Home LiteratureArticle Details
PMID: 7524604 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Variability of EWS chimaeric transcripts in Ewing tumours: a comparison of clinical and molecular data.

British journal of cancer ·Vol. 70 ·No. 5 ·1994-11-00 ·Pages 908-13

Zoubek A, Pfleiderer C, Salzer-Kuntschik M, Amann G, Windhager R, Fink FM, Koscielniak E, Delattre O, Strehl S, Ambros PF

Abstract

Ewing tumours (ET), including Ewing's sarcoma and peripheral primitive neuroectodermal tumour, are well characterised at the molecular level by a unique chromosomal rearrangement which fuses the EWS gene to one of two closely related ETS proto-oncogenes, FLI-1 or ERG. Expression of the resulting chimaeric transcripts can be readily detected by reversed transcriptase polymerase chain reaction (RT-PCR). This approach led to the identification of a number of different exon combinations at the junction site of coding sequences. The physiological consequences of the observed variability in the hinge region of EWS chimaeric proteins are not known. We have analysed tumour-derived material from 30 ET patients with well-documented clinical course (18 with localised and 12 with metastatic disease at diagnosis) for the presence of EWS/FLI-1 or EWS/ERG RNA. Karyotypes were obtained in 21 out of 27 cases and analysed by routine cytogenetics. A chromosome 22 rearrangement was demonstrated in 18 cases (67%). In contrast, RT-PCR revealed the presence of chimaeric transcripts in 28 tumours (93%), with fusions of EWS exon 7 to FLI-1 exons 6 (19/28), 5 (4/28) and 7 (1/28). In addition, EWS/FLI-1 exon combinations 10/5 and 9/4 were observed in one case each. In the last tumour, the presence of at least four additional splicing variants corresponding to fusion of EWS exon 7 to FLI-1 exons 4, 6, 8 and 9 was demonstrated. Two tumours expressed EWS/ERG fusion transcripts involving EWS exon 7 and ERG exon 6. In this study, EWS/FLI-1 exon combinations 7/6 (type I) predominated over 7/5 (type II) in localised ET (14 versus 1) and were more abundant in tumours affecting the long bones (9 versus 0), whereas in central axis tumours and metastatic disease there was only little difference in the frequency of the two types. So far, no correlations between different chimaeric EWS transcripts and any other clinical parameters have been identified.

Related Genes
MeSH Terms
Adolescent Adult Base Sequence Child Child, Preschool Chimera Chromosomes, Human, Pair 22 Exons Female Gene Rearrangement Genetic Variation Humans Karyotyping Male Molecular Sequence Data Polymerase Chain Reaction/methods RNA Splicing RNA, Messenger/genetics RNA-Directed DNA Polymerase Recombinant Fusion Proteins/genetics Sarcoma, Ewing/genetics Transcription, Genetic
Chemicals
RNA, Messenger Recombinant Fusion Proteins RNA-Directed DNA Polymerase
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Zoubek A
Children's Cancer Research Institute (CCRI), St. Anna Children's Hospital, Vienna, Austria.
Pfleiderer C
Salzer-Kuntschik M
Amann G
Windhager R
Fink F M
Koscielniak E
Delattre O
Strehl S
Ambros P F
References (20)
20 references, click to expand
  1. Chromosome translocation in peripheral neuroepithelioma.
    N Engl J Med. 1984 Aug 30;311(9):584-5 PMID: 6749231
  2. A second Ewing's sarcoma translocation, t(21;22), fuses the EWS gene to another ETS-family transcription factor, ERG.
    Nat Genet. 1994 Feb;6(2):146-51 PMID: 8162068
  3. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.
    Anal Biochem. 1987 Apr;162(1):156-9 PMID: 2440339
  4. Multidisciplinary treatment of primary Ewing's sarcoma of bone. A 6-year experience of a European Cooperative Trial.
    Cancer. 1988 Jan 1;61(1):23-32 PMID: 3334950
  5. Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases of remarkable consistency of t(11;22)(q24;q12).
    Cancer Genet Cytogenet. 1988 Jun;32(2):229-38 PMID: 3163261
  6. Overexpression of the pseudoautosomal gene MIC2 in Ewing's sarcoma and peripheral primitive neuroectodermal tumor.
    Oncogene. 1990 Jul;5(7):1067-70 PMID: 1695726
  7. MIC2 is a specific marker for Ewing's sarcoma and peripheral primitive neuroectodermal tumors. Evidence for a common histogenesis of Ewing's sarcoma and peripheral primitive neuroectodermal tumors from MIC2 expression and specific chromosome aberration.
    Cancer. 1991 Apr 1;67(7):1886-93 PMID: 1848471
  8. High-dose melphalan, etoposide +/- carboplatin (MEC) combined with 12-gray fractionated total-body irradiation in children with generalized solid tumors.
    Pediatr Hematol Oncol. 1991 Jan-Mar;8(1):13-22 PMID: 2029464
  9. Mononuclear cell (MNC) concentration from the marrow harvest by automatic system.
    Haematologica. 1991 Mar;76 Suppl 1:15-7 PMID: 1864550
  10. Unexpected heterogeneity in E2A/PBX1 fusion messenger RNA detected by the polymerase chain reaction in pediatric patients with acute lymphoblastic leukemia.
    Blood. 1992 Sep 15;80(6):1413-7 PMID: 1520867
  11. Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours.
    Nature. 1992 Sep 10;359(6391):162-5 PMID: 1522903
  12. Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints.
    Genes Chromosomes Cancer. 1992 Nov;5(4):271-7 PMID: 1283315
  13. Partial physical map of human chromosome 21 from fibroblast and lymphocyte DNA.
    Hum Genet. 1993 Apr;91(3):245-53 PMID: 8478008
  14. 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 Jun 15;90(12):5752-6 PMID: 8516324
  15. Narrow spectrum of infrequent p53 mutations and absence of MDM2 amplification in Ewing tumours.
    Oncogene. 1993 Oct;8(10):2683-90 PMID: 8378080
  16. Combinatorial generation of variable fusion proteins in the Ewing family of tumours.
    EMBO J. 1993 Dec;12(12):4481-7 PMID: 8223458
  17. Detection of the (11;22)(q24;q12) translocation of Ewing's sarcoma and peripheral neuroectodermal tumor by reverse transcription polymerase chain reaction.
    Am J Pathol. 1993 Nov;143(5):1294-300 PMID: 8238248
  18. EWS/Fli-1 chimeric protein is a transcriptional activator.
    Cancer Res. 1993 Dec 15;53(24):5859-63 PMID: 7503813
  19. Genomic structure of the EWS gene and its relationship to EWSR1, a site of tumor-associated chromosome translocation.
    Genomics. 1993 Dec;18(3):609-15 PMID: 8307570
  20. Alternative splicing of RNAs transcribed from the human abl gene and from the bcr-abl fused gene.
    Cell. 1986 Oct 24;47(2):277-84 PMID: 3021337
Article Info
Journal
British journal of cancer
Abbr.
Br J Cancer
ISSN
0007-0920
Published
1994-11-00
Pages
908-13
Language
English
Region
England
NLM ID
0370635
PMCID
PMC2033557
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]