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Despite aggressive multimodal treatments the overall survival of patients with high-risk neuroblastoma remains poor. The aim of this study was to identify novel combination chemotherapy to improve survival rate in patients with high-risk neuroblastoma.
We took a synthetic lethal approach using a siRNA library targeting 418 apoptosis-related genes and identified genes and pathways whose inhibition synergized with topotecan. Microarray analyses of cells treated with topotecan were performed to identify if the same genes or pathways were altered by the drug. An inhibitor of this pathway was used in combination with topotecan to confirm synergism by in vitro and in vivo studies.
We found that there were nine genes whose suppression synergized with topotecan to enhance cell death, and the NF-κB signaling pathway was significantly enriched. Microarray analysis of cells treated with topotecan revealed a significant enrichment of NF-κB target genes among the differentially altered genes, suggesting that NF-κB pathway was activated in the treated cells. Combination of topotecan and known NF-κB inhibitors (NSC 676914 or bortezomib) significantly reduced cell growth and induced caspase 3 activity in vitro. Furthermore, in a neuroblastoma xenograft mouse model, combined treatment of topotecan and bortezomib significantly delayed tumor formation compared to single-drug treatments.
Synthetic lethal screening provides a rational approach for selecting drugs for use in combination therapy and warrants clinical evaluation of the efficacy of the combination of topotecan and bortezomib or other NF-κB inhibitors in patients with high risk neuroblastoma.
Neuroblastoma is the most common extra-cranial solid tumor in childhood, accounting for 7-10% of childhood cancers . Based on age, staging, MYCN amplification status, histology, and DNA ploidy, neuroblastoma is classified into low, intermediate and high risk groups [2,3]. At present, high risk neuroblastoma is treated with high dose chemotherapy, surgery, autologous stem cell transplantation, radiation, immune and differentiating therapy. Currently used chemotherapeutic agents in standard and salvage regimens include toposisomerase I and II inhibitors, topotecan, etoposide, irinotecan and doxorubicin; alkylating agents, cisplatin, carboplatin, melphalan and cyclophosphamide and the microtubule inhibitor vincristine [4,5]. The differentiating agent 13-cis-retinoic acid is also administered during the maintenance period post chemotherapy. Recent clinical trials have shown that the combination of anti-GD2 antibodies and immunocytokines significantly increase the survival of patients with high risk neuroblastoma [6,7]. Despite these aggressive combined multimodal treatments the survival rate for these high risk neuroblastoma patients remains less than 50%.
Topoisomerase inhibitors are currently a mainstay of many salvage regimens for neuroblastoma and are being evaluated as up-front therapy in an ongoing trial [8-11]. They function by perturbing the cellular machinery responsible for maintaining DNA structure during transcription and replication. Topotecan is an inhibitor for the enzyme topoisomerase-I which is involved in the replication and repair of nuclear DNA. As DNA is replicated in dividing cells, topoisomerase-I binds to super-coiled DNA causing single-stranded breaks. As a result, topoisomerase-I relieves the torsional stresses that are introduced into DNA ahead of the replication complex or moving replication fork. Topotecan inhibits topoisomerase-I by stabilizing the covalent complex of enzyme and strand-cleaved DNA, which is an intermediate of the catalytic mechanism, thereby inducing breaks in the protein-associated DNA single-strands, resulting in cell death . This agent is currently used for the treatment of many cancers including metastatic ovarian cancer and platinum-sensitive relapsed small-cell lung cancer , recurrent or persistent cervical cancer , and neuroblastoma . In addition, topotecan is being evaluated in pediatric cancer patients for treating leukemia, lymphoma, Ewing's sarcoma, rhabdomyosarcomas and gliomas (http://www.clinicaltrials.gov). However, the primary dose-limiting toxicity of topotecan is myelosuppression, restricting its use at high doses. Therefore, identification of other chemotherapeutic agents synergizing with topotecan may potentially maintain or increase efficacy while limiting toxicity.
In this study, we performed a loss-of-function synthetic lethal siRNA screening of 418 apoptosis related genes with and without topotecan to identify genes or pathways whose inhibition synergized with topotecan to enhance growth suppression or apoptosis in neuroblastoma. The goal of the study was to identify drugs that would potentially be synergistic when used in combination with topotecan to inhibit the growth of neuroblastoma.
The neuroblastoma cell lines SK-N-AS and SH-SY5Y were maintained in RPMI-1640; and NB-1691 was maintained in DMEM, both supplemented with 10% FBS, 1% penicillin/streptomycin (P/S) and 1% L-glutamine (all from Quality Biological Inc., Gaithersburg, MD) at 37°C. To ensure consistency, a batch of cells was expanded, aliquoted and stored in liquid nitrogen prior to the screening. In each experiment, a vial of cells was defrosted and passaged 1:4 when 70% confluency was reached. Cells between passages 3 and 7 were used for all experiments.
Topotecan hydrocholoride (Hycamtin; GlaxoSmithKline, Philadelphia, PA) and Bortezomib (Velcade; Millenium Pharmaceuticals, Cambridge, MA) were reconstituted and stored according to the manufacturers' instructions. NSC 676914 was obtained from the Developmental Therapeutics Program, Division of Cancer Treatment and Diagnostics, NCI/NIH.
A set of synthetic siRNAs targeting 418 genes related to the apoptotic pathway (Qiagen Apoptosis Set V.1; Qiagen, Valencia, CA), with 2 siRNAs of different sequences per gene, was used for the first screen. For the second screen, 2 new siRNA pre-designed sequences were used (Qiagen). In the third confirmatory screen, one siRNA from each of the previous two screens was chosen. siRNAs were transfected at passage 4. Briefly, transfection reagent Dharmafect 1 (Dharmacon RNA Technologies, Lafayette, CO) was diluted in DCCR reagent medium at a ratio of 1:208 in volume. siRNA (20 nM) and 25 μL of the diluted transfection reagent were added to an individual well in a 96-well plate for complex formation with incubation for 20 min at RT. SK-N-AS cells were trypsinized, counted and resuspended in P/S free culture medium. 5000 cells were added to each individual well in 100 μL medium. The plate was incubated at RT for 30 min for cell attachment before being placed at 37°C for 24 h. Topotecan was then added to each well for additional 72 h incubation. Cell proliferation assay was performed at 96 h post siRNA transfection. The IC50 of topotecan for SK-N-AS cells at 24 h was 2 μM. In the 1st and 2nd screens, topotecan doses of 0, 1, 5 and 10 μM were used, whereas in the 3 rd screen, lower drug doses of topotecan at 0, 0.01, 0.1 and 1 μM were used to identify synergy. The criterion of hit selection for the enhancer genes was ≤0.8 fold cell growth compared to its own siRNA effect in the presence of topotecan. The final enhancer gene list was subjected to pathway analysis for identification of overrepresented genes within a target pathway. An inhibitor to the pathway was chosen and tested individually or in combination with topotecan in vitro and in vivo.
Cell proliferation was measured using Cell Titer Glo proliferation assay (Promega Corporation, Madison, WI) or a real-time cell sensing system (RT-CES; ACEA Biosciences, Inc. San Diego, CA) according to the manufacturer's instruction. We performed cell proliferation assays at a volume of 35 μL per well for 10 min and was measured at 562 nm on a Tecan plate reader (Tecan Inc., Durham, NC). Each treatment was performed in triplicates, averaged and normalized using untreated cells. For real-time cell electronic sensing assays, cells treated with drugs alone or in combinations or transfected with siRNA were added in triplicates to a 96-well plate device compatible with the real-time cell electronic sensing analyzer (RT-CES; ACEA Biosciences, Inc. San Diego, CA). Cell growth was monitored hourly for indicated durations via calculation of "cell index" (normalized impedance) for each well.
SK-N-AS cells were collected at 60 h post siRNA transfection. Total RNA was reverse transcribed using SuperScript II reverse transcriptase system (Life Technologies, Foster City, CA). The target regions were then pre-amplified using a standard PCR for 10 cycles. The pre-amplified cDNA was quantified by Taqman gene expression assay (Life Technologies) using Fluidigm digital array (South San Francisco, CA) according to the manufacturer's protocol. Fold expression was calculated using a comparative threshold cycle method (2-Δ ΔCT) .
The pathway analysis was performed using MetaCore (http://www.genego.com/metacore.php, GeneGo Inc., St Joseph, MI). MetaCore is an integrated software suite for functional analysis of experimental data and it contains curated protein interaction networks on the basis of manually curated database of human protein-protein, protein-DNA, protein-RNA and protein-compound interactions. Metacore uses a hypergeometric model to determine the significance of enrichment. The enhancer genes from our experiment and the genes in the GeneGo maps from the MetaCore database were used to identify the enriched GeneGo pathway maps.
To investigate gene set enrichment, GSEA (http://www.broad.mit.edu/gsea/) was performed for genes, ranked by log2 ratio of gene expressions between topotecan-treated (1 μM and 10 μM) and untreated control SK-N-AS cells, using a weighted Kolmogorov-Smirnov-like statistics . The gene set of NF-κB target genes used in GSEA were downloaded from http://bioinfo.lifl.fr/NF-KB.
Cells were seeded on a 100 mm2 culture dish for overnight and were treated with topotecan alone or with bortezomib. For topotecan alone effect, SK-N-AS were treated with 5 μM of topotecan for 0, 3, 6, or 24 h at 37°C. For the combined effect of bortezomib and topotecan, cells were treated with bortezomib at 0, 1 and 10 nM for 24 h, followed by the addition of topotecan at 5 μM for 6 h. Total cell lysate was collected with RIPA buffer containing 1% phosphatase inhibitor and 1% protease inhibitor (all from Thermo Fisher Scientific, Rockford, IL). Protein concentration was measured by BCA Protein Assay Kit (Thermo Fisher Scientific, Waltham, MA) and protein lysates (20 ug per lane) were resolved on 4-12% TRIS-gradient gel (Invitrogen Life Technologies, Carlsbad, CA) and were transferred to nitrocellulose membranes by iBlot blotting system (Invitrogen Life Technologies). The membranes were blocked with 5% non-fat dry milk in PBS with 0.1% Tween 20 (PBST) for 1 h at RT, followed by incubation with mouse monoclonal antibodies against total or phosphorylated IκB-α (Ser32/36), rabbit monoclonal antibodies against total or phosphorylated p65/RelA or rabbit monoclonal antibody against NFKB1 (all from Cell Signaling Technology, Danvers, MA) at 4°C overnight. Peroxidase-conjugated goat anti-mouse or anti-rabbit antibody was used as secondary antibodies (Santa Cruz Biotechnology, Santa Cruz, CA) for 1 h incubation at RT. Immunoreactive bands were visualized by ECL analysis system (GE Healthcare, Piscataway, NJ) and enhanced chemiluminescence. For loading control, the membranes were washed with Restore Western blot stripping buffer (Thermo Fisher Scientific) and probed with goat anti-human actin HRP conjugated antibody (Santa Cruz Biotechnology).
Neuroblastoma cells were trypsinized, counted and resuspended in P/S free culture medium. 5000 cells per well in 100 μL medium were seeded in 96-well white plates for overnight. Topotecan and NSC 676914 or bortezomib were added individually or in combination at various doses and the plates were incubated at 37°C for 24 h and 48 h respectively. Cell proliferation assay was performed as described above. Combination index was calculated using CompuSyn software (ComboSyn Inc., Paramus, NJ). Briefly, the combination index theorem was used to quantify synergy or antagonism for two drugs by the formula C.I. = (D)1/(Dx)1 + (D)2/(Dx)2, where D1 and D2 are drug 1 and drug 2, and × is growth inhibition by X% .
The caspase-3 activity was measured using the PE Active Caspase-3 Apoptosis kit (BD Pharmingen, San Diego, CA). Briefly, SK-N-AS cells (untreated or treated with topotecan and bortezomib alone or in combination for 24 h) were trypsinized, fixed, and stained with PE rabbit anti-active caspase-3 antibody. Fluorescence intensity was measured by FACS Calibur and data were analyzed using CellQuest software (BD Biosciences, Franklin Lakes, NJ).
All animal experiments have been reviewed and approved by the NIH Animal Care and User Committees. A minimal residual disease xenograft model in mice bearing neuroblastoma was established in 8-10 week-old female SCID Beige mice (Charles River Laboratories, Fredrick, MD). Briefly, five million SK-N-AS cells expressing luciferase (gift from Dr. Bryan Clary, Duke University Medical Center) were injected intravenously via the lateral tail vein into the mice. Tumors were allowed to grow for 7 d, and then mice were randomly assigned to cohorts treated with topotecan and bortezomib administered individually or in combination, or with saline solution (control mice). Bortezomib (0.6 mg/kg) was injected intraperitoneally three times a week for two weeks, rested for two weeks and repeated with another course of treatment. Topotecan (0.5 mg/kg) was injected intraperitoneally five times a week for two weeks, rested for two weeks, followed by another course of treatment. Body weight and general wellness of the mice were monitored, and tumor size was monitored by Xenogen IVIS 100 imaging system (Caliper Life Sciences Inc., Hopkinton, MA). The in vivo xenograft experiment was repeated, and results from two independent experiments were combined (n = 43).
Non-parametric Mann-Whitney test was used to compare among various groups in cell growth assay. For relative luciferase intensity results from two independent in vivo experiments, we normalized the log2 transformed intensities from each experiment using median-centered method and then combined the results. T-test was used to compare the difference of two groups.
Neuroblastoma cell line SK-N-AS was used to screen a siRNA library against 418 apoptosis related genes to identify genes whose inhibition can enhance the effect of topotecan in inhibiting neuroblastoma cell growth. Two siRNAs were initially used against each gene, either alone or in combination with various doses of topotecan. For the first screen, 64 out of the 418 siRNAs potentiated the growth inhibition induced by topotecan at any one of the three doses. To minimize possible off-target effects, the candidate genes were further screened with 2 new siRNA sequences in a second screen, and 18 hits continued to show efficacy. To validate theses hits, we performed a third confirmatory screen by using the two most effective siRNAs for each gene from the two screens and lower doses of topotecan. Nine hits including BIRC4, CTSD, NFKB1, NOS2A, RIPK1, TGFB1, TNFRSF10A, TNFRSF25 and TNFRSF8, were confirmed to potentiate the inhibition of cell growth by topotecan (Table (Table11).
We next explored if there were any signaling pathways associated with these nine hits using MetaCore (see Methods). The top of the list was anti-apoptotic TNFs/NF-κB/IAP pathway (p = 6.03E-06; Table Table2).2). Out of the total 27 curated genes in this pathway, five of them were among the nine hits, including BIRC4, NFKB1, RIPK1, TNFRSF25 and TNFRSF8. The knockdown on these five target genes by siRNAs was confirmed using Taqman assays (Figure (Figure1A).1A). Therefore we hypothesized that the NF-κB pathway might be activated as a response to topotecan in SK-N-AS cells. To test this hypothesis, we performed Gene Set Enrichment Analysis (GSEA)  on microarray gene expression data of SK-N-AS cells treated with topotecan to determine if there was enrichment for NF-κB target genes (http://bioinfo.lifl.fr/NF-KB/). We found that these NF-κB target genes were significantly up-regulated in the leading edge subset genes in the GSEA analysis in the topotecan-treated cells (p < 0.0001; Figure Figure1B).1B). Because activation of the NF-κB pathway results in degradation of IκB-α (through phosphorylation) and increase of p65/RelA phosphorylation, we further examined the effect of topotecan on the NF-κB pathway using Western blotting for these two key components of the pathway. Indeed, the Western blotting showed decreased amount of total IκB-α and increased phosphorylation of p65/RelA after topotecan treatment, confirming activation of NF-κB by topotecan (Figure (Figure1C).1C). These results suggested that the NF-κB pathway was activated by topotecan possibly as a protective mechanism against topoisomerase-I inhibition resulting in single stranded DNA breaks. To verify if the up-regulation of NF-κB pathway was protective from topotecan-mediated growth inhibition, we specifically knocked down NFKB1, another key component in the pathway, by siRNA. Knocking down NFKB1 resulted in further inhibition of cell proliferation in topotecan-treated cells (p < 0.01, Figure Figure1D),1D), and a Western blot confirmed the effective knockdown of NFKB1 by the siRNA at the protein level (Figure (Figure1E).1E). Taken together, our results indicated that combination of topotecan with a NF-κB inhibitor might be synergistic, and this synergistic effect provided a rational combination therapy against neuroblastoma.
In order to examine if the cell growth inhibition in neuroblastoma mediated by topotecan can be synergized with NF-κB pathway inhibition, we tested a specific NF-κB inhibitor, NSC 676914  and a FDA approved proteasome inhibitor which also inhibits the NF-κB pathway, bortezomib, in combination with topotecan. We tested these combinations in SK-N-AS and two additional neuroblastoma cell lines NB-1691 (MYCN amplified) and SH-SY5Y (MYCN non-amplified) to ensure that the synergistic effect was not specific to any cell line. We first measured the IC50 of topotecan and NSC676914 in these cells at 24 hours, and they were 2 μM and 7 μM for SK-N-AS; 550 nM and 4 μM for NB-1691; 200 nM and 2 μM for SH-SY5Y respectively. Sub-IC50 doses of topotecan and NSC 676914 were then used in combination in all three cell lines and the combination index was calculated for each dose combination . All the combination treatment data points in normalized isobolograms were away from the diagonal additive line and towards the origin indicating that low doses of NSC676914 and topotecan act synergistically in all three cell lines (Figure (Figure2A).2A). To facilitate future translation of our findings to the clinic, we tested bortezomib, an FDA-approved drug known to inhibit NF-κB as one of its mechanisms, in the subsequent in vitro and in vivo studies. In addition, this drug has been reported to inhibit all of the top four pathways identified in our synthetic lethal screen (Table (Table2)2) [20-22]. Therefore, we predicted bortezomib would have synergistic effects in combination with topotecan in neuroblastoma cells. To test this hypothesis, we first measured the IC50 of bortezomib for these three cell lines at 24 hours as 7 nM, 3.5 nM and 3.5 nM for SK-N-AS, NB-1691 and SH-SY5Y respectively. As expected, we found from normalized isobolograms that sub-IC50 doses of topotecan and bortezomib acted synergistically to inhibit cell growth as the data points in normalized isobolograms were also away from the diagonal additive line (Figure (Figure2B).2B). This synergistic inhibitory effect between topotecan and bortezomib was confirmed in an independent experiment using electronic cell sensing to monitor cell growth (P < 0.01) (Figure (Figure2C).2C). Furthermore, we were able to detect an increase in apoptosis with the combination of topotecan and bortezomib as evidenced by elevated caspase-3 activity (Figure (Figure2D).2D). To confirm that bortezomib enhances topotecan-induced growth inhibition through NF-κB pathway, Western blotting was performed to show that SK-N-AS cells treated with both bortezomib and topotecan inhibited the degradation of total IκB-α protein, suggesting that the NF-κB was indeed inactivated (Figure (Figure2E).2E). Taken together, these data demonstrated that topotecan and NF-κB inhibitors could synergistically inhibit growth through inhibition of the NF-κB pathway and induction of apoptosis in neuroblastoma cells.
In order to investigate the synergistic effect of topotecan and bortezomib in vivo, we tested the drug combination in SCID beige mice bearing human neuroblastoma xenografts. SK-N-AS cells were intravenously injected into the mice and monitored by Xenogen. Treatments started seven days after injection, and our treatment scheme encompassed only two courses of drug administration allowing us to focus on the immediate effect of the drug combination on tumor formation and progression. One week after the first course of treatment, tumors were observed in mice treated with control and bortezomib alone. By the end of the second course of treatment, these mice became morbid and were euthanized (data not shown). We also found that the mice treated with combination of topotecan and bortezomib showed a delay in tumor progression when compared to mice treated with topotecan alone (Figure (Figure3A).3A). Results from two independent in vivo experiments showed that the relative luciferase signals from tumor cells were significantly decreased in mice treated with combination of topotecan and bortezomib (p = 0.01; Figure Figure3B).3B). Therefore, we concluded that combination therapy of topotecan and bortezomib caused a significant reduction of tumor growth compared to individual drugs alone, which confirmed our hypothesis that bortezomib potentiated the effects of topotecan, via targeting the NF-κB pathway as one mechanism together with the topoisomerase-1 inhibition.
More than half of the neuroblastoma patients over 1 year old have advanced metastatic disease at the time of diagnosis . For these patients, the overall survival rate remains less than 50%. Therefore, a new therapeutic strategy is critically needed. Current treatment regimens used in high risk neuroblastoma include topotecan, a topoisomerase I inhibitor and cyclophosphamide, a nitrogen mustard alkylating agent. Cyclophosphamide induces DNA cross-linking and DNA single-strand breaks; while topotecan inhibits religation of the topoisomerase I-mediated DNA single-strand breaks. Both result in increased numbers of strand breaks and stabilization of these unrepaired breaks, leading to enhanced cytotoxicity. The combination was first proven effective in a phase II trial in neuroblastoma, in which there were six partial responses in 13 patients with neuroblastoma with the combination of cyclophosphamide and topotecan compared with two responses (one complete and one partial) in 37 patients treated with topotecan alone.. Subsequently, topotecan together with other topoisomerase inhibitors have become the basis of many salvage regimens and is being evaluated as up-front therapy in ongoing trials in neuroblastoma and other cancers.
Here we utilized a high throughput loss of function approach using siRNAs to identify genes whose inhibition would synergize with topotecan with the ultimate goal of discovering potent synergistic drug combinations for treating patients with neuroblastoma. SiRNA screening can identify genes, and pathways critical for cancer cell growth and survival. This approach provides a rational method of choosing inhibitors to target the identified genes and pathways. The objective of combination chemotherapy is to simultaneously target multiple pathways that are important for cancer cell growth and survival, in the hope to synergistically inhibit tumor cell growth. In our study, there was an enrichment of NF-κB pathway genes in the positive hits and an induction of NF-κB gene signature upon treatment with topotecan. This pathway plays an important role in inflammation, autoimmune response, cell proliferation, and apoptosis depending on the cell type and context . In cancers including neuroblastoma, the NF-κB pathway is found to activate transcription of genes encoding tumor-promoting cytokines, playing critical roles in neoplastic transformation and cancer cell survival . Hence, targeting this signaling pathway should be effective for growth inhibition and increasing apoptosis for cancers. However, NF-κB inhibitors are generally used as adjuvants because inhibition of NF-κB alone may be insufficient for a pronounced apoptotic response unless it is combined with apoptosis-inducing drugs or radiation . Our results indicated that the NF-κB pathway was activated as a possible protective mechanism against topoisomerase-I inhibition resulting in single stranded DNA breaks. This together with our siRNA screening results suggested that the combination of topotecan and an NF-κB inhibitor might be a good combination to kill neuroblastoma cells.
In this study, we found that a specific NF-κB inhibitor, NSC 676914, synergized growth inhibition mediated by topotecan in both MYCN and non-MYCN amplified neuroblastoma cell lines. NSC 676914 has been identified as a novel, specific and stable small-molecular NF-κB inhibitor through the inhibition of IKK-β to induce growth inhibition of multiple myeloma cells in vitro and in vivo [19,26]. Our findings were consistent with a recent publication which suggested that inhibition of NF-κB pathway could lead to increased chemosensitivity . In addition, we used bortezomib, a FDA-approved drug known to have NF-κB inhibition effects through preventing IκB-α protein degradation in the proteasome , for the subsequent in vitro and in vivo studies. Bortezomib, the first FDA-approved proteasome inhibitor, is a boronic-acid derivative that reversibly inhibits the active sites in the 20S proteasome [29,30]. Down-regulation of NF-κB pathway is its prevailing mechanism of action in multiple myeloma and relapsed mantle cell lymphoma . In addition to NF-κB inhibition, bortezomib has been shown to inhibit other pathways which may partially contribute to the effect observed in this study. For example, the topoisomerase I cleavable complex also serves as a substrate for the proteasome , an inhibitory target of bortezomib. Stabilization of these complexes has been shown to enhance the cytotoxic effect of another topoisomerase I inhibitor camptothecin, an analog of topotecan . Furthermore, bortezomib inhibits tumor growth, causing cell cycle arrest in colon, ovarian, breast, renal cell and pancreatic carcinomas , as well as in lymphomas and leukemias and pediatric tumors including neuroblastoma in vitro and in vivo .
Our in vivo xenograft experiments demonstrated a delay in tumor progression when topotecan was combined with bortezomib. Therefore, bortezomib could be a logical choice of NF-κB inhibitors to be used with topotecan as a rational combination therapy. With regards to drug toxicity, myelosuppression, primarily reversible, noncumulative neutropenia, is the predominant toxicity observed with topotecan treatment [11,36]. For bortezomib, while peripheral neuropathy is the most often seen toxicity, recent study suggests that it is manageable and reversible . Bortezomib-induced thrombocytopenia and neutropenia are cyclic, reversible, typically do not lead to treatment discontinuation and recover prior to initiation of the subsequent cycle [38,39]. The combination of topotecan and bortezomib is currently under investigation in clinical trials for other advanced solid tumors in adults . Thus this combination should be well tolerated in patients with neuroblastoma.
In conclusion, our synthetic lethal siRNA screening led to the discovery that NF-κB inhibition synergized cell death when used with topotecan in neuroblastoma. Furthermore we showed that the NF-κB pathway was induced in neuroblastoma cells treated with topotecan. Finally we demonstrated evidence of the synergistic effects of topotecan and bortezomib in in-vitro and in a pre-clinical mouse model. Our study therefore provides the rationale for future clinical trials evaluating this combination therapy for patients with high risk neuroblastoma.
The authors declare that they have no competing interests.
PT contributed to conception and design, acquisition, interpretation and analysis of the results, and wrote the manuscript. AC contributed to the design of the in vivo experiment and carried out a subset of experiments. QC contributed to conception and performed the pathway analysis; gene set enrichment analysis and statistical analyses. YKS contributed to a subset of experiments. TB revised the manuscript. JSW contributed to conception, design, and interpretation of the results for the study; and revised the manuscript. JK devised and directed the study. All authors read and approved the final manuscript.
The pre-publication history for this paper can be accessed here:
We would like to thank Dr Paul Meltzer, Dr Natasha Caplen and Dr Scott Martin for providing the siRNA library and for useful discussions; and Dr David Azorsa for helpful technical advice. This work was supported by the Intramural Research Program of the National Institutes of Health, National Cancer Institute, Center for Cancer Research. The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. government.