Literature DB >> 30325210

Making way for suppressing the FGF19/FGFR4 axis in cancer.

Nestor Prieto-Dominguez1,2, Austin Y Shull3, Yong Teng1,4.   

Abstract

FGF19 is a noncanonical FGF ligand that can control a broad spectrum of physiological responses, which include bile acid homeostasis, liver metabolism and glucose uptake. Many of these responses are mediated by FGF19 binding to its FGFR4/β-klotho receptor complex and controlling activation of an array of intracellular signaling events. Overactivation of the FGF19/FGFR4 axis has been implicated in tumorigenic formation, progression and metastasis, and inhibitors of this axis have recently been developed for single agent use or in combination with other anticancer drugs. Considering the critical role of this receptor complex in cancer, this review focuses on recent developments and applications of FGF19/FGFR4-targeted therapeutics.

Entities:  

Keywords:  FGF19; FGFR4; anticancer; inhibitors; oncogenic role; signaling transduction; treatment regimens

Mesh:

Substances:

Year:  2018        PMID: 30325210     DOI: 10.4155/fmc-2018-0099

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  8 in total

Review 1.  Fibroblast Growth Factor Receptor 4 Targeting in Cancer: New Insights into Mechanisms and Therapeutic Strategies.

Authors:  Liwei Lang; Yong Teng
Journal:  Cells       Date:  2019-01-09       Impact factor: 6.600

Review 2.  Fibroblast Growth Factor Receptor Signaling in Skin Cancers.

Authors:  Malgorzata Czyz
Journal:  Cells       Date:  2019-06-04       Impact factor: 6.600

3.  Involvement of FGFR4 Gene Variants on the Clinicopathological Severity in Urothelial Cell Carcinoma.

Authors:  Ming-Dow Tsay; Ming-Ju Hsieh; Chia-Yi Lee; Shian-Shiang Wang; Chuan-Shu Chen; Sheng-Chun Hung; Chia-Yen Lin; Shun-Fa Yang
Journal:  Int J Environ Res Public Health       Date:  2019-12-23       Impact factor: 3.390

4.  6-Amino-2,4,5-trimethylpyridin-3-ol and 2-amino-4,6-dimethylpyrimidin-5-ol derivatives as selective fibroblast growth factor receptor 4 inhibitors: design, synthesis, molecular docking, and anti-hepatocellular carcinoma efficacy evaluation.

Authors:  Chhabi Lal Chaudhary; Dongchul Lim; Prakash Chaudhary; Diwakar Guragain; Bhuwan Prasad Awasthi; Hee Dong Park; Jung-Ae Kim; Byeong-Seon Jeong
Journal:  J Enzyme Inhib Med Chem       Date:  2022-12       Impact factor: 5.051

5.  DCZ0415, a small-molecule inhibitor targeting TRIP13, inhibits EMT and metastasis via inactivation of the FGFR4/STAT3 axis and the Wnt/β-catenin pathway in colorectal cancer.

Authors:  Sumit Agarwal; Farrukh Afaq; Prachi Bajpai; Hyung-Gyoon Kim; Amr Elkholy; Michael Behring; Darshan Shimoga Chandrashekar; Sameer Al Diffalha; Moh'd Khushman; Shajan P Sugandha; Sooryanarayana Varambally; Upender Manne
Journal:  Mol Oncol       Date:  2022-03-07       Impact factor: 7.449

Review 6.  Dissecting the Role of the FGF19-FGFR4 Signaling Pathway in Cancer Development and Progression.

Authors:  Yanan Liu; Meng Cao; Yuepiao Cai; Xiaokun Li; Chengguang Zhao; Ri Cui
Journal:  Front Cell Dev Biol       Date:  2020-02-20

Review 7.  Fibroblast growth factor receptor signaling as therapeutic targets in female reproductive system cancers.

Authors:  Dong-Li Zhu; Xiao-Mei Tuo; Yu Rong; Kun Zhang; Yan Guo
Journal:  J Cancer       Date:  2020-10-21       Impact factor: 4.207

8.  FGF19/FGFR4 signaling axis confines and switches the role of melatonin in head and neck cancer metastasis.

Authors:  Liwei Lang; Yuanping Xiong; Nestor Prieto-Dominguez; Reid Loveless; Caleb Jensen; Chloe Shay; Yong Teng
Journal:  J Exp Clin Cancer Res       Date:  2021-03-10
  8 in total

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