Multiple "Omics" data-based biomarker screening for hepatocellular carcinoma diagnosis

被引:56
作者
Liu, Xiao-Na [1 ]
Cui, Dan-Ni [1 ]
Li, Yu-Fang [1 ]
Liu, Yun-He [1 ]
Liu, Gang [1 ]
Liu, Lei [1 ]
机构
[1] Fudan Univ, Inst Biomed Sci, 131 Dongan Rd, Shanghai 200032, Peoples R China
关键词
Hepatocellular carcinoma; Diagnosis; Circulating tumor cells; Exosomes; Circulating tumor DNA; RNA; Metabolomics; Protein; CIRCULATING-TUMOR-CELLS; ISLAND DNA HYPERMETHYLATION; ALPHA-FETOPROTEIN; POTENTIAL BIOMARKERS; LIVER-CANCER; PROMOTER METHYLATION; PERIPHERAL-BLOOD; GUT MICROBIOME; CHROMOSOME; 8P; HEPATITIS-C;
D O I
10.3748/wjg.v25.i30.4199
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The huge prognostic difference between early and late stage hepatocellular carcinoma (HCC) is a challenging diagnostic problem. Alpha-fetopmtein is the mostly widely used biomarker for HCC used in the clinic however it's sensitivity and specificity of is not optimal. The development and application of multiple biotechnologies, including next generation sequencing, multiple "omics" data, that include genomics, epigenomics, transcriptomics, proteomics, metabolomics, metagenomics has been used for HCC diagnostic biomarker screening. Effective biomarkers/panels/models have been identified and validated at different clinical levels. A large proportion of these have a good diagnostic performance for HCC, especially for early HCC. In this article, we reviewed the various HCC biomarkers derived from "omics" data and discussed the advantages and disadvantages for diagnosis HCC.
引用
收藏
页码:4199 / 4212
页数:14
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