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Articles Published Processes
6/21/2016 6:11:00 PM | Browse: 1008 | Download: 1579
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Received |
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2016-03-25 15:42 |
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Peer-Review Started |
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2016-03-25 16:51 |
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To Make the First Decision |
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2016-05-12 14:25 |
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Return for Revision |
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2016-05-12 15:31 |
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Revised |
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2016-05-17 08:28 |
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Second Decision |
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2016-05-23 08:46 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2016-06-02 15:32 |
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Articles in Press |
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2016-06-02 15:33 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2016-06-12 10:34 |
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Publish the Manuscript Online |
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2016-06-21 18:11 |
ISSN |
1007-9327 (print) and 2219-2840 (online) |
Open Access |
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
Copyright |
© The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved. |
Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
Website |
http://www.wjgnet.com |
Category |
Virology |
Manuscript Type |
Topic Highlights |
Article Title |
X region mutations of hepatitis B virus related to clinical severity
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Manuscript Source |
Invited Manuscript |
All Author List |
Hong Kim, Seoung-Ae Lee and Bum-Joon Kim |
Funding Agency and Grant Number |
Funding Agency |
Grant Number |
National Research Foundation (NRF) grant of Ministry of Science, ICT and Future Planning, South Korea |
NRF-2015R1C1A1A02037267 |
Korea Health Technology R&D Project through the Korea Health Industry Development Institute, funded by the Ministry of Health and Welfare, South Korea |
HI14C0955 |
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Corresponding Author |
Bum-Joon Kim, PhD, Department of Biomedical Sciences, Microbiology and Immunology, Liver Research Institute and Cancer Research Institute, College of Medicine, Seoul National University, 28 Yongon-dong, Chongno-gu, Seoul 110-799, South Korea. kbumjoon@snu.ac.kr |
Key Words |
Hepatitis B virus infection; Hepatitis B virus-X protein mutation; Hepatocellular carcinoma; Clinical severity |
Core Tip |
Of hepatitis B virus (HBV)-X protein (HBx) mutations related to clinical severity, the A1762T/G1764A BCP mutation is one of the most frequently encountered HBx mutations and plays a significant role in liver disease progression in chronic patients with HBV infections. It also further contributes to disease progression by inducing mutations of other HBx mutations related to clinical severity, such as G1386A/C (V5M/L), C1653T (H94Y), T1753V (I127V) and HBx C-terminal deletion or insertion. Moreover, T1753V (I127L,T,N,S) and C1653T (H94Y) mutations in the enhancer Ⅱ/BCP region and A1383C, G1386A/C (V5M/L) and C1485T (P38S) in the negative regulation domain are significantly related to severe types of liver diseases, including hepatocellular carcinoma. Furthermore, deletions or insertions affecting the C-terminal region of HBx may also contribute to the severity of the clinical outcome in chronic patients. In addition, our recent study indicated that a novel mutation type (X8Del) composed of an 8-bp deletion in the C-terminal region of the HBx could contribute to occult HBV infection in vaccinated Korean individuals via a reduced secretion of HBsAg and virions. Therefore, several distinct types of HBx mutations may contribute to HBV pathogenesis by regulating HBV replication or host genes related to cell homeostasis. |
Publish Date |
2016-06-21 18:11 |
Citation |
Kim H, Lee SA, Kim BJ. X region mutations of hepatitis B virus related to clinical severity. World J Gastroenterol 2016; 22(24): 5467-5478 |
URL |
http://www.wjgnet.com/1007-9327/full/v22/i24/5467.htm |
DOI |
http://dx.doi.org/10.3748/wjg.v22.i24.5467 |
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