4.3 Article

Screening differential circular RNA expression profiles reveals hsa_ circ_ 0004018 is associated with hepatocellular carcinoma

Journal

ONCOTARGET
Volume 8, Issue 35, Pages 58405-58416

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.16881

Keywords

hsa_circ_0004018; circular RNA; hepatocellular carcinom; microRNA; biomarker

Funding

  1. Foundation for Hepatitis Prevention and Control Project of China [TQGB20150219]
  2. Zhejiang Medical Scientific Research Foundation [2017KY140]
  3. Regional Medical Center Project of Zhejiang Province [201498]
  4. Natural Science Foundation of Ningbo [2015A10236]

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Circular RNAs (circRNAs) have been emerged as an indispensable part of endogenous RNA network. However, the expression significance of circRNAs in hepatocellular carcinoma (HCC) is rarely revealed. The aim of this study was to determine the circRNA expression profile in HCC, and to investigate their clinical significances and relevant mechanisms for cancer progression. The global circRNA expression profile in HCC was measured by circRNA microarray. Levels of one representative circRNAs, hsa_circ_0004018, were confirmed by real-time reverse transcription-polymerase chain reaction. The expression levels of hsa_circ_0004018 in HCC were significantly lower compared with para-tumorous tissue (P<0.001). Our data further showed that lower expression of hsa_circ_0004018 was correlated with serum alpha-fetoprotein (AFP) level, tumor diameters, differentiation, Barcelona Clinic Liver Cancer stage and Tumor-node-metastasis stage. More importantly, we detected liver tissues from chronic hepatitis, cirrhosis and HCC patients; and found that hsa_circ_0004018 harbored HCC-stage-specific expression features in diverse chronic liver diseases (P<0.001). The area under receiver operating characteristic curve was up to 0.848 (95% CI=0.803-0.894, P<0.001). The sensitivity and specificity were 0.716 and 0.815, respectively. Finally, hsa_circ_0004018 might be involved in cancer-related pathways via interactions with miRNAs.

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