ING4 expressing oncolytic vaccinia virus promotes anti-tumor efficiency and synergizes with gemcitabine in pancreatic cancer
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Yinfang Wu1,2,3, Xiaozhou Mou3,4, Shibing Wang3,4, Xing-E Liu5 and Xiaodong Sun1,2,4
1Department of Hepatobiliary and Pancreatic Surgery, Zhejiang Provincial People’s Hospital, People’s Hospital of Hangzhou Medical College, Hangzhou 310014, P. R. China
2The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou 310053, P. R. China
3Clinical Research Institute, Zhejiang Provincial People’s Hospital, People’s Hospital of Hangzhou Medical College, Hangzhou 310014, P. R. China
4Key Laboratory of Tumor Molecular Diagnosis and Individualized Medicine of Zhejiang Province, Hangzhou 310014, P. R. China
5Department of Medical Oncology, Zhejiang Hospital, Hangzhou 310007, P. R. China
Xiaodong Sun, email: [email protected]
Xing-E Liu, email: [email protected]
Keywords: oncolytic vaccinia virus, ING4, gene therapy, gemcitabine, pancreatic cancer
Received: May 25, 2017 Accepted: August 26, 2017 Published: September 20, 2017
With no effective treatments available for most pancreatic cancer patients, pancreatic cancer continues to be one of the most difficult malignancies to treat. Oncolytic virus mediated-gene therapy has exhibited ubiquitous antitumor potential. In this study, we constructed a novel oncolytic vaccinia virus harboring the inhibitor of growth family member 4 gene (VV-ING4) to investigate its therapeutic efficacy alone or in combination with gemcitabine against pancreatic cancer cells in vitro and in vivo. ING4 expression was determined via quantitative real-time polymerase chain reaction (qPCR) and western blot. The cytotoxicity of VV-ING4 was measured using a cell proliferation assay. Both flow cytometry and western blot were applied to analyze the cell cycle and apoptosis. Furthermore, the combination inhibitory effect of VV-ING4 and gemcitabine was assessed using Chou-Talalay analysis in vitro and a BLAB/c mice model in vivo. We found that VV-ING4 significantly increases ING4 expression, displayed greater cytotoxic efficiency, and induced pancreatic cancer cell apoptosis and G2/M phase arrest. Additionally, the combination of VV-ING4 and gemcitabine synergistically effect in vitro and in vivo. Taken together, our data implicate VV-ING4 as a conceivable pancreatic cancer therapeutic candidate alone or in combination with gemcitabine.
Pancreatic cancer is an extremely lethal disease. It is the fourth most prevalent cause of cancer death, with a 5-year survival rate of only 5% [1, 2]. Complete surgical abscission remains the only curative treatment. Sadly, only 10% to 20% of pancreatic tumors are in a position in which they can be surgically removed at the time of diagnosis . For patients with unresectable or metastatic pancreatic tumors, chemotherapy with gemcitabine (Gem) is the first-line therapy. However, acquired resistance to gemcitabine has become an increasing challenge in treating pancreatic tumors . Thus, more potent treatments are needed to improve the outcome of patients with pancreatic cancer.
Gene therapy represents a novel and promising remedial modality for cancer treatment. Gene therapy can be divided into monogene therapy  and multigene-based combination therapy . The ING tumor-suppressor family (ING1-5) identified during the past decade act as regulators of transcription, DNA repair, cell cycle checkpoints, apoptosis, angiogenesis, and cellular senescence . ING4, a recently discovered protein, inhibits angiogenesis by correlating with NF-κB subunit p65 (RelA) , the loss of contact suppression evoked by MYCN or MYC , and the activation of hypoxia inducible factor (HIF) . In addition, substantial studies have reported that ING4 displays pervasive antitumor properties also by inducing apoptosis in a p53-dependent way and significant G2/M cell cycle arrest in a spectrum of cancer cells [6, 8, 11–13]. ING4 also increases cancer cell sensitivity to chemotherapeutic drugs [14, 15]. Conversely, deletion or down-regulation of ING4 is firmly associated with high tumor grade, metastasis, and poor prognosis in a number of cancers, including breast carcinoma , glioblastoma  and gastric carcinoma . According to the Human Protein Atlas Database (HPA, http://www.proteinatlas.org), ING4 expression is low in pancreatic cancer, indicating its potential functions in transformation and development of pancreatic cancer.
Vaccinia virus (VACV), a member of the poxvirus superfamily, holds several inherent advantages as a vector for cancer gene therapy. Specifically, the virus contains the TK gene which codes for a phosphotransferase that enables viral replication. When the gene is disrupted, it inhibits viral replication in normal, non-dividing cells . However, cancer cells have a high concentration of functional nucleotides that enables VACV to selectively replicate in tumor cells. The size of the VACV genome, 200 kb, is permissive to the introduction of foreign genes up to 25 kb in length . Other advantages include an excellent safety profile , high capability of transgene expression , and the capability to function under hypoxia conditions . VACV-based gene therapy has been shown to significantly inhibit cancer cell growth with low cytotoxic effects against healthy tissue in many different tumor types including myeloma , pancreatic carcinoma , hepatocellular carcinoma  and gastric carcinoma . Despite its potential as a cancer therapy, the role of VACV-mediated ING4 gene therapy for human pancreatic cancer has not been reported.
In this study, we constructed a novel oncolytic vaccinia virus expressing ING4 (VV-ING4), and evaluated its therapeutic efficacy alone or in combination with gemcitabine against pancreatic cancer cells in vitro and in vivo. Our data implicate that VV-ING4 is a potential candidate alone and in combination with gemcitabine for pancreatic cancer therapy.
Construction and characterization of VV-ING4
We constructed an expression cassette consisting of the ING4 gene and the gpt selection gene promoted by the viral promoter Pse/L or P7.5k, respectively. These genes were inserted into the viral TK gene (Figure 1A). VV, a control virus, was constructed similarly but without ING4 gene insertion. The whole expression cassette was constructed into the pCB vector, which is a shuttle plasmid for VV and VV-ING4 packaging. We verified significant expression of ING4 gene in pancreatic cancer cells after infection with VV-ING4 using qPCR (Figure 1B) and western blot (Figure 1C).
Figure 1: Characterization of VV-ING4. (A) Linear schematic of VV-ING4 structure. VV: oncolytic vaccinia virus. gpt works as a screen gene. ****, sites of anticipated homologous recombination. 5′TK and 3′TK, viral flanking sequences of the thymidine kinase gene. ITR, inverted terminal repeat. (B–C) The expression of ING4. Cells were infected with VV or VV-ING4 at a MOI of 5 for 48 hrs. The ING4 expression was determined using qPCR and western blot. GAPDH (B) and β-actin (C) served as internal controls. Data are presented as mean ± standard deviation (SD) or the representative of three separate experiments (*** represents P < 0.001). (D) Replication profiles of VV and VV-ING4 in HEK293A cells. Cells were infected at a MOI of 0.02. The titer at each time point is presented as mean ± SD of at least three separate experiments.
The titer and replication rate of each virus was measured. As shown in Table 1, VV and VV-ING4 grew efficiently in HEK293A cells with expected and equivalent titers. The two recombinant viruses have similar replication rates (Figure 1D, P > 0.05).
Table 1: Virus particle titers and vp/pfu ratios
Recombinant vaccinia virus
Physical titer (vp/ml)
Infectious titer (pfu/ml)
5.03 × 109
1.61 × 108
4.27 × 109
1.76 × 108
Note: vp, virus particle; pfu, plaque forming units.
Pancreatic cancer-specific cytotoxicity of VV-ING4 in vitro
The cytotoxicity of VV-ING4 was evaluated in three pancreatic cancer cell lines (PANC-1, BXPC-3 and SW1990) and a normal liver cell line (QSG-7701) at 48 hrs post-infection using the MTS cell proliferation assay. The results showed that growth of VV-ING4-infected pancreatic cancer cells was inhibited in a dose-dependent manner, with EC50 values lower than that of VV (Figure 2A). However, growth of normal cells QSG-7701 was not inhibited significantly (Figure 2B). These findings indicate that VV-ING4 efficiently represses in vitro pancreatic cancer cell growth with minimal influence on normal cells.
Figure 2: Pancreatic cancer-specific cytotoxicity of VV-ING4. Cells were seeded in 96-well plates and infected with VV or VV-ING4 at a series of MOIs. Cell viability was determined by MTS cell proliferation assay at 48 hrs post-infection. (A) Cytotoxicity and EC50 of VV and VV-ING4 in three pancreatic cancer cell lines. (B) Cytotoxicity of VV and VV-ING4 in QSG-7701 cells. The results were presented as mean ± SD of three separate experiments (* represents P < 0.05, ** represents P < 0.01 and *** represents P < 0.001, one-way analysis of variance (ANOVA) and multiple comparisons).
VV-ING4 induced apoptosis in pancreatic cancer cells in vitro
We then examined whether VV-ING4 inhibits cell growth by inducing apoptosis by treating pancreatic cancer cells with VV-ING4 for 48 hrs. As shown in Figure 3A–3C, VV-ING4 induced significant apoptosis in SW1990 cells, compared with VV- or PBS-treated cells. Western blot analysis revealed activation of Caspase 8/9/3 and enhanced poly (ADP-ribose) polymerase (PARP) cleavage, and Bax in VV-ING4-infected cells (Figure 3D). Expression of pro-survival proteins Bcl-2 and XIAP was remarkably decreased (Figure 3D). Taken together, these observations indicate that VV-ING4 induces apoptosis in pancreatic cancer cells.
Figure 3: VV-ING4 induced apoptosis in pancreatic cancer cells in vitro. (A) Apoptosis analysis using Annexin V-FITC/PI double staining. SW1990 cells were infected with VV or VV-ING4 (MOI = 5) for 48 hrs. The florescence was analyzed by flow cytometry (Data are presented as mean ± SD of three separate experiments; ** represents P < 0.01, *** represents P < 0.001). (B–C) Apoptosis detection through measurement of DNA fragmentation. Cells were treated as indicated above, stained with TUNEL solution (B) or Hoechst 33258 (C). The arrows signify fragmented nucleic, scale bar: 500 μm; average values of TUNEL+ cells rate were determined by flow cytometry and expressed as mean ± SD of three separate experiments; ** represents P < 0.01, *** represents P < 0.001. (D) Apoptosis detection by Western blot. β-actin served as a loading control. Results are representative of three separate experiments.
VV-ING4 induced G2/M cell cycle arrest in pancreatic cancer cells
To assess the effect of VV-ING4 on cell cycle regulation, SW1990 cells were treated as indicated above. The cells were then stained with Propidium Iodide (PI) and analyzed by flow cytometry. VV-ING4-treated cells contained a remarkably smaller S phase population and a significantly larger G2/M phase population than VV- or PBS-treated cells (Figure 4A). Western blot analysis showed that expression of cyclin D1, cyclin D3, CDK2 and CDK4 in VV-ING4-treated cells was significantly lower, whereas the expression of p21 was higher when compared with VV- or PBS-treated cells (Figure 4B). Taken together, these findings suggest that VV-ING4inhibits pancreatic cancer cells in part through alteration of cell cycle protein expression.
Figure 4: Regulation of the cell cycle by VV-ING4 in SW1990 cells. (A) Analysis of cell cycle distribution. SW1990 cells were infected with VV or VV-ING4 (MOI = 5) for 48 hrs. Cells were stained with PI. The florescence was analyzed by flow cytometry (Data are presented as mean ± SD of three separate experiments; ** represents P < 0.01). (B) Expression analysis of cell cycle-related proteins by western blot. Cells were infected as described above. β-actin was normalised as an internal reference. Data are representative of three determinations.
Combination therapy of gemcitabine and VV-ING4 synergistically suppress pancreatic cancer cell proliferation
To determine whether VV-ING4 enhances the antitumor effects of gemcitabine, SW1990 and PANC-1 cells were treated as indicated in the MATERIALS AND METHODS section. Cell viability was determined 2 days later. As shown in Figure 5A, a negative dose-response effect was evident in all cases. Combination treatment significantly inhibited cell growth in both cell lines examined.
Figure 5: Evaluation of synergistic effect between gemcitabine and VV-ING4 in vitro. (A) Dose–response histogram of cell viability. SW1990 and PANC-1 cells were seeded at 10,000 cells/well into 96-well plates. For synergism research, gemcitabine and VV-ING4 were analyzed as a constant ratio of 2.5/1. Cell viability was measured 2 days later. Data shown are representative of three independent experiments. (B) Synergism detection was conducted by Chou–Talalay Combination Index (CI) analysis using CalcuSyn software (Biosoft, Cambridge Place, Cambrige, UK). The middle curve line stands for the simulated CI values, which were expressed as the log10 (CI) ± 1.96 SD. The log10 (CI) values represent an antagonism between the treatments when > 0, an additive efficiency when equal to 0 and a synergism when < 0.
We evaluated the potential synergism between VV-ING4 and gemcitabine by Chou–Talalay Combination Index (CI) analysis. At all the fractions considered, the Chou–Talalay CI was less than one in both SW1990 (CI 0.903–0.633, log10 (CI) < 0) and PANC-1 cells (CI 0.538–0.439, log10 (CI) < 0) (Figure 5B), indicating a potentiation effect of gemcitabine when combined with VV-ING4. Hence, the combined treatment of gemcitabine and VV-ING4 synergistically represses pancreatic cancer cell proliferation.
Combination therapy of gemcitabine and VV-ING4 showed an enhanced tumor-killing effect in vivo
To analyze the impact of the combined treatment in vivo, animal experiments (BALB/c athymic nude mice) were performed following the protocol described in Figure 6A. We found that mean tumor volume rapidly declined in animals treated with the combination therapy when compared to tumors from animals treated with either individual therapy (Figure 6B–6C). To affirm the underlying mechanism, we evaluated the effect of combined treatment on tumor cell apoptosis in vivo by flow cytometry analysis. As shown in Figure 6D, the percentage of apoptotic SW1990 cells was significantly higher in the combination treatment group, compared with either individual treatment group.
Figure 6: Combination therapy of gemcitabine and VV-ING4 showed an enhanced tumor-killing effect in vivo. (A) Schematic of injections with experimental timeline. BALB/c athymic nude mice were intratumorally injected with PBS (100 μl), VV (1 × 107 pfu) or VV-ING4 (1 × 107 pfu) every other day for a total of 6 times, or intraperitoneally injected with a single dose of gemcitabine (40 mg/Kg) every other three days for 3 times or a combination therapy based on gemcitabine and VV-ING4. The tumor volume (B) was determined. Mice were sacrificed at 4 weeks post-injection. Tumors were removed and weighted (C). Tumor cell apoptosis in vivo was detected by flow cytometry (D) (*** represents P < 0.001. Results are presented as mean ± SD of three separate experiments). (E) Histopathological analysis. Tumor samples from different groups were subjected to H&E staining, immunohistochemical analysis and TUNEL assay. Quantitative graph for percentage of Ki67, ING4 and TUNEL positive cells are given (5 random fields, 4 sections for each sample, *** represents P < 0.001, scale bars: 500 μm, 400× magnification).
Hematoxylin and eosin (H&E) and immunohistochemical (IHC) staining for Ki-67 were applied to assess and compare tumor tissue histopathology. Decreased Ki-67 expression and H&E staining revealed that combination therapy had a more cytotoxic effect on tumor proliferation than either treatment alone (Figure 6E). IHC analysis using anti-ING4 antibody confirmed expression of ING4 in the tumor tissues following by combined treatment (Figure 6E).
Apoptosis was further examined using the terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay. Results from this experiment showed significantly higher apoptosis rates in the combination treatment when compared with either individual treatment (Figure 6E).
In this study, we constructed an oncolytic vaccina virus expressing tumor suppressor ING4 (VV-ING4) and revealed that ING4 expression exhibits anti-tumor effects alone and in combination with gemcitabine against pancreatic cancer cells in vitro and in vivo.
ING4 expression induced significant apoptosis in SW1990 human pancreatic cancer cells, consistent with the findings of previous studies [12, 27, 28]. Chen et al. showed miR-214 inhibits apoptosis in pancreatic cancer tissues by downregulating ING4 expression . In this study, we found that infection of VV-ING4 reduced the ratio of Bcl-2/Bax and induced the activation of Caspase 8/9/3 and PARP in SW1990 human pancreatic cancer cells (Figure 3D), suggesting that Caspase-dependent apoptosis and the Bcl-2 family is participated in VV-ING4-induced cytotoxicity. This finding is in line with a previous study which identified the Fas/Caspase-8 pathway as a mechanism of ING4-induced apoptosis in human melanoma cells . Another potential mechanism by which ING4 induces apoptosis is promotion of p53. An earlier study by Shiseki et al. reported that ING4 induced apoptosis of RKO colon cancer cells via enhancing the function of p53 . The tumor suppressor p53 is well known to have a pro-apoptotic function through regulation of Bcl-2 and Bax expression [31, 32]. These results support the involvement of Bcl-2 family proteins in ING4-induced apoptosis . ING4 may also induce apoptosis through negative regulation of NF-κB signaling  and via cooperating with other tumor suppressors . More research is needed to tease out the mechanism underlying ING4 pro-apoptotic effects.
We also found that ING4 expression induces significant cell cycle arrest in pancreatic cancer cells. This is consistent with previous studies that have shown that ING4 promotes cell cycle arrest in other cancer cells [14, 28]. It is well known that cyclins, cyclin-dependent kinases (CDKs) and CDK inhibitors are crucial for cell cycle progression. The activities of various cyclin/CDK complexes are inhibited by the CDK inhibitors, such as p16, p21, and p27. It has been proved that ING4 upregulated p21 in a p53-dependent manner . p21 restricts the activity of cyclin E-CDK2, cyclin D3-CDK4 and cyclin B1/CDC2 complexes leading to G2/M arrest [35, 36]. p21 also inhibits cyclin D1 activity , which can cause G2/M arrest [38, 39]. Interestingly, ING4 was reported to connect with p300  and NF-κB subunit p65 (RelA) . Whether ING4-induced upregulation of p21 was related with these p53-independent signaling pathways still needs to be further studied. In our study, flow cytometry analysis showed VV-ING4 infection altered the cell cycle with S-phase reduction and G2/M phase arrest, which differs from the preceding report using RKO colon cancer cells . This may be due to the use of different tumor cell lines with specific characteristics in these studies. Further study indicated that ING4 expression significantly decreased the expression of cyclin D1, cyclin D3, CDK2 and CDK4, whereas the expression of p21 was increased. Therefore, ING4-induced upregulation of p21 may contribute to the G2/M cell cycle arrest in VV-ING4-treated human pancreatic cancer cells.
Finally, combination therapy of VV-ING4 and gemcitabine synergistically promoted cell death in pancreatic cancer cells in vitro and in vivo. Multiple mechanisms may account for this improved anti-tumor efficiency. Xu et al. reported that ING4 enhances the sensitivity of cells to chemotherapy by decreasing p-Stat3 expression . In addition, cooperative regulation of apoptosis pathways and the inhibition of tumor angiogenesis between IGN4 and chemotherapy may also contribute to the synergistic effect . Gemcitabine is a standard first-line treatment for pancreatic cancer. However, one disadvantage to gemcitabine efficacy is its disappointing penetration into tumor parenchyma . VV-ING4 may selectively replicate in and lyse tumor cells, which disrupt tumor architecture thus facilitating gemcitabine penetration to generate a synergistic effect. Additionally, gemcitabine has been shown to enhance vaccine efficacy by obviating CD11b+/Gr-1+ myeloid-derived suppressor cells (MDSCs) in a murine model of pancreatic carcinoma , and vice versa . In addition, suboptimal doses of gemcitabine invigorate viral uptake in pancreatic cancer cell lines . Furthermore, the synergism in the combination therapy may also be caused by unblocking host pathways, transporting viruses with greater efficiency and/or increasing virus generation at the tumor site . In this study, flow cytometry analysis and TUNEL assay indicate that the percentage of apoptotic cells in the combined therapy group was significantly higher compared with either individual sample, exhibiting an apoptosis-induction synergism, which is consistent with the previous study .
To our knowledge, this is the first study to show that VV-ING4 can induce the death of pancreatic cancer cells and in combination with gemcitabine shows a synergistic effect in vitro and in vivo. However, there still remain many obstacles to be conquered for in applying VV-ING4 to clinical practice, such as efficient delivery and expression of ING4, the cytotoxicity of viral vector, or immune responses against viral antigens. Hence, future studies aim to develop a tumor-specific delivery system using carrier cells or nanotechnologies to promote the transfection efficiency of VV-ING4 and weaken the potential systemic toxicity in our future work.
In conclusion, our data suggest that VV-ING4 is a conceivable candidate alone and in combination with gemcitabine for pancreatic cancer therapy.
MATERIALS AND METHODS
Cell lines and vectors
The human embryonic kidney cell line 293A and the liver cell line QSG-7701 were retained in our lab. SW1990, BXPC-3 and PANC-1 human pancreatic cancer cell lines were purchased from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China). The cell lines were authenticated by short-tandem repeat profiling. Cells were cultivated in Dulbecco’s modified Eagle’s medium (DMEM), supplied with 10% fetal bovine serum (FBS), penicillin (100 U/ml), streptomycin (100 μg/ml), and L-glutamine (2 mM, Gibco, Invitrogen), incubated at 37°C in a humidified 5% CO2 atmosphere in air. The wild-type vaccinia virus (VACV) and pCB vector were kindly offered by academician Xinyuan Liu.
Cell cycle and apoptosis detection kit and the TUNEL kit were purchased from Beyotime biotechnology company (Beyotime, Jiangsu, China). Tissue dissociation kit was purchased from Miltenyi (Miltenyi, Bergisch Gladbach, Germany). Antibodies against ING4 (1:1000), Bax (1:1000), cyclin D1 (1:5000), cyclin D3 (1:5000), CDK2 (1:5000) and CDK4 (1:5000) were purchased from Abcam (Shanghai, China). Antibodies against Caspase 8 (1:1000), Caspase 3 (1:1000) and Bcl-2 (1:1000) were obtained from the Bioworld Company (Minnesota, USA). Caspase 9 (1:1000), XIAP (1:1000) and p21 (1:1000) antibodies were purchased from EMD Millipore Corporation (Billerica, MA, USA). PARP antibody (1:1000) was purchased from Sino Biological Inc. (Beijing, China). β-actin (1:5000) antibody was obtained from HuaAn Biotechnology Co., Ltd. (Hangzhou, China). The primers used in this study were synthesized in Generay Biotech Co.,Ltd (Shanghai, China).
Construction, identification and purification of oncolytic vaccinia viruses
The entire ING4 cDNA sequence was PCR-amplified with specific primer pairs: 5′-GGCCTCGAGATGG CTGCGGGGATGTATTTG-3′ [forward] and 5′-GG CGGTACCCTATTTCTTCTTCCGTTCTTGGGAG- 3′ [reverse]. The artificial DNA was digested with BglII and ECORI (Takara, Japan), then inserted into pCB plasmid to create pCB-ING4. After sequence confirmation, pCB or pCB-ING4 homologously recombined with VACV in HEK293A cells using Lipofectamine 3000 (Invitrogen, Shanghai, China). After observing cytopathic effect, cell culture medium was gathered to obtain recombinant viruses. Mycophenolic acid, dioxopurine and hypoxanthine were applied to get rid of VACV. Recombinant vaccinia viruses were amplified in HEK293A cells and purified by ultracentrifugation. OD260 assay and plaque formation assay were used to determine viral titers.
Viral replication rate
Viral growth curves were determined as described previously . Briefly, HEK293A cells at a density of 62,500/cm2 were infected with VV or VV-ING4 at a MOI of 0.02. At 12 hrs intervals post-infection, the supernatant was collected and titered by plaque assay in HEK293A cells at a density of 50,000/cm2. Virus titers were expressed as plaque forming units (pfu) per mL (pfu/ml).
RNA was extracted with Trizol reagent (Invitrogen, Shanghai, China) following the manufacturer’s instructions. cDNA was generated using the PrimeScript RT reagent kit (Tokyo, Japan). The qPCR reactions were conducted in a total volume of 20 μl by using the following procedure: 1 cycle at 95°C (10 min), then 60°C (30 sec), followed by 39 cycles at 95°C (10 sec), 60°C (30 sec). PCR amplicons were determined based on SYBR Green I detection (Roche Diagnostic, Indianapolis, USA), and the authenticity was certified by melting curve analysis. Quantitative PCR was operated using the CFX-96 qPCR system and iQ SYBR Green Supermix (Bio-Rad). Relative gene expression was determined via the 2-ΔΔCt method. The primers used are as follows: Gene: Sequence; ING4: 5′-AGTATGGGATGCCCTCAGTG-3′ (forward), 5′-GACCTGGTGACAAAGGCAAT-3′ (reverse);GAPDH: 5′-CTTTGGTATCGTGGAAGGACTC-3′ (forward), 5′-G TAGAGGCAGGGGATGATGTTCT-3′ (forward).
Western blot analysis
Floating and adherent cells were harvested in lysis buffer (Beyotime, Jiangsu, China) involving 1% Complete Mini-Protease Inhibitor Cocktail (Roche Diagnosis, Switzerland), and 5 mM NaF. Protein extractions were quantified using the BCA kit (Thermo scientific, MA, USA) and heated for 10 min at 100°C. 30 μg of protein was resolved in 12% SDS-PAGE and transferred to nitrocellulose membrane (Merk Millipore, Germany). After blocked for 1 hour at 37°C, the membranes were immunobloted with different antibodies overnight at 4°C. Membranes were then washed with TBST and incubated with HRP-conjugated goat anti-rabbit or anti-mouse antibody (1:5000) for 1 hour at room temperature. Finally, blots were detected using ChemiDoc™ MP Imaging System (Bio-Rad) with a SuperEnhanced chemiluminescence detection kit (Applygen, Beijing, China).
MTS cell proliferation assay
PANC-1, BXPC-3 and SW1990 cells and normal liver cells QSG-7701 were dispensed in 96-well culture plates at a density of 1 × 104 cells/well. After attachment, cells were infected with VV or VV-ING4 at a MOI of 0.1, 1, 5, 10 or 20. The medium added with PBS was a blank control. At 48 hrs post-infection, cells were further incubated with 20 μl/well MTS reagent (Promega, Madison, WI, USA) at 37°C for 4 hrs. After shaked for 1 min, plates were read at 490 nm using a Microplate Reader Model 550 (Bio-Rad, Shanghai, China). Cell viability% = [(experimental group OD - blank control OD)/(negative control OD - blank control OD)] × 100%. The viral MOIs required to kill 50% of cells (the median effective concentration [EC50]) were determined.
Hoechst DNA staining
SW1990 cells at a density of 2 × 104 cells/coverslip were treated with VV or VV-ING4 at a MOI of 5. At 48 hrs post-infection, cells were fixed with 4% paraformaldehyde, stained with Hoechst 33258 (Beyotime, Jiangsu, China, 1 μg/ml) for 15 min at room temperature. The chromatin changes were visualized under a Nikon standard fluorescence microscope (Ti-U, Nikon, Japan) with NIS-Elements BR 4.50.00 imaging software. Four random microscopic fields (400× magnification) were selected per sample. Three replicates were performed.
Flow cytometry analysis
At 48 hrs post-infection, SW1990 cells were harvested at a density of 6 × 105 cells/ml. 2 ml collected cells were centrifuged, incubated in 300 μl of 1X binding buffer with 5 μl of Annexin V-FITC and 10 μl of PI for 10 min. For TUNEL assay, 2 ml collected cells were fixed in 4% paraformaldehyde solution for 30 min and permeabilizated in 0.1% Triton X-100 solution for 10 min. Cells were incubated in TUNEL reaction mixture (50 μl) for 60 min at 37°C, then transferred into a tube to a total volume of 500 μl in PBS. The florescence was analyzed by NovoCyte Flow Cytometer (ACEA Biosciences Inc. San Diego, CA).
For cell cycle analysis, 1 ml collected cells were centrifuged, fixed with cold 75% alcohol overnight, incubated in 500 μl of staining buffer containing 25 μl of PI and 10 μl of RNase A for 30 min. The florescence was analyzed by flow cytometry.
Dose–response and combination index analysis
SW1990 and PANC-1 cells in 96-well plates were treated with different doses of gemcitabine (μM) (Eli Lilly, Indianapolis, USA) or VV-ING4 (MOI), or combination with a constant ratio of gemcitabine/VV-ING4 of 2.5/1. Cell viability was measured 48 hrs later, based on which the synergism between gemcitabine and VV-ING4 was analyzed with Calcusyn Software (Biosoft, Cambridge, UK). For combination index plots, CI is expressed as the log10 (CI) ± 1.96 SD, the 95% confidence intervals are shown where estimable. CI values were calculated over a scope of levels of growth inhibition (GI) from 20% to 80% of the fraction affected.
All animal experiments were approved by the Institutional Animal Care and Use Committee, performed according to the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health, and followed the guidelines of the Animal Welfare Act. BALB/c athymic nude mice (male, 5-week old and 17–20 g) were purchased from Shanghai Experimental Animal Center (Shanghai, China). One week later, mice were randomly grouped (7 mice per group) and subcutaneously injected on the neck with 1 × 106 SW1990 cells. When tumors grew up to about 200 mm3, mice were injected following the schematic of injections in Figure 6A. On day 7 post-intervention, xenografted tumors from two mice per group were digested enzymatically for apoptosis detection. Tumor volumes were calculated every other three days. Mice were sacrificed at 4 weeks post-injection according to ethical instructions. Tumors were separated, fixed by 4% paraformaldehyde, imbedded in paraffin, finally cut into 4 μm sections for hematoxylin and eosin staining, immunohistochemistry analysis and TUNEL assay according to manufacturers’ instructions. For immunohistochemistry analysis, slides were incubated with primary antibodies: anti-Ki 67 (1:100, HuaAn, Hangzhou, China) or anti-ING4 (1:100, Abcam, Shanghai, China) overnight at 4°C, then incubated with biotinylated secondary antibody, further visualized using a diaminobenzidine (DAB) Kit (Thermo scientific, Waltham, MA).
An analysis of variance (ANOVA) was applied for comparison of 3 or more groups. The analysis of the combined effects was performed with CalcuSyn software 2.0 (Biosoft, Cambridge, UK). Data are expressed as mean ± SD. Statistical analysis was performed with IBM SPSS Statistics software version 20 (SPSS Inc., Chicago, IL). Statistical significance was prescribed at P < 0.05.
ING4: inhibitor of growth family member 4; VV: oncolytic vaccinia virus; MOI: multiplicity of infection; PBS: phosphate buffered saline.
ACKNOWLEDGMENTS AND FUNDING
This article was supported by the Zhejiang Provincial Natural Science Foundation of China (No. LY15H160051, LY14H160041, LY17H160066), National Science Foundation of China (NO. 81602706, 81672430, 81172137), Funds of Science Technology Department of Zhejiang Province (NO. 2017C33116), Zhejiang Medical Technology Plan Project (No. 2016KYA018, 2016140143, 2013KYB007, 2014PYA001), State administration of Traditional Chinese Medicine of Zhejiang (NO. 2017ZB006).
CONFLICTS OF INTEREST
The authors declare no conflicts of interest.
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