Natural Oncolytic Activity of Live-Attenuated Measles Virus against Human Lung and Colorectal Adenocarcinomas

Boisgerault, Nicolas; Guillerme, Jean-Baptiste; Pouliquen, Daniel; Mesel-Lemoine, Mariana; Achard, Carole; Combredet, Chantal; Fonteneau, Jean-François; Tangy, Frédéric; Grégoire, Marc

doi:https://doi.org/10.1155/2013/387362

BioMed Research International

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Abstract Introduction Materials and Methods Results Discussion Conclusions Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2013 | Article ID 387362 | https://doi.org/10.1155/2013/387362

Natural Oncolytic Activity of Live-Attenuated Measles Virus against Human Lung and Colorectal Adenocarcinomas

Nicolas Boisgerault,^1,2,3Jean-Baptiste Guillerme,^1,2,3Daniel Pouliquen,^1,2,3Mariana Mesel-Lemoine,⁴Carole Achard,^1,2,3Chantal Combredet,⁴Jean-François Fonteneau,^1,2,3Frédéric Tangy,⁴and Marc Grégoire^1,2,3

Academic Editor: Changqing Su

Received11 Oct 2012

Revised30 Dec 2012

Accepted14 Jan 2013

Published17 Mar 2013

Abstract

Lung and colorectal cancers are responsible for approximately 2 million deaths each year worldwide. Despite continual improvements, clinical management of these diseases remains challenging and development of novel therapies with increased efficacy is critical to address these major public health issues. Oncolytic viruses have shown promising results against cancers that are resistant to conventional anticancer therapies. Vaccine strains of measles virus (MV) exhibit such natural antitumor properties by preferentially targeting cancer cells. We tested the ability of live-attenuated Schwarz strain of MV to specifically infect tumor cells derived from human lung and colorectal adenocarcinomas and demonstrated that live-attenuated MV exhibits oncolytic properties against these two aggressive neoplasms. We also showed that Schwarz MV was able to prevent uncontrollable growth of large, established lung and colorectal adenocarcinoma xenografts in nude mice. Moreover, MV oncolysis is associated with in vivo activation of caspase-3 in colorectal cancer model, as shown by immunohistochemical staining. Our results provide new arguments for the use of MV as an antitumor therapy against aggressive human malignancies.

1. Introduction

Lung and colorectal cancers are leading causes of death worldwide with approximately 1.6 million and 1.2 million new cases per year resulting in 1.4 million and 610,000 estimated deaths, respectively [1]. In developed countries, lung cancers rank first for males and second for females in overall cancer-related deaths while colorectal cancers rank second for male and third for female. These cancers are found to be extremely resistant to conventional therapies including surgery, chemotherapy, and radiotherapy with a 5-year survival of only 15% and 50%, respectively.

Difficult clinical management of these two malignancies makes them ideal candidates for development of alternative approaches such as cancer virotherapy [2–5]. Live-attenuated vaccinal strains of measles virus (MV) are of particular interest due to their ability to specifically target different types of human tumors [6, 7] through recognition of the CD46 membrane complement regulatory molecule [8, 9] which is frequently overexpressed on cancer cells [10]. Oncolytic viruses are also powerful inducers of tumor cell death and thus could help to cure cancers that are refractory to conventional treatments. Furthermore, in addition to inducing cell death, the infection of tumor cells by MV is able to activate components of the antitumor immune response, such as myeloid and plasmacytoid dendritic cells, that may play a role in the efficacy of cancer virotherapy [6, 11].

Several Phase I clinical trials targeting different cancers with MV virotherapy are in progress and two of them have been published. In the initial Phase I clinical trial, intratumoral injection of low doses of MV into five patients with cutaneous-T-cell-lymphoma, patients induced stabilization of the disease in two patients and a partial response in one [12]. The authors of the second published Phase I clinical trial, carried out in patients with refractory ovarian cancers [13], noticed a dose-dependent biological activity of oncolytic MV. They also reported that the treatment was well tolerated, thus confirming previous reports that demonstrated the safety of using live-attenuated vaccinal strains of MV in the clinical setting.

Sparse data from the literature show that wild-type MV is able to infect some human lung and colorectal adenocarcinoma cells [14, 15]. MV fusogenic membrane glycoproteins by themselves were also demonstrated to improve treatment of human colorectal cancer xenografts when used in combination with chemotherapy or virotherapy [16]. Moreover, urokinase receptor-retargeted MV was shown to display oncolytic activity against murine colorectal cancer cells in vivo [17]. However, whereas MV virotherapy has been tested against a wide variety of human cancers, no comprehensive work has been achieved until now to investigate how oncolytic strains of MV target human lung and colorectal adenocarcinomas.

To our knowledge, we demonstrate here for the first time that live-attenuated Schwarz vaccinal strain of MV is able to specifically infect and kill tumor cells derived from human lung and colorectal adenocarcinomas, both in vitro and in vivo against large tumor burdens. Specifically, these oncolytic properties are associated with in vivo activation of caspase-3. Altogether, our results confirm the ability of oncolytic MV to target aggressive neoplasms and thus provide new perspectives for the treatment of two major malignancies.

2. Materials and Methods

2.1. Cell Culture

ADK3, ADK117, and ADK153 lung adenocarcinoma cell lines were established in our laboratory from pleural effusions collected by thoracocentesis of cancer patients, with their informed consent, and genetically characterized [18]. The A549 lung adenocarcinoma, Caco-2, HT29, SW480, and SW620 colorectal adenocarcinoma cell lines were purchased from ATCC. All cell lines were maintained in RPMI-1640 medium (Gibco-Invitrogen, Cergy-Pontoise, France) supplemented with 10% (v/v) heat-inactivated fetal calf serum (PAA Laboratories, Les Mureaux, France), 2 mM L-glutamine, 100 U/mL penicillin, and 100 μg/mL streptomycin (all purchased from Gibco). Normal bronchial epithelial cells (BEC) were obtained from a healthy lung graft (Dr Magnan, INSERM UMR 915, Nantes) and cultured in CnT-17 medium (CELLnTEC, Switzerland). Cells were cultured at 37°C in a humidified, 5% CO₂ atmosphere and were routinely checked for Mycoplasma contamination by PCR.

2.2. In Vitro Measles Virus Infection

Live-attenuated Schwarz vaccinal strain of measles virus recombinant for enhanced green fluorescent protein (MV-eGFP) was produced as previously described [19] and titered on Vero cells (TCID₅₀/mL). In vitro infections were performed at MOI = 1.0 TCID₅₀ for 2 h at 37°C. Viral inoculum was then replaced by fresh culture medium with no further renewal during the experiments.

2.3. Time-Lapse Microscopy

All experiments were performed at the Cellular and Tissular Imaging Core Facility (MicroPICell, IFR26, Nantes, France) using a Leica DMI6000B station. Images were acquired every 15 min for 72 hours with MetaMorph Microscopy Automation & Image Analysis Software (Molecular Devices) and further treated with ImageJ (National Institute of Health).

2.4. Cell Death Analysis

Percentages of dying cells were determined 3 days after infection using the Apoptosis Detection Kit (BD Biosciences) following manufacturer’s instructions. Briefly, cells were double stained with annexin-V-FITC and propidium iodide (PI) for 15 min and analyzed by flow cytometry within 1 hour.

2.5. Flow Cytometry

Cells were incubated for 30 min with FITC-conjugated anti-CD46, PE-conjugated anti-CD150/SLAM (BD Biosciences, Le Pont de Claix, France), or PE-conjugated anti-Nectin-4 (R&D Systems Europe, Lille, France) antibodies in PBS/0.1% BSA for extracellular staining. Cells were then washed 3 times with PBS before analysis by flow cytometry (FACSCalibur, BD Biosciences).

2.6. Animal Model and In Vivo Experiments

All in vivo experiments complied with European Union regulations on the welfare and use of animals in cancer research. Six-week-old female RJ:NMRi-nu nude mice were purchased from Centre d’Élevage Janvier (Le Genest-Saint-Isle, France). Mice were challenged subcutaneously with 10⁶ tumor cells in the left flank. When volumes reached approximately 150–200 mm³ for Caco-2 or 100 mm³ for A549, MV-eGFP (1.5 × 10⁷ TCID₅₀) or saline buffer (PBS) was injected intratumorally (50 μL). Tumors were measured twice weekly with a microcaliper and tumor volumes were calculated using the formula. Animals were sacrificed when tumors reached 1-2 cm³ in volume. Tumors were then harvested, fixed in 4% paraformaldehyde (Electron Microscopy Sciences, Hatfield, USA) and embedded in paraffin wax.

2.7. Immunohistochemistry

Immunohistochemical stainings were performed by the MicroPICell core facility with a Bond Max automaton (Menarini, Rungis, France). Briefly, paraffin-embedded tumor slides were incubated in a demasking citrate buffer (pH = 6.0) before blocking of endogenous peroxidase for 5 min. Slides were then incubated for 1 h with a polyclonal, rabbit antiactive-caspase-3 antibody (Abcam, Paris, France) diluted to 1 : 50 and subsequently with Histofine Rabbit-to-Mouse secondary antibody (Nichirei Biosciences, Tokyo, Japan). After 10 min 3,3′-Diaminobenzidine (DAB) incubation, tumors were counterstained with hematoxylin. Slides were analyzed using a Leica DM2500 microscope coupled to a Leica DCF295 camera. Images were acquired with Leica Application Suite Version 3 software.

2.8. Statistical Analyses

One-sided, unpaired Mann-Whitney t-test was used to compare groups in the in vivo experiments. Differences were considered significant when * or **. All data are presented as mean ± SEM.

3. Results

3.1. Human Adenocarcinoma Cells Are Efficiently Infected by MV

Cancer cells derived from human lung and colorectal adenocarcinomas were first infected with live-attenuated Schwarz strain of MV recombinant for EGFP (MV-eGFP) to test their sensitivity to oncolytic MV. We infected four different colorectal adenocarcinoma cell lines and showed that they were all susceptible to MV infection (Figure 1(a)). Whereas SW480 and metastatic SW620 cells showed high infection yield after 3 days with 87% and 93% of cells infected, respectively, we observed less EGFP⁺ HT29 (51%) and Caco-2 (37%) cells at the same time point. To determine how MV infection spreads in these two cell lines, we further analyzed MV infection by time-lapse microscopy. In Caco-2 culture, infection progressed slowly despite tight cell interactions and typical syncytia formation resulting from fusion of infected tumor cells with neighboring cells (Figures 1(b) and S1). On the other hand, HT29 cells underwent a rapid oncolytic process with infected cells dying shortly after infection (not shown). We observed with fluorescent microscopy that HT29 cell death resulted in the release of EGFP in the extracellular medium, especially at 72 h, thus lowering the amount of EGFP⁺ cells determined by flow cytometry (not shown).

(a)

(b)

(c)

Figure 1

In vitro oncolytic properties of measles virus against human adenocarcinomas. (a) One million human lung or colorectal adenocarcinoma cells were infected in vitro with a live-attenuated strain of MV recombinant for EGFP (MV-eGFP; MOI = 1). Percentages of infected cells (EGFP⁺) were determined by flow cytometry at 24, 48, and 72 h after infection. Data are presented as mean ± SEM, (). (b) Infected cells were observed for 72 h by time-lapse microscopy to study cytopathic effects of MV infection. Complete experiments are presented in Figures (Caco-2) and (A549) in Supplementary Material available online at http://dx.doi.org/10.1155/2013/387362. (c) Human lung and colorectal adenocarcinoma cells were either infected with live-attenuated MV (MOI = 1, black bars) as described above or left uninfected (white bars). Cells were cultured for 72 h without medium renewal. Cells were then double stained with annexin V/propidium Iodide and analyzed by flow cytometry.

We also tested oncolytic properties of MV against one commercial (A549) and three (ADK3, ADK117, and ADK153) lung adenocarcinoma cell lines obtained in our laboratory. These cell lines exhibited heterogeneous infection rates following exposure to MV-eGFP. While A549 and ADK153 cells were efficiently infected with 88% and 65% EGFP⁺ cells after 72 h, respectively, infection spread slowly in ADK3 cells with only 29% of infected cells at the same time (Figure 1(a)). ADK117 cells were found to be resistant to infection with only 6% of infected cells at 72 h after infection. Time-lapse experiments confirmed efficient infection of A549 cells by MV, even though only minimal syncytia formation was observed (Figures 1(b) and S2). On the contrary, normal bronchial epithelial cells (BEC) were not infected by MV (0.4% at 72 h, MOI = 1, data not shown). Thus, our results show that 4 out of 4 colorectal and 3 out of 4 lung adenocarcinoma tested cell lines, but not normal epithelial cells, are sensitive to live-attenuated MV infection.

3.2. MV Induces Cell Death of Infected Lung and Colorectal Cancer Cells

To further investigate oncolytic properties of MV against lung and colorectal cancer cells, we studied the ability of the virus to induce death of the infected cells. We initially characterized MV-related cytopathic effects by fluorescence microscopy. As expected, MV infection induced the formation of giant, multinucleated cells, namely, syncytia, in colorectal adenocarcinoma cells (Figures 1(b) and S1). Ultimately, MV infection caused detachment of MV-induced syncytia from the plate support, thereby demonstrating the induction of tumor cell death by MV infection. Infected A549 lung adenocarcinoma cells only formed small syncytia resulting from fusion of two to five tumor cells, though these cells were eventually driven to apoptotic-like cell death, as shown by consistent observations of plasma membrane blebbing (Figures 1(b) and S2).

To better characterize the cell death induced after MV infection, we performed annexin-V/propidium iodide double staining (Figure 1(c)). Oncolytic MV infection efficiently induced cell death in A549, ADK153, Caco-2, HT29, SW480, and metastatic SW620 cells as shown by a substantial increase of annexin-V⁺ cell percentages compared to uninfected cells. Conversely, death induction in ADK3 and ADK117 cells was minimal, consistent with the relatively low infection rates observed in previous experiments (Figure 1(a)). Thus, analysis of cell death induction demonstrates that oncolytic MV effectively kills infected cancer cells derived from human lung and colorectal adenocarcinomas through an apoptotic-like process.

3.3. CD46 Is Highly Expressed in Lung and Colorectal Cancer Cell Lines

Despite recent advances in the identification of MV cellular receptors [14, 20], CD46 is still considered to be critical in determining the sensitivity of tumor cells to oncolytic strains of MV. As expected, a majority of efficiently infected tumor cells exhibited a high CD46 surface level (Figures 2(a) and 2(b)). Indeed, A549 (MFI = 159), Caco-2 (115), HT29 (255), SW480 (227), and SW620 (219) were efficiently infected and killed, which is consistent with their high expression of the CD46 receptor. Interestingly, CD46 expression analysis was not sufficient to predict the infection levels of some lung adenocarcinoma cell lines. For instance, fairly high levels of CD46 were expressed on ADK3 (MFI = 66) and ADK117 (68) but these cells were less efficiently infected than ADK153 cells which exhibit low CD46 expression (MFI = 45). Consistent with their resistance to infection, normal bronchial epithelial cells barely expressed CD46 (MFI = 21).

(a)

(b)

(c)

Figure 2

Expression of CD46 and CD150/SLAM receptors on human adenocarcinoma cells. (a) Lung (left) and colorectal (right) tumor cell lines were stained with anti-CD46-FITC, anti-CD150/SLAM-PE, and anti-Nectin-4-PE antibodies (thick black lines) in PBS/0.1% BSA for 30 min before analysis by flow cytometry. Isotypic stainings are shown as grey filled curves. (b)-(c) CD46 (b) and Nectin-4 (c) expression levels were determined for each lung (white bars) or colorectal (black bars) tumor cell line in three independent experiments. Expression levels of CD46 and Nectin-4 for normal bronchial epithelial cells (BEC) are indicated. MFI: median fluorescence intensity.

To better determine which receptor(s) were involved in the infection of these lung adenocarcinoma cell lines, we subsequently screened them for expression of CD150/SLAM (Signaling Lymphocytic Activation Molecule) and Nectin-4 receptors. CD150/SLAM is known to be involved in the infection of immune cells by wild-type MV [21] while Nectin-4 has been recently described as essential for host-to-host spread of MV [20, 22]. None of the tumor cell lines studied in our experiments exhibited CD150/SLAM expression (Figure 2(a)) and Nectin-4 was only found to be weakly expressed on HT29 cells (Figures 2(a) and 2(c)) as determined by flow cytometry.

3.4. In Vivo Oncolytic Activity of MV

To confirm our in vitro results regarding oncolytic properties of live-attenuated MV, we studied the ability of the virus to efficiently target and kill human lung and colorectal adenocarcinoma subcutaneous xenografts in vivo in nude mice (Figure 3). As our ultimate goal is to develop therapy against aggressive established tumors, we decided to treat large (100 to 200 mm³) A549 and Caco-2 tumors.

(a)

(b)

Figure 3

Measles virus exhibits oncolytic properties against human adenocarcinomas in vivo. (a) Nude mice were challenged subcutaneously with 1 million A549 (lung) or Caco-2 (colorectal) human adenocarcinoma cells. When tumors reached a volume of 100 mm³ for A549 or 150–200 mm³ for Caco-2, MV-eGFP or PBS was injected intratumorally (day 0, 1.5 × 10⁷ TCID₅₀). Tumor volumes were measured twice weekly. Additional intratumoral MV injections were performed with A549 mice at days 22, 28, and 35 after initial injection as indicated by arrowheads. (b) When tumors reach 1–1.5 cm³ or after 31 (Caco-2 tumor) or 42 (A549 tumors) days, animals were sacrificed and tumors were harvested and weighed. (*; **).

Human Caco-2 colorectal adenocarcinomas xenografts were treated by a single intratumoral injection of oncolytic MV ( TCID₅₀). Whereas we previously observed slow transmission of the virus in vitro for this cell line (Figure 1), a single injection of the virus resulted in growth arrest of the tumor for up to 31 days (Figure 3(a)). Conversely, tumor growth was constant in mice treated with control saline buffer (PBS). After 31 days, significant differences were observed between control and MV-treated mice regarding either tumor volumes ( mm³ versus mm³; ; Figure 3(a)) or tumor weights ( mg versus mg; ; Figure 3(b)).

Treatment of human A549 lung adenocarcinoma xenografts using identical experimental settings was not found to be effective. Indeed, even though MV induced a delayed tumor growth, we did not obtain any significant difference between PBS- ( mm³) and MV-treated ( mm³) mice (Figure 3(a)). This could be explained by the higher proliferation capacities of A549 cells as observed previously by time-lapse microscopy (Figure ). Considering that steady proliferation of A549 cells could result in reduced viral particles/cells ratio into the tumor, we decided to carry out multiple injections of oncolytic MV by performing three extra intratumoral MV injections at days 22, 28, and 35 after the initial injection. This treatment schedule efficiently stopped tumor growth, as shown by the differences in tumor volumes between control animals ( mm³) and multiple-injections group ( mm³; ) at day 42 (Figure 3(a)). At this point, tumors were weighed and tumor masses were found to be significantly different between control and MV-treated mice ( mg versus mg; ; Figure 3(b)).

3.5. MV Infection Induces Caspase-3 Activation in Colorectal Tumor Cells

Cell death triggered by MV infection has been previously described to be apoptosis [23]. Our results above are consistent with these observations as we found increased percentages of annexin-V⁺/PI⁻ lung and colorectal carcinoma cells following MV infection (Figure 1(c)). To investigate induction of apoptotic tumor cell death in vivo, we analyzed activation of caspase-3 in MV-treated and PBS-injected tumors by immunohistochemistry (Figure 4). Caspase-3 is involved in late events of apoptosis and thus can be activated by both extrinsic and intrinsic apoptotic pathways.

Caco-2 colorectal tumors grew in a specific way by forming round structures as shown by microscopy (Figures 1(b) and S1). In control mice, we observed minimal caspase-3 activation in the centers of these structures, which could be related to hypoxia or nutrient deprivation (Figure 4). In contrast, we observed strong activation of caspase-3 in MV-treated tumors, likely as a result of in vivo oncolytic activity of MV against Caco-2 colorectal adenocarcinoma cells. This strong and extended activation of caspase-3 throughout the tumor correlates with significant tumor growth arrest (Figure 3(a)). We did not observe any activation of caspase-3 in control and MV-infected A549 tumors (not shown).

4. Discussion

We report here that Schwarz live-attenuated vaccinal strain of measles virus (MV) exhibits both in vitro and in vivo antitumor activity against human lung and colorectal adenocarcinomas. MV was able to infect and efficiently induce cell death in different cell lines derived from these two types of cancers. Significantly, our in vivo experiments showed that MV is able to control the growth of large, established tumors derived from these human malignancies. These findings are of particular interest as lung and colorectal cancers are widespread aggressive diseases which are still in need of innovative antitumor treatments [24, 25]. Our work supports previous studies where oncolytic properties of MV vaccinal strains, derived from Edmonston lineage, have been demonstrated against a wide range of human cancers including lymphoma [26], glioblastoma multiforme [27], multiple myeloma [28], ovarian [29] and breast [30] carcinomas, prostate cancer [31], leukemia [32], and more recently melanoma [33].

MV-induced cell death has been characterized as apoptosis [23] and we regularly observed common features of apoptotic cell death, for example blebbing and early exposure of phosphatidylserine on the outer leaflet of plasma membrane. However, we also repeatedly observed atypical events that could possibly challenge the “apoptosis model”, at least when using live-attenuated MV against malignant cells. Indeed, we previously showed how mesothelioma cells infected with MV were able to induce spontaneous maturation of human monocyte-derived and plasmacytoid dendritic cells and, subsequently, the cross-presentation of tumor antigen to specific CD8⁺ T cells [6, 11]. Here, we observed that some of the infected cells undergoing cell death after syncytia formation showed rapid release of intracellular content into the culture medium, as shown by rapid leakage of cytoplasmic GFP. This could partially explain the immunogenicity of “apoptosis” that we harnessed in our previous work [6]. Recent advances in the characterization of tumor cell death pathways [34]—for instance description of necroptosis—could help to improve our comprehension of oncolytic MV-related cell death. Altered apoptotic pathways in tumor cells could also impact this process, as we observed divergent mechanisms in Caco-2 and A549 regarding syncytia formation in vitro and cleavage of caspase-3 in vivo. However, the fact that we did not observe activated caspase 3 in A549 tumor in mice could be due to the rapid growth of this cell line compared to Caco-2. It is thus possible that rapidly dividing A549 cells outgrow activated caspase-3 apoptotic tumor cell and are thus more difficult to detect in histologic samples. Since more and more groups now focus on improving proapoptotic capacities of oncolytic viruses to circumvent resistance of tumor cells to cancer therapies [35], such information would be of great interest for clinical utility. Even if viruses are potent inducers of cell death and are often able to demonstrate cytotoxicity even in unfavorable conditions, it has been shown recently, for instance, that overexpression of antiapoptotic molecules from Bcl-2 protein family can impair MV-induced cell death in leukemia cells [32].

Better understanding of the features of MV-induced cell death will help to design appropriate clinical strategies for targeting aggressive human neoplasms. Antitumor effects of virotherapy have been shown to be enhanced by combination with other antitumor treatments in different models [36]. Combination with chemotherapy, the use of histone deacetylase inhibitors, for example, was found to improve the oncolytic properties of both vesicular stomatitis virus [37] and herpes virus [38]. Combinations with radiotherapy are also now widely described [39, 40]. Associations with immunotherapy, to combine direct oncolysis with an adaptive, antitumor immune response, is also an interesting alternative, with some groups demonstrating a critical role for the immune system in the therapeutic effects of oncolytic viruses [6, 41, 42]. Others have used engineered oncolytic viruses expressing proimmune molecules [5, 43]. Synergistic action of virotherapy and antitumor immune response in vivo has been extensively shown for oncolytic VSV [44] and reovirus [45, 46]. In vitro studies with MV tend to confirm this trend even though a suitable immunocompetent model to study interactions between the virus and the immune system is lacking [47]. For example, we (manuscript in preparation) and others [33] have observed the release of danger signals by MV-infected cells in vitro, although the in vivo consequences remain largely unknown.

Recent identification of Nectin-4 as a new receptor for measles virus has been a major step forward for a better understanding of MV biology [14, 20]. Nonetheless, CD46 membrane complement regulatory protein expression still remains the key determinant for cancer cell sensitivity (i) to primary infection by MV and subsequently (ii) to the efficient transmission of new viruses to neighboring cells by formation of multinucleated syncytia [48]. Overexpression of CD46 had been previously described in human lung and colorectal adenocarcinomas [10, 14] and we were able to confirm these observations in several cell lines derived from these two malignancies. Moreover, we showed that cell lines exhibiting high CD46 expression also displayed high infection rates by oncolytic MV. The virus was also able to induce substantial regressions of these human adenocarcinomas engrafted in nude mice. Surprisingly, one of our lung adenocarcinoma cell lines (ADK153) was found to be efficiently infected by MV while displaying a lower expression level of CD46 receptor (Figures 1 and 2). This unexpected observation supports preliminary experiments in melanoma where low expression of CD46 and the absence of SLAM and Nectin-4 receptors do not correlate with efficient infection by live-attenuated vaccinal MV (manuscript in preparation). This indicates that additional parameters have to be taken into account when tumor cells are screened for their susceptibility to oncolytic MV. Sensitivity to innate antiviral mechanisms—such as the ability to respond to Type-I interferon signaling—should be considered, even if one cannot exclude that, out of CD46, CD150/SLAM, and Nectin-4 receptors, other unidentified surface molecules could play a role in MV infection mechanisms. Nevertheless, the majority of the tumor cell lines we studied showed increase in sensitivity to oncolytic MV infection when overexpressing CD46, thereby showing that lung and colorectal cancers, which are highly resistant to conventional treatments, are suitable targets for MV cancer virotherapy.

5. Conclusions

Our experiments demonstrate that live-attenuated oncolytic MV is able to efficiently target human lung and colorectal carcinomas, thus highlighting novel options for the treatment of these aggressive malignancies. Further studies to better characterize cell death pathways activated by MV infection and parameters involved in MV susceptibility would again reinforce the interest in development of live-attenuated MV for cancer therapy.

Conflict of Interests

The authors declare no competing financial interests.

Acknowledgments

This project was supported by Grants from the Association pour la Recherche sur le Cancer (ARC), La Ligue contre le Cancer, and ARSMESO44. N. Boisgerault was personally supported by a Grant from the ARC. The author thank Philippe Hulin, Myriam Robard, and Cécile Deleine from the MicroPICell core facility for microscopic and immunohistochemical analyses and Virginie Maurier for animal experiments. The author also thank Kate Vassaux and Diana Rommelfanger for English editing.

Supplementary Materials

Figures S1 & S2: Analysis of adenocarcinoma cells infection by time-lapse microscopy. To analyze kinetics of infection by oncolytic measles virus, Caco-2 colorectal (Figure S1) and A549 lung (Figure S2) adenocarcinoma cells were infected with MV-EGFP (MOI = 1.0). Pictures were taken every 15 minutes for 72 hours using a time-lapse microscope (time is indicated as days:hours:minutes). Bright field and fluorescence pictures are merged.

References

A. Jemal, F. Bray, M. M. Center, J. Ferlay, E. Ward, and D. Forman, “Global cancer statistics,” CA Cancer Journal for Clinicians, vol. 61, no. 2, pp. 69–90, 2011.
View at: Publisher Site | Google Scholar
V. Beljanski and J. Hiscott, “The use of oncolytic viruses to overcome lung cancer drug resistance,” Current Opinion in Virology, vol. 2, no. 5, pp. 629–635, 2012.
View at: Google Scholar
S. Miyamoto, H. Inoue, T. Nakamura et al., “Coxsackievirus B3 is an oncolytic virus with immunostimulatory properties that is active against lung adenocarcinoma,” Cancer Research, vol. 72, no. 10, pp. 2609–2621, 2012.
View at: Publisher Site | Google Scholar
K. B. Stephenson, N. G. Barra, E. Davies, A. A. Ashkar, and B. D. Lichty, “Expressing human interleukin-15 from oncolytic vesicular stomatitis virus improves survival in a murine metastatic colon adenocarcinoma model through the enhancement of anti-tumor immunity,” Cancer Gene Therapy, vol. 19, no. 4, pp. 238–246, 2012.
View at: Google Scholar
N. Boisgerault, F. Tangy, and M. Gregoire, “New perspectives in cancer virotherapy: bringing the immune system into play,” Immunotherapy, vol. 2, no. 2, pp. 185–199, 2010.
View at: Publisher Site | Google Scholar
A. Gauvrit, S. Brandler, C. Sapede-Peroz, N. Boisgerault, F. Tangy, and M. Gregoire, “Measles virus induces oncolysis of mesothelioma cells and allows dendritic cells to cross-prime tumor-specific CD8 response,” Cancer Research, vol. 68, no. 12, pp. 4882–4892, 2008.
View at: Publisher Site | Google Scholar
P. J. Lech and S. J. Russell, “Use of attenuated paramyxoviruses for cancer therapy,” Expert Review of Vaccines, vol. 9, no. 11, pp. 1275–1302, 2010.
View at: Publisher Site | Google Scholar
R. E. Dorig, A. Marcil, A. Chopra, and C. D. Richardson, “The human CD46 molecule is a receptor for measles virus (Edmonston strain),” Cell, vol. 75, no. 2, pp. 295–305, 1993.
View at: Publisher Site | Google Scholar
D. Naniche, G. Varior-Krishnan, F. Cervoni et al., “Human membrane cofactor protein (CD46) acts as a cellular receptor for measles virus,” Journal of Virology, vol. 67, no. 10, pp. 6025–6032, 1993.
View at: Google Scholar
Z. Fishelson, N. Donin, S. Zell, S. Schultz, and M. Kirschfink, “Obstacles to cancer immunotherapy: expression of membrane complement regulatory proteins (mCRPs) in tumors,” Molecular Immunology, vol. 40, no. 2–4, pp. 109–123, 2003.
View at: Publisher Site | Google Scholar
J. Guillerme, N. Boisgerault, D. Roulois et al., “Measles virus vaccine-infected tumor cells induce tumor antigen cross-presentation by human plasmacytoïd dendritic cells,” Clinical Cancer Research. In press.
View at: Google Scholar
L. Heinzerling, V. Künzi, P. A. Oberholzer, T. Kündig, H. Naim, and R. Dummer, “Oncolytic measles virus in cutaneous T-cell lymphomas mounts antitumor immune responses in vivo and targets interferon-resistant tumor cells,” Blood, vol. 106, no. 7, pp. 2287–2294, 2005.
View at: Publisher Site | Google Scholar
E. Galanis, L. C. Hartmann, W. A. Cliby et al., “Phase I trial of intraperitoneal administration of an oncolytic measles virus strain engineered to express carcinoembryonic antigen for recurrent ovarian cancer,” Cancer Research, vol. 70, no. 3, pp. 875–882, 2010.
View at: Publisher Site | Google Scholar
R. S. Noyce, D. G. Bondre, M. N. Ha et al., “Tumor cell marker PVRL4 (nectin 4) is an epithelial cell receptor for measles virus,” PLoS Pathogens, vol. 7, no. 8, Article ID e1002240, 2011.
View at: Google Scholar
Y. Shirogane, M. Takeda, M. Tahara, S. Ikegame, T. Nakamura, and Y. Yanagi, “Epithelial-mesenchymal transition abolishes the susceptibility of polarized epithelial cell lines to measles virus,” Journal of Biological Chemistry, vol. 285, no. 27, pp. 20882–20890, 2010.
View at: Publisher Site | Google Scholar
D. Hoffmann, J. M. Bangen, W. Bayer, and O. Wildner, “Synergy between expression of fusogenic membrane proteins, chemotherapy and facultative virotherapy in colorectal cancer,” Gene Therapy, vol. 13, no. 21, pp. 1534–1544, 2006.
View at: Publisher Site | Google Scholar
Y. Jing, C. Tong, J. Zhang et al., “Tumor and vascular targeting of a novel oncolytic measles virus retargeted against the urokinase receptor,” Cancer Research, vol. 69, no. 4, pp. 1459–1468, 2009.
View at: Publisher Site | Google Scholar
F. Gueugnon, S. Leclercq, C. Blanquart et al., “Identification of novel markers for the diagnosis of malignant pleural mesothelioma,” American Journal of Pathology, vol. 178, no. 3, pp. 1033–1042, 2011.
View at: Publisher Site | Google Scholar
C. Combredet, V. Labrousse, L. Mollet et al., “A Molecularly cloned Schwarz strain of measles virus vaccine induces strong immune responses in macaques and transgenic mice,” Journal of Virology, vol. 77, no. 21, pp. 11546–11554, 2003.
View at: Publisher Site | Google Scholar
M. D. Muhlebach, M. Mateo, P. L. Sinn et al., “Adherens junction protein nectin-4 is the epithelial receptor for measles virus,” Nature, vol. 480, no. 7378, pp. 530–533, 2011.
View at: Google Scholar
G. G. Welstead, C. Iorio, R. Draker et al., “Measles virus replication in lymphatic cells and organs of CD150 (SLAM) transgenic mice,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 45, pp. 16415–16420, 2005.
View at: Publisher Site | Google Scholar
V. Racaniello, “Virology. An exit strategy for measles virus,” Science, vol. 334, no. 6063, pp. 1650–1651, 2011.
View at: Google Scholar
L. M. Esolen, S. W. Park, J. M. Hardwick, and D. E. Griffin, “Apoptosis as a cause of death in measles virus-infected cells,” Journal of Virology, vol. 69, no. 6, pp. 3955–3958, 1995.
View at: Google Scholar
M. A. Bareschino, C. Schettino, A. Rossi et al., “Treatment of advanced non small cell lung cancer,” Journal of Thoracic Disease, vol. 3, no. 2, pp. 122–133, 2011.
View at: Publisher Site | Google Scholar
S. Leong, W. A. Messersmith, A. C. Tan, and S. G. Eckhardt, “Novel agents in the treatment of metastatic colorectal cancer,” Cancer Journal, vol. 16, no. 3, pp. 273–282, 2010.
View at: Publisher Site | Google Scholar
D. Grote, S. J. Russell, T. I. Cornu et al., “Live attenuated measles virus induces regression of human lymphoma xenografts in immunodeficient mice,” Blood, vol. 97, no. 12, pp. 3746–3754, 2001.
View at: Publisher Site | Google Scholar
L. K. Phuong, C. Allen, K. W. Peng et al., “Use of a vaccine strain of measles virus genetically engineered to produce carcinoembryonic antigen as a novel therapeutic agent against glioblastoma multiforme,” Cancer Research, vol. 63, no. 10, pp. 2462–2469, 2003.
View at: Google Scholar
K. W. Peng, G. J. Ahmann, L. Pham, P. R. Greipp, R. Cattaneo, and S. J. Russell, “Systemic therapy of myeloma xenografts by an attenuated measles virus,” Blood, vol. 98, no. 7, pp. 2002–2007, 2001.
View at: Publisher Site | Google Scholar
K. W. Peng, C. J. TenEyck, E. Galanis, K. R. Kalli, L. C. Hartmann, and S. J. Russell, “Intraperitoneal therapy of ovarian cancer using an engineered measles virus,” Cancer Research, vol. 62, no. 16, pp. 4656–4662, 2002.
View at: Google Scholar
C. J. McDonald, C. Erlichman, J. N. Ingle et al., “A measles virus vaccine strain derivative as a novel oncolytic agent against breast cancer,” Breast Cancer Research and Treatment, vol. 99, no. 2, pp. 177–184, 2006.
View at: Publisher Site | Google Scholar
P. Msaouel, I. D. Iankov, C. Allen et al., “Engineered measles virus as a novel oncolytic therapy against prostate cancer,” Prostate, vol. 69, no. 1, pp. 82–91, 2009.
View at: Publisher Site | Google Scholar
B. Patel, A. Dey, E. Ghorani et al., “Differential cytopathology and kinetics of measles oncolysis in two primary B-cell malignancies provides mechanistic insights,” Molecular Therapy, vol. 19, no. 6, pp. 1034–1040, 2011.
View at: Publisher Site | Google Scholar
O. G. Donnelly, F. Errington-Mais, L. Steele et al., “Measles virus causes immunogenic cell death in human melanoma,” Gene Therapy, vol. 20, no. 1, pp. 7–15, 2011.
View at: Google Scholar
P. Kreuzaler and C. J. Watson, “Killing a cancer: what are the alternatives?” Nature Reviews Cancer, no. 6, pp. 411–424, 201212.
View at: Google Scholar
T. C. Liu and D. Kirn, “Viruses with deletions in antiapoptotic genes as potential oncolytic agents,” Oncogene, vol. 24, no. 40, pp. 6069–6079, 2005.
View at: Publisher Site | Google Scholar
T. L. A. Nguyen, V. F. Tumilasci, D. Singhroy, M. Arguello, and J. Hiscott, “The emergence of combinatorial strategies in the development of RNA oncolytic virus therapies,” Cellular Microbiology, vol. 11, no. 6, pp. 889–897, 2009.
View at: Publisher Site | Google Scholar
T. L. A. Nguyên, H. Abdelbary, M. Arguello et al., “Chemical targeting of the innate antiviral response by histone deacetylase inhibitors renders refractory cancers sensitive to viral oncolysis,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 39, pp. 14981–14986, 2008.
View at: Publisher Site | Google Scholar
A. Otsuki, A. Patel, K. Kasai et al., “Histone deacetylase inhibitors augment antitumor efficacy of herpes-based oncolytic viruses,” Molecular Therapy, vol. 16, no. 9, pp. 1546–1555, 2008.
View at: Publisher Site | Google Scholar
M. H. Dai, D. Zamarin, S. P. Gao et al., “Synergistic action of oncolytic herpes simplex virus and radiotherapy in pancreatic cancer cell lines,” British Journal of Surgery, vol. 97, no. 9, pp. 1385–1394, 2010.
View at: Publisher Site | Google Scholar
S. Kuroda, T. Fujiwara, Y. Shirakawa et al., “Telomerase-dependent oncolytic adenovirus sensitizes human cancer cells to ionizing radiation via inhibition of DNA repair machinery,” Cancer Research, vol. 70, no. 22, pp. 9339–9348, 2010.
View at: Publisher Site | Google Scholar
F. Errington, L. Steele, R. Prestwich et al., “Reovirus activates human dendritic cells to promote innate antitumor immunity,” Journal of Immunology, vol. 180, no. 9, pp. 6018–6026, 2008.
View at: Google Scholar
Z. G. Fridlender, J. Sun, S. Singhal et al., “Chemotherapy delivered after viral immunogene therapy augments antitumor efficacy via multiple immune-mediated mechanisms,” Molecular Therapy, vol. 18, no. 11, pp. 1947–1959, 2010.
View at: Publisher Site | Google Scholar
I. D. Iankov, C. Allen, M. J. Federspiel et al., “Expression of immunomodulatory neutrophil-activating protein of Helicobacter pylori enhances the antitumor activity of oncolytic measles virus,” Molecular Therapy, vol. 20, no. 6, pp. 1139–1147, 2012.
View at: Google Scholar
P. Wongthida, R. M. Diaz, F. Galivo et al., “VSV oncolytic virotherapy in the B16 model depends upon intact MyD88 signaling,” Molecular Therapy, vol. 19, no. 1, pp. 150–158, 2011.
View at: Publisher Site | Google Scholar
S. A. Gujar, P. Marcato, D. Pan, and P. W. K. Lee, “Reovirus virotherapy overrides tumor antigen presentation evasion and promotes protective antitumor immunity,” Molecular Cancer Therapeutics, vol. 9, no. 11, pp. 2924–2933, 2010.
View at: Publisher Site | Google Scholar
R. J. Prestwich, E. J. Ilett, F. Errington et al., “Immune-mediated antitumor activity of reovirus is required for therapy and is independent of direct viral oncolysis and replication,” Clinical Cancer Research, vol. 15, no. 13, pp. 4374–4381, 2009.
View at: Publisher Site | Google Scholar
G. Ungerechts, C. Springfeld, M. E. Frenzke et al., “An immunocompetent murine model for oncolysis with an armed and targeted measles virus,” Molecular Therapy, vol. 15, no. 11, pp. 1991–1997, 2007.
View at: Publisher Site | Google Scholar
B. D. Anderson, T. Nakamura, S. J. Russell, and K. W. Peng, “High CD46 receptor density determines preferential killing of tumor cells by oncolytic measles virus,” Cancer Research, vol. 64, no. 14, pp. 4919–4926, 2004.
View at: Publisher Site | Google Scholar

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Copyright © 2013 Nicolas Boisgerault et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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