肾透明细胞癌
代谢组
代谢组学
转录组
生物
癌症研究
肾细胞癌
代谢物
谷胱甘肽
医学
生物信息学
病理
内分泌学
生物化学
基因表达
基因
酶
作者
A. Ari Hakimi,Ed Reznik,Chung‐Han Lee,Chad J. Creighton,A. Rose Brannon,Augustin Luna,Bülent Arman Aksoy,Eric Minwei Liu,Ronglai Shen,William Lee,Czau‐Siung Yang,Steve Stirdivant,Paul Russo,Ying-Bei Chen,Satish K. Tickoo,Victor E. Reuter,Emily H. Cheng,Chris Sander,James J. Hsieh
出处
期刊:Cancer Cell
[Cell Press]
日期:2016-01-01
卷期号:29 (1): 104-116
被引量:482
标识
DOI:10.1016/j.ccell.2015.12.004
摘要
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.
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