| Literature DB >> 28410298 |
Wei Zhao1, Matthew Fitzgibbon, Lindsay Bergan, Nigel Clegg, David Crispin, Gordon B Mills, Martin McIntosh.
Abstract
RNA-seq and mass-spectrometry proteomics combined with growing data repositories have greatly increased the capacity to identify candidate proteins or protein sequence variants that share properties of ideal therapy targets, which include being abundant in cancer cells, absent or rare in adult organs (especially vital organs), and shared by many patient tumors. RNA-seq and fixed content arrays can identify genes that are overexpressed or misexpressed in cancer. RNA-seq is uniquely suited to identifying cancer-specific sequence variants. We review factors relevant for determining whether products of genes that are abundant or differentially abundant in RNA-seq are concordant or discordant with proteins that are identified as abundant or differentially abundant in mass-spectrometry proteomics assays.Entities:
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Year: 2017 PMID: 28410298 PMCID: PMC5839124 DOI: 10.1097/PPO.0000000000000258
Source DB: PubMed Journal: Cancer J ISSN: 1528-9117 Impact factor: 3.360