Lee Byron H
Urol Oncol. 2017 Sep;35(9):579-580. doi: 10.1016/j.urolonc.2017.07.023. Epub 2017 Aug 5.
Dysregulated metabolism is a hallmark of cancer, manifested through alterations in metabolites. We performed metabolomic profiling on 138 matched clear cell renal cell carcinoma (ccRCC)/normal tissue pairs and found that ccRCC is characterized by broad shifts in central carbon metabolism, one-carbon metabolism, and antioxidant response. Tumor progression and metastasis were associated with metabolite increases in glutathione and cysteine/methionine metabolism pathways. We develop an analytic pipeline and visualization tool (metabolograms) to bridge the gap between TCGA transcriptomic profiling and our metabolomic data, which enables us to assemble an integrated pathway-level metabolic atlas and to demonstrate discordance between transcriptome and metabolome. Lastly, expression profiling was performed on a high-glutathione cluster, which corresponds to a poor-survival subgroup in the ccRCC TCGA cohort.
代谢失调是癌症的一个标志,通过代谢物的改变表现出来。我们对138对匹配的透明细胞肾细胞癌(ccRCC)/正常组织进行了代谢组学分析,发现ccRCC的特征是中心碳代谢、一碳代谢和抗氧化反应发生广泛变化。肿瘤进展和转移与谷胱甘肽以及半胱氨酸/甲硫氨酸代谢途径中的代谢物增加有关。我们开发了一个分析流程和可视化工具(代谢图)来弥合TCGA转录组分析与我们的代谢组学数据之间的差距,这使我们能够构建一个综合的通路水平代谢图谱,并证明转录组和代谢组之间的不一致。最后,对一个高谷胱甘肽簇进行了表达分析,该簇对应于ccRCC TCGA队列中预后较差的亚组。