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- W2507788101 abstract "Cancer cell metabolism has received increasing attention. Despite a boost in the application of clinical metabolic profiling (CMP) in cancer patients, a meta‐analysis has not been performed. The primary goal of this study was to assess whether public accessibility of metabolomics data and identification and reporting of metabolites were sufficient to assess which metabolites were consistently altered in cancer patients. We therefore retrospectively curated data from CMP studies in cancer patients published during 5 recent years and used an established vote‐counting method to perform a semiquantitative meta‐analysis of metabolites in tumor tissue and blood. This analysis confirmed well‐known increases in glycolytic metabolites, but also unveiled unprecedented changes in other metabolites such as ketone bodies and amino acids (histidine, tryptophan). However, this study also highlighted that insufficient public accessibility of metabolomics data, and inadequate metabolite identification and reporting hamper the discovery potential of meta‐analyses of CMP studies, calling for improved standardization of metabolomics studies.![][1] The results of clinical metabolic profiling studies in cancer were curated and a meta‐analysis was subsequently performed to identify deregulated metabolites in blood, tissue, and urine.EMBO Mol Med (2016) 8: 1134–1142 [1]: /embed/graphic-1.gif" @default.
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- W2507788101 date "2016-09-06" @default.
- W2507788101 modified "2023-10-11" @default.
- W2507788101 title "Meta‐analysis of clinical metabolic profiling studies in cancer: challenges and opportunities" @default.
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- W2507788101 doi "https://doi.org/10.15252/emmm.201606798" @default.
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