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Efficacy of ONC201 in Desmoplastic Small Round Cell Tumor()
Desmoplastic Small Round Cell Tumor (DSRCT) is a rare sarcoma tumor of adolescence and young adulthood, which harbors a recurrent chromosomal translocation between the Ewing’s sarcoma gene (EWSR1) and the Wilms’ tumor suppressor gene (WT1). Patients usually develop multiple abdominal tumors with liv...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Neoplasia Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915995/ https://www.ncbi.nlm.nih.gov/pubmed/29626752 http://dx.doi.org/10.1016/j.neo.2018.02.006 |
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author | Hayes-Jordan, Andrea A. Ma, Xiao Menegaz, Brian A. Lamhamedi-Cherradi, Salah-Eddine Kingsley, Charles V. Benson, Jalen A. Camacho, Pamela E. Ludwig, Joseph A. Lockworth, Cynthia R. Garcia, Gloria E. Craig, Suzanne L. |
author_facet | Hayes-Jordan, Andrea A. Ma, Xiao Menegaz, Brian A. Lamhamedi-Cherradi, Salah-Eddine Kingsley, Charles V. Benson, Jalen A. Camacho, Pamela E. Ludwig, Joseph A. Lockworth, Cynthia R. Garcia, Gloria E. Craig, Suzanne L. |
author_sort | Hayes-Jordan, Andrea A. |
collection | PubMed |
description | Desmoplastic Small Round Cell Tumor (DSRCT) is a rare sarcoma tumor of adolescence and young adulthood, which harbors a recurrent chromosomal translocation between the Ewing’s sarcoma gene (EWSR1) and the Wilms’ tumor suppressor gene (WT1). Patients usually develop multiple abdominal tumors with liver and lymph node metastasis developing later. Survival is poor using a multimodal therapy that includes chemotherapy, radiation and surgical resection, new therapies are needed for better management of DSRCT. Triggering cell apoptosis is the scientific rationale of many cancer therapies. Here, we characterized for the first time the expression of pro-apoptotic receptors, tumor necrosis-related apoptosis-inducing ligand receptors (TRAILR1-4) within an established human DSRCT cell line and clinical samples. The molecular induction of TRAIL-mediated apoptosis using agonistic small molecule, ONC201 in vitro cell-based proliferation assay and in vivo novel orthotopic xenograft animal models of DSRCT, was able to inhibit cell proliferation that was associated with caspase activation, and tumor growth, indicating that a cell-based delivery of an apoptosis-inducing factor could be relevant therapeutic agent to control DSRCT. |
format | Online Article Text |
id | pubmed-5915995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Neoplasia Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59159952018-04-27 Efficacy of ONC201 in Desmoplastic Small Round Cell Tumor() Hayes-Jordan, Andrea A. Ma, Xiao Menegaz, Brian A. Lamhamedi-Cherradi, Salah-Eddine Kingsley, Charles V. Benson, Jalen A. Camacho, Pamela E. Ludwig, Joseph A. Lockworth, Cynthia R. Garcia, Gloria E. Craig, Suzanne L. Neoplasia Original article Desmoplastic Small Round Cell Tumor (DSRCT) is a rare sarcoma tumor of adolescence and young adulthood, which harbors a recurrent chromosomal translocation between the Ewing’s sarcoma gene (EWSR1) and the Wilms’ tumor suppressor gene (WT1). Patients usually develop multiple abdominal tumors with liver and lymph node metastasis developing later. Survival is poor using a multimodal therapy that includes chemotherapy, radiation and surgical resection, new therapies are needed for better management of DSRCT. Triggering cell apoptosis is the scientific rationale of many cancer therapies. Here, we characterized for the first time the expression of pro-apoptotic receptors, tumor necrosis-related apoptosis-inducing ligand receptors (TRAILR1-4) within an established human DSRCT cell line and clinical samples. The molecular induction of TRAIL-mediated apoptosis using agonistic small molecule, ONC201 in vitro cell-based proliferation assay and in vivo novel orthotopic xenograft animal models of DSRCT, was able to inhibit cell proliferation that was associated with caspase activation, and tumor growth, indicating that a cell-based delivery of an apoptosis-inducing factor could be relevant therapeutic agent to control DSRCT. Neoplasia Press 2018-04-05 /pmc/articles/PMC5915995/ /pubmed/29626752 http://dx.doi.org/10.1016/j.neo.2018.02.006 Text en © 2018 Published by Elsevier Inc. on behalf of Neoplasia Press, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original article Hayes-Jordan, Andrea A. Ma, Xiao Menegaz, Brian A. Lamhamedi-Cherradi, Salah-Eddine Kingsley, Charles V. Benson, Jalen A. Camacho, Pamela E. Ludwig, Joseph A. Lockworth, Cynthia R. Garcia, Gloria E. Craig, Suzanne L. Efficacy of ONC201 in Desmoplastic Small Round Cell Tumor() |
title | Efficacy of ONC201 in Desmoplastic Small Round Cell Tumor() |
title_full | Efficacy of ONC201 in Desmoplastic Small Round Cell Tumor() |
title_fullStr | Efficacy of ONC201 in Desmoplastic Small Round Cell Tumor() |
title_full_unstemmed | Efficacy of ONC201 in Desmoplastic Small Round Cell Tumor() |
title_short | Efficacy of ONC201 in Desmoplastic Small Round Cell Tumor() |
title_sort | efficacy of onc201 in desmoplastic small round cell tumor() |
topic | Original article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915995/ https://www.ncbi.nlm.nih.gov/pubmed/29626752 http://dx.doi.org/10.1016/j.neo.2018.02.006 |
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