Novel patient-derived models of desmoplastic small round cell tumor confirm a targetable dependency on ERBB signaling Journal Article


Authors: Smith, R. S.; Odintsov, I.; Liu, Z.; Lui, A. J. W.; Hayashi, T.; Vojnic, M.; Suehara, Y.; Delasos, L.; Mattar, M. S.; Hmeljak, J.; Ramirez, H. A.; Shaw, M.; Bui, G.; Hartono, A. B.; Gladstone, E.; Kunte, S.; Magnan, H.; Khodos, I.; De Stanchina, E.; La Quaglia, M. P.; Yao, J.; Laé, M.; Lee, S. B.; Spraggon, L.; Pratilas, C. A.; Ladanyi, M.; Somwar, R.
Article Title: Novel patient-derived models of desmoplastic small round cell tumor confirm a targetable dependency on ERBB signaling
Abstract: Desmoplastic small round cell tumor (DSRCT) is characterized by the t(11;22)(p13;q12) translocation, which fuses the transcriptional regulatory domain of EWSR1 with the DNA-binding domain of WT1, resulting in the oncogenic EWSR1-WT1 fusion protein. The paucity of DSRCT disease models has hampered preclinical therapeutic studies on this aggressive cancer. Here, we developed preclinical disease models and mined DSRCT expression profiles to identify genetic vulnerabilities that could be leveraged for new therapies. We describe four DSRCT cell lines and one patient-derived xenograft model. Transcriptomic, proteomic and biochemical profiling showed evidence of activation of the ERBB pathway. Ectopic expression of EWSR1-WT1 resulted in upregulation of ERRB family ligands. Treatment of DSRCT cell lines with ERBB ligands resulted in activation of EGFR, ERBB2, ERK1/2 and AKT, and stimulation of cell growth. Antagonizing EGFR function with shRNAs, small-molecule inhibitors (afatinib, neratinib) or an anti-EGFR antibody (cetuximab) inhibited proliferation of DSRCT cells. Finally, treatment of mice bearing DSRCT xenografts with a combination of cetuximab and afatinib significantly reduced tumor growth. These data provide a rationale for evaluating EGFR antagonists in patients with DSRCT. © 2022. Published by The Company of Biologists Ltd
Keywords: egfr; ewsr1-wt1; dsrct pdx; sarcoma proteomics
Journal Title: Disease Models & Mechanisms
Volume: 15
Issue: 1
ISSN: 1754-8403
Publisher: Company of Biologists  
Date Published: 2022-01-01
Start Page: dmm047621
Language: English
DOI: 10.1242/dmm.047621
PUBMED: 34841430
PROVIDER: scopus
PMCID: PMC8807576
DOI/URL:
Notes: Article -- Export Date: 1 March 2022 -- Source: Scopus
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MSK Authors
  1. Marick E. Lae
    16 Lae
  2. Jinjuan Yao
    58 Yao
  3. Marc Ladanyi
    1326 Ladanyi
  4. Romel Somwar
    110 Somwar
  5. Yoshiyuki Suehara
    10 Suehara
  6. Heather Magnan
    31 Magnan
  7. Lukas   Delasos
    14 Delasos
  8. Roger Stephen Smith
    20 Smith
  9. Inna   Khodos
    36 Khodos
  10. Marissa   Mattar
    56 Mattar
  11. Morana Vojnic
    17 Vojnic
  12. Jo Weng Allan Lui
    15 Lui
  13. Siddharth Kunte
    8 Kunte
  14. Zebing Liu
    5 Liu