Background
Acute lymphoblastic leukemia (ALL) is caused by malignant transformation and proliferation of lymphoid progenitor cells of either B or T cells. In children, ALL patients enjoy an approximately 90% long-term survival with the current pediatric chemotherapy protocols [
1]. However, ALL is a devastating disease when it occurs in the adults, with reportedly only 30–40% long-term survival rate [
2]. Despite many advances in management, the backbone of ALL therapy remains as multi-agent chemotherapy with vincristine, corticosteroids, cyclophosphamide and anthracycline, and may involve allogeneic stem cell transplantation for eligible candidates [
2]. While dose intensification strategies have led to a significant improvement in outcomes for pediatric patients, the elderly patients usually do not benefit from or sometimes can be even over-treated by these therapies, as they are unable to tolerate such regimens and consequently may carry an extremely poor prognosis. Therefore, there is an urgent need to develop additional therapeutic regimens for adult ALL patients.
The essential role of angiogenesis, a process of blood vessel formation, in the growth and maintenance of solid tumors was well established. Over the past decades, emerging evidence also suggests an involvement of angiogenesis in leukemogenesis and leukemia progression [
3]. Increased angiogenesis in bone marrow niche correlates with both acute lymphoblastic leukemia and acute myeloid leukemia progression and resistance to treatment [
4‐
8]. Moreover, a recent study identified an important role of the VEGF/VEGFR2 axis in regulating ALL cell migration through the cerebral microvascular endothelial barrier, contributing to central nervous system (CNS) leukemia [
9]. Thus, targeting angiogenesis with anti-angiogenic drugs or VEGFR inhibitors may be a new approach for ALL treatment. Apatinib, also known as YN968D1, is an orally administrated small molecule receptor tyrosine kinase inhibitor selectively targeting VEGFR-2 [
10]. It was approved in China as a subsequent-line treatment for patients with advanced gastric cancer [
11], and has been tested for many other types of cancers in phase II/III clinical trials in China, such as non-small-cell lung cancer, breast cancer, and hepatocellular carcinoma [
12]. Promising results obtained from these clinical trials demonstrated that Apatinib has anti-tumor activity across a broad range of advanced cancers. This prompts us to investigate whether Apatinib can be used for ALL treatment and the potential underlying mechanisms.
Methods
Reagents
Apatinib was kindly provided by Jiangsu Hengrui Medicine Company (Jiangsu, China) and dissolved in DMSO (Invitrogen, USA) as a 100 mM stock solution. It was diluted to desired concentrations in subsequent experiments with growth media.
Cell lines and cell culture
The following human B and T lineage acute lymphoblastic leukemia cell lines were used in this study: Nalm6, Reh, Molt4 and Jurkat. Cells were cultured in RPMI-1640 (Hyclone, Thermo Scientific, MA, USA) supplemented with 10% fetal bovine serum (FBS, Gibco, Life Technologies, NY, USA) and 100 units/mL penicillin and 100 μg/mL streptomycin at 37 °C in a water-saturated atmosphere with 5% CO2.
Primary samples
Mobilized peripheral blood mononuclear cells were obtained from healthy donors for hematopoietic stem cell transplantation with a standard 5 day G-CSF treatment. Bone marrow samples with B or T lineage acute lymphoblastic leukemia were obtained from patients after informed consent in accordance with the guidelines of the first affiliated hospital of Xiamen University. The study protocols were approved by the Ethics Committee and accorded with the Declaration of Helsinki. Mononuclear cells were isolated by standard Ficoll-Hypaque density centrifugation (BD, Franklin Lakes, NJ, USA) and cultured in IMDM [HyClone, Thermo Scientific, MA, USA) supplemented with 10% FBS (Gibco, Life Technologies, NY, USA)], 100 U/mL penicillin and 100 µg/mL streptomycin (1 × P/S) at 37 °C.
In vitro cell viability assay
Cytotoxicity of Apatinib against ALL cell lines was determined using a CCK8 kit (Dojindo, Kumamoto, Japan). Briefly, cells were first aliquot into 96-well plates at 5 × 104 cells/well with 100 μL of growth medium and then treated with designated dosages of Apatinib for 48 or 72 h. After that CCK-8 reagents (10 µL/well) were added and cells were further incubated for 2 h in the incubator. Finally, absorbance at 450 nm was read by a microplate reader (ELX800, Bio TEK, USA). All experiments were repeated at least three times with triplicate in each experiment. The IC50 value (half maximal inhibitory concentration) of each cell line was calculated using the GraphPad Prism 5 software.
Apoptosis assay
Annexin V and Propidium iodide (PI) (Ebioscience, San Diego, USA) dual staining was performed to detect apoptotic cells following manufacturer’s instructions. Briefly, cells (2 × 105 cells/well) were seeded into 24-well plates and treated with different concentrations of Apatinib for 48 or 72 h. Then cells were harvested, washed twice with ice-cold PBS, double-labeled with Annexin V/PI for 30 min at 4 °C in the dark, followed by analysis with flow cytometry using the FACS C6 software (BD, Oxford, UK).
Western blot analysis
Whole cell lysates (50 μg/line) from each sample were electrophoresed in 8% or 10% SDS-PAGE and transferred to PVDF membrane (Millipore, Billerica, MA, USA). After blocking for 1 h for non-specific binding in TBS-T with 5% non-fat milk, membranes were incubated with primary antibodies [VEGFR, rabbit monoclonal, 1:1000; p-VEGFR, rabbit monoclonal, 1:1000; p-AKT (ser473), rabbit monoclonal, 1:1000; AKT, rabbit monoclonal, 1:1000; p-ERK, rabbit monoclonal, 1:1000; ERK, rabbit monoclonal, 1:1000; GAPDH, rabbit monoclonal, 1:1000; β-actin, rabbit monoclonal, 1:1000, Cell Signaling Technology, Inc. Herts, UK] overnight at 4 °C and followed by secondary HRP-conjugated monoclonal antibody (1:10000, Cell Signaling Technology) for 1 h at room temperature. The expression of target proteins was detected by enhanced chemiluminescence western blotting detection kit (Amersham, Little Chalfont, UK) following the manufacturer’s instructions.
Mass cytometry (CyTOF) analysis
Bone marrow mononuclear cells from one patient with B-ALL was collected and used for the Mass Cytometry (CyTOF) analysis. Briefly, cells with 95% or higher viability were treated with 0 or 20 μM of Apatinib for 48 h and washed three times with washing buffer (phosphate-buffered saline plus 0.5% bovine serum albumin). Samples of 3 × 10
6 cells were incubated with 0.75 μM 195 Pt monoisotopic cisplatin (Fluidigm, San Francisco, CA) at room temperature for 2 min, followed by staining with the mass cytometry antibody cocktail against surface and intracellular proteins (Additional file
1: Table S1) following the manufacturer’s protocol. Cells were subsequently washed and stained with 125 nM Iridium intercalator (Fluidigm, San Francisco, CA) overnight at 4 °C. Lastly, cells were washed twice with H
2O and re-suspended in 500 μL H
2O for CyTOF analysis. Helios™ Software V6.5.358 acquisition software (Fluidigm, San Francisco, CA) was used to normalize to internal bead standards. Data were evaluated using Cytobank software (Cytobank Inc.).
Human acute lymphoblastic leukemia xenograft experiments
NODscid-IL2Rg−/− (NSI) mice, which has a high tumor engraftment index (TEI) score [
13], were used to establish ALL xenografted model according to our previous study [
14]. For briefly, 6–8 week old male were provided by Guangzhou Institutes of Biomedicine and Health (GIBH) and housed under specific-pathogen-free (SPF) conditions following the animal care guidelines. The protocols for the animal studies were approved by the Animal Welfare Committee of GIBH. Before inoculation, mice received 1 Gy of total body irradiation at a dose rate of 325 cGy/min by parallel opposed 4 MV X-ray. Within 24 h, mice were intravenously injected via retro-orbital vein with 5 × 10
6 ALL cells (Nalm6 cell line). Seven days post transplantation of ALL cells, mice were randomly assigned to either control or Apatinib treatment group (n = 6 per group), and treated with either vehicle (PBS and 0.5% methyl cellulose/0.5% Tween 80 in PBS) or 100 mg/kg/day Apatinib by oral gavage from Monday to Friday for 2 consecutive weeks. At the end of the experiments, mice were euthanized and their spleens were photographed and weighed. The leukemia load (human CD45+ cells) in peripheral blood (PB), bone marrow (BM) and spleen was determined by flow cytometry staining with anti-human-CD45 antibody. The bone marrow and spleen were fixed in 10% paraformaldehyde for 24 h, followed by paraffin-embedding and H&E staining.
Statistical analysis
Data were represented as mean ± S.D of at least three independent experiments. The statistical analyses were performed using the SPSS 19.0 and GraphPad Prism 5.0 software. Comparison between two groups were analyzed by 2-tailed Student’s t test. Statistical analyses of multiple-group comparisons were performed by one-way analysis of variance (ANOVA) followed by the Bonferroni posthoc test. P values < 0.05 was considered as statistically significant.
Discussion
Angiogenesis plays a critical role in the growth, progression, and metastasis of cancers [
15], including hematological leukemia [
3]. Vascular endothelial growth factor (VEGF) and its receptors (VEGFRs) function as key regulators of this process. The VEGFR-family proteins consist of three members: VEGFR-1 (Flt-1), VEGFR-2 (KDR/Flk-1), and VEGFR-3 (Flt-4), among which VEGFR-2 is thought to be principally responsible for angiogenesis in malignancies [
16]. Inhibition of VEGF/VEGFRs mediated signaling shows promise as an anti-angiogenic strategy for solid tumors [
17]. Several small molecule VEGF/VEGFR pathway inhibitors have been approved for the treatment of metastatic colorectal cancer, gastrointestinal stromal tumors, hepatocellular carcinoma, non-small-cell lung cancer, renal cell carcinoma, soft tissue sarcoma, and medullary thyroid cancer, and are under the development of a number of other oncology indications, including pancreatic cancer, ovarian cancer, breast cancer, prostate, head and neck cancers [
17]. These anti-angiogenic drugs have improved progression-free survival and in some cases overall survival for several cancer types. However, clinical experience with the current anti-angiogenic agent, Apatinib, remains limited in treating aggressive leukemias, especially ALL [
18]. Therefore, the development of new drugs targeting angiogenesis may open up a new era of anti-angiogenic combination therapy of human leukemia. In the present study, we showed that a novel anti-angiogenic drug, Apatinib, inhibited both B and T lineage ALL cell growth and progression in in vitro and in vivo preclinical models.
Apatinib is a potent tyrosine kinases inhibitor of VEGFR-2, PDGFR-β, RET, c-Src and c-Kit [
10,
19,
20]. It can effectively inhibit the proliferation, migration and tube formation of human umbilical vein endothelial cells (HUVEC), block the microvessel budding of rat aortic ring, and show anti-tumor efficacy in vivo against a variety of established tumor xenografts with good tolerance [
8]. Moreover, Apatinib could reverse ABCB1- and ABCG2-mediated multidrug resistance in solid tumors as well as in leukemia cell lines [
21,
22], thereby enhancing the efficacy of chemotherapeutic agents. Based on this mechanism, Apatinib has proved to be effective and safe in the treatment of advanced gastric cancer patients [
11,
12]. However, anti-tumor activity of Apatinib in ALL had not been explored. Here, we showed that Apatinib not only suppresses the proliferation but also induces apoptosis of ALL cells, with low cytotoxicity towards normal hematopoietic cells. Our results may extend the field of indications for Apatinib to the treatment of leukemia. As expected, we found that primary leukemia cells from adult ALL patients are all sensitive to Apatinib in cell culture. Currently, 750 mg once daily of Apatinib mesylate is recommended for clinical studies in patients with advanced solid tumors and well tolerated [
23]. Pharmacokinetic analysis showed a peak plasma concentration (C
max) of 3.8–4.0 μM was achieved in patients continuously treated with this dose of Apatinib [
24]. In the present study, the IC
50 of Apatinib varied in a range of 17–56 μM in vitro in this setting directly targeting ALL cells, while it could be active at concentration as low as 2.5 μM, which appears to be within the range of C
max in vivo. In this context, it has also been demonstrated earlier that Apatinib induces apoptosis and cell cycle arrest of osteosarcoma cells at a concentrations range of 5–20 μM [
25]. Moreover, the dose-escalation experiment of Apatinib displayed no obvious toxicity towards normal hematopoietic stem cells, suggesting that this dose range might be tolerated in vivo. Nevertheless, these results raise a possibility that it might require a dose higher than 750 mg daily of Apatinib to be effective in treatment of ALL.
Interestingly, it seems that acute lymphoblastic T leukemias are more susceptible to Apatinib-induced apoptosis in our experiments. A low activity of p-VEGFR in T lymphoblastic leukemia cell lines might account for a relatively lower IC
50 of Apatinib against T lymphoblastic leukemia cells. In addition, previous studies showed that a high functional P-glycoprotein activity is frequently present in T-ALL [
26]. Therefore, Apatinib might block the efflux function of P-glycoprotein in T-ALL cells, rendering T-ALL cells more vulnerable to Apatinib-induced apoptosis.
Extramedullary infiltration is a common phenomenon in relapse ALL even after allogeneic hematopoietic stem cell transplantation, contributing to poor prognosis and mortality [
27]. In general, the sites most frequently affected by extramedullary relapse are the testicles and the central nervous system [
28,
29]. Relapse in other tissues has also been reported, including kidney, breast and the gastrointestinal system [
30‐
32]. Several molecular pathways are involved in solid tumor metastasis, including the VEGF signaling pathway [
33]. However, the mechanism underlying extramedullary infiltration of ALL cells remains poorly understood. More recently, Münch et al. [
9] found that VEGF signaling regulates trans-endothelial leukemia cell migration and contributes to extramedullary infiltration of ALL cells. In line with it, the inhibition of VEGF signaling by Apatinib led to a specific effect in vivo, namely significantly decreased leukemia burden in bone marrow and spleen of leukemic mice. On the other hand, high VEGF levels have also been associated with poor prognosis and ALL patients with high VEGF levels after induction therapy relapse earlier than those with low VEGF levels [
34]. Accordingly, Apatinib, in combination with conventional therapy, offers the promise of effective anti-leukemia activity, as well as improvements in remission and survival of ALL patients.
The primary mechanism for the anti-tumor effect of Apatinib is the suppression VEGF/VEGFR2 signaling, which activates the PI3K-AKT-mTOR and PLC-ERK1/2 pathways [
35,
36]. Similarly, our study indicated that AKT and ERK1/2 inactivation contributes to Apatinib-induced inhibition of cell proliferation and promotion of apoptosis of ALL cells. A recent study suggested that Apatinib promotes autophagy and induces apoptosis through VEGFR2/STAT3/BCL-2 signaling in osteosarcoma [
25]. These studies suggest multiple signaling cascades downstream of the VEGF/VEGFR2 signaling. To pinpoint the mechanism underlying Apatinib inhibition of ALL leukemia cells, mass cytometry (CyTOF), a powerful technology able to detect up to 50 different parameters at the single-cell level [
37], was used in our study. Our CyTOF analysis of an ALL patient’s primary cells showed that multiple signaling cascades downstream of VEGFR2 were repressed by Apatinib, including the PI3K, MAPK and STAT3 pathways. Collectively, our study demonstrates that Apatinib exerts an anti-leukemia effect by inhibiting VEGFR2 signaling and its multiple downstream signaling cascades.
Authors’ contributions
XB directed the project, analyzed the data, wrote the paper and supported the experiments. DZQ directed the project, contributed useful suggestions and wrote the paper. FZH directed the project, contributed useful suggestions and wrote the manuscript. CXL contributed useful suggestions and revised the paper. PL contributed useful suggestions. DMM conceptualized and designed the study, performed the CCK8 and flow cytometric analysis experiments, analyzed the data. ZJ performed flow cytometric analysis experiments. JX performed the Mass cytometry (CyTOF) analysis. SYF did the western blot assay. JZW performed animal experiments. All authors read and approved the final manuscript.