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
相关论文
共 50 条
  • [1] c-Met: A Promising Therapeutic Target in Bladder Cancer
    Feng, Yanfei
    Yang, Zitong
    Xu, Xin
    CANCER MANAGEMENT AND RESEARCH, 2022, 14 : 2379 - 2388
  • [2] HGF/c-Met Axis: The Advanced Development in Digestive System Cancer
    Shao, Zhiwei
    Pan, Haoqi
    Tu, Sheng
    Zhang, Jingying
    Yan, Sheng
    Shao, Anwen
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2020, 8
  • [3] c-met and HGF-α in advanced Cervical cancer FIGO III and IV - a therapeutic Target?
    Horn, L. -C.
    Hommel, N.
    Einenkel, J.
    Hentschel, B.
    ONKOLOGIE, 2010, 33 : 115 - 116
  • [4] Therapeutic Strategies for Ovarian Cancer in Point of HGF/c-MET Targeting
    Kim, Hyun Jung
    MEDICINA-LITHUANIA, 2022, 58 (05):
  • [5] The role of HGF/c-MET signaling system in somite myogenesis
    Shiozuka, M
    Yokoyama, S
    Kimura, I
    MOLECULAR BIOLOGY OF THE CELL, 2002, 13 : 531A - 531A
  • [6] Activated c-Met; a Potential Therapeutic Target in Chordoma
    Riddle, Nicole
    Jones, Krister
    Staddon, Arthur
    Zhang, Paul
    Brooks, John
    Huang, Jui-Han
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2012, 138 : A303 - A303
  • [7] c-Met: A potential therapeutic target for hepatocellular carcinoma
    Gao, Jianjun
    Inagaki, Yoshinori
    Xue, Xia
    Qu, Xianjun
    Tang, Wei
    DRUG DISCOVERIES AND THERAPEUTICS, 2011, 5 (01): : 2 - 11
  • [8] The HGF/c-MET axis as a potential target to overcome survival signals and improve therapeutic efficacy in multiple myeloma
    Giannoni, Paolo
    de Totero, Daniela
    CANCER DRUG RESISTANCE, 2021, 4 (04) : 923 - 933
  • [9] Regulation of HGF and c-MET Interaction in Normal Ovary and Ovarian Cancer: Importance of Targeting c-MET and HGF Interaction
    Youngjoo Kwon
    Andrew K. Godwin
    Reproductive Sciences, 2017, 24 : 494 - 501
  • [10] Regulation of HGF and c-MET Interaction in Normal Ovary and Ovarian Cancer: Importance of Targeting c-MET and HGF Interaction
    Kwon, Youngjoo
    Godwin, Andrew K.
    REPRODUCTIVE SCIENCES, 2017, 24 (04) : 494 - 501