Skip to main content

Advertisement

Log in

Multiple splice variants of EWSR1-ETS fusion transcripts co-existing in the Ewing sarcoma family of tumors

  • Original Paper
  • Published:
Cellular Oncology Aims and scope Submit manuscript

Abstract

Purpose

The Ewing sarcoma family of tumors (EFT) is characterized by fusions of the EWSR1 gene on chromosome 22q12 with either one of the genes encoding members of the ETS family of transcription factors, in the majority of cases FLI1 or ERG. Many alternative EWSR1-ETS gene fusions have been encountered, due to variations in the locations of the EWSR1 and ETS genomic breakpoints. The resulting heterogeneity in EWSR1-ETS fusion transcripts may further be increased by the occurrence of multiple splice variants within the same tumor. Here we present a retrospective study designed to detect all of the EWSR1-FLI1 and EWSR1-ERG fusion transcripts in a series of 23 fresh frozen EFT tissues.

Methods

RT-PCR and nested fluorescent multiplex PCR were used to amplify EWSR1-FLI1 and EWSR1-ERG transcripts from EFT tissues. Fusion transcripts were identified by laser-induced fluorescent capillary electrophoresis and confirmed by sequence analysis.

Results

Nine different EWSR1-FLI1 fusion transcripts and one EWSR1-ERG fusion transcript were identified in 21 out of 23 fresh frozen EFT tissue samples. In five cases multiple fusion transcripts were found to coexist in the same tumor sample. We additionally reviewed previous reports on twelve cases with multiple EWSR1-ETS fusion transcripts.

Conclusions

Alternative splicing may frequently affect the process of EFT-associated fusion gene transcription and, as such, may significantly contribute to the pathogenic role of EFT-associated chromosome translocations. In a considerable number of cases this may result in multiple splice variants within the same tumor.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. O. Delattre, J. Zucman, B. Plougastel, C. Desmaze, T. Melot, M. Peter, H. Kovar, I. Joubert, P. de Jong, G. Rouleau, A. Aurias, G. Thomas, Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours. Nature 359, 162–165 (1992)

    Article  PubMed  CAS  Google Scholar 

  2. P.H. Sorensen, S.L. Lessnick, D. Lopez-Terrada, X.F. Liu, T.J. Triche, C.T. Denny, A second Ewing’s sarcoma translocation, t(21;22), fuses the EWS gene to another ETS-family transcription factor. ERG. Nat. Genet. 6, 146–151 (1994)

    Article  CAS  Google Scholar 

  3. J. Zucman, T. Melot, C. Desmaze, J. Ghysdael, B. Plougastel, M. Peter, J.M. Zucker, T.J. Triche, D. Sheer, C. Turc-Carel, P. Ambros, V. Combaret, G. Lenoir, A. Aurias, G. Thomas, O. Delattre, Combinatorial generation of variable fusion proteins in the Ewing family of tumours. EMBO J. 12, 4481–4487 (1993)

    PubMed  CAS  Google Scholar 

  4. J.P. Ginsberg, E. de Alava, M. Ladanyi, L.H. Wexler, H. Kovar, M. Paulussen, A. Zoubek, B. Dockhorn-Dworniczak, H. Juergens, J.S. Wunder, I.L. Andrulis, R. Malik, P.H. Sorensen, R.B. Womer, F.G. Barr, EWS-FLI1 and EWS-ERG gene fusions are associated with similar clinical phenotypes in Ewing’s sarcoma. J. Clin. Oncol. 17, 1809–1814 (1999)

    PubMed  CAS  Google Scholar 

  5. M.C. Le Deley, O. Delattre, K.L. Schaefer, S.A. Burchill, G. Koehler, P.C. Hogendoorn, T. Lion, C. Poremba, J. Marandet, S. Ballet, G. Pierron, S.C. Brownhill, M. Nesslböck, A. Ranft, U. Dirksen, O. Oberlin, I.J. Lewis, A.W. Craft, H. Jürgens, H. Kovar, Impact of EWS-ETS fusion type on disease progression in Ewing’s sarcoma/peripheral primitive neuroectodermal tumor: prospective results from the cooperative Euro-E.W.I.N.G. 99 trial. J. Clin. Oncol. 28, 1982–1988 (2010)

    Article  PubMed  Google Scholar 

  6. C. Turc-Carel, A. Aurias, F. Mugneret, S. Lizard, I. Sidaner, C. Volk, J.P. Thiery, S. Olschwang, I. Philip, M.P. Berger, T. Philip, G.M. Lenoir, A. Mazabraud, Chromosomes in Ewing’s sarcoma. I. An evaluation of 85 cases of remarkable consistency of t(11;22)(q24;q12). Cancer Genet. Cytogenet. 32, 229–238 (1988)

    Article  PubMed  CAS  Google Scholar 

  7. J.R. Downing, D.R. Head, D.M. Parham, E.C. Douglass, M.G. Hulshof, M.P. Link, T.A. Motroni, H.E. Grier, A.M. Curcio-Brint, D.N. Shapiro, 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. 143, 1294–1300 (1993)

    PubMed  CAS  Google Scholar 

  8. I.S. Jeon, J.N. Davis, B.S. Braun, J.E. Sublett, M.F. Roussel, C.T. Denny, D.N. Shapiro, A variant Ewing’s sarcoma translocation (7;22) fuses the EWS gene to the ETS gene ETV1. Oncogene 10, 1229–1234 (1995)

    PubMed  CAS  Google Scholar 

  9. F. Urano, A. Umezawa, W. Hong, H. Kikuchi, J. Hata, A novel chimera gene between EWS and E1A-F, encoding the adenovirus E1A enhancer-binding protein, in extraosseous Ewing’s sarcoma. Biochem. Biophys. Res. Commun. 219, 608–612 (1996)

    Article  PubMed  CAS  Google Scholar 

  10. M. Peter, J. Couturier, H. Pacquement, J. Michon, G. Thomas, H. Magdelenat, O. Delattre, A new member of the ETS family fused to EWS in Ewing tumors. Oncogene 14, 1159–1164 (1997)

    Article  PubMed  CAS  Google Scholar 

  11. D.C. Shing, D.J. McMullan, P. Roberts, K. Smith, S.F. Chin, J. Nicholson, R.M. Tillman, P. Ramani, C. Cullinane, N. Coleman, FUS/ERG gene fusions in Ewing’s tumors. Cancer Res. 63, 4568–4576 (2003)

    PubMed  CAS  Google Scholar 

  12. T.L. Ng, M.J. O’Sullivan, C.J. Pallen, M. Hayes, P.W. Clarkson, M. Winstanley, P.H. Sorensen, T.O. Nielsen, D.E. Horsman, Ewing sarcoma with novel translocation t(2;16) producing an in-frame fusion of FUS and FEV. J. Mol. Diagn. 9, 459–463 (2007)

    Article  PubMed  Google Scholar 

  13. T. Mastrangelo, P. Modena, S. Tornielli, F. Bullrich, M.A. Testi, A. Mezzelani, P. Radice, A. Azzarelli, S. Pilotti, C.M. Croce, M.A. Pierotti, G. Sozzi, A novel zinc finger gene is fused to EWS in small round cell tumor. Oncogene 19, 3799–3804 (2000)

    Article  PubMed  CAS  Google Scholar 

  14. L. Wang, R. Bhargava, T. Zheng, L. Wexler, M.H. Collins, D. Roulston, M. Ladanyi, Undifferentiated small round cell sarcomas with rare EWS gene fusions: identification of a novel EWS-SP3 fusion and of additional cases with the EWS-ETV1 and EWS-FEV fusions. J. Mol. Diagn. 9, 498–509 (2007)

    Article  PubMed  Google Scholar 

  15. K. Szuhai, M. Ijszenga, D. de Jong, A. Karseladze, H.J. Tanke, P.C. Hogendoorn, The NFATc2 gene is involved in a novel cloned translocation in a Ewing sarcoma variant that couples its function in immunology to oncology. Clin. Cancer Res. 15, 2259–2268 (2009)

    Article  PubMed  CAS  Google Scholar 

  16. J. Sumegi, J. Nishio, M. Nelson, R.W. Frayer, D. Perry, J.A. Bridge, A novel t(4;22)(q31;q12) produces an EWSR1-SMARCA5 fusion in extraskeletal Ewing sarcoma/primitive neuroectodermal tumor. Mod. Pathol. 24, 333–342 (2011)

    Article  PubMed  CAS  Google Scholar 

  17. A. Zoubek, C. Pfleiderer, M. Salzer-Kuntschik, G. Amann, R. Windhager, F.M. Fink, E. Koscielniak, O. Delattre, S. Strehl, P.F. Ambros, H. Gadner, H. Kovar, Variability of EWS chimaeric transcripts in Ewing tumours: a comparison of clinical and molecular data. Br. J. Cancer 70, 908–913 (1994)

    Article  PubMed  CAS  Google Scholar 

  18. G. Gamberi, S. Cocchi, S. Benini, G. Magagnoli, L. Morandi, J. Kreshak, M. Gambarotti, P. Picci, L. Zanella, M. Alberghini, Molecular diagnosis in Ewing family tumors: the Rizzoli experience–222 consecutive cases in four years. J. Mol. Diagn. 13, 313–324 (2011)

    Article  PubMed  CAS  Google Scholar 

  19. A. Zoubek, B. Dockhorn-Dworniczak, O. Delattre, H. Christiansen, F. Niggli, I. Gatterer-Menz, T.L. Smith, H. Jürgens, H. Gadner, H. Kovar, Does expression of different EWS chimeric transcripts define clinically distinct risk groups of Ewing tumor patients? J. Clin. Oncol. 14, 1245–1251 (1996)

    PubMed  CAS  Google Scholar 

  20. W.A. May, S.L. Lessnick, B.S. Braun, M. Klemsz, B.C. Lewis, L.B. Lunsford, R. Hromas, C.T. Denny, The Ewing’s sarcoma EWS/FLI-1 fusion gene encodes a more potent transcriptional activator and is a more powerful transforming gene than FLI-1. Mol. Cell. Biol. 13, 7393–7398 (1993)

    PubMed  CAS  Google Scholar 

  21. W.A. May, M.L. Gishizky, S.L. Lessnick, L.B. Lunsford, B.C. Lewis, O. Delattre, J. Zucman, G. Thomas, C.T. Denny, 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. 90, 5752–5756 (1993)

    Article  PubMed  CAS  Google Scholar 

  22. B. Patócs, K. Németh, M. Garami, G. Arató, I. Kovalszky, M. Szendrői, G. Fekete, Utilization of fluorescent multiplex PCR and laser-induced capillary electrophoresis for the diagnosis of Ewing family of tumours in formalin-fixed paraffin-embedded tissues. J. Clin. Path. 65, 1112–1118 (2012)

    Article  PubMed  Google Scholar 

  23. S. Ushigome, R. Machinami, P.H. Sorensen, Ewing Sarcoma/Primitive Neuroectodermal Tumour (PNET), in World Health Organisation Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone, ed. by C.D.M. Fletcher, K.K. Unni, F. Mertens (IARC Press, Lyon, 2002), pp. 297–300

    Google Scholar 

  24. M. Giovannini, J.A. Biegel, M. Serra, J.Y. Wang, Y.H. Wei, L. Nycum, B.S. Emanuel, G.A. Evans, EWS-erg and EWS-Fli1 fusion transcripts in Ewing’s sarcoma and primitive neuroectodermal tumors with variant translocations. J. Clin. Invest. 94, 489–496 (1994)

    Article  PubMed  CAS  Google Scholar 

  25. J. Zucman-Rossi, P. Legoix, J.M. Victor, B. Lopez, G. Thomas, Chromosome translocation based on illegitimate recombination in human tumors. Proc. Natl. Acad. Sci. U. S. A 95, 11786–11791 (1998)

    Article  PubMed  CAS  Google Scholar 

  26. J. Liu, M.M. Nau, J.C. Yeh, C.J. Allegra, E. Chu, J.J. Wright, Molecular heterogeneity and function of EWS-WT1 fusion transcripts in desmoplastic small round cell tumors. Clin. Cancer Res. 6, 3522–3529 (2000)

    PubMed  CAS  Google Scholar 

  27. K. Yang, W.O. Lui, Y. Xie, A. Zhang, B. Skytting, N. Mandahl, C. Larsson, O. Larsson, Co-existence of SYT-SSX1 and SYT-SSX2 fusions in synovial sarcomas. Oncogene 21, 4181–4190 (2002)

    Article  PubMed  CAS  Google Scholar 

  28. W.L. Wang, E. Mayordomo, W. Zhang, V.S. Hernandez, D. Tuvin, L. Garcia, D.C. Lev, A.J. Lazar, D. López-Terrada, Detection and characterization of EWSR1/ATF1 and EWSR1/CREB1 chimeric transcripts in clear cell sarcoma (melanoma of soft parts). Mod. Pathol. 22, 1201–1209 (2009)

    Article  PubMed  CAS  Google Scholar 

  29. A. Jakubauskas, V. Valceckiene, K. Andrekute, D. Seinin, A. Kanopka, L. Griskevicius, Discovery of two novel EWSR1/ATF1 transcripts in four chimerical transcripts-expressing clear cell sarcoma and their quantitative evaluation. Exp. Mol. Pathol. 90, 194–200 (2011)

    Article  PubMed  CAS  Google Scholar 

  30. E. De Braekeleer, N. Douet-Guilbert, D. Rowe, N. Bown, F. Morel, C. Berthou, C. Férec, M. De Braekeleer, ABL1 fusion genes in hematological malignancies: a review. Eur. J. Haematol. 86, 361–371 (2011)

    Article  PubMed  Google Scholar 

  31. P.P. Pandolfi, M. Alcalay, M. Fagioli, D. Zangrilli, A. Mencarelli, D. Diverio, A. Biondi, F. Lo Coco, A. Rambaldi, F. Grignani, C. Rochette-Egly, M.P. Gaube, P. Chambon, P.G. Pelicci, Genomic variability and alternative splicing generate multiple PML/RAR alpha transcripts that encode aberrant PML proteins and PML/RAR alpha isoforms in acute promyelocytic leukaemia. EMBO J. 11, 1397–1407 (1992)

    PubMed  CAS  Google Scholar 

  32. E. de Alava, A. Kawai, J.H. Healey, I. Fligman, P.A. Meyers, A.G. Huvos, W.L. Gerald, S.C. Jhanwar, P. Argani, C.R. Antonescu, F.J. Pardo-Mindan, J. Ginsberg, R. Womer, E.R. Lawlor, J. Wunder, I. Andrulis, P.H. Sorensen, F.G. Barr, M. Ladanyi, EWS-FLI1 fusion transcript structure is an independent determinant of prognosis in Ewing’s sarcoma. J. Clin. Oncol. 16, 1248–1255 (1998)

    PubMed  Google Scholar 

  33. N. Yoshino, T. Kojima, S. Asami, S. Motohashi, Y. Yoshida, M. Chin, H. Shichino, Y. Yoshida, N. Nemoto, M. Kaneko, H. Mugishima, T. Suzuki, Diagnostic significance and clinical applications of chimeric genes in Ewing’s sarcoma. Biol. Pharm. Bull. 26, 585–588 (2003)

    Article  PubMed  CAS  Google Scholar 

  34. F. Minoletti, G. Sozzi, S. Tornielli, S. Pilotti, A. Azzarelli, M.A. Pierotti, P. Radice, A novel EWS-ERG rearrangement generating two hybrid mRNAs in a peripheral primitive neuroectodermal tumour (pPNET) with a t(15;22) translocation. J. Pathol. 186, 434–437 (1998)

    Article  PubMed  CAS  Google Scholar 

  35. S.S. Bielack, M. Paulussen, G. Köhler, A patient with two Ewing’s sarcomas with distinct EWS fusion transcripts. N. Engl. J. Med. 350, 1364–1365 (2004)

    Article  PubMed  CAS  Google Scholar 

  36. T.B. Lewis, C.M. Coffin, P.S. Bernard, Differentiating Ewing’s sarcoma from other round blue cell tumors using a RT-PCR translocation panel on formalin-fixed paraffin-embedded tissues. Mod. Pathol. 20, 397–404 (2007)

    Article  PubMed  CAS  Google Scholar 

  37. R.I. Skotheim, M. Nees, Alternative splicing in cancer: noise, functional, or systematic? Int. J. Biochem. Cell Biol. 39, 1432–1449 (2007)

    Article  PubMed  CAS  Google Scholar 

  38. M. Roy, Q. Xu, C. Lee, Evidence that public database records for many cancer-associated genes reflect a splice form found in tumors and lack normal splice forms. Nucleic Acids Res. 33, 5026–5033 (2005)

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

The authors would like to thank Prof. Dezső Schuler for critical reading of the manuscript, Tibor Fülep and Dr. Ilona Milánkovics for their helpful suggestions and Krisztina Staub and Zsoltné Vincze for their technical assistance.

Disclosure/Conflict of interest

The authors declare that they have no conflict of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Barbara Patócs.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Patócs, B., Németh, K., Garami, M. et al. Multiple splice variants of EWSR1-ETS fusion transcripts co-existing in the Ewing sarcoma family of tumors. Cell Oncol. 36, 191–200 (2013). https://doi.org/10.1007/s13402-013-0126-8

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13402-013-0126-8

Keywords

Navigation