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HGF/c-MET: A Promising Therapeutic Target in the Digestive System Cancers
Hongli Zhang1, Qingqing Feng2, Wei-Dong Chen3,4
1State Key Laboratory of Chemical Resource Engineering, College of Life Science and Technology, Beijing University of Chemical Technology, Beijing 100029, China. hlz13084@163.com.
Abstract:
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.
Insights
Inhibiting the HGF/c-MET pathway shows promise for digestive system cancers. MicroRNAs offer a novel therapeutic strategy by targeting this pathway, potentially improving cancer treatment outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Gastroenterology
Background:
- The HGF/c-MET signaling pathway is implicated in the pathogenesis of digestive system cancers.
- Current c-MET inhibitors have shown limitations in efficacy and tolerability for these cancers.
Purpose of the Study:
- To review recent advancements in HGF/c-MET signaling inhibitors for digestive system cancers.
- To explore the role of microRNAs in regulating the HGF/c-MET pathway for cancer therapeutics.
Main Methods:
- Review of preclinical and clinical studies on HGF/c-MET inhibitors.
- Analysis of research on microRNA's role in the HGF/c-MET axis.
- Discussion of combination therapy strategies.
Main Results:
- New HGF/c-MET inhibitors in preclinical development show therapeutic potential.
- MicroRNAs demonstrate a capacity to inhibit HGF/c-MET signaling in digestive cancers.
- Combination therapies may offer improved safety and tolerability.
Conclusions:
- Targeting the HGF/c-MET pathway is a viable strategy for digestive system cancers.
- MicroRNAs represent a novel and promising therapeutic avenue for these cancers.
- Further research into miRNA-based therapies and combination strategies is warranted.
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