A novel RNA sequencing‐based mi RNA signature predicts with recurrence and outcome of hepatocellular carcinoma
Hepatocellular carcinoma ( HCC ) is the fifth most common type of cancer and the second leading cause of cancer‐related deaths worldwide. Given that the rate of HCC recurrence 5 years after liver resection is as high as 70%, patient with HCC typically has a poor outcome. A biomarker or set of biomar...
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Veröffentlicht in: | Molecular oncology 2018-06, Vol.12 (7), p.1125-1137 |
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Sprache: | eng |
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Zusammenfassung: | Hepatocellular carcinoma (
HCC
) is the fifth most common type of cancer and the second leading cause of cancer‐related deaths worldwide. Given that the rate of
HCC
recurrence 5 years after liver resection is as high as 70%, patient with
HCC
typically has a poor outcome. A biomarker or set of biomarkers that could predict disease recurrence would have a substantial clinical impact, allowing earlier detection of recurrence and more effective treatment. With the aim of identifying a new micro
RNA
(mi
RNA
) signature associated with
HCC
recurrence, we analyzed data on 306 patients with
HCC
for whom both mi
RNA
expression profiles and complete clinical information were available from The Cancer Genome Atlas database. Through this analysis, we identified a six‐mi
RNA
signature that could effectively predict patients’ recurrence risk; the high‐risk and low‐risk groups had significantly different recurrence‐free survival rates. Time‐dependent receiver operating characteristic analysis indicated that this signature had a good predictive performance. Multivariable Cox regression and stratified analyses demonstrated that the six‐mi
RNA
signature was independent of other clinical features. Functional enrichment analysis of the gene targets of the six prognostic mi
RNA
indicated enrichment mainly in cancer‐related pathways and important cell biological processes. Our results support use of this six‐mi
RNA
signature as an independent factor for predicting recurrence and outcome of patients with
HCC
. |
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ISSN: | 1574-7891 1878-0261 |
DOI: | 10.1002/1878-0261.12315 |