메뉴 건너뛰기




Volumn 47, Issue 8, 2015, Pages 864-871

Relapsed neuroblastomas show frequent RAS-MAPK pathway mutations

(46)  Eleveld, Thomas F a   Oldridge, Derek A b,c   Bernard, Virginie d   Koster, Jan a   Daage, Leo Colmet d   Diskin, Sharon J b,c   Schild, Linda a   Bentahar, Nadia Bessoltane d   Bellini, Angela d   Chicard, Mathieu d   Lapouble, Eve d   Combaret, Valérie e   Legoix Né, Patricia d   Michon, Jean d   Pugh, Trevor J f   Hart, Lori S b   Rader, Julieann b   Attiyeh, Edward F b,c   Wei, Jun S g   Zhang, Shile g   more..


Author keywords

[No Author keywords available]

Indexed keywords

BINIMETINIB; COBIMETINIB; MITOGEN ACTIVATED PROTEIN KINASE; PROTEIN P14; PROTEIN TYROSINE KINASE; PROTEIN TYROSINE PHOSPHATASE SHP 2; RAS PROTEIN; TRAMETINIB; ANAPLASTIC LYMPHOMA KINASE; BENZIMIDAZOLE DERIVATIVE; CYCLIN DEPENDENT KINASE INHIBITOR 2A;

EID: 84938268035     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.3333     Document Type: Article
Times cited : (423)

References (43)
  • 1
    • 41149137119 scopus 로고    scopus 로고
    • Localized infant neuroblastomas often show spontaneous regression: Results of the prospective trials NB95-S and NB97
    • Hero, B. et al. Localized infant neuroblastomas often show spontaneous regression: Results of the prospective trials NB95-S and NB97. J. Clin. Oncol. 26, 1504-1510 (2008).
    • (2008) J. Clin. Oncol , vol.26 , pp. 1504-1510
    • Hero, B.1
  • 2
    • 84876430459 scopus 로고    scopus 로고
    • Children's Oncology Group's 2013 blueprint for research: Neuroblastoma
    • Park, J.R. et al. Children's Oncology Group's 2013 blueprint for research: Neuroblastoma. Pediatr. Blood Cancer 60, 985-993 (2013).
    • (2013) Pediatr. Blood Cancer , vol.60 , pp. 985-993
    • Park, J.R.1
  • 3
    • 79551628428 scopus 로고    scopus 로고
    • Treatment and outcomes of patients with relapsed, high-risk neuroblastoma: Results of German trials
    • Simon, T. et al. Treatment and outcomes of patients with relapsed, high-risk neuroblastoma: Results of German trials. Pediatr. Blood Cancer 56, 578-583 (2011).
    • (2011) Pediatr. Blood Cancer , vol.56 , pp. 578-583
    • Simon, T.1
  • 4
    • 77953523121 scopus 로고    scopus 로고
    • Recent advances in neuroblastoma
    • Maris, J.M. Recent advances in neuroblastoma. N. Engl. J. Med. 362, 2202-2211 (2010).
    • (2010) N. Engl. J. Med , vol.362 , pp. 2202-2211
    • Maris, J.M.1
  • 5
    • 58249093955 scopus 로고    scopus 로고
    • The International Neuroblastoma Risk Group (INRG) classification system: An INRG Task Force report
    • Cohn, S.L. et al. The International Neuroblastoma Risk Group (INRG) classification system: An INRG Task Force report. J. Clin. Oncol. 27, 289-297 (2009).
    • (2009) J. Clin. Oncol , vol.27 , pp. 289-297
    • Cohn, S.L.1
  • 6
    • 0033600283 scopus 로고    scopus 로고
    • Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma
    • Bown, N. et al. Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma. N. Engl. J. Med. 340, 1954-1961 (1999).
    • (1999) N. Engl. J. Med , vol.340 , pp. 1954-1961
    • Bown, N.1
  • 7
    • 28144453057 scopus 로고    scopus 로고
    • Chromosome 1p and 11q deletions and outcome in neuroblastoma
    • Attiyeh, E.F. et al. Chromosome 1p and 11q deletions and outcome in neuroblastoma. N. Engl. J. Med. 353, 2243-2253 (2005).
    • (2005) N. Engl. J. Med , vol.353 , pp. 2243-2253
    • Attiyeh, E.F.1
  • 8
    • 0022388606 scopus 로고
    • Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas
    • Seeger, R.C. et al. Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas. N. Engl. J. Med. 313, 1111-1116 (1985).
    • (1985) N. Engl. J. Med , vol.313 , pp. 1111-1116
    • Seeger, R.C.1
  • 9
    • 13344275864 scopus 로고    scopus 로고
    • Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma
    • Caron, H. et al. Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. N. Engl. J. Med. 334, 225-230 (1996).
    • (1996) N. Engl. J. Med , vol.334 , pp. 225-230
    • Caron, H.1
  • 10
    • 84858248558 scopus 로고    scopus 로고
    • Association of age at diagnosis and genetic mutations in patients with neuroblastoma
    • Cheung, N.K. et al. Association of age at diagnosis and genetic mutations in patients with neuroblastoma. J. Am. Med. Assoc. 307, 1062-1071 (2012).
    • (2012) J. Am. Med. Assoc , vol.307 , pp. 1062-1071
    • Cheung, N.K.1
  • 11
    • 84859216598 scopus 로고    scopus 로고
    • Sequencing of neuroblastoma identifies chromothripsis and defects in neuritogenesis genes
    • Molenaar, J.J. et al. Sequencing of neuroblastoma identifies chromothripsis and defects in neuritogenesis genes. Nature 483, 589-593 (2012).
    • (2012) Nature , vol.483 , pp. 589-593
    • Molenaar, J.J.1
  • 12
    • 84874664731 scopus 로고    scopus 로고
    • The genetic landscape of high-risk neuroblastoma
    • Pugh, T.J. et al. The genetic landscape of high-risk neuroblastoma. Nat. Genet. 45, 279-284 (2013).
    • (2013) Nat. Genet , vol.45 , pp. 279-284
    • Pugh, T.J.1
  • 13
    • 84871982155 scopus 로고    scopus 로고
    • Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
    • Sausen, M. et al. Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma. Nat. Genet. 45, 12-17 (2013).
    • (2013) Nat. Genet , vol.45 , pp. 12-17
    • Sausen, M.1
  • 14
    • 60549088714 scopus 로고    scopus 로고
    • Radiolabeled metaiodobenzylguanidine for imaging and therapy of neuroblastoma
    • Taggart, D., Dubois, S. & Matthay, K.K. Radiolabeled metaiodobenzylguanidine for imaging and therapy of neuroblastoma. Q. J. Nucl. Med. Mol. Imaging 52, 403-418 (2008).
    • (2008) Q. J. Nucl. Med. Mol. Imaging , vol.52 , pp. 403-418
    • Taggart, D.1    Dubois, S.2    Matthay, K.K.3
  • 15
    • 84906819212 scopus 로고    scopus 로고
    • Emergence of new ALK mutations at relapse of neuroblastoma
    • Schleiermacher, G. et al. Emergence of new ALK mutations at relapse of neuroblastoma. J. Clin. Oncol. 32, 2727-2734 (2014).
    • (2014) J. Clin. Oncol , vol.32 , pp. 2727-2734
    • Schleiermacher, G.1
  • 16
    • 84860782006 scopus 로고    scopus 로고
    • Absolute quantification of somatic DNA alterations in human cancer
    • Carter, S.L. et al. Absolute quantification of somatic DNA alterations in human cancer. Nat. Biotechnol. 30, 413-421 (2012).
    • (2012) Nat. Biotechnol , vol.30 , pp. 413-421
    • Carter, S.L.1
  • 18
    • 1542515338 scopus 로고    scopus 로고
    • A census of human cancer genes
    • Futreal, P.A. et al. A census of human cancer genes. Nat. Rev. Cancer 4, 177-183 (2004).
    • (2004) Nat. Rev. Cancer , vol.4 , pp. 177-183
    • Futreal, P.A.1
  • 19
    • 84912059340 scopus 로고    scopus 로고
    • ALK mutations confer differential oncogenic activation and sensitivity to ALK inhibition therapy in neuroblastoma
    • Bresler, S.C. et al. ALK mutations confer differential oncogenic activation and sensitivity to ALK inhibition therapy in neuroblastoma. Cancer Cell 26, 682-694 (2014).
    • (2014) Cancer Cell , vol.26 , pp. 682-694
    • Bresler, S.C.1
  • 20
    • 77955038485 scopus 로고    scopus 로고
    • NF1 is a tumor suppressor in neuroblastoma that determines retinoic acid response and disease outcome
    • Hölzel, M. et al. NF1 is a tumor suppressor in neuroblastoma that determines retinoic acid response and disease outcome. Cell 142, 218-229 (2010).
    • (2010) Cell , vol.142 , pp. 218-229
    • Hölzel, M.1
  • 21
    • 31544452561 scopus 로고    scopus 로고
    • Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease
    • Tartaglia, M. et al. Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease. Am. J. Hum. Genet. 78, 279-290 (2006).
    • (2006) Am. J. Hum. Genet , vol.78 , pp. 279-290
    • Tartaglia, M.1
  • 22
    • 76749166680 scopus 로고    scopus 로고
    • High frequency of p53/MDM2/p14ARF pathway abnormalities in relapsed neuroblastoma
    • Carr-Wilkinson, J. et al. High frequency of p53/MDM2/p14ARF pathway abnormalities in relapsed neuroblastoma. Clin. Cancer Res. 16, 1108-1118 (2010).
    • (2010) Clin. Cancer Res , vol.16 , pp. 1108-1118
    • Carr-Wilkinson, J.1
  • 23
    • 84859187259 scopus 로고    scopus 로고
    • Systematic identification of genomic markers of drug sensitivity in cancer cells
    • Garnett, M.J. et al. Systematic identification of genomic markers of drug sensitivity in cancer cells. Nature 483, 570-575 (2012).
    • (2012) Nature , vol.483 , pp. 570-575
    • Garnett, M.J.1
  • 24
    • 77955477995 scopus 로고    scopus 로고
    • Accumulation of segmental alterations determines progression in neuroblastoma
    • Schleiermacher, G. et al. Accumulation of segmental alterations determines progression in neuroblastoma. J. Clin. Oncol. 28, 3122-3130 (2010).
    • (2010) J. Clin. Oncol , vol.28 , pp. 3122-3130
    • Schleiermacher, G.1
  • 25
    • 84874102335 scopus 로고    scopus 로고
    • Evolution and impact of subclonal mutations in chronic lymphocytic leukemia
    • Landau, D.A. et al. Evolution and impact of subclonal mutations in chronic lymphocytic leukemia. Cell 152, 714-726 (2013).
    • (2013) Cell , vol.152 , pp. 714-726
    • Landau, D.A.1
  • 26
    • 84923341318 scopus 로고    scopus 로고
    • Increased MAPK reactivation in early resistance to dabrafenib/trametinib combination therapy of BRAF-mutant metastatic melanoma
    • Long, G.V. Increased MAPK reactivation in early resistance to dabrafenib/trametinib combination therapy of BRAF-mutant metastatic melanoma. Nat. Commun. 5, 5694 (2014).
    • (2014) Nat. Commun , vol.5 , pp. 5694
    • Long, G.V.1
  • 27
    • 54049120220 scopus 로고    scopus 로고
    • Activating mutations in ALK provide a therapeutic target in neuroblastoma
    • George, R.E. et al. Activating mutations in ALK provide a therapeutic target in neuroblastoma. Nature 455, 975-978 (2008).
    • (2008) Nature , vol.455 , pp. 975-978
    • George, R.E.1
  • 28
    • 84876966952 scopus 로고    scopus 로고
    • Safety and activity of crizotinib for paediatric patients with refractory solid tumours or anaplastic large-cell lymphoma: A Children's Oncology Group phase 1 consortium study
    • Mossé, Y.P. et al. Safety and activity of crizotinib for paediatric patients with refractory solid tumours or anaplastic large-cell lymphoma: A Children's Oncology Group phase 1 consortium study. Lancet Oncol. 14, 472-480 (2013).
    • (2013) Lancet Oncol , vol.14 , pp. 472-480
    • Mossé, Y.P.1
  • 29
    • 84863753157 scopus 로고    scopus 로고
    • The ALKF1174L mutation potentiates the oncogenic activity of MYCN in neuroblastoma
    • Berry, T. et al. The ALKF1174L mutation potentiates the oncogenic activity of MYCN in neuroblastoma. Cancer Cell 22, 117-130 (2012).
    • (2012) Cancer Cell , vol.22 , pp. 117-130
    • Berry, T.1
  • 30
    • 84908011214 scopus 로고    scopus 로고
    • Molecular rationale for the use of PI3K/AKT/mTOR pathway inhibitors in combination with crizotinib in ALK-mutated neuroblastoma
    • Moore, N.F. et al. Molecular rationale for the use of PI3K/AKT/mTOR pathway inhibitors in combination with crizotinib in ALK-mutated neuroblastoma. Oncotarget 5, 8737-8749 (2014).
    • (2014) Oncotarget , vol.5 , pp. 8737-8749
    • Moore, N.F.1
  • 31
    • 74949138753 scopus 로고    scopus 로고
    • Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
    • Drmanac, R. et al. Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays. Science 327, 78-81 (2010).
    • (2010) Science , vol.327 , pp. 78-81
    • Drmanac, R.1
  • 32
    • 84922572688 scopus 로고    scopus 로고
    • Sequenza: Allele-specific copy number and mutation profiles from tumor sequencing data
    • Favero, F. et al. Sequenza: Allele-specific copy number and mutation profiles from tumor sequencing data. Ann. Oncol. 26, 64-70 (2015).
    • (2015) Ann. Oncol , vol.26 , pp. 64-70
    • Favero, F.1
  • 33
    • 69649109364 scopus 로고    scopus 로고
    • Circos: An information aesthetic for comparative genomics
    • Krzywinski, M. et al. Circos: An information aesthetic for comparative genomics. Genome Res. 19, 1639-1645 (2009).
    • (2009) Genome Res , vol.19 , pp. 1639-1645
    • Krzywinski, M.1
  • 34
    • 67649884743 scopus 로고    scopus 로고
    • Fast and accurate short read alignment with Burrows-Wheeler transform
    • Li, H. & Durbin, R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25, 1754-1760 (2009).
    • (2009) Bioinformatics , vol.25 , pp. 1754-1760
    • Li, H.1    Durbin, R.2
  • 35
    • 77956295988 scopus 로고    scopus 로고
    • The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
    • McKenna, A. et al. The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res. 20, 1297-1303 (2010).
    • (2010) Genome Res , vol.20 , pp. 1297-1303
    • McKenna, A.1
  • 36
    • 84874025843 scopus 로고    scopus 로고
    • Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
    • Cibulskis, K. et al. Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat. Biotechnol. 31, 213-219 (2013).
    • (2013) Nat. Biotechnol , vol.31 , pp. 213-219
    • Cibulskis, K.1
  • 37
    • 77956534324 scopus 로고    scopus 로고
    • ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data
    • Wang, K., Li, M. & Hakonarson, H. ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res. 38, e164 (2010).
    • (2010) Nucleic Acids Res , vol.38 , pp. e164
    • Wang, K.1    Li, M.2    Hakonarson, H.3
  • 38
    • 84975795680 scopus 로고    scopus 로고
    • An integrated map of genetic variation from 1, 092 human genomes
    • 1000 Genomes Project Consortium.
    • 1000 Genomes Project Consortium. An integrated map of genetic variation from 1, 092 human genomes. Nature 491, 56-65 (2012).
    • (2012) Nature , vol.491 , pp. 56-65
  • 39
    • 84866440781 scopus 로고    scopus 로고
    • DELLY: Structural variant discovery by integrated paired-end and split-read analysis
    • Rausch, T. et al. DELLY: Structural variant discovery by integrated paired-end and split-read analysis. Bioinformatics 28, i333-i339 (2012).
    • (2012) Bioinformatics , vol.28 , pp. i333-i339
    • Rausch, T.1
  • 40
    • 84860782006 scopus 로고    scopus 로고
    • Absolute quantification of somatic DNA alterations in human cancer
    • Carter, S.L. et al. Absolute quantification of somatic DNA alterations in human cancer. Nat. Biotechnol. 30, 413-421 (2012).
    • (2012) Nat. Biotechnol , vol.30 , pp. 413-421
    • Carter, S.L.1
  • 41
    • 84897954204 scopus 로고    scopus 로고
    • PyClone: Statistical inference of clonal population structure in cancer
    • Roth, A. et al. PyClone: Statistical inference of clonal population structure in cancer. Nat. Methods 11, 396-398 (2014).
    • (2014) Nat. Methods , vol.11 , pp. 396-398
    • Roth, A.1
  • 42
    • 84858707750 scopus 로고    scopus 로고
    • Targeted BIRC5 silencing using YM155 causes cell death in neuroblastoma cells with low ABCB1 expression
    • Lamers, F. et al. Targeted BIRC5 silencing using YM155 causes cell death in neuroblastoma cells with low ABCB1 expression. Eur. J. Cancer 48, 763-771 (2012).
    • (2012) Eur. J. Cancer , vol.48 , pp. 763-771
    • Lamers, F.1
  • 43
    • 59849113821 scopus 로고    scopus 로고
    • Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
    • Gnirke, A. et al. Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing. Nat. Biotechnol. 27, 182-189 (2009).
    • (2009) Nat. Biotechnol , vol.27 , pp. 182-189
    • Gnirke, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.