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Publication Name World Journal of Gastrointestinal Oncology
Manuscript ID 108649
Country China
Category Gastroenterology & Hepatology
Manuscript Type Review
Article Title Fibroblast growth factor 19-fibroblast growth factor receptor 4 axis: From oncogenesis to targeted-immunotherapy in advanced hepatocellular carcinoma
Manuscript Source Unsolicited Manuscript
All Author List Tian-Ao Zhan, Feng Xia, Hong-Wei Huang, Jun-Cheng Zhan, Xin-Kang Liu and Qi Cheng
Funding Agency and Grant Number
Funding Agency Grant Number
Chen Xiao-Ping Foundation for The Development of Science and Technology of Hubei Province CXPJJH124001-2406
National Natural Science Foundation of China U23A20483
Corresponding Author Qi Cheng, MD, PhD, Professor, Hepatic Surgery Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1095 Jiefang Avenue, Wuhan 430030, Hubei Province, China. chengqi@hust.edu.cn
Key Words Hepatocellular carcinoma; Fibroblast growth factor 19; Selective fibroblast growth factor receptor 4 inhibitor; Adverse events; Resistance; Targeted-immunotherapy; Tumor microenvironment; Biomarker
Core Tip The aberrant Fibroblast growth factor 19 (FGF19)-fibroblast growth factor receptor 4 (FGFR4) axis plays a crucial role in progression of hepatocellular carcinoma. Multi-kinase inhibitors enhance anti-tumor effects by targeting the FGF19-FGFR4 axis and FGF19 overexpression contributes to the development of immune suppression. These findings highlight the association between FGF19 and targeted-immunotherapy in hepatocellular carcinoma (HCC). Selective FGFR4 inhibitors, either alone or combining with targeted-immunotherapy, have demonstrated therapeutic potential for advanced HCC, although the clinical application is hindered by challenges such as adverse effects and drug resistance. Furthermore, FGF19 serves as a promising biomarker for HCC, underscoring its potential for precision treatment.
Citation Zhan TA, Xia F, Huang HW, Zhan JC, Liu XK, Cheng Q. Fibroblast growth factor 19-fibroblast growth factor receptor 4 axis: From oncogenesis to targeted-immunotherapy in advanced hepatocellular carcinoma. World J Gastrointest Oncol 2025; In press
Received
2025-04-21 03:31
Peer-Review Started
2025-04-21 03:31
To Make the First Decision
Return for Revision
2025-05-11 13:08
Revised
2025-05-25 04:09
Second Decision
2025-07-18 02:43
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief
2025-07-18 08:51
Articles in Press
2025-07-18 08:51
Publication Fee Transferred
2025-05-26 12:18
Edit the Manuscript by Language Editor
Typeset the Manuscript
ISSN 1948-5204 (online)
Open Access This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (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: https://creativecommons.org/Licenses/by-nc/4.0/
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