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Salivary orosomucoid 1 as a biomarker of hepatitis B associated hepatocellular carcinoma
Saliva is rich in proteins, DNA, RNA and microorganisms, and can be regarded as a biomarker library. In order to explore a noninvasive and simple means of early screening for liver cancer, proteomics was used to screen salivary markers of hepatitis B associated liver cancer. We used mass spectrometr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467997/ https://www.ncbi.nlm.nih.gov/pubmed/36096917 http://dx.doi.org/10.1038/s41598-022-18894-2 |
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author | He, Jiaoxia Zheng, Zhongling Liu, Tingting Ao, Yupei Yang, Yixuan Hu, Huaidong |
author_facet | He, Jiaoxia Zheng, Zhongling Liu, Tingting Ao, Yupei Yang, Yixuan Hu, Huaidong |
author_sort | He, Jiaoxia |
collection | PubMed |
description | Saliva is rich in proteins, DNA, RNA and microorganisms, and can be regarded as a biomarker library. In order to explore a noninvasive and simple means of early screening for liver cancer, proteomics was used to screen salivary markers of hepatitis B associated liver cancer. We used mass spectrometry coupled isobaric tags for relative and absolute quantitation (iTRAQ)-technology to identify differentially expressed proteins (DEPs). Western blot, immunohistochemistry and enzyme linked immunosorbent assay were used to detect marker expression of in tissues and saliva. Statistical analysis was used to analyze the diagnostic efficacy of the markers was analyzed through statistical analyses. By comparing the hepatocellular carcinoma (HCC) group with non-HCC groups, we screened out 152 salivary DEPs. We found orosomucoid 1(ORM1) had significantly higher expression in saliva of HCC patients compared with non-HCC groups (p < 0.001) and the expression of ORM1 in liver cancer tissues was significantly higher than that in adjacent normal tissues (p < 0.001). The combination of salivary ORM1 and alpha-fetoprotein (AFP) showed reasonable specificities and sensitivities for detecting HCC. In a word, salivary ORM1 as a new biomarker of hepatitis B associated hepatocellular carcinoma, combination of salivary ORM1 and AFP as an improved diagnostic tool for hepatocellular carcinoma. |
format | Online Article Text |
id | pubmed-9467997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94679972022-09-14 Salivary orosomucoid 1 as a biomarker of hepatitis B associated hepatocellular carcinoma He, Jiaoxia Zheng, Zhongling Liu, Tingting Ao, Yupei Yang, Yixuan Hu, Huaidong Sci Rep Article Saliva is rich in proteins, DNA, RNA and microorganisms, and can be regarded as a biomarker library. In order to explore a noninvasive and simple means of early screening for liver cancer, proteomics was used to screen salivary markers of hepatitis B associated liver cancer. We used mass spectrometry coupled isobaric tags for relative and absolute quantitation (iTRAQ)-technology to identify differentially expressed proteins (DEPs). Western blot, immunohistochemistry and enzyme linked immunosorbent assay were used to detect marker expression of in tissues and saliva. Statistical analysis was used to analyze the diagnostic efficacy of the markers was analyzed through statistical analyses. By comparing the hepatocellular carcinoma (HCC) group with non-HCC groups, we screened out 152 salivary DEPs. We found orosomucoid 1(ORM1) had significantly higher expression in saliva of HCC patients compared with non-HCC groups (p < 0.001) and the expression of ORM1 in liver cancer tissues was significantly higher than that in adjacent normal tissues (p < 0.001). The combination of salivary ORM1 and alpha-fetoprotein (AFP) showed reasonable specificities and sensitivities for detecting HCC. In a word, salivary ORM1 as a new biomarker of hepatitis B associated hepatocellular carcinoma, combination of salivary ORM1 and AFP as an improved diagnostic tool for hepatocellular carcinoma. Nature Publishing Group UK 2022-09-12 /pmc/articles/PMC9467997/ /pubmed/36096917 http://dx.doi.org/10.1038/s41598-022-18894-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article He, Jiaoxia Zheng, Zhongling Liu, Tingting Ao, Yupei Yang, Yixuan Hu, Huaidong Salivary orosomucoid 1 as a biomarker of hepatitis B associated hepatocellular carcinoma |
title | Salivary orosomucoid 1 as a biomarker of hepatitis B associated hepatocellular carcinoma |
title_full | Salivary orosomucoid 1 as a biomarker of hepatitis B associated hepatocellular carcinoma |
title_fullStr | Salivary orosomucoid 1 as a biomarker of hepatitis B associated hepatocellular carcinoma |
title_full_unstemmed | Salivary orosomucoid 1 as a biomarker of hepatitis B associated hepatocellular carcinoma |
title_short | Salivary orosomucoid 1 as a biomarker of hepatitis B associated hepatocellular carcinoma |
title_sort | salivary orosomucoid 1 as a biomarker of hepatitis b associated hepatocellular carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467997/ https://www.ncbi.nlm.nih.gov/pubmed/36096917 http://dx.doi.org/10.1038/s41598-022-18894-2 |
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