- Open Access
Genetically modified "obligate" anaerobic Salmonella typhimurium as a therapeutic strategy for neuroblastoma
Journal of Hematology & Oncology volume 8, Article number: 99 (2015)
Neuroblastoma currently has poor prognosis, therefore we proposed a new strategy by targeting neuroblastoma with genetically engineered anaerobic Salmonella (Sal-YB1).
Nude and nonobese diabetic-severe combined immunodeficiency (NOD-SCID) orthotopic mouse models were used, and Sal-YB1 was administered via tail vein. The therapeutic effectiveness, bio-safety, and mechanisms were studied.
No mice died of therapy-related complications. Tumor size reduction was 70 and 30 % in nude and NOD-SCID mice, respectively. No Salmonella was detected in the urine; 75 % mice had positive stool culture if diaminopimelic acid was added, but all turned negative subsequently. Tumor tissues had more Sal-YB1 infiltration, necrosis, and shrinkage in Sal-YB1-treated mice. Significantly higher expression of TLR4, TNF-stimulated gene 6 protein (TSG6), and cleaved caspase 1, 3, 8, and 9 was found in the tumor masses of the Sal-YB1-treated group with a decrease of interleukin 1 receptor-associated kinase (IRAK) and nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor alpha (IκBα). There was a high release of TNFα both in human macrophages and mouse tumor tissues with Sal-YB1 treatment. The antitumor effect of the supernatant derived from macrophages treated with Sal-YB1 could be reversed with TNFα and pan-caspase inhibitors.
This new approach in targeting neuroblastoma by bio-engineered Salmonella with the assistance of macrophages indirectly may have a clinical therapeutic impact in the future.
Neuroblastoma is an aggressive pediatric malignant tumor with high variability in biological and clinical behaviors [1–3]. Despite intensive multi-modality therapies, the outcome of advanced stage neuroblastoma remains extremely poor. Novel therapeutic approach to improve the survival of this group of children is urgently needed.
It is known that cancer stem cells remain viable in the hypoxic tumor core with minimal blood supply. Hence, this affects the drug delivery and has been considered a resistant mechanism to conventional chemotherapy for cancer [4–7]. Attenuated pathogens such as Salmonella typhimurium and measles virus have been adopted as a form of biotherapy among the burgeoning anti-cancer strategies [8–10]. However, many of such “bio-bullets” still face the challenge of balance between potential side-effects and anti-cancer effectiveness [11, 12]. Systematically evaluating their effectiveness and safety prior to their actual clinical application to cancer patients is mandatory. To overcome such adversity and also mimic the actual disease characteristics, we proposed to use a genetically engineered anaerobe S. typhimurium strain YB1 (Sal-YB1) as a form of biotherapy for the intra-adrenal orthotopic xenograft human neuroblastoma mouse models using either nude or nonobese diabetic-severe combined immunodeficiency (NOD-SCID) mice .
The genetically modified Sal-YB1 can only proliferate in hypoxic environment (oxygen <0.5 %) . Otherwise, it must be supplemented with diaminopimelic acid (DAP) when it is cultured under aerobic condition [12, 13]. For bacteria, DAP is an indispensible component in the synthesis of cell wall. In the wild type Salmonella strain, DAP is normally developed by the essential gene asd. The expression of asd is modified and regulated by the hypoxia-conditioned promoter in the Sal-YB1 strain. Compared with the two more commonly used VNP20009 and SL7207 Salmonella strain, this genetically modified Sal-YB1 exhibited excellent in vivo cytotoxic effect and had low therapy-related death rate on a human breast cancer model .
The orthotopic mouse model has been developed by implanting neuroblastoma into the fat pad of the mice adrenal glands, which is the most common primary site of neuroblastoma in patients. This xenograft model could simulate the actual microenvironment of the tumor. Furthermore, nude mouse together with NOD-SCID mouse model are relatively robust tools to mimic the deficient immune states of patients undergoing chemotherapy [14, 15]. There are specific immune deficiencies found in both the nude and NOD-SCID mouse. For example, the nude mouse cannot generate mature T lymphocytes whereas the NOD-SCID mouse has deficient T- and B-lymphocytes; abnormal natural killer (NK) cells and macrophages (MΦ) both in terms of numbers and function. The neuroblastoma cell line SK-N-LP/luciferase that we used is transduced with the luciferase gene. The bioluminescence is closely correlated to the tumor growth under in vivo imaging system Xenogen 100 (IVIS 100).
In the present study, we chose the new generation Sal-YB1 as the mono-biotherapy for the orthotopic murine models using mice with different immunological backgrounds. Our purpose was to investigate the therapeutic effectiveness and biosafety on both kinds of mice when they were treated with virulent bacteria. The possible immunological mechanism was also explored to guide our clinical application of this potential “bio-bullet”—Sal-YB1.
Orthotopic neuroblastoma mouse models with or without Sal-YB1 treatment
Ten nude mice and ten NOD-SCID mice were implanted with human neuroblastoma initially. However, before the Sal-YB1 treatment was started, both groups had one mouse each which died due to paralysis. The paralysis was subsequently due to metastasis of orthotopic adrenal neuroblastoma cells to the brain within 2 to 3 weeks. Three-week post-tumor cells transplantation, the nude (n = 8) and NOD-SCID (n = 8) mice were divided into two groups. At week 2 after inoculation with or without Sal-YB1, all mice survived. Rate of region of interest (ROI) change was significantly different within either nude or NOD-SCID mice and also between these two groups (P < 0.05). The post mortem tumor size increase rate post-YB1 treatment was reduced to 30 % in nude mice and 70 % in NOD-SCID mice (Fig. 1). Such reduction was mainly due to tumor necrosis as suggested in the following paragraphs.
Mouse body weight and temperature were recorded daily. The urine and stool were also collected daily for 2 weeks after Sal-YB1 was administered. Although the body weight declined in the initial 2 days post-YB1 injection, the nude and NOD-SCID mice of the treated group regained body weight from day 3 onwards. Body surface temperature showed no obvious change during the treatment course. On the first day post-YB1 injection, we could still observe that the mice turned inactive. Rash could be transiently found on the skin of nude mice, but it was relatively difficult to observe in NOD-SCID due to the presence of fur. These febrile reactions might reflect transient bacteremia-triggering immune reaction. However, they have no evidence in inducing organ damage as reflected by the tissues examination when the mice were sacrificed.
Ex vivo Sal-YB1 side effect evaluation on mouse models
Flow cytometry, hematoxylin and eosin (H&E), and immunohistochemistry (IHC) staining were applied to evaluate the cytotoxic activities and tissue distribution of Sal-YB1. Sal-YB1-treated tumor tissues showed necrosis, which was tested by annexin V/PI assay and H&E staining (Fig. 2a, b). IHC staining revealed that Sal-YB1 formed clusters within the tumor mass (Fig. 2c) for both nude and NOD-SCID mice without too much differences in their extent of necrosis. It is interesting to note that there are more late apoptotic cells (annexin V+/PI+) for the nude mice but relatively more early apoptotic cells (annexin V+/PI−) for the NOD-SCID mice as found in the annexin V/PI assay. However, the total numbers of apoptotic cells (annexin V+/PI− plus V+/PI+) were more for the nude mice group (Fig. 2d). The findings suggested that tumor in nude mice is more susceptible to Sal-YB1 treatment, reflecting some other factors relating that the immune system might play a role in the anti-tumor effect.
Salmonella was not detected in the urine. However, 75 % of the mice had positive Sal-YB1 in their stool. They all turned negative within 2 weeks. Particularly, Salmonella was undetectable in stool colony-forming unit (CFU) test without DAP supplement suggesting that these residual Sal-YB1 found in the stool will not be able to survive and proliferate when they were passed under normoxic environment. No matter if mice with tumor implantation or not, both nude and NOD-SCID group did not have Sal-YB1 detected in the heart, spleen, liver, lung, kidney, brain, spinal cord, and blood at 2 weeks post-treatment. However, hepatosplenomegaly was observed in Sal-YB1-treated mice but there was no evidence of either inflammation or necrosis as shown by annexin V/PI and H&E stain.
Sal-YB1 therapy mechanism on neuroblastoma
Sal-YB1 could significantly upregulate Toll-like receptor 4 (TLR4) expression in tumor tissues by flow cytometry. Interleukin 1 receptor-associated kinase (IRAK) (P < 0.05) and nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor alpha (IκBα) (P < 0.001) were downregulated in the xenograft triggered by Sal-YB1 as shown by Western blotting (Fig. 3). There were high release of TNFα from both human macrophage and mouse tumor tissues in the Sal-YB1-treated group as shown by ELISA (P < 0.05). The expression of TNFα in nude mice and 2-day hypoxia-cultured macrophages were significantly higher than that of the NOD-SCID mice (Fig. 4a) and normoxia-cultured macrophages (Fig. 4b), respectively. Besides, the Sal-YB1 could only be detected in hypoxia-cultured macrophages by CFU counting. The viability of neuroblastoma was decreased when co-cultured with 50 % supernatant of the YB1 pre-treated macrophages (P < 0.01); however, it could be rescued by TNFα inhibitor (P < 0.01) (Fig. 4c, d). These data suggested that the endotoxin (LPS) from salmonella could activate the TLR4 and the downstream signalling pathway leading to the release of TNFα by macrophages and the TNFα will subsequently induce indirect tumor cell killing in the cancer microenvironment.
Using the supernatant from Sal-YB1 pre-treated macrophages or Sal-YB1 direct treatment on neuroblastoma could induce apoptosis as shown by the JC-1 assay (Fig. 5). This finding implies the involvement of the intrinsic apoptotic pathway. Sal-YB1-treated mouse tumor tissues showed high expression of caspase 3 by flow cytometry (Fig. 6a). Cleaved caspase 1 (p20) (P < 0.05), cleaved caspase 3 (p17, 19) (P < 0.01), cleaved caspase 8 (p18, 43) (P < 0.05), cleaved caspase 9 (p37, 39) (P < 0.05), and TNF-stimulated gene 6 protein (TSG6) (P < 0.05) could be significantly identified in Sal-YB1-treated tumor mass by Western blotting (Fig. 6b–g). Pan-caspase inhibitor could block the apoptosis of neuroblastoma, which is treated by post-activated macrophage culture supernatant (P < 0.001) and Sal-YB1 (P < 0.05) (Fig. 4e, f). These findings further supported that the TNFα by macrophages induced indirect tumor cell killing in the cancer microenvironment via caspase-dependent apoptotic pathway.
In the past decades, the paradigms of cancer treatments are mainly based on surgical resection, irradiation, chemotherapy, immunotherapy, and targeted therapy. There are also advocates on using alternative approaches including homeopathic therapy, hyperthermia, or some other strategies but all with doubtful impact [16, 17]. Neuroblastoma is the most common childhood extracranial solid tumor derived from neural crest cells [2, 18]. Although a minority of cases spontaneously regress, more than half of the children suffered from metastatic disease at diagnosis, and they have poor prognosis despite current therapeutic approaches [19–21].
Recently, novel treatment such as using an attenuated measles virus to patients with disseminated myeloma raised the possibility of applying biotherapy with genetically modified microorganism . Such approach has been attempted, but its clinical application has been limited by low efficacy and potential adverse effects. Currently, SL7207 has been tested as a form of lived bacterial vaccine in pre-clinical studies [22–24]. Here, we proposed a novel treatment strategy by using an engineered anaerobe Salmonella strain Sal-YB1. Such “bio-bullet” has a survival advantage in a hypoxic environment, which is a common phenomenon within the cancer core where the cancer stem cells reside. Similar to most stem cells, cancer stem cells thrive better in a hypoxic environment. Therefore, Sal-YB1 may overcome the current limitations of conventional treatment by getting rid of the cancer cells within the hypoxic microenvironment. Sal-YB1 only replicates under a hypoxic environment and therefore is unlikely to cause serious infection in the recipient. Furthermore, any potential infection can also be easily controlled by conventional antibiotics. Compared to chemotherapy, it has the advantage of having less off-target organ toxicity. In addition, unlike measles virus therapy, the issue of immune rejection effect of Salmonella is unlikely as there is no routine vaccination for Salmonella. As in our animal model, Sal-YB1 can effectively target at the tumor mass with minimal side effect on the mice.
How the Sal-YB1 induced cell death of cancer such as neuroblastoma cells remains unknown. There may be direct or indirect effects on the cancer cells. To find out the likely influence of the host immune system on such cytotoxicity, we make use of two different types of immune-deficient mice to find out the possible involvement of the host immune system. Nude mice (deficient in T cells) and NOD-SCID mice (deficient in T, B, NK cells, and MΦ) were used in our orthotopic xenograft neuroblastoma mouse model [14, 15]. The mice were applied to mimic the induced immune-deficient state of cancer patients after chemotherapy. Despite the severe immune-deficient state of the mice, none of them died of infection. Interestingly, we noted a much higher tumor necrosis rate among nude mice than NOD-SCID mice, suggesting the contribution of non-T immune cells in the event. On the first day post-YB1 injection, we observed that all the mice turned inactive and four nude mice developed transient skin rash, suggesting transient bacteremia associated with immune activation leading to inflammation. All the mice subsequently regained their body weight 3 days after Sal-YB1 inoculation. As the treatment effect was demonstrated in the mice, the increased body weight should not be contributed by the progression in tumor burden especially compared to the control group. While we know that wild type Salmonella can cause infection, or even a chronic carrier state, in people with normal immunity, our findings suggested that the anaerobic Sal-YB1 is safe even if applied to these severely immune-deficient mice. But whether Sal-YB1 may be rejected by immune-competent mice remains unanswered. Testing of such an approach on transgenic mice with spontaneous neuroblastoma development may help to answer this question. However, we can adopt this approach as an adjuvant to chemotherapy. Then, the immune rejection issue will be resolved because chemotherapy can induce an iatrogenic immune-deficient state.
Referring to the bio-safety concern of potential Salmonella-induced environmental pollution, the excreta was screened. There was no Salmonella found in the urine of the mice. Seventy-five percent of mice showed positive Sal-YB1 in their stool, but they all turned negative within 2 weeks. The genetically modified Sal-YB1 can only proliferate under hypoxic condition or by supplementing with DAP under aerobic condition. The usual Sal-YB1 detection was by using DAP-supplemented plate in normal incubation at 37 °C. Here, we double-checked the stool by parallel DAP-free CFU test. Unlike detection rate in DAP+ plate, Sal-YB1 is nearly undetectable in DAP-negative stool culture. Therefore, the worry of Salmonella causing environmental pollution remains theoretical.
We further explored the possible mechanism of Sal-YB1-induced cytotoxicity in vivo (Fig. 7). Increased TLR4 expression may account for the resistance of mice to Gram-negative bacterial infection, for it elicits stronger immune response from the host [25, 26]. Tumor necrosis factor can enhance the lethal effect of endotoxin in mice, but there is no difference in TNFα expression in S. typhimurium-infected TLR4+/− mice [27, 28]. Gram-positive and -negative bacteria could both activate MyD88/IRAK/IKK/NFκB signalling pathways [29, 30]. Our data showed that Sal-YB1 could upregulate TLR4 expression in the tumor tissues. The direct cytotoxicity was observed via the activation of TLR4. The treatment effect was significantly different between nude and NOD-SCID mice. It is probably due to the number and function of B cell, NK and macrophages are relatively preserved in the nude mice [31, 32]. Our investigation suggested that the indirect anti-cancer effect of Salmonella was due to the activation of macrophages. To test our hypothesis in vitro, we treated the human macrophages with Sal-YB1 and found that Sal-YB1 had significant direct stimulatory effect on macrophages. Then, we collected the supernatant from the macrophages and co-cultured it with human neuroblastoma cells. The viability of neuroblastoma was significantly decreased in the group co-cultured with the supernatant derived from macrophages pre-treated with Sal-YB1. Moreover, there was a high release of TNFα from both human macrophages and mouse tumor tissues in the Sal-YB1-treated group. TNFα and pan-caspase inhibitors could both reverse the anti-neuroblastoma effect induced by macrophages. TNFα release from macrophages as suggested by our in vitro and in vivo experiments is likely to be one of the cytotoxic components found in our animal model. Our results highlighted that the anti-tumor function of Sal-YB1 therapy was mediated via TLR signalling pathway and the activation of IRAK and IκBα are determinant for TNFα release. The TNFα could further trigger the expression of caspase 1 and 8 [33, 34]. Caspase 1 could induce the mitochondria to release caspase 9 through the complex multistep process. Both caspase 8 and 9 could activate caspase 3-induced apoptosis [35–38]. On the contrary, TSG6, the negative feedback loop during the inflammatory/apoptosis network, could be upregulated by LPS and TNFα [39, 40]. These downstream apoptotic related proteins could all be detected to have enhanced expression in our nude mice tumor tissues. Thus, one of the possible mechanisms of Sal-YB1-induced cytotoxic effect on neuroblastoma may be due to the activation of macrophages by Sal-YB1.
The limitation of the current study is that the status of immunodeficient mice is not totally similar to the post-chemotherapy-treated immunosuppressed mice for they are often having neutropenia as well. Currently, there are several mouse models with spontaneous neuroblastoma development such as those with amplified MYCN  or mutated ALK . In future study, we can make use of such models to simulate the actual clinical setting and test our approach. Our proposed possible underlying mechanisms can also be revisited and verified.
In conclusion, our approach provides a new paradigm in targeting cancer cells residing within the hypoxic microenvironment. Even in mice with severe immune-deficient backgrounds such as nude or NOD-SCID, the Sal-YB1 could still induce tumor necrosis without causing severe infection. The macrophages recruited by Sal-YB1-directed therapy may play a significant role in fighting against the cancer. Even Sal-YB1 is not tumor specific, it helps to control both primary refractory tumors and metastatic tumors via direct and indirect pathways. Sal-YB1 can also serve as a therapeutic vector in carrying drugs to poorly vascularized hypoxia regions, so it may open up another new frontier in eradicating cancer in the future.
Culture of Salmonella strains SL7207 and YB1
S. typhimurium strain YB1 was kindly provided by Prof. JD Huang. Sal-YB1 was cultivated at 37 °C in Luria-Bertani (LB) broth (USB, Cleveland, USA) containing 25 μg/mL chloramphenicol, 50 μg/mL streptomycin (Sigma-Aldrich, St. Louis, USA), and 50 μg/mL DAP (DACO, Tokyo, Japan). OD600 was measured to determine the bacterial count. The final calculation was based on 1 OD unit of bacteria medium equivalent to 109 bacteria.
Maintenance of human neuroblastoma cell lines and macrophages
SK-N-LP/luciferase cell line passages 7–10 were cultured in Dulbecco’s modified Eagle’s medium-high glucose (DMEM-HG), supplemented with 100 U/mL penicillin, 100 mg/mL streptomycin (Invitrogen, New York, USA), 10 % heat-inactivated fetal bovine serum (Hyclone, Logan, USA), and 1000 μg/mL G418 (Roche, Mannheim, Germany). Macrophages were isolated from healthy human peripheral blood mononuclear cell and kept in RPMI 1640 (Invitrogen, New York, USA) medium containing 5 % autologous serum and 1 % penicillin-streptomycin. The medium was renewed every other day. Normal incubator was supplied with a humidified atmosphere at 37 °C with 5 % CO2, but the hypoxic chamber was precalibrated with less than 0.5 % O2.
Establishment of orthotopic neuroblastoma mouse model and treated with Sal-YB1
Four-week-old male nude and NOD-SCID mice were purchased from the Laboratory Animal Unit of the University of Hong Kong with the approval of the Hong Kong Department of Health and Committee on the Use of Live Animals in Teaching and Research of the University of Hong Kong (CULATR 2587-11 and 2887-12). Mice were routinely anesthetized and disinfected for abdominal operation. With the surgical operation microscope, 2E+05 SK-N-LP/luciferase cells diluted in 50 % Matrigel (BD Biosciences, San Diego, USA) were administered directly to the fat pad of the mice’s left side adrenal glands. By intraperitoneal injection of the luciferin (Invitrogen, New York, USA), the xenograft condition (no more than 4000 mm3) was monitored via Xenogen in vivo imaging system bi-weekly. The ROI was generated automatically, and its value was normalized under the luminescence interval 12,256 to 2.4512E+07. Three weeks post-tumor cells transplantation, the mice were divided into two groups according to the similar tumor ROI value. Sal-YB1 (5E+07 CFU) dissolved in 100 μL PBS was inoculated via the tail vein of the mice, whereas the control group was treated with 100 μL PBS only. The body weight and temperature were recorded and also the urine and stool were collected daily for 2 weeks. Then, the mice were sacrificed by an overdose of pentobarbital. Tissues of the tumor, heart, lung, spleen, liver, kidney, brain, and spinal cord were harvested for extro-vivo experiments. The length, width, and height of the tumor were measured for the calculation of the final xenograft volumes, using formula: 4/3 × π (Length × Width × Height)/8.
Around 1–2 cm3 tissues of the tumor, heart, lung, spleen, liver, kidney, brain, and spinal cord were resected and immediately immersed in 4 % paraformaldehyde for overnight fixation. Paraffin-embedded block was sectioned into approximately 4 μm slices and mounted on polylysine pre-coated slide. H&E staining was performed to examine the overall structure and necrosis of the tissues. Salmonella distribution was detected with rabbit anti-Salmonella (Abcam 35156, Cambridge, UK). Bound primary antibody (1:700) was detected with horseradish peroxidase-conjugated goat anti-rabbit secondary antibody (1:8000) and then developed in DAB solution (DACO, Tokyo, Japan). Pictures were taken under a ×200 light microscope.
LB agar plates containing 25 μg/mL chloramphenicol and 50 μg/mL streptomycin were prepared with ±50 μg/mL DAP supplement. Ten microliters of urine, blood, and bile were pipettied on DAP+ plate. Stool and tissues of the tumor, heart, lung, spleen, liver, kidney, brain, and spinal cord were weighed, homogenized, serially diluted in PBS, and plated on the previous descried LB agar plates. Salmonella colonies were counted after 12–18 h incubation at 37 °C.
Salmonella targeting neuroblastoma/macrophages in vitro
SK-N-LP/Luciferase cells were cultured in antibiotic-free DMEM medium the day before they were co-cultured with Salmonella at a ratio of 1:500. Salmonella was eliminated by adding 500 μg/mL gentamycin-supplemented medium for 20–30 min 2–2.5 h later. Then, the cells were replenished with DMEM containing 100 μg/mL gentamycin under a normoxia incubator or a precalibrated hypoxic chamber (O2 < 0.5 %). Similarly, the DMEM was changed to RPMI1640 for macrophages, and the supernatant of macrophages was also collected after 2 days. Fifty percent supernatant of the YB1 pre-treated macrophages was supplemented to the SK-N-LP/luciferase cells for another 2 days.
XTT cell proliferation assay
SK-N-LP/luciferase cells were seeded in a 96-well plate (around 4000 cells/well). After overnight culture, SK-N-LP/luciferase cells were pre-treated with DMSO, TNFα antibody (Sigma-Aldrich, St. Louis, USA), caspase 1 (Biovision, San Diego, USA), and pan-caspase (Calbiochem, Darmstad, Germany) inhibitors for 2 h, respectively. The viability of neuroblastoma with Salmonella or macrophages supernatant treatment was observed by XTT kit (Roche, Mannheim, Germany) for three continuous days or after 2 days, respectively. The optical density was measured using a microplate reader at wavelength 450 nm.
For the JC-1 (BD, San Diego, USA) analysis, the experiment involved one no-treatment negative control arm and two experimental treatment arms. The two treatment arms involved 1 or 2 days treatment, respectively, as illustrated in the following. The no-treatment control served as a control for comparison of both 1- and 2-day treatment with Sal-YB1. The data were analyzed by using FlowJo 8.8.2.
|Day 1||Seed cells||Well 1||Well 2||Well 3|
|Day 2||Treatment to well 3||–||–||+|
|Day 3||Treatment to well 2||–||+||+|
|Day 4||Flow (JC-1)||Control group||1-day treatment group||2-day treatment group|
Mouse tissues of the tumor, heart, lung, spleen, liver, kidney, brain, and spinal cord were weighed, homogenized, and filtered with 70 μm cell strainer on ice. Suspension containing around 5E+04 single cells was prepared to perform flow cytometry within 1 h. The apoptosis of neuroblastoma triggered by Sal-YB1 was analyzed by annexin V/PI (BD, San Diego, USA). Annexin V+/PI−, annexin V+/PI+, and annexin V−/PI+ cells are divided as early apoptosis group, late apoptosis group, and dead group, respectively. The TLR4 expression induced by Sal-YB1 was detected by anti-human CD284 (TLR4) PE (HTA 125), using mouse IgG2a K isotype control PE (eBM2a) (Ebioscience, San Diego, USA). The count of TLR4 positive expression rate was gated according to the isotype control. The FITC active caspase 3 apoptosis kits were purchased from BD Pharmingen. The data were analyzed by using FlowJo 8.8.2.
Approximately 1.5 g tumor tissues were homogenized, filtered, and centrifuged at 4 °C. Concentration of TNFα in the collected supernatant was measured using mouse TNFα ELISA kit (Ebioscience, San Diego, USA) according to the manufacturer’s instructions. Macrophages were seeded in a 24-well plate (around 5E+05 cells/well). The supernatant of macrophages with/without Sal-YB1 treatment was detected by human TNFα ELISA kit (R&D Systems, Minneapolis, USA). The optical density was measured using a microplate reader at wavelength 450 nm with correction at 570 nm.
Cell lysis, SDS-PAGE, and Western blotting
Approximately 5 mg tumor tissues were weighed, homogenized, and lysed directly with radio immune precipitation assay buffer for 2 h with constant agitation in cold room. Lysates were clarified by centrifugation for 20 min at 12,000 rpm at 4 °C, and the protein concentrations were quantificated by protein assay kit (Bio-Rad, Hercules, USA). SDS-PAGE and Western blotting were performed by standard techniques. Spectra multicolor prestained protein ladder (Thermo, New York, USA) was used as the size standard in gel electrophoresis and Western blotting. Primary rabbit polyclonal antibodies (1:1000) of IRAK (Millipore 06-872, Bedford, USA), IκBα (Santa Cruzs c-203, Santa Rosa, USA), and caspase 1, 3, 8, and 9 (CST, Danvers, USA), and mouse monocolonal antibody of TSG6 (R & D Systems 259820, Minneapolis, USA) in PBS-Tween 20 (Bio-Rad, Hercules, USA) containing 5 % bovine serum albumin (Sigma-Aldrich, St. Louis, USA) were prepared. Diluted β-actin (1:8000) (CST 4967, Danvers, USA) was compared as internal control. Subsequently, 1:4000 secondary anti-rabbit antibody was used, and immunocomplex was visualized by enhanced chemiluminescence (Pierce, Chicago, USA). The density of the protein bands was calculated by Quantity One (Bio-Rad, Hercules, USA).
Statistical analysis was performed with GraphPad Prism 5 (GraphPad Software, San Diego, USA). Differences between groups were analyzed by the unpaired, two-tailed Student t test. All data was presented as the means ± SEM. P value less than 0.05 was considered as statistically significant.
cysteinyl aspartate specific proteinase
enzyme-linked immunosorbent assay
hematoxylin and eosin
nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor alpha
interleukin 1 receptor-associated kinase
- IVIS 100:
in vivo imaging system Xenogen 100
myeloid differentiation primary response gene 88
nuclear factor kappa B
natural killer cell
TGF-β-activated kinase 1
Toll-like receptor 4
tumor necrosis factor alpha-induced protein 6
tumor necrosis factor alpha
tumor necrosis factor receptor
TNF-stimulated gene 6 protein
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We would like to thank Professor Jian-Gang Shen for the provision of hypoxia chamber. This project was supported by the CRCG Grant (200907176170), the Edward Sai Kim Hotung Paediatric Education and Research Fund (200000663), the National Basic Research Program of China from the Ministry of Science and Technology of PRC (973 project, 2014CB745200), the Collaborative Research Fund of the Research Grant Council Hong Kong to JDH (HKU1/CRF/10, HKU3/CRF11R), and the National Science Foundation of China grant to BY and LS (31200639).
The authors declare that they have no competing interests.
GCF, JDH, ZLG, BY, and BTN are involved in the study conception and design. ZLG, SC, and BY are involved in data acquisition. GCF, ZLG, JCB, and QBL performed the analysis and interpretation of data. ZLG drafted the manuscript. GCF and JDH helped in the critical revision of the manuscript. All authors read and approved the final manuscript.
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Guo, Z., Yu, B., Ning, B. et al. Genetically modified "obligate" anaerobic Salmonella typhimurium as a therapeutic strategy for neuroblastoma. J Hematol Oncol 8, 99 (2015) doi:10.1186/s13045-015-0196-3
- Anaerobic salmonella
- Orthotopic mouse model
- Immune-compromised host
- Cancer treatment