TAE226, a bis-anilino pyrimidine compound, has been developed as an inhibitor of focal adhesion kinase (FAK) and insulin-like growth factor-I receptor (IGF-IR). In this study, we investigated the effect of TAE226 on non-small-cell lung cancer (NSCLC), especially focusing on the EGFR mutational status. TAE226 was more effective against cells with mutant EGFR, including the T790M mutant, than against cells with wild-type one. TAE226 preferentially inhibited phospho-EGFR and its downstream signaling mediators in the cells with mutant EGFR than in those with wild-type one. Phosphorylation of FAK and IGF-IR was not inhibited at the concentration at which the proliferation of EGFR-mutant cells was inhibited. Results of the in vitro binding assay indicated significant differences in the affinity for TAE226 between the wild-type and L858R (or delE746_A750) mutant, and the reduced affinity of ATP to the L858R (or delE746_A750) mutant resulted in good responsiveness of the L858R (or delE746_A750) mutant cells to TAE226. Of interest, the L858R/T790M or delE746_A750/T790M mutant enhanced the binding affinity for TAE226 compared with the L858R or delE746_A750 mutant, resulting in the effectiveness of TAE226 against T790M mutant cells despite the T790M mutation restoring the ATP affinity for the mutant EGFR close to that for the wild-type. TAE226 also showed higher affinity of about 15-fold for the L858R/T790M mutant than for the wild-type one by kinetic interaction analysis. The anti-tumor effect against EGFR-mutant tumors including T790M mutation was confirmed in mouse models without any significant toxicity. In summary, we showed that TAE226 inhibited the activation of mutant EGFR and exhibited anti-proliferative activity against NSCLCs carrying EGFR mutations, including T790M mutation.
Citation: Otani H, Yamamoto H, Takaoka M, Sakaguchi M, Soh J, Jida M, et al. (2015) TAE226, a Bis-Anilino Pyrimidine Compound, Inhibits the EGFR-Mutant Kinase Including T790M Mutant to Show Anti-Tumor Effect on EGFR-Mutant Non-Small Cell Lung Cancer Cells. PLoS ONE 10(6): e0129838. https://doi.org/10.1371/journal.pone.0129838
Academic Editor: Pier Giorgio Petronini, University of Parma, ITALY
Received: August 19, 2014; Accepted: May 13, 2015; Published: June 19, 2015
Copyright: © 2015 Otani et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This study was supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (grant number: 18790993 to ST), http://www.mext.go.jp/english/. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Novartis Pharma AG provided support in the form of salaries for authors SH and EK, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.
Competing interests: Although the authors of this manuscript (SH and EK) are employees of Novartis Pharma AG, this does not alter the authors’ adherence to PLOS ONE policies on sharing data and materials. Novartis Pharma AG provided support in the form of salaries for authors SH and EK, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.
Lung cancer is the leading cause of cancer death worldwide . Lung cancer is divided into two major histological categories, non-small-cell lung cancer (NSCLC) and small-cell lung cancer. Despite great efforts to improve the survival of patients with lung cancer, a satisfactory survival rate has not yet been achieved because the majority of patients present with an advanced disease stage and their tumors exhibit an inherent resistance to conventional chemotherapy . To improve the prognosis of patients with lung cancer, many clinical and basic investigations, including translational research, have been undertaken [3, 4].
Molecular-targeting therapy based on molecular alterations in cancer is a promising strategy for the treatment of lung cancers as well as other malignant tumors. For instance, 4-anilinoquinazoline inhibitors, such as gefitinib and erlotinib, have been designed to inhibit the tyrosine kinase domain of epidermal growth factor receptor (EGFR), which is overexpressed in NSCLC; such inhibitors are currently being used for the treatment of NSCLC [5–8]. Of particular interest, these EGFR tyrosine kinase inhibitors (EGFR-TKIs) produce drastic anti-tumor effects against NSCLCs carrying common EGFR mutations, small deletions at exon 19 and L858R mutation at exon 21. Besides these EGFR-TKI-sensitive mutations, T790M mutation at exon 20 is known as EGFR-TKI-resistant mutation [9, 10]. Previous studies have reported that common EGFR mutations in the tyrosine kinase domain are more frequent in patients with adenocarcinoma histology, a never smoking history, and an East Asian ethnicity [11–13]. The frequency of common EGFR mutation in adenocarcinoma, which depends on the patients’ background, ranges from 15 to 45%, suggesting that the common EGFR mutation is a frequent and important event of lung adenocarcinomas [11, 13, 14]. In contrast, inherent T790M mutations are very rare . However, T790M mutations are found in approximately 50% cases among NSCLCs that acquired resistance to EGFR-TKI .
Besides EGFR-TKIs targeting EGFR protein, various kinds of small molecule compounds have been developed to target cancer-specific molecular alterations. TAE226, a bis-anilino pyrimidine compound, competes with ATP for focal adhesion kinase (FAK) and insulin-like growth factor-I receptor (IGF-IR). This compound reportedly inhibits cell proliferation, migration, and the invasion of many cancers such as glioma, Barrett’s esophageal adenocarcinoma, ovarian, colorectal and breast cancers [17–22].
FAK is a non-receptor tyrosine kinase that transduces signals from integrin receptor and participates in multiple cell functions required for cell proliferation, survival, motility, and invasion . IGF-IR is a transmembrane receptor tyrosine kinase that participates in signaling cascades that lead to the activation of both AKT and mitogen-activated protein kinase (MAPK) . These tyrosine kinases are known to be overexpressed in many malignant tumors including some NSCLCs and to play an oncogenic role in cancer cells [25–27]. These facts and background encouraged us to examine the anti-tumor effect of TAE226 in NSCLC, and we unexpectedly found that TAE226 preferably inhibits the proliferation of EGFR-mutant NSCLC cell lines including the T790M mutant, compared with EGFR-wild-type NSCLC cell lines.
In this study, we describe the anti-tumor effect of TAE226 on EGFR-mutant cells in vitro and in vivo and investigated the anti-tumor mechanism of TAE226 in EGFR-mutant cells.
Materials and Methods
This study was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocol was approved by the Animal Care and Use Committee of Okayama University (Permit Number: OKU-2007232). All surgery was performed under ketamine and xylazine anesthesia, and all efforts were made to minimize suffering.
NVP-TAE226 was kindly provided by Novartis Pharma AG (Basel, Switzerland). ZD1839 (gefitinib) was kindly provided by AstraZeneca (Wilmington, DE). The stock solution of these compounds was respectively reconstituted in the concentration of 20 mM and 10 mM with dimethyl sulfoxide (DMSO) (Sigma-Aldrich, St. Louis, MO) and stored at -20°C until used for in vitro experiments.
The primary antibodies to the following proteins were used for western blotting: polyclonal anti-EGFR, phospho-EGFR (Tyr1068), IGF-IRβ, phospho-IGF-IRβ (Tyr1131), AKT, phospho-AKT (Ser473), p44/p42 mitogen-activated protein kinase (MAPK), and phospho-p44/p42 MAPK antibodies were purchased from Cell Signaling Technology (Beverly, MA). Monoclonal anti-focal adhesion kinase (FAK), phospho-FAK (pY397) antibodies were purchased from Biosource (Berkeley, CA), and anti-actin antibody, used as equal loading controls, was purchased from Sigma-Aldrich.
Cell lines and cell culture
To assess the effect of TAE226, the following 17 NSCLC cell lines, one breast cancer cell line (SK-BR-3), one gastric cancer cell line (MKN45) and HEK-293T cell line were used for in vitro and in vivo experiments. HCC827, HCC4006, NCI-H3255, NCI-H1975, NCI-H820, NCI-H1819, NCI-H1666, NCI-H1395, NCI-H2228, NCI-H1648, NCI-H1993, NCI-H838 and NCI-H1299 cell lines were kindly provided by Dr. Adi F. Gazdar (University of Texas Southwestern Medical Center at Dallas, Dallas, TX, USA), who established those NSCLC cell lines with Dr. John D. Minna [28–30] except for NCI-H3255, which was established by Dr. Bruce E. Johnson [11, 31]. These cell lines were proven to have individual genetic origins by the Powerplex 1.2 system (Promega, Madison, WI) at University of Texas Southwestern Medical Center at Dallas, before we obtained these cell lines . PC-9 (catalog number: 37012) was purchased from Immuno-Biological Laboratories (Takasaki, Japan). MKN45 (catalog number: JCRB0254) was purchased from Japanese Collection of Research Bioresources Cell Bank, National Institute of Biomedical Innovation (Ibaraki, Japan). SK-BR-3 (catalog number: HTB-30), A549 (catalog number: CCL-185), Calu-3 (catalog number: HTB-55) and HEK-293T (catalog number: CRL-3216) were purchased from the American Type Culture Collection (Manassas, VA). The gefitinib-resistant PC-9 cell line (RPC-9) was established by one of the authors (K.K.) . PC-9, HCC827, HCC4006, NCI-H3255, NCI-H1975, NCI-H820 and RPC-9 have EGFR-TKIs-sensitive mutations. Besides, NCI-H1975, NCI-H820 and RPC-9 cell lines also have T790M EGFR-TKIs-resistant mutation. The details of genetic alterations in these cell lines except for HCC4006 (delL747_A750, P ins) and NCI-H820 (delE746_E749/T790M) are shown in Table 1.
NCI-H3255 was grown in ACL-4 medium [33, 34] supplemented with 10% fetal bovine serum (FBS) and the other cancer cell lines were maintained in RPMI-1640 medium (Sigma-Aldrich) supplemented with 10% FBS, 100 U/ml penicillin, and 100 μg/ml streptomycin (Sigma-Aldrich). HEK-293T cell line was maintained in Dulbecco's Modified Eagle's Medium (Sigma-Aldrich) supplemented with 10% FBS. All the cell lines were maintained at 37°C in a fully humidified atmosphere of 5% CO2 in air. All in vitro experiments were conducted with about 80% confluent cultures.
The effect of TAE226 on IGF-IR after serum-starvation
To assess the effect of TAE226 on IGF-IR under ligand-free condition, we analyzed the induced IGF-IR phosphorylation after serum-starvation followed by TAE226 treatment. After cell lines were serum-starved for three hours and treated with increased concentration of TAE226 for two hours, they were stimulated by 100 ng/ml IGF-I recombinant (Sigma-Aldrich) for 15 minutes and then were analyzed by western blotting.
Determining the drug sensitivity to TAE226 and gefitinib in various cell lines
Drug sensitivity was determined by a modified MTS assay with CellTiter 96 AQueous One Solution Reagent (Promega, Madison, WI). Cells were generally seeded on 96-well plates at a density that would yield 80% confluence by the completion of the experiment, varying by each cell line from 3000 to 4000 per well. After that, the medium in the wells was replaced with the medium containing diluted drug solutions of TAE226 or gefitinib in a 4-log range or complete medium, which were distributed in 8-replicate wells. Cells were incubated in the presence of each concentration of TAE226 for 48 hours and of gefitinib for 72 hours at 37°C in a humidified atmosphere of 5% CO2 in air. After that, MTS dye was added to each well. The cultures were incubated for another 1 hour at 37°C in a humidified atmosphere with 5% CO2. Optical densities of samples were measured at 490 nm using Immuno Mini NJ-2300 (Nalge Nunc International KK, Rochester, NY). Mean optical density at each drug concentration was calculated after discarding the highest and lowest values. The anti-tumor effects of TAE226 and gefitinib for each cell line were shown in terms of inhibitory concentration at 50% (IC50), which was determined by plotting the graph of percentage of cell growth inhibition (Y-axis) versus drug concentration (X-axis). IC50 values were expressed as mean and standard deviations. The assays were repeated until the standard deviation became less than the mean.
Western blot analysis
Cells were cultured in 60 mm dishes overnight, and then, treated with DMSO or each concentration of TAE226 and gefitinib. Next, they were washed out with cold PBS and lysed in 1 × cell lysis buffer [20 mM Tris-HCl (pH 7.5), 150 mM NaCl, 1 mM Na2EDTA, 1 mM EGTA, 1% Triton, 2.5 mM sodium pyrophosphate, 1 mM beta-glycerophosphate, 1 mM Na3VO4, 1 μg/ml leupeptin] (Cell signaling Technology) supplemented with Complete, Mini (Roche, Basel, Switzerland) to extract protein. After the protein concentration was measured, equal amounts of total protein (30 μg) were separated by SDS-PAGE and transferred to PVDF membranes. The proteins on membranes were incubated overnight at 4°C with the primary antibodies. The following secondary antibodies were used: goat antirabbit or antimouse IgG-conjugated horseradish peroxidase (HRP) (Santa Cruz Biotechnology, Santa Cruz, CA). To detect specific signals, the membranes were incubated by ECL plus Western Blotting Detection Reagents (Amersham Biosciences UK Limited, Buckinghamshire, UK).
In vitro binding assay of the variant EGFR-TK domains
The binding ability of TAE 226 for variant EGFR-TK domains was examined with in vitro binding assay. Variant EGFR-TK domains consisted of wild-type, delE746_A750, L858R, delE746_A750/T790M, and L858R/T790M. The detailed method is described in S1 Method.
Kinetic interaction analysis of TAE226 and gefitinib against wild-type EGFR and L858R/ T790M EGFR mutant
To characterize the mechanism of the action of TAE226 on EGFR, we performed kinetic interaction analysis of TAE226 and gefitinib (as a control) against wild-type EGFR and L858R/T790M EGFR mutant by Proteros Reporter Displacement Assay (Proteros biostructures GmbH, Munich, Germany), which was used to determine the following parameters: Kd, kon, koff and residence time. The Proteros Reporter Displacement Assay was performed as described previously [35, 36]. Detailed method was described in S1 Method.
Animal xenograft mouse model
In this experiment, we used BALB/c-nu/nu female nude mice at 4–6 weeks of age that were purchased from Charles River Laboratories Japan, Inc (Yokohama, Japan). They were maintained under specific-pathogen-free conditions in accordance with the guidelines of the Animal Care and Use Committee at Okayama University. PC-9 and RPC-9 cell lines (4.0×106/100 μl) mixed with 100 μl Matrigel (Corning Life Sciences, Tewksbury, MA) were inoculated subcutaneously into 24 nude mice [4 different groups (n = 6 in each group) by the concentration of TAE226], which had about 20 g body weight. TAE226 was diluted by methylcellulose in the concentration of 0 mg/kg (vehicle), 30 mg/kg, 60 mg/kg and 90 mg/kg. After the tumor volume has reached 200–400 mm3, TAE226 was orally administered to each nude mouse once a day for serial 14 days. Every three days, body weight of the mice and the major axis and minor axis of each tumor were measured and calculated tumor volume using the following formula; (major axis) × (minor axis)2 × 1/2 [37, 38]. For the 14 days, tumor volume, tumor growth rate and the body weight were analyzed as an average of the each group.
Anti-proliferative effect of TAE226 on NSCLC cell lines
We evaluated the anti-tumor effect of TAE226 using an MTS assay in 15 NSCLC cell lines, one breast cancer cell line and one gastric cancer cell line (Table 1). Number of MTS assays performed and each IC50 value obtained from independent assays are shown in S2 Table. Three NSCLC cell lines (PC-9, HCC827, and NCI-H3255) with only EGFR-TKI-sensitive EGFR mutations and two NSCLC cell lines (RPC-9 and NCI-H1975) with both TKI-sensitive and TKI-resistant EGFR mutations showed similar IC50 values, ranging from 0.086 to 0.31 μM. In contrast, the IC50 values for EGFR wild-type NSCLC cell lines (n = 10: ranged from 0.28 to 6.2 μM) were higher than those of EGFR-mutant NSCLC cell lines although two BRAF mutant cell lines and one EML4-ALK translocated cell line showed intermediate level of IC50 values (range, 0.28 to 0.48 μM). These results suggested that TAE226 was more effective in EGFR-mutant cell lines, regardless of the presence of the TKI-resistant EGFR T790M mutation, than in EGFR wild-type cell lines, especially which did not have BRAF or EML4-ALK alterations.
We also examined the anti-tumor effect of gefitinib against 14 NSCLC cell lines (Table 1). Three NSCLC cell lines harboring only EGFR-TKI-sensitive EGFR mutation were sensitive to gefitinib (the IC50 values were ranged from 0.0014 to 0.0028 μM), while other NSCLC cell lines harboring wild-type EGFR (n = 9) or TKI-resistant EGFR mutation (n = 2) were resistant (the IC50 were ranged from 5.3 to 32.6 μM). These data were consistent with those of previous reports [10, 28].
Deregulation of FAK, IGF-IR, and EGFR-related proteins after TAE226 treatment in NSCLC cell lines
We investigated the effect of TAE226 on FAK, IGF-IR, and EGFR-related proteins using 6 cell lines (PC-9, HCC827, NCI-H1975, RPC-9, NCI-H1299, and NCI-H1819). The phosphorylation of FAK (Thy397) and IGF-IR (Tyr1131), which are targets of TAE226, was not significantly inhibited up to a concentration of 5 μM in all 6 cell lines tested (Fig 1). For FAK, phosphorylation was inhibited at a concentration of 20 μM (data not shown). For IGF-IR, phosphorylation was completely inhibited by TAE226 after serum-starvation in all 4 cell lines tested (PC-9, RPC-9, NCI-H1299, and NCI-H1819), regardless of ligand stimulation (S1 Fig). This result indicated that TAE226 inhibited phoshorylation of IGF-IR as expected.
The NSCLC cell lines with EGFR-TKI-sensitive (exon 19 deletions) mutation (PC-9 and HCC827), cell lines with both EGFR-TKI-sensitive and-resistant (T790M) mutations (NCI-H1975 and RPC-9), and cell lines with wild-type EGFR (NCI-H1299 and NCI-H1819) were treated with TAE226 at several concentrations and western blotting analysis was performed. The phosphorylations of FAK and IGF-IR were not suppressed in all NSCLC cell lines tested. In contrast, the phosphorylations of EGFR and its downstream proteins, AKT and MAPK, were suppressed at lower concentration of TAE226 in EGFR-mutant cell lines regardless of the presence of T790M mutation compared with EGFR-wild-type cell lines. We incubated the membrane for Actin (42 KDa) after we incubated MAPK (42 and 44 KDa) and the stripping buffer was used for that membrane.
Of particular interest, the phosphorylation of EGFR was predominantly inhibited by TAE226 in all four EGFR-mutant cell lines (PC-9, HCC827, NCI-H1975, and RPC-9), regardless of the presence of TKI-resistant mutations. In addition, the phosphorylations of AKT and MAPK, which are downstream molecules of EGFR, were also inhibited in these EGFR-mutant cell lines. In contrast, the phosphorylations of EGFR, AKT, and MAPK were not inhibited in cell lines with wild-type EGFR (NCI-H1299 and NCI-H1819) (Fig 1). These data suggested that TAE226 might have a stronger effect on mutant EGFR than wild-type EGFR.
We confirmed the expression level of FAK, p-FAK, IGF-IR, and p-IGF-IR in cell lines without drug exposure using ten NSCLC cell lines (EGFR-mutant cell lines, PC-9, HCC827, NCI-H3255, HCC4006, NCI-H1975, NCI-H820 and RPC-9; EGFR wild-type cell lines, NCI-H1819, NCI-H1299 and A549). No significant difference in the expression level of each of the proteins was observed among the cell lines (S2 Fig).
Effect of TAE226 on mutant EGFR-transfected HEK-293T cell line
We examined the anti-proliferative effect of TAE226 on two HEK-293T cell lines stably transfected with wild-type EGFR or mutant EGFR (L858R) that we had previously established . The HEK-293T with mutant EGFR was more sensitive to gefitinib than the HEK-293T with wild-type EGFR (the IC50 values were 0.38 ± 0.087 and 18.2 ± 3.9 μM, respectively) (Table 1). TAE226 exerted a higher anti-tumor effect on the HEK-293T with the mutant EGFR than on the HEK-293T with the wild-type EGFR (the IC50 values were 0.41 ± 0.06 and 3.0 ± 0.11 μM, respectively) (Table 1). TAE226 inhibited the phosphorylations of EGFR and AKT in the HEK-293T cell with the mutant EGFR but not in the HEK-293T cell with the wild-type EGFR (S3 Fig). These results also indicated that TAE226 inhibited the cell growth or survival of EGFR-mutant cells by suppressing mutant EGFR protein.
Binding affinity of TAE226 to mutant EGFR
To assess the binding affinity of TAE226 to EGFR kinases, we performed an in vitro binding assay of the variant EGFR kinases (Fig 2). The supernatant fraction contained EGFR kinase that did not bind to bead-modified ATP because of interference from TAE226 (or exogenous ATP). The precipitated fraction contained EGFR kinase that had bound to bead-modified ATP, indicating that TAE226 (or exogenous ATP) did not interfere with the ATP binding. Thus, the band intensity at each TAE226 (or exogenous ATP) concentration reflects the ability of TAE226 (or exogenous ATP) to compete with bead-modified ATP for the EGFR kinases.
A) common EGFR mutant kinases and B) T790M containing EGFR mutant kinases. The five types of EGFR kinases, wild-type, exon 21 L858R mutation (L858R) or exon 19 deletion (delE746_A750), T790M in tandem with the L858R mutation (L858R/T790M), and T790M in tandem with delE746_A750 (delE746_A750/T790M), which competitively bind to ATP or TAE226, were extracted and were incubated with beads-modified ATP. TAE226 or the recombinant ATP was added to compete with beads-modified ATP for the binding to EGFR kinases. The EGFR kinase binging with the beads-modified ATP was present in precipitation, and the EGFR kinase binding with TAE226 (or recombinant ATP) was present in supernatant. Western blotting was performed to detect EGFR kinases in each component using a HA antibody. *, at the concentration of 10 μM for ATP; **, at the concentration of 0.005 μM for TAE226.
Among the variant EGFR kinases that were tested (wild-type, L858R, delE746_A750, L858R/T790M and delE746_A750/T790M), no difference in the amounts of EGFR kinases that bound to the bead-modified ATP was noted under the control condition (Fig 2A and 2B). Exogenous ATP weakly bound to EGFR kinases at a concentration of 1000 μM in all the variants tested (Fig 2A). In contrast, TAE226 started to bind to wild-type EGFR kinase at a concentration of 0.1 μM and at lower concentrations for mutant EGFRs, indicating that TAE226 possess a higher affinity to EGFR kinases than ATP. We estimated the binding affinity of TAE226 to EGFR variants by comparing the ratio of the semi-quantified band intensity between the supernatant fraction and the precipitated fraction at 0.1 μM of TAE226 among wild-type, L858R, or delE746_A750 (S4A Fig). Quantification using ImageJ software (National Institutes of Health, Bethesda, MD) showed that the binding affinity of TAE226 was approximately 7.5-fold higher to both mutant EGFRs than to wild-type EGFR (S4A Fig). The effect of acquired T790M mutation on the binding affinity for TAE226 to common mutant EGFR kinases (L858R or delE746_A750) was also evaluated at the concentration of 0.005 μM for TAE226 and 10 μM for ATP (Fig 2B). Interestingly, the binding affinity for TAE226 was higher in T790M containing EGFR mutant kinases (L858R/T790M or delE746_A750/T790M) than in common EGFR mutant kinases (L858R or delE746_A750) (S4B Fig).
Interaction kinetics of TAE226 and gefitinib with wild-type EGFR and L858R/T790M EGFR mutant
IC50 and Kd values for TAE226 and gefitinib against wild-type EGFR and L858R/T790M EGFR mutant were shown in Table 2. IC50 and Kd values for TAE226 were 0.326 μM and 0.163 μM in wild-type EGFR, and 0.0193 μM and 0.00966 μM in L858R/T790M EGFR mutant, respectively. Regarding gefitinib, those were 0.0244 μM and 0.0122 μM in wild-type EGFR, and 0.927 μM and 0.463 μM in L858R/T790M EGFR mutant, respectively. Gefitinib showed a higher affinity of about 40-fold for wild-type EGFR than for L858R/T790M EGFR mutant. On the contrary, TAE226 showed higher affinity of about 15-fold for L858R/T790M EGFR mutant than for wild-type EGFR. The values of kon and koff could not be calculated in TAE226 for the both type of EGFR and in gefitinib for L858R/T790M EGFR mutant because of the short residence time (< 1.4 min).
Anti-tumor effect of TAE226 on NSCLC mouse xenograft models
Based on our in vitro data, we examined the anti-tumor effect of TAE226 on mouse xenograft models. After the subcutaneous tumor volume of the inoculated PC-9 and RPC-9 cell lines in nude mice had reached a volume of 200–400 mm3, we treated the nude mice with the oral administration of TAE226 (30 mg/kg, 60 mg/kg or 90 mg/kg) or methylcellulose as vehicle for 14 days. The tumor volume and body weight of both xenografts were measured on the day before the oral administration of TAE226 and every three days thereafter. Obvious side effects, including the loss of body weight, did not occur in the vehicle-treated group or in the groups treated with 30mg/kg or 60mg/kg of TAE226, while a loss of body weight was observed in mice treated with 90 mg/kg of TAE226. The tumor volume in both xenografts significantly decreased over time and in a dose-dependent manner, compared with the vehicle-treated mice (Fig 3). Furthermore, both xenografts of EGFR-TKI-sensitive (PC-9) and EGFR-TKI-resistant (RPC-9) cell lines showed similar anti-tumor effects in response to TAE226 in vivo.
The oral administration of TAE226 for 14 days significantly inhibited the tumor growth of the subcutaneously inoculated mice xenografts with PC-9 (exon19 deletion) or RPC-9 (exon19 deletion and T790M mutation) at every dose (30, 60 and 90 mg/kg). In addition, TAE226 showed the similar anti-tumor effect on both xenograft models irrespective of the presence of EGFR T790M mutation.
As shown in the relationship between small EGFR-TKI and EGFR mutation , the ability of TAE226 to compete with ATP, resulting in its anti-tumor potential, is determined by two factors: 1) the binding ability for TAE226 to mutant EGFR and 2) the affinity for ATP to mutant EGFR. It is well known that the affinity for ATP is lower to common EGFR mutants than to wild-type EGFR .
There seems to be another important factor that strongly influences the effects of molecular targeting drugs on cancer cells. According to the concept of “oncogene addiction”, EGFR-mutant cell lines are highly dependent on mutant EGFR for cell proliferation and survival . Whereas the reason for poor inhibition to FAK or IGF-IR activity in NSCLC is not clear, our findings indicated that TAE226 strongly inhibited the mutant EGFR, compared to FAK and IGF-IR, in cells that are “addicted” to the mutant EGFR, resulting in the anti-tumor activity of TAE226. Of note, there were some discrepancies between IC50 of in vitro non-cellular kinase assay and cellular inhibition assay for some oncogenes. This phenomenon seems to be explained by the concept of “oncogene addition” that the degree of dependency to specific oncogenes can be different among tumors and oncogenes. IC50 values for c-Src (0.91), HER2 (0.95), FGFR-1 (0.75), c-Met (0.16) and ALK (0.15), which are often activated in NSCLC, are less than that for EGFR (1.7) (S1 Table, updated data from ref. 20), indicating that TAE226 may also inhibit these kinases in addition to EGFR in NSCLCs, especially if the tumors are “addicted” to these kinases.
Regarding the mechanism whereby the T790M mutation is thought to influence small molecule TKIs such as gefitinib and erlotinib, the T790M mutation has been thought to cause resistance by sterically blocking the binding of TKIs [9, 10, 42]. In addition, Yun and colleagues reported that an increase in ATP affinity is the primary mechanism by which the T790M mutation causes resistance to TKIs; while the single L858R mutation reduces the binding affinity of ATP by about 30-fold compared with the wild-type EGFR, introduction of the additional T790M mutation restores the binding affinity of ATP comparable to that of the wild-type EGFR . Interestingly, our data showed that IC50 values of TAE226 for EGFR T790M in tandem with the L858R (or delE746_A750) mutant cells are similar to those for EGFR L858R (or delE746_A750) mutant cells, providing the contrasting results compared to the IC50 values of gefitinib for them. Our in vitro binding assay also indicates that the double mutant reveals higher binding affinity to TAE226 than that of the L858R (or delE746_A750) mutant. It is well known and documented that increased hydrophobic interactions between a protein and a ligand lead to an enhanced binding affinity of the ligand, occasionally by several orders of magnitude . Kinetic interaction analysis of TAE226 and gefitinib using wild-type EGFR and L858R/T790M EGFR mutant confirmed that the L858R/T790M double mutant showed higher binding affinity to TAE226 than wild-type EGFR. By taking into account the fact about the binding affinity of ATP to the L858R and L858R/T790M mutants described above, we can reasonably assume that, in the presence of ATP, TAE226 will show comparable inhibition to both mutants, by canceling out the two type of factors–the binding of ATP to the mutants as well as the binding of TAE226 to the mutants. Actually, the IC50 of the RPC-9 cells was higher than the IC50 of the PC-9 cells for TAE226. However, the difference of IC50 between PC-9 and RPC-9 for TAE226 is slight compared to that for gefitinib. As for in vivo study, the obtained results suggest the safety of TAE226 doses suitable for the treatment of EGFR-mutant cells, regardless of the presence of EGFR T790M mutation in vivo, opening the possibility for clinical application. In addition to TAE226, related bis-anilino pyrimidine compounds have also been developed . Further study is warranted to examine whether these bis-anilino pyrimidine compounds inhibit mutant EGFR kinase.
In conclusion, we found that TAE226 inhibited the activation of EGFR-mutant kinase and exerted anti-tumor activity on EGFR-mutant NSCLC regardless of the presence of T790M mutation. Our results showed that the EGFR L858R/T790M (or delE746_A750/T790M) mutant retains the binding affinity to TAE226 comparable to that of the L858R (or delE746_A750) mutant, suggesting that TAE226, or its relatives, is promising to overcome acquired TKI resistance mediated by EGFR T790M mutation.
S1 Fig. The effect of TAE226 to IGF-IR-related proteins after the stimulation of IGF-I recombinant in NSCLC cell lines.
Serum-starved NSCLC cell lines were treated with TAE226 for two hours and stimulated with IGF-I recombinant for 15 minutes. The phosphorylations of IGF-IR and AKT were completely inhibited in all cell lines regardless of EGFR mutational status.
S2 Fig. The expression profiles of p-FAK, FAK, p-IGF-IR and IGF-IR in NSCLC cell lines.
There were no significant differences in the expression levels of p-FAK, FAK, p-IGF-IR and IGF-IR in 10 NSCLC cell lines regardless of EGFR mutational status.
S3 Fig. The effect of TAE226 on mutant EGFR-transfected HEK-293T cell line.
The mutant EGFR-transfected HEK-293T was more sensitive to gefitinib treatment than wild-type EGFR-transfected HEK-293T. TAE226 significantly inhibited phosphorylations of EGFR and AKT in mutant EGFR-trasnsfected HEK-293T compared with wild-type EGFR-transfected HEK-293T.
S4 Fig. Comparison of the binding affinity of TAE226 to EGFR variants by the quantification of EGFR protein expression.
(A) Density of EGFR protein bands between the supernatant fraction and the precipitated fraction at 0.1 μM of TAE226 in Fig 2A was semi-quantified by densitometry analysis. The binding affinity of TAE226 to EGFR variants was approximately 7.5-fold higher to both mutant EGFRs than to wild-type EGFR. (B) Density of EGFR protein bands in supernatant fraction for TAE226 in Fig 2B was semi-quantified by densitometry analysis. Band density of EGFR protein for TAE226 was higher in T790M-containing EGFR mutant kinases (L858R/T790M or delE746_A750/T790M) than in common EGFR mutant kinases (L858R or delE746_A750).
S1 Method. Methods for “In vitro binding assay of the variant EGFR-TK domains” and “Kinetic interaction analysis of TAE226 and gefitinib against wild-type EGFR and L858R/ T790M EGFR mutant”.
Detailed methods are described.
S1 Table. In vitro non-cellular kinase assay for TAE226.
This table is updated data from ref. 20.
We thank Chieko Takahashi for technical assistance, Dr. Motowo Nakajima for useful advice, and Dr. Adi F. Gazdar for providing the cell lines that were used in this study.
Conceived and designed the experiments: HO HY MT MS JS HA KT YN SM ST. Performed the experiments: HO MS MJ TU TK SH EK. Analyzed the data: HO HY MS SH EK ST. Contributed reagents/materials/analysis tools: KK SH EK YN. Wrote the paper: HO HY MS JS SH EK ST.
- 1. Siegel R, Ma J, Zou Z, Jemal A (2014) Cancer statistics, 2014. CA Cancer J Clin 64: 9–29. pmid:24399786
- 2. Schiller JH, Harrington D, Belani CP, Langer C, Sandler A, Krook J, et al. (2002) Comparison of four chemotherapy regimens for advanced non-small-cell lung cancer. N Engl J Med 346: 92–98. pmid:11784875
- 3. Fukui T, Mitsudomi T (2008) Mutations in the epidermal growth factor receptor gene and effects of EGFR-tyrosine kinase inhibitors on lung cancers. Gen Thorac Cardiovasc Surg 56: 97–103. pmid:18340507
- 4. Suehisa H, Toyooka S, Hotta K, Uchida A, Soh J, Fujiwara Y, et al. (2007) Epidermal growth factor receptor mutation status and adjuvant chemotherapy with uracil-tegafur for adenocarcinoma of the lung. J Clin Oncol 25: 3952–3957. pmid:17761979
- 5. Fong T, Morgensztern D, Govindan R (2008) EGFR inhibitors as first-line therapy in advanced non-small cell lung cancer. J Thorac Oncol 3: 303–310. pmid:18317074
- 6. Gridelli C, Bareschino MA, Schettino C, Rossi A, Maione P, Ciardiello F (2007) Erlotinib in non-small cell lung cancer treatment: current status and future development. Oncologist 12: 840–849. pmid:17673615
- 7. Inoue A, Suzuki T, Fukuhara T, Maemondo M, Kimura Y, Morikawa N, et al. (2006) Prospective phase II study of gefitinib for chemotherapy-naive patients with advanced non-small-cell lung cancer with epidermal growth factor receptor gene mutations. J Clin Oncol 24: 3340–3346. pmid:16785471
- 8. Tamura K, Okamoto I, Kashii T, Negoro S, Hirashima T, Kudoh S, et al. (2008) Multicentre prospective phase II trial of gefitinib for advanced non-small cell lung cancer with epidermal growth factor receptor mutations: results of the West Japan Thoracic Oncology Group trial (WJTOG0403). Br J Cancer 98: 907–914. pmid:18283321
- 9. Kobayashi S, Boggon TJ, Dayaram T, Janne PA, Kocher O, Meyerson M, et al. (2005) EGFR mutation and resistance of non-small-cell lung cancer to gefitinib. N Engl J Med 352: 786–792. pmid:15728811
- 10. Pao W, Miller VA, Politi KA, Riely GJ, Somwar R, Zakowski MF, et al. (2005) Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain. PLoS Med 2: e73. pmid:15737014
- 11. Paez JG, Janne PA, Lee JC, Tracy S, Greulich H, Gabriel S, et al. (2004) EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science 304: 1497–1500. pmid:15118125
- 12. Pao W, Miller V, Zakowski M, Doherty J, Politi K, Sarkaria I, et al. (2004) EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib. Proc Natl Acad Sci U S A 101: 13306–13311. pmid:15329413
- 13. Shigematsu H, Lin L, Takahashi T, Nomura M, Suzuki M, Wistuba II, et al. (2005) Clinical and biological features associated with epidermal growth factor receptor gene mutations in lung cancers. J Natl Cancer Inst 97: 339–346. pmid:15741570
- 14. Tokumo M, Toyooka S, Kiura K, Shigematsu H, Tomii K, Aoe M, et al. (2005) The relationship between epidermal growth factor receptor mutations and clinicopathologic features in non-small cell lung cancers. Clin Cancer Res 11: 1167–1173. pmid:15709185
- 15. Toyooka S, Kiura K, Mitsudomi T (2005) EGFR mutation and response of lung cancer to gefitinib. N Engl J Med 352: 2136; author reply 2136. pmid:15901872
- 16. Engelman JA, Zejnullahu K, Mitsudomi T, Song Y, Hyland C, Park JO, et al. (2007) MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling. Science 316: 1039–1043. pmid:17463250
- 17. Watanabe N, Takaoka M, Sakurama K, Tomono Y, Hatakeyama S, Ohmori O, et al. (2008) Dual tyrosine kinase inhibitor for focal adhesion kinase and insulin-like growth factor-I receptor exhibits anticancer effect in esophageal adenocarcinoma in vitro and in vivo. Clin Cancer Res 14: 4631–4639. pmid:18628478
- 18. Halder J, Lin YG, Merritt WM, Spannuth WA, Nick AM, Honda T, et al. (2007) Therapeutic efficacy of a novel focal adhesion kinase inhibitor TAE226 in ovarian carcinoma. Cancer Res 67: 10976–10983. pmid:18006843
- 19. Golubovskaya VM, Virnig C, Cance WG (2008) TAE226-induced apoptosis in breast cancer cells with overexpressed Src or EGFR. Mol Carcinog 47: 222–234. pmid:17849451
- 20. Liu TJ, LaFortune T, Honda T, Ohmori O, Hatakeyama S, Meyer T, et al. (2007) Inhibition of both focal adhesion kinase and insulin-like growth factor-I receptor kinase suppresses glioma proliferation in vitro and in vivo. Mol Cancer Ther 6: 1357–1367. pmid:17431114
- 21. Shi Q, Hjelmeland AB, Keir ST, Song L, Wickman S, Jackson D, et al. (2007) A novel low-molecular weight inhibitor of focal adhesion kinase, TAE226, inhibits glioma growth. Mol Carcinog 46: 488–496. pmid:17219439
- 22. Hehlgans S, Lange I, Eke I, Cordes N (2009) 3D cell cultures of human head and neck squamous cell carcinoma cells are radiosensitized by the focal adhesion kinase inhibitor TAE226. Radiother Oncol 92: 371–378. pmid:19729215
- 23. Parsons JT, Martin KH, Slack JK, Taylor JM, Weed SA (2000) Focal adhesion kinase: a regulator of focal adhesion dynamics and cell movement. Oncogene 19: 5606–5613. pmid:11114741
- 24. Werner H, Bruchim I (2009) The insulin-like growth factor-I receptor as an oncogene. Arch Physiol Biochem 115: 58–71. pmid:19485702
- 25. van Nimwegen MJ, van de Water B (2007) Focal adhesion kinase: a potential target in cancer therapy. Biochem Pharmacol 73: 597–609. pmid:16997283
- 26. Siesser PM, Hanks SK (2006) The signaling and biological implications of FAK overexpression in cancer. Clin Cancer Res 12: 3233–3237. pmid:16740741
- 27. Guerreiro AS, Boller D, Doepfner KT, Arcaro A (2006) IGF-IR: potential role in antitumor agents. Drug News Perspect 19: 261–272. pmid:16941048
- 28. Gandhi J, Zhang J, Xie Y, Soh J, Shigematsu H, Zhang W, et al. (2009) Alterations in genes of the EGFR signaling pathway and their relationship to EGFR tyrosine kinase inhibitor sensitivity in lung cancer cell lines. PLoS One 4: e4576. pmid:19238210
- 29. Gazdar AF, Girard L, Lockwood WW, Lam WL, Minna JD (2010) Lung cancer cell lines as tools for biomedical discovery and research. J Natl Cancer Inst 102: 1310–1321. pmid:20679594
- 30. Phelps RM, Johnson BE, Ihde DC, Gazdar AF, Carbone DP, McClintock PR, et al. (1996) NCI-Navy Medical Oncology Branch cell line data base. J Cell Biochem Suppl 24: 32–91. pmid:8806092
- 31. Fujishita T, Loda M, Turner RE, Gentler M, Kashii T, Breathnach OS, et al. (2003) Sensitivity of non-small-cell lung cancer cell lines established from patients treated with prolonged infusions of Paclitaxel. Oncology 64: 399–406. pmid:12759538
- 32. Ogino A, Kitao H, Hirano S, Uchida A, Ishiai M, Kozuki T, et al. (2007) Emergence of epidermal growth factor receptor T790M mutation during chronic exposure to gefitinib in a non small cell lung cancer cell line. Cancer Res 67: 7807–7814. pmid:17699786
- 33. Gazdar AF, Oie HK (1986) Re: Growth of cell lines and clinical specimens of human non-small cell lung cancer in a serum-free defined medium. Cancer Res 46: 6011–6012. pmid:3019544
- 34. Brower M, Carney DN, Oie HK, Gazdar AF, Minna JD (1986) Growth of cell lines and clinical specimens of human non-small cell lung cancer in a serum-free defined medium. Cancer Res 46: 798–806. pmid:3940644
- 35. Schneider EV, Bottcher J, Huber R, Maskos K, Neumann L (2013) Structure-kinetic relationship study of CDK8/CycC specific compounds. Proc Natl Acad Sci U S A 110: 8081–8086. pmid:23630251
- 36. Neumann L, von Konig K, Ullmann D (2011) HTS reporter displacement assay for fragment screening and fragment evolution toward leads with optimized binding kinetics, binding selectivity, and thermodynamic signature. Methods Enzymol 493: 299–320. pmid:21371596
- 37. Tomayko MM, Reynolds CP (1989) Determination of subcutaneous tumor size in athymic (nude) mice. Cancer Chemother Pharmacol 24: 148–154. pmid:2544306
- 38. Euhus DM, Hudd C, LaRegina MC, Johnson FE (1986) Tumor measurement in the nude mouse. J Surg Oncol 31: 229–234. pmid:3724177
- 39. Uchida A, Hirano S, Kitao H, Ogino A, Rai K, Toyooka S, et al. (2007) Activation of downstream epidermal growth factor receptor (EGFR) signaling provides gefitinib-resistance in cells carrying EGFR mutation. Cancer Sci 98: 357–363. pmid:17270025
- 40. Carey KD, Garton AJ, Romero MS, Kahler J, Thomson S, Ross S, et al. (2006) Kinetic analysis of epidermal growth factor receptor somatic mutant proteins shows increased sensitivity to the epidermal growth factor receptor tyrosine kinase inhibitor, erlotinib. Cancer Res 66: 8163–8171. pmid:16912195
- 41. Gazdar AF, Shigematsu H, Herz J, Minna JD (2004) Mutations and addiction to EGFR: the Achilles 'heal' of lung cancers? Trends Mol Med 10: 481–486. pmid:15464447
- 42. Kwak EL, Sordella R, Bell DW, Godin-Heymann N, Okimoto RA, Brannigan BW, et al. (2005) Irreversible inhibitors of the EGF receptor may circumvent acquired resistance to gefitinib. Proc Natl Acad Sci U S A 102: 7665–7670. pmid:15897464
- 43. Yun CH, Mengwasser KE, Toms AV, Woo MS, Greulich H, Wong KK, et al. (2008) The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP. Proc Natl Acad Sci U S A 105: 2070–2075. pmid:18227510
- 44. Klebe G, Bohm HJ (1997) Energetic and entropic factors determining binding affinity in protein-ligand complexes. J Recept Signal Transduct Res 17: 459–473. pmid:9029508
- 45. Lietha D, Eck MJ (2008) Crystal structures of the FAK kinase in complex with TAE226 and related bis-anilino pyrimidine inhibitors reveal a helical DFG conformation. PLoS One 3: e3800. pmid:19030106