Inhibitors targeting hepatocyte growth factor receptor and their potential therapeutic applications

被引:62
作者
Cui, Jingrong Jean [1 ]
机构
[1] Pfizer Inc, PGRD La Jolla Lab, San Diego, CA 92121 USA
关键词
c-Met; hepatocyte growth factor; hepatocyte growth factor receptor; metastasis; proliferation; receptor tyrosine kinase; scatter factor; vascular enclothelial growth factor receptor;
D O I
10.1517/13543776.17.9.1035
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
The hepatocyte growth factor (HGF)/c-Met signaling pathway is important in mediating a wide range of biological activities, including embryological development, wound healing, tissue regeneration, angiogenesis, proliferation, survival, scattering, motility, invasion and morphogenic differentiation. HGF and/or c-Met are expressed at abnormally high levels in a large variety of solid tumors. Various c-Met mutations have been described in many solid tumors and some hematologic malignancies. Therefore, inhibition of the HGF/c-Met signaling pathway has great potential in molecular targeted cancer therapy. Many patent applications associated with inhibition of the HGF/c-Met axis have been published in the past few years. There are four small molecule c-Met inhibitors presently in clinical trials. This review focusses on recent patent applications for small molecule c-Met inhibitors and their potential applications in cancer therapy.
引用
收藏
页码:1035 / 1045
页数:11
相关论文
共 46 条
[1]
The new paradigm in the treatment of colorectal cancer: are we hitting the right target? [J].
Baranda, Joaquina ;
Williamson, Stephen .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2007, 16 (03) :311-324
[2]
A peptide representing the carboxyl-terminal tail of the met receptor inhibits kinase activity and invasive growth [J].
Bardelli, A ;
Longati, P ;
Williams, TA ;
Benvenuti, S ;
Comoglio, PM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (41) :29274-29281
[3]
BELLON S, 2007, 98 ANN M AM ASS CANC, pA3162
[4]
The Met kinase inhibitor SU11274 exhibits a selective inhibition pattern toward different receptor mutated variants [J].
Berthou, S ;
Aebersold, DM ;
Schmidt, LS ;
Stroka, D ;
Heigl, C ;
Streit, B ;
Stalder, D ;
Gruber, G ;
Liang, CX ;
Howlett, AR ;
Candinas, D ;
Greiner, RH ;
Lipson, KE ;
Zimmer, Y .
ONCOGENE, 2004, 23 (31) :5387-5393
[5]
Met, metastasis, motility and more [J].
Birchmeier, C ;
Birchmeier, W ;
Gherardi, E ;
Vande Woude, GF .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (12) :915-925
[6]
Opinion -: Invasive growth:: a MET-driven genetic programme for cancer and stem cells [J].
Boccaccio, Carla ;
Comoglio, Paolo M. .
NATURE REVIEWS CANCER, 2006, 6 (08) :637-645
[7]
Fully human monoclonal antibodies to hepatocyte growth factor with therapeutic potential against hepatocyte growth factor/c-Met-dependent human tumors [J].
Burgess, T ;
Coxon, A ;
Meyer, S ;
Sun, J ;
Rex, K ;
Tsuruda, T ;
Chen, Q ;
Ho, SY ;
Li, L ;
Kaufman, S ;
McDorman, K ;
Cattley, RC ;
Sun, JL ;
Elliott, G ;
Zhang, K ;
Feng, X ;
Jia, XC ;
Green, L ;
Radinsky, R ;
Kendall, R .
CANCER RESEARCH, 2006, 66 (03) :1721-1729
[8]
Christensen JG, 2003, CANCER RES, V63, P7345
[9]
MOLECULAR-CLONING OF A NEW TRANSFORMING GENE FROM A CHEMICALLY TRANSFORMED HUMAN CELL-LINE [J].
COOPER, CS ;
PARK, M ;
BLAIR, DG ;
TAINSKY, MA ;
HUEBNER, K ;
CROCE, CM ;
VANDEWOUDE, GF .
NATURE, 1984, 311 (5981) :29-33
[10]
CUI J, 2007, 2 RSC SCI S KIN INH