1
|
Collini P, Sorensen PH, Patel S, et al:
Sarcomas with spindle cell morphology. Semin Oncol. 36:324–337.
2009. View Article : Google Scholar : PubMed/NCBI
|
2
|
Fletcher CD, Bridge JA, Hogendoorn P and
Mertens F: WHO Classification of Tumours of Soft Tissue and Bone.
4th edition. IARC; Lyon: 2013
|
3
|
Heim S and Mitelman F: Cancer
Cytogenetics. 3rd edition. Wiley-Blackwell; New York: 2009
|
4
|
Sirvent N, Maire G and Pedeutour F:
Genetics of dermatofibrosarcoma protuberans family of tumors: from
ring chromosomes to tyrosine kinase inhibitor treatment. Genes
Chromosomes Cancer. 37:1–19. 2003. View Article : Google Scholar : PubMed/NCBI
|
5
|
Chmielecki J, Crago AM, Rosenberg M, et
al: Whole-exome sequencing identifies a recurrent NAB2-STAT6 fusion
in solitary fibrous tumors. Nat Genet. 45:131–132. 2013. View Article : Google Scholar
|
6
|
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. 45:180–185.
2013. View
Article : Google Scholar : PubMed/NCBI
|
7
|
Eyden BP, Banerjee SS, Harris M and Mene
A: A study of spindle cell sarcomas showing myofibroblastic
differentiation. Ultrastruct Pathol. 15:367–378. 1991. View Article : Google Scholar : PubMed/NCBI
|
8
|
Fletcher CD, Dal Cin P, de Wever I, et al:
Correlation between clinicopathological features and karyotype in
spindle cell sarcomas. A report of 130 cases from the CHAMP study
group. Am J Pathol. 154:1841–1847. 1999. View Article : Google Scholar
|
9
|
Alaggio R, Rosolen A, Sartori F, et al:
Spindle cell tumor with EWS-WT1 transcript and a favorable clinical
course: a variant of DSCT, a variant of leiomyosarcoma, or a new
entity? Report of 2 pediatric cases. Am J Surg Pathol. 31:454–459.
2007. View Article : Google Scholar : PubMed/NCBI
|
10
|
Lestou VS, O’Connell JX, Ludkovski O,
Gosling H, Lesack D and Horsman DE: Coamplification of 12p11 and
12q13 approximately q22 in multiple ring chromosomes in a spindle
cell sarcoma resolved by novel multicolor fluorescence in situ
hybridization analysis. Cancer Genet Cytogenet. 139:44–47. 2002.
View Article : Google Scholar
|
11
|
Nord KH, Macchia G, Tayebwa J, et al:
Integrative genome and transcriptome analyses reveal two distinct
types of ring chromosome in soft tissue sarcomas. Hum Mol Genet.
23:878–888. 2014. View Article : Google Scholar : PubMed/NCBI
|
12
|
Mandahl N: Methods in solid tumour
cytogenetics. Human Cytogenetics: Malignancy and Acquired
Abnormalities. Rooney DE: Oxford University Press; New York: pp.
165–203. 2001
|
13
|
Schaffer LG, Slovak ML and Campbell LJ:
ISCN 2009: An International System for Human Cytogenetic
Nomenclature. Karger; Basel: 2009
|
14
|
Ge H, Liu K, Juan T, Fang F, Newman M and
Hoeck W: FusionMap: detecting fusion genes from next-generation
sequencing data at base-pair resolution. Bioinformatics.
27:1922–1928. 2011. View Article : Google Scholar : PubMed/NCBI
|
15
|
Hostein I, Pelmus M, Aurias A, Pedeutour
F, Mathoulin-Pelissier S and Coindre JM: Evaluation of MDM2 and
CDK4 amplification by real-time PCR on paraffin wax-embedded
material: a potential tool for the diagnosis of atypical lipomatous
tumours/well-differentiated liposarcomas. J Pathol. 202:95–102.
2004. View Article : Google Scholar
|
16
|
Nilbert M, Rydholm A, Willen H, Mitelman F
and Mandahl N: MDM2 gene amplification correlates with ring
chromosome in soft tissue tumors. Genes Chromosomes Cancer.
9:261–265. 1994. View Article : Google Scholar : PubMed/NCBI
|
17
|
Gisselsson D, Höglund M, Mertens F,
Mitelman F and Mandahl N: Chromosomal organization of amplified
chromosome 12 sequences in mesenchymal tumors detected by
fluorescence in situ hybridization. Genes Chromosomes Cancer.
23:203–212. 1998. View Article : Google Scholar : PubMed/NCBI
|
18
|
Pedeutour F, Forus A, Coindre JM, et al:
Structure of the supernumerary ring and giant rod chromosomes in
adipose tissue tumors. Genes Chromosomes Cancer. 24:30–41. 1999.
View Article : Google Scholar : PubMed/NCBI
|
19
|
Gisselsson D, Pettersson L, Höglund M, et
al: Chromosomal breakage-fusion-bridge events cause genetic
intratumor heterogeneity. Proc Natl Acad Sci USA. 97:5357–5362.
2000. View Article : Google Scholar : PubMed/NCBI
|
20
|
Lee YS and Dutta A: The tumor suppressor
microRNA let-7 represses the HM GA2 oncogene. Genes Dev.
21:1025–1030. 2007. View Article : Google Scholar : PubMed/NCBI
|
21
|
Gray TA, Saitoh S and Nicholls RD: An
imprinted, mammalian bicistronic transcript encodes two independent
proteins. Proc Natl Acad Sci USA. 96:5616–5621. 1999. View Article : Google Scholar : PubMed/NCBI
|
22
|
Ritchie H and Wang LH: A mammalian
bicistronic transcript encoding two dentin-specific proteins.
Biochem Biophys Res Commun. 231:425–428. 1997. View Article : Google Scholar : PubMed/NCBI
|
23
|
Guerra E, Trerotola M, Dell’Arciprete R,
et al: A bicistronic CYCLIN D1-TROP2 mRNA chimera demonstrates a
novel oncogenic mechanism in human cancer. Cancer Res.
68:8113–8121. 2008. View Article : Google Scholar : PubMed/NCBI
|
24
|
Kim HY and Gladyshev VN: Methionine
sulfoxide reduction in mammals: characterization of
methionine-R-sulfoxide reductases. Mol Biol Cell. 15:1055–1064.
2004. View Article : Google Scholar : PubMed/NCBI
|