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Publication Name World Journal of Gastroenterology
Manuscript ID 36612
Country China
Category Gastroenterology & Hepatology
Manuscript Type Basic Study
Article Title Hepatitis C virus core protein-induced miR-93-5p inhibits IFN signaling pathway through targeting IFNAR1
Manuscript Source Unsolicited Manuscript
All Author List Chang-Long He, Ming Liu, Zhao-Xia Tan, Ya-jun Hu, Qiao-Yue Zhang, Xue-Mei Kuang, Wei-Long Kong and Qing Mao
Funding Agency and Grant Number
Funding Agency Grant Number
Natural Science Foundation of China 81371849
the TMMU Key Project for Clinical Research 2012XLC05
Corresponding Author Qing Mao, MD, PhD, Doctor, Doctor, Institute of Infectious Diseases, Southwest Hospital, Army Medical University (Former: The Third Military Medical University), Gaotanyan street, Shapingba distinct, Chongqing 400037, China. qingmao@tmmu.edu.cn
Key Words IFN signaling pathway; Interferon receptor 1; miR-93-5p; Hepatitis C virus
Core Tip Hepatitis C virus-1b core protein increases miR-93-5p expression and induces inactivation of the IFN signaling pathway. miR-93-5p expression is involved in pegylated interferon-α resistance and directly targets interferon receptor 1 (IFNAR1). miR-93-5p-IFNAR1 axis regulates STAT1 phosphorylation.
Citation He CL, Liu M, Tan ZX, Hu YJ, Zhang QY, Kuang XM, Kong WL, Mao Q. Hepatitis C virus core protein-induced miR-93-5p up-regulation inhibits interferon signaling pathway by targeting IFNAR1. World J Gastroenterol 2018; 24(2): 226-236
Received
2017-10-27 02:08
Peer-Review Started
2017-10-27 06:08
To Make the First Decision
2017-11-22 01:10
Return for Revision
2017-11-27 10:47
Revised
2017-12-05 08:29
Second Decision
2017-12-12 07:46
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief
2017-12-12 19:51
Articles in Press
2017-12-12 19:51
Publication Fee Transferred
Edit the Manuscript by Language Editor
2017-12-16 13:22
Typeset the Manuscript
2018-01-05 07:03
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/
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