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A single nucleotide polymorphism genotyping platform for the authentication of patient derived xenografts
Patient derived xenografts (PDXs) have become a vital, frequently used, component of anti-cancer drug development. PDXs can be serially passaged in vivo for years, and shared across laboratories. As a consequence, the potential for mis-identification and cross-contamination is possible, yet authenti...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312397/ https://www.ncbi.nlm.nih.gov/pubmed/27528024 http://dx.doi.org/10.18632/oncotarget.11125 |
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author | El-Hoss, Jad Jing, Duohui Evans, Kathryn Toscan, Cara Xie, Jinhan Lee, Hyunjoo Taylor, Renea A. Lawrence, Mitchell G. Risbridger, Gail P. MacKenzie, Karen L. Sutton, Rosemary Lock, Richard B. |
author_facet | El-Hoss, Jad Jing, Duohui Evans, Kathryn Toscan, Cara Xie, Jinhan Lee, Hyunjoo Taylor, Renea A. Lawrence, Mitchell G. Risbridger, Gail P. MacKenzie, Karen L. Sutton, Rosemary Lock, Richard B. |
author_sort | El-Hoss, Jad |
collection | PubMed |
description | Patient derived xenografts (PDXs) have become a vital, frequently used, component of anti-cancer drug development. PDXs can be serially passaged in vivo for years, and shared across laboratories. As a consequence, the potential for mis-identification and cross-contamination is possible, yet authentication of PDXs appears limited. We present a PDX Authentication System (PAS), by combining a commercially available OpenArray assay of single nucleotide polymorphisms (SNPs) with in-house R studio programs, to validate PDXs established in individual mice from acute lymphoblastic leukemia biopsies. The PAS is sufficiently robust to identify contamination at levels as low as 3%, similar to the gold standard of short tandem repeat (STR) profiling. We have surveyed a panel of PDXs established from 73 individual leukemia patients, and found that the PAS provided sufficient discriminatory power to identify each xenograft. The identified SNP-discrepant PDXs demonstrated distinct gene expression profiles, indicating a risk of contamination for PDXs at high passage number. The PAS also allows for the authentication of tumor cells with complex karyotypes from solid tumors including prostate cancer and Ewing's sarcoma. This study highlights the demands of authenticating PDXs for cancer research, and evaluates a reliable authentication platform that utilizes a commercially available and cost-effective system. |
format | Online Article Text |
id | pubmed-5312397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53123972017-03-06 A single nucleotide polymorphism genotyping platform for the authentication of patient derived xenografts El-Hoss, Jad Jing, Duohui Evans, Kathryn Toscan, Cara Xie, Jinhan Lee, Hyunjoo Taylor, Renea A. Lawrence, Mitchell G. Risbridger, Gail P. MacKenzie, Karen L. Sutton, Rosemary Lock, Richard B. Oncotarget Research Paper Patient derived xenografts (PDXs) have become a vital, frequently used, component of anti-cancer drug development. PDXs can be serially passaged in vivo for years, and shared across laboratories. As a consequence, the potential for mis-identification and cross-contamination is possible, yet authentication of PDXs appears limited. We present a PDX Authentication System (PAS), by combining a commercially available OpenArray assay of single nucleotide polymorphisms (SNPs) with in-house R studio programs, to validate PDXs established in individual mice from acute lymphoblastic leukemia biopsies. The PAS is sufficiently robust to identify contamination at levels as low as 3%, similar to the gold standard of short tandem repeat (STR) profiling. We have surveyed a panel of PDXs established from 73 individual leukemia patients, and found that the PAS provided sufficient discriminatory power to identify each xenograft. The identified SNP-discrepant PDXs demonstrated distinct gene expression profiles, indicating a risk of contamination for PDXs at high passage number. The PAS also allows for the authentication of tumor cells with complex karyotypes from solid tumors including prostate cancer and Ewing's sarcoma. This study highlights the demands of authenticating PDXs for cancer research, and evaluates a reliable authentication platform that utilizes a commercially available and cost-effective system. Impact Journals LLC 2016-08-09 /pmc/articles/PMC5312397/ /pubmed/27528024 http://dx.doi.org/10.18632/oncotarget.11125 Text en Copyright: © 2016 El-Hoss et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper El-Hoss, Jad Jing, Duohui Evans, Kathryn Toscan, Cara Xie, Jinhan Lee, Hyunjoo Taylor, Renea A. Lawrence, Mitchell G. Risbridger, Gail P. MacKenzie, Karen L. Sutton, Rosemary Lock, Richard B. A single nucleotide polymorphism genotyping platform for the authentication of patient derived xenografts |
title | A single nucleotide polymorphism genotyping platform for the authentication of patient derived xenografts |
title_full | A single nucleotide polymorphism genotyping platform for the authentication of patient derived xenografts |
title_fullStr | A single nucleotide polymorphism genotyping platform for the authentication of patient derived xenografts |
title_full_unstemmed | A single nucleotide polymorphism genotyping platform for the authentication of patient derived xenografts |
title_short | A single nucleotide polymorphism genotyping platform for the authentication of patient derived xenografts |
title_sort | single nucleotide polymorphism genotyping platform for the authentication of patient derived xenografts |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312397/ https://www.ncbi.nlm.nih.gov/pubmed/27528024 http://dx.doi.org/10.18632/oncotarget.11125 |
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