메뉴 건너뛰기




Volumn 59, Issue 6, 2000, Pages 539-543

Loss of heterozygosity on chromosome 19 in secondary glioblastomas

Author keywords

LOH on chromosome 19; Primary glioblastoma; Secondary glioblastoma

Indexed keywords

ARTICLE; CHROMOSOME 19; GENE AMPLIFICATION; GENE DELETION; GENE LOCUS; GENE MUTATION; GENE OVEREXPRESSION; GLIOBLASTOMA; HETEROZYGOSITY LOSS; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; PRIORITY JOURNAL;

EID: 0034084423     PISSN: 00223069     EISSN: None     Source Type: Journal    
DOI: 10.1093/jnen/59.6.539     Document Type: Article
Times cited : (126)

References (47)
  • 2
    • 0028087884 scopus 로고
    • Pathways leading to glioblastoma multiforme: A molecular analysis of genetic alterations in 65 astrocytic tumors
    • Lang FF, Miller DC, Koslow M, Newcomb EW. Pathways leading to glioblastoma multiforme: A molecular analysis of genetic alterations in 65 astrocytic tumors. J Neurosurg 1994;81:427-36
    • (1994) J Neurosurg , vol.81 , pp. 427-436
    • Lang, F.F.1    Miller, D.C.2    Koslow, M.3    Newcomb, E.W.4
  • 3
    • 0030017885 scopus 로고    scopus 로고
    • Overexpression of the EGF receptor and p53 mutations are mutually exclusive in the evolution of primary and secondary glioblastomas
    • Watanabe K, Tachibana O, Sato K, Yonekawa Y, Kleihues P, Ohgaki H. Overexpression of the EGF receptor and p53 mutations are mutually exclusive in the evolution of primary and secondary glioblastomas. Brain Pathol 1996;6:217-24
    • (1996) Brain Pathol , vol.6 , pp. 217-224
    • Watanabe, K.1    Tachibana, O.2    Sato, K.3    Yonekawa, Y.4    Kleihues, P.5    Ohgaki, H.6
  • 4
    • 0030881477 scopus 로고    scopus 로고
    • Alterations of cell cycle regulatory genes in primary (de novo) and secondary glioblastomas
    • Biernat W, Tohma Y, Yonekawa Y, Kleihues P, Ohgaki H. Alterations of cell cycle regulatory genes in primary (de novo) and secondary glioblastomas. Acta Neuropathol 1997;94:303-9
    • (1997) Acta Neuropathol , vol.94 , pp. 303-309
    • Biernat, W.1    Tohma, Y.2    Yonekawa, Y.3    Kleihues, P.4    Ohgaki, H.5
  • 5
    • 0031840405 scopus 로고    scopus 로고
    • PTEN (MMAC1) mutations are frequent in primary glioblastomas (de novo) but not in secondary glioblastomas
    • Tohma Y, Gratas C, Biernat W, et al. PTEN (MMAC1) mutations are frequent in primary glioblastomas (de novo) but not in secondary glioblastomas. J Neuropathol Exp Neurol 1998;57:684-89
    • (1998) J Neuropathol Exp Neurol , vol.57 , pp. 684-689
    • Tohma, Y.1    Gratas, C.2    Biernat, W.3
  • 6
    • 0032601166 scopus 로고    scopus 로고
    • Primary and secondary glioblastomas: From concept to clinical diagnosis
    • Kleihues P, Ohgaki H. Primary and secondary glioblastomas: From concept to clinical diagnosis. Neuro-Oncology 1999;1:44-51
    • (1999) Neuro-Oncology , vol.1 , pp. 44-51
    • Kleihues, P.1    Ohgaki, H.2
  • 7
    • 0030917734 scopus 로고    scopus 로고
    • Incidence and timing of p53 mutations during astrocytoma progression in patients with multiple biopsies
    • Watanabe K, Sato K, Biernat W, et al. Incidence and timing of p53 mutations during astrocytoma progression in patients with multiple biopsies. Clin Cancer Res 1997;3:523-30
    • (1997) Clin Cancer Res , vol.3 , pp. 523-530
    • Watanabe, K.1    Sato, K.2    Biernat, W.3
  • 8
    • 0033968345 scopus 로고    scopus 로고
    • Loss of heterozygosity on chromosome 10 is more extensive in primary (de novo) than in secondary glioblastomas
    • Fujisawa H, Reis R, Nakamura M, et al. Loss of heterozygosity on chromosome 10 is more extensive in primary (de novo) than in secondary glioblastomas. Lab Invest 2000;80:65-72
    • (2000) Lab Invest , vol.80 , pp. 65-72
    • Fujisawa, H.1    Reis, R.2    Nakamura, M.3
  • 9
    • 0032788101 scopus 로고    scopus 로고
    • Acquisition of the glioblastoma phenotype during astrocytoma progression is associated with LOH on chromosome 10q25-qter
    • Fujisawa H, Kurrer M, Reis RM, Yonekawa Y, Kleihues P, Ohgaki H. Acquisition of the glioblastoma phenotype during astrocytoma progression is associated with LOH on chromosome 10q25-qter. Am J Pathol 1999;155:387-94
    • (1999) Am J Pathol , vol.155 , pp. 387-394
    • Fujisawa, H.1    Kurrer, M.2    Reis, R.M.3    Yonekawa, Y.4    Kleihues, P.5    Ohgaki, H.6
  • 10
    • 0028335222 scopus 로고
    • Deletion mapping of chromosome 19 in human gliomas
    • von Deimling A, Nagel J, Bender B, et al. Deletion mapping of chromosome 19 in human gliomas. Int J Cancer 1994;57:676-80
    • (1994) Int J Cancer , vol.57 , pp. 676-680
    • Von Deimling, A.1    Nagel, J.2    Bender, B.3
  • 12
    • 0030070484 scopus 로고    scopus 로고
    • CDKN2/p16 or RB alterations occur in the majority of glioblastomas and are inversely correlated
    • Ueki K, Ono Y, Henson JW, Efird JT, von Deimling A, Louis DN. CDKN2/p16 or RB alterations occur in the majority of glioblastomas and are inversely correlated. Cancer Res 1996;56:150-53
    • (1996) Cancer Res , vol.56 , pp. 150-153
    • Ueki, K.1    Ono, Y.2    Henson, J.W.3    Efird, J.T.4    Von Deimling, A.5    Louis, D.N.6
  • 13
    • 0027943938 scopus 로고
    • The retinoblastoma gene is involved in malignant progression of astrocytomas
    • Henson JW, Schnitker BL, Correa KM, et al. The retinoblastoma gene is involved in malignant progression of astrocytomas. Ann Neurol 1994;36:714-21
    • (1994) Ann Neurol , vol.36 , pp. 714-721
    • Henson, J.W.1    Schnitker, B.L.2    Correa, K.M.3
  • 14
    • 0029736653 scopus 로고    scopus 로고
    • INK4A, MTS1) and CDK4 genes have frequent mutations of the retinoblastoma gene
    • INK4A, MTS1) and CDK4 genes have frequent mutations of the retinoblastoma gene. Oncogene 1996;13:1065-72
    • (1996) Oncogene , vol.13 , pp. 1065-1072
    • Ichimura, K.1    Schmidt, E.E.2    Goike, H.M.3    Collins, V.P.4
  • 15
    • 0028954148 scopus 로고
    • Region-specific loss of heterozygosity on chromosome 19 is related to the morphologic type of human glioma
    • Ritland SR, Ganju V, Jenkins RB. Region-specific loss of heterozygosity on chromosome 19 is related to the morphologic type of human glioma. Genes Chromosomes Cancer 1995;12:277-82
    • (1995) Genes Chromosomes Cancer , vol.12 , pp. 277-282
    • Ritland, S.R.1    Ganju, V.2    Jenkins, R.B.3
  • 16
    • 0028799791 scopus 로고
    • Shared allelic losses on chromosomes 1p and 19q suggest a common origin of oligodendroglioma and oligoastrocytoma
    • Kraus JA, Koopmann J, Kaskel P, et al. Shared allelic losses on chromosomes 1p and 19q suggest a common origin of oligodendroglioma and oligoastrocytoma. J Neuropathol Exp Neurol 1995;54:91-95
    • (1995) J Neuropathol Exp Neurol , vol.54 , pp. 91-95
    • Kraus, J.A.1    Koopmann, J.2    Kaskel, P.3
  • 17
    • 0029029912 scopus 로고
    • Chromosome 19q deletions in human gliomas overlap telomeric to D19S219 and may target a 425 kb region centromeric to D19S112
    • Yong WH, Chou D, Ucki K, et al. Chromosome 19q deletions in human gliomas overlap telomeric to D19S219 and may target a 425 kb region centromeric to D19S112. J Neuropathol Exp Neurol 1995;54:622-26
    • (1995) J Neuropathol Exp Neurol , vol.54 , pp. 622-626
    • Yong, W.H.1    Chou, D.2    Ucki, K.3
  • 18
    • 0030444184 scopus 로고    scopus 로고
    • Refined deletion mapping of the chromosome 19q glioma tumor suppressor gene to the D19S412-STD interval
    • Rosenberg JE, Lisle DK, Burwick JA, et al. Refined deletion mapping of the chromosome 19q glioma tumor suppressor gene to the D19S412-STD interval. Oncogene 1996;13:2483-85
    • (1996) Oncogene , vol.13 , pp. 2483-2485
    • Rosenberg, J.E.1    Lisle, D.K.2    Burwick, J.A.3
  • 19
    • 0033566061 scopus 로고    scopus 로고
    • Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype
    • Smith JS, Alderete B, Minn Y, et al. Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype. Oncogene 1999;18:4144-52
    • (1999) Oncogene , vol.18 , pp. 4144-4152
    • Smith, J.S.1    Alderete, B.2    Minn, Y.3
  • 21
    • 17144463441 scopus 로고    scopus 로고
    • Molecular genetic analysis as a tool for evaluating stereotactic biopsies of glioma specimens
    • Müller MB, Schmidt MC, Schmidt O, et al. Molecular genetic analysis as a tool for evaluating stereotactic biopsies of glioma specimens. J Neuropathol Exp Neurol 1999;58:40-45
    • (1999) J Neuropathol Exp Neurol , vol.58 , pp. 40-45
    • Müller, M.B.1    Schmidt, M.C.2    Schmidt, O.3
  • 22
    • 0030883778 scopus 로고    scopus 로고
    • Molecular genetic evidence for subtypes of oligoastrocytomas
    • Maintz D, Fiedler K, Koopmann J, et al. Molecular genetic evidence for subtypes of oligoastrocytomas. J Neuropathol Exp Neurol 1997;56:1098-1104
    • (1997) J Neuropathol Exp Neurol , vol.56 , pp. 1098-1104
    • Maintz, D.1    Fiedler, K.2    Koopmann, J.3
  • 23
    • 0032494479 scopus 로고    scopus 로고
    • Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas
    • Cairncross JG, Ueki K, Zlatescu MC, et al. Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas. J Natl Cancer Inst 1998;90: 1473-79
    • (1998) J Natl Cancer Inst , vol.90 , pp. 1473-1479
    • Cairncross, J.G.1    Ueki, K.2    Zlatescu, M.C.3
  • 24
    • 0026580876 scopus 로고
    • Primitive neuroectodermal tumors after prophylactic central nervous system irradiation in children. Association with an activated K-ras gene
    • Brüstle O, Ohgaki H, Schmitt HP, Walter GF, Ostertag H, Kleihues P. Primitive neuroectodermal tumors after prophylactic central nervous system irradiation in children. Association with an activated K-ras gene. Cancer 1992;69:2385-92
    • (1992) Cancer , vol.69 , pp. 2385-2392
    • Brüstle, O.1    Ohgaki, H.2    Schmitt, H.P.3    Walter, G.F.4    Ostertag, H.5    Kleihues, P.6
  • 25
    • 0027166048 scopus 로고
    • Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death
    • Oltvai ZN, Milliman CL, Korsmeyer SJ. Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death. Cell 1993;74:609-19
    • (1993) Cell , vol.74 , pp. 609-619
    • Oltvai, Z.N.1    Milliman, C.L.2    Korsmeyer, S.J.3
  • 26
    • 0029902618 scopus 로고    scopus 로고
    • The BAX gene maps to the glioma candidate region at 19q13.3, but is not altered in human gliomas
    • Chou D, Miyashita T, Mohrenweiser HW, et al. The BAX gene maps to the glioma candidate region at 19q13.3, but is not altered in human gliomas. Cancer Genet Cytogenet 1996;88:136-40
    • (1996) Cancer Genet Cytogenet , vol.88 , pp. 136-140
    • Chou, D.1    Miyashita, T.2    Mohrenweiser, H.W.3
  • 27
    • 0029121531 scopus 로고
    • Cloning of a highly conserved human protein Serine-Threonine phosphatase gene from the Glioma candidate region on chromosome 19q13.3
    • Yong WH, Ueki K, Chou D, et al. Cloning of a highly conserved human protein Serine-Threonine phosphatase gene from the Glioma candidate region on chromosome 19q13.3. Genomics 1995;29: 533-36
    • (1995) Genomics , vol.29 , pp. 533-536
    • Yong, W.H.1    Ueki, K.2    Chou, D.3
  • 28
    • 0028205559 scopus 로고
    • Molecular analysis of chromosome I abnormalities in human gliomas reveals frequent loss of 1p in oligodendroglial tumors
    • Bello MJ, Vaquero J, de Campos JM, et al. Molecular analysis of chromosome I abnormalities in human gliomas reveals frequent loss of 1p in oligodendroglial tumors. Int J Cancer 1994;57: 172-75
    • (1994) Int J Cancer , vol.57 , pp. 172-175
    • Bello, M.J.1    Vaquero, J.2    De Campos, J.M.3
  • 29
    • 0029092061 scopus 로고
    • Allelic status of chromosome 1 in neoplasms of the nervous system
    • Bello MJ, Leone PE, Nebreda P, et al. Allelic status of chromosome 1 in neoplasms of the nervous system. Cancer Genet Cytogenet 1995;83:160-64
    • (1995) Cancer Genet Cytogenet , vol.83 , pp. 160-164
    • Bello, M.J.1    Leone, P.E.2    Nebreda, P.3
  • 30
    • 0030812331 scopus 로고    scopus 로고
    • Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers
    • Kaghad M, Bonnet H, Yang A, et al. Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers. Cell 1997;90:809-19
    • (1997) Cell , vol.90 , pp. 809-819
    • Kaghad, M.1    Bonnet, H.2    Yang, A.3
  • 31
    • 0027362625 scopus 로고
    • The retinoblastoma protein binds to a family of E2F transcription factors
    • Lees JA, Saito M, Vidal M, et al. The retinoblastoma protein binds to a family of E2F transcription factors. Mol Cell Biol 1993;13: 7813-25
    • (1993) Mol Cell Biol , vol.13 , pp. 7813-7825
    • Lees, J.A.1    Saito, M.2    Vidal, M.3
  • 32
    • 0030984895 scopus 로고    scopus 로고
    • A newly identified member of the tumor necrosis factor receptor superfamily with a wide tissue distribution and involvement in lymphocyte activation
    • Kwon BS, Tan KB, Ni J, et al. A newly identified member of the tumor necrosis factor receptor superfamily with a wide tissue distribution and involvement in lymphocyte activation. J Biol Chem 1997;272:14272-76
    • (1997) J Biol Chem , vol.272 , pp. 14272-14276
    • Kwon, B.S.1    Tan, K.B.2    Ni, J.3
  • 33
    • 0025946360 scopus 로고
    • The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2-p36.3
    • Kemper O, Derre J, Cherif D, Engelmann H, Wallach D, Berger R. The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2-p36.3. Hum Genet 1991;87: 623-24
    • (1991) Hum Genet , vol.87 , pp. 623-624
    • Kemper, O.1    Derre, J.2    Cherif, D.3    Engelmann, H.4    Wallach, D.5    Berger, R.6
  • 34
    • 0030896087 scopus 로고    scopus 로고
    • TRAMP, a novel apoptosis-mediating receptor with sequence homology to tumor necrosis factor receptor 1 and Fas(Apo-1/CD95)
    • Bodmer JL, Burns K, Schneider P, et al. TRAMP, a novel apoptosis-mediating receptor with sequence homology to tumor necrosis factor receptor 1 and Fas(Apo-1/CD95). Immunity 1997;6:79-88
    • (1997) Immunity , vol.6 , pp. 79-88
    • Bodmer, J.L.1    Burns, K.2    Schneider, P.3
  • 35
    • 0031253977 scopus 로고    scopus 로고
    • KILLER/DR5 is a DNA damage-inducible p53-reguluted death receptor gene
    • Wu GS, Burns TF, McDonald ER, et al. KILLER/DR5 is a DNA damage-inducible p53-reguluted death receptor gene. Nat Genet 1997;17:141-43
    • (1997) Nat Genet , vol.17 , pp. 141-143
    • Wu, G.S.1    Burns, T.F.2    McDonald, E.R.3
  • 36
    • 14444278729 scopus 로고    scopus 로고
    • Characterization of the human homologue of RAD54: A gene located on chromosome 1p32 at a region of high loss of heterozygosity in breast tumors
    • Rasio D, Murakumo Y, Robbins D, et al. Characterization of the human homologue of RAD54: A gene located on chromosome 1p32 at a region of high loss of heterozygosity in breast tumors. Cancer Res 1997;57:2378-83
    • (1997) Cancer Res , vol.57 , pp. 2378-2383
    • Rasio, D.1    Murakumo, Y.2    Robbins, D.3
  • 37
    • 0029795614 scopus 로고    scopus 로고
    • A p18 mutant defective in CDK6 binding in human breast cancer cells
    • Lapointe J, Lachance Y, Labrie Y, Labrie C. A p18 mutant defective in CDK6 binding in human breast cancer cells. Cancer Res 1996;56:4586-89
    • (1996) Cancer Res , vol.56 , pp. 4586-4589
    • Lapointe, J.1    Lachance, Y.2    Labrie, Y.3    Labrie, C.4
  • 38
    • 0031766420 scopus 로고    scopus 로고
    • Expression level, allelic origin, and mutation analysis of the p73 gene in neuroblastoma tumors and cell lines
    • Kovalev S, Marchenko N, Swendeman S, LaQuaglia M, Moll UM. Expression level, allelic origin, and mutation analysis of the p73 gene in neuroblastoma tumors and cell lines. Cell Growth Differ 1998;9:897-903
    • (1998) Cell Growth Differ , vol.9 , pp. 897-903
    • Kovalev, S.1    Marchenko, N.2    Swendeman, S.3    LaQuaglia, M.4    Moll, U.M.5
  • 39
    • 0032143910 scopus 로고    scopus 로고
    • Genomic organization and mutation analysis of p73 in oligodendrogliomas with chromosome 1 p-arm deletions
    • Mai M, Huang H, Reed C, et al. Genomic organization and mutation analysis of p73 in oligodendrogliomas with chromosome 1 p-arm deletions. Genomics 1998;51:359-63
    • (1998) Genomics , vol.51 , pp. 359-363
    • Mai, M.1    Huang, H.2    Reed, C.3
  • 40
    • 13144293030 scopus 로고    scopus 로고
    • Mutational analysis of the p73 gene localized at chromosome 1p36.3 in colorectal carcinomas
    • Sunahara M, Ichimiya S, Nimura Y, et al. Mutational analysis of the p73 gene localized at chromosome 1p36.3 in colorectal carcinomas. Int J Oncol 1998;13:319-23
    • (1998) Int J Oncol , vol.13 , pp. 319-323
    • Sunahara, M.1    Ichimiya, S.2    Nimura, Y.3
  • 41
    • 0032053793 scopus 로고    scopus 로고
    • Search for mutations and examination of allelic expression imbalance of the p73 gene at 1p36.33 in human lung cancers
    • Nomoto S, Haruki N, Kondo M, et al. Search for mutations and examination of allelic expression imbalance of the p73 gene at 1p36.33 in human lung cancers. Cancer Res 1998;58:1380-83
    • (1998) Cancer Res , vol.58 , pp. 1380-1383
    • Nomoto, S.1    Haruki, N.2    Kondo, M.3
  • 42
    • 0032523842 scopus 로고    scopus 로고
    • Mutation, allelotyping, and transcription analyses of the p73 gene in prostatic carcinoma
    • Takahashi H, Ichimiya S, Nimura Y, et al. Mutation, allelotyping, and transcription analyses of the p73 gene in prostatic carcinoma. Cancer Res 1998;58:2076-77
    • (1998) Cancer Res , vol.58 , pp. 2076-2077
    • Takahashi, H.1    Ichimiya, S.2    Nimura, Y.3
  • 43
    • 0031906358 scopus 로고    scopus 로고
    • Molecular genetic correlates of p16, cdk4, and prb immunohistochemistry in glioblastomas
    • Burns KL, Ueki K, Jhung SL, Koh J, Louis DN. Molecular genetic correlates of p16, cdk4, and pRb immunohistochemistry in glioblastomas. J Neuropathol Exp Neurol 1998;57:122-30
    • (1998) J Neuropathol Exp Neurol , vol.57 , pp. 122-130
    • Burns, K.L.1    Ueki, K.2    Jhung, S.L.3    Koh, J.4    Louis, D.N.5
  • 44
    • 0022506980 scopus 로고
    • A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
    • Friend SH, Bernards R, Rogelj S, et al. A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma. Nature 1986;323:643-46
    • (1986) Nature , vol.323 , pp. 643-646
    • Friend, S.H.1    Bernards, R.2    Rogelj, S.3
  • 45
    • 0029007696 scopus 로고
    • Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13
    • Collins N, McManus R, Wooster R, et al. Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13. Oncogene 1995;10: 1673-75
    • (1995) Oncogene , vol.10 , pp. 1673-1675
    • Collins, N.1    McManus, R.2    Wooster, R.3
  • 46
    • 0028819984 scopus 로고
    • Different tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12-q13
    • Gudmundsson J, Johannesdottir G, Bergthorsson JT, et al. Different tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12-q13. Cancer Res 1995;55:4830-32
    • (1995) Cancer Res , vol.55 , pp. 4830-4832
    • Gudmundsson, J.1    Johannesdottir, G.2    Bergthorsson, J.T.3
  • 47
    • 0030056824 scopus 로고    scopus 로고
    • Alterations of retinoblastoma, p53, p16(CDKN2), and p15 genes in human astrocytomas
    • Tsuzuki T, Tsunoda S, Sukaki T, Konishi N, Hiasa Y, Nakamura M. Alterations of retinoblastoma, p53, p16(CDKN2), and p15 genes in human astrocytomas. Cancer 1996;78:287-93
    • (1996) Cancer , vol.78 , pp. 287-293
    • Tsuzuki, T.1    Tsunoda, S.2    Sukaki, T.3    Konishi, N.4    Hiasa, Y.5    Nakamura, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.