NSC-87877 inhibits DUSP26 function in neuroblastoma resulting in p53-mediated apoptosis

Dual specificity protein phosphatase 26 (DUSP26) is overexpressed in high-risk neuroblastoma (NB) and contributes to chemoresistance by inhibiting p53 function. In vitro, DUSP26 has also been shown to effectively inhibit p38 MAP kinase. We hypothesize that inhibiting DUSP26 will result in decreased NB cell growth in a p53 and/or p38-mediated manner. NSC-87877 (8-hydroxy-7-[(6-sulfo-2-naphthyl)azo]-5-quinolinesulfonic acid), a novel DUSP26 small molecule inhibitor, shows effective growth inhibition and induction of apoptosis in NB cell lines. NB cell lines treated with small hairpin RNA (shRNA) targeting DUSP26 also exhibit a proliferation defect both in vitro and in vivo. Treatment of NB cell lines with NSC-87877 results in increased p53 phosphorylation (Ser37 and Ser46) and activation, increased activation of downstream p38 effector proteins (heat shock protein 27 (HSP27) and MAP kinase-activated protein kinase 2 (MAPKAPK2)) and poly ADP ribose polymerase/caspase-3 cleavage. The cytotoxicity resulting from DUSP26 inhibition is partially reversed by knocking down p53 expression with shRNA and also by inhibiting p38 activity with SB203580 (4-[4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-1H-imidazol-5-yl]pyridine). In an intrarenal mouse model of NB, NSC-87877 treatment results in decreased tumor growth and increased p53 and p38 activity. Together, these results suggest that DUSP26 inhibition with NSC-87877 is an effective strategy to induce NB cell cytotoxicity in vitro and in vivo through activation of the p53 and p38 mitogen-activated protein kinase (MAPK) tumor-suppressor pathways.

Neuroblastoma (NB) remains the most common extracranial solid tumor in children and is associated with a very poor prognosis in high-risk patients. 1 Current treatment strategy for this subgroup of patients includes intense myeloablative chemotherapy, radical surgical resection of primary tumor, radiation therapy and stem cell rescue. In spite of these therapies, survival in high-risk NB patients is o50% at 5 years from diagnosis. 2 These therapies confer major long-term toxicities in over 90% of long-term survivors; therefore, efforts are underway to identify more specific biologic therapies with less toxicity and better efficacy at targeting NB.
A therapeutic strategy that is gaining much interest is utilizing small molecule inhibitors to activate innate, nonmutated cell senescence and death pathways, such as the p53 tumor suppressor. Mutations in the p53 gene are seen in over 60% of adult cancers; however, pediatric solid tumors, particularly NB, do not exhibit frequent p53 mutations and actually have an intact pathway that is suppressed by other mechanisms. 3 Mouse double minute 2 (MDM2) inhibition is a strategy to activate p53 using compounds such as Nutlin-3a, RITA and RG7112, which has already been tested in a phase I clinical trial in adults. [4][5][6] The p38 stress kinase, MAP kinase, pathway is another tumor-suppressive pathway that is upstream from p53 and can function through p53-dependent and -independent mechanisms to induce apoptosis. Although described as oncogenic in some cancers, there is evidence that p38 activation leads to tumor cell apoptosis in NB. [7][8][9][10] Both of these tumor-suppressive pathways are regulated through phosphorylation and dephosphorylation events by an array of kinases and phosphatases.
Phosphatase targeting in NB has had very limited application because of the limited number of phosphatases found to have an oncogenic role. Protein phosphatase 2A (PP2A), protein tyrosine phosphatase receptor delta (PTPRD) and dual specificity protein phosphatase 12 (DUSP12) have been found to be involved in NB cell differentiation and tumor suppression. [11][12][13][14] First discovered in breast cancer, PPM1D, or Wip-1 phosphatase, is active in NB, and small molecule inhibition results in p53 activation and chemosensitivity. [15][16][17] In this report, we show DUSP26 functions by inhibiting p53 and p38 function to promote growth of NB tumor cells.
A novel DUSP26 function shown in NB is enzymatic regulation of the p53 tumor suppressor. 22 We demonstrated that DUSP26 physically binds p53, dephosphorylates p53 at Ser20 and Ser37, and causes inhibition of downstream p53 signaling. DUSP26 activity leads to increased chemoresistance to doxorubicin and VP-16 (etoposide) treatment, and overexpression was seen in high-risk NB tumor tissue samples correlating with a worse prognosis in these patients. Here, we show how DUSP26 has pro-proliferative effects in NB by inhibiting the p53 tumor-suppressor pathway, as well as the p38 mitogen-activated protein kinase (MAPK) pathway. Inhibition with small hairpin RNA (shRNA) targeting DUSP26 or NSC-87877 results in decreased proliferation and cell viability in NB cell lines in vitro and in vivo. Inhibiting the p53 or p38 pathways reverses this phenotype seen with inhibition of DUSP26. These data establish DUSP26 inhibition as a promising novel therapeutic approach for NB.

Results
NSC-87877 inhibits DUSP26 function in NB cell lines resulting in decreased proliferation. To test the effects of NSC-87877, a chemical inhibitor of DUSP26, we exposed three p53 wild-type NB cell lines, IMR32, NB-19 and SH-SY5Y, known to express DUSP26 (Supplementary Figure 1) with low concentrations of the chemical inhibitor. In all cell lines, we saw a decrease in cell proliferation by day 5 when exposed to 0.25 μM of NSC-87877 (Figures 1a-c). In NB-19 and SH-SY5Y, the decrease in cell proliferation seemed more pronounced with a 0.5 μM dose. The same cell lines were then plated in soft agar, which recapitulates in vivo tumor growth to a greater degree than twodimensional cell growth, 23 with 0.5 μM of NSC-87877 and grown for 14 days. After staining with MTT (3-(4,5dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide), the colony formation was significantly decreased in the three cell lines tested when compared with the control group (Figures 1d-e, Po0.01). In order to demonstrate that NSC-87877 can inhibit DUSP26 function in NB cell lines, we used the SK-N-AS cell line that expresses DUSP26 and transduced this cell line with a DUSP26 overexpression construct (Supplementary Figure 2a). DUSP26 overexpression in SK-N-AS causes a decrease in p38 MAPK phosphorylation as previously demonstrated in HEK293T cells. 18 However, when this cell line was treated with NSC-87877, we saw an increase in p38 phosphorylation indicating that DUSP26 function is inhibited. This finding is consistent with the results reported by Song et al. 20 describing NSC-87877 as a DUSP26 inhibitor.
DUSP26 shRNA-treated NB cell lines also display a proliferation defect. In order to validate the above data, we designed shRNA targeting DUSP26 to achieve decreased mRNA expression. Figure 2a shows a 450% expression knockdown with the shDUSP26-1 (shD26-1) sequence in the SH-SY5Y cell line. A non-targeting, control shRNA (shC) sequence was used as a comparison. These cell lines were then grown and tested for proliferation. At day 9, there was a significant difference comparing the shC cell line to shD26-1 (Po0.01). This was also true in the IMR32 cell line tested in a similar manner ( Supplementary Figures 3a and b (Figures 2c and d).
As NSC-87877 was originally described as an inhibitor of Src homology region 2 domain-containing phosphatases (SHP-1 and SHP-2), we tested the effects of shRNA targeting SHP-1 in SH-SY5Y. Using a previously published shRNA sequence targeting SHP-1 (shSHP-1), 24 gene expression was decreased per immunoblot (Supplementary Figure 4a). These cells did not display decreased proliferation when compared with control cells and shD26-1 (Supplementary Figure 4b); however, when grown in soft agar, the shSHP-1 cells made much larger colonies than the control further indicating a lack of a proliferation defect and very different phenotype than DUSP26 inhibition (Supplementary Figure 4c).
DUSP26 shRNA causes decreased tumor growth in vivo. As the soft agar colony formation assay mimics in vivo tumor growth, we tested the shD26-1 versus the shC sequence in an intrarenal model of NB using the SH-SY5Y cell line with luciferase expression. After transduction and selection of these cell lines, female nude mice were injected with 1 × 10 6 cells into the left kidney and allowed to grow. Tumor growth was monitored periodically with intraperitoneal (i.p.) injections of luciferin and bioluminescence images were taken showing a decrease in tumor size of the shD26-1 cell line compared with shC (Figure 3a). At 4 weeks, a necropsy was performed and the tumors were weighed. The shD26-1 tumors weighed significantly less than the shC tumors (Po0.05; Figure 3b).

NSC-87877 can induce apoptosis in NB cell lines.
Having shown that nanomolar doses of NSC-87877 can result in a proliferation defect in NB cell lines similar to shRNA knockdown of DUSP26, we tested higher doses of NSC-87877 on NB to see if cytotoxicity could be induced. As seen in our previous studies using shRNA targeting DUSP26, 22 concomitant treatment with NSC-87877 and doxorubicin resulted in enhanced cytotoxicity when compared with doxorubicin treatment alone (Figures 4a-d). As a single agent, we found that increasing doses of NSC-87877 resulted in apoptosis in many cell lines at varying IC 50 levels ( Figure 4e). In order to further confirm that DUSP26 inhibition is leading to cytotoxicity, we treated IMR32 cells with NSC-87877 and collected cells at time points over a 12-h period. By immunoblot, poly ADP ribose polymerase (PARP) cleavage was seen after 6 h of treatment confirming cell death ( Figure 4f, Supplementary Figure 5a). We then tested the phosphorylation status of the two serine DUSP26 target sites on p53 (Ser20 and Ser37). 22 There was a noticeable increase in Ser37 phosphorylation over the time course. In addition, we saw a significant increase in Ser46 phosphorylation 1 h after treatment compared with the 0 time point (Supplementary Figure 5a). Ser46 is described as an apoptosis activation site for p53 and is a direct target of p38 kinase. 15,25,26 Therefore, in addition to increased Ser46-p53 phosphorylation, we saw an increase in p38 phosphorylation at the activation sites, Thr180/Tyr182, starting at 1 h after treatment with a concomitant increase and stabilization in total p38 (Supplementary Figure 2b). This effect was transient as the level of phosphorylated p38 decreased at 12 h when the most PARP cleavage was seen. This decrease at 12 h was also seen in Ser46-p53, as well (Supplementary Figure 5a). In summary, DUSP26 inhibition with NSC-87877 results in increased phosphorylation of Ser37 and Ser46 on p53, and subsequent cell death as evidenced by increased PARP cleavage.
Inhibition of p53 or p38 MAPK results in increased cell viability in the setting of NSC-87877 treatment. As NSC-87877 inhibits DUSP26 activity resulting in increased p53 and p38 activation and cell death, we tested if inhibiting either the p53 or p38 pathways in this setting could reverse the cell death. We first sought to determine the effect of NSC-87877 on NB cell lines with defective p53 signaling. The SK-N-AS cell line contains a deactivating deletion at the C-terminus of p53. 27 The SHEP cell line is another unique cell line with an inactive p53 pathway because of a homozygous deletion of the CDKN2A gene resulting in loss of p14 ARF , a known MDM2 inhibitor. 28 This results in increased p53 degradation through unregulated MDM2. Both of these cell lines had much higher IC 50 values (26.03 and 32.24 μM) with NSC-87877 monotherapy than the other cell lines tested (Figures 5a and 4e). From this, we hypothesized that p53 inactivation can also reverse the effects of NSC-87877 treatment. We used an shRNA targeting p53 (sh-p53) to inhibit p53 expression in IMR32 cells and achieved a significant decrease in protein expression (Supplementary Figure 4d). These cells were plated with shRNA non-targeting, control (shRNA control) cells and treated with increasing concentrations of NSC-87877. Figure 5b shows that the sh-p53 cells were much more resistant to cell death than the shRNA control cells with an IC 50 increasing from 1.37 to 14.7 μM.
In order to test the effects of p38 pathway inhibition on NSC-87877-induced cell death through Ser46-p53 activation, we pre-incubated IMR32 and NB-19 cells with SB203580 (4-[4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-1H-imidazol-5-yl]pyridine), a well-described p38 inhibitor, 29 and then exposed them to increasing concentrations of NSC-87877. DUSP26 regulates p53 and p38 activity in NB. Owing to the reversal of cell death with p38 inhibition, we then tested the expression and activation of downstream effector proteins. The NB-19 cell line was treated with 10 μM of NSC-87877 alone or after a pre-incubation period with SB203580. Similar to the previous immunoblot analysis, we again saw in an increase in Ser46-p53 phosphorylation; however, in this cell line we also saw an increase in p53 stability (Figure 6a, Supplementary Figure 5b). With the addition of SB203580, Ser46-p53 phosphorylation decreased as did total p53 levels (Supplementary Figure 5c). In addition, p53 upregulated modulator of apoptosis (PUMA) levels increased with NSC-87877 alone and decreased with SB203580 pre-treatment. With NSC-87877 treatment, the direct downstream target proteins of p38, MAP kinaseactivated protein kinase 2 (MAPKAPK2) and heat shock protein 27 (HSP27), had increasing phosphorylation at their respective activation sites, as well as total protein stability. The downstream function of p38 was inhibited by SB203580 pre-treatment as evidenced by decreased phosphorylation of MAPKAPK2 and HSP27. When we analyzed p38 phosphorylation at the known activation sites, Thr180/Tyr182, in these cells, we did not see a robust increase in p38 phosphorylation (Supplementary Figure 2c). As SB203580 only inhibits p38 downstream function and does not affect phosphorylation status of p38, 29 the p-p38 and total p38 expression looked almost identical in the SB203580/NSC-87877-treated group.
With NSC-87877 treatment and p38 inhibition with SB203580, we tested for expression of cleaved PARP and caspase-3. We again saw an increase in PARP cleavage with increasing time points after administration of NSC-87877, particularly at 8, 12 and 24 h (Figure 6b, Supplementary  Figures 5d and e). Confirming that this is indeed apoptosis and not cellular necrosis from small molecule treatment, we found that cleaved caspase-3 (20 kDa) also increased with progressing time points after NSC-87877 treatment (Figure 6b, Supplementary Figures 5d and e). This phenomenon was reversed with the addition of SB203580. These data suggest that DUSP26 most likely has a role in directly inhibiting p53 phosphorylation at Ser37 and indirectly inhibiting p53 phosphorylation at Ser46 by affecting p38 MAPK function in order to promote NB tumor cell growth (Figure 6c).  Figure 7b). In order to test phosphorylation status of p38 and p53 with in vivo NSC-87877 treatment, we generated xenografts with SH-SY5Y luciferase-tagged cells as above and grew the tumors for 14 days. After confirming a significant tumor size by bioluminescence, three mice were treated with an i.p. injection of NSC-87877 (30 mg/kg). The mice were placed under anesthesia and a piece of tumor was harvested through the same flank incision as the intrarenal implantation at time points. By immunoblot, the tumors displayed increased phosphorylation and stabilization of Ser46-p53, total p53, p-MAPKAPK2, total MAPKAPK2, p-HSP27 and total HSP27 as seen in the in vitro experiments (Figure 7c, Supplementary  Figure 5f). We also found increased p38 phosphorylation (Thr180/Tyr182) at 24 h of treatment with NSC-87877 (Supplementary Figure 2d). Tumor samples harvested after 15 days of NSC-87877 treatment from the experiment in Figure 7a were tested for PARP and caspase-7 cleavage to show presence of cellular apoptosis in vivo. In two of the experimental samples, we saw more PARP and caspase-7 cleavage when compared with the control sample (Figure 7d). In summary, we demonstrated a significant decrease in tumor growth in NSC-87877-treated mice and showed a similar mechanism of p53 and p38 activation resulting in cellular apoptosis.

Discussion
NB continues to be a prevalent cancer in children with a poor prognosis in 50% of patients because of treatment refractory and/or metastatic disease. 1 Although intensive chemotherapy and immunotherapy have modestly improved survival, the associated increase in toxicity of our current approach suggests that future improvements in cure rates will require novel molecular targeted approaches. One approach to targeted therapy is to activate intrinsic death pathways, such as the p53 tumor-suppressor pathway. Several studies have investigated the mechanisms repressing p53 activation in NB. Key inhibitory proteins such as PARC, MDM2 and apoptosisantagonistic transcription factor (AATF) have been described to sequester, degrade or suppress transcription factor activity of the p53 protein. [31][32][33][34] The results of our study suggest that DUSP26 is an important regulator of p53-mediated apoptosis in NB. The proposed mechanism of action is similar to how Wip-1  15 In our previous studies, we have established that DUSP26 expression is highly specific to NB and is preferentially overexpressed in high-risk NB patients with the worst outcome. 18,22 The identified substrates for DUSP26 are p38 and p53 both of which are strong tumor suppressors in NB and many other cancers. 35 In this study, we were able to show that the DUSP26 target site Ser37-p53 shows increased phosphorylation indicating p53 activation with NSC-87877 treatment. Moreover, the Ser46 site also undergoes increased phosphorylation suggesting that p38 MAPK is also activated with NSC-87877 treatment. 36 This was supported by downstream activation of MAPKAPK2 and HSP27. In addition, p38 and/or p53 inhibition resulted in a significant reversal of the cell death seen with NSC-87877 treatment strongly suggesting that DUSP26 inhibition results in activation of these tumorsuppressor pathways. This article focuses on the use of a small molecule inhibitor, NSC-87877, which targets and inhibits DUSP26 function. 20 Our data show that NSC-87877 causes a proliferation defect in NB cell lines similar to knocking down expression with DUSP26-specific shRNA. In regards to 'off target effects' of using NSC-87877, silencing SHP-1 expression resulted in a pro-proliferative phenotype in contrast to that seen with DUSP26 knockdown suggesting that NSC-87877 specifically targets DUSP26 in NB with less affect on other known substrates. Even with the validation data presented, it is still quite possible that NSC-87877 activates other pathways than what we have described. However, our experiments showing that p53 inhibition with shRNA and p38 MAPK inhibition with SB203580 both partially reverse the cytotoxicity seen with NSC-87877 treatment, strongly suggest that NSC-87877 inhibits DUSP26 function resulting in unregulated p53 activation and cell death.
In our experiments analyzing the regulation of the p53 and p38 pathways by DUSP26 inhibition with NSC-87877, we were not able to show a consistent pattern of p38 phosphorylation. Several experiments both in vitro and in vivo showed that p38 phosphorylation increased with NSC-87877 treatment (Supplementary Figures 2a, b, and d) similar to previously published reports. 25 However, significant p38 phosphorylation changes were not seen in the NB-19 cell line treated with NSC-87877 (Supplementary Figure 2c). Instead, significant changes in Ser46-p53, total p53, PUMA, MAP-KAPK2 and HSP27 were seen. These data suggest that DUSP26 may have a unique regulation of p38 that is not yet undescribed. The experiments with the IMR32 cell line also revealed increasing total p38 stability accompanying increasing phosphorylation of p38 at Thr180/Tyr182 with NSC-87877 treatment. This finding is unique and we feel possible because phosphorylation of many enzymatic proteins leads to stability. Other studies have shown discrepancies in total p38 stability with activating phosphorylation thus demonstrating that the mechanisms behind this regulation are not known and can vary with cell types. 37,38 Some controversy has been raised in the literature on the mechanism of action of DUSP26 on the MAPK's. Patterson Immunoblotting was performed using an antibody specific to caspase-3 (FL-caspase-3) and cleaved caspase-3 (CL-caspase-3). Panels are representative of two independent experiments. (c) The inferred mechanism of NSC-87877 action on DUSP26 is outlined. Active DUSP26 causes inactivation of p38 and p53 with their respective downstream proapoptic proteins, resulting in tumor growth. The p53-activating activity of p38 is also suppressed. The addition of NSC-87877 results in competitive inhibition of DUSP26 activity and removes the inhibitory effect of DUSP26 on p38 and p53 NSC-87877 inhibits DUSP26 function in neuroblastoma Y Shi et al et al. 39 state in their paper that DUSP26 does not function in a MAPK-dependent manner and does not dephosphorylate p38. They also state that DUSP26 is not overexpressed in NB cell lines by qPCR. In addition to our studies showing that DUSP26 clearly dephosphorylates p38, multiple other studies have shown p38 dephosphorylation with DUSP26 overexpression. 18,20,21 As far as expression in NB, our group has clearly shown by immunohistochemistry that DUSP26 is overexpressed in NB tissue samples versus normal adrenal gland controls particularly in high-risk patients. Studies in the literature also describe DUSP26 as a potential tumor suppressor in breast cancer and cervical carcinoma. 39,40 This data, however, convincing and well described, does not mandate that DUSP26 must serve as a tumor suppressor in every cancer especially when comparing an embryonal, neural crest-derived malignancy to epithelial malignancies seen in adults.
Currently, targeted molecular therapies for NB are limited. The active trials through the Children's Oncology Group utilize anti-GD2 inhibition with monoclonal antibody, ALK inhibition with crizotunib and differentiation induction with retinoic acid. 1,2 Agents targeting the p53 pathway show promise, such as, RG7112 and RITA targeting the MDM2-p53 complex, P22077 targeting USP7 (a p53 regulating ubiquitin-specific protease), miRNA antagonist targeting miR-380-5p (an epigenetic regulator of p53) and NSC697923 targeting UBE2N (a p53 structural modulator). 6,33,[41][42][43] The data presented in this article suggest that DUSP26 inhibition is a potential therapeutic strategy for NB targeting both the p53 and p38 tumor-suppressor pathways. Our hope is that this study will spawn an interest in DUSP26 inhibition to help develop novel therapies for this devastating disease. Colony formation assay. For the soft agar assay, a base layer of 1% (w/v) agarose/cell culture media was plated into six-well plates and allowed to solidify. A top layer of NB cells were resuspended in a mixture of 0.7% (w/v) agarose/cell culture media to give a final concentration of 20 000 cells/2 ml. After 2-3 weeks, 1 ml of 5 mg/ml MTT was added to each well and incubated at 37°C for 1 h. Photos were then taken of each well. The NIST Integrated Colony Enumerator (National Institute of Standards and Technology, Gaithersburg, MD, USA) was used to count the colonies in each plate.
Cytotoxicity assays using NSC-87877 on NB cell lines. The cell lines IMR32, SH-SY5Y, NB-19, LAN-1, SK-N-AS, SK-N-SH and SHEP were individually plated at 1 x 10 4 cells per well in flat bottom 96-well plates to evaluate the cytotoxicity of NSC-87877, with and without doxorubicin. Treatment was initiated after cells were allowed to settle for 24 h. Plates were then read between 24 and 48 h after the two drugs were added. An MTT assay was performed using a multimode plate reader (Beckman Coulter) as described in the proliferation and cell viability assay. This experiment was repeated using IMR32 and NB-19 using NSC-87877 and the p38 inhibitor SB203580 (0 and 5 μM).
Quantitative reverse transcription-PCR. Total RNA was extracted from cell lines using Direct-zol RNA Miniprep Kit as per the manufacturer's instructions (cat# 11-331, Zymo Research, Irvine, CA, USA), and RNA purity and quantity were determined using a spectrophotometer measuring absorbance at 260/280 nm. SYBR green primers were designed to measure the quantity of specific mRNA, which are as follows: DUSP26 mRNA (forward, 5′-GCAGCGCTTGCAAAGAGCAG-3′; reverse, 5′-ACAGGAGACCTTGAGCTACT-3′). Glyceraldehyde 3-phosphate dehydrogenase was used as the internal control.
Immunoblotting assay. For immunoblotting, IMR32 and NB-19 cells were cultured for 48 h. All agents were added while cells were in logarithmic growth phase. For IMR32, NSC-87877 (50 μM) was added to each plate and cells were collected at 0, 1, 2, 4, 6, 8 and 12 h. For NB-19, NSC-87877 (10 μM) and a vehicle control was added to respective plates, and then collected at various time points (0-12 h). In a subsequent experiment, the p38 inhibitor, SB203580, and a vehicle control was added to each plate. After 12 h of treatment, NSC-87877 was added to all plates that were collected at various time points (0-12 h). The cell proteins were lysed with protein lysis buffer (50 mM Tris-HCl at pH 7.4, 150 mM NaCl, 1 mM EDTA, 1% NP-40, 0.25% sodium deoxycholate, 1 mM phenylmethylsulfonyl fluoride, 1 mM benzamidine, 10 mg/ml leupeptin, 1 mM dithiothreitol, 50 mM sodium fluoride, 0.1 mM sodium orthovanadate and phosphatase inhibitor cocktail 2 and 3 (p5726 and p0044, Sigma-Aldrich)) for 20 min at 4°C. Equal concentrations of protein extracts (100 μg) were resolved by sodium dodecyl sulfate-PAGE and transferred to a nitrocellulose membrane (Bio-Rad, Hercules, CA, USA). Depending on the antibody, the membrane was blocked with buffer containing 5% non-fat milk in TBST (10 mM Tris, pH 7.8, 150 mM NaCl and 0.05% Tween) or 5% bovine serum albumin (A9418) (Sigma-Aldrich) in TBST for 1 h at room temperature. The specific antibody was then incubated with the membrane at 4°C overnight. This was then followed by incubation with horse radish peroxidase (HRP)-conjugated, anti-mouse secondary antibody (Ab) or HRP-conjugated, anti-rabbit secondary antibody (Ab). The membrane was developed using the Pierce ECL Western Blotting Substrate chemiluminescent detection system (#32106) (Thermo Fisher Scientific).
Effect of RNA interference and NSC-87877 on NB cell growth in an orthotopic mouse model. Female Nu-nude mice (Taconic Biosciences, Hudson, NY, USA) were used for in vivo testing of NSC-87877 compared with control. SH-SY5Y transduced luciferase cells (SY5Y-Luc) and SH-SY5Y transduced with shDUSP26-1 were implanted into the left kidney as previously described. 30 The mice were imaged 10 days after implantation and flux measured. A threshold of 5 × 10 7 total flux (p/s) was used to standardize the mice who would be treated. Two groups were treated, one with NSC-87877 using a dose of 30 mg/kg/day, and the other with a carrier control composed of an equivalent volume of 0.9% NaCl via i.p. injection. After 15 days, necropsy was performed and tumor weights measured. For phosphor-immunoblotting, SH-SY5Y-Luc were implanted into the kidneys of three mice, once the previously indicated threshold for flux was reached, two mice were treated with 30 mg/kg of NSC-87877 and one control mouse was treated with carrier control. The mice were killed, at 12 and 24 h after administration of NSC-87877, and necropsy was performed. Tumors were immediately flash frozen with liquid nitrogen for later protein extraction. Protein was extracted by grinding 10 mg of tumor tissue, which was mixed with protein lysis buffer, passed through a 22 G needle, and incubated on ice for 30 min.
Statistical analysis. A two-tailed Student's t-test was used to determine statistical significance of in vitro cell viability and cytotoxicity experiments. The Kruskall-Wallis test was used to determine the statistical significance of in vivo tumor size differences between control and treatment groups. IC 50 were calculated using nonlinear regression in Prism (Graphpad, La Jolla, CA, USA). A P-value o0.05 was considered statistically significant.

Conflict of Interest
The authors declare no conflict of interest.