메뉴 건너뛰기




Volumn 238, Issue 5, 2016, Pages 700-710

Paediatric and adult soft tissue sarcomas with NTRK1 gene fusions: A subset of spindle cell sarcomas unified by a prominent myopericytic/haemangiopericytic pattern

Author keywords

haemangiopericytoma; infantile fibrosarcoma; myopericytic sarcoma; NTRK1; sarcoma

Indexed keywords

BRAIN DERIVED NEUROTROPHIC FACTOR RECEPTOR; CD34 ANTIGEN; LAMIN A; NEUROTROPHIC TYROSINE KINASE RECEPTOR 1; SMOOTH MUSCLE ACTIN; STAT6 PROTEIN; UNCLASSIFIED DRUG; CYCLIN DEPENDENT KINASE INHIBITOR 2A; LMNA PROTEIN, HUMAN; PROTEIN TYROSINE KINASE A; TPM3 PROTEIN, HUMAN; TROPOMYOSIN; TUMOR MARKER;

EID: 84961770663     PISSN: 00223417     EISSN: 10969896     Source Type: Journal    
DOI: 10.1002/path.4701     Document Type: Article
Times cited : (115)

References (27)
  • 1
    • 33645061279 scopus 로고    scopus 로고
    • Solitary fibrous tumour and haemangiopericytoma: Evolution of a concept
    • Gengler C, Guillou L,. Solitary fibrous tumour and haemangiopericytoma: evolution of a concept. Histopathology. 2006; 48: 63-74.
    • (2006) Histopathology. , vol.48 , pp. 63-74
    • Gengler, C.1    Guillou, L.2
  • 2
    • 84873096886 scopus 로고    scopus 로고
    • Identification of recurrent NAB2-STAT6 gene fusions in solitary fibrous tumor by integrative sequencing
    • Robinson DR, Wu YM, Kalyana-Sundaram S, et al., Identification of recurrent NAB2-STAT6 gene fusions in solitary fibrous tumor by integrative sequencing. Nat Genet 2013; 45: 180-185.
    • (2013) Nat Genet , vol.45 , pp. 180-185
    • Robinson, D.R.1    Wu, Y.M.2    Kalyana-Sundaram, S.3
  • 3
    • 84873081601 scopus 로고    scopus 로고
    • Whole-exome sequencing identifies a recurrent NAB2-STAT6 fusion in solitary fibrous tumors
    • Chmielecki J, Crago AM, Rosenberg M, et al., Whole-exome sequencing identifies a recurrent NAB2-STAT6 fusion in solitary fibrous tumors. Nat Genet 2013; 45: 131-132.
    • (2013) Nat Genet , vol.45 , pp. 131-132
    • Chmielecki, J.1    Crago, A.M.2    Rosenberg, M.3
  • 4
    • 84897877577 scopus 로고    scopus 로고
    • Solitary fibrous tumors/hemangiopericytomas with different variants of the NAB2-STAT6 gene fusion are characterized by specific histomorphology and distinct clinicopathological features
    • Barthelmess S, Geddert H, Boltze C, et al., Solitary fibrous tumors/hemangiopericytomas with different variants of the NAB2-STAT6 gene fusion are characterized by specific histomorphology and distinct clinicopathological features. Am J Pathol 2014; 184: 1209-1218.
    • (2014) Am J Pathol , vol.184 , pp. 1209-1218
    • Barthelmess, S.1    Geddert, H.2    Boltze, C.3
  • 5
    • 84911363194 scopus 로고    scopus 로고
    • Phenotypical and molecular distinctness of sinonasal haemangiopericytoma compared to solitary fibrous tumour of the sinonasal tract
    • Agaimy A, Barthelmeß S, Geddert H, et al., Phenotypical and molecular distinctness of sinonasal haemangiopericytoma compared to solitary fibrous tumour of the sinonasal tract. Histopathology 2014; 65: 667-673.
    • (2014) Histopathology , vol.65 , pp. 667-673
    • Agaimy, A.1    Barthelmeß, S.2    Geddert, H.3
  • 6
    • 84922333915 scopus 로고    scopus 로고
    • Recurrent mutations within the amino-terminal region of β-catenin are probable key molecular driver events in sinonasal hemangiopericytoma
    • Haller F, Bieg M, Moskalev EA, et al., Recurrent mutations within the amino-terminal region of β-catenin are probable key molecular driver events in sinonasal hemangiopericytoma. Am J Pathol 2015; 185: 563-571.
    • (2015) Am J Pathol , vol.185 , pp. 563-571
    • Haller, F.1    Bieg, M.2    Moskalev, E.A.3
  • 7
    • 0036431476 scopus 로고    scopus 로고
    • Malignant myopericytoma: Expanding the spectrum of tumours with myopericytic differentiation
    • McMenamin ME, Fletcher CD,. Malignant myopericytoma: expanding the spectrum of tumours with myopericytic differentiation. Histopathology 2002; 41: 450-460.
    • (2002) Histopathology , vol.41 , pp. 450-460
    • McMenamin, M.E.1    Fletcher, C.D.2
  • 8
    • 0031953233 scopus 로고    scopus 로고
    • A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma
    • Knezevich SR, McFadden DE, Tao W, et al., A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma. Nat Genet 1998; 18: 184-187.
    • (1998) Nat Genet , vol.18 , pp. 184-187
    • Knezevich, S.R.1    McFadden, D.E.2    Tao, W.3
  • 9
    • 84943338865 scopus 로고    scopus 로고
    • An oncogenic NTRK fusion in a soft tissue sarcoma patient with response to the tropomyosin-related kinase (TRK) inhibitor LOXO-101
    • Doebele RC, Davis LE, Vaishnavi A, et al., An oncogenic NTRK fusion in a soft tissue sarcoma patient with response to the tropomyosin-related kinase (TRK) inhibitor LOXO-101. Cancer Discov 2015; 5: 1049-1057.
    • (2015) Cancer Discov , vol.5 , pp. 1049-1057
    • Doebele, R.C.1    Davis, L.E.2    Vaishnavi, A.3
  • 10
    • 84922341647 scopus 로고    scopus 로고
    • TRKing down an old oncogene in a new era of targeted therapy
    • Vaishnavi A, Le AT, Doebele RC,. TRKing down an old oncogene in a new era of targeted therapy. Cancer Discov 2015; 5: 25-34.
    • (2015) Cancer Discov , vol.5 , pp. 25-34
    • Vaishnavi, A.1    Le, A.T.2    Doebele, R.C.3
  • 11
    • 84892882633 scopus 로고    scopus 로고
    • Kinase fusions are frequent in Spitz tumours and spitzoid melanomas
    • Wiesner T, He J, Yelensky R, et al., Kinase fusions are frequent in Spitz tumours and spitzoid melanomas. Nat Commun 2014; 5: 3116.
    • (2014) Nat Commun , vol.5 , pp. 3116
    • Wiesner, T.1    He, J.2    Yelensky, R.3
  • 12
    • 77950939830 scopus 로고    scopus 로고
    • Rearrangements of NTRK1 gene in papillary thyroid carcinoma
    • Greco A, Miranda C, Pierotti MA,. Rearrangements of NTRK1 gene in papillary thyroid carcinoma. Mol Cell Endocrinol 2010; 321: 44-49.
    • (2010) Mol Cell Endocrinol , vol.321 , pp. 44-49
    • Greco, A.1    Miranda, C.2    Pierotti, M.A.3
  • 13
    • 84887445619 scopus 로고    scopus 로고
    • Oncogenic and drug-sensitive NTRK1 rearrangements in lung cancer
    • Vaishnavi A, Capelletti M, Le AT, et al., Oncogenic and drug-sensitive NTRK1 rearrangements in lung cancer. Nat Med 2013; 19: 1469-1472.
    • (2013) Nat Med , vol.19 , pp. 1469-1472
    • Vaishnavi, A.1    Capelletti, M.2    Le, A.T.3
  • 14
    • 0028114005 scopus 로고
    • Infantile hemangiopericytoma versus infantile myofibromatosis. Study of a series suggesting a continuous spectrum of infantile myofibroblastic lesions
    • Mentzel T, Calonje E, Nascimento AG, et al., Infantile hemangiopericytoma versus infantile myofibromatosis. Study of a series suggesting a continuous spectrum of infantile myofibroblastic lesions. Am J Surg Pathol 1994; 18: 922-930.
    • (1994) Am J Surg Pathol , vol.18 , pp. 922-930
    • Mentzel, T.1    Calonje, E.2    Nascimento, A.G.3
  • 15
    • 0028913120 scopus 로고
    • Are infantile myofibromatosis, congenital fibrosarcoma and congenital haemangiopericytoma histogenetically related?
    • Variend S, Bax NM, van Gorp J,. Are infantile myofibromatosis, congenital fibrosarcoma and congenital haemangiopericytoma histogenetically related? Histopathology. 1995; 26: 57-62.
    • (1995) Histopathology. , vol.26 , pp. 57-62
    • Variend, S.1    Bax, N.M.2    Van Gorp, J.3
  • 16
    • 84878865983 scopus 로고    scopus 로고
    • A recurrent PDGFRB mutation causes familial infantile myofibromatosis
    • Cheung YH, Gayden T, Campeau PM, et al., A recurrent PDGFRB mutation causes familial infantile myofibromatosis. Am J Hum Genet 2013; 92: 996-1000.
    • (2013) Am J Hum Genet , vol.92 , pp. 996-1000
    • Cheung, Y.H.1    Gayden, T.2    Campeau, P.M.3
  • 17
    • 84878859923 scopus 로고    scopus 로고
    • Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis
    • Martignetti JA, Tian L, Li D, et al., Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis. Am J Hum Genet 2013; 92: 1001-1007.
    • (2013) Am J Hum Genet , vol.92 , pp. 1001-1007
    • Martignetti, J.A.1    Tian, L.2    Li, D.3
  • 18
    • 84907007265 scopus 로고    scopus 로고
    • Role of BRAF V600E in the first preclinical model of multifocal infiltrating myopericytoma development and microenvironment
    • Sadow PM, Priolo C, Nanni S, et al., Role of BRAF V600E in the first preclinical model of multifocal infiltrating myopericytoma development and microenvironment. J Natl Cancer Inst 2014; DOI: 10.1093/jnci/dju182.
    • (2014) J Natl Cancer Inst
    • Sadow, P.M.1    Priolo, C.2    Nanni, S.3
  • 19
    • 84914705747 scopus 로고    scopus 로고
    • Myofibromas with atypical features: Expanding the morphologic spectrum of a benign entity
    • Linos K, Carter JM, Gardner JM, et al., Myofibromas with atypical features: expanding the morphologic spectrum of a benign entity. Am J Surg Pathol 2014; 38: 1649-1654.
    • (2014) Am J Surg Pathol , vol.38 , pp. 1649-1654
    • Linos, K.1    Carter, J.M.2    Gardner, J.M.3
  • 20
    • 0027078524 scopus 로고
    • Myofibromatosis-like hemangiopericytoma metastasizing as differentiated vascular smooth-muscle and myosarcoma. Myopericytes as a subset of 'myofibroblasts'
    • Dictor M, Elner A, Andersson T, et al., Myofibromatosis-like hemangiopericytoma metastasizing as differentiated vascular smooth-muscle and myosarcoma. Myopericytes as a subset of 'myofibroblasts'. Am J Surg Pathol 1992; 16: 1239-1247.
    • (1992) Am J Surg Pathol , vol.16 , pp. 1239-1247
    • Dictor, M.1    Elner, A.2    Andersson, T.3
  • 21
    • 33746647820 scopus 로고    scopus 로고
    • Neurotrophin signaling: Many exciting surprises!
    • Arévalo JC, Wu SH,. Neurotrophin signaling: many exciting surprises! Cell Mol Life Sci 2006; 63: 1523-1537.
    • (2006) Cell Mol Life Sci , vol.63 , pp. 1523-1537
    • Arévalo, J.C.1    Wu, S.H.2
  • 22
    • 0022641294 scopus 로고
    • A human oncogene formed by the fusion of truncated tropomyosin and protein tyrosine kinase sequences
    • Martin-Zanca D, Hughes SH, Barbacid M,. A human oncogene formed by the fusion of truncated tropomyosin and protein tyrosine kinase sequences. Nature 1986; 319: 743-748.
    • (1986) Nature , vol.319 , pp. 743-748
    • Martin-Zanca, D.1    Hughes, S.H.2    Barbacid, M.3
  • 23
    • 84898657475 scopus 로고    scopus 로고
    • NTRK1 fusion in glioblastoma multiforme
    • e91940
    • Kim J, Lee Y, Cho HJ, et al., NTRK1 fusion in glioblastoma multiforme. PLoS One 2014; 9: e91940.
    • (2014) PLoS One , vol.9
    • Kim, J.1    Lee, Y.2    Cho, H.J.3
  • 24
    • 84899526966 scopus 로고    scopus 로고
    • The genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade glioma
    • Wu G, Diaz AK, Paugh BS, et al., The genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade glioma. Nat Genet 2014; 46: 444-450.
    • (2014) Nat Genet , vol.46 , pp. 444-450
    • Wu, G.1    Diaz, A.K.2    Paugh, B.S.3
  • 25
    • 84922373207 scopus 로고    scopus 로고
    • The landscape of kinase fusions in cancer
    • Stransky N, Cerami E, Schalm S, et al., The landscape of kinase fusions in cancer. Nat Commun 2014; 5: 4846.
    • (2014) Nat Commun , vol.5 , pp. 4846
    • Stransky, N.1    Cerami, E.2    Schalm, S.3
  • 27
    • 84956594380 scopus 로고    scopus 로고
    • Evaluation of a congenital infantile fibrosarcoma by comprehensive genomic profiling reveals an LMNA-NTRK1 gene fusion responsive to crizotinib
    • Wong V, Pavlick D, Brennan T, et al., Evaluation of a congenital infantile fibrosarcoma by comprehensive genomic profiling reveals an LMNA-NTRK1 gene fusion responsive to crizotinib. J Natl Cancer Inst 2015; 108: 1.
    • (2015) J Natl Cancer Inst , vol.108 , pp. 1
    • Wong, V.1    Pavlick, D.2    Brennan, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.