Cargando…

A blood-based 22-gene expression signature for hepatocellular carcinoma identification

BACKGROUND: Hepatocellular carcinoma (HCC) is one of the most common and lethal malignancies. Early detection of HCC could largely reduce mortalities. Ultrasonography (US) and serum Alpha Fetoprotein (AFP) test are the screening methods that are most frequently applied to high-risk populations. Due...

Descripción completa

Detalles Bibliográficos
Autores principales: Zheng, Jie, Zhu, Ming-Yu, Wu, Fei, Kang, Bin, Liang, Ji, Heskia, Fabienne, Shan, Yun-Feng, Zhang, Xin-Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154425/
https://www.ncbi.nlm.nih.gov/pubmed/32309342
http://dx.doi.org/10.21037/atm.2020.01.93
_version_ 1783521814526296064
author Zheng, Jie
Zhu, Ming-Yu
Wu, Fei
Kang, Bin
Liang, Ji
Heskia, Fabienne
Shan, Yun-Feng
Zhang, Xin-Xin
author_facet Zheng, Jie
Zhu, Ming-Yu
Wu, Fei
Kang, Bin
Liang, Ji
Heskia, Fabienne
Shan, Yun-Feng
Zhang, Xin-Xin
author_sort Zheng, Jie
collection PubMed
description BACKGROUND: Hepatocellular carcinoma (HCC) is one of the most common and lethal malignancies. Early detection of HCC could largely reduce mortalities. Ultrasonography (US) and serum Alpha Fetoprotein (AFP) test are the screening methods that are most frequently applied to high-risk populations. Due to the poor performance of AFP testing, and the highly operator-dependent nature of US, a biomarker for HCC early diagnosis is highly sought after. We developed a method for HCC screening using a 22-gene expression signature. METHODS: Peripheral whole blood of 98 patients were processed through microarrays for the first round of feature selection via two strategies, Minimal Redundancy Maximal Relevance and Least Absolute Shrinkage and Selection Operator combined with Support Vector Machine (SVM). Candidate genes were combined for further validation through qPCR in an enlarged population with 316 samples with 104 chronic hepatitis, 112 liver cirrhosis (LC), and 100 HCC. RESULTS: A 22-gene signature was established in classifying HCC and non-cancer samples with good performance. The area under curve reached 0.94 in all of the samples and 0.93 in the AFP -negative samples. CONCLUSIONS: We have established a blood mRNA signature with high performance for HCC screening. Our results show transcriptome of peripheral blood could be valuable source for biomarkers.
format Online
Article
Text
id pubmed-7154425
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher AME Publishing Company
record_format MEDLINE/PubMed
spelling pubmed-71544252020-04-17 A blood-based 22-gene expression signature for hepatocellular carcinoma identification Zheng, Jie Zhu, Ming-Yu Wu, Fei Kang, Bin Liang, Ji Heskia, Fabienne Shan, Yun-Feng Zhang, Xin-Xin Ann Transl Med Original Article BACKGROUND: Hepatocellular carcinoma (HCC) is one of the most common and lethal malignancies. Early detection of HCC could largely reduce mortalities. Ultrasonography (US) and serum Alpha Fetoprotein (AFP) test are the screening methods that are most frequently applied to high-risk populations. Due to the poor performance of AFP testing, and the highly operator-dependent nature of US, a biomarker for HCC early diagnosis is highly sought after. We developed a method for HCC screening using a 22-gene expression signature. METHODS: Peripheral whole blood of 98 patients were processed through microarrays for the first round of feature selection via two strategies, Minimal Redundancy Maximal Relevance and Least Absolute Shrinkage and Selection Operator combined with Support Vector Machine (SVM). Candidate genes were combined for further validation through qPCR in an enlarged population with 316 samples with 104 chronic hepatitis, 112 liver cirrhosis (LC), and 100 HCC. RESULTS: A 22-gene signature was established in classifying HCC and non-cancer samples with good performance. The area under curve reached 0.94 in all of the samples and 0.93 in the AFP -negative samples. CONCLUSIONS: We have established a blood mRNA signature with high performance for HCC screening. Our results show transcriptome of peripheral blood could be valuable source for biomarkers. AME Publishing Company 2020-03 /pmc/articles/PMC7154425/ /pubmed/32309342 http://dx.doi.org/10.21037/atm.2020.01.93 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Zheng, Jie
Zhu, Ming-Yu
Wu, Fei
Kang, Bin
Liang, Ji
Heskia, Fabienne
Shan, Yun-Feng
Zhang, Xin-Xin
A blood-based 22-gene expression signature for hepatocellular carcinoma identification
title A blood-based 22-gene expression signature for hepatocellular carcinoma identification
title_full A blood-based 22-gene expression signature for hepatocellular carcinoma identification
title_fullStr A blood-based 22-gene expression signature for hepatocellular carcinoma identification
title_full_unstemmed A blood-based 22-gene expression signature for hepatocellular carcinoma identification
title_short A blood-based 22-gene expression signature for hepatocellular carcinoma identification
title_sort blood-based 22-gene expression signature for hepatocellular carcinoma identification
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154425/
https://www.ncbi.nlm.nih.gov/pubmed/32309342
http://dx.doi.org/10.21037/atm.2020.01.93
work_keys_str_mv AT zhengjie abloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT zhumingyu abloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT wufei abloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT kangbin abloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT liangji abloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT heskiafabienne abloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT shanyunfeng abloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT zhangxinxin abloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT zhengjie bloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT zhumingyu bloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT wufei bloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT kangbin bloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT liangji bloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT heskiafabienne bloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT shanyunfeng bloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification
AT zhangxinxin bloodbased22geneexpressionsignatureforhepatocellularcarcinomaidentification