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Expression of P62 in hepatocellular carcinoma involving hepatitis B virus infection and aflatoxin B1 exposure
This study aims to clarify the relationship and mechanism between expression of autophagy‐related protein P62 and prognosis of patients with hepatocellular carcinoma (HCC) involving chronic hepatitis B virus (HBV) infection and aflatoxin B1 (AFB1) exposure. HCC patients who underwent resection were...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633547/ https://www.ncbi.nlm.nih.gov/pubmed/28941211 http://dx.doi.org/10.1002/cam4.1176 |
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author | Xiang, Xiao Qin, Hong‐Gui You, Xue‐Mei Wang, Yan‐Yan Qi, Lu‐Nan Ma, Liang Xiang, Bang‐De Zhong, Jian‐Hong Li, Le‐Qun |
author_facet | Xiang, Xiao Qin, Hong‐Gui You, Xue‐Mei Wang, Yan‐Yan Qi, Lu‐Nan Ma, Liang Xiang, Bang‐De Zhong, Jian‐Hong Li, Le‐Qun |
author_sort | Xiang, Xiao |
collection | PubMed |
description | This study aims to clarify the relationship and mechanism between expression of autophagy‐related protein P62 and prognosis of patients with hepatocellular carcinoma (HCC) involving chronic hepatitis B virus (HBV) infection and aflatoxin B1 (AFB1) exposure. HCC patients who underwent resection were divided into three groups: HBV(+)/AFB1(+) (n = 26), HBV(+)/AFB1(−) (n = 68), and HBV(−)/AFB1(−) (n = 14). The groups were compared in terms of mRNA and protein levels of P62, disease‐free survival (DFS), and overall survival (OS) and the expression of NRF2, Nqo1, and AKR7A3 in P62 high‐expression and low‐expression group. HBV(+)/AFB1(+) group has lower DFS and OS, and higher P62 expression than in the other two groups. P62 expression generally correlated with elevated NRF2 and Nqo1 expression, and reduced AKR7A3 expression. Patients expressing high levels of P62 showed significantly lower DFS and OS rates than patients expressing low levels. HCC involving HBV infection and AFB1 exposure is associated with relatively high risk of tumor recurrence, and this poor prognosis may relate to high P62 expression. High P62 expression activates the NRF2 pathway, promotes tumor recurrence. The downregulation of AKR7A3 also reduced liver detoxification of aflatoxin B1. |
format | Online Article Text |
id | pubmed-5633547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56335472017-10-17 Expression of P62 in hepatocellular carcinoma involving hepatitis B virus infection and aflatoxin B1 exposure Xiang, Xiao Qin, Hong‐Gui You, Xue‐Mei Wang, Yan‐Yan Qi, Lu‐Nan Ma, Liang Xiang, Bang‐De Zhong, Jian‐Hong Li, Le‐Qun Cancer Med Cancer Biology This study aims to clarify the relationship and mechanism between expression of autophagy‐related protein P62 and prognosis of patients with hepatocellular carcinoma (HCC) involving chronic hepatitis B virus (HBV) infection and aflatoxin B1 (AFB1) exposure. HCC patients who underwent resection were divided into three groups: HBV(+)/AFB1(+) (n = 26), HBV(+)/AFB1(−) (n = 68), and HBV(−)/AFB1(−) (n = 14). The groups were compared in terms of mRNA and protein levels of P62, disease‐free survival (DFS), and overall survival (OS) and the expression of NRF2, Nqo1, and AKR7A3 in P62 high‐expression and low‐expression group. HBV(+)/AFB1(+) group has lower DFS and OS, and higher P62 expression than in the other two groups. P62 expression generally correlated with elevated NRF2 and Nqo1 expression, and reduced AKR7A3 expression. Patients expressing high levels of P62 showed significantly lower DFS and OS rates than patients expressing low levels. HCC involving HBV infection and AFB1 exposure is associated with relatively high risk of tumor recurrence, and this poor prognosis may relate to high P62 expression. High P62 expression activates the NRF2 pathway, promotes tumor recurrence. The downregulation of AKR7A3 also reduced liver detoxification of aflatoxin B1. John Wiley and Sons Inc. 2017-09-21 /pmc/articles/PMC5633547/ /pubmed/28941211 http://dx.doi.org/10.1002/cam4.1176 Text en © 2017 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cancer Biology Xiang, Xiao Qin, Hong‐Gui You, Xue‐Mei Wang, Yan‐Yan Qi, Lu‐Nan Ma, Liang Xiang, Bang‐De Zhong, Jian‐Hong Li, Le‐Qun Expression of P62 in hepatocellular carcinoma involving hepatitis B virus infection and aflatoxin B1 exposure |
title | Expression of P62 in hepatocellular carcinoma involving hepatitis B virus infection and aflatoxin B1 exposure |
title_full | Expression of P62 in hepatocellular carcinoma involving hepatitis B virus infection and aflatoxin B1 exposure |
title_fullStr | Expression of P62 in hepatocellular carcinoma involving hepatitis B virus infection and aflatoxin B1 exposure |
title_full_unstemmed | Expression of P62 in hepatocellular carcinoma involving hepatitis B virus infection and aflatoxin B1 exposure |
title_short | Expression of P62 in hepatocellular carcinoma involving hepatitis B virus infection and aflatoxin B1 exposure |
title_sort | expression of p62 in hepatocellular carcinoma involving hepatitis b virus infection and aflatoxin b1 exposure |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633547/ https://www.ncbi.nlm.nih.gov/pubmed/28941211 http://dx.doi.org/10.1002/cam4.1176 |
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