Biedler JL, Ross RA, Shanske S, Spengler BA. Human neuroblastoma cytogenetics: search for significance of homogeneously staining regions and double minute chromosomes. In: Evan AE, ed. Advances in neuroblastoma research. New York: Raven Press, 1980:81-96.
    • (1980) Advances in Neuroblastoma Research , pp. 81-96
    • Biedler, J.L.1    Ross, R.A.2    Shanske, S.3    Spengler, B.A.4
  • 6
    • 0021683414 scopus 로고
    • Human neuroblastomas and abnormalities of chromosomes 1 and 17
    • Gilbert F, Feder M, Balaban G, et al. Human neuroblastomas and abnormalities of chromosomes 1 and 17. Cancer Res 1984;44:5444-9.
    • (1984) Cancer Res , vol.44 , pp. 5444-5449
    • Gilbert, F.1    Feder, M.2    Balaban, G.3
  • 7
    • 0028023048 scopus 로고
    • Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells
    • Savelyeva L, Corvi R, Schwab M. Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells. Am J Hum Genet 1994;55:334-40.
    • (1994) Am J Hum Genet , vol.55 , pp. 334-340
    • Savelyeva, L.1    Corvi, R.2    Schwab, M.3
  • 8
    • 0028176145 scopus 로고
    • 1;17 Translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell lines
    • Van Roy N, Laureys G, Cheng NC, et al. 1;17 Translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell lines. Genes Chromosomes Cancer 1994;10:103-14.
    • (1994) Genes Chromosomes Cancer , vol.10 , pp. 103-114
    • Van Roy, N.1    Laureys, G.2    Cheng, N.C.3
  • 9
    • 10544222830 scopus 로고    scopus 로고
    • Additional copies of a 25 Mb chromosomal region originating from 17q23.1-17qter are present in 90% of high-grade neuroblastomas
    • Meddeb M, Danglot G, Chudoba I, et al. Additional copies of a 25 Mb chromosomal region originating from 17q23.1-17qter are present in 90% of high-grade neuroblastomas. Genes Chromosomes Cancer 1996;17:156-65.
    • (1996) Genes Chromosomes Cancer , vol.17 , pp. 156-165
    • Meddeb, M.1    Danglot, G.2    Chudoba, I.3
  • 10
    • 0030966604 scopus 로고    scopus 로고
    • Comparative genomic hybridization (CGH) analysis of neuroblastomas - An important methodological approach in paediatric tumour pathology
    • Brinkschmidt C, Christiansen H, Terpe HJ, et al. Comparative genomic hybridization (CGH) analysis of neuroblastomas - an important methodological approach in paediatric tumour pathology. J Pathol 1997; 181:394-400.
    • (1997) J Pathol , vol.181 , pp. 394-400
    • Brinkschmidt, C.1    Christiansen, H.2    Terpe, H.J.3
  • 11
    • 0031031692 scopus 로고    scopus 로고
    • Gain of chromosome 17 is the most frequent abnormality detected in neuroblastoma by comparative genomic hybridization
    • Plantaz D, Mohapatra G, Matthay KK, Pellarin M, Seeger RC, Feuerstein BG. Gain of chromosome 17 is the most frequent abnormality detected in neuroblastoma by comparative genomic hybridization. Am J Pathol 1997;150:81-9.
    • (1997) Am J Pathol , vol.150 , pp. 81-89
    • Plantaz, D.1    Mohapatra, G.2    Matthay, K.K.3    Pellarin, M.4    Seeger, R.C.5    Feuerstein, B.G.6
  • 12
    • 0030939571 scopus 로고    scopus 로고
    • Comparative genomic hybridization study of primary neuroblastoma tumors
    • Łastowska M, Nacheva E, McGuckin A, et al. Comparative genomic hybridization study of primary neuroblastoma tumors. Genes Chromosomes Cancer 1997;18:162-9.
    • (1997) Genes Chromosomes Cancer , vol.18 , pp. 162-169
    • ŁAstowska, M.1    Nacheva, E.2    McGuckin, A.3
  • 13
    • 0031418167 scopus 로고    scopus 로고
    • Sensitive and reliable detection of genomic imbalances in human neuroblastomas using comparative genomic hybridisation analysis
    • Van Gele M, Van Roy N, Jauch A, et al. Sensitive and reliable detection of genomic imbalances in human neuroblastomas using comparative genomic hybridisation analysis. Eur J Cancer 1997;33:1979-82.
    • (1997) Eur J Cancer , vol.33 , pp. 1979-1982
    • Van Gele, M.1    Van Roy, N.2    Jauch, A.3
  • 14
    • 0031665929 scopus 로고    scopus 로고
    • Genetic heterogeneity of neuroblastoma studied by comparative genomic hybridization
    • Vandesompele J, Van Roy N, Van Gele M, et al. Genetic heterogeneity of neuroblastoma studied by comparative genomic hybridization. Genes Chromosomes Cancer 1998;23:141-52.
    • (1998) Genes Chromosomes Cancer , vol.23 , pp. 141-152
    • Vandesompele, J.1    Van Roy, N.2    Van Gele, M.3
  • 16
    • 0028944776 scopus 로고
    • Allelic loss of chromosome 1 and additional chromosome 17 material are both unfavorable prognostic markers in neuroblastoma
    • Caron H. Allelic loss of chromosome 1 and additional chromosome 17 material are both unfavorable prognostic markers in neuroblastoma. Med Pediatr Oncol 1995;24:215-21.
    • (1995) Med Pediatr Oncol , vol.24 , pp. 215-221
    • Caron, H.1
  • 17
    • 13344275864 scopus 로고    scopus 로고
    • Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma
    • Caron H, van Sluis P, de Kraker J, et al. Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. N Engl J Med 1996;334:225-30.
    • (1996) N Engl J Med , vol.334 , pp. 225-230
    • Caron, H.1    Van Sluis, P.2    De Kraker, J.3
  • 18
    • 0031409099 scopus 로고    scopus 로고
    • Gain of chromosome arm 17q predicts unfavorable outcome in neuroblastoma patients
    • Łastowski M, Cotterill S, Pearson ADJ, et al. Gain of chromosome arm 17q predicts unfavorable outcome in neuroblastoma patients. Eur J Cancer 1997;33:1627-33.
    • (1997) Eur J Cancer , vol.33 , pp. 1627-1633
    • ŁAstowski, M.1    Cotterill, S.2    Pearson, A.D.J.3
  • 19
    • 0027239723 scopus 로고
    • Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment
    • Brodeur GM, Pritchard J, Berthold F, et al. Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment. J Clin Oncol 1993;11:1466-77.
    • (1993) J Clin Oncol , vol.11 , pp. 1466-1477
    • Brodeur, G.M.1    Pritchard, J.2    Berthold, F.3
  • 20
    • 0027537408 scopus 로고
    • Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization
    • du Manoir S, Speicher MR, Joos S, et al. Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. Hum Genet 1993;90:590-610.
    • (1993) Hum Genet , vol.90 , pp. 590-610
    • Du Manoir, S.1    Speicher, M.R.2    Joos, S.3
  • 21
    • 0026495364 scopus 로고
    • Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
    • Kallioniemi A, Kallioniemi OP, Sudar D, et al. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 1992;258:818-21.
    • (1992) Science , vol.258 , pp. 818-821
    • Kallioniemi, A.1    Kallioniemi, O.P.2    Sudar, D.3
  • 22
    • 0027516967 scopus 로고
    • Fluorescence in situ hybridization combined with immunohistochemistry for highly sensitive detection of chromosome 1 aberrations in neuroblastoma
    • Strehl S, Ambros PF. Fluorescence in situ hybridization combined with immunohistochemistry for highly sensitive detection of chromosome 1 aberrations in neuroblastoma. Cytogenet Cell Genet 1993;63:24-8.
    • (1993) Cytogenet Cell Genet , vol.63 , pp. 24-28
    • Strehl, S.1    Ambros, P.F.2
  • 23
    • 0026744941 scopus 로고
    • PCR assay for chromosome 1p deletion in small neuroblastoma samples
    • Peter M, Michon J, Vielh P, et al. PCR assay for chromosome 1p deletion in small neuroblastoma samples. Int J Cancer 1992;52:544-8.
    • (1992) Int J Cancer , vol.52 , pp. 544-548
    • Peter, M.1    Michon, J.2    Vielh, P.3
  • 24
    • 33845382806 scopus 로고
    • Nonparametric estimation from incomplete observations
    • Kaplan EL, Meier P. Nonparametric estimation from incomplete observations. J Am Stat Assoc 1958;53:457-81.
    • (1958) J Am Stat Assoc , vol.53 , pp. 457-481
    • Kaplan, E.L.1    Meier, P.2
  • 25
    • 0026584404 scopus 로고
    • A population-based study of neuroblastoma incidence, survival, and mortality in North America
    • Erratum, J Clin Oncol 1992;10:1202
    • Bernstein ML, Leclerc JM, Bunin G, et al. A population-based study of neuroblastoma incidence, survival, and mortality in North America. J Clin Oncol 1992;10:323-9. [Erratum, J Clin Oncol 1992;10:1202.]
    • (1992) J Clin Oncol , vol.10 , pp. 323-329
    • Bernstein, M.L.1    Leclerc, J.M.2    Bunin, G.3
  • 26
    • 0031687133 scopus 로고    scopus 로고
    • Molecular cytogenetic delineation of 17q translocation breakpoints in neuroblastoma cell lines
    • Łastowska M, Van Roy N, Bown N, et al. Molecular cytogenetic delineation of 17q translocation breakpoints in neuroblastoma cell lines. Genes Chromosomes Cancer 1998;23:116-22.
    • (1998) Genes Chromosomes Cancer , vol.23 , pp. 116-122
    • ŁAstowska, M.1    Van Roy, N.2    Bown, N.3
  • 27
    • 0031778631 scopus 로고    scopus 로고
    • Stage 4S neuroblastoma: What makes it special?
    • Matthay KK. Stage 4S neuroblastoma: what makes it special? J Clin Oncol 1998;16:2003-6.
    • (1998) J Clin Oncol , vol.16 , pp. 2003-2006
    • Matthay, K.K.1
  • 28
    • 0031749828 scopus 로고    scopus 로고
    • Prognostic significance of age, MYCN oncogene amplification, tumor cell ploidy, and histology in 110 infants with stage D(S) neuroblastoma: The Pediatric Oncology Group experience - A Pediatric Oncology Group study
    • Katzenstein HM, Bowman LC, Brodeur GM, et al. Prognostic significance of age, MYCN oncogene amplification, tumor cell ploidy, and histology in 110 infants with stage D(S) neuroblastoma: the Pediatric Oncology Group experience - a Pediatric Oncology Group study. J Clin Oncol 1998;16:2007-17.
    • (1998) J Clin Oncol , vol.16 , pp. 2007-2017
    • Katzenstein, H.M.1    Bowman, L.C.2    Brodeur, G.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.