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pmid:31556110

A P53-related microRNA model for predicting the prognosis of hepatocellular carcinoma patients.

Shuang-Sang Fang · Jin-Cheng Guo · Jian-Hua Zhang · Jin-Na Liu · Shuai Hong · Bo Yu · Yuhan Gao · Su-Pei Hu · Hai-Zhong Liu · Liang Sun · Yi Zhao

Journal of cellular physiology · 2020 doi:10.1002/jcp.29245

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:31556110
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title
A P53-related microRNA model for predicting the prognosis of hepatocellular carcinoma patients.
doi
10.1002/jcp.29245
pmid
31556110
authors array · 11 items
[0]
Shuang-Sang Fang
[1]
Jin-Cheng Guo
[2]
Jian-Hua Zhang
[3]
Jin-Na Liu
[4]
Shuai Hong
[5]
Bo Yu
[6]
Yuhan Gao
[7]
Su-Pei Hu
[8]
Hai-Zhong Liu
[9]
Liang Sun
[10]
Yi Zhao
journal
Journal of cellular physiology
year
2020
abstract
Studies have shown that microRNAs (miRNAs) play a vital role in tumor progression and patients' prognosis. Therefore, we aimed to construct a miRNA model for forecasting the survival of hepatocellular carcinoma (HCC) patients. The gene expression data of 433 patients with HCC from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus public databases were remined by survival analysis and receptor manipulation characteristic curve (ROC). A prognostic model including six miRNAs (hsa-mir-26a-1-3p, hsa-mir-188-5p, hsa-mir-212-5p, hsa-mir-149-5p, hsa-mir-105-5p, and hsa-mir-132-5p) were constructed in the training dataset (TCGA, n = 333). HCC patients were stratified into a high-risk group and a low-risk group with significantly different survival (median: 2.75 vs. 8.93 years, log-rank test p < .001). Then we proved its performance of stratification in another independent dataset (GSE116182, median: 2.55 vs 6.96 years, log-rank test p = .008). Cox regression analysis showed that the prognostic model was an independent prognostic indicator for HCC patients. Then time-dependent ROC analyses were performed to test the prognostic ability of the model with that of TNM staging, we found the model had a better performance, especially at 5 years (AUC = 0.76). Functional prediction showed that the genes targeted by the six prognostic miRNAs in the prognostic model were highly expressed in the P53-related pathway. In conclusion, we constructed a prognostic miRNA model that could indicate the survival of HCC patients.
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The gene expression data of 433 patients with HCC from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus public databases were remined by survival analysis and receptor manipulation characteristic curve (ROC).
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A prognostic model including six miRNAs (hsa‐mir‐26a‐1‐3p, hsa‐mir‐188‐5p, hsa‐mir‐212‐5p, hsa‐mir‐149‐5p, hsa‐mir‐105‐5p, and hsa‐mir‐132‐5p) were constructed in the training dataset (TCGA, n = 333).
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A prognostic model including six miRNAs (hsa‐mir‐26a‐1‐3p, hsa‐mir‐188‐5p, hsa‐mir‐212‐5p, hsa‐mir‐149‐5p, hsa‐mir‐105‐5p, and hsa‐mir‐132‐5p) were constructed in the training dataset (TCGA, n = 333).
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A prognostic model including six microRNAs predicted survival time and more precisely and finely stratified HCC patient stage when combined with TNM stages.
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In conclusion, the prognostic model including six microRNAs could predict the survival time of hepatocellular carcinoma (HCC) patients with more precision and fine stratify HCC patient stage combined with TNM stages.
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A prognostic model including six miRNAs (hsa‐mir‐26a‐1‐3p, hsa‐mir‐188‐5p, hsa‐mir‐212‐5p, hsa‐mir‐149‐5p, hsa‐mir‐105‐5p, and hsa‐mir‐132‐5p) were constructed in the training dataset (TCGA, n = 333).
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MicroRNA expression profile in human hepatocellular carcinoma
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