Abstract

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.

Highlights

  • Cancer is the leading cause of disease-related mortality in children

  • Using either mean or median to split the cohort, PDX for Childhood Cancer Therapeutics (PCAT) shows high TERT expression is significantly associated with worse overall survival in the TARGET neuroblastoma dataset (Figure 4C)

  • We describe PCAT, a new resource for childhood cancer Patient-derived xenograft (PDX) models

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Summary

Introduction

Cancer is the leading cause of disease-related mortality in children. Approximately 300,000 children under age of 14 are diagnosed with cancer globally each year [1]. PCAT currently stores information of 324 PDX models spanning all major cancer types seen in children, including some very rare subtypes. 309 have at least one type of genomic profiling data (somatic mutation, n=289; expression/fusion, n=244; copy number, n=282). In addition to PDX models, PCAT curated patient tumor data from TARGET (Supplementary Figure 2).

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