PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
August 21, 2015Scientific Reports127 citationsOpen Access

Large-scale RNA-Seq Transcriptome Analysis of 4043 Cancers and 548 Normal Tissue Controls across 12 TCGA Cancer Types

View Full Paper
LPLi PengHunan Normal UniversityXBXiu Wu BianSouthwest General Health CenterDLDi Kang LiSouthwest University

Key Points

Key points are not available for this paper at this time.

Abstract

Abstract The Cancer Genome Atlas (TCGA) has accrued RNA-Seq-based transcriptome data for more than 4000 cancer tissue samples across 12 cancer types, translating these data into biological insights remains a major challenge. We analyzed and compared the transcriptomes of 4043 cancer and 548 normal tissue samples from 21 TCGA cancer types and created a comprehensive catalog of gene expression alterations for each cancer type. By clustering genes into co-regulated gene sets, we identified seven cross-cancer gene signatures altered across a diverse panel of primary human cancer samples. A 14-gene signature extracted from these seven cross-cancer gene signatures precisely differentiated between cancerous and normal samples, the predictive accuracy of leave-one-out cross-validation (LOOCV) were 92.04%, 96.23%, 91.76%, 90.05%, 88.17%, 94.29% and 99.10% for BLCA, BRCA, COAD, HNSC, LIHC, LUAD and LUSC, respectively. A lung cancer-specific gene signature, containing SFTPA1 and SFTPA2 genes, accurately distinguished lung cancer from other cancer samples, the predictive accuracy of LOOCV for TCGA and GSE5364 data were 95.68% and 100%, respectively. These gene signatures provide rich insights into the transcriptional programs that trigger tumorigenesis and metastasis and many genes in the signature gene panels may be of significant value to the diagnosis and treatment of cancer.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Peng et al. (2015) studied this question.

synapsesocial.com/papers/6a0cb19195872b300be8e033https://doi.org/10.1038/srep13413
Ask AI
Helpful
Bookmark
Share
View Full Paper