- Research article
- Open Access
Halofuginone inhibits phosphorylation of SMAD-2 reducing angiogenesis and leukemia burden in an acute promyelocytic leukemia mouse model
- Patricia A. Assis†1,
- Lorena L. De Figueiredo-Pontes†1,
- Ana Silvia G. Lima1,
- Vitor Leão1,
- Larissa A. Cândido1,
- Carolina T. Pintão1,
- Aglair B. Garcia1,
- Fabiano P. Saggioro2,
- Rodrigo A Panepucci1,
- Fernando Chahud2,
- Arnon Nagler3,
- Roberto P. Falcão1 and
- Eduardo M. Rego1Email author
© Assis et al. 2015
- Received: 19 September 2014
- Accepted: 11 June 2015
- Published: 23 June 2015
Halofuginone (HF) is a low-molecular-weight alkaloid that has been demonstrated to interfere with Metalloproteinase-2 (MMP-2) and Tumor Growth Factor-β (TGF-β) function and, to present antiangiogenic, antiproliferative and proapoptotic properties in several solid tumor models. Based on the fact that high levels of Vascular Endothelial Growth Factor (VEGF) and increased angiogenesis have been described in acute myeloid leukemia and associated with disease progression, we studied the in vivo effects of HF using an Acute Promyelocytic Leukemia (APL) mouse model.
NOD/SCID mice were transplanted with leukemic cells from hCG-PML/RARA transgenic mice (TM) and treated with HF 150 μg/kg/day for 21 days. The leukemic infiltration and the percentage of VEGF+ cells were evaluated by morphology and flow cytometry. The effect of HF on the gene expression of several pro- and antiangiogenic factors, phosphorylation of SMAD2 and VEGF secretion was assessed in vitro using NB4 and HUVEC cells.
HF treatment resulted in hematological remission with decreased accumulation of immature cell and lower amounts of VEGF in BM of leukemic mice. In vitro, HF modulated gene expression of several pro- and antiangiogenic factors, reduced VEGF secretion and phosphorylation of SMAD2, blocking TGF-β-signaling.
Taken together, our results demonstrate that HF inhibits SMAD2 signaling and reduces leukemia growth and angiogenesis.
- Acute Promyelocytic Leukemia
Halofuginone (HF) is a low-molecular-weight quinazolinone alkaloid that has been demonstrated to present potent antitumor effects due antiproliferative [1, 2] and proapoptotic  properties. Treatment with HF impaired proliferation and induced apoptosis of several multiple myeloma cell lines and showed antitumor activity in a myeloma xenograft mouse model . In addition, HF antiangiogenic properties also have been shown to contribute to control of tumor growth [4–6]. In a rat brain tumor model, HF treatment markedly reduced vascularization and vessel maturation resulting in reduced tumor burden and metastasis .
Angiogenesis is one of the most important mechanisms of tumor progression [7, 8] and has been associated to development of hematological malignancies . Several studies have reported an increase in bone marrow (BM) microvessel density (MVD) and high VEGF (Vascular Endothelial Growth Factor) expression in multiple myeloma , non-Hodgkin lymphoma , and acute leukemias [12, 13]. Particularly, in acute myeloid leukemia (AML), high levels of VEGF and increased MVD were found in leukemic BM biopsies  and correlated with lower rates of complete remission and lower overall survival . In a study analyzing 12 BM biopsies from patients with acute promyelocytic leukemia (APL), Kini et al.  detected increased MVD associated with high VEGF expression. After standard treatment with ATRA (all-trans retinoic acid), VEGF levels and BM MVD were normalized. Another clinical study with 17 new cases of APL associated the efficacy of the arsenic trioxide treatment with its antiangiogenic effect, demonstrated by the reduced MVD in the BM and increased survival .
Despite the fact that all-trans retinoic acid (ATRA) is largely applied for the treatment of APL, the use of ATRA alone does not achieve long-term remission [17, 18]. Thus, associations of ATRA with chemotherapy or arsenic trioxide have been more successful in improve long-term survival . However, these treatment regiments have limited application for elderly patients or those with serious heart conditions . In addition, the therapy with arsenic trioxide is not available in several developing countries  and the 10-20 % of patients treated with ATRA-chemotherapy or ATRA-arsenic trioxide association will relapse [22, 23]. Therefore, the development of new strategies for APL therapeutics is necessary and angiogenesis is a potential target to achieve a better outcome.
The exact mechanism by which HF impairs angiogenesis has not yet been fully characterized. Elkin et al.  reported that HF treatment led to the reduction in metalloproteinase-2 (MMP-2) expression and inhibition of bladder carcinoma metastasis in an animal model. However, HF effects may not be specific to malignant tissues, since the implant of silicone coated with HF resulted in reduced expression of MMP-2, bFGF and TGF-β in normal muscle . In APL the TGF-β pathway is deregulated by the cytoplasmic PML isoform (cPML)  and we have demonstrated that HF inhibited cell proliferation and induced apoptosis in the APL cell line NB4 through modulation of TGF-β-target genes, such as c-Myc and p21 . In addition, it is noteworthy to point out that the promoter region of the VEGF gene contains DNA-binding sequences for hypoxia-inducible factor 1 alpha (HIF-1α) and for the TGF-β-signaling mediators SMADs [27, 28]. Thus, activation of TGF-β pathway may be associated with increased VEGF expression and angiogenesis in acute leukemias. Here we analyzed the in vivo antileukemic effect of HF and its association with the modulation of proangiogenic and antiangiogenic factors using APL as a bone fide example of acute leukemia with increased angiogenesis.
Halofuginone (HF-dl-trans-7-bromo-6-chloro-3-(3-(3-hydroxy-piperidyl)acetonyl)-(3H)-quinazolinone hydrobromide) was solubilized in lactic acid priors to dilute into phosphate buffer solution. In vitro ED50 was previous determined  in vivo doses were delineated based on previous reports of the use of this drug in solid tumors and fibrosis models [29–32].
Mice and leukemia transplant model
BM angiogenesis was first analyzed in leukemic hCG-PML/RARA transgenic mice (TM). Notably, in this transgenic model, a lethal form of leukemia that closely resembles human APL occurs after a long pre-leukemic phase (12–15 months) and affects only 10–15 % of the TM . To analyze in vivo effects of HF we developed an APL transplanted model. Thus, NOD/SCID mice aged 10 to 12 weeks were irradiated with 250 cGy and 24 hours later, 2 × 106 viable cells from leukemic hCG-PML/RARA transgenic mice (TM) were intravenously injected. Twenty-four hours after transplantation, NOD/SCID mice were then submitted to daily treatment with 150 μg/kg/day HF (n = 5) or vehicle only (0.9 % NaCl; n = 5) as an intraperitoneal injection for 21 consecutive days. Previous experiments were performed to confirm leukemic infiltration in transplanted animals and to test the efficacy and toxicity of HF. All animal experiments using mice were conducted according to national guidelines for the care and use of laboratory animals (Brazilian College of Animal Experimentation) and were approved by the institutional Animal Experimentation Ethics Committee (protocol number 062/2008).
NB4 cells, a permanent cell line harboring PML-RARα t (15;17), characterizing an APL cell line , was used for in vitro assays. Briefly, cells were cultured in RPMI 1640 with 10 % fetal calf serum (FCS, Gibco, BRL, UK). Human Umbilical Vein Endothelial Cells (HUVEC) were maintained in EBM medium supplemented with 20 % FCS . All cells were maintained at 37 °C under 5 % CO2.
Quantification of VEGF, angiogenin, and TGF-β
NB4 cells were treated with HF for 72 hours at doses ranging from 25 to 100 ng/mL. VEGF, angiogenin and TGF-β concentrations in supernatants were determinate by CBA (Cytometric Bead Array, BD Biosciences, San Jose, CA, USA) and/or ELISA (BD Biosciences, San Jose, CA, USA), following manufacturer’s recommendations.
Phospho-SMAD2 (P-SMAD2) identification
The phosphorylation of SMAD2 was assessed in total protein extracts obtained from NB4 cells treated with 50, 100, and 200 ng/mL doses of HF for 6, 12, and 24 hours. We used the PathScan® Phospho-Smad2 (Ser465/467) Sandwich ELISA Kit (Cell Signaling, Danvers, MA, USA) that provides the P-SMAD2 level as a direct absorbance reason. To assess the phosphorylated protein, TGF-β1 cytokine (Sigma-Aldrich, St. Louis, MO, USA) was added to the culture (1ng/mL) one hour before the ending of HF treatment.
Real time PCR and PCR array
mRNA expression was assessed by real time PCR. Briefly, total RNA was isolated using Trizol reagent (Invitrogen, Carlsbad, CA, USA) and was reverse transcribed using the cDNA High Capacity Archive kit (Applied Biosystems, Foster City, CA, USA). cDNA samples were used to quantify gene expression using specific primers and probes TaqMan® (Applied Biosystems, Foster City, CA, USA). Gapdh was included as endogenous internal control. PCR array was performed using the angiogenesis RT2 Profiler™ PCR Arrays kit (SA Biosciences, Frederick, MD, USA), in which each cDNA sample was processed in a 96-well plate containing 84 angiogenesis-related genes and B2M, HPRT1, RPL13A, ACTB, and GAPDH were included as endogenous internal controls in all plates. mRNA expression of non-treated cells or non-leukemic mice are expressed as Fold Change = 1. Amplification was performed in plate duplicates in a 7500 Real-Time PCR System (Applied Biosystems, Foster City, CA, USA).
Immunohistochemistry staining for VEGF in bone marrow sections
Vertebra samples were collected from mice, fixed and serial 5-μm sections were prepared in paraffin. Immunohistochemistry was performed with primary anti-VEGF antibodies (Santa Cruz Biotechnology, Santa Cruz, CA, USA) and anti-α-actin (for TM mice) and anti-CD34 (for transplante mice) (Becton Dickinson, San Jose, CA, USA) at 1:500, 1:800 and 1:50, respectively. Peroxidase activity was revealed by 3,3′-diaminobenzidine as chromogen. Alpha-actin and CD34 expression was used for assessing microvessel density (MVD), quantified as the number of microvessels/mm2 after analyzing three high-power fields (400 ×).
Analysis of the hematological responses to HF in vivo
At day 21 mice were sacrificed after being subjected to a cardiac puncture to obtain peripheral blood  samples. Age-matched NOD/SCID healthy animals were used as controls (WT; n = 3). Automated counts for white blood cells (WBC) were performed using a T-890 Coulter cell counter (Coulter Corporation, Hialeah, FL, USA), and differential counts were obtained from Leishman-Wright-Giemsa-stained smears. For morphological analysis, 100 cells of PB were counted, and then myeloid cells were classified as immature, intermediate, or mature, according to the Bethesda criteria . Bone marrow (BM) cells were obtained by flushing of the bone cavities and the cells were used for cytospin slide preparation and staining with Leishman-Wright-Giemsa. Imprint slides of the spleen were also performed to quantify the hematological response to HF.
Immnunophenotyping of bone marrow cells
BM cells were characterized by immnunophenotyping using the following combinations of mAbs: CD117-PE/CD16/32-FITC/CD45-Per-CP; CD11b-PE/Gr-1-FITC/CD45-PerCP. Fluorochrome-conjugated isotypic antibodies were used as negative controls. All antibodies were purchased from BD Biosciences Pharmingen (San Diego, CA, USA). A minimum of 10,000 events/tube were acquired with a FACScalibur flow cytometer. Viable CD45-positive cells were gated and the percentage of each cell subset was determined using the CellQuest software (Becton Dickinson).
NB4 cells were stimulated with Halofuginone (200 ng/mL), TGF-β (50 ng/ml) or Halofuginone (200ng/mL) + TGF-β (50ng/mL), for 6 hours and the chormatin immunoprecipitation was performed with Magna ChIP™ G (Millipore, Billerica, MA, USA) according to the instructions of manufacturer. Briefely, the crosslink was made with 1 % formaldehyde followed by addition of 125mM glicine to quench unreacted formaldehyde. Samples were then resuspended in cell lysis buffer containing Proteases Inhibitors before addition of Nuclear Lysis Buffer. The final lysates were sonicated to shear the genomic DNA into around 200-1000pb fragments. ChIP assay was performed on the supernatants by addition of 5 μg of each antibody: Anti-P-Smad2 (phospho S467 - ab192191); Anti-Smad2 + Smad3 (ab63672); Anti-HIF-1α (ab2185) and IgG rabbit polyclonal (ab27478). Primers for Vegf promoter region were custom designed (Additional file 1: Table S1). Graphics show Fold enrichment over IgG antibodie control for each sample and primer. Primers were purchased from Sigma- Aldrich (St. Louis, MO, USA).
All experiments were evaluated by analysis of the variance (ANOVA) between groups followed by the Bonferroni’s correction post-test or Mann-Whitney unpaired t-test. In all comparisons, a significance level of P < 0.05 was considered to be significant. Statistical analyses were performed using SPSS 13.0 software.
Angiogenesis is aberrantly increased in the APL transgenic mouse model
Halofuginone modulates expression of genes associated with angiogenesis
Halofuginone inhibits pro-angiogenic mediators in the APL cell line NB4
Halofuginone displays an anti-leukemic effect in the in vivo model of APL
Here we report that HF reduced tumor burden in an APL mouse model as showed by the cytomorphological and immunophenotyping analysis of the BM after 21 days of treatment. This is the first study to show that leukemic hCG-PML/RARA TM had increased VEGF expression in BM, reinforcing that VEGF may be a mediator supporting leukemogenesis . Using a transplant model of PML-RARα leukemic cells, the treatment with HF reduced the number of VEGF+ cells and VEGF gene expression in BM of leukemic mice. However, HF treatment did not result in a significant reduction of MVD. This may be a consequence of the transplant model used, which led to a massive infiltration of the BM with a shorter survival compared to solid tumor models. In this regard it is worthy pointing out that in the study by Elkin et al. the animals with bladder cancer were treated with oral HF for 26 and 29 weeks .
In addition, the treatment of the endothelial cell HUVEC with HF did not change the gene expression of ANGPT-1, HIF-1α, TIMP2 and CXCL10, whereas increased VEGF gene expression and protein secretion. These data suggests that HF effects may present variation according to the cell type, which is in accord with the previous demonstrated increase in VEGF production by fibrotic liver cells from rats treated with HF . Furthermore, it is well established that tumor cells-derived VEGF stimulates endothelial cells to produce VEGF . Considering that the basal production of VEGF showed by NB4 cells is over 100-fold higher, the induction of VEGF by HF treatment in endothelial cells may not have impact in the angiogenesis process.
In non-APL AML Schuch et al.  demonstrated that VEGF administration resulted in enhanced tumor growth and vascularization whereas treatment with a VEGF antagonist soluble NRP-1 inhibited tumor angiogenesis and growth in a chloroma mouse model. Moreover, these authors showed that the injection of adenovirus encoding NRP-1 reduced the leukemic burden and prolonged the survival of leukemic mice. Recently, Oka et al. described a high level of VEGF-A in the serum of an APL patient at diagnosis and the ex-vivo treatment with an anti-VEGF-A reduced leukemic cell proliferation . Unfortunately, in the phase II HOVON/SAKK AML study, the administration of the anti-VEGF agent bevacizumab along with standard chemotherapy did not result in better outcome in older patients . Thus, despite experimental results indicating that VEGF have a potential therapeutic benefit, the HOVON/SAKK study suggests that inhibition of VEGF may not be sufficient to control angiogenesis or tumor growth.
Considering HF antiangiogenic properties, we used a PCR array to screening angiogenic mediators in the APL cell line NB4. Our data showed a down-regulation mediated by HF in several pro-angiogenic factors, including HFG, HIF-1α, ANGPT-1 and -2, whereas the anti-angiogenic factors TIMP2 and CXCL10 were over expressed. Indeed, HGF is a well-recognized proangiogenic mediator which inhibition reduces tumor growth and metastasis , as well HIF-1α, which is associated with poor prognosis in cancer due stimulation of VEGFR+ cells migration to the tumor . Contrary, CXCL10 and TIMP2 had they antiangiogenic potential demonstrated. Mice with fibrosarcoma treated with CXCL10 combined with hypothermia presented reduced tumor burden and MVD , whereas the MMP2-inhibitor TIMP2, have been recently described as important prognostic factors in acute lymphoblastic leukemia . In the leukemia mouse model, we did observe increased gene expression of VEGF, HIF-1α and ANGPT-2, which were significantly reduced after HF treatment. These PCR data support that HF antiangiogenic effect implicates multiple targets, as demonstrated by Jordan ans Zeplin , MMP-2, bFGF and TGF-β were down-modulated by HF in physiologic conditions.
On the other hand, addition of HF to NB4 cells cultures did not result in morphological differentiation  likewise, no differentiation was observed in BM and blood smears of recipient mice at seven and 14 days of HF treatment (data not shown). Therefore, we believe that increase in differentiated cells in BM of HF treated mice reflects the restoration of normal hematopoiesis secondary to the significant reduction of the leukemic infiltration. Together, our results corroborate with previous studies reporting the anti-proliferative and proapoptotic actions of HF in solid tumors [32, 52] and in leiomyoma cell line  and with recent observations from our group demonstrating that HF induced the blockade of cell cycle progression at G1/S transition and apoptosis in NB4 cells . Here we showed that NB4 cells treated with HF had SMAD2 phosphorylation abrogated indicating that the TGF-β-signaling was inhibited, which is in agreement with previous studies [54–56]. It is proposed that VEGF gene expression is targeted by TGF-β- signaling [57–59] and that low concentration of TGF-β cooperate with VEGF to stimulate epithelial cell proliferation and migration . Thus, one possible explanation for the VEGF reduction induced by HF is the inhibition of the TGF-β-signaling. One result suggest that HF acts by decreasing SMAD-2 phosphorylation triggered by TGF-β. However, ChIP analysis showed that, despite reduction of SMAD phosphorylation, HF treatment increases P-SMAD2 binding to VEGF promoter region. Importantly, it has been demonstrated that SMAD2 is not required for VEGF gene expression, and that SMAD3 is the potential transcription factor linking TGF-β-signaling and VEGF .
It has been proposed that the PML-RARα fusion protein, similarly to cPML interacts and co-localizes with SMAD2/3 and SARA thus interfering with the phosphorylation and nuclear translocation of this complex Lin et al. . The authors hypothesized that PML/RARα in the cytosol inhibits TGF-β-signaling by sequestering cPML away from the TFβR1/SARA/SMAD2/3 complex thus preventing the trafficking to the early endosome. This inhibition could be further enhanced by interfering with nuclear isoform PML4, which has been demonstrated to transactivate TGF-β target genes. Our results showed that NB4 cells responded to the addition of TGF-β in culture medium with an increase of about 20-fold in SMAD2 phosphorylation. HF was capable of inhibiting TGF-β-induced SMAD2 phosphorylation. Taken together with our previous report that HF blocked NB4 proliferation and reduced the leukemia burden in vivo we postulated that despite the interference of PML/RARα with TFβR1/SARA/SMAD2/3 complex, the TGF-β pathway remain active in APL and contributes for leukemia progression.
Here we showed HF can affect multiply mechanism and that HF treatment reduced proangiogenic factors expression and TGF-β-signaling in vitro, in addition to displaying antiangiogenic and antileukemic effects in an animal model of APL. Considering the importance of angiogenesis and deregulation of TGF-β-signaling in tumor progression, we propose HF as a potential new anti-cancer drug
Halofuginone was obtained as a kind donation from Prof. Arnon Nagler, Chaim Sheba Medical Center, Tel Hashomer, Israel. The transgenic hCG-PML-RARα mice were kindly provided by Prof. Pier Paolo Pandolfi (Beth Israel Deaconess Medical Center, Harvard Stem Cell Institute, Boston, MA, USA). This work was supported by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP, grant No. 2013/08135-2). P.A.A. was an FAPESP fellowship recipient (Grant No. 08/52634-5).
- De Figueiredo-Pontes LL, Assis PA, Santana-Lemos BA, Jacomo RH, Lima AS, Garcia AB, et al. Halofuginone has anti-proliferative effects in acute promyelocytic leukemia by modulating the transforming growth factor beta signaling pathway. PLoS One. 2011;6:e26713.PubMed CentralPubMedView ArticleGoogle Scholar
- Chu TL, Guan Q, Nguan CY, Du C. Halofuginone suppresses T cell proliferation by blocking proline uptake and inducing cell apoptosis. Int Immunopharmacol. 2013;16:414–23.PubMedView ArticleGoogle Scholar
- Leiba M, Jakubikova J, Klippel S, Mitsiades CS, Hideshima T, Tai YT, et al. Halofuginone inhibits multiple myeloma growth in vitro and in vivo and enhances cytotoxicity of conventional and novel agents. Br J Haematol. 2012;157:718–31.PubMed CentralPubMedView ArticleGoogle Scholar
- Abramovitch R, Dafni H, Neeman M, Nagler A, Pines M. Inhibition of neovascularization and tumor growth, and facilitation of wound repair, by halofuginone, an inhibitor of collagen type I synthesis. Neoplasia. 1999;1:321–9.PubMed CentralPubMedView ArticleGoogle Scholar
- Elkin M, Miao HQ, Nagler A, Aingorn E, Reich R, Hemo I, et al. Halofuginone: a potent inhibitor of critical steps in angiogenesis progression. FASEB J. 2000;14:2477–85.PubMedView ArticleGoogle Scholar
- Abramovitch R, Itzik A, Harel H, Nagler A, Vlodavsky I, Siegal T. Halofuginone inhibits angiogenesis and growth in implanted metastatic rat brain tumor model–an MRI study. Neoplasia. 2004;6:480–9.PubMed CentralPubMedView ArticleGoogle Scholar
- Folkman J. Tumor angiogenesis: therapeutic implications. N Engl J Med. 1971;285:1182–6.PubMedView ArticleGoogle Scholar
- Jakovljevic G, Culic S, Stepan J, Bonevski A, Seiwerth S. Vascular endothelial growth factor in children with neuroblastoma: a retrospective analysis. J Exp Clin Cancer Res. 2009;28:143.PubMed CentralPubMedView ArticleGoogle Scholar
- Ayala F, Dewar R, Kieran M, Kalluri R. Contribution of bone microenvironment to leukemogenesis and leukemia progression. Leukemia. 2009;23:2233–41.PubMed CentralPubMedView ArticleGoogle Scholar
- Rajkumar SV, Witzig TE. A review of angiogenesis and antiangiogenic therapy with thalidomide in multiple myeloma. Cancer Treat Rev. 2000;26:351–62.PubMedView ArticleGoogle Scholar
- Jorgensen JM, Sorensen FB, Bendix K, Nielsen JL, Olsen ML, Funder AM, et al. Angiogenesis in non-Hodgkin’s lymphoma: clinico-pathological correlations and prognostic significance in specific subtypes. Leuk Lymphoma. 2007;48:584–95.PubMedView ArticleGoogle Scholar
- Padro T, Ruiz S, Bieker R, Burger H, Steins M, Kienast J, et al. Increased angiogenesis in the bone marrow of patients with acute myeloid leukemia. Blood. 2000;95:2637–44.PubMedGoogle Scholar
- Hatfield KJ, Olsnes AM, Gjertsen BT, Bruserud O. Antiangiogenic therapy in acute myelogenous leukemia: targeting of vascular endothelial growth factor and interleukin 8 as possible antileukemic strategies. Curr Cancer Drug Targets. 2005;5:229–48.PubMedView ArticleGoogle Scholar
- Aguayo A, Kantarjian HM, Estey EH, Giles FJ, Verstovsek S, Manshouri T, et al. Plasma vascular endothelial growth factor levels have prognostic significance in patients with acute myeloid leukemia but not in patients with myelodysplastic syndromes. Cancer. 2002;95:1923–30.PubMedView ArticleGoogle Scholar
- Kini AR, Peterson LA, Tallman MS, Lingen MW. Angiogenesis in acute promyelocytic leukemia: induction by vascular endothelial growth factor and inhibition by all-trans retinoic acid. Blood. 2001;97:3919–24.PubMedView ArticleGoogle Scholar
- Alimoghaddam K, Shariftabrizi A, Tavangar SM, Sanaat Z, Rostami S, Jahani M, et al. Anti-leukemic and anti-angiogenesis efficacy of arsenic trioxide in new cases of acute promyelocytic leukemia. Leuk Lymphoma. 2006;47:81–8.PubMedView ArticleGoogle Scholar
- Estey E, Levine RL, Lowenberg B. Current challenges in clinical development of “targeted therapies”: the case of acute myeloid leukemia. Blood. 2015;125:2461–6.PubMedView ArticleGoogle Scholar
- Estey EH, Giles FJ, Kantarjian H, O’Brien S, Cortes J, Freireich EJ, et al. Molecular remissions induced by liposomal-encapsulated all-trans retinoic acid in newly diagnosed acute promyelocytic leukemia. Blood. 1999;94:2230–5.PubMedGoogle Scholar
- Lo-Coco F, Avvisati G, Vignetti M, Thiede C, Orlando SM, Iacobelli S, et al. Retinoic acid and arsenic trioxide for acute promyelocytic leukemia. N Engl J Med. 2013;369:111–21.PubMedView ArticleGoogle Scholar
- Mathews V, Desire S, George B, Lakshmi KM, Rao JG, Viswabandya A, et al. Hepatotoxicity profile of single agent arsenic trioxide in the treatment of newly diagnosed acute promyelocytic leukemia, its impact on clinical outcome and the effect of genetic polymorphisms on the incidence of hepatotoxicity. Leukemia. 2006;20:881–3.PubMedView ArticleGoogle Scholar
- Ribeiro RC, Rego E. Management of APL in developing countries: epidemiology, challenges and opportunities for international collaboration. In: Hematology / the Education Program of the American Society of Hematology American Society of Hematology Education Program. 2006. p. 162–8.Google Scholar
- Mathews V, George B, Chendamarai E, Lakshmi KM, Desire S, Balasubramanian P, et al. Single-agent arsenic trioxide in the treatment of newly diagnosed acute promyelocytic leukemia: long-term follow-up data. J Clin Oncol. 2010;28:3866–71.PubMedView ArticleGoogle Scholar
- Tallman MS. Treatment of relapsed or refractory acute promyelocytic leukemia. Best Pract Res Clin Haematol. 2007;20:57–65.PubMedView ArticleGoogle Scholar
- Elkin M, Reich R, Nagler A, Aingorn E, Pines M, De-Groot N, et al. Inhibition of matrix metalloproteinase-2 expression and bladder carcinoma metastasis by halofuginone. Clin Cancer Res. 1999;5:1982–8.PubMedGoogle Scholar
- Jordan MC, Zeplin PH. Local inhibition of angiogenesis by halofuginone coated silicone materials. J Mater Sci Mater Med. 2012;23:1203–10.PubMedView ArticleGoogle Scholar
- Lin HK, Bergmann S, Pandolfi PP. Cytoplasmic PML function in TGF-beta signalling. Nature. 2004;431:205–11.PubMedView ArticleGoogle Scholar
- Pepper MS. Transforming growth factor-beta: vasculogenesis, angiogenesis, and vessel wall integrity. Cytokine Growth Factor Rev. 1997;8:21–43.PubMedView ArticleGoogle Scholar
- Semenza GL. Expression of hypoxia-inducible factor 1: mechanisms and consequences. Biochem Pharmacol. 2000;59:47–53.PubMedView ArticleGoogle Scholar
- Xavier S, Piek E, Fujii M, Javelaud D, Mauviel A, Flanders KC, et al. Amelioration of radiation-induced fibrosis: inhibition of transforming growth factor-beta signaling by halofuginone. J Biol Chem. 2004;279:15167–76.PubMedView ArticleGoogle Scholar
- Sheffer Y, Leon O, Pinthus JH, Nagler A, Mor Y, Genin O, et al. Inhibition of fibroblast to myofibroblast transition by halofuginone contributes to the chemotherapy-mediated antitumoral effect. Mol Cancer Ther. 2007;6:570–7.PubMedView ArticleGoogle Scholar
- Taras D, Blanc JF, Rullier A, Dugot-Senant N, Laurendeau I, Bieche I, et al. Halofuginone suppresses the lung metastasis of chemically induced hepatocellular carcinoma in rats through MMP inhibition. Neoplasia. 2006;8:312–8.PubMed CentralPubMedView ArticleGoogle Scholar
- Nagler A, Ohana M, Shibolet O, Shapira MY, Alper R, Vlodavsky I, et al. Suppression of hepatocellular carcinoma growth in mice by the alkaloid coccidiostat halofuginone. Eur J Cancer. 2004;40:1397–403.PubMedView ArticleGoogle Scholar
- He LZ, Tribioli C, Rivi R, Peruzzi D, Pelicci PG, Soares V, et al. Acute leukemia with promyelocytic features in PML/RARalpha transgenic mice. Proc Natl Acad Sci U S A. 1997;94:5302–7.PubMed CentralPubMedView ArticleGoogle Scholar
- Lanotte M, Martin-Thouvenin V, Najman S, Balerini P, Valensi F, Berger R. NB4, a maturation inducible cell line with t(15;17) marker isolated from a human acute promyelocytic leukemia (M3). Blood. 1991;77:1080–6.PubMedGoogle Scholar
- Wang YH, Dong YY, Wang WM, Xie XY, Wang ZM, Chen RX, et al. Vascular endothelial cells facilitated HCC invasion and metastasis through the Akt and NF-kappaB pathways induced by paracrine cytokines. J Exp Clin Cancer Res. 2013;32:51.PubMed CentralPubMedView ArticleGoogle Scholar
- Kunkel SL, Campbell Jr DA, Chensue SW, Higashi GI. Species-dependent regulation of monocyte/macrophage Ia antigen expression and antigen presentation by prostaglandin E. Cell Immunol. 1986;97:140–5.PubMedView ArticleGoogle Scholar
- Kogan SC, Ward JM, Anver MR, Berman JJ, Brayton C, Cardiff RD, et al. Bethesda proposals for classification of nonlymphoid hematopoietic neoplasms in mice. Blood. 2002;100:238–45.PubMedView ArticleGoogle Scholar
- Rego EM, Ruggero D, Tribioli C, Cattoretti G, Kogan S, Redner RL, et al. Leukemia with distinct phenotypes in transgenic mice expressing PML/RAR alpha, PLZF/RAR alpha or NPM/RAR alpha. Oncogene. 2006;25:1974–9.PubMedView ArticleGoogle Scholar
- Roberts AB. TGF-beta signaling from receptors to the nucleus. Microbes Infect. 1999;1:1265–73.PubMedView ArticleGoogle Scholar
- Santana BA, Pintao MC, Lima RS AE, Scheucher PS, Santos GA, Garcia AB, et al. Asynchronous expression of myeloid antigens in leukemic cells in a PML/RARalpha transgenic mouse model. Braz J Med Biol Res. 2006;39:615–20.PubMedView ArticleGoogle Scholar
- Dong X, Han ZC, Yang R. Angiogenesis and antiangiogenic therapy in hematologic malignancies. Crit Rev Oncol Hematol. 2007;62:105–18.PubMedView ArticleGoogle Scholar
- Elkin M, Ariel I, Miao HQ, Nagler A, Pines M, De-Groot N, et al. Inhibition of bladder carcinoma angiogenesis, stromal support, and tumor growth by halofuginone. Cancer Res. 1999;59:4111–8.PubMedGoogle Scholar
- Ohayon O, Mawasi N, Pevzner A, Tryvitz A, Gildor T, Pines M, et al. Halofuginone upregulates the expression of heparanase in thioacetamide-induced liver fibrosis in rats. Lab Investig: J Tech Meth Pathol. 2008;88:627–33.View ArticleGoogle Scholar
- Bergers G, Benjamin LE. Tumorigenesis and the angiogenic switch. Nat Rev Cancer. 2003;3:401–10.PubMedView ArticleGoogle Scholar
- Schuch G, Machluf M, Bartsch Jr G, Nomi M, Richard H, Atala A, et al. In vivo administration of vascular endothelial growth factor (VEGF) and its antagonist, soluble neuropilin-1, predicts a role of VEGF in the progression of acute myeloid leukemia in vivo. Blood. 2002;100:4622–8.PubMedView ArticleGoogle Scholar
- Oka Y, Tashiro H, Shirasaki R, Sugao T, Nishi R, Akiyama N, et al. Vascular endothelial growth factor acted as autocrine growth factor in an acute promyelocytic leukemia case. Leuk Lymphoma. 2010;51:717–9.PubMedView ArticleGoogle Scholar
- Ossenkoppele GJ, Stussi G, Maertens J, Van Montfort K, Biemond BJ, Breems D, et al. Addition of bevacizumab to chemotherapy in acute myeloid leukemia at older age: a randomized phase 2 trial of the Dutch-Belgian Cooperative Trial Group for Hemato-Oncology (HOVON) and the Swiss Group for Clinical Cancer Research (SAKK). Blood. 2012;120:4706–11.PubMedView ArticleGoogle Scholar
- You WK, McDonald DM. The hepatocyte growth factor/c-Met signaling pathway as a therapeutic target to inhibit angiogenesis. BMB Rep. 2008;41:833–9.PubMed CentralPubMedView ArticleGoogle Scholar
- Du R, Lu KV, Petritsch C, Liu P, Ganss R, Passegue E, et al. HIF1alpha induces the recruitment of bone marrow-derived vascular modulatory cells to regulate tumor angiogenesis and invasion. Cancer Cell. 2008;13:206–20.PubMed CentralPubMedView ArticleGoogle Scholar
- Chen P, Yang LL, Yang HS, Wang YS, Li G, Wu Y, et al. Synergistic antitumor effect of CXCL10 with hyperthermia. J Cancer Res Clin Oncol. 2008;134:679–87.PubMedView ArticleGoogle Scholar
- Scrideli CA, Cortez MA, Yunes JA, Queiroz RG, Valera ET, Da Mata JF, et al. mRNA expression of matrix metalloproteinases (MMPs) 2 and 9 and tissue inhibitor of matrix metalloproteinases (TIMPs) 1 and 2 in childhood acute lymphoblastic leukemia: potential role of TIMP1 as an adverse prognostic factor. Leuk Res. 2010;34:32–7.PubMedView ArticleGoogle Scholar
- Gavish Z, Pinthus JH, Barak V, Ramon J, Nagler A, Eshhar Z, et al. Growth inhibition of prostate cancer xenografts by halofuginone. Prostate. 2002;51:73–83.PubMedView ArticleGoogle Scholar
- Grudzien MM, Low PS, Manning PC, Arredondo M, Belton Jr RJ, Nowak RA. The antifibrotic drug halofuginone inhibits proliferation and collagen production by human leiomyoma and myometrial smooth muscle cells. Fertil Steril. 2010;93:1290–8.PubMed CentralPubMedView ArticleGoogle Scholar
- McGaha TL, Phelps RG, Spiera H, Bona C. Halofuginone, an inhibitor of type-I collagen synthesis and skin sclerosis, blocks transforming-growth-factor-beta-mediated Smad3 activation in fibroblasts. J Invest Dermatol. 2002;118:461–70.PubMedView ArticleGoogle Scholar
- Roffe S, Hagai Y, Pines M, Halevy O. Halofuginone inhibits Smad3 phosphorylation via the PI3K/Akt and MAPK/ERK pathways in muscle cells: effect on myotube fusion. Exp Cell Res. 2010;316:1061–9.PubMedView ArticleGoogle Scholar
- Juarez P, Mohammad KS, Yin JJ, Fournier PG, McKenna RC, Davis HW, et al. Halofuginone inhibits the establishment and progression of melanoma bone metastases. Cancer Res. 2012;72:6247–56.PubMed CentralPubMedView ArticleGoogle Scholar
- Kobayashi T, Liu X, Wen FQ, Fang Q, Abe S, Wang XQ, et al. Smad3 mediates TGF-beta1 induction of VEGF production in lung fibroblasts. Biochem Biophys Res Commun. 2005;327:393–8.PubMedView ArticleGoogle Scholar
- Jeon SH, Chae BC, Kim HA, Seo GY, Seo DW, Chun GT, et al. Mechanisms underlying TGF-beta1-induced expression of VEGF and Flk-1 in mouse macrophages and their implications for angiogenesis. J Leukoc Biol. 2007;81:557–66.PubMedView ArticleGoogle Scholar
- Clifford RL, Deacon K, Knox AJ. Novel regulation of vascular endothelial growth factor-A (VEGF-A) by transforming growth factor (beta)1: requirement for Smads, (beta)-CATENIN, AND GSK3(beta). J Biol Chem. 2008;283:35337–53.PubMedView ArticleGoogle Scholar
- Pepper MS, Vassalli JD, Orci L, Montesano R. Biphasic effect of transforming growth factor-beta 1 on in vitro angiogenesis. Exp Cell Res. 1993;204:356–63.PubMedView ArticleGoogle Scholar
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