Enhanced therapeutic effect of an antiangiogenesis peptide on lung cancer in vivo combined with salmonella VNP20009 carrying a Sox2 shRNA construct
© The Author(s). 2016
Received: 29 March 2016
Accepted: 21 June 2016
Published: 2 July 2016
HM-3 is a polypeptide inhibiting angiogenesis. Recent reports suggest that the antitumor effect of angiogenesis inhibitors administered alone might be limited. Cancer stem cells can survive the lack of oxygen and nutrients. To achieve better anti-tumor effect, HM-3 was administered in combination with the attenuated Salmonella typhimurium VNP20009 transformed with a shRNA construct against sex determining region Y-box 2 (Sox2).
Cell invasion assay and soft agar colony formation assay were used to assess the migration and growth capability of A549 cells once Sox2 was knocked down with the shRNA construct. The shRNA construct targeting Sox2 was transformed into VNP20009. After the mouse xenograft model of A549 was established, HM-3 was co-administered with VNP20009 carrying the shRNA construct. The growth of tumor was checked to compare the effectiveness of different therapies. Western blotting assay and immunohistochemistry staining of the tumor tissue were used to measure the levels of proteins associated with the apoptosis pathway.
Sox2 was necessary for the migration and growth of A549 cells. The expression of Sox2 was down regulated in the tumor tissue of the combined treatment group of HM-3 with VNP20009 carrying the Sox2 shRNA construct. Together with the accumulation of salmonella in tumor and the inhibition of angiogenesis by HM-3, more tumor cells went through cell apoptosis with increased expression of Bax, cleaved Caspase 3 and decreased expression of Bcl2.
The results suggest the combination of antiangiogenesis agent HM-3 with gene therapy targeting Sox2 delivered by salmonella as a promising strategy for the treatment of lung cancer.
KeywordsSox2 Lung cancer Antiangiogenesis Salmonella typhimurium Apoptosis
Lung cancer is one of the leading causes of cancer-related death throughout the world. The average 5-year survival rate of non-small cell lung carcinoma (NSCLC) which accounts for 85 % of lung cancers is only 4 %, highlighting the need for more effective treatment options . HM-3 is an 18-amino acid peptide generated by the fusion of the Arg-Gly-Asp (RGD) sequence to the C-terminus of an endostatin-derived peptide. Our previous research has shown that HM-3 has no effect on the growth of tumor cells in vitro. However, HM-3 can inhibit tumor growth by inhibiting angiogenesis in vivo [2, 3]. The binding of HM-3 to integrin αvβ3 expressed on the surface of vascular endothelium cells (VECs) results in the down-regulation of MEK1 and AKT1, leading to the inhibition of the migration of VECs [4–6]. HM-3 has been approved for phase I clinical study in China (Register number: CTR20150368). Recent studies reported that the antitumor effect of angiogenesis inhibitors (AIs) administered alone might be limited implicating that additional tumor targeting drugs should be co-administered with AIs [7–9].
Tumor growth is sustained by a small number of tumor-initiating cells known as cancer stem cells (CSCs). Sox2, a gene expressed at high level in stem cells, also plays a vital role in the regenesis of lung CSCs [10–12]. It has been reported that the growth and metastasis of certain cancer cells were suppressed when Sox2 was down regulated suggesting Sox2 may be a potential target for cancer treatment [13, 14]. Finding an effective way to deliver Sox2 shRNA constructs into lung cancer cells may achieve better anti-tumor effect. Among the gene therapy delivery systems reported, attenuated salmonella offers more advantages as it can preferentially accumulate and amplify in solid tumor with little toxicity to normal organs. Also, it has been used as gene therapy delivering system for many shRNA constructs targeting different genes such as indoleamine 2, 3-dioxygenase 1 (IDO1) , multiple drug resistance 1 (MDR1)  and murine double minute 2 (MDM2) .
Here, we explored the antitumor effect of the novel combination therapy of HM-3 with VNP20009 carrying a Sox2 shRNA construct in a mouse xenograft model of NSCLC. Our results showed that the combined therapy had the optimal antitumor effect compared to HM-3 alone or docetaxel alone. The optimal therapeutic effect was achieved through accumulation of VNP20009 in tumor tissue, suppression of the expression of Sox2 and inhibition of angiogenesis in tumors. More tumor cells went through cell apoptosis in the combined treatment group. Also, no apparent toxic side-effect was observed in the mice.
Cell lines, animals and drugs
The NSCLC cell line A549 was purchased from Shanghai Institute of Cell Biology, Chinese Academy of Sciences (Shanghai, China). A549 cells were maintained in RPMI-1640 medium containing 10 % FBS. Athymic BALB/c nude female mice (5 weeks) were purchased from CAVENS (Changzhou, China). HM-3 (sequence: IVRRADRAAVPGGGGRGD) with purity of more than 99 % was chemically synthesized in our lab. The antibodies against Sox2 and CD31 were purchased from Santa Cruz (Dallas, USA). The antibodies against Bax and Bcl2 were obtained from Wanleibio (Dalian, China). The antibody against cleaved Caspase 3 was obtained from Elabscience (Wuhan, China). Docetaxel Injection was purchased from Hengrui (Jiangsu, China).
Plasmids and bacterial strains
The mammalian shRNA expression plasmid (pGPU6/Neo) targeting Sox2 was constructed by GenePharma (Shanghai, China). The shRNA sense sequence targeting Sox2 was TGGACAGTTACGCGCACATGA as reported and the scrambled shRNA sense sequence was GTTCTCCGAACGTGTCACGT . The scrambled shRNA construct was referred as shScr while the Sox2 shRNA construct was referred as shSox2. The shRNA construct was electroporated into VNP20009 with a Gene Pulser Xcell system (Bio-Rad) at 2.5 kV, 186 ohms . VNP20009 transformed with the shScr (shScr-V) and VNP20009 transformed with the shSox2 (shSox2-V) was cultured in Luria-Bertani (LB) broth supplemented with ampicillin (50 μg/ml) . The shRNA constructs were isolated and the targeting sequence was confirmed by sequencing. To calculate the number of colony forming unit (cfu) in culture, an optical density of 1.0 measured at 600 nm equal to 109 cfu/ml was used.
Cell invasion assay and soft agar colony formation assay
The cell invasion assay was performed using 24-transwell chambers (Corning, Newyork, USA). The procedures were carried out as previously reported . For soft agar colony formation assay, a layer of media with 0.5 % agarose was first plated onto the bottom of a 6-well plate. 1 × 104 cells/well were plated in a top layer of media with 0.33 % agarose. After stained with 0.005 % crystal violet, images were taken under an inverted microscope (Olympus IX53) after three weeks. The number of colonies was counted from multiple random fields.
Tumor models and treatment
Normal saline (NS) was administered as control
VNP20009 carrying the scrambled shRNA construct was administered
VNP20009 carrying the Sox2 shRNA construct was administered
HM-3 was administered
HM-3 + shScr-V
Both HM-3 and shScr-V were administered
HM-3 + shSox2-V
Both HM-3 and shSox2-V were administered
Docetaxel was administered
Assay of VNP20009 in tissues and blood
After the A549 tumor model in nude mice was established, VNP20009 was administered by intravenous injection at a dose of 2.5 × 106 cfu per mouse. On days 2, 7 and 14 after injection, tumors and major organs were aseptically removed, weighted and homogenized in PBS. 1 ml homogenized tissue of the same weight (100 mg) was diluted in gradient and 100 μl was plated onto LB agar plates containing ampicillin (50 μg/ml). In the case of blood analysis from mice, 200 μl blood was collected as the mice were killed and was plated directly onto the LB plates. The LB plates were incubated at 37 Celsius overnight and the bacteria colonies were quantified.
Western blotting assay (WB)
The tumor samples were snapped into small pieces and incubated with RIPA cell lysis buffer supplemented with protease inhibitors on ice for 20 min. After that, the samples were homogenized with a glass tissue grinder. After centrifuging (14,000 × g) for 20 min, the supernatant was removed and boiled with protein loading buffer. The western blotting was carried out as described before . ImageJ software (Wayne Rasband, USA) was used to analyze the result. The relative protein expression was calculated by dividing the optical density of the protein analysed with the optical density of β-actin of the same group. The results of three independent experiments were calculated.
Tumor and organ tissue was fixed in 4 % formalin and embedded in paraffin. Sections were deparaffinized and rehydrated. For hematoxylin and eosin (H&E) staining, sections were stained in hematoxylin and then counterstained with eosin. For immunohistochemistry staining, after treatment with 3 % H2O2, sections were boiled in 10 mM sodium citrate buffer (pH 6.0) for antigen retrieval. After blocking, sections were incubated with the primary antibody as recommended by the supplier, washed with PBS, and then incubated with the horseradish peroxidase labeled secondary antibody. Sections were finally incubated with DAB and counterstained with hematoxylin.
All the data was collected and processed with the Statistical Program for Social Sciences (SPSS version 13.0, Chicago, USA). The difference between samples of the same group was tested by one-way analysis of variance. It would be considered statistically significant when P < 0.05 and statistically highly significant when P < 0.01.
The invasion and anchorage-independent growth capability of A549 cells was inhibited as Sox2 was knocked down
VNP20009 selectively accumulated in tumors
Antitumor activity of HM-3 combined with shSox2-V in vivo
The expression of Sox2 and microvessel formation in the A549 xenografts of different treatment groups
CD31 has been used extensively to evaluate the degree of angiogenesis in tumors. As shown in the WB and IHC results, the amount of CD31 was much lower in the HM-3, HM-3 + shScr-V and HM-3 + shSox2-V groups compared to those treated with NS, shScr-V, shSox2-V and docetaxel (Fig. 4a and c, P < 0.05). The microvessel number per field for the mock, shScr-V, shSox2-V, HM-3, HM-3 + shScr-V, HM-3 + shSox2-V and docetaxel groups was 10.25, 9.75, 10.75, 3.5, 3.25, 2.5 and 9.75 respectively (Fig. 5b). The results confirmed that HM-3 could inhibit the microvessel formation in tumors. The difference of microvessel density between HM-3 + shScr-V and HM-3 + shSox2-V group was not significant suggesting that the antiangiogenesis activity of HM-3 was not affected in both groups.
Effects of HM-3 with shSox2-V on the expression of apoptosis-related protein in the A549 xenografts
Systematic toxicity in the mice treated with HM-3 + shSox2-V
At the early stages of tumor progression, microvessels are formed around tumor. If angiogenesis inhibitors are administered at this stage, the growth of tumor could be effectively inhibited. However, the microenvironment in the inner tumor mass changes as tumor progresses. The actions of antitumor drugs may be affected as the expression of various factors and microRNAs are influenced by the microenvironment [24, 25]. Also, the survival of CSCs further limits the effectiveness of chemotherapy and anti-angiogenesis therapy [26–28]. In this study, the treatment was started after the tumor volume was greater than 300 mm3. On one hand, polypeptide HM-3 was administered to suppress the microvessel formation in tumor which cut the supply of oxygen and nutrients for tumor growth. On the other hand, attenuated facultative anaerobe VNP20009 was administered which can specifically accumulate in tumor because of its natural tropism for hypoxic areas in contrast to chemo drugs . The inhibition of microvessel formation in tumor could not affect the tumor targeting potential of VNP20009 as it was cleared away from the blood quickly and accumulated in tumors shortly after injection. To further inhibit the survival of CSCs in tumor tissue, a shRNA construct targeting Sox2 was transformed into VNP20009. The expression of Sox2 was down regulated in the tumor tissue of the combined treatment group while with much smaller tumor volume.
The engineered salmonella enhanced the antitumor effect of HM-3 on lung cancer compared to the individual therapy group. The inhibition rate of the HM-3 + shSox2-V group was 58.73 %, while that in the shScr-V, shSox2-V, HM-3, HM-3 + shScr-V and docetaxel groups was 24.3 %, 36.69 %, 26.97 %, 44.86 % and 48.1 % respectively. Our results suggested that this combination was effective in inhibiting tumor growth in vivo. According to our knowledge, this was the first report that attenuated salmonella with a shRNA construct targeting Sox2 was co-administered with a polypeptide inhibiting angiogenesis in the treatment of lung cancer.
Sox2 is a poor prognostic indicator in stage I lung cancer . Also, it has been reported that the expression of Sox2 promoted drug resistance of certain tumors [31, 32]. By knocking down the expression of Sox2 with shRNA, the growth of lung cancer cells was inhibited. In consistent with previous reports, the down regulation of Sox2 was related to the expression of apoptosis related marker C-caspase 3 . However, our results suggested that knocking down Sox2 alone was not enough to significantly inhibit A549 tumor growth in vivo. Considering the redundancy of signaling factors in tumor cells, other members of the same protein family or different pathways may compensate for the loss of Sox2 leading to the survival of tumor cells [33, 34].
Cell death mediated by apoptosis is important in the regulation of tumor growth. It has been reported that VNP20009 could migrate from the vascular and induce apoptosis in tumor . Our results showed that the apoptosis induced by VNP20009 alone was not evident. This might be due to the difference of tumor model and treatment regimens. More tumor cell went through apoptosis in the HM-3 + shSox2-V group implicating that the inhibition of angiogenesis by HM-3 had synergistic antitumor effects with shSox2-V. The cell apoptosis pathway was also activated in the group treated with docetaxel due to its cytotoxicity. It has been reported that the combination therapy of cytotoxic agents with salmonella was effective in inhibiting the growth of prostate cancer . However, whether this combination can be applied to lung cancer still requires further verification.
Our study suggested that HM-3 together with a gene therapy targeting Sox2 delivered by VNP20009 was an attractive treatment option for patients with lung cancer. However, to achieve better antitumor effect, multi-targeting therapies with cytotoxic drugs and the use of other gene therapy delivering system may be considered . Also, the key factors of other signal pathways that are involved in lung cancer growth can be evaluated as potential targets .
AIs, angiogenesis inhibitors; C-caspase 3, cleaved Caspase 3; Cfu, colony forming unit; CSCs, cancer stem cells; H&E, hematoxylin and eosin; IDO1, indoleamine 2, 3-dioxygenase 1; IHC, immunohistochemistry; L, length; LB, Luria-Bertani; MDM2, murine double minute 2; MDR1, multiple drug resistance 1; NS, normal saline; NSCLC, non-small cell lung carcinoma; RGD, Arg-Gly-Asp; s.c, subcutaneously; shScr, the scrambled shRNA construct; shScr-V, VNP20009 transformed with the shScr; shSox2, the Sox2 shRNA construct; shSox2-V, VNP20009 transformed with the shSox2; Sox2, sex determining region Y-box 2; TV, tumor volume; VECs, vascular endothelium cells; W, width; WB, western blotting assay
This work was mainly supported by 863 High-Technology Development Planning (No. SQ2011SF11B02030), the Project Program of State Key Laboratory of Natural Medicines (No. SKLNMBZ201403) and the National Science and Technology Major Projects of New Drugs (No. 2012ZX09103301-004 and No. 2014ZX09508007) in China. This project was also funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD).
HMX and CHZ conceived and designed the experiments. CHZ, JJH and HRC carried out the in vivo study. CHZ and ZHZ performed the WB, IHC and statistical analysis. CHZ and HMX prepared the manuscript. All authors read and approved the manuscript.
The authors declare that there are no competing interests.
Ethics approval and consent to participate
The study involved with animals was approved by the Animal Ethics Committees of China Pharmaceutical University. All the experimental animals were kept according to the Guide for the Care and Use of Laboratory animals.
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