HGF/c-MET: A Promising Therapeutic Target in the Digestive System Cancers

被引:35
|
作者
Zhang, Hongli [1 ]
Feng, Qingqing [1 ]
Chen, Wei-Dong [2 ,3 ]
Wang, Yan-Dong [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Life Sci & Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Inner Mongolia Med Univ, Sch Basic Med Sci, Key Lab Mol Pathol, Hohhot 010110, Peoples R China
[3] Henan Univ, Key Lab Receptors Mediated Gene Regulat & Drug Di, Sch Med, Kaifeng 475004, Peoples R China
基金
中国国家自然科学基金;
关键词
HGF; c-MET; digestive system cancers; miRNA; EXHIBITS ANTITUMOR-ACTIVITY; RECEPTOR TYROSINE KINASE; HEPATOCYTE GROWTH-FACTOR; TIVANTINIB ARQ 197; C-MET; HEPATOCELLULAR-CARCINOMA; INHIBITS MIGRATION; GASTRIC-CANCER; TUMOR-GROWTH; MESENCHYMAL TRANSITION;
D O I
10.3390/ijms19113295
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The HGF/c-MET pathway is active in the development of digestive system cancers, indicating that inhibition of HGF/c-MET signaling may have therapeutic potential. Various HGF/c-MET signaling inhibitors, mainly c-MET inhibitors, have been tested in clinical trials. The observed efficacy and adverse events of some c-MET inhibitors were not very suitable for treating digestive system cancers. The development of new HGF/c-MET inhibitors in preclinical studies may bring promising treatments and synergistic combination (traditional anticancer drugs and c-MET inhibitors) strategies provided anacceptable safety and tolerability. Insights into miRNA biology and miRNA therapeutics have made miRNAs attractive tools to inhibit HGF/c-MET signaling. Recent reports show that several microRNAs participate in inhibiting HGF/c-MET signaling networks through antagonizing c-MET or HGF in digestive system cancers, and the miRNAs-HGF/c-MET axis plays crucial and novel roles for cancer treatment. In the current review, we will discuss recent findings about inhibitors of HGF/c-MET signaling in treating digestive system cancers, and how miRNAs regulate digestive system cancers via mediating HGF/c-MET pathway.
引用
收藏
页数:17
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