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A Seven-microRNA Expression Signature Predicts Survival in Hepatocellular Carcinoma
Hepatocellular carcinoma (HCC) is the fifth common cancer. The differential expression of microRNAs (miRNAs) has been associated with the prognosis of various cancers. However, limited information is available regarding genome-wide miRNA expression profiles in HCC to generate a tumor-specific miRNA...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4457814/ https://www.ncbi.nlm.nih.gov/pubmed/26046780 http://dx.doi.org/10.1371/journal.pone.0128628 |
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author | Zhang, Jian Chong, Charing C. N. Chen, George G. Lai, Paul B. S. |
author_facet | Zhang, Jian Chong, Charing C. N. Chen, George G. Lai, Paul B. S. |
author_sort | Zhang, Jian |
collection | PubMed |
description | Hepatocellular carcinoma (HCC) is the fifth common cancer. The differential expression of microRNAs (miRNAs) has been associated with the prognosis of various cancers. However, limited information is available regarding genome-wide miRNA expression profiles in HCC to generate a tumor-specific miRNA signature of prognostic values. In this study, the miRNA profiles in 327 HCC patients, including 327 tumor and 43 adjacent non-tumor tissues, from The Cancer Genome Atlas (TCGA) Liver hepatocellular carcinoma (LIHC) were analyzed. The associations of the differentially expressed miRNAs with patient survival and other clinical characteristics were examined with t-test and Cox proportional regression model. Finally, a tumor-specific miRNA signature was generated and examined with Kaplan–Meier survival, univariate\multivariate Cox regression analyses and KEGG pathway analysis. Results showed that a total of 207 miRNAs were found differentially expressed between tumor and adjacent non-tumor HCC tissues. 78 of them were also discriminatively expressed with gender, race, tumor grade and AJCC tumor stage. Seven miRNAs were significantly associated with survival (P value <0.001). Among the seven significant miRNAs, six (hsa-mir-326, hsa-mir-3677, hsa-mir-511-1, hsa-mir-511-2, hsa-mir-9-1, and hsa-mir-9-2) were negatively associated with overall survival (OS), while the remaining one (hsa-mir-30d) was positively correlated. A tumor-specific 7-miRNAs signature was generated and validated as an independent prognostic predictor. Collectively, we have identified and validated an independent prognostic model based on the expression of seven miRNAs, which can be used to assess patients’ survival. Additional work is needed to translate our model into clinical practice. |
format | Online Article Text |
id | pubmed-4457814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44578142015-06-09 A Seven-microRNA Expression Signature Predicts Survival in Hepatocellular Carcinoma Zhang, Jian Chong, Charing C. N. Chen, George G. Lai, Paul B. S. PLoS One Research Article Hepatocellular carcinoma (HCC) is the fifth common cancer. The differential expression of microRNAs (miRNAs) has been associated with the prognosis of various cancers. However, limited information is available regarding genome-wide miRNA expression profiles in HCC to generate a tumor-specific miRNA signature of prognostic values. In this study, the miRNA profiles in 327 HCC patients, including 327 tumor and 43 adjacent non-tumor tissues, from The Cancer Genome Atlas (TCGA) Liver hepatocellular carcinoma (LIHC) were analyzed. The associations of the differentially expressed miRNAs with patient survival and other clinical characteristics were examined with t-test and Cox proportional regression model. Finally, a tumor-specific miRNA signature was generated and examined with Kaplan–Meier survival, univariate\multivariate Cox regression analyses and KEGG pathway analysis. Results showed that a total of 207 miRNAs were found differentially expressed between tumor and adjacent non-tumor HCC tissues. 78 of them were also discriminatively expressed with gender, race, tumor grade and AJCC tumor stage. Seven miRNAs were significantly associated with survival (P value <0.001). Among the seven significant miRNAs, six (hsa-mir-326, hsa-mir-3677, hsa-mir-511-1, hsa-mir-511-2, hsa-mir-9-1, and hsa-mir-9-2) were negatively associated with overall survival (OS), while the remaining one (hsa-mir-30d) was positively correlated. A tumor-specific 7-miRNAs signature was generated and validated as an independent prognostic predictor. Collectively, we have identified and validated an independent prognostic model based on the expression of seven miRNAs, which can be used to assess patients’ survival. Additional work is needed to translate our model into clinical practice. Public Library of Science 2015-06-05 /pmc/articles/PMC4457814/ /pubmed/26046780 http://dx.doi.org/10.1371/journal.pone.0128628 Text en © 2015 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zhang, Jian Chong, Charing C. N. Chen, George G. Lai, Paul B. S. A Seven-microRNA Expression Signature Predicts Survival in Hepatocellular Carcinoma |
title | A Seven-microRNA Expression Signature Predicts Survival in Hepatocellular Carcinoma |
title_full | A Seven-microRNA Expression Signature Predicts Survival in Hepatocellular Carcinoma |
title_fullStr | A Seven-microRNA Expression Signature Predicts Survival in Hepatocellular Carcinoma |
title_full_unstemmed | A Seven-microRNA Expression Signature Predicts Survival in Hepatocellular Carcinoma |
title_short | A Seven-microRNA Expression Signature Predicts Survival in Hepatocellular Carcinoma |
title_sort | seven-microrna expression signature predicts survival in hepatocellular carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4457814/ https://www.ncbi.nlm.nih.gov/pubmed/26046780 http://dx.doi.org/10.1371/journal.pone.0128628 |
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