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PCAT: an integrated portal for genomic and preclinical testing data of pediatric cancer patient-derived xenograft models
Although cancer is the leading cause of disease-related mortality in children, the relative rarity of pediatric cancers poses a significant challenge for developing novel therapeutics to further improve prognosis. Patient-derived xenograft (PDX) models, which are usually developed from high-risk tum...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778893/ https://www.ncbi.nlm.nih.gov/pubmed/32810235 http://dx.doi.org/10.1093/nar/gkaa698 |
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author | Yang, Juechen Li, Qilin Noureen, Nighat Fang, Yanbing Kurmasheva, Raushan Houghton, Peter J Wang, Xiaojing Zheng, Siyuan |
author_facet | Yang, Juechen Li, Qilin Noureen, Nighat Fang, Yanbing Kurmasheva, Raushan Houghton, Peter J Wang, Xiaojing Zheng, Siyuan |
author_sort | Yang, Juechen |
collection | PubMed |
description | Although cancer is the leading cause of disease-related mortality in children, the relative rarity of pediatric cancers poses a significant challenge for developing novel therapeutics to further improve prognosis. Patient-derived xenograft (PDX) models, which are usually developed from high-risk tumors, are a useful platform to study molecular driver events, identify biomarkers and prioritize therapeutic agents. Here, we develop PDX for Childhood Cancer Therapeutics (PCAT), a new integrated portal for pediatric cancer PDX models. Distinct from previously reported PDX portals, PCAT is focused on pediatric cancer models and provides intuitive interfaces for querying and data mining. The current release comprises 324 models and their associated clinical and genomic data, including gene expression, mutation and copy number alteration. Importantly, PCAT curates preclinical testing results for 68 models and 79 therapeutic agents manually collected from individual agent testing studies published since 2008. To facilitate comparisons of patterns between patient tumors and PDX models, PCAT curates clinical and molecular data of patient tumors from the TARGET project. In addition, PCAT provides access to gene fusions identified in nearly 1000 TARGET samples. PCAT was built using R-shiny and MySQL. The portal can be accessed at http://pcat.zhenglab.info or http://www.pedtranscriptome.org. |
format | Online Article Text |
id | pubmed-7778893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77788932021-01-06 PCAT: an integrated portal for genomic and preclinical testing data of pediatric cancer patient-derived xenograft models Yang, Juechen Li, Qilin Noureen, Nighat Fang, Yanbing Kurmasheva, Raushan Houghton, Peter J Wang, Xiaojing Zheng, Siyuan Nucleic Acids Res Database Issue Although cancer is the leading cause of disease-related mortality in children, the relative rarity of pediatric cancers poses a significant challenge for developing novel therapeutics to further improve prognosis. Patient-derived xenograft (PDX) models, which are usually developed from high-risk tumors, are a useful platform to study molecular driver events, identify biomarkers and prioritize therapeutic agents. Here, we develop PDX for Childhood Cancer Therapeutics (PCAT), a new integrated portal for pediatric cancer PDX models. Distinct from previously reported PDX portals, PCAT is focused on pediatric cancer models and provides intuitive interfaces for querying and data mining. The current release comprises 324 models and their associated clinical and genomic data, including gene expression, mutation and copy number alteration. Importantly, PCAT curates preclinical testing results for 68 models and 79 therapeutic agents manually collected from individual agent testing studies published since 2008. To facilitate comparisons of patterns between patient tumors and PDX models, PCAT curates clinical and molecular data of patient tumors from the TARGET project. In addition, PCAT provides access to gene fusions identified in nearly 1000 TARGET samples. PCAT was built using R-shiny and MySQL. The portal can be accessed at http://pcat.zhenglab.info or http://www.pedtranscriptome.org. Oxford University Press 2020-08-18 /pmc/articles/PMC7778893/ /pubmed/32810235 http://dx.doi.org/10.1093/nar/gkaa698 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Database Issue Yang, Juechen Li, Qilin Noureen, Nighat Fang, Yanbing Kurmasheva, Raushan Houghton, Peter J Wang, Xiaojing Zheng, Siyuan PCAT: an integrated portal for genomic and preclinical testing data of pediatric cancer patient-derived xenograft models |
title | PCAT: an integrated portal for genomic and preclinical testing data of pediatric cancer patient-derived xenograft models |
title_full | PCAT: an integrated portal for genomic and preclinical testing data of pediatric cancer patient-derived xenograft models |
title_fullStr | PCAT: an integrated portal for genomic and preclinical testing data of pediatric cancer patient-derived xenograft models |
title_full_unstemmed | PCAT: an integrated portal for genomic and preclinical testing data of pediatric cancer patient-derived xenograft models |
title_short | PCAT: an integrated portal for genomic and preclinical testing data of pediatric cancer patient-derived xenograft models |
title_sort | pcat: an integrated portal for genomic and preclinical testing data of pediatric cancer patient-derived xenograft models |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778893/ https://www.ncbi.nlm.nih.gov/pubmed/32810235 http://dx.doi.org/10.1093/nar/gkaa698 |
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