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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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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 |
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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 |
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