Assessment of patient-derived tumour xenografts (PDXs) as a discovery tool for cancer epigenomics

作者：Guilhamon Paul; Butcher Lee M; Presneau Nadege; Wilson Gareth A; Feber Andrew; Paul Dirk S; Scuette Moritz; Haybaeck Johannes; Keilholz Ulrich; Hoffman Jens; Ross Mark T; Flanagan Adrienne M; Beck Stephan^*

来源：Genome Medicine, 2014, 6(12): 116.

DOI：10.1186/s13073-014-0116-0

Background: The use of tumour xenografts is a well-established research tool in cancer genomics but has not yet been comprehensively evaluated for cancer epigenomics. %26lt;br%26gt;Methods: In this study, we assessed the suitability of patient-derived tumour xenografts (PDXs) for methylome analysis using Infinium 450 K Beadchips and MeDIP-seq. %26lt;br%26gt;Results: Controlled for confounding host (mouse) sequences, comparison of primary PDXs and matching patient tumours in a rare (osteosarcoma) and common (colon) cancer revealed that an average 2.7% of the assayed CpG sites undergo major (Delta beta %26gt;= 0.51) methylation changes in a cancer-specific manner as a result of the xenografting procedure. No significant subsequent methylation changes were observed after a second round of xenografting between primary and secondary PDXs. Based on computational simulation using publically available methylation data, we additionally show that future studies comparing two groups of PDXs should use 15 or more samples in each group to minimise the impact of xenografting-associated changes in methylation on comparison results. %26lt;br%26gt;Conclusions: Our results from rare and common cancers indicate that PDXs are a suitable discovery tool for cancer epigenomics and we provide guidance on how to overcome the observed limitations.

• 出版日期2014-12-12