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Evaluation of the Antitumor Effects of BPR1J-340, a Potent and Selective FLT3 Inhibitor, Alone or in Combination with an HDAC Inhibitor, Vorinostat, in AML Cancer

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Potent and Selective FLT3 Inhibitor, Alone or in

Combination with an HDAC Inhibitor, Vorinostat, in AML

Cancer

Wen-Hsing Lin1., Teng-Kuang Yeh1., Weir-Torn Jiaang1., Kuei-Jung Yen1, Chun-Hwa Chen1, Chin-Ting Huang1, Shih-Chieh Yen1, Shu-Yi Hsieh1, Ling-Hui Chou1, Ching-Ping Chen1, Chun-Hsien Chiu1, Li-Chun Kao1, Yu-Sheng Chao1, Chiung-Tong Chen1*, John T.-A. Hsu1,2*

1 Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan, 2 Department of Biological Science and Technology, National Chiao Tung University, Hsinchu, Taiwan

Abstract

Overexpression or/and activating mutation of FLT3 kinase play a major driving role in the pathogenesis of acute myeloid leukemia (AML). Hence, pharmacologic inhibitors of FLT3 are of therapeutic potential for AML treatment. In this study, BPR1J-340 was identified as a novel potent FLT3 inhibitor by biochemical kinase activity (IC50approximately 25 nM) and

cellular proliferation (GC50 approximately 5 nM) assays. BPR1J-340 inhibited the phosphorylation of FLT3 and STAT5 and

triggered apoptosis in FLT3-ITD+AML cells. The pharmacokinetic parameters of 340 in rats were determined. BPR1J-340 also demonstrated pronounced tumor growth inhibition and regression in FLT3-ITD+AML murine xenograft models. The combination treatment of the HDAC inhibitor vorinostat (SAHA) with BPR1J-340 synergistically induced apoptosis via Mcl-1 down-regulation in MOLM-13 AML cells, indicating that the combination of selective FLT3 kinase inhibitors and HDAC inhibitors could exhibit clinical benefit in AML therapy. Our results suggest that BPR1J-340 may be further developed in the preclinical and clinical studies as therapeutics in AML treatments.

Citation: Lin W-H, Yeh T-K, Jiaang W-T, Yen K-J, Chen C-H, et al. (2014) Evaluation of the Antitumor Effects of BPR1J-340, a Potent and Selective FLT3 Inhibitor, Alone or in Combination with an HDAC Inhibitor, Vorinostat, in AML Cancer. PLoS ONE 9(1): e83160. doi:10.1371/journal.pone.0083160

Editor: Zhengqi Wang, Emory University, United States of America

Received July 18, 2013; Accepted October 31, 2013; Published January 8, 2014

Copyright: ß 2014 Lin 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.

Funding: The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Competing Interests: The authors have declared that no competing interests exist.

* E-mail: ctchen@nhri.org.tw (CTC); tsuanhsu@nhri.org.tw (JT-AH) .These authors contributed equally to this work.

Introduction

Acute myeloid leukemia (AML) is the most common hemato-logic malignancy in adults with a high incidence rate and low survival probability [1,2,3]. AML progresses rapidly due to the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of red blood cells, platelets, and normal white blood cells. If left untreated, AML is usually fatal within weeks or months after diagnosis. FLT3 (FMS-like tyrosine kinase 3), a cell surface receptor belonging to the class III receptor tyrosine kinase family, plays a pivotal role in the differentiation and survival of the hematopoietic stem cells in bone marrow [4,5]. FLT3 is one of the most commonly mutated genes in AML [6,7]. Activating FLT3 mutations, FLT3-ITD (an internal tandem duplication mutation in the juxtamembrane domain) and FLT3-TKD (a missense mutation within the kinase domain), are frequently observed in approximately 30% of adult AML patients [8,9,10,11]. FLT3-activating mutantions critically regulate leuke-mic transformation by accelerating proliferation and suppressing apoptosis and are significantly associated with poor prognosis [12,13]. These findings highlight FLT3-ITD and FLT3-TKD as

highly attractive therapeutic targets for drug development in human AML.

There are now several classes of small molecule FLT3 inhibitors that have entered clinical trials. However, effective drugs have not yet been identified in clinics [14,15,16]. Although these inhibitors have demonstrated promising anti-cancer activity in in vitro and in vivo preclinical models, clinically positive responses in AML patients receiving single-agent FLT3 inhibitors are limited due to the transient reduction of peripheral blasts but not bone marrow blasts or the occurrence of inhibitor-resistant FLT3 mutations in patients [17,18,19,20]. Therefore, combinatorial strategies of FLT3 inhibitors and other chemotherapeutic agents may be beneficial approaches to improve FLT3 inhibitor therapy and to overcome treatment failures [21,22]. The FLT3 inhibitor CEP-701 (lestaurtinib) combined with standard AML chemotherapeutic agents has the potential to improve clinical outcomes in AML patients [23]. In addition, histone deacetylase inhibitors (HDACi), a class of compounds that can induce cancer cell growth arrest and cell death by altering the acetylation status of both histone and non-histone proteins, can enhance the activity of FLT3 inhibitors on AML cell apoptosis [24,25,26]. The HDACi vorinostat (SAHA) exhibits clinical activity in AML; however, its efficacy as a single

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agent is only moderate [27,28]. In this study, we report data characterizing the pharmacological profile of a new FLT3 kinase inhibitor, BPR1J-340, and elucidate the possible molecular mechanism of the strongly synergistic effects in combination with SAHA in FLT3-ITD+cells.

The BPR1J-340 compound exhibits potent FLT3 inhibitory activity, with a 50% inhibitory concentration (IC50) of 2565 nM

and growth inhibitory effects on FLT3-ITD+leukemia MOLM-13 and MV4;11 cells with a GC50value of 3.461.5 and 2.861.2 nM,

respectively. The IC50 values were approximately 1 nM against

FLT3-ITD and 1 nM against STAT5 phosphorylation in MV4;11 cells. In addition, BPR1J-340 exhibits favorable pharmacokinetic properties and significant anti-tumor activity in FLT3-ITD murine xenograft models. The combination of the HDAC inhibitor SAHA with BPR1J-340 exhibits strongly synergistic anti-leukemia effect in FLT3-ITD+ cells. These results highlight the therapeutic potential of BPR1J-340 and SAHA in AML and support its preclinical or clinical development.

Materials and Methods Chemicals and reagents

The FLT3 inhibitors, BPR1J-340 and AC220, were synthesized by our laboratory. The histone deacetylase inhibitor vorinostat (SAHA) was purchased from SelleckBio (Houston, TX, USA). All inhibitors were dissolved in dimethylsulfoxide (DMSO) at a stock concentration of 10 mM. The anti-FLT3 (sc-480, Santa Cruz Biotechnology, Santa Cruz, CA, USA), anti-pFLT3-Tyr591 (#3461, Cell Signaling Technology, Beverly, MA, USA) anti-STAT5 (#9363, Cell Signaling Technology), anti-panti-STAT5– Tyr694 (#9351, Cell Signaling Technology), anti-cleaved poly ADP-ribose polymerase (PARP) (#9542, Cell Signaling Technol-ogy), anti-Mcl-1 (#4572, Cell Signaling TechnolTechnol-ogy), anti-caspase 3 (#9662, Cell Signaling Technology) and anti-b-actin (Gtx110546, GeneTex, Irvine, CA, USA) antibodies were purchased for Western blotting analysis. The preparation of recombinant proteins, FLT3 (residues Y567-S993), VEGFR1 (residues R781-I1338) and VEGFR2 (residues V789-V1356), for biochemical kinase assay was described previously [29]. The VEGFR3 (residues M800-Y1363) proteins were purchased from Upstate (Billerica, MA, USA).

Cell culture

RS4;11, MV4;11, U937 and K562 cells were obtained from American Type Culture Collection (ATCC, Manassas, VA, USA). MOLM-13 cells were purchased from the Deutsche Sammlung von Microorganismen und Zellkulturen GmbH (DSMZ, Braunschweig, Germany). All leukemic cell lines were grown in RPMI 1640 (Invitrogen, USA) with 10% fetal bovine serum (FBS) (Fisher Scientific, Pittsburgh, PA, USA). The HEK293T and FLT3-transfected HEK293T cells were cultured in DMEM (Invitrogen, USA) medium with 10% fetal bovine serum (FBS). The other 14 non-leukemic cell lines, HCC827, H1975, H1650, H2228, NCIH460, A431, HCT-116, MKN45, MiaPaCa-2, RT4, MCF-7, Huh7, Hep3B, and Detroit 551, were cultured in medium according to the ATCC recommendations.

In vitro kinase activity assay

The FLT3 and VEGFR1/2 Kinase-Glo kinase assays were performed as reported by our earlier study [30]. The VEGFR3 activity analysis was conducted using the same protocol described in the VEGFR1/2 assay. The kinase inhibition profiling and inhibitory activity of FLT3-D835Y, CSF1R, and TRKA were

determined by Invitrogen SelectScreenH kinase profiling service (Carlsbad, California, USA).

Cell viability and cell growth assays

Cell viability was assessed with an MTS assay as carried out as the method described previously [31]. Cells were seeded in 96-well plates at a density of 10,000 cells per well for 16 hours and then treated with vehicle or various concentrations of compound in medium. The change in viable cells was quantitated using the MTS method (Promega, Madison, WI, USA) according to the manufacturer’s recommended protocol or by cell counting under a microscope. The GC50 value was defined as the amount of

compound that caused a 50% reduction in cell viability in comparison with DMSO-treated (vehicle) control and was calculated using Prism version 4 software (Graph-Pad Software, Inc., San Diego, CA, USA). The data are presented as the mean 6 S.D. from three independent experiments. Cell growth were measured by trypan blue dye exclusion method. Cells (16104mL21) were cultured in 12-well plates for 24 hours and then treated with different amounts of test compound and the same volumes of vehicle for 72 hours. The number of viable cells was counted by trypan blue dye staining using a hemocytometer at the indicated time point after drug treatment. The result was expressed as the mean 6 S.D. from triplicate determinations.

Western blotting

Cells were lysed in lysis buffer (50 mM Tris, pH 8.0, 150 mM NaCl, 1% Triton X-100, 0.5% sodium deoxycholate, 0.1% SDS, 1 mM sodium orthovanadate, 1 mM PMSF, and 1 mM DTT). Protein lysates were resolved by SDS-PAGE and transferred onto a polyvinylidene difluoride (PVDF) membrane (Millipore, Bed-ford, MA, USA). The membranes were immunoblotted with appropriate antibodies and detected using the SuperSignal reagent (Pierce, Rockford, IL, USA) followed by exposure to X-ray film.

Apoptosis assay

The number of apoptotic cells was determined by fluorescence-activated cell sorting (FACS) analyses using Annexin V-FITC staining. In brief, cells were centrifuged after drug treatment and resuspended in 16 binding buffer containing 2.5 mM of calcium (Ca2+). Cells were incubated with Annexin V-FITC (Biolegend, San Diego, CA) and propidium iodide (PI) (Sigma–Aldrich, St. Louis, MO) in the dark at room temperature for 20 minutes. Next, samples were reconstituted with 16 binding buffer and subjected to flow cytometry FACS Calibus (BD Bioscience, Franklin Lakes, NJ) to analyze the Annexin V-positive population using CellQuest Pro (BD Bioscience) and FlowJo (Treestar, Inc., San Carlos, CA).

Pharmacokinetic analysis of BPR1J-340

The uses of animals were approved by The Institutional Care and Use Committee of the National Health Research Institutes. Briefly, male Sprague-Dawley rats weighing 300–400 g each were obtained from BioLASCO, Taiwan Co., Ltd., Ilan, Taiwan. One day prior dosing, rats were surgically prepared with a jugular-vein cannula and fasted overnight (,18–20 hr). Water was available ad libitum. Food was provided at 4 hours after dosing. Single 1.5 mg/ kg intravenous dose of BPR1J-340, as a PEG400/water (80/20, v/ v) solution, was separately administered to groups of 3 rats each via the jugular-vein cannula. At 0 (prior to dosing), 2, 5, 15 and 30 min. and at 1, 2, 4, 6, 8 and 24 hr after dosing, a blood sample was collected. Plasma was separated from the blood by centrifu-gation (14,000 g for 15 min at 4uC in a Beckman Model AllegraTM 6R centrifuge) and stored in a freezer (220uC) until

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analysis. All plasma samples were analyzed by LC-MS/MS. Plasma concentration data were analyzed with non-compartmen-tal method for pharmacokinetic determination.

Subcutaneously tumor xenograft experiments

Male nude mice (Nu-Fox1nu) of eight weeks old were purchased from BioLasco (Ilan, Taiwan). The nude mice (n = 5,7 per group) were inoculated subcutaneously with MOLM-13 (16106 cells/ flank). All human cancer cells were determined to be free of Mycoplasma spp before the inoculation. When tumors size reached 100,200 mm3 and a large size of .500 mm3, the animals were grouped and treated with the BPR1J-340 (5 and 20 mg/kg, i.v.) or vehicle as control once daily for 5 days per week for two or three weeks. Tumor sizes were measured and calculated with the formula of length6width2/2 after the initiation of the treatments. Tumor size and animal body weight were measured twice a week after the tumor cell inoculation. At the end of the study, animals were euthanized by carbon dioxide inhalation followed by cervical dislocation. The significant difference between the treated and vehicle control were analyzed by using one-way ANOVA and Student-Newman-Keuls test. The level of a statistical significance was set at p,0.05.

Results

In vitro kinase profiling of BPR1J-340

BPR1J-340, a urea-substituted 3-phenyl-1H-5-pyrazolylamine-based compound, was designed through chemical modification of sulfonamide series of derivatives (BPR1J-097 series) by a structure-activity relationship (SAR) study (Fig. 1) [31,32]. For kinase inhibition specificity screening, BPR1J-340 was tested against 59 protein kinases covering the major oncogenic kinases of human protein kinome. This kinase inhibition profile revealed that BPR1J-340 is a highly selective kinase inhibitor and most of tested kinases were not significantly inhibited at the concentration of 100 nM (Table S1). Subsequently, the most potent kinases from the 59 kinases screening were further evaluated. As shown in Table 1, BPR1J-340 potently inhibited wild-type FLT3 (IC50= 2965 nM, as compared to ABT869 with an IC50 of

3863 nM,), mutant FLT3-D835Y (IC50= 19 nM), CSF1R (FMS)

(IC50= 78 nM), KDR (VEGFR2) (IC50= 2869 nM), and FLT4

(VEGFR3) (IC50= 2967 nM). In addition, BPR1J-340 inhibited

TRKA, which is associated with the growth and metastasis of breast cancers, with an IC50 value of 8 nM. Given the high

similarity of the ATP binding pockets of FLT3 and the Aurora kinases, the inhibitory activity toward Aurora A and Aurora B were measured. The IC50s of BPRJ-340 were determined to be

1,040 nM and 1,344 nM for Aurora A kinase and Aurora B kinase, respectively. Taken together, BPRJ-340 is a selective kinase inhibitor with in vitro activity against FLT3, VEGFR2, VEGFR3 and TRKA receptor tyrosine kinases.

BPR1J-340 inhibits the proliferation of FLT3-ITD+cells

After the selective and potent growth inhibitory effects of BPR1J-340 were demonstrated in FLT3-ITD-bearing leukemic cells, the cell proliferation inhibitory activity was tested in a panel of leukemic and non-leukemic cells. BPR1J-340 inhibited the cellular proliferation of FLT3-ITD+cells (MOLM-13 and MV4;11 FLT3-dependent cell lines) with an GC50of approximately 5 nM.

Cells that were not dependent on FLT3 signaling for growth, including RS4;11, U937, and K562 leukemic cells [33,34,35], and the non-leukemic cell lines tested were either weakly inhibited or were not inhibited by BPR1J-340 (Table 2). The growth of the FLT3-independent RS4;11 cell line which contains wild-type

FLT3 was only weakly inhibited by BPR1J-340 with an GC50

value of 7706360 nM. The sensitivity toward BPR1J-340 varies between the FLT3-dependent cells MOLM-13/MV4;11 and FLT3-independent cells RS4;11, suggesting that the FLT3 signaling pathway in FLT3-ITD+ cells is almost completely disturbed by BPR1J-340. Furthermore, our results suggest that BPR1J-340 could inhibit FLT-ITD activity by in vitro biochemical and cellular assays. Overall, BPR1J-340 is a potent and highly selective inhibitor for the proliferation for FLT3-driven cells.

BPR1J-340 inhibits FLT3-STAT5 signaling

To address whether BPR1J-340 was able to inhibit the FLT3 signaling pathway in FLT3-driven cells, MV4;11 cells were treated

Figure 1. Chemical structure of BPR1J-340 and BPR1J-097. BPR1J-340: N1-(3-4-[([(5-ethyl-3-isoxazolyl)amino]carbonylamino)- methyl]phenyl-1H-5-pyrazolyl)-4-[(4-methylpiperazino)methyl]benza-mide. BPR1J-097: N1-(3-3-[(phenylsulfonyl)amino]phenyl-1H-5-pyrazo-lyl)-4-(4-methylpiperazino)benzamide.

doi:10.1371/journal.pone.0083160.g001

Table 1. Specificity of kinase inhibition of BPR1J-340.

Kinase Percentage of inhibitiona IC50, nM FLT3 97 2965b TRKA 89 8* FLT3-D835Y 78 19* CSF1R (FMS) 73 78* KDR (VEGFR2) 69 2869b FLT4 (VEGFR3) 45 2967b FLT1 (VEGFR1) 15 164624b a

Inhibition of kinase at 100 nM, carried out by Invitrogen SelectScreenH kinase profiling service.

b

IC50 determination was performed by kinase-Glo assay.

*IC50determination was performed by Invitrogen SelectScreenH kinase assay.

Note: IC50of DBPR1J-340 against multiple oncogenic kinases; the 7 most potent

kinases from the 59 kinases screened are shown. doi:10.1371/journal.pone.0083160.t001

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with different concentrations of BPR1J-340 for 1 hour, and the phosphorylation status of FLT3 and STAT5 (Signal Transducer and Activator of Transcription 5), a critical down-stream modulator that plays a major role in FLT3-ITD signal transduc-tion for cell expansion and survival, was examined by Western blot analysis. As shown in Figure 2A, BPR1J-340 suppressed the phosphorylation of FLT3 and STAT5 in a dose-dependent manner with an IC50value of approximately 1 nM. To investigate

the difference in sensitivity between FLT3-WT and the activating mutants FLT3-ITD and FLT3-D835Y to BPR1J-340, HEK293T cells engineered to express FLT3-WT or mutants FLT3 (FLT3-ITD, FLT3-D835Y) were analyzed [31]. The HEK293T-FLT3 cells were treated with BPR1J-340 at various concentrations for 1 hr, and FLT3 ligand (50 ng/mL) was added for 5 min to prepare the cell lysate for detection of changes in FLT3 phosphorylation by Western analysis. As shown in Figure 2B, the phosphorylation of all the WT, ITD and FLT3-D835Y was inhibited by BPR-1J340, with IC50 values of 10 to

100 nM. Taken together these data demonstrate that BPR-1J340 inhibits cellular FLT3 phosphorylation and modulates the FLT3 signaling pathway, particularly the FLT3-ITD pathway.

BPR1J-340 induces apoptosis in FLT3-ITD expressing cells

As the inhibition of FLT3 signaling results in a loss of growth potential and an induction of apoptosis in FLT3-ITD expressing cells, the effects of BPR1J-340 on cell apoptotic response in FLT3-ITD+ cells was investigated. The MOLM-13 and MV4;11 cells were treated with BPR1J-340 at different concentrations for 24 hours and analyzed for the induction of apoptosis using active caspase-3 and cleaved PARP (poly-ADP-ribose polymerase) analysis. The ability of BPR1J-340 to induce apoptosis is evident

as shown in Figure 3 where significant cleavage of caspase-3 (active caspase-3) and PARP (active PARP) was observed in MOLM-13 and MV4;11 cells treated with BPR1J-340 at 10 nM.

SAHA in combination with BPR1J-340 enhances cytotoxicity against FLT3-ITD+expressing cells

Some histone deacetylase inhibitors (HDACi) will enhance the cytotoxic activity of FLT3 inhibitor on FLT3-ITD+ cell via degradation of FLT3-ITD and STAT5 [24,26,36,37]. To determine whether SAHA, an HDACi, can synergize with BPR1J-340 to enhance cytotoxicity in FLT3-ITD expressing cells by interfering with the FLT3-ITD and STAT5 axis, the combined effects of SAHA and BPR1J-340 on cytotoxicity were examined. The cell growth rate of MOLM-13 and MV4;11 with SAHA and BPR1J-340 combinational treatment was decreased compared with the single-drug treatment (Fig. 4A). Next, we examined the SAHA treatment effect on BPR1J-340-induced apoptosis in FLT3-ITD-expressing cells. Sole treatment with SAHA (at 300 nM) for 48 hours did not increase the rate of apoptotic cells in control population 10%, whereas SAHA/BPR1J-340 co-treatment resulted in a greater induction of apoptosis (increased 20% in MOLM-13 and 12% in MV4;11 cells, respectively) as compared with BPR1J-340 drug treatment alone (Fig. 4B and Fig. 4C). These data suggested that SAHA enhance BPR1J-340-induced apoptosis in FLT3-ITD+cells. We further elucidated the protein levels of FLT3-ITD and STAT5 in this SAHA/BPR1J-340 co-treatment enhanced cytotoxicity. We treated MOLM-13 cells with SAHA, BPR1J-340, or their combination for 20 hours. Compared with single-drug treatment, the combination of SAHA and BPR1J-340 remarkedly decreased the protein levels of FLT3-ITD and STAT5 (Fig. 4D). Furthermore, BPR1J-340/SAHA treatment profoundly reduced Mcl-1 (myeloid cell leukemia-1, an anti-apoptotic member of the BCL-2 family) protein levels in FLT3-ITD+cells (Fig. 4D). This results of Mcl-1 reduction may explain the enhanced cytotoxicity even the STAT5 phosphoryla-tion at Tyr694 was completely block by BPR1J-340 (Fig. 4D) Mcl-1 plays an essential role in resistance to chemotherapy in AML cells [38]. Thus, targeting MCL-1 using SAHA/BPR1J-340 may be a promising strategy to overcome drug resistance in FLT3-ITD-positive AML. Our results suggest that the reduction in the total protein levels of FLT3-ITD, STAT5 and Mcl-1 by SAHA addition provides a possible mechanism to explain the enhanced cytotoxicity with SAHA/BPR1J-340 coadministration.

Pharmacokinetic parameters of BPR1J-340

To evaluate the pharmacokinetic properties of BPR1J-340, we measured the plasma concentration of BPR1J-340 over a 24-hr period after a single intravenous administration (Fig. 5 and Table 3). After a 1.5 mg/kg intravenous dose administered to Sprague-Dawley rats, BPR1J-340 achieved a maximum plasma concentration of 7.9mM (4,296 ng/mL) at 2 min after dosing. The plasma concentration exceeded 80 ng/mL for 6 hours and remained steady at 9.9 ng/mL (C24 hour, 18 nM) after 24 hour

dosing. Therefore, the plasma concentration of BPR1J-340 reaches sufficient levels to inhibit proliferation and induce apoptosis of FLT3-ITD+ cells based on cellular experiments. The total body clearance was 20.465.2 mL/min/kg and the volume of distribution at the steady state (Vss) was 10.362.5 L/kg for BPR1J-340 in rats. The apparent plasma half-life was approximately 8.8 hr.

Table 2. Anti-proliferative activity of BPR1J-340 against a panel of tumor cell lines.

Cell lines Proliferation GI50, nM Leukemias MOLM-13 3.461.5 MV4;11 2.861.2 RS4;11 7706360 U937 2,4006780 K562 6,37062,070 Non-Leukemias HCC827 2,4706380 H1975 2,6106270 H1650 3,7256977 H2228 2,5206420 NCIH460 13,16062,840 A431 6,5706680 HCT-116 9,33062,320 MKN45 3,58061,210 MiaPaCa-2 9,9606570 RT4 7,03061,510 MCF-7 11,30061,110 Huh7 9,74061,680 Hep3B 8,3106490 Detroit551 8,3406680 doi:10.1371/journal.pone.0083160.t002

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Tumor growth suppressive activity of BPR1J-340

FLT3-ITD+ MV4;11 and MOLM-13 xenografts have been widely used to evaluate the in vivo efficacy of FLT3 inhibitors against AML [39,40]. We and other groups have found the MV4;11 xenograft model is noticeably more sensitive to FLT3 inhibitors [30,31,39,41]. To assess the ability of BPR1J-340 to inhibit tumor growth in an AML xenograft model, we therefore selected the MOLM-13 tumor xenograft model. BPR1J-340 was administered intravenously (5 mg/kg qd) on days 1–5 of each week for 3 weeks; by the end of this period the MOLM-13 tumors

had reached an average volume of 200 mm3. Treatment via this regimen resulted in complete regression of the tumor in all animals by day 22; complete regression (CR) occurred in 4 of 6 treated animals within 31 days of post-treatment observation (Fig. 6A). In this efficacy study, mice with larger tumors (average tumor volume 630 mm3, n = 3) were given a single intravenous dose of 20 mg/kg BPR1J-340 on days 1–5 of each week for 2 weeks, which resulted in complete and durable tumor regression with no palpable tumors detected during the 48-day follow up (Fig. 6B). No loss of body weight or mortality was observed in animals treated with any dose

Figure 2. BPR1J-340 inhibits FLT3-dependent signaling. (A) MV4;11 cells were treated with BPR1J-340 at the indicated concentrations for 1 hour. The phosphorylation status of FLT3 and STAT5 were evaluated by Western blot analysis. (B) HEK 293T cells were transfected with FLT3-WT-, FLT3-ITD-, or FLT3-D835Y-expressing plasmids for 24 hours and then incubated with various concentrations of BPR1J-340 for 1 hour. The FLT3 phosphorylation status in the transfected cells was evaluated by Western blot analysis.

doi:10.1371/journal.pone.0083160.g002

Figure 3. BPR1J-340 induces apoptosis in MOLM-13 and MV4;11 cells. Western blotting revealed that BPR1J-340 was able to induce apoptosis in FLT3-ITD-driven FLT3-ITD+AML cells. MOLM-13 (A) and MV4;11 (B) cells were treated with BPR1J-340 at the indicated concentrations for 24 hours, and the cell lysates were then subjected to Western blot analysis using antibodies against caspase-3 and PARP (poly-ADP-ribose polymerase). (full length caspase-3 (FL-caspase-3), cleavage of caspase-3 (CL-caspase-3), full length poly(ADP-ribose) polymerase (FL-PARP), cleavage of PARP (CL-PARP)).

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of BPR1J-340 (data not shown). These results demonstrate that BPR1J-340 effectively reduces tumor size at intravenous doses of 5 and 20 mg/kg/day; BPR1J-340 is well-tolerated in mice at these effective doses.

Discussion

Given that the abnormal expression of FLT3 kinase, including amplified or aberrantly activated FLT3, is frequently observed in

Figure 4. The effect of BPR1J-340 and SAHA versus drug combination on AML FLT3-ITD+ cells. MOLM-13 or MV4;11 cells were seeded at an initial concentration of 16105cell mL21for 24 hours and then treated with BPR-1J340 either alone or in combination with SAHA in the indicated concentrations. (A) Viable cells were counted after staining with trypan blue dye at indicated time point (B) At 48-hours after treatment, cells were stained with FITC-labeled annexin V and propidium iodide and percentages of apoptotic cells were analyzed by flow cytometry. (C) The representative flow cytometry histograms of assays of annexin positive apoptotic cells at 48 hours drug treatment (D) MOLM-13 cells were treated with drugs for 20 hours, and then followed by Western blot analysis to assess changes in protein levels with the indicated antibodies. Statistical analysis was performed using Student’s t-test. *Indicates significant difference compared to vehicle control (* p,0.05, * * * p,0.01). Data shown are representative of multiple independent experiments.

doi:10.1371/journal.pone.0083160.g004

Figure 5. Pharmacokinetic profile of BPR1J-340 in rats. A single intravenous bolus dose (1.5 mg/kg) of BPR1J-340 was administered to adult male Sprague-Dawley rats (n = 3). Data illustrate mean values (n = 3) 6 S.D. of plasma concentrations of BPR1J-340 at each timepoint. doi:10.1371/journal.pone.0083160.g005

Table 3. Pharmacokinetic parameters of BPR1J-340 in rats.

Rat IV (dose: 1.5 mg/kg)

Compound T1/2 CL Vss AUC(0–24)

(hr) (mL/min/kg) (L/kg) (ng/mL6hr) BRP1J-340 8.860.6 20.465.2 10.362.5 11306260 doi:10.1371/journal.pone.0083160.t003

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the blast cells of AML patients, FLT3 represents an attractive therapeutic target of choice for drugs development in AML. To date, several potential FLT3 inhibitors have been developed and examined in AML patients, including lestaurtinib (CEP701) and midostaurin (PKC412) in phase III clinical trials and sunitinib malate (Sutent), sorafenib (Nexavar), quizartinib (AC220), and crenolanib (CP-868596) in phase II trials. However, FLT3 kinase targeting by mono-therapy with current experimental agents does not yield therapeutic benefits in AML patients. It indicated that the aberrant activation of FLT3 and/or drug-resistant FLT3, including pre-existing and acquired drug-resistant mutants, could rarely be fully inhibited by single-agent treatment. Thus, there is a need for the identification of more effective inhibitors of FLT3 and the development of novel therapeutic approaches, including drug combination strategies that target not only FLT3 but also molecules relevant to the FLT3 survival pathway to override current drug resistance. In this study, we demonstrated the efficacy of the novel FLT3 inhibitor BPR1J-340 in various in vitro and in vivo models of AML and identify synergistic effects with HDACi SAHA on the cytotoxicity of FL3-ITD-expressing cells in in vitro analyses.

Previously, we identified a sulfonamide series of 3-phenyl-1H-5-pyrazolylamine-based compounds as potent inhibitors of FLT3 such as BPR1J-097 [31]. In continuing to our efforts to develop potent FLT3 inhibitors, we intended to search other series of inhibitors that not only increased the in vitro growth-inhibitory effect on AML cells but also prolonged the duration of action in vivo. Through rational design, we discovered BPR1J-340, which is a urea series of 3-phenyl-1H-5-pyrazolylamine-based FLT3 inhibitor, with effectively inhibits FLT3-WT or FLT3-ITD activity in vitro and in vivo. Because multiple signaling pathways influence the growth and metastatic potential of tumor cells, many of the inhibitors in clinical development are designed as multi-targeted inhibitors that block a limited number of oncogenic kinases. Thus, the kinase selectivity profiling of BPR1J-340 was performed to identify additional targets in a panel of 59 tested oncogenic kinases. In further biochemical assay, BPR1J-340 demonstrated potent inhibition (20–190 nM) against the angiogenic kinases VEGFR1, VEGFR2, and VEGFR3, which all play an important role in the tumor microenvironment (Table 1). In addition,

BPR1J-340 potently inhibited TRKA activity with an IC50value

of 8 nM. Taken together, BPRJ-340 is characterized as a selective multi-targeted inhibitor with potent inhibition activity against FLT3-WT, FLT3-D835Y, VEGFR2, VEGFR3, and TRKA. This inhibition profile may allow BPRJ-340 to inhibit tumor growth directly by blocking the aberrant FLT3 signaling pathway and indirectly by targeting tumor angiogenesis. BPR1J-340 may also have clinical potential in tumor driven by abnormally expressed TRKA receptors, which can occur in brain, prostate, pancreatic, and breast cancer [42,43,44,45].

BPR-1J340 inhibited cellular FLT3 phosphorylation and modulated the FLT3 signaling pathway, which resulted in inhibition of proliferation and induction of apoptosis. BPR1J-340 demonstrated potent growth inhibition, predominantly in dependent cells (MOLM-13 and MV4;11) but not in FLT3-independent cells. BPR1J-340 inhibited the proliferation of mutant FLT3-ITD+cells with an GC50of 2–6 nM and inhibited

FLT3-ITD phosphorylation with an IC50 of 10 nM; even the cells

transfected with the FLT3-D835Y mutant were also inhibited by BPR1J-340 with an IC50 of approximately 100 nM. Consistent

with these results, BPR1J-340 effectively induced apoptosis in FLT3-ITD+cells.

HDAC inhibitors may exhibit growth inhibition activity against AML cells and significantly improve the therapeutic efficacy of FLT3 inhibitors [24,46]. A recent study reported that HDACi LBH589 plus an FLT3 inhibitor (PPKC412, AC220) combination treatment could synergistically induce apoptosis through FLT3-ITD and STAT5 degradation [26]. It also demonstrated that activated caspase-3 (CL-caspase 3) contributes to the degrdation of FLT3-ITD and STAT5 [26]. FLT3-ITD degradation was also reported secondary to HDACi-induced up-regulation of UBCH8 and down-regulation of HSP90 [36,47]. Mcl-1, an anti-apoptotic protein that promotes survival of FLT3-ITD+ cells via STAT5 activation, is down-regulated by FLT3 inhibition [25]. The HDACi SAHA also induced down-regulation of Mcl-1 [48]. Furthermore, Mcl-1 protein is a direct cleavage substrate of activated caspase-3 [49]. We noted that the amount of Mcl-1 correlated with iuduction of activated caspase-3 (Figure 4D). Our results demonstrate that SAHA enhances BPR1J-340 inhibition activity in FLT3-ITD+cells and suggests that the enhancement is

Figure 6. Antitumor activity of BPR1J-340 against FLT3-ITD-driven leukemia tumor growth in nude mice. BPR1J-340 (i.v.) is active against human acute leukemia MOLM-13 tumors growing subcutaneously and can reduce the size of tumors even after the tumors were allowed to grow to a size of .630 mm3. (A) The in vivo antitumor effect of BPR1J-340 in the MOLM-13 xenograft nude mice model. The growth of the tumor xenograft was inhibited by BPR1J-340 [5 mg/kg, i.v.]; p,0.05 compared with vehicle treatment. (B) The subcutaneously growth of a MOLM-13 tumor of large size (.630 mm3) in nude mice could be significantly reversed by BPR1J-340 [20 mg/kg, i.v.].

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due to HDACi-induced reduction of FLT3-ITD, STAT5, and Mcl-1. However, the underlying mechanism of enhanced action by combination treatment remains to be further elucidated.

The maximum achievable plasma concentration of BPR1J-340 after a single 1.5 mg/kg in rat is more than 272-fold above the IC50for FLT3-ITD inhibition in biochemical and cellular assays.

Even at 24 hour after the single dosing, the plasma levels of BPR1J-340 were close to the IC50value for inhibition of

FLT3-ITD. In addition, the high Vss indicated that the distribution of BPR1J-340 into deep tissue compartments, including tumor tissue, is expected. These pharmacokinetic properties suggest that BPR1J-340 dosing once a day is sufficient for continuous inhibition of FLT3 activity in rats or mice.

To examine whether BPR1J-340 exhibits antitumor activity in vivo, MOLM-13 cells were subcutaneously implanted into nude mice. Our results demonstrated that BPR1J-340 administration resulted in significant tumor regression and tumor shrinkage in this MOLM-13 tumor model. In comparison with sulfonamide 97 (1/8 CR, 25 mg/kg) in the same model [31], BPR1J-340 results in a higher CR ratio (67%) at a lower dose (5 mg/kg). These data demonstrated that BPR1J-340 is superior to the sulfonamide compound BPR1J-097 in an in vivo efficacy study.

In conclusion, results from this study demonstrate that BPR1J-340 exhibits high potency and excellent selectivity against FLT3 kinase, strong suppression of the FLT3-ITD survival signaling pathway, favorable pharmacokinetic properties, and complete

tumor regression in a FLT3-ITD+xenograft model. These data together support further clinical investigation of PR1J-340 in patients with AML. In addition, the BPR1J-340 potentiated the anti-proliferative activity of the HDAC inhibitor SAHA against human leukemia cells. The combination of SAHA and BPR1J-340 should be a good candidate therapy to develop as a treatment in AML and further investigation in clinical study is warranted.

Supporting Information

Table S1 Kinase inhibition profiles of BPR1J-340. Percentage inhibition was determined by Invitrogen SelectScreen kinase profiling service.

(XLS)

Acknowledgments

The National Health Research Institutes and National Science Council of Taiwan (NSC 100-2325-B-400-002-) financially supported this study. Author Contributions

Conceived and designed the experiments: WHL WTJ TKY CTC JT-AH. Performed the experiments: WHL KJY Chun-Hwa Chen CTH SCY SYH LHC CPC Chun-Hsien Chiu, LCK. Analyzed the data: WHL CPC TKY CTC JT-AH. Contributed reagents/materials/analysis tools: WTJ YSC CTC JT-AH. Wrote the paper: WHL WTJ TKY CTC JT-AH. References

1. Lowenberg B, Downing JR, Burnett A (1999) Acute myeloid leukemia. N Engl J Med 341: 1051–1062.

2. Estey E, Dohner H (2006) Acute myeloid leukaemia. Lancet 368: 1894–1907. 3. Shipley JL, Butera JN (2009) Acute myelogenous leukemia. Exp Hematol 37:

649–658.

4. Scheijen B, Griffin JD (2002) Tyrosine kinase oncogenes in normal hematopoiesis and hematological disease. Oncogene 21: 3314–3333. 5. Markovic A, MacKenzie KL, Lock RB (2005) FLT-3: a new focus in the

understanding of acute leukemia. Int J Biochem Cell Biol 37: 1168–1172. 6. Stirewalt DL, Radich JP (2003) The role of FLT3 in haematopoietic

malignancies. Nat Rev Cancer 3: 650–665.

7. Kiyoi H, Yanada M, Ozekia K (2005) Clinical significance of FLT3 in leukemia. Int J Hematol 82: 85–92.

8. Nakao M, Yokota S, Iwai T, Kaneko H, Horiike S, et al. (1996) Internal tandem duplication of the flt3 gene found in acute myeloid leukemia. Leukemia 10: 1911–1918.

9. Kiyoi H, Towatari M, Yokota S, Hamaguchi M, Ohno R, et al. (1998) Internal tandem duplication of the FLT3 gene is a novel modality of elongation mutation which causes constitutive activation of the product. Leukemia 12: 1333–1337. 10. Yamamoto Y, Kiyoi H, Nakano Y, Suzuki R, Kodera Y, et al. (2001) Activating

mutation of D835 within the activation loop of FLT3 in human hematologic malignancies. Blood 97: 2434–2439.

11. Gilliland DG, Griffin JD (2002) The roles of FLT3 in hematopoiesis and leukemia. Blood 100: 1532–1542.

12. Thiede C, Steudel C, Mohr B, Schaich M, Schakel U, et al. (2002) Analysis of FLT3-activating mutations in 979 patients with acute myelogenous leukemia: association with FAB subtypes and identification of subgroups with poor prognosis. Blood 99: 4326–4335.

13. Yanada M, Matsuo K, Suzuki T, Kiyoi H, Naoe T (2005) Prognostic significance of FLT3 internal tandem duplication and tyrosine kinase domain mutations for acute myeloid leukemia: a meta-analysis. Leukemia 19: 1345– 1349.

14. Chu SH, Small D (2009) Mechanisms of resistance to FLT3 inhibitors. Drug Resist Updat 12: 8–16.

15. Kindler T, Lipka DB, Fischer T (2010) FLT3 as a therapeutic target in AML: still challenging after all these years. Blood 116: 5089–5102.

16. Wiernik PH (2010) FLT3 inhibitors for the treatment of acute myeloid leukemia. Clin Adv Hematol Oncol 8: 429–436, 444.

17. Weisberg E, Boulton C, Kelly LM, Manley P, Fabbro D, et al. (2002) Inhibition of mutant FLT3 receptors in leukemia cells by the small molecule tyrosine kinase inhibitor PKC412. Cancer Cell 1: 433–443.

18. Grundler R, Thiede C, Miething C, Steudel C, Peschel C, et al. (2003) Sensitivity toward tyrosine kinase inhibitors varies between different activating mutations of the FLT3 receptor. Blood 102: 646–651.

19. Stone RM, DeAngelo DJ, Klimek V, Galinsky I, Estey E, et al. (2005) Patients with acute myeloid leukemia and an activating mutation in FLT3 respond to a small-molecule FLT3 tyrosine kinase inhibitor, PKC412. Blood 105: 54–60. 20. Knapper S, Burnett AK, Littlewood T, Kell WJ, Agrawal S, et al. (2006) A phase

2 trial of the FLT3 inhibitor lestaurtinib (CEP701) as first-line treatment for older patients with acute myeloid leukemia not considered fit for intensive chemotherapy. Blood 108: 3262–3270.

21. Levis M, Pham R, Smith BD, Small D (2004) In vitro studies of a FLT3 inhibitor combined with chemotherapy: sequence of administration is important to achieve synergistic cytotoxic effects. Blood 104: 1145–1150.

22. Mollgard L, Deneberg S, Nahi H, Bengtzen S, Jonsson-Videsater K, et al. (2008) The FLT3 inhibitor PKC412 in combination with cytostatic drugs in vitro in acute myeloid leukemia. Cancer Chemother Pharmacol 62: 439–448. 23. Stone RM, Fischer T, Paquette R, Schiller G, Schiffer CA, et al. (2012) Phase IB

study of the FLT3 kinase inhibitor midostaurin with chemotherapy in younger newly diagnosed adult patients with acute myeloid leukemia. Leukemia 26: 2061–2068.

24. Bali P, George P, Cohen P, Tao J, Guo F, et al. (2004) Superior activity of the combination of histone deacetylase inhibitor LAQ824 and the FLT-3 kinase inhibitor PKC412 against human acute myelogenous leukemia cells with mutant FLT-3. Clin Cancer Res 10: 4991–4997.

25. Zhou J, Bi C, Chng WJ, Cheong LL, Liu SC, et al. (2011) PRL-3, a metastasis associated tyrosine phosphatase, is involved in FLT3-ITD signaling and implicated in anti-AML therapy. PLoS One 6: e19798.

26. Pietschmann K, Bolck HA, Buchwald M, Spielberg S, Polzer H, et al. (2012) Breakdown of the FLT3-ITD/STAT5 axis and synergistic apoptosis induction by the histone deacetylase inhibitor panobinostat and FLT3-specific inhibitors. Mol Cancer Ther 11: 2373–2383.

27. Schaefer EW, Loaiza-Bonilla A, Juckett M, DiPersio JF, Roy V, et al. (2009) A phase 2 study of vorinostat in acute myeloid leukemia. Haematologica 94: 1375– 1382.

28. Wei Y, Kadia T, Tong W, Zhang M, Jia Y, et al. (2010) The combination of a histone deacetylase inhibitor with the Bcl-2 homology domain-3 mimetic GX15-070 has synergistic antileukemia activity by activating both apoptosis and autophagy. Clin Cancer Res 16: 3923–3932.

29. Coumar MS, Wu JS, Leou JS, Tan UK, Chang CY, et al. (2008) Aurora kinase A inhibitors: identification, SAR exploration and molecular modeling of 6,7-dihydro-4H-pyrazolo-[1,5-a]pyrrolo[3,4-d]pyrimidine-5,8-dione scaffold. Bioorg Med Chem Lett 18: 1623–1627.

30. Lin WH, Hsieh SY, Yen SC, Chen CT, Yeh TK, et al. (2011) Discovery and evaluation of 3-phenyl-1H-5-pyrazolylamine-based derivatives as potent, selective and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3). Bioorg Med Chem 19: 4173–4182.

31. Lin WH, Jiaang WT, Chen CW, Yen KJ, Hsieh SY, et al. (2012) BPR1J-097, a novel FLT3 kinase inhibitor, exerts potent inhibitory activity against AML. Br J Cancer 106: 475–481.

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32. Lin WH, Hsu JT, Hsieh SY, Chen CT, Song JS, et al. (2013) Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3). Bioorg Med Chem 21: 2856–2867.

33. Odgerel T, Kikuchi J, Wada T, Shimizu R, Futaki K, et al. (2008) The FLT3 inhibitor PKC412 exerts differential cell cycle effects on leukemic cells depending on the presence of FLT3 mutations. Oncogene 27: 3102–3110. 34. Pallis M, Seedhouse C, Grundy M, Russell N (2003) Flow cytometric

measurement of phosphorylated STAT5 in AML: lack of specific association with FLT3 internal tandem duplications. Leuk Res 27: 803–805.

35. Yee KW, O’Farrell AM, Smolich BD, Cherrington JM, McMahon G, et al. (2002) SU5416 and SU5614 inhibit kinase activity of wild-type and mutant FLT3 receptor tyrosine kinase. Blood 100: 2941–2949.

36. Buchwald M, Pietschmann K, Muller JP, Bohmer FD, Heinzel T, et al. (2010) Ubiquitin conjugase UBCH8 targets active FMS-like tyrosine kinase 3 for proteasomal degradation. Leukemia 24: 1412–1421.

37. Nishioka C, Ikezoe T, Yang J, Takeuchi S, Koeffler HP, et al. (2008) MS-275, a novel histone deacetylase inhibitor with selectivity against HDAC1, induces degradation of FLT3 via inhibition of chaperone function of heat shock protein 90 in AML cells. Leuk Res 32: 1382–1392.

38. Kasper S, Breitenbuecher F, Heidel F, Hoffarth S, Markova B, et al. (2012) Targeting MCL-1 sensitizes FLT3-ITD-positive leukemias to cytotoxic thera-pies. Blood Cancer J 2: e60.

39. Shankar DB, Li J, Tapang P, Owen McCall J, Pease LJ, et al. (2007) ABT-869, a multitargeted receptor tyrosine kinase inhibitor: inhibition of FLT3 phosphor-ylation and signaling in acute myeloid leukemia. Blood 109: 3400–3408. 40. Shiotsu Y, Kiyoi H, Ishikawa Y, Tanizaki R, Shimizu M, et al. (2009) KW-2449,

a novel multikinase inhibitor, suppresses the growth of leukemia cells with FLT3 mutations or T315I-mutated BCR/ABL translocation. Blood 114: 1607–1617.

41. Hart S, Goh KC, Novotny-Diermayr V, Tan YC, Madan B, et al. (2011) Pacritinib (SB1518), a JAK2/FLT3 inhibitor for the treatment of acute myeloid leukemia. Blood Cancer J 1: e44.

42. Weeraratna AT, Arnold JT, George DJ, DeMarzo A, Isaacs JT (2000) Rational basis for Trk inhibition therapy for prostate cancer. Prostate 45: 140–148. 43. Nakagawara A (2001) Trk receptor tyrosine kinases: a bridge between cancer

and neural development. Cancer Lett 169: 107–114.

44. Liu D, Zhang Y, Dang C, Ma Q, Lee W, et al. (2007) siRNA directed against TrkA sensitizes human pancreatic cancer cells to apoptosis induced by gemcitabine through an inactivation of PI3K/Akt-dependent pathway. Oncol Rep 18: 673–677.

45. Lagadec C, Meignan S, Adriaenssens E, Foveau B, Vanhecke E, et al. (2009) TrkA overexpression enhances growth and metastasis of breast cancer cells. Oncogene 28: 1960–1970.

46. Kosugi H, Towatari M, Hatano S, Kitamura K, Kiyoi H, et al. (1999) Histone deacetylase inhibitors are the potent inducer/enhancer of differentiation in acute myeloid leukemia: a new approach to anti-leukemia therapy. Leukemia 13: 1316–1324.

47. George P, Bali P, Annavarapu S, Scuto A, Fiskus W, et al. (2005) Combination of the histone deacetylase inhibitor LBH589 and the hsp90 inhibitor 17-AAG is highly active against human CML-BC cells and AML cells with activating mutation of FLT-3. Blood 105: 1768–1776.

48. Al-Yacoub N, Fecker LF, Mobs M, Plotz M, Braun FK, et al. (2012) Apoptosis induction by SAHA in cutaneous T-cell lymphoma cells is related to downregulation of c-FLIP and enhanced TRAIL signaling. J Invest Dermatol 132: 2263–2274.

49. Weng C, Li Y, Xu D, Shi Y, Tang H (2005) Specific cleavage of Mcl-1 by caspase-3 in tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis in Jurkat leukemia T cells. J Biol Chem 280: 10491–10500.

數據

Table 1. Specificity of kinase inhibition of BPR1J-340.
Table 2. Anti-proliferative activity of BPR1J-340 against a panel of tumor cell lines.
Figure 2. BPR1J-340 inhibits FLT3-dependent signaling. (A) MV4;11 cells were treated with BPR1J-340 at the indicated concentrations for 1 hour
Figure 4. The effect of BPR1J-340 and SAHA versus drug combination on AML FLT3-ITD+ cells
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