메뉴 건너뛰기




Volumn 19, Issue 3, 2010, Pages 225-233

Pediatric oncology

Author keywords

Childhood cancer; Epigenetics; Genetics; Hereditary; Transformation

Indexed keywords

CHIMERIC PROTEIN; DNA; HISTONE; MICRORNA; PROTEIN P53; PROTEIN TYROSINE KINASE; RAS PROTEIN; TRANSCRIPTION FACTOR FKHR; TRANSCRIPTION FACTOR FLI 1; TRANSCRIPTION FACTOR PAX3; TRANSCRIPTION FACTOR PAX6; TRANSCRIPTION FACTOR PAX7;

EID: 77953939471     PISSN: 10558586     EISSN: None     Source Type: Journal    
DOI: 10.1053/j.sempedsurg.2010.03.007     Document Type: Article
Times cited : (37)

References (43)
  • 1
    • 0022539934 scopus 로고
    • Cancer incidence, survival, and mortality for children younger than age 15 years
    • Young J.L., Ries L.G., Silverberg E., et al. Cancer incidence, survival, and mortality for children younger than age 15 years. Cancer 1986, 58(suppl):598-602.
    • (1986) Cancer , vol.58 , Issue.SUPPL. , pp. 598-602
    • Young, J.L.1    Ries, L.G.2    Silverberg, E.3
  • 3
    • 0025637635 scopus 로고
    • The impact of childhood cancer on the United States and the world
    • Bleyer W.A. The impact of childhood cancer on the United States and the world. CA Cancer J Clin 1990, 40:355-367.
    • (1990) CA Cancer J Clin , vol.40 , pp. 355-367
    • Bleyer, W.A.1
  • 4
    • 0023099075 scopus 로고
    • Different karyotypic patterns in early and advanced stage neuroblastomas
    • Kaneko Y., Kanda N., Maseki N., et al. Different karyotypic patterns in early and advanced stage neuroblastomas. Cancer Res 1987, 47:311-318.
    • (1987) Cancer Res , vol.47 , pp. 311-318
    • Kaneko, Y.1    Kanda, N.2    Maseki, N.3
  • 5
    • 0021201236 scopus 로고
    • Cellular DNA content as a predictor of response to chemotherapy in infants with unresectable neuroblastoma
    • Look A.T., Hayes F.A., Nitschke R., et al. Cellular DNA content as a predictor of response to chemotherapy in infants with unresectable neuroblastoma. N Engl J Med 1984, 311:231-235.
    • (1984) N Engl J Med , vol.311 , pp. 231-235
    • Look, A.T.1    Hayes, F.A.2    Nitschke, R.3
  • 6
    • 0027230568 scopus 로고
    • Ewing sarcoma 11; 22 translocation produces a chimeric transcription factor that requires the DNA-binding domain encoded by FLI1 for transformation
    • May W.A., Gishizky M.L., Lessnick S.L., et al. Ewing sarcoma 11; 22 translocation produces a chimeric transcription factor that requires the DNA-binding domain encoded by FLI1 for transformation. Proc Natl Acad Sci U S A 1993, 90:5752-5756.
    • (1993) Proc Natl Acad Sci U S A , vol.90 , pp. 5752-5756
    • May, W.A.1    Gishizky, M.L.2    Lessnick, S.L.3
  • 7
    • 0027362619 scopus 로고
    • The Ewing's sarcoma EWS/FLI-1 fusion gene encodes a more potent transcriptional activator and is a more powerful transforming gene than FLI-1
    • May W.A., Lessnick S.L., Braun B.S., et al. The Ewing's sarcoma EWS/FLI-1 fusion gene encodes a more potent transcriptional activator and is a more powerful transforming gene than FLI-1. Mol Cell Biol 1993, 13:7393-7398.
    • (1993) Mol Cell Biol , vol.13 , pp. 7393-7398
    • May, W.A.1    Lessnick, S.L.2    Braun, B.S.3
  • 8
    • 0028307384 scopus 로고
    • A second Ewing's sarcoma translocation, t(21;22), fuses the EWS gene to another ETS-family transcription factor, ERG
    • Sorensen P.H., Lessnick S.L., Lopez-Terrada D., et al. A second Ewing's sarcoma translocation, t(21;22), fuses the EWS gene to another ETS-family transcription factor, ERG. Nat Genet 1994, 6:146-151.
    • (1994) Nat Genet , vol.6 , pp. 146-151
    • Sorensen, P.H.1    Lessnick, S.L.2    Lopez-Terrada, D.3
  • 9
    • 0027521658 scopus 로고
    • Fusion of a fork head domain gene to Pax3 in the solid tumour alveolar rhabdomyosarcoma
    • Galili N., Davis R.J., Fredericks W.J., et al. Fusion of a fork head domain gene to Pax3 in the solid tumour alveolar rhabdomyosarcoma. Nat Genet 1993, 5:230-235.
    • (1993) Nat Genet , vol.5 , pp. 230-235
    • Galili, N.1    Davis, R.J.2    Fredericks, W.J.3
  • 10
    • 0033118781 scopus 로고    scopus 로고
    • The role of chimeric paired box transcription factors in the pathogenesis of pediatric rhabdomysarcoma
    • Barr F.G. The role of chimeric paired box transcription factors in the pathogenesis of pediatric rhabdomysarcoma. Cancer Res 1999, 59(suppl):1711s-1715s.
    • (1999) Cancer Res , vol.59 , Issue.SUPPL.
    • Barr, F.G.1
  • 11
    • 0036605806 scopus 로고    scopus 로고
    • Pax3-FKHR and PAX7-FKHR gene fusions are prognostic indicators in alveolar rhabdomyosarcoma: A report from the Children's Oncology Group
    • Sorensen P.H., Lynch J.C., Qualman S.J., et al. Pax3-FKHR and PAX7-FKHR gene fusions are prognostic indicators in alveolar rhabdomyosarcoma: A report from the Children's Oncology Group. J Clin Oncol 2002, 20:2672-2679.
    • (2002) J Clin Oncol , vol.20 , pp. 2672-2679
    • Sorensen, P.H.1    Lynch, J.C.2    Qualman, S.J.3
  • 12
    • 0034906257 scopus 로고    scopus 로고
    • Molecular genetic aspects of solid tumors in childhood
    • Davidoff A.M., Hill D.A. Molecular genetic aspects of solid tumors in childhood. Semin Pediatr Surg 2001, 10:106-118.
    • (2001) Semin Pediatr Surg , vol.10 , pp. 106-118
    • Davidoff, A.M.1    Hill, D.A.2
  • 13
    • 33646589708 scopus 로고    scopus 로고
    • Mutations of the PTPN11 and RAS genes in rhabdomyosarcoma and pediatric hematological malignancies
    • Chen Y., Takita J., Hiwatari M., et al. Mutations of the PTPN11 and RAS genes in rhabdomyosarcoma and pediatric hematological malignancies. Genes Chromosomes Cancer 2006, 45:583-591.
    • (2006) Genes Chromosomes Cancer , vol.45 , pp. 583-591
    • Chen, Y.1    Takita, J.2    Hiwatari, M.3
  • 14
    • 0021047844 scopus 로고
    • Transposition and amplification of oncogene-related sequences in human neuroblastomas
    • Kohl N.E., Kanda N., Schreck R.R., et al. Transposition and amplification of oncogene-related sequences in human neuroblastomas. Cell 1983, 35:359-367.
    • (1983) Cell , vol.35 , pp. 359-367
    • Kohl, N.E.1    Kanda, N.2    Schreck, R.R.3
  • 15
    • 0029743372 scopus 로고    scopus 로고
    • Conditional expression of N-myc in human neuroblastoma cells increases expression of alpha-prothymosin and ornithine decarboxylase and accelerates progression into S-phase early after mitogenic stimulation of quiescent cells
    • Lutz W., Stohr M., Schurmann J., et al. Conditional expression of N-myc in human neuroblastoma cells increases expression of alpha-prothymosin and ornithine decarboxylase and accelerates progression into S-phase early after mitogenic stimulation of quiescent cells. Oncogene 1996, 13:803-812.
    • (1996) Oncogene , vol.13 , pp. 803-812
    • Lutz, W.1    Stohr, M.2    Schurmann, J.3
  • 16
    • 0023260866 scopus 로고
    • Consistent N-myc copy number in simultaneous or consecutive neuroblastoma samples from sixty individual patients
    • Brodeur G.M., Hayes F.A., Green A.A., et al. Consistent N-myc copy number in simultaneous or consecutive neuroblastoma samples from sixty individual patients. Cancer Res 1987, 47:4248-4253.
    • (1987) Cancer Res , vol.47 , pp. 4248-4253
    • Brodeur, G.M.1    Hayes, F.A.2    Green, A.A.3
  • 17
    • 0022388606 scopus 로고
    • Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas
    • Seeger R.C., Brodeur G.M., Sather H., et al. Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas. N Engl J Med 1985, 313:1111-1116.
    • (1985) N Engl J Med , vol.313 , pp. 1111-1116
    • Seeger, R.C.1    Brodeur, G.M.2    Sather, H.3
  • 18
    • 0030724929 scopus 로고    scopus 로고
    • Mutation analysis of p53 gene in childhood malignant solid tumors
    • Kusafuka T., Fukuzawa M., Oue T., et al. Mutation analysis of p53 gene in childhood malignant solid tumors. J Pediatr Surg 1997, 32:1175-1180.
    • (1997) J Pediatr Surg , vol.32 , pp. 1175-1180
    • Kusafuka, T.1    Fukuzawa, M.2    Oue, T.3
  • 19
    • 0025633582 scopus 로고
    • Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms
    • Malkin D., Li F.P., Strong L.C., et al. Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science 1990, 250:1233-1238.
    • (1990) Science , vol.250 , pp. 1233-1238
    • Malkin, D.1    Li, F.P.2    Strong, L.C.3
  • 20
    • 0017698493 scopus 로고
    • Chromosomal aberrations in human neuroblastomas
    • Brodeur G.M., Sekhon G., Goldstein M.N. Chromosomal aberrations in human neuroblastomas. Cancer 1977, 40:2256-2263.
    • (1977) Cancer , vol.40 , pp. 2256-2263
    • Brodeur, G.M.1    Sekhon, G.2    Goldstein, M.N.3
  • 21
    • 0024670859 scopus 로고
    • Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: Correlation with N-myc amplification
    • Fong C.T., Dracopoli N.C., White P.S., et al. Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: Correlation with N-myc amplification. Proc Natl Acad Sci U S A 1989, 86:3753-3757.
    • (1989) Proc Natl Acad Sci U S A , vol.86 , pp. 3753-3757
    • Fong, C.T.1    Dracopoli, N.C.2    White, P.S.3
  • 22
    • 46849107117 scopus 로고    scopus 로고
    • CHD5, a tumor suppressor gene deleted from 1p36.31 in neuroblastomas
    • Fujita T., Igarashi J., Okawa E.R., et al. CHD5, a tumor suppressor gene deleted from 1p36.31 in neuroblastomas. J Natl Cancer Inst 2008, 100:940-949.
    • (2008) J Natl Cancer Inst , vol.100 , pp. 940-949
    • Fujita, T.1    Igarashi, J.2    Okawa, E.R.3
  • 23
    • 28144453057 scopus 로고    scopus 로고
    • Chromosome 1p and 11q deletions and outcome in neuroblastoma
    • Attiyeh E.F., London W.B., Mosse Y.P., et al. Chromosome 1p and 11q deletions and outcome in neuroblastoma. N Engl J Med 2005, 353:2243-2253.
    • (2005) N Engl J Med , vol.353 , pp. 2243-2253
    • Attiyeh, E.F.1    London, W.B.2    Mosse, Y.P.3
  • 25
    • 31444451325 scopus 로고    scopus 로고
    • Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorable-histology Wilms tumor: A report from the National Wilms Tumor Study Group
    • Grundy P.E., Breslow N.E., Li S., et al. Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorable-histology Wilms tumor: A report from the National Wilms Tumor Study Group. J Clin Oncol 2005, 23:7312-7321.
    • (2005) J Clin Oncol , vol.23 , pp. 7312-7321
    • Grundy, P.E.1    Breslow, N.E.2    Li, S.3
  • 26
    • 0034066405 scopus 로고    scopus 로고
    • Caspase 8 is deleted or silenced preferentially in childhood neuroblastomas with amplification of MYCN
    • Teitz T., Wei T., Valentine M.B., et al. Caspase 8 is deleted or silenced preferentially in childhood neuroblastomas with amplification of MYCN. Nat Med 2000, 6:529-535.
    • (2000) Nat Med , vol.6 , pp. 529-535
    • Teitz, T.1    Wei, T.2    Valentine, M.B.3
  • 27
    • 0035855626 scopus 로고    scopus 로고
    • Sensitization for death receptor- or drug-induced apoptosis by re-expression of caspase-8 through demethylation or gene transfer
    • Fulda S., Kufer M., Meyer E., et al. Sensitization for death receptor- or drug-induced apoptosis by re-expression of caspase-8 through demethylation or gene transfer. Oncogene 2001, 20:5865-5877.
    • (2001) Oncogene , vol.20 , pp. 5865-5877
    • Fulda, S.1    Kufer, M.2    Meyer, E.3
  • 28
    • 0035955406 scopus 로고    scopus 로고
    • Molecular biology. Glimpses of a tiny RNA world
    • Ruvkun G. Molecular biology. Glimpses of a tiny RNA world. Science 2001, 294:797-799.
    • (2001) Science , vol.294 , pp. 797-799
    • Ruvkun, G.1
  • 29
    • 11844278458 scopus 로고    scopus 로고
    • Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets
    • Lewis B.P., Burge C.B., Bartel D.P. Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets. Cell 2005, 120:15-20.
    • (2005) Cell , vol.120 , pp. 15-20
    • Lewis, B.P.1    Burge, C.B.2    Bartel, D.P.3
  • 30
    • 69949089785 scopus 로고    scopus 로고
    • MicroRNA profiling identifies cancer-specific and prognostic signatures in pediatric malignancies
    • Wei J.S., Johansson P., Chen Q.R., et al. MicroRNA profiling identifies cancer-specific and prognostic signatures in pediatric malignancies. Clin Cancer Res 2009, 15:5560-5568.
    • (2009) Clin Cancer Res , vol.15 , pp. 5560-5568
    • Wei, J.S.1    Johansson, P.2    Chen, Q.R.3
  • 31
    • 0030766029 scopus 로고    scopus 로고
    • Genetic predisposition to cancer and familial cancer syndromes
    • Quesnel S., Malkin D. Genetic predisposition to cancer and familial cancer syndromes. Pediatr Clin North Am 1997, 44:791-808.
    • (1997) Pediatr Clin North Am , vol.44 , pp. 791-808
    • Quesnel, S.1    Malkin, D.2
  • 32
    • 0028059816 scopus 로고
    • Genetic events in the development of Wilms' tumor
    • Coppes M.J., Haber D.A., Grundy P.E. Genetic events in the development of Wilms' tumor. N Engl J Med 1994, 331:586-590.
    • (1994) N Engl J Med , vol.331 , pp. 586-590
    • Coppes, M.J.1    Haber, D.A.2    Grundy, P.E.3
  • 33
    • 0025099787 scopus 로고
    • Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
    • Call K.M., Glaser T., Ito C.Y., et al. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell 1990, 60:509-520.
    • (1990) Cell , vol.60 , pp. 509-520
    • Call, K.M.1    Glaser, T.2    Ito, C.Y.3
  • 34
    • 0025291908 scopus 로고
    • The candidate Wilms' tumour gene is involved in genitourinary development
    • Pritchard-Jones K., Fleming S., Davidson D., et al. The candidate Wilms' tumour gene is involved in genitourinary development. Nature 1990, 346:194-197.
    • (1990) Nature , vol.346 , pp. 194-197
    • Pritchard-Jones, K.1    Fleming, S.2    Davidson, D.3
  • 35
    • 0026315044 scopus 로고
    • Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region
    • Ton C.C., Hirvonen H., Miwa H., et al. Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region. Cell 1991, 67:1059-1074.
    • (1991) Cell , vol.67 , pp. 1059-1074
    • Ton, C.C.1    Hirvonen, H.2    Miwa, H.3
  • 36
    • 0026094584 scopus 로고
    • Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
    • Pelletier J., Bruening W., Kashtan C.E., et al. Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell 1991, 67:437-447.
    • (1991) Cell , vol.67 , pp. 437-447
    • Pelletier, J.1    Bruening, W.2    Kashtan, C.E.3
  • 37
    • 0028298044 scopus 로고
    • Fine structure analysis of the WT1 gene in sporadic Wilms tumors
    • Varanasi R., Bardeesy N., Ghahremani M., et al. Fine structure analysis of the WT1 gene in sporadic Wilms tumors. Proc Natl Acad Sci U S A 1994, 91:3554-3558.
    • (1994) Proc Natl Acad Sci U S A , vol.91 , pp. 3554-3558
    • Varanasi, R.1    Bardeesy, N.2    Ghahremani, M.3
  • 38
    • 0026685962 scopus 로고
    • Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination
    • Coppes M.J., Bonetta L., Huang A., et al. Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination. Genes Chromosomes Cancer 1992, 5:326-334.
    • (1992) Genes Chromosomes Cancer , vol.5 , pp. 326-334
    • Coppes, M.J.1    Bonetta, L.2    Huang, A.3
  • 39
    • 0024517062 scopus 로고
    • Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5
    • Koufos A., Grundy P., Morgan K., et al. Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. Am J Hum Genet 1989, 44:711-719.
    • (1989) Am J Hum Genet , vol.44 , pp. 711-719
    • Koufos, A.1    Grundy, P.2    Morgan, K.3
  • 40
    • 54049094708 scopus 로고    scopus 로고
    • Identification of ALK as a major familial neuroblastoma predisposition gene
    • Mosse Y.P., Laudenslager M., Longo L., et al. Identification of ALK as a major familial neuroblastoma predisposition gene. Nature 2008, 455:930-935.
    • (2008) Nature , vol.455 , pp. 930-935
    • Mosse, Y.P.1    Laudenslager, M.2    Longo, L.3
  • 41
    • 45149123645 scopus 로고    scopus 로고
    • Chromosome 6p22 locus associated with clinically aggressive neuroblastoma
    • Maris J.M., Mosse Y.P., Bradfield J.P., et al. Chromosome 6p22 locus associated with clinically aggressive neuroblastoma. N Engl J Med 2008, 358:2585-2593.
    • (2008) N Engl J Med , vol.358 , pp. 2585-2593
    • Maris, J.M.1    Mosse, Y.P.2    Bradfield, J.P.3
  • 42
    • 67349156045 scopus 로고    scopus 로고
    • Common variations in BARD1 influence susceptibility to high-risk neuroblastoma
    • Capasso M., Devoto M., Hou C., et al. Common variations in BARD1 influence susceptibility to high-risk neuroblastoma. Nat Genet 2009, 41:718-723.
    • (2009) Nat Genet , vol.41 , pp. 718-723
    • Capasso, M.1    Devoto, M.2    Hou, C.3
  • 43
    • 67649289900 scopus 로고    scopus 로고
    • Copy number variation at 1q21.1 associated with neuroblastoma
    • Diskin S.J., Hou C., Glessner J.T., et al. Copy number variation at 1q21.1 associated with neuroblastoma. Nature 2009, 459:987-991.
    • (2009) Nature , vol.459 , pp. 987-991
    • Diskin, S.J.1    Hou, C.2    Glessner, J.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.