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The oncogenic properties of EWS/WT1 of desmoplastic small round cell tumors are unmasked by loss of p53 in murine embryonic fibroblasts.

Publication ,  Journal Article
Bandopadhayay, P; Jabbour, AM; Riffkin, C; Salmanidis, M; Gordon, L; Popovski, D; Rigby, L; Ashley, DM; Watkins, DN; Thomas, DM; Algar, E; Ekert, PG
Published in: BMC Cancer
December 9, 2013

BACKGROUND: Desmoplastic small round cell tumor (DSRCT) is characterized by the presence of a fusion protein EWS/WT1, arising from the t (11;22) (p13;q12) translocation. Here we examine the oncogenic properties of two splice variants of EWS/WT1, EWS/WT1-KTS and EWS/WT1 + KTS. METHODS: We over-expressed both EWS/WT1 variants in murine embryonic fibroblasts (MEFs) of wild-type, p53+/- and p53-/- backgrounds and measured effects on cell-proliferation, anchorage-independent growth, clonogenicity after serum withdrawal, and sensitivity to cytotoxic drugs and gamma irradiation in comparison to control cells. We examined gene expression profiles in cells expressing EWS/WT1. Finally we validated our key findings in a small series of DSRCT. RESULTS: Neither isoform of EWS/WT1 was sufficient to transform wild-type MEFs however the oncogenic potential of both was unmasked by p53 loss. Expression of EWS/WT1 in MEFs lacking at least one allele of p53 enhanced cell-proliferation, clonogenic survival and anchorage-independent growth. EWS/WT1 expression in wild-type MEFs conferred resistance to cell-cycle arrest after irradiation and daunorubicin induced apoptosis. We show DSRCT commonly have nuclear localization of p53, and copy-number amplification of MDM2/MDMX. Expression of either isoform of EWS/WT1 induced characteristic mRNA expression profiles. Gene-set enrichment analysis demonstrated enrichment of WNT pathway signatures in MEFs expressing EWS/WT1 + KTS. Wnt-activation was validated in cell lines with over-expression of EWS/WT1 and in DSRCT. CONCLUSION: In conclusion, we show both isoforms of EWS/WT1 have oncogenic potential in MEFs with loss of p53. In addition we provide the first link between EWS/WT1 and Wnt-pathway signaling. These data provide novel insights into the function of the EWS/WT1 fusion protein which characterize DSRCT.

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Published In

BMC Cancer

DOI

EISSN

1471-2407

Publication Date

December 9, 2013

Volume

13

Start / End Page

585

Location

England

Related Subject Headings

  • Wnt Signaling Pathway
  • Tumor Suppressor Protein p53
  • Transcriptome
  • Radiation Tolerance
  • Proto-Oncogene Proteins c-mdm2
  • Proto-Oncogene Proteins
  • Oncology & Carcinogenesis
  • Oncogene Proteins, Fusion
  • Nuclear Proteins
  • Mice, Transgenic
 

Citation

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Bandopadhayay, P., Jabbour, A. M., Riffkin, C., Salmanidis, M., Gordon, L., Popovski, D., … Ekert, P. G. (2013). The oncogenic properties of EWS/WT1 of desmoplastic small round cell tumors are unmasked by loss of p53 in murine embryonic fibroblasts. BMC Cancer, 13, 585. https://doi.org/10.1186/1471-2407-13-585
Bandopadhayay, Pratiti, Anissa M. Jabbour, Christopher Riffkin, Marika Salmanidis, Lavinia Gordon, Dean Popovski, Lin Rigby, et al. “The oncogenic properties of EWS/WT1 of desmoplastic small round cell tumors are unmasked by loss of p53 in murine embryonic fibroblasts.BMC Cancer 13 (December 9, 2013): 585. https://doi.org/10.1186/1471-2407-13-585.
Bandopadhayay P, Jabbour AM, Riffkin C, Salmanidis M, Gordon L, Popovski D, et al. The oncogenic properties of EWS/WT1 of desmoplastic small round cell tumors are unmasked by loss of p53 in murine embryonic fibroblasts. BMC Cancer. 2013 Dec 9;13:585.
Bandopadhayay, Pratiti, et al. “The oncogenic properties of EWS/WT1 of desmoplastic small round cell tumors are unmasked by loss of p53 in murine embryonic fibroblasts.BMC Cancer, vol. 13, Dec. 2013, p. 585. Pubmed, doi:10.1186/1471-2407-13-585.
Bandopadhayay P, Jabbour AM, Riffkin C, Salmanidis M, Gordon L, Popovski D, Rigby L, Ashley DM, Watkins DN, Thomas DM, Algar E, Ekert PG. The oncogenic properties of EWS/WT1 of desmoplastic small round cell tumors are unmasked by loss of p53 in murine embryonic fibroblasts. BMC Cancer. 2013 Dec 9;13:585.
Journal cover image

Published In

BMC Cancer

DOI

EISSN

1471-2407

Publication Date

December 9, 2013

Volume

13

Start / End Page

585

Location

England

Related Subject Headings

  • Wnt Signaling Pathway
  • Tumor Suppressor Protein p53
  • Transcriptome
  • Radiation Tolerance
  • Proto-Oncogene Proteins c-mdm2
  • Proto-Oncogene Proteins
  • Oncology & Carcinogenesis
  • Oncogene Proteins, Fusion
  • Nuclear Proteins
  • Mice, Transgenic