The Pan-Cancer analysis of pseudogene expression reveals biologically and clinically relevant tumour subtypes

被引:0
作者
Leng Han
Yuan Yuan
Siyuan Zheng
Yang Yang
Jun Li
Mary E. Edgerton
Lixia Diao
Yanxun Xu
Roeland G. W. Verhaak
Han Liang
机构
[1] The University of Texas MD Anderson Cancer Center,Department of Bioinformatics and Computational Biology
[2] 1400 Pressler Street,Division of Biostatistics
[3] Houston,Department of Pathology
[4] Texas 77030,undefined
[5] USA,undefined
[6] Graduate Program in Structural and Computational Biology and Molecular Biophysics,undefined
[7] Baylor College of Medicine,undefined
[8] The University of Texas Health Science Center at Houston,undefined
[9] School of Public Health,undefined
[10] The University of Texas MD Anderson Cancer Center,undefined
[11] 1515 Holcombe Boulevard,undefined
[12] Houston,undefined
[13] Texas 77030,undefined
[14] USA,undefined
来源
Nature Communications | / 5卷
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摘要
Although individual pseudogenes have been implicated in tumour biology, the biomedical significance and clinical relevance of pseudogene expression have not been assessed in a systematic way. Here we generate pseudogene expression profiles in 2,808 patient samples of seven cancer types from The Cancer Genome Atlas RNA-seq data using a newly developed computational pipeline. Supervised analysis reveals a significant number of pseudogenes differentially expressed among established tumour subtypes and pseudogene expression alone can accurately classify the major histological subtypes of endometrial cancer. Across cancer types, the tumour subtypes revealed by pseudogene expression show extensive and strong concordance with the subtypes defined by other molecular data. Strikingly, in kidney cancer, the pseudogene expression subtypes not only significantly correlate with patient survival, but also help stratify patients in combination with clinical variables. Our study highlights the potential of pseudogene expression analysis as a new paradigm for investigating cancer mechanisms and discovering prognostic biomarkers.
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