RNA-seq profiling reveals PBMC RNA as a potential biomarker for hepatocellular carcinoma

Abstract Hepatocellular carcinoma (HCC) is one of the most common malignant tumors and has extremely high morbidity and mortality. Although many existing studies have focused on the identification of biomarkers, little information has been uncovered regarding the PBMC RNA profile of HCC. We attempte...

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Autores principales: Zhiyi Han, Wenxing Feng, Rui Hu, Qinyu Ge, Wenfeng Ma, Wei Zhang, Shaomin Xu, Bolin Zhan, Lai Zhang, Xinfeng Sun, Xiaozhou Zhou
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/c341afc478664a56b2965c0c74e05690
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spelling oai:doaj.org-article:c341afc478664a56b2965c0c74e056902021-12-02T18:03:05ZRNA-seq profiling reveals PBMC RNA as a potential biomarker for hepatocellular carcinoma10.1038/s41598-021-96952-x2045-2322https://doaj.org/article/c341afc478664a56b2965c0c74e056902021-09-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-96952-xhttps://doaj.org/toc/2045-2322Abstract Hepatocellular carcinoma (HCC) is one of the most common malignant tumors and has extremely high morbidity and mortality. Although many existing studies have focused on the identification of biomarkers, little information has been uncovered regarding the PBMC RNA profile of HCC. We attempted to create a profile throughout using expression of peripheral blood mononuclear cell (PBMC) RNA using RNA-seq technology and compared the transcriptome between HCC patients and healthy controls. Seventeen patients and 17 matched healthy controls were included in this study, and PBMC RNA was sequenced from all samples. Sequencing data were analyzed using bioinformatics tools, and quantitative reverse transcription PCR (qRT-PCR) was used for selected validation of DEGs. A total of 1,578 dysregulated genes were found in the PBMC samples, including 1,334 upregulated genes and 244 downregulated genes. GO enrichment and KEGG studies revealed that HCC is closely linked to differentially expressed genes (DEGs) implicated in the immune response. Expression of 6 selected genes (SELENBP1, SLC4A1, SLC26A8, HSPA8P4, CALM1, and RPL7p24) was confirmed by qRT-PCR, and higher sensitivity and specificity were obtained by ROC analysis of the 6 genes. CALM1 was found to gradually decrease as tumors enlarged. Nearly the opposite expression modes were obtained when compared to tumor sequencing data. Immune cell populations exhibited significant differences between HCC and controls. These findings suggest a potential biomarker for the diagnosis of HCC. This study provides new perspectives for liver cancer development and possible future successful clinical diagnosis.Zhiyi HanWenxing FengRui HuQinyu GeWenfeng MaWei ZhangShaomin XuBolin ZhanLai ZhangXinfeng SunXiaozhou ZhouNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Zhiyi Han
Wenxing Feng
Rui Hu
Qinyu Ge
Wenfeng Ma
Wei Zhang
Shaomin Xu
Bolin Zhan
Lai Zhang
Xinfeng Sun
Xiaozhou Zhou
RNA-seq profiling reveals PBMC RNA as a potential biomarker for hepatocellular carcinoma
description Abstract Hepatocellular carcinoma (HCC) is one of the most common malignant tumors and has extremely high morbidity and mortality. Although many existing studies have focused on the identification of biomarkers, little information has been uncovered regarding the PBMC RNA profile of HCC. We attempted to create a profile throughout using expression of peripheral blood mononuclear cell (PBMC) RNA using RNA-seq technology and compared the transcriptome between HCC patients and healthy controls. Seventeen patients and 17 matched healthy controls were included in this study, and PBMC RNA was sequenced from all samples. Sequencing data were analyzed using bioinformatics tools, and quantitative reverse transcription PCR (qRT-PCR) was used for selected validation of DEGs. A total of 1,578 dysregulated genes were found in the PBMC samples, including 1,334 upregulated genes and 244 downregulated genes. GO enrichment and KEGG studies revealed that HCC is closely linked to differentially expressed genes (DEGs) implicated in the immune response. Expression of 6 selected genes (SELENBP1, SLC4A1, SLC26A8, HSPA8P4, CALM1, and RPL7p24) was confirmed by qRT-PCR, and higher sensitivity and specificity were obtained by ROC analysis of the 6 genes. CALM1 was found to gradually decrease as tumors enlarged. Nearly the opposite expression modes were obtained when compared to tumor sequencing data. Immune cell populations exhibited significant differences between HCC and controls. These findings suggest a potential biomarker for the diagnosis of HCC. This study provides new perspectives for liver cancer development and possible future successful clinical diagnosis.
format article
author Zhiyi Han
Wenxing Feng
Rui Hu
Qinyu Ge
Wenfeng Ma
Wei Zhang
Shaomin Xu
Bolin Zhan
Lai Zhang
Xinfeng Sun
Xiaozhou Zhou
author_facet Zhiyi Han
Wenxing Feng
Rui Hu
Qinyu Ge
Wenfeng Ma
Wei Zhang
Shaomin Xu
Bolin Zhan
Lai Zhang
Xinfeng Sun
Xiaozhou Zhou
author_sort Zhiyi Han
title RNA-seq profiling reveals PBMC RNA as a potential biomarker for hepatocellular carcinoma
title_short RNA-seq profiling reveals PBMC RNA as a potential biomarker for hepatocellular carcinoma
title_full RNA-seq profiling reveals PBMC RNA as a potential biomarker for hepatocellular carcinoma
title_fullStr RNA-seq profiling reveals PBMC RNA as a potential biomarker for hepatocellular carcinoma
title_full_unstemmed RNA-seq profiling reveals PBMC RNA as a potential biomarker for hepatocellular carcinoma
title_sort rna-seq profiling reveals pbmc rna as a potential biomarker for hepatocellular carcinoma
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/c341afc478664a56b2965c0c74e05690
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