LY2801653 is an orally bioavailable multi-kinase inhibitor with potent activity against MET, MST1R, and other oncoproteins, and displays anti-tumor activities in mouse xenograft models
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- Yan, S.B., Peek, V.L., Ajamie, R. et al. Invest New Drugs (2013) 31: 833. doi:10.1007/s10637-012-9912-9
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The HGF/MET signaling pathway regulates a wide variety of normal cellular functions that can be subverted to support neoplasia, including cell proliferation, survival, apoptosis, scattering and motility, invasion, and angiogenesis. MET over-expression (with or without gene amplification), aberrant autocrine or paracrine ligand production, and missense MET mutations are mechanisms that lead to activation of the MET pathway in tumors and are associated with poor prognostic outcome. We report here preclinical development of a potent, orally bioavailable, small-molecule inhibitor LY2801653 targeting MET kinase. LY2801653 is a type-II ATP competitive, slow-off inhibitor of MET tyrosine kinase with a dissociation constant (Ki) of 2 nM, a pharmacodynamic residence time (Koff) of 0.00132 min−1 and t1/2 of 525 min. LY2801653 demonstrated in vitro effects on MET pathway-dependent cell scattering and cell proliferation; in vivo anti-tumor effects in MET amplified (MKN45), MET autocrine (U-87MG, and KP4) and MET over-expressed (H441) xenograft models; and in vivo vessel normalization effects. LY2801653 also maintained potency against 13 MET variants, each bearing a single-point mutation. In subsequent nonclinical characterization, LY2801653 was found to have potent activity against several other receptor tyrosine oncokinases including MST1R, FLT3, AXL, MERTK, TEK, ROS1, DDR1/2 and against the serine/threonine kinases MKNK1/2. The potential value of MET and other inhibited targets within a number of malignancies (such as colon, bile ducts, and lung) is discussed. LY2801653 is currently in phase 1 clinical testing in patients with advanced cancer (trial I3O-MC-JSBA, NCT01285037).
KeywordsMET inhibitor LY2801653 MST1R MKNK ROS1
The human MET proto-oncogene encodes the MET kinase, also known as HGF receptor. HGF binds with high affinity to this trans-membrane tyrosine kinase receptor and is the only known ligand for this receptor. Binding of HGF to the extracellular domain of MET induces receptor multimerization, activates the intrinsic kinase activity of the receptor and results in the phosphorylation of multiple tyrosine residues in the intracellular region. The HGF/MET signaling pathway regulates a wide variety of normal cellular functions that can be subverted to support neoplasia including cell proliferation, survival, apoptosis, scattering and motility, invasion, and angiogenesis . Dysregulated MET/HGF signaling leads to an abnormally activated cellular invasive program that plays a role in cellular transformation; epithelial-mesenchymsal transition; and tumor invasion, progression and metastasis. MET over-expression (with or without gene amplification), aberrant autocrine or paracrine ligand production, and missense MET mutations are mechanisms that lead to activation of the MET pathway in tumors and are associated with poor prognostic outcome . Over-expression of MET, ligand-dependent activation, or MET amplification have also been implicated as potential mechanisms of resistance to epidermal growth factor receptor (EGFR) inhibitor therapies [3, 4, 5, 6]. Receptor cross-activation of other oncoproteins such as MST1R (also known as RON), AXL and PDGFRA by MET has also been reported [7, 8]. We report the discovery and initial in vitro and in vivo evaluation of a small-molecule inhibitor LY2801653, whose development was initiated with the intent of targeting the MET kinase. We provide data to illustrate the in vitro effects of LY2801653 on the MET pathway-dependent cell scattering and cell proliferation, as well as its in vivo anti-tumor effects in mouse xenograft models. In subsequent nonclinical characterization, LY2801653 was screened against a larger panel of kinases and was found to have potent activity against several other receptor tyrosine oncokinases including MST1R (MET related tyrosine kinase), FLT3, AXL, MERTK, TEK, and ROS1, and against the serine/threonine kinases MKNK1/2. The potential value of MET and other inhibited targets within a number of malignancies is discussed. LY2801653 is currently in phase 1 clinical testing in patients with advanced cancer (trial I3O-MC-JSBA, NCT01285037).
Materials and methods
The cell lines U-87MG, H441, H1299, MV4-11, HT29, H460, TT, Calu1, U118MG, A375, HCT-116, DU145, T47D and H1993 were obtained from ATCC (Manassas, VA). S114 cells were licensed from National Institute of Health; HCC78 and BaF3 cells were from DSMZ (Deutsche Sammlung von Mikroorganismen und Zellkulturen, Braunschweig, Germany); MKN45 cells from the Japanese Health Science Research Resources Bank (Osaka, Japan); A2780 cells from NCI DCTD repository, and the KP4 cells from RIKEN Cell Bank (Tsukuba, Japan); HUVECs were obtained from Invitrogen (Madison, WI). Cells were cultured according to manufacturers’ guidelines.
Chemical synthesis of LY2801653
The synthesis of LY2801653 is described in Example 1 of the patent .
MET inhibition enzyme kinetics studies
The dissociation constant (Ki) value, mode of inhibition (competitive, noncompetitive or uncompetitive) and the pharmacodynamic residence time (Koff) value of LY2801653 for the MET kinase activity were determined using radiometric-filter binding and spin column assays. Methods for these assays are described in detail in the Supplementary Methods section.
Co-crystallization of LY2801653 with MET and crystal structure determination
MET kinase domain (amino acid boundaries 1056–1364) was co-expressed with protein-tyrosine phosphatase 1B (PTP1B) and purified by Kinasia (Carmel, IN) similarly to previous work by Wang et al. . MET protein was purified by nickel affinity and MonoQ chromatography and concentrated to 8 mg/mL in 20 mM MES (pH 6.0), 500 mM NaCl, 10 % glycerol, and 2 mM DTT. The buffer was adjusted to 10 mM HEPES (pH 7.0), 500 mM NaCl, 5 % glycerol, 5 mM DTT, and 0.2 mM n-dodecyl-β-D-maltoside for crystallization with 10 mg/mL MET incubated with 1 mM LY2801653 (1 % DMSO). Crystals were grown by hanging drop vapor diffusion at 20 °C, with reservoir solution of 16 % PEG 10,000, 0.1 M HEPES (pH 7.0), 5 % ethylene glycol, and optimized by microseeding. Crystals were flash frozen in liquid nitrogen with 20 % glycerol. Crystals of MET/LY2801653 belong to space group P212121 with unit cell parameters a = 40.51 Å, b = 63.89 Å, c = 111.63 Å. The diffraction data (1.8 Å, 99.7 % complete) were collected and processed on SGX-CAT beam line at APS in Argonne National Laboratory. The crystal structure was determined by the method of molecular replacement using 1 internal MET structure as a search model. The Flynn program (OpenEye Scientific Software) was used for ligand fitting and Coot  was used in model building. Structure refinement (Rwork = 0.216 and Rfree = 0.249, RMSbond = 0.009, RMSangle = 1.218) was carried out by Refmac5 . Protein Data Bank accession code for the co-crystal structure is 4EEV.
Cell-based assays to determine the inhibition (IC50) of MET auto-phosphorylation by LY2801653
Inhibition of auto-phosphorylation of MET by LY2801653 was assessed in two cell lines by ELISA. One measured the HGF stimulated MET auto-phosphorylation of Y1349 in H460 cells. Another measured the MET auto-phosphorylation at Y1230/Y1234/Y1235 in NIH3T3-derived S114 cells engineered to stably express human MET and HGF . For details, see the Supplementary Method section.
In vitro inhibitory activity of LY2801653 on MET-activating mutations
Translocated promoter region-MET (TPR-MET) oncogene  was cloned into the pLNCX2 vector (Clontech Laboratories, Inc., Mountain View, CA) and various reported MET mutations in hereditary papillary renal cell carcinoma were introduced using the QuikChange™ Site-Directed Mutagenesis Kit (Agilent, Santa Clara, CA). BaF3 cells are an immortalized murine bone marrow–derived pro-B-cell line, the proliferation of which depends on the presence of IL3. These cells were transduced with retrovirus containing each of the TPR-MET mutation-bearing constructs as previously described . BaF3 cell lines expressing these MET mutations were confirmed with bidirectional DNA sequencing, using 3730xl DNA analyzers (Applied Biosystems, Foster City, CA). Cells were maintained in RPMI 1640 media + 10 % dialyzed FBS (Invitrogen # 26400-044) and antibiotic/antimycotic (Invitrogen # 15240-067). 4.5 × 103 cells (-IL3) or 1.8 × 103 cells (+IL3) (10 ng/mL, R&D Systems, # 403-ml) were plated onto 96-well plates, treated with LY2801653, and incubated for 48 h at 37 °C. WST1 reagent (Roche, #11644807001) was added and incubated for 2 h; absorbance was read at OD450. The IC50 values were determined with the JOCKYSS program.
In vitro biochemical kinase specificity profiling of LY2801653
The specificity of the inhibitory activity of LY2801653 was determined using single-point or 3-point profiling and confirmatory 10-point or 11-point IC50 assays available at EMD Millipore Inc. (Dundee, UK), Cerep (Poitiers, France), or KinomeScan (DiscoveRx, San Diego, CA). These assays used active full-length or receptor tyrosine kinase domain enzymes, and peptide or protein substrates unique to each enzyme. Reactions were run at or near the Km for ATP to allow for direct comparisons of IC50 potency between the enzymes. For details, see the Supplementary Method section.
In vitro HGF induced cell scattering assay
2 × 103 DU145 cells/well on poly-D-lysine 96-well black/clear plates were treated with LY2801653 (in 0.4 % DMSO), immediately followed by the addition of human HGF (20 ng/ml), and incubated for 48 h at 37 °C. 2 % formaldehyde fixed cells were stained with AlexaFluor 488 Phalloidin (#A12379, Invitrogen, Molecular Probes, Carlsbad, CA) and counterstained with Propidium Iodide (# P3566 Invitrogen). Colony counts were quantified on Acumen Explorer™ laser-scanning fluorescence microplate cytometer (TTP Labtech Ltd, Cambridge, MA). A colony was defined as ≥ 4 cells.
Cell-based assays to determine the inhibition (IC50) of non-MET kinases by LY2801653
Cell-based assays (anti-proliferative or inhibition of phosphorylation of target kinase) were performed to evaluate the inhibitory activity of LY2801653 against MST1R, AXL, ROS1, PDGFRA, MKNK1/2, FLT3, MERTK, TYRO3, TEK, KDR, CSF1R, RET, DDR1, DDR2. for details, see the Supplementary Method section.
In vivo mouse studies
All animal studies were performed in accordance with American Association for Laboratory Animal Care institutional guidelines. All in vivo experimental protocols were approved by the Eli Lilly and Company Animal Care and Use Committee. Athymic nude mice and CD-1 nude mice were obtained from Harlan (Indianapolis, IN) and Charles River (Wilmington, MA), respectively. In all in vivo studies, LY2801653 was formulated in 10 % acacia daily and dosed orally. The in vivo mouse studies explored the MET target inhibition and pharmacokinetics of LY2801653 in the S114 xenograft model; as well as the antitumor growth activity in xenograft (U-87MG, KP4, H441, MKN45, H1993, HT-29, and MV4-11) and in orthotopic (H1299) models. For details, see the Supplementary Method section.
Multiplexed immunofluorescence tumor tissue imaging
U-87MG xenograft tumors were excised from mice after 28 days of dosing and placed into Zinc-Tris fixative (BD Pharmingen, San Jose, CA), stained and quantified as previously described . For the apoptotic and proliferative markers, slides were stained with a combination of Hoechst 33324 (Invitrogen), rat anti-mouse CD31 (Pharmingen) /anti-rat Alexa-488 (Invitrogen), rabbit anti-Ki67 (NeoMarkers)/anti-rabbit Alexa 647 (Invitrogen), and TUNEL-TMR red (Roche). For the angiogenesis markers, slides were stained with a combination of Hoechst 33324, rat anti-mouse CD31/anti-rat Alexa-488, rabbit anti-glucose transporter 1 (GLUT1) (Chemicon) /anti-rabbit Alexa 647, and mouse anti-Smooth Muscle Actin/Cy3 (Sigma).
In vitro MET inhibitory activities
LY2801653 was evaluated for its ability to inhibit biochemical and cellular functions of MET including cell scattering/migration and proliferation. Biochemical assays using purified human MET kinase domain and a synthetic peptide substrate demonstrated LY2801653 to be a potent, competitive, slow-off inhibitor of MET tyrosine kinase (Supplementary Fig. S1) with a dissociation constant (Ki) of 2 nM, a pharmacodynamic residence time (Koff) of 0.00132 min−1 and a half-life (t1/2) of 525 min. The crystal structure of MET bound to LY2801653 was determined to 1.8 Å (Fig. 1b) and demonstrated that the inhibitor bound MET is in an inactive form with the activation loop DFG motif adopting a DFG-out conformation indicating that LY2801653 is a type II kinase inhibitor [17, 18].
In vitro inhibitory activity of LY2801653 for TPR-MET bearing activating mutations in BaF3 cells cultured without IL3
TPR-MET wild type
Anti-proliferative effect of LY2801653 was evaluated against a panel of MET expressing cell lines (Supplementary Table S1). LY2801653 demonstrated more potent anti-proliferative activity in cell lines with MET gene amplification (MKN45, Hs746T and H1993) than the cell lines without MET gene amplification (U-87MG, KATO-III).
In vivo MET target inhibition study in S114 xenograft model
Anti-tumor activity in MET-dependent mouse xenograft models
Two non-continuous dosing regimens were also explored in the U-87MG and H441 xenograft models. The U-87MG study (Fig. 4b-2) evaluated the 9/5 schedule for 2 cycles and the 5/2 schedule for 4 cycles. The H441 study (Fig. 4e) evaluated the 9/5 schedule for 3 cycles and the 5/2 schedule for 6 cycles. Results indicated that when dosed at 12 mg/kg (around TED95), the anti-tumor growth effect in the two non-continuous dosing regimens was similar to that in the twice-daily uninterrupted dosing groups. The tumor growth delay lasted for at least a week after discontinuing dosing. When the dose was lowered to 3 mg/kg, the 9/5 schedule displayed better anti-tumor growth effect than the 5/2 schedule in U-87MG xenograft tumor models (Fig. 4b-2).
Vessel normalization and anti-apoptotic/anti-proliferative effect
Kinase specificity profile for LY2801653
In vitro inhibitory activity of LY2801653 against MET and other kinases
Biochemical activity IC50 or Kdk (nM)
Cell-base activitye IC50 (nM)
Findings from subsequent testing of LY2801653 in xenograft or orthotopic models selected based on their dependence on MST1R (H1993, HT-29), FLT3 (MV4-11), and AXL (H1299) were consistent with the anti-growth activity of LY2801653 in the presence of these targets (Figs. 4f, and g and Supplementary Figs. S4A-C). NSCLC-derived H1993 xenograft tumors have previously been shown to have high levels of pMST1R due to transactivation by highly amplified MET . The HT-29 colon xenograft tumors not only express MET, but also express a constitutively activated splice variant of MST1R, p160MST1R . Growth of MV4-11 xenograft tumors, an acute myeloid leukemia cell line is driven by a FLT3-activating mutation , and in vitro anti-proliferative activity of LY2801653 for MV4-11 cells was determined to have an IC50 of 4 nM. Lastly, the NSCLC H1299 xenograft tumors over-express AXL and its ligand Gas6.
MET inhibitory activity
The normal physiologic regulation of HGF and MET signaling found in development and organogenesis is prone to dysregulation in cancer and may contribute to invasion and metastasis [1, 18]. For these reasons, LY2801653 was developed through a strategy of targeting the MET receptor, and data presented here demonstrate that LY2801653 is a potent ATP-competitive inhibitor of the MET receptor tyrosine kinase, which is further capable of inhibiting MET-dependent tumor cell proliferation and migration/scattering. In addition, LY2801653 was able to induce vessel normalization in xenograft tumors. Whereas MET signaling is involved in angiogenesis, this latter effect of LY2801653 may not be exclusively due to MET inhibition. Indeed, inhibition of angiogenesis by LY2801653 may include contributions from among the limited range of other targets that it inhibits, such as TEK and AXL, that are involved in modulating angiogenesis.
In vitro biochemical measurements showed LY2801653 to be a potent inhibitor of MET with a 2 nM Ki, this activity was confirmed in cell-based assessments, in which LY2801653 had an IC50 for inhibition of MET phosphorylation of 35.2–59.2 nM. The S114 cell line is an engineered mouse cell line expressing both human MET and HGF. In mice implanted subcutaneously with S114 tumorigenic cells, LY2801653 given orally at 12 mg/kg resulted in 95 % inhibition of MET phosphorylation in the tumors for up to 8 h. With elimination t1/2 being the shortest in mice of 2.9 h (e.g. compared to 14.3 h in non-primate), but with the kinase active site occupancy t1/2 of approximately 8.5 h, LY2801653 can be dosed orally twice a day in mouse tumor model studies.
The crystal structure of MET bound with LY2801653 indicates that LY2801653 is a type II inhibitor and illustrates that the mechanism of inhibition is through the stabilization of the inactive ‘DFG-out’ conformation [17, 18]. This binding mode often leads to a long dissociation time constant, a feature that was experimentally confirmed by the observation that LY2801653 has a slow-off rate with an active site occupancy t1/2 of approximately 8.5 h.
Type-II kinase inhibitors are typically more tolerant of mutations in the kinase domain than type-I inhibitors . For LY2801653, this feature was experimentally confirmed, and the molecule does retain inhibitory activity with a variety of MET-activating point mutations. Of the 13 point mutations examined, 12 are within the kinase domain. The exception, S1040P, is in the juxtamembrane domain. The MET crystal structure with bound LY2801653 provides a basis to interpret the impact of these mutations on the IC50 of LY2801653. The 2 mutants causing the greatest increases in IC50 (L1195V and M1131T) are located at the hydrophobic binding site of the inhibitor where changing from a hydrophobic side chain to a polar one, or reducing the size of hydrophobic side chain, is expected to weaken the inhibitor binding. The 2 mutants (D1228N, M1250T) with the next largest increases in IC50 bear mutations in the activation loop. This region is distal from the inhibitor. One of the mutations (D1228N) was not observed in the structure due to loop disorder. Thus the impact of the mutation is not through direct interaction with the inhibitor. One hypothesis for the increased IC50 is that these activating mutations stabilize the active conformation of the activation loop (DFG-in conformation), therefore reducing the potency of the inhibitor. The 2 mutations with noticeable decreases in IC50 (V1092I, V1220I) are located near the inhibitor. Both mutations slightly increase the bulk of the hydrophobic side chain, likely leading to stronger Van der Waals and/or hydrophobic interactions with the inhibitor.
Activating mutations of MET have been reported in sporadic and inherited papillary renal carcinomas, hepatocellular carcinomas, head and neck squamous cell carcinomas (HNSCC) and other neoplasms . The majority of these mutations are kinase domain mutations with homology to cancer-inducing mutations in other receptor tyrosine kinases such as EGFR. In HNSCC, cells harboring multiple kinase domain mutations have been observed and are postulated to be selected during metastatic spread . The 13 MET mutations evaluated here represent approximately half of the kinase domain mutations currently reported in the literature . The LY2801653-binding configuration to MET appears to contribute 2 clinically intriguing features; specifically, the potential ability to retain potency versus a spectrum of mutations and the ability to sustain target inhibition due to its slow off-rate.
Because the HGF/MET pathway has also been shown to be involved in cancer cell survival and growth, LY2801653 was evaluated for its ability to inhibit cell growth against a panel of MET expressing tumor cell lines. LY2801653 showed several-fold more potent anti-proliferative activity against tumor cell lines with high MET gene amplification (MKN45, Hs746T, H1993) than the cell lines without MET amplification (U-87MG, KATO III). These potency differences were less evident in the in vivo evaluation in xenograft models.
The in vivo effects in xenograft mouse models observed for LY2801653 were otherwise consistent with the in vitro data. LY2801653 treatment demonstrated significant anti-tumor growth effect in two MET autocrine models (U-87MG, KP4), a model with very high MET gene amplification (MKN45), and a model with MET low MET amplification, but over-expression, (H441). Similar tumor growth inhibition effect was observed following LY2801653 dosing of 4 to 12 mg/kg either once or twice a day. In the U-87MG and H441 models, similar anti-tumor effects were seen with interrupted dosing on a 9/5 or 5/2 schedule. Whereas the mechanism for maintaining tumor growth suppression with the non-continuous dosing schedules is unclear, it may be related to the observed slow off-rate of LY2801653 released from the ATP-binding site of the kinase target.
Kinase selectivity profile
Whereas type-II inhibitors are often characterized by a broad spectrum of kinase activity, LY2801653 retains a limited repertoire of engagement. The selectivity profile was examined through biochemical screening against 442 kinases, followed by confirmation with cell-based activity assays. LY2801653 was found to have potent activity against 11 additional kinases besides MET. A dendrogram shows that the 11 kinases are clustered in 3 regions, 2 of them in the receptor tyrosine kinase (RTKs) families and 1 (MKNK1/2) in the CAMK family (calcium/calmodulin-dependent protein kinases). Because LY2801653 does not have significant activity against ALK and LTK, it is somewhat surprising to find potent activity against ROS1, which is in the member of the ALK/LTK family. The x-ray crystal structure data may offer some insight. The inactive form of the ALK structure has been shown to be distinct from the typical features, such as the DFG-out conformation, observed in other RTKs . Instead, it appears that the DFG-in conformation is more stable in the inactive form of ALK, explaining the lack of inhibition by LY2801653. As MKNK1/2 are inhibited by LY2801653 despite these being serine/threonine kinases rather than tyrosine kinases, this inhibition is likely due to the inactive form of MKNK1/2 adopting a DFG-out (DFD in MKNK1/2) conformation, stabilized in part by the replacement of Asp (D) for Gly (G) in the canonical DFG motif [25, 26].
LY2801653 is an inhibitor of MET and MST1R (Table 2) in vitro and demonstrates tumor activity in 2 xenograft models (H1993, HT29) that co-express MET and MST1R. Tumor cells such as H1993 that have high levels of MET gene amplification have been shown to cross-activate MST1R . The ability to potently block both MET and MST1R pathway signaling may be advantageous in treating tumors with this phenotype.
Some of the other kinase targets of LY2801653 presented in Table 2 were also examined further in in vivo models. The potent in vitro anti-proliferative activity (IC50 = 4 nM) and in vivo anti-tumor growth activity of LY2801653 with the MV4-11 tumor cells may be explained by its inhibitory activity against FLT3 as this tumor cell line bears a FLT3-activating mutation . The in vivo anti-tumor growth activity of LY2801653 against AXL was demonstrated in a murine orthotopic model of NSCLC (H1299) with AXL over-expression. MET has been reported to be capable of transactivating AXL and PDGFRA in vitro in tumor cells . In human bladder cancer, co-expression of these RTKs was associated with poor patient survival, and over-expression of MET/AXL/PDGFRA was shown to correlate with poor survival, and contributed to the progression of human bladder cancer . Up-regulation of AXL was reported recently to be a resistance mechanism to EGFR targeted therapy .
MKNK1/2 are activated by ERK or p38 , leading to the phosphorylation of several substrates including eIF4E and Sprouty2, thereby enhancing tumorigenesis . An increase in Sprouty-2 protein in tumor cells was associated with an increase in MET expression and in tumor malignancy, especially in colon cancer cells . LY2801653 treatment produces anti-tumor effect in multiple murine xenograft models bearing KRAS-activating mutation as illustrated in H441 NSCLC cells and KP4 pancreatic cells, and treatment outcomes for such tumors may benefit from combined MET and MKNK1/2 inhibition.
ROS1 is an orphan RTK that has been reported to be constitutively activated via gene translocation leading to formation of fusion proteins in glioblastoma, NSCLC, ovarian cancer and cholangiocarcinoma [30, 31, 32, 33]. Over-expression of DDR1/2 has been reported in multiple tumor types such as sarcoma . Activating mutations for DDR2 in squamous cell lung cancer were also reported [34, 35]. In view of the reported transforming activity of constitutively activated ROS1 kinase with various fusion partners, and the potent inhibitory activity of LY2801653 for ROS1 and DDR1/2, there may be clinical merit in evaluating LY2801653 in tumor types bearing ROS1 or DDR1/2 aberrations.
Tumor vessel normalization describes a process whereby a tortuous, poorly perfused vascular network is converted to one that consists of directionally-aligned, highly perfused, pericyte-covered vessels . Treatment of U-87MG tumor-bearing mice with daily doses of 12 mg/kg LY2801653 resulted in phenotypic events that are hallmarks of vessel normalization. Whereas the tumors treated with 12 mg/kg LY2801653 displayed a more functional vasculature, the tumors themselves had less apoptotic and proliferative markers compared with vehicle-treated tumors, consistent with a cytostatic phenotype. As LY2801653 has little or no inhibitory activity against KDR, the displayed anti-angiogenic effects in vivo were most probably via a non-VEGFR-dependent mechanism. The HGF/MET , the AXL and MERTK , and the TEK  pathways were all reported to play a role in tumor angiogenesis and were inhibited by LY2801653.
In summary, we report here a potent type II ATP-competitive inhibitor of MET, LY2801653, that has in vivo anti-tumor activities in multiple mouse xenograft models, as well as anti-angiogenic, and anti-proliferative/cytostatic activities. In addition, this -molecule has potent inhibitory activity against several other oncogenic proteins, including MST1R, FLT3, AXL, PDGFRA, ROS1, TEK, DDR1/2 and MKNK-1/2. Nonclinical testing suggests that LY2801653 may have merits for clinical evaluation in tumors with a number of MET pathway phenotypic profiles such as over-expression, activating mutation, and gene amplification. Furthermore, as MKNK-1/2 is down-stream of the RAS/MEK/ERK signaling pathway, LY2801653 may have anti-tumor activity in tumors bearing KRAS-activating mutations in addition to the over-expression of the above mentioned RTK targets. These observations have supported the progression of LY2801653 into clinical testing in an ongoing phase 1 study (JSBA, NCT01285037).
The authors wish to thank Robert Foreman, Adam Phillips, Jennifer Stephens, Spring Weir for performing the mouse xenograft studies; Patti Moore for editing and managing the manuscript writing; Colleen Burns/Nick Loizos, Jason Cunningham and Jacqueline Doody/Yanxia Li for performing cell-based assays for PDGFRA, MST1R and CSF1R respectively; Laura Bloem for in vitro biochemical kinase assay management; Steve Demarest/Arlene Sereno for providing recombinant human Gas6; Beverly Falcon for constructing the figure of the tumor images; Shaoyou Chu for development of the cell scattering assay and Megan Thobe for review of the manuscript.
Disclosure of potential conflicts of interest
All authors: current or former employees of Eli Lilly and Company
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