Doxorubicin-enriched, ALDHbr mouse breast cancer stem cells are treatable to oncolytic herpes simplex virus type 1
© Zhuang et al.; licensee BioMed Central Ltd. 2012
Received: 7 June 2012
Accepted: 18 October 2012
Published: 23 November 2012
The primary objective of this study was to test whether oncolytic herpes simplex virus type 1 (HSV1) could eradicate chemoresistant cancer stem cells (CSCs).
The fluorescent aldefluor reagent-based technique was used to identify and isolate ALDHbr cells as CSCs from the 4T1 murine breast cancer cell line. The presence of ALDHbr 4T1 cells was also examined in 4T1 breast cancer transplanted in immune-competent syngeneic mice.
Compared with ALDHlo cells, ALDHbr cells had a markedly higher ability to form tumor spheres in vitro and a higher tumorigenic potential in vivo. ALDHbr cells also exhibited increased doxorubicin resistance in vitro, which correlated with a selective increase in the percentage of ALDHbr cells after doxorubicin treatment and an increased expression of P-glycoprotein (P-gp), a known chemoresistance factor. In contrast, oncolytic HSV1 was able to kill ALDHbr cells in vitro and even more markedly in vivo. Furthermore, in in vivo studies, systemic administration of doxorubicin followed by intratumoral injection of oncolytic HSV1 resulted in much more significant suppression of tumor growth with increased median survival period compared with each treatment given alone (p<0.05). Though more CD8+ T lymphocytes were induced by oncolytic HSV1, no significant specific T cell response against CSCs was detected in vivo.
These results suggested that the use of oncolytic HSV1 following doxorubicin treatment may help eradicate residual chemoresistant CSCs in vivo.
KeywordsCancer stem cells Breast cancer Chemoresistant ALDH Oncolytic virus Doxorubicin Herpes simplex virus
Breast cancer is the 3rd most commonly diagnosed type of cancer and the leading cause of cancer death among females aged 20 to 59 years old . With the improvement of early detection and/or comprehensive treatment, the breast cancer death rate has been greatly reduced. However, there are no effective therapeutic treatments once cancer is recurrent or metastatic. Cancer stem cells (CSCs) have been considered responsible for cancer progression, recurrence, metastasis and resistance to a number of conventional therapies [2–7]. CSCs have been identified in many tumor types and cell lines based on the expression of unique cell surface markers such as CD44, CD24 and CD133 or their ability to efflux lipophilic, fluorescent dyes such as Hoechst 33342 [8–11]. Another useful approach for the identification of CSCs is based on a high level of aldehyde dehydrogenase (ALDHbr) activity, which has been associated with chemoresistance and poor prognosis in many types of cancer [12–18]. The 4T1 mouse breast cancer cell line was chosen for this study because its growth and metastatic spread in mice closely mimic stage IV human breast cancer . Several markers, including Sca-1 and ALDHbr, have been used for 4T1 CSC isolation in recent reports [20, 21]. In this study, we used ALDHbr to identify and isolate CSCs from 4T1 cells. Because most conventional treatment regimens, including chemotherapy, target the non-CSC population of the tumor and fail to eliminate CSCs [5, 6], discovering new ways to eliminate CSCs that are left behind following chemotherapy is important. The use of oncolytic viruses (OVs) is likely the treatment of choice [22–24]. OVs are either naturally occurring or genetically engineered viruses that selectively infect and lyse tumor cells without deleterious effects on normal cells [25, 26]. In the OV family, the oncolytic herpes simplex virus type 1 (HSV1) is one of the most extensively studied, and it has strong oncolytic activity and promising therapeutic effects [27–29]. Given that the anticancer mechanism of viral oncolysis differs from that of chemotherapeutic agents, we reasoned that chemoresistant CSCs may be still treatable to oncolytic HSV1 [30–34]. In this study, we compared the role of oncolytic HSV1 and doxorubicin in the eradication of CSCs in vitro and in vivo and then employed doxorubicin to kill non-CSCs, followed by oncolytic HSV1 administration to eradicate residual chemoresistant CSCs in vivo. CD8+ cytotoxic T lymphocytes (CTLs) have been shown to play a critical role in immunity against cancer and viruses [35–37]. We therefore further investigated whether the immunological mechanism induced by our oncolytic HSV1 mediated the eradication of CSCs.
Cells and drugs
4T1, a mammary gland tumor cell line from Balb/c mice with high metastatic potency, was purchased from ATCC. 4T1 cells were maintained in DMEM/F12 supplemented with 10% FCS and gentamycin at 37°C in a humidified atmosphere of 5% CO2. The cells were subcultured at a ratio 1:6–8 when they were close to 80% confluent, approximately every 2 to 3 days. Cells of the 3rd-6th passages in the log growth phase were used for experiments.
Doxorubicin, a classic chemotherapy agent for human breast cancers, was purchased from Shenzhen Main Luck Pharmaceuticals Inc. and prepared at 1.5 mg/ml in saline just prior to use.
Construction of recombinant oncolytic HSV1-GFP and HSV1-hGM-CSF
Oncolytic HSV1-GFP and HSV1-hGM-CSF, constructed in our laboratory, were attenuated oncolytic herpes simplex type 1 viruses (17+, ECACC 0104151v). All virus vectors were grown in BHK-21 [C13] (ATCC: CCL-10) or Vero (ATCC: CCL-81) cells in DMEM/F12 containing 10% FCS. Viral DNA was purified using DNAzol (BioTeke Corporation, China).
To construct HSV1-GFP and HSV1-hGM-CSF, the genes encoding infection cell protein 34.5 (ICP34.5) and ICP47 were removed, the expression cassette for human granulocyte–macrophage colony-stimulating factor (hGM-CSF) or green fluorescent protein (GFP) was inserted into the sites for ICP34.5.
The primers used for the construction of pdICP34.5 and pdICP47 are listed
To delete ICP34.5, the US and DS FLRs were amplified from 17+ strain genome with primer pairs ICP34.5USf versus ICP34.5USr and ICP34.5DSf versus ICP34.5DSr, respectively (Table 1). Then the ICP34.5 US and DS FLRs were jointed together using an overlapping PCR with the primer pair ICP34.5USf/ICP34.5DSr and subsequently inserted into pSP72 (Promega) pre-digested with BamHI/XhoI and treated with T4 DNA polymerase for blunt-end cloning. The resulted plasmid was named as pdICP34.5 and sequencing verified. The hGM-CSF gene (Invivogen)was used to replace eGFP of pcDNA3.1-eGFP giving plasmid pcDNA3.1-hGM-CSF. The eGFP and hGM-CSF expression cassettes from pcDNA3.1-eGFP and pcDNA3.1- hGM-CSF were cloned into pdICP34.5 AfeI site to generate pdICP34.5-eGFP and pdICP34.5-hGM-CSF, respectively. The pdICP34.5-eGFP and pd.ICP34.5-hGM-CSF were used to delete ICP34.5 from 17-d47 vector giving viruses HSV1-GFP and HSV1-hGM-CSF (Figure 1).
Flow cytometry sorting of cells with ALDHbractivity
4T1 cells were harvested, and a single-cell suspension was obtained for the aldefluor assay according to the manufacturer's instructions (Stem Cell Technologies). Briefly, 106 cells were resuspended in 1 ml of aldefluor assay buffer containing activated aldefluor substrate. As a negative control for each sample, an aliquot of “aldefluor-exposed” cells was immediately quenched with a specific ALDH inhibitor, diethylaminobenzaldehyde (DEAB). Following a 30-minute incubation at 37°C, the cells were centrifuged, the pellets were resuspended in 0.5 ml aldefluor assay buffer, and the ALDHbr and ALDHlo subpopulations were sorted using a FACSDiVa flow cytometer (Becton Dickinson).
Mammosphere formation assay
4T1 or isolated cells were resuspended in DMEM/F12 serum free medium (SFM) supplemented with human recombinant epidermal growth factor (EGF; 20 ng/ml) and basic fibroblast growth factor (bFGF; 20 ng/ml) and then seeded in ultra-low attachment 6-well plates (Costar, Corning Incorporated) with 5 × 104 cells/well in 2 ml. Both EGF and bFGF were purchased from Sigma Biochemicals. Fresh aliquots of EGF and bFGF were added every other day. After 8 days of culture, mammospheres were observed. Carboxymethyl cellulose (CMC) was added at a final concentration of 0.8% to keep the fluid flow slow, and the spheres were quantified using an inverted phase contrast microscope (Olympus Co.).
Tumorigenicity studies with isolated cells
The sorted ALDHbr and ALDHlo cells were resuspended, serially diluted in DMEM/F12 SFM and inoculated subcutaneously (s.c.) into the right flanks of 6-7-week-old immune-competent female Balb/c mice (n=5-6) at varying numbers (5, 000, 1, 000 and 100) in a volume of 100 μl. The tumor-initiating capacity of the two populations was monitored weekly and compared. Animals were euthanized when tumors exceeded 1, 800 mm3 or the 60-day endpoint was reached.
Western blot assay for P-gp in sorted cells
Both ALDHbr and ALDHlo subpopulations isolated from 4T1 cells were washed with phosphate-buffered saline (PBS). The cells were collected by centrifugation, and the pellet was suspended in RIPA lysis buffer (Biomiga, Inc.) containing a cocktail of proteinase inhibitors i.e., leupeptin, aprotinin and pepstatin (the first two agents were purchased from Roche, and pepstatin was purchased from Amresco). The cells were lysed on ice for 15 minutes. The lysates were centrifuged at 12, 000 rpm for 10 minutes at 4°C, and the protein in the supernatant was collected. The protein concentration was quantified using the bicinchoninic acid (BCA) assay kit (Applygen Technologies, Inc.) to ensure that equal amounts of protein from both subpopulations were loaded in the gel. The remaining supernatants were boiled in sample buffer containing sodium dodecyl sulfate (SDS) and β-mercaptoethanol and then used for western blot analysis.
Western blot analysis was performed as previously described with slight modifications . Briefly, the proteins were separated using a 7% sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE). Following electrophoresis, the samples were transferred onto a polyvinylidene difluoride (PVDF) membrane. After the transfer, non-specific binding sites were blocked at room temperature for 1 hour with 5% non-fat dry milk in PBS with gentle agitation. The membranes were incubated overnight at 4°C with the following primary antibodies: monoclonal mouse anti-P-gp (JSB-1, Abcam) (1:200 dilution in 3% non-fat dry milk) and anti-β-actin (1:1, 000 dilution, Zhongshan goldenbridge biotechnology Co., Ltd.), which was used for normalization. The membrane was washed with PBS (3 × 10 minutes) and then incubated with a horseradish peroxidase-conjugated goat anti-mouse IgG (1:5, 000 dilution, Zhongshan goldenbridge biotechnology Co., Ltd.) for 1 hour at room temperature with gentle agitation followed by rinsing as before. The protein bands were visualized using an enhanced chemiluminescence (ECL) detection system (Applygen Technologies Inc.), according to the manufacturer’s instructions, followed by exposure to X-ray film.
In vitrocytotoxicity of oncolytic HSV1
For 4T1 monolayers, the day before infection, 2 × 105 4T1 cells were seeded into 6-well plates. After a 24-hour incubation, the cells of one well were trypsinized and counted to facilitate the calculation of the MOIs for infection. The media in the other wells were replaced with 1 ml fresh DMEM/F12 SFM containing viruses at different MOIs. One control well was added only DMEM/F12 SFM. After a 1-hour incubation, 1 ml of DMEM/F12 full growth medium (FGM) was added to each well. The CPE was observed at different times after infection using an inverted phase contrast microscope.
For the mammospheres, after 7 days of culture, 4T1 mammospheres of one well were collected and digested with Accutase® solution (Sigma), and the cells were counted to calculate the MOIs for virus infection. The mammospheres of the other wells were infected with HSV1-GFP at an MOI of 1, and a well with the addition of vehicle was used as a control. HSV1-GFP was directly added without changing the medium. The GFP expression was observed at different time points.
For ALDHbr and ALDHlo cells, the cells were resuspended in DMEM/F12 FGM and seeded into dishes (33 mm in diameter) at a density of 5 × 104 cells/ml in 2 ml/dish. The media was then replaced with 1 ml of fresh DMEM/F12 SFM containing HSV1-GFP at different MOIs when most cells were adherent. One control dish contained DMEM/F12 SFM only. After a 1-hour incubation, the medium was changed with 2 ml of fresh DMEM/F12 FGM, which contained just 3% FCS to keep the cells alive but to slow cell differentiation. After incubation for another 10 hours, GFP expression was examined, and images were obtained using an inverted fluorescence microscope.
Establishment of a subcutaneous cancer model and tumor therapy protocols
5–6 weeks old immune-competent female Balb/c mice were obtained from the Institute of Zoology, Chinese Academy of Sciences. All protocols for the animal experiments were approved by the Animal Care and Use Committee of the Cancer Institute and Hospital, Chinese Academy of Medical Sciences. All mice were housed and handled according to the institutionally recommended guidelines. A total of 5 × 104 4T1 cells were s.c. injected into the right flank of mice. After 4–5 days, when tumors appeared, the mice were distributed by tumor size into the following treatment groups (n=12-13 per group): (a) doxorubicin followed by HSV1, (b) doxorubicin alone, (c) HSV1 alone and (d) control. Chemotherapy with 8 mg/kg doxorubicin was i.v. administered twice at days 0 and 3. Oncolytic HSV1-hGM-CSF treatment at a dose of 1 × 107 plaque forming units (PFU) per mouse was subsequently given by direct intratumoral injection on days 5, 7, 9, 11 and 13. We treated the control mice with the solvent for doxorubicin and oncolytic HSV1 (NS and DMEM/F12 SFM, respectively). The primary tumor size and body weight were routinely measured every 4 days following treatment. The tumor volume was calculated using the following formula: tumor volume (mm3) = [L × W2] / 2, where L equals length and W equals width in mm.
After the third treatment with oncolytic HSV1-hGM-CSF (on day 11), the primary tumors were surgically removed from each group (n=4-5) and used for the aldefluor assay. The remaining animals in each group were used for the survival analysis (n=5-7).
Flow cytometry analysis of 4T1 cells with ALDHbractivity
4T1 cells at a density of 1 × 105 cells/ml were seeded in T-75 cm2 cell culture flasks at 15 ml/flask. On the second day, the medium was changed with fresh DMEM/F12 FGM, and the cells were cultured for an additional 24 hours in the presence or absence of doxorubicin (1.0 μg/ml) or HSV1-hGM-CSF (MOI=0.3). The controls were incubated with vehicle only. Then the cells were harvested, and a single-cell suspension was obtained for the aldefluor assay as described above.
Primary tumor tissue comprising 4T1 cells was isolated, minced into tiny fragments and digested with collagenase IV (1 mg/ml) and DNase I (300 U/ml) (all obtained from Sigma) for approximately 1.5 hours at 37°C in 5% CO2 with intermittent pipetting. The single cells obtained by filtering through a 200-mesh screen were lysed with Ammonium Chloride Solution (Stem Cell Technologies) to exclude red blood cells. After the aldefluor assay was performed, the cells were stained with APC anti-mouse CD45 (BioLegend) and its isotype antibody at 4°C for 30 minutes to exclude leukocytes. The ALDHbr cells were then analyzed by flow cytometry as described above.
Characterization of CD8+T lymphocytes in splenocytes by flow cytometry analysis
After the second treatment with oncolytic HSV1 (on day 8), the spleens (n=3-4) were surgically removed and used for CD8+ T lymphocyte measurement, and their cytotoxicity to 4T1 ALDHbr cells was measured by flow cytometry. The single cell suspension was prepared through a 400-gauge mesh. Lymphocytes from the spleens were isolated by centrifugation in gradient lymphocyte isolation solution for mice (Tianjin Hao Yang Biological Manufacture Co., Ltd., China) at room temperature and washed twice with PBS. The cell suspensions in PBS were then stained at 4°C for 30 minutes using the following antibodies: FITC anti-mouse CD3, PE anti-mouse CD8b and their corresponding isotype control antibodies (all monoclonal antibodies were obtained from Biolegend). After washing with PBS, the cells were fixed with 10% formaldehyde and the CD8+ T lymphocyte frequency was determined by flow cytometry.
CTL cytotoxicity assay by flow cytometry
In vitro CTL detection was performed as previously described with some modification . ALDHbr cells were sorted from 4T1 cells on the day of the assay. To label target cells, the isolated cells were resuspended in PBS containing 5-(and −6) -carboxyfluorescein diacetate succinimidyl ester (CFSE, Sigma) at a final concentration of 10 μmol/l and incubated at 37°C/5% CO2 for 10 minutes. After incubation, the reaction was stopped by adding a large volume of DMEM/F12 FGM, and the labeled target cells were then washed in DMEM/F12 FGM to sequester any free CFSE. After resuspension in DMEM/F12 FGM, the cell number and viability were assessed using trypan blue exclusion, and the cell concentration was adjusted to 2 × 104 viable cells/100 μl with DMEM/F12 FGM. Effector cells (lymphocytes) were obtained from euthanized tumor-bearing mice from the different treatment groups as described above. Isolated lymphocytes were washed and resuspended in DMEM/F12 FGM, the cell number and viability were assessed as described above, and the cell concentration was adjusted to 2 × 106 viable cells/100 μl. Effector and target cells were mixed at an E:T ratio of 100:1 (2 × 106 for effector cells and 2 × 104 for target cells, respectively) in a total volume of 200 μl per test. After incubation for 3.5 hours at 37°C/5% CO2, DMEM/F12 FGM was added to a final volume of 0.5 ml and stained with propidium iodide (PI, Sigma) at a final concentration of 2 μg/ml. Finally, cytotoxicity against the target cells was assessed by flow cytometry. The determination of cytotoxicity was based on enumeration of dead target cells (CFSE+PI+). To determine specific lysis, the survival of allogeneic splenocytes in tumor-free naive mice was used as a baseline. All of the assays were performed in triplicate.
All statistical tests were performed using GraphPad Prism 5 software. The Student's unpaired t-test was performed on the following experimental data: the frequency of ALDHbr cells and CD8+ T lymphocytes and tumor volume. The results are presented as the mean ± SEM (standard error of the mean). The Kaplan–Meier method and the log-rank test were used to compare survival, which was defined as the time from tumor inoculation until the endpoint. All statistical tests were two-sided, and statistical significance was defined as a p < 0.05.
The scheme for construction of the two recombinant oncolytic viruses, HSV1-GFP and HSV1-hGM-CSF, is shown in Figure 1. They are attenuated by the deletion of both copies of the ICP34.5, which is neurovirulence gene, and of ICP 47 gene. Deletion of gene encoding ICP34.5 provides tumor selectivity. ICP47 functions to block antigen processing in HSV1 infected cells, and therefore deletion of it is aiming to improve anti-tumor immunity . Deletion of ICP47 also results in the US11 gene being under the control of the ICP47 immediate early promoter that results in enhanced virus replication. Insertion of GFP gene or hGM-CSF is to serve as an infection marker or to improve vector’s immune stimulating potency, respectively.
4T1 ALDHbrcells have CSC characteristics
Tumor-initiating capacity of freshly sorted ALDH br versus ALDH lo subpopulations in vivo
Collectively, the 4T1 ALDHbr cells had increased mammosphere-forming capacity and tumor-initiating potency compared with ALDHlo cells; thus, they possessed CSC properties.
4T1 ALDHbrcells are resistant to chemotherapy
Both 4T1 monolayers and mammospheres are infectable to HSV1 in vitro
Mammosphere cultures from the 4T1 cell line were established and infected by oncolytic HSV1-GFP. Strong green fluorescence due to constitutive GFP expression was detected in many cells of the spheres compared with the mock-infected control (Figure 4B). At an MOI of 1 for 24 hours, HSV1-GFP could infect a few cells of mammospheres, while at a later time of infection (48 hours), it had spread into more cells of the mammospheres. Collectively, these data indicate that both 4T1 monolayers and mammospheres can be infected by oncolytic HSV1-GFP.
ALDHbr and ALDHlocells can be uniformly infected by HSV1-GFP
4T1 cells stained with aldefluor substrate demonstrated bright green fluorescence, which could not be distinguished from the GFP expression in cells infected with HSV1-GFP. However, the green fluorescence quickly disappeared from post-sorted ALDHbr cells because they were no longer in the aldefluor buffer, which blocked ABC transporters and retained the fluorescent substrate in the cells, but were instead in sheath fluid and medium when plated in dishes. Therefore, the isolated ALDHbr cells were fluorescent-free and HSV1 drived GFP expression could be used to evaluate the HSV1 infectivity to ALDHbr cells. Sorted ALDHbr and ALDHlo cells were infected with HSV1-GFP at different MOIs for different times. As shown in Figure 4C, after 10 hours, GFP expression had appeared in both subpopulations infected with HSV1-GFP at MOIs of 0.3 and 1. After infection for 34 hours, when cell proliferation and differentiation had occurred, GFP expression was more apparent in both subpopulations. Moreover, the HSV1-GFP infection efficiency in both ALDHbr and ALDHlo cells was similar (38.8% for ALDHbr cells versus 29.4% for ALDHlo cells, respectively, p=0.0664, n=4-6).
4T1 ALDHbr cells are resistant to doxorubicin but treatable to HSV1 in vitro and in vivo
ALDHbr subpopulation increased with the development of a primary tumor in vivo
We speculated that the reason the percentage of ALDHbr 4T1 cells in the control group was unexpectedly high (32.10%, Figure 6B) may be because of their larger tumor volume. Therefore, 4T1 tumor-bearing mice with different primary tumor volumes (1 week and 2 weeks after the tumor occurred) were selected, and the change in the percentage of ALDHbr 4T1 cells in the primary tumors was analyzed. As expected, the frequency of ALDHbr tumor cells grew with the development of primary tumors (Figure 6C). The mean primary tumor volume was 73.0 mm3 at 1 week and 360.5 mm3 at 2 weeks after the tumor appeared (n=3, p=0.0437), and the frequency of ALDHbr tumor cells was 10.02% and 17.11%, respectively (n=3, p<0.0001). Therefore, the percentage of ALDHbr 4T1 cells increased with the growth of primary tumors.
CD8+ T lymphocytes induced by HSV1 does not appear to be responsible for ALDHbrtumor cell eradication
To explore whether the eradication of ALDHbr tumor cells was mediated by CD8+ T lymphocytes generated in mice after oncolytic HSV1 treatment, we assessed the CD8+ T lymphocyte percentage and activity after different treatments.
CD8+ T lymphocytes induced by doxorubicin demonstrated significant cytotoxic activity to 4T1 ALDHbr cells with an E/T ratio of 100:1 (24.17%) (n=3, p<0.05), while lymphocytes from mice treated with oncolytic HSV1 did not seem to demonstrate significant CTL activity against the same target cells at the same E/T ratio (12.27%), which was even less than that of the control group (20.13%) (n=3, p<0.05) (Figure 7B). Moreover, cytotoxic activity induced by doxorubicin plus oncolytic HSV1 treatment increased slightly compared with the nonspecific cytotoxicity (14.67% versus 9.80%, respectively; n=3; p>0.05), which was also lower than that of the control group (n=3, p>0.05).
Doxorubicin followed by HSV1 demonstrated the greatest therapeutic effect in vivo
None of the animal tumors completely regressed, and all animals died due to excessive tumor growth. Mice treated with doxorubicin or HSV1-hGM-CSF alone demonstrated a prolonged median survival time compared with mock-treated mice (35 days for the control group, 39.5 days for the doxorubicin-alone group and 40 days for the HSV1-alone group; n=5-7; p<0.05, log-rank test) (Figure 8B). The median survival time between mice that received either treatment alone was not significantly different. For the combination group, the median survival time was significantly longer (47 days) compared with either treatment alone (n=5-7, p<0.01 versus doxorubicin-alone, p>0.05 versus HSV1-alone, log-rank test). The results above demonstrated that treatment with either doxorubicin or HSV1 exhibited significant anticancer effects, and the combination treatment group demonstrated the greatest anticancer efficacy in vivo.
CSC chemoresistance has become the main obstacle in successful anticancer treatment and is largely responsible for human breast cancer mortality [47–49]. Cells with high ALDH1 activity have been shown to possess CSC characteristics in many tumor types [13–18]. In our study, ALDHbr cells isolated from 4T1 cells were shown to have CSC properties, including their mammosphere-forming ability in vitro and tumorigenicity in vivo. In addition, CSCs typically overexpress cell membrane ATP-binding cassette (ABC) drug transporters such as P-gp, which mediate the efflux of a large number of cytotoxic compounds, including doxorubicin. Our study indicated that P-gp expression was only detected in 4T1 ALDHbr cells.
Among the therapeutic agents used for human breast cancer, doxorubicin, an anthracycline drug, remains a first-line choice [50, 51]. Despite its excellent anticancer activity in the clinic, doxorubicin treatment is confronted with toxicities, including severe myelosuppression and dose-cumulative cardio-toxicity [52–54]. Most importantly, similar to many other chemotherapeutic drugs, the treatment of breast cancer with doxorubicin was unable to eradicate CSCs but instead led to an enrichment of CSCs [55, 56]. HSV1 is a potent oncolytic virus that has been evaluated in many types of tumors in mice and humans [27–29, 57]. We compared the effects of oncolytic HSV1 and doxorubicin on the ALDHbr population in vitro and in vivo. Our in vitro results, in agreement with previous reports [55, 56, 58], indicated that doxorubicin can enrich the CSCs of 4T1 cells, which were still treatable by oncolytic HSV1. Phenotypic analysis revealed an obvious decrease in the frequency of ALDHbr tumor cells in mice treated with oncolytic HSV1. It has been reported that oncolytic HSV can induce a robust anti-tumor immune responses against 4T1 mammary tumors in vivo[27, 59, 60] and CTLs mediated cytotoxicity to cancer cells . In our study, though the CD8+ T lymphocyte frequency in spleens treated with oncolytic HSV1 demonstrated a significant elevation compared with the control group, no significant specific CTL response appeared to participate in ALDHbr cell elimination. This may be due to the following reasons: (1) The CD8+ T lymphocytes induced by oncolytic HSV1 may be mainly specific to the virus itself (a strong immunogen compared with 4T1 cells) and this was supported by marked splenomegaly observed after oncolytic virus alone treatment (data not shown), and (2) the hGM-CSF carried by oncolytic HSV1 was ineffective in mice due to species differences . Unexpectedly, there was no increase in the percentage of ALDHbr cells in tumors treated with doxorubicin alone compared with those treated with vehicle. This unexpected result may be due to the following factors: (1) The time between the last chemotherapy and aldefluor assay was too long (8 days) to exam the enrichment of CSCs from doxorubicin, (2) Doxorubicin by itself can enhance the anticancer immune response [62, 63] and may also enhance the anti-CSC activity (Figure 7B), which may explain why ALDHbr subpopulation in the doxorubicin-treated group was not greater than that of the control group, and (3) The larger primary tumor volume in vehicle-treated control mice may influence the percentage of ALDHbr tumor cells due to tumor necrosis or hypoxia . In our study, it was demonstrated for the first time that the frequency of ALDHbr tumor cells increased with the development of primary tumors in 4T1 tumor-bearing mice.
Although our oncolytic HSV1 can reduce the primary 4T1 tumor volume effectively, which is consistent with the previous reports [27, 59, 60, 65, 66], and decrease the frequency of ALDHbr cells compared with chemotherapy, it also has its own limitations, including physical barriers such as the extracellular matrix, which restrict the initial distribution and subsequent spread of viruses in the tumor mass when the oncolytic virus is directly injected into the tumor, and anti-HSV1 immunity, which can limit virus replication when locally or systematically given repeatedly [67, 68]. These limitations may be overcome by combination of viral and chemotherapies. Ideally, the combined therapies could lead to synergistic effects in the following considerations: (1) The majority of the non-CSCs were first eradicated by chemotherapy and then the residual CSCs were killed by oncolytic HSV1. (2) Oncolytic viral replication and subsequent spread in the tumor mass may be enhanced by chemotherapy leading to antiviral immune response inhibition, the destruction of physical barriers, alteration in the tumor cell physiology and induced activation of DNA repair pathways [34, 69, 70]. (3) Oncolytic viruses circumvent typical chemoresistance mechanisms, they may be effective for chemoresistant CSCs [22, 71]. (4) Chemotherapy and oncolytic HSV1 with different mechanisms of action could synergistically act to kill cancer cells and thus may achieve much more efficient antitumor activity [70, 72]. In our in vivo study, treatment with doxorubicin chemotherapy followed by oncolytic HSV1 achieved more significant benefits than either single agent alone. (5) Oncolytic HSV1 had slight and different toxicities compared with chemotherapy . The combination of the two modalities may minimize toxic side effects [70, 74]. In our experiment, the administration of oncolytic HSV1-hGM-CSF alone was well tolerated, and administering HSV1-hGM-CSF followed by doxorubicin did not enhance the toxicity of the latter (Additional file 1: Figure S1). The strategy of targeting CSCs with oncolytic HSV1-hGM-CSF in combination with standard chemotherapy that kills non-CSCs may be applied to the treatment of human breast cancer in the clinic.
In conclusion, this study suggested that 4T1 ALDHbr cells possess CSC characteristics. These ALDHbr cells were doxorubicin-resistant but still treatable to oncolytic HSV1. The treatment of 4T1 breast tumors with oncolytic HSV1 followed by doxorubicin chemotherapy generated a potent anticancer effect in vivo.
Cancer stem cells
Herpes simplex virus
Multiplicity of infection
Green fluorescent protein
human granulocyte-macrophage colony stimulating factor
Plaque forming units
Fetal calf serum
Full growth medium
Human recombinant epidermal growth factor
Human recombinant basic fibroblast growth factor
Standard error of the mean
Sodium dodecyl sulfate– polyacrylamide gel electrophoresis.
This work was supported by grants from the Tianjin Municipal Science and Technology Commission (10ZCKFSY08000) and National Natural Sciene Foundation of China (81172160). We thank Jianming Liang at our institute and Drs. Li Su and Shiliang Ma at Peking University Health Science Center for providing technical assistance for flow cytometry. We also thank Dr. Jun Liang at our institute for assistance with fluorescence microscope.
- Jemal A, Siegel R, Xu J, Ward E: Cancer statistics, 2010. CA Cancer J Clin. 2010, 60 (5): 277-300. 10.3322/caac.20073.View ArticlePubMedGoogle Scholar
- Awad O, Yustein JT, Shah P, Gul N, Katuri V, O'Neill A, Kong Y, Brown ML, Toretsky JA, Loeb DM: High ALDH activity identifies chemotherapy-resistant Ewing's sarcoma stem cells that retain sensitivity to EWS-FLI1 inhibition. PLoS One. 2010, 5 (11): e13943-10.1371/journal.pone.0013943.View ArticlePubMedPubMed CentralGoogle Scholar
- Dalerba P, Cho RW, Clarke MF: Cancer stem cells: models and concepts. Annu Rev Med. 2007, 58: 267-284. 10.1146/annurev.med.58.062105.204854.View ArticlePubMedGoogle Scholar
- Dallas NA, Xia L, Fan F, Gray MJ, Gaur P, 2nd Van Buren G, Samuel S, Kim MP, Lim SJ, Ellis LM: Chemoresistant colorectal cancer cells, the cancer stem cell phenotype, and increased sensitivity to insulin-like growth factor-I receptor inhibition. Cancer Res. 2009, 69 (5): 1951-1957. 10.1158/0008-5472.CAN-08-2023.View ArticlePubMedPubMed CentralGoogle Scholar
- Jordan CT, Guzman ML, Noble M: Cancer stem cells. N Engl J Med. 2006, 355 (12): 1253-1261. 10.1056/NEJMra061808.View ArticlePubMedGoogle Scholar
- Dean M, Fojo T, Bates S: Tumour stem cells and drug resistance. Nat Rev Cancer. 2005, 5 (4): 275-284. 10.1038/nrc1590.View ArticlePubMedGoogle Scholar
- Bao S, Wu Q, McLendon RE, Hao Y, Shi Q, Hjelmeland AB, Dewhirst MW, Bigner DD, Rich JN: Glioma stem cells promote radioresistance by preferential activation of the DNA damage response. Nature. 2006, 444 (7120): 756-760. 10.1038/nature05236.View ArticlePubMedGoogle Scholar
- Xin L, Lawson DA, Witte ON: The Sca-1 cell surface marker enriches for a prostate-regenerating cell subpopulation that can initiate prostate tumorigenesis. Proc Natl Acad Sci U S A. 2005, 102 (19): 6942-6947. 10.1073/pnas.0502320102.View ArticlePubMedPubMed CentralGoogle Scholar
- Hirschmann-Jax C, Foster AE, Wulf GG, Nuchtern JG, Jax TW, Gobel U, Goodell MA, Brenner MK: A distinct "side population" of cells with high drug efflux capacity in human tumor cells. Proc Natl Acad Sci U S A. 2004, 101 (39): 14228-14233. 10.1073/pnas.0400067101.View ArticlePubMedPubMed CentralGoogle Scholar
- Al-Hajj M, Wicha MS, Benito-Hernandez A, Morrison SJ, Clarke MF: Prospective identification of tumorigenic breast cancer cells. Proc Natl Acad Sci U S A. 2003, 100 (7): 3983-3988. 10.1073/pnas.0530291100.View ArticlePubMedPubMed CentralGoogle Scholar
- Singh SK, Hawkins C, Clarke ID, Squire JA, Bayani J, Hide T, Henkelman RM, Cusimano MD, Dirks PB: Identification of human brain tumour initiating cells. Nature. 2004, 432 (7015): 396-401. 10.1038/nature03128.View ArticlePubMedGoogle Scholar
- Huang EH, Hynes MJ, Zhang T, Ginestier C, Dontu G, Appelman H, Fields JZ, Wicha MS, Boman BM: Aldehyde dehydrogenase 1 is a marker for normal and malignant human colonic stem cells (SC) and tracks SC overpopulation during colon tumorigenesis. Cancer Res. 2009, 69 (8): 3382-3389. 10.1158/0008-5472.CAN-08-4418.View ArticlePubMedPubMed CentralGoogle Scholar
- Jiang F, Qiu Q, Khanna A, Todd NW, Deepak J, Xing L, Wang H, Liu Z, Su Y, Stass SA, et al: Aldehyde dehydrogenase 1 is a tumor stem cell-associated marker in lung cancer. Mol Cancer Res. 2009, 7 (3): 330-338. 10.1158/1541-7786.MCR-08-0393.View ArticlePubMedPubMed CentralGoogle Scholar
- Ginestier C, Hur MH, Charafe-Jauffret E, Monville F, Dutcher J, Brown M, Jacquemier J, Viens P, Kleer CG, Liu S, et al: ALDH1 is a marker of normal and malignant human mammary stem cells and a predictor of poor clinical outcome. Cell Stem Cell. 2007, 1 (5): 555-567. 10.1016/j.stem.2007.08.014.View ArticlePubMedPubMed CentralGoogle Scholar
- Ran D, Schubert M, Pietsch L, Taubert I, Wuchter P, Eckstein V, Bruckner T, Zoeller M, Ho AD: Aldehyde dehydrogenase activity among primary leukemia cells is associated with stem cell features and correlates with adverse clinical outcomes. Exp Hematol. 2009, 37 (12): 1423-1434. 10.1016/j.exphem.2009.10.001.View ArticlePubMedGoogle Scholar
- Carpentino JE, Hynes MJ, Appelman HD, Zheng T, Steindler DA, Scott EW, Huang EH: Aldehyde dehydrogenase-expressing colon stem cells contribute to tumorigenesis in the transition from colitis to cancer. Cancer Res. 2009, 69 (20): 8208-8215. 10.1158/0008-5472.CAN-09-1132.View ArticlePubMedPubMed CentralGoogle Scholar
- van den Hoogen C, van der Horst G, Cheung H, Buijs JT, Lippitt JM, Guzman-Ramirez N, Hamdy FC, Eaton CL, Thalmann GN, Cecchini MG, et al: High aldehyde dehydrogenase activity identifies tumor-initiating and metastasis-initiating cells in human prostate cancer. Cancer Res. 2010, 70 (12): 5163-5173. 10.1158/0008-5472.CAN-09-3806.View ArticlePubMedGoogle Scholar
- Clay MR, Tabor M, Owen JH, Carey TE, Bradford CR, Wolf GT, Wicha MS, Prince ME: Single-marker identification of head and neck squamous cell carcinoma cancer stem cells with aldehyde dehydrogenase. Head Neck. 2010, 32 (9): 1195-1201. 10.1002/hed.21315.View ArticlePubMedPubMed CentralGoogle Scholar
- Pulaski BA, Ostrand-Rosenberg S: Mouse 4T1 breast tumor model. Curr Protoc Immuno. 2001, 20: 20-21.Google Scholar
- Matilainen H, Yu XW, Tang CW, Berridge MV, McConnell MJ: Sphere formation reverses the metastatic and cancer stem cell phenotype of the murine mammary tumour 4T1, independently of the putative cancer stem cell marker Sca-1. Cancer Lett. 2012, 323 (1): 20-28. 10.1016/j.canlet.2012.03.028.View ArticlePubMedGoogle Scholar
- Park SJ, Kim RJ, Nam JS: Inhibitor of DNA-binding 4 contributes to the maintenance and expansion of cancer stem cells in 4T1 mouse mammary cancer cell line. Laboratory animal research. 2011, 27 (4): 333-338. 10.5625/lar.2011.27.4.333.View ArticlePubMedPubMed CentralGoogle Scholar
- Mahller YY, Williams JP, Baird WH, Mitton B, Grossheim J, Saeki Y, Cancelas JA, Ratner N, Cripe TP: Neuroblastoma cell lines contain pluripotent tumor initiating cells that are susceptible to a targeted oncolytic virus. PLoS One. 2009, 4 (1): e4235-10.1371/journal.pone.0004235.View ArticlePubMedPubMed CentralGoogle Scholar
- Cripe TP, Wang PY, Marcato P, Mahller YY, Lee PW: Targeting cancer-initiating cells with oncolytic viruses. Mol Ther. 2009, 17 (10): 1677-1682. 10.1038/mt.2009.193.View ArticlePubMedPubMed CentralGoogle Scholar
- Liu TC, Kirn D: Targeting the untargetable: oncolytic virotherapy for the cancer stem cell. Mol Ther. 2007, 15 (12): 2060-2061. 10.1038/sj.mt.6300337.View ArticlePubMedGoogle Scholar
- Parato KA, Senger D, Forsyth PA, Bell JC: Recent progress in the battle between oncolytic viruses and tumours. Nat Rev Cancer. 2005, 5 (12): 965-976. 10.1038/nrc1750.View ArticlePubMedGoogle Scholar
- Sugiura S, Goshima F, Takakuwa H, Sata T, Nakashima T, Nishiyama Y: Treatment of solid sarcomas in immunocompetent mice with novel, oncolytic herpes simplex viruses. Otolaryngol Head Neck Surg. 2004, 130 (4): 470-478. 10.1016/j.otohns.2004.01.001.View ArticlePubMedGoogle Scholar
- Israyelyan A, Chouljenko VN, Baghian A, David AT, Kearney MT, Kousoulas KG: Herpes simplex virus type-1(HSV-1) oncolytic and highly fusogenic mutants carrying the NV1020 genomic deletion effectively inhibit primary and metastatic tumors in mice. Virol J. 2008, 5: 68-10.1186/1743-422X-5-68.View ArticlePubMedPubMed CentralGoogle Scholar
- Todo T: "Armed" oncolytic herpes simplex viruses for brain tumor therapy. Cell Adh Migr. 2008, 2 (3): 208-213. 10.4161/cam.2.3.6353.View ArticlePubMedPubMed CentralGoogle Scholar
- Todo T, Martuza RL, Rabkin SD, Johnson PA: Oncolytic herpes simplex virus vector with enhanced MHC class I presentation and tumor cell killing. Proc Natl Acad Sci U S A. 2001, 98 (11): 6396-6401. 10.1073/pnas.101136398.View ArticlePubMedPubMed CentralGoogle Scholar
- Wakimoto H, Kesari S, Farrell CJ, Curry WT, Zaupa C, Aghi M, Kuroda T, Stemmer-Rachamimov A, Shah K, Liu TC, et al: Human glioblastoma-derived cancer stem cells: establishment of invasive glioma models and treatment with oncolytic herpes simplex virus vectors. Cancer Res. 2009, 69 (8): 3472-3481. 10.1158/0008-5472.CAN-08-3886.View ArticlePubMedPubMed CentralGoogle Scholar
- Coukos G, Makrigiannakis A, Kang EH, Rubin SC, Albelda SM, Molnar-Kimber KL: Oncolytic herpes simplex virus-1 lacking ICP34.5 induces p53-independent death and is efficacious against chemotherapy-resistant ovarian cancer. Clin Cancer Res. 2000, 6 (8): 3342-3353.PubMedGoogle Scholar
- Chahlavi A, Todo T, Martuza RL, Rabkin SD: Replication-competent herpes simplex virus vector G207 and cisplatin combination therapy for head and neck squamous cell carcinoma. Neoplasia. 1999, 1 (2): 162-169. 10.1038/sj.neo.7900016.View ArticlePubMedPubMed CentralGoogle Scholar
- Gutermann A, Mayer E, von Dehn-Rothfelser K, Breidenstein C, Weber M, Muench M, Gungor D, Suehnel J, Moebius U, Lechmann M: Efficacy of oncolytic herpesvirus NV1020 can be enhanced by combination with chemotherapeutics in colon carcinoma cells. Hum Gene Ther. 2006, 17 (12): 1241-1253. 10.1089/hum.2006.17.1241.View ArticlePubMedGoogle Scholar
- Aghi M, Rabkin S, Martuza RL: Effect of chemotherapy-induced DNA repair on oncolytic herpes simplex viral replication. J Natl Cancer Inst. 2006, 98 (1): 38-50. 10.1093/jnci/djj003.View ArticlePubMedGoogle Scholar
- Melief CJ, Kast WM: T-cell immunotherapy of tumors by adoptive transfer of cytotoxic T lymphocytes and by vaccination with minimal essential epitopes. Immunol Rev. 1995, 145: 167-177. 10.1111/j.1600-065X.1995.tb00081.x.View ArticlePubMedGoogle Scholar
- Martin S, Zhu XX, Silverstein SJ, Courtney RJ, Yao F, Jenkins FJ, Rouse BT: Murine cytotoxic T lymphocytes specific for herpes simplex virus type 1 recognize the immediate early protein ICP4 but not ICP0. J Gen Virol. 1990, 71 (Pt 10): 2391-2399.View ArticlePubMedGoogle Scholar
- Osorio Y, Cai S, Ghiasi H: Treatment of mice with anti-CD86 mAb reduces CD8+ T cell-mediated CTL activity and enhances ocular viral replication in HSV-1-infected mice. Ocul Immunol Inflamm. 2005, 13 (2–3): 159-167.View ArticlePubMedGoogle Scholar
- Tribble ND, Burka JF, Kibenge FS, Wright GM: Identification and localization of a putative ATP-binding cassette transporter in sea lice (Lepeophtheirus salmonis) and host Atlantic salmon (Salmo salar). Parasitology. 2008, 135 (2): 243-255.View ArticlePubMedGoogle Scholar
- Godoy-Ramirez K, Makitalo B, Thorstensson R, Sandstrom E, Biberfeld G, Gaines H: A novel assay for assessment of HIV-specific cytotoxicity by multiparameter flow cytometry. Cytometry A. 2005, 68 (2): 71-80.View ArticlePubMedGoogle Scholar
- Liu BL, Robinson M, Han ZQ, Branston RH, English C, Reay P, McGrath Y, Thomas SK, Thornton M, Bullock P, et al: ICP34.5 deleted herpes simplex virus with enhanced oncolytic, immune stimulating, and anti-tumour properties. Gene Ther. 2003, 10 (4): 292-303. 10.1038/sj.gt.3301885.View ArticlePubMedGoogle Scholar
- Beier D, Wischhusen J, Dietmaier W, Hau P, Proescholdt M, Brawanski A, Bogdahn U, Beier CP: CD133 expression and cancer stem cells predict prognosis in high-grade oligodendroglial tumors. Brain Pathol. 2008, 18 (3): 370-377. 10.1111/j.1750-3639.2008.00130.x.View ArticlePubMedGoogle Scholar
- Levina V, Marrangoni AM, DeMarco R, Gorelik E, Lokshin AE: Drug-selected human lung cancer stem cells: cytokine network, tumorigenic and metastatic properties. PLoS One. 2008, 3 (8): e3077-10.1371/journal.pone.0003077.View ArticlePubMedPubMed CentralGoogle Scholar
- Kim RJ, Kim SR, Roh KJ, Park SB, Park JR, Kang KS, Kong G, Tang B, Yang YA, Kohn EA, et al: Ras activation contributes to the maintenance and expansion of Sca-1pos cells in a mouse model of breast cancer. Cancer Lett. 2010, 287 (2): 172-181. 10.1016/j.canlet.2009.06.010.View ArticlePubMedGoogle Scholar
- Clarke MF, Dick JE, Dirks PB, Eaves CJ, Jamieson CH, Jones DL, Visvader J, Weissman IL, Wahl GM: Cancer stem cells–perspectives on current status and future directions: AACR Workshop on cancer stem cells. Cancer Res. 2006, 66 (19): 9339-9344. 10.1158/0008-5472.CAN-06-3126.View ArticlePubMedGoogle Scholar
- Croker AK, Allan AL: Cancer stem cells: implications for the progression and treatment of metastatic disease. J Cell Mol Med. 2008, 12 (2): 374-390. 10.1111/j.1582-4934.2007.00211.x.View ArticlePubMedGoogle Scholar
- Bao L, Haque A, Jackson K, Hazari S, Moroz K, Jetly R, Dash S: Increased expression of P-glycoprotein is associated with doxorubicin chemoresistance in the metastatic 4T1 breast cancer model. Am J Pathol. 2011, 178 (2): 838-852. 10.1016/j.ajpath.2010.10.029.View ArticlePubMedPubMed CentralGoogle Scholar
- Dean M: Cancer stem cells: Implications for cancer causation and therapy resistance. Discov Med. 2005, 5 (27): 278-282.PubMedGoogle Scholar
- Kakarala M, Wicha MS: Implications of the cancer stem-cell hypothesis for breast cancer prevention and therapy. J Clin Oncol. 2008, 26 (17): 2813-2820. 10.1200/JCO.2008.16.3931.View ArticlePubMedPubMed CentralGoogle Scholar
- Morrison BJ, Schmidt CW, Lakhani SR, Reynolds BA, Lopez JA: Breast cancer stem cells: implications for therapy of breast cancer. Breast Cancer Res. 2008, 10 (4): 210-223. 10.1186/bcr2111.View ArticlePubMedPubMed CentralGoogle Scholar
- Minotti G, Menna P, Salvatorelli E, Cairo G, Gianni L: Anthracyclines: molecular advances and pharmacologic developments in antitumor activity and cardiotoxicity. Pharmacol Rev. 2004, 56 (2): 185-229. 10.1124/pr.56.2.6.View ArticlePubMedGoogle Scholar
- Mouridsen HT: Systemic therapy of advanced breast cancer. Drugs. 1992, 44 (Suppl 4): 17-28. discussion 66–19.View ArticlePubMedGoogle Scholar
- Chen JH, Ling R, Yao Q, Li Y, Chen T, Wang Z, Li KZ: Effect of small-sized liposomal Adriamycin administered by various routes on a metastatic breast cancer model. Endocr Relat Cancer. 2005, 12 (1): 93-100. 10.1677/erc.1.00871.View ArticlePubMedGoogle Scholar
- Molyneux G, Andrews M, Sones W, York M, Barnett A, Quirk E, Yeung W, Turton J: Haemotoxicity of busulphan, doxorubicin, cisplatin and cyclophosphamide in the female BALB/c mouse using a brief regimen of drug administration. Cell Biol Toxicol. 2011, 27 (1): 13-40. 10.1007/s10565-010-9167-1.View ArticlePubMedGoogle Scholar
- Swain SM, Whaley FS, Ewer MS: Congestive heart failure in patients treated with doxorubicin: a retrospective analysis of three trials. Cancer. 2003, 97 (11): 2869-2879. 10.1002/cncr.11407.View ArticlePubMedGoogle Scholar
- Kruger JA, Kaplan CD, Luo Y, Zhou H, Markowitz D, Xiang R, Reisfeld RA: Characterization of stem cell-like cancer cells in immune-competent mice. Blood. 2006, 108 (12): 3906-3912. 10.1182/blood-2006-05-024687.View ArticlePubMedGoogle Scholar
- Bandyopadhyay A, Wang L, Agyin J, Tang Y, Lin S, Yeh IT, De K, Sun LZ: Doxorubicin in combination with a small TGFbeta inhibitor: a potential novel therapy for metastatic breast cancer in mouse models. PLoS One. 2010, 5 (4): e10365-10.1371/journal.pone.0010365.View ArticlePubMedPubMed CentralGoogle Scholar
- Kaufman HL, Kim DW, DeRaffele G, Mitcham J, Coffin RS, Kim-Schulze S: Local and distant immunity induced by intralesional vaccination with an oncolytic herpes virus encoding GM-CSF in patients with stage IIIc and IV melanoma. Ann Surg Oncol. 2010, 17 (3): 718-730. 10.1245/s10434-009-0809-6.View ArticlePubMedGoogle Scholar
- Friedman GK, Langford CP, Coleman JM, Cassady KA, Parker JN, Markert JM, Yancey Gillespie G: Engineered herpes simplex viruses efficiently infect and kill CD133+ human glioma xenograft cells that express CD111. J Neurooncol. 2009, 95 (2): 199-209. 10.1007/s11060-009-9926-0.View ArticlePubMedPubMed CentralGoogle Scholar
- Li H, Dutuor A, Fu X, Zhang X: Induction of strong antitumor immunity by an HSV-2-based oncolytic virus in a murine mammary tumor model. J Gene Med. 2007, 9 (3): 161-169. 10.1002/jgm.1005.View ArticlePubMedGoogle Scholar
- Nakamori M, Fu X, Rousseau R, Chen SY, Zhang X: Destruction of nonimmunogenic mammary tumor cells by a fusogenic oncolytic herpes simplex virus induces potent antitumor immunity. Mol Ther. 2004, 9 (5): 658-665. 10.1016/j.ymthe.2004.02.019.View ArticlePubMedGoogle Scholar
- Loudon PT, McLean CS, Martin G, Curry J, Leigh Shaw M, Hoogstraten C, Verdegaal E, Osanto S: Preclinical evaluation of DISC-GMCSF for the treatment of breast carcinoma. J Gene Med. 2003, 5 (5): 407-416.View ArticlePubMedGoogle Scholar
- Zitvogel L, Apetoh L, Ghiringhelli F, Kroemer G: Immunological aspects of cancer chemotherapy. Nat Rev Immunol. 2008, 8 (1): 59-73. 10.1038/nri2216.View ArticlePubMedGoogle Scholar
- Bagalkot V, Lee IH, Yu MK, Lee E, Park S, Lee JH, Jon S: A combined chemoimmunotherapy approach using a plasmid-doxorubicin complex. Mol Pharm. 2009, 6 (3): 1019-1028. 10.1021/mp800177f.View ArticlePubMedGoogle Scholar
- Soeda A, Park M, Lee D, Mintz A, Androutsellis-Theotokis A, McKay RD, Engh J, Iwama T, Kunisada T, Kassam AB, et al: Hypoxia promotes expansion of the CD133-positive glioma stem cells through activation of HIF-1alpha. Oncogene. 2009, 28 (45): 3949-3959. 10.1038/onc.2009.252.View ArticlePubMedGoogle Scholar
- Israyelyan A, Shannon EJ, Baghian A, Kearney MT, Kousoulas KG: Thalidomide suppressed the growth of 4T1 cells into solid tumors in Balb/c mice in a combination therapy with the oncolytic fusogenic HSV-1 OncdSyn. Cancer Chemother Pharmacol. 2009, 64 (6): 1201-1210. 10.1007/s00280-009-0987-8.View ArticlePubMedGoogle Scholar
- Walker JD, Sehgal I, Kousoulas KG: Oncolytic herpes simplex virus 1 encoding 15-prostaglandin dehydrogenase mitigates immune suppression and reduces ectopic primary and metastatic breast cancer in mice. J Virol. 2011, 85 (14): 7363-7371. 10.1128/JVI.00098-11.View ArticlePubMedPubMed CentralGoogle Scholar
- Yun CO: Overcoming the extracellular matrix barrier to improve intratumoral spread and therapeutic potential of oncolytic virotherapy. Curr Opin Mol Ther. 2008, 10 (4): 356-361.PubMedGoogle Scholar
- Fukuhara H, Todo T: Oncolytic herpes simplex virus type 1 and host immune responses. Curr Cancer Drug Targets. 2007, 7 (2): 149-155. 10.2174/156800907780058907.View ArticlePubMedGoogle Scholar
- Fulci G, Breymann L, Gianni D, Kurozomi K, Rhee SS, Yu J, Kaur B, Louis DN, Weissleder R, Caligiuri MA, et al: Cyclophosphamide enhances glioma virotherapy by inhibiting innate immune responses. Proc Natl Acad Sci U S A. 2006, 103 (34): 12873-12878. 10.1073/pnas.0605496103.View ArticlePubMedPubMed CentralGoogle Scholar
- Kanai R, Wakimoto H, Cheema T, Rabkin SD: Oncolytic herpes simplex virus vectors and chemotherapy: are combinatorial strategies more effective for cancer?. Future Oncol. 2010, 6 (4): 619-634. 10.2217/fon.10.18.View ArticlePubMedPubMed CentralGoogle Scholar
- Ribacka C, Hemminki A: Virotherapy as an approach against cancer stem cells. Curr Gene Ther. 2008, 8 (2): 88-96. 10.2174/156652308784049372.View ArticlePubMedGoogle Scholar
- Toyoizumi T, Mick R, Abbas AE, Kang EH, Kaiser LR, Molnar-Kimber KL: Combined therapy with chemotherapeutic agents and herpes simplex virus type 1 ICP34.5 mutant (HSV-1716) in human non-small cell lung cancer. Hum Gene Ther. 1999, 10 (18): 3013-3029. 10.1089/10430349950016410.View ArticlePubMedGoogle Scholar
- Hu JC, Coffin RS, Davis CJ, Graham NJ, Groves N, Guest PJ, Harrington KJ, James ND, Love CA, McNeish I, et al: A phase I study of OncoVEXGM-CSF, a second-generation oncolytic herpes simplex virus expressing granulocyte macrophage colony-stimulating factor. Clin Cancer Res. 2006, 12 (22): 6737-6747. 10.1158/1078-0432.CCR-06-0759.View ArticlePubMedGoogle Scholar
- Kumar S, Gao L, Yeagy B, Reid T: Virus combinations and chemotherapy for the treatment of human cancers. Curr Opin Mol Ther. 2008, 10 (4): 371-379.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/12/549/prepub
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