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Volumn 22, Issue 3, 2010, Pages 268-273

Pediatric genitourinary tumors

Author keywords

Childhood cancer; Genitourinary; Germ cell tumor; Rhabdomyosarcoma; Testicle; Wilms tumor

Indexed keywords

CARBOPLATIN; CYCLOPHOSPHAMIDE; DACTINOMYCIN; DOXORUBICIN; ETOPOSIDE; FORKHEAD TRANSCRIPTION FACTOR; HYBRID PROTEIN; IFOSFAMIDE; INTEGRIN LINKED KINASE; IRINOTECAN; MICRORNA; PLATELET DERIVED GROWTH FACTOR ALPHA RECEPTOR; TRANSCRIPTION FACTOR PAX3; TRANSCRIPTION FACTOR PAX7; TUMOR PROTEIN; TUMOR SUPPRESSOR PROTEIN; VINCRISTINE;

EID: 77951467568     PISSN: 10408746     EISSN: None     Source Type: Journal    
DOI: 10.1097/CCO.0b013e32833841a1     Document Type: Review
Times cited : (7)

References (41)
  • 2
    • 50449097025 scopus 로고    scopus 로고
    • Use of positron emission tomography for staging, preoperative response assessment and posttherapeutic evaluation in children with Wilms tumour
    • Misch D, Steffen IG, Schonberger S, et al. Use of positron emission tomography for staging, preoperative response assessment and posttherapeutic evaluation in children with Wilms tumour. Eur J Nucl Med Mol Imaging 2008; 35:1642-1650.
    • (2008) Eur J Nucl Med Mol Imaging , vol.35 , pp. 1642-1650
    • Misch, D.1    Steffen, I.G.2    Schonberger, S.3
  • 3
    • 51649130716 scopus 로고    scopus 로고
    • Pre or postoperative therapy for Wilms' tumor?
    • D'Angio GJ. Pre or postoperative therapy for Wilms' tumor? J Clin Oncol 2008; 26:4055-4057.
    • (2008) J Clin Oncol , vol.26 , pp. 4055-4057
    • D'Angio, G.J.1
  • 4
    • 72549092942 scopus 로고    scopus 로고
    • Subsets of very low risk Wilms tumor show distinctive gene expression, histologic, and clinical features
    • Sredni ST, Gadd S, Huang CC, et al. Subsets of very low risk Wilms tumor show distinctive gene expression, histologic, and clinical features. Clin Cancer Res 2009; 15:6800-6809.
    • (2009) Clin Cancer Res , vol.15 , pp. 6800-6809
    • Sredni, S.T.1    Gadd, S.2    Huang, C.C.3
  • 5
    • 42449123046 scopus 로고    scopus 로고
    • The feasibility and outcome of nephron-sparing surgery for children with bilateral Wilms tumor. the St Jude Children's Research Hospital experience: 1999-2006
    • Davidoff AM, Giel DW, Jones DP, etal. The feasibility and outcome of nephron-sparing surgery for children with bilateral Wilms tumor. The St Jude Children's Research Hospital experience: 1 999-2006. Cancer 2008; 112:2060-2070.
    • (2008) Cancer , vol.112 , pp. 2060-2070
    • Davidoff, A.M.1    Giel, D.W.2    Jones, D.P.3
  • 7
    • 37549055839 scopus 로고    scopus 로고
    • Treatment of Wilms tumor relapsing after initial treatment with vincristine, actinomycin D, and doxorubicin
    • A report from the National Wilms Tumor Study Group
    • Malogolowkin M, Cotton CA, Green DM, et al. Treatment of Wilms tumor relapsing after initial treatment with vincristine, actinomycin D, and doxorubicin. A report from the National Wilms Tumor Study Group. Pediatr Blood Cancer 2008; 50:236-241.
    • (2008) Pediatr Blood Cancer , vol.50 , pp. 236-241
    • Malogolowkin, M.1    Cotton, C.A.2    Green, D.M.3
  • 9
    • 43049157909 scopus 로고    scopus 로고
    • Wilms tumor genetics: Mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors
    • Ruteshouser EC, Robinson SM, Huff V. Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors. Genes Chromosomes Cancer 2008; 47:461-470.
    • (2008) Genes Chromosomes Cancer , vol.47 , pp. 461-470
    • Ruteshouser, E.C.1    Robinson, S.M.2    Huff, V.3
  • 10
    • 61349113324 scopus 로고    scopus 로고
    • Canonical WNT signalling determines lineage specificity in Wilms tumour
    • Fukuzawa R, Anaka MR, Weeks RJ, et al. Canonical WNT signalling determines lineage specificity in Wilms tumour. Oncogene 2009; 28:1063-1075.
    • (2009) Oncogene , vol.28 , pp. 1063-1075
    • Fukuzawa, R.1    Anaka, M.R.2    Weeks, R.J.3
  • 11
    • 68549123567 scopus 로고    scopus 로고
    • WNT/beta-catenin pathway activation in Wilms tumors: A unifying mechanism with multiple entries?
    • Corbin M, de Reynies A, Rickman DS, et al. WNT/beta-catenin pathway activation in Wilms tumors: a unifying mechanism with multiple entries? Genes Chromosomes Cancer 2009; 48:816-827.
    • (2009) Genes Chromosomes Cancer , vol.48 , pp. 816-827
    • Corbin, M.1    De Reynies, A.2    Rickman, D.S.3
  • 12
    • 52049100974 scopus 로고    scopus 로고
    • Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein beta1 gene CTNNB1 for patients with Wilms tumors: Results of long-term surveillance of 71 patients from International Society of Pediatric Oncology Study 9/Society for Pediatric Oncology
    • Royer-Pokora B, Weirich A, Schumacher V, et al. Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein beta1 gene CTNNB1 for patients with Wilms tumors: results of long-term surveillance of 71 patients from International Society of Pediatric Oncology Study 9/Society for Pediatric Oncology. Cancer 2008; 113:1080-1089.
    • (2008) Cancer , vol.113 , pp. 1080-1089
    • Royer-Pokora, B.1    Weirich, A.2    Schumacher, V.3
  • 13
    • 55049098900 scopus 로고    scopus 로고
    • Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor
    • Scott RH, Douglas J, Baskcomb L, etal. Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor. Nat Genet 2008; 40:1329-1334.
    • (2008) Nat Genet , vol.40 , pp. 1329-1334
    • Scott, R.H.1    Douglas, J.2    Baskcomb, L.3
  • 14
    • 70350236512 scopus 로고    scopus 로고
    • WTX inactivation is a frequent, but late event in Wilms tumors without apparent clinical impact
    • Wegert J, Wittmann S, Leuschner I, etal. WTX inactivation is a frequent, but late event in Wilms tumors without apparent clinical impact. Genes Chromosomes Cancer 2009; 48:1102-1111.
    • (2009) Genes Chromosomes Cancer , vol.48 , pp. 1102-1111
    • Wegert, J.1    Wittmann, S.2    Leuschner, I.3
  • 15
    • 66249117651 scopus 로고    scopus 로고
    • The tumor suppressor WTX shuttles to the nucleus and modulates WT1 activity
    • Rivera MN, Kim WJ, Wells J, et al. The tumor suppressor WTX shuttles to the nucleus and modulates WT1 activity. Proc Natl Acad Sci USA 2009; 106:8338-8343.
    • (2009) Proc Natl Acad Sci USA , vol.106 , pp. 8338-8343
    • Rivera, M.N.1    Kim, W.J.2    Wells, J.3
  • 16
    • 58149157778 scopus 로고    scopus 로고
    • Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis
    • Jenkins ZA, van Kogelenberg M, Morgan T, etal. Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis. Nat Genet 2009; 41:95-100.
    • (2009) Nat Genet , vol.41 , pp. 95-100
    • Jenkins, Z.A.1    Van Kogelenberg, M.2    Morgan, T.3
  • 17
    • 73649141296 scopus 로고    scopus 로고
    • Frequent long-range epigenetic silencing of protocadherin gene clusters on chromosome 5q31 in Wilms' tumor
    • Dallosso AR, Hancock AL, Szemes M, et al. Frequent long-range epigenetic silencing of protocadherin gene clusters on chromosome 5q31 in Wilms' tumor. PLoS Genet 2009; 5:e1000745.
    • (2009) PLoS Genet , vol.5
    • Dallosso, A.R.1    Hancock, A.L.2    Szemes, M.3
  • 18
    • 49449102827 scopus 로고    scopus 로고
    • Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes
    • Fukuzawa R, Anaka MR, Heathcott RW, et al. Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes. J Pathol 2008; 215:377-387.
    • (2008) J Pathol , vol.215 , pp. 377-387
    • Fukuzawa, R.1    Anaka, M.R.2    Heathcott, R.W.3
  • 19
    • 64549113699 scopus 로고    scopus 로고
    • Paediatric renal tumours: Recent developments, new entities and pathological features
    • Sebire NJ, Vujanic GM. Paediatric renal tumours: recent developments, new entities and pathological features. Histopathology 2009; 54:516-528.
    • (2009) Histopathology , vol.54 , pp. 516-528
    • Sebire, N.J.1    Vujanic, G.M.2
  • 20
    • 47049104788 scopus 로고    scopus 로고
    • Imaging accuracy and incidence of Wilms' and non-Wilms' renal tumors in children
    • Miniati D, Gay AN, Parks KV, et al. Imaging accuracy and incidence of Wilms' and non-Wilms' renal tumors in children. J Pediatr Surg 2008; 43:1301-1307.
    • (2008) J Pediatr Surg , vol.43 , pp. 1301-1307
    • Miniati, D.1    Gay, A.N.2    Parks, K.V.3
  • 24
    • 70449698239 scopus 로고    scopus 로고
    • Vincristine, actinomycin, and cyclophosphamide compared with vincristine, actinomycin, and cyclopho sphamide alternating with vincristine, topotecan, and cyclophosphamide for intermediate-risk rhabdomyosarcoma: Children's oncology group study D9803
    • Arndt CA, Stoner JA, Hawkins DS, et al. Vincristine, actinomycin, and cyclophosphamide compared with vincristine, actinomycin, and cyclopho sphamide alternating with vincristine, topotecan, and cyclophosphamide for intermediate-risk rhabdomyosarcoma: children's oncology group study D9803. J Clin Oncol 2009; 27:5182-5188.
    • (2009) J Clin Oncol , vol.27 , pp. 5182-5188
    • Arndt, C.A.1    Stoner, J.A.2    Hawkins, D.S.3
  • 25
    • 68949090556 scopus 로고    scopus 로고
    • Prognostic significance of tumor response at the end of therapy in group III rhabdomyosarcoma: A report from the children's oncology group
    • Rodeberg DA, Stoner JA, Hayes-Jordan A, et al. Prognostic significance of tumor response at the end of therapy in group III rhabdomyosarcoma: a report from the children's oncology group. J Clin Oncol 2009; 27:3705-3711.
    • (2009) J Clin Oncol , vol.27 , pp. 3705-3711
    • Rodeberg, D.A.1    Stoner, J.A.2    Hayes-Jordan, A.3
  • 26
    • 70350602712 scopus 로고    scopus 로고
    • Sequential high-dose chemotherapy for children with metastatic rhabdomyosarcoma
    • Bisogno G, Ferrari A, Prete A, et al. Sequential high-dose chemotherapy for children with metastatic rhabdomyosarcoma. Eur J Cancer 2009; 45:3035-3041.
    • (2009) Eur J Cancer , vol.45 , pp. 3035-3041
    • Bisogno, G.1    Ferrari, A.2    Prete, A.3
  • 27
    • 77951448582 scopus 로고    scopus 로고
    • High-dose chemotherapy with blood or bone marrow transplants for rhabdomyosarcoma
    • [Epub ahead of print]
    • Stiff PJ, Agovi MA, Antman KH, et al. High-dose chemotherapy with blood or bone marrow transplants for rhabdomyosarcoma. Biol Blood Marrow Transplant 2009. [Epub ahead of print]
    • (2009) Biol Blood Marrow Transplant
    • Stiff, P.J.1    Agovi, M.A.2    Antman, K.H.3
  • 28
    • 41849086234 scopus 로고    scopus 로고
    • Bortezomib-mediated proteasome inhibition as a potential strategy for the treatment of rhabdomyosarcoma
    • Bersani F, Taulli R, Accornero P, et al. Bortezomib-mediated proteasome inhibition as a potential strategy for the treatment of rhabdomyosarcoma. Eur J Cancer 2008; 44:876-884.
    • (2008) Eur J Cancer , vol.44 , pp. 876-884
    • Bersani, F.1    Taulli, R.2    Accornero, P.3
  • 29
    • 59649085853 scopus 로고    scopus 로고
    • Molecular classification of rhabdomyosarcoma: Genotypic and phenotypic determinants of diagnosis-a report from the Children's Oncology Group
    • Davicioni E, Anderson MJ, Finckenstein FG, et al. Molecular classification of rhabdomyosarcoma: genotypic and phenotypic determinants of diagnosis-a report from the Children's Oncology Group. Am J Pathol 2009; 174:550-564.
    • (2009) Am J Pathol , vol.174 , pp. 550-564
    • Davicioni, E.1    Anderson, M.J.2    Finckenstein, F.G.3
  • 30
    • 67651006358 scopus 로고    scopus 로고
    • JNK1 determines the oncogenic or tumor-suppressive activity of the integrin-linked kinase in human rhabdomyosarcoma
    • Durbin AD, SomersGR, Forrester M, et al. JNK1 determines the oncogenic or tumor-suppressive activity of the integrin-linked kinase in human rhabdomyosarcoma. J Clin Invest 2009; 119:1558-1570.
    • (2009) J Clin Invest , vol.119 , pp. 1558-1570
    • Durbin, A.D.1    Somers, G.R.2    Forrester, M.3
  • 31
    • 68849118992 scopus 로고    scopus 로고
    • The muscle-specific microRNA miR-206 blocks human rhabdomyosarcoma growth in xenotransplanted mice by promoting myogenic differentiation
    • Taulli R, Bersani F, Foglizzo V, et al. The muscle-specific microRNA miR-206 blocks human rhabdomyosarcoma growth in xenotransplanted mice by promoting myogenic differentiation. J Clin Invest 2009; 119:2366-2378.
    • (2009) J Clin Invest , vol.119 , pp. 2366-2378
    • Taulli, R.1    Bersani, F.2    Foglizzo, V.3
  • 32
    • 55249083566 scopus 로고    scopus 로고
    • PDGFR-A is a therapeutic target in alveolar rhabdomyosarcoma
    • Taniguchi E, Nishijo K, McCleish AT, et al. PDGFR-A is a therapeutic target in alveolar rhabdomyosarcoma. Oncogene 2008; 27:6550-6560.
    • (2008) Oncogene , vol.27 , pp. 6550-6560
    • Taniguchi, E.1    Nishijo, K.2    McCleish, A.T.3
  • 33
    • 57149093809 scopus 로고    scopus 로고
    • Defining the cooperative genetic changes that temporally drive alveolar rhabdomyosarcoma
    • Naini S, Etheridge KT, Adam SJ, et al. Defining the cooperative genetic changes that temporally drive alveolar rhabdomyosarcoma. Cancer Res 2008; 68:9583-9588.
    • (2008) Cancer Res , vol.68 , pp. 9583-9588
    • Naini, S.1    Etheridge, K.T.2    Adam, S.J.3
  • 34
    • 67649227118 scopus 로고    scopus 로고
    • Prepubertal testicular tumors
    • Ross JH. Prepubertal testicular tumors. Urology 2009; 74:94-99.
    • (2009) Urology , vol.74 , pp. 94-99
    • Ross, J.H.1
  • 36
    • 67649562737 scopus 로고    scopus 로고
    • SALL4 is a novel diagnostic marker for testicular germ cell tumors
    • Cao D, Li J, Guo CC, et al. SALL4 is a novel diagnostic marker for testicular germ cell tumors. Am J Surg Pathol 2009; 33:1065-1077.
    • (2009) Am J Surg Pathol , vol.33 , pp. 1065-1077
    • Cao, D.1    Li, J.2    Guo, C.C.3
  • 37
    • 62449183529 scopus 로고    scopus 로고
    • Early and late mortality after diagnosis of Wilms tumor
    • Cotton CA, Peterson S, Norkool PA, et al. Early and late mortality after diagnosis of Wilms tumor. J Clin Oncol 2009; 27:1304-1309.
    • (2009) J Clin Oncol , vol.27 , pp. 1304-1309
    • Cotton, C.A.1    Peterson, S.2    Norkool, P.A.3
  • 38
    • 40749109443 scopus 로고    scopus 로고
    • Second primary neoplasms in survivors of Wilms' tumour: A population-based cohort study from the British Childhood Cancer Survivor Study
    • Taylor AJ, Winter DL, Pritchard-Jones K, et al. Second primary neoplasms in survivors of Wilms' tumour: a population-based cohort study from the British Childhood Cancer Survivor Study. Int J Cancer 2008; 122:2085-2093.
    • (2008) Int J Cancer , vol.122 , pp. 2085-2093
    • Taylor, A.J.1    Winter, D.L.2    Pritchard-Jones, K.3
  • 39
    • 67650360364 scopus 로고    scopus 로고
    • Comprehensive clinical follow-up of late effects in childhood cancer survivors shows the need for early and well timed intervention
    • Han JW, Kwon SY, Won SC, et al. Comprehensive clinical follow-up of late effects in childhood cancer survivors shows the need for early and well timed intervention. Ann Oncol 2009; 20:1170-1177.
    • (2009) Ann Oncol , vol.20 , pp. 1170-1177
    • Han, J.W.1    Kwon, S.Y.2    Won, S.C.3
  • 40
    • 65549147667 scopus 로고    scopus 로고
    • Psychological status in childhood cancer survivors: A report from the Childhood Cancer Survivor Study
    • Zeltzer LK, RecklitisC, Buchbinder D, et al. Psychological status in childhood cancer survivors: a report from the Childhood Cancer Survivor Study. J Clin Oncol 2009; 27:2396-2404.
    • (2009) J Clin Oncol , vol.27 , pp. 2396-2404
    • Zeltzer, L.K.1    Recklitis, C.2    Buchbinder, D.3


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