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The predictive powers of plasma trefoil factor 3 or its related micro RNAs for patients with hepatocellular carcinoma

BACKGROUND: Earlier diagnosis is beneficial for the prognosis of hepatocellular carcinoma (HCC). Alpha fetoprotein (AFP) is the most widely used biomarker for HCC, but its sensitivity and specificity are only 60 and 90%, respectively. Therefore, it is of great clinical significance to identify early...

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Autores principales: Zhang, Chenghua, Xia, Ran, Zhang, Bo, Wang, Haibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6234585/
https://www.ncbi.nlm.nih.gov/pubmed/30424721
http://dx.doi.org/10.1186/s12885-018-5017-y
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author Zhang, Chenghua
Xia, Ran
Zhang, Bo
Wang, Haibo
author_facet Zhang, Chenghua
Xia, Ran
Zhang, Bo
Wang, Haibo
author_sort Zhang, Chenghua
collection PubMed
description BACKGROUND: Earlier diagnosis is beneficial for the prognosis of hepatocellular carcinoma (HCC). Alpha fetoprotein (AFP) is the most widely used biomarker for HCC, but its sensitivity and specificity are only 60 and 90%, respectively. Therefore, it is of great clinical significance to identify early prognostic biomarkers for HCC, especially a blood-based biomarker as it offers several advantages over tissue-based biomarkers. Trefoil factor 3 (TFF3), a novel secretory protein, was over-expressed in HCC tissues, indicating it might be a blood-based biomarker for HCC. In addition, circulating microRNAs have been investigated as biomarkers for HCC, indicating that miR-7-5p and miR-203a-3p, which are reported or predicted to target TFF3, also hold promise as blood-based biomarkers for HCC. METHODS: We enrolled 43 patients who were firstly diagnosed HCC and matched 47 control subjects without HCC. The levels of TFF3, miR-7-5p and miR-203a-3p were tested in the plasma of HCC patients. Moreover, we assayed the correlation of TFF3 with its related micro RNAs, miR-7-5p and miR-203a-3p, and evaluated their predictive powers for HCC. RESULTS: Decrease of TFF3 was associated with increase of miR-203a-3p in the plasma of HCC patients and they displayed potent predictive powers for HCC diagnosis. However, there was no significant change of plasma miR-7-5p between HCC and control group. CONCLUSION: Decrease of TFF3 correlated with increase of miR-203a-3p in the plasma of HCC patients and they could be additional biomarkers to improve sensitivity and specificity in the diagnosis of HCC.
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spelling pubmed-62345852018-11-23 The predictive powers of plasma trefoil factor 3 or its related micro RNAs for patients with hepatocellular carcinoma Zhang, Chenghua Xia, Ran Zhang, Bo Wang, Haibo BMC Cancer Research Article BACKGROUND: Earlier diagnosis is beneficial for the prognosis of hepatocellular carcinoma (HCC). Alpha fetoprotein (AFP) is the most widely used biomarker for HCC, but its sensitivity and specificity are only 60 and 90%, respectively. Therefore, it is of great clinical significance to identify early prognostic biomarkers for HCC, especially a blood-based biomarker as it offers several advantages over tissue-based biomarkers. Trefoil factor 3 (TFF3), a novel secretory protein, was over-expressed in HCC tissues, indicating it might be a blood-based biomarker for HCC. In addition, circulating microRNAs have been investigated as biomarkers for HCC, indicating that miR-7-5p and miR-203a-3p, which are reported or predicted to target TFF3, also hold promise as blood-based biomarkers for HCC. METHODS: We enrolled 43 patients who were firstly diagnosed HCC and matched 47 control subjects without HCC. The levels of TFF3, miR-7-5p and miR-203a-3p were tested in the plasma of HCC patients. Moreover, we assayed the correlation of TFF3 with its related micro RNAs, miR-7-5p and miR-203a-3p, and evaluated their predictive powers for HCC. RESULTS: Decrease of TFF3 was associated with increase of miR-203a-3p in the plasma of HCC patients and they displayed potent predictive powers for HCC diagnosis. However, there was no significant change of plasma miR-7-5p between HCC and control group. CONCLUSION: Decrease of TFF3 correlated with increase of miR-203a-3p in the plasma of HCC patients and they could be additional biomarkers to improve sensitivity and specificity in the diagnosis of HCC. BioMed Central 2018-11-13 /pmc/articles/PMC6234585/ /pubmed/30424721 http://dx.doi.org/10.1186/s12885-018-5017-y Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhang, Chenghua
Xia, Ran
Zhang, Bo
Wang, Haibo
The predictive powers of plasma trefoil factor 3 or its related micro RNAs for patients with hepatocellular carcinoma
title The predictive powers of plasma trefoil factor 3 or its related micro RNAs for patients with hepatocellular carcinoma
title_full The predictive powers of plasma trefoil factor 3 or its related micro RNAs for patients with hepatocellular carcinoma
title_fullStr The predictive powers of plasma trefoil factor 3 or its related micro RNAs for patients with hepatocellular carcinoma
title_full_unstemmed The predictive powers of plasma trefoil factor 3 or its related micro RNAs for patients with hepatocellular carcinoma
title_short The predictive powers of plasma trefoil factor 3 or its related micro RNAs for patients with hepatocellular carcinoma
title_sort predictive powers of plasma trefoil factor 3 or its related micro rnas for patients with hepatocellular carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6234585/
https://www.ncbi.nlm.nih.gov/pubmed/30424721
http://dx.doi.org/10.1186/s12885-018-5017-y
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