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10.1038/srep43353

http://scihub22266oqcxt.onion/10.1038/srep43353
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C5320559!5320559!28225065
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suck abstract from ncbi


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pmid28225065      Sci+Rep 2017 ; 7 (ä): ä
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  • A Comprehensive Analysis of Metabolomics and Transcriptomics in Cervical Cancer #MMPMID28225065
  • Yang K; Xia B; Wang W; Cheng J; Yin M; Xie H; Li J; Ma L; Yang C; Li A; Fan X; Dhillon HS; Hou Y; Lou G; Li K
  • Sci Rep 2017[]; 7 (ä): ä PMID28225065show ga
  • Cervical cancer (CC) still remains a common and deadly malignancy among females in developing countries. More accurate and reliable diagnostic methods/biomarkers should be discovered. In this study, we performed a comprehensive analysis of metabolomics (285 samples) and transcriptomics (52 samples) on the potential diagnostic implication and metabolic characteristic description in cervical cancer. Sixty-two metabolites were different between CC and normal controls (NOR), in which 5 metabolites (bilirubin, LysoPC(17:0), n-oleoyl threonine, 12-hydroxydodecanoic acid and tetracosahexaenoic acid) were selected as candidate biomarkers for CC. The AUC value, sensitivity (SE), and specificity (SP) of these 5 biomarkers were 0.99, 0.98 and 0.99, respectively. We further analysed the genes in 7 significantly enriched pathways, of which 117 genes, that were expressed differentially, were mainly involved in catalytic activity. Finally, a fully connected network of metabolites and genes in these pathways was built, which can increase the credibility of our selected metabolites. In conclusion, our biomarkers from metabolomics could set a path for CC diagnosis and screening. Our results also showed that variables of both transcriptomics and metabolomics were associated with CC.
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