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AJR Am J Roentgenol. Author manuscript; available in PMC Jun 17, 2011.
Published in final edited form as:
PMCID: PMC3117397

Sodium Iodide Symporter (NIS)-Mediated Radiovirotherapy for Pancreatic Cancer

Alan R. Penheiter, Ph.D.,1 Troy R. Wegman,1 Kelly L. Classic, M.S.,2 David Dingli, M.D., Ph.D.,1,3 Claire E. Bender, M.D., M.P.H.,4 Stephen J. Russell, M.D., Ph.D.,1,3 and Stephanie K. Carlson, M.D., M.S.1,4



We have previously shown the therapeutic efficacy of an engineered oncolytic measles virus expressing the sodium iodide symporter reporter gene (MV-NIS) in mice with human pancreatic cancer xenografts. The goal of this study was to determine the synergy between MV-NIS-induced oncolysis and NIS-mediated 131I radiotherapy in this tumor model.


Subcutaneous human BxPC-3 pancreatic tumors were injected twice with MV-NIS. Viral infection, NIS expression, and intratumoral iodide uptake were quantitated with 123I micro-SPECT/CT. Mice with MV-NIS infected tumors were treated with 0, 37, or 74 MBq 131I and monitored for tumor progression and survival. Additional studies were performed with stable NIS-expressing tumors (BxPC-3-NIS) treated with 0, 3.7, 18.5, 37, or 74 MBq of 131I.


Mice treated with intratumoral MV-NIS exhibited significant tumor growth delay (p<0.01) and prolonged survival (p=0.02) compared with untreated mice. Synergy between MV-NIS-induced oncolysis and NIS-mediated 131I ablation was not seen; however, a significant correlation was observed between NIS-mediated intratumoral iodide localization (% ID/g) and peak tumor volume reduction (p=0.04) with combination MV-NIS and 131I therapy. Stably-transduced NIS-expressing BxPC-3 tumors exhibited rapid regression with ≥18.5 MBq 131I.


Delivery of 131I radiotherapy to NIS-expressing tumors can be optimized using micro-SPECT/CT image guidance. Significant hurdles exist for NIS as a therapeutic gene for combined radiovirotherapy in this human pancreatic cancer model. The lack of synergy observed with MV-NIS and 131I in this model was not due to a lack of radiosensitivity, but rather to a non-uniform intratumoral distribution of MV-NIS infection.

Keywords: hNIS, sodium-iodide symporter (NIS), 131I, pancreatic cancer, measles virus


Pancreatic adenocarcinoma is the fourth most common cause of cancer-related death in men and women [1] and has a dismal prognosis with an overall 5-year survival rate of < 5% [2]. Conventional therapies for locally advanced, recurrent, or metastatic disease including chemotherapy, external beam radiation, or a combination of chemo-radiation therapy [3] have demonstrated minimal efficacy and are associated with considerable locoregional and systemic toxicity [4]. New targeted therapies for pancreatic cancer with increased efficacy and less toxicity are needed.

One targeted therapy that has shown great promise in numerous pre-clinical studies is the use of replicating oncolytic viruses [58] which also have the ability to serve as vectors for the transfer of reporter and/or therapeutic genes to infected tumor cells. A cell culture propagated molecular clone (Edmtag) [9, 10] of an attenuated Edmonston vaccine lineage of measles virus has been studied extensively at our institution and has shown significant oncolytic activity in multiple tumor cell types [7, 11, 12] including pancreatic adenocarcinoma [13]. To facilitate in vivo monitoring of viral delivery and tumor response, oncolytic measles was genetically engineered to express the human thyroidal sodium-iodide symporter (MV-NIS) [14].

In addition to the role of NIS an imaging reporter, which has recently been validated in a human clinical trial [15], several groups have attempted to utilize NIS as a therapeutic transgene for tumor ablation with 131I.[14, 1621]. Early studies with doses of 131I to rodents bearing NIS-expressing xenografts (based on mass-adjusted human maximum doses of 37–111 MBq 131I/kg body mass) were unsuccessful [2225]. However, later studies that employed much higher doses of 131I (1.85–5.55 GBq/kg) have shown consistent xenograft regression (albeit at rather low calculated tumor absorbed doses of <10 Gy), in mice with stable NIS-expressing tumors or adenovirus transfected tumors [21, 26, 27]. These therapeutic xenograft studies provide a foundation for the concept of NIS-mediated isotope concentrator gene therapy, and several groups are attempting to build on this foundation by exploring strategies to trap intracellular iodide [14, 2832].

In addition to the gene therapy approaches, a previous report from our group demonstrated a profound synergy between oncolytic MV-NIS therapy and systemically delivered 131I in an multiple myeloma xenograft (MM1) model [14]. In the MM1 model, systemically delivered virus infected and replicated in the tumor, but had only a modest oncolytic effect. When 37 MBq 131I was administered systemically at the peak of MV-NIS infection, the combined effects resulted in complete tumor regression in all animals. This was the first report of a synergistic relationship between an oncolytic virus (in which all NIS-expressing cells are destined for destruction) and systemic 131I.

We previously reported the efficacy of MV-NIS virotherapy alone for the treatment of human pancreatic cancer xenografts in athymic nude mice [13]. Although therapy with MV-NIS slowed BxPC-3 human pancreatic cancer xenograft tumor growth and extended survival in mice compared with control mice, it did not completely eradicate the tumors, and there was considerable tumor-to-tumor variability in response to MV-NIS. The primary goal of the present study was to determine the synergy between MV-NIS-induced oncolysis and NIS-mediated 131I radiotherapy in this tumor model. A secondary goal was to determine the role of micro-SPECT/CT imaging in optimizing the timing of radiovirotherapy.


Cell Culture

BxPC-3 human pancreatic cancer cells and 293T cells were purchased from American Type Culture Collection. BxPC-3 cells were maintained in RPMI 1640 supplemented with 10% fetal bovine serum (FBS) and 1X penicillin/streptomycin cocktail. The 293T cells were maintained in Dulbecco modified Eagle medium supplemented with 10% FBS and penicillin/streptomycin cocktail. FBS was obtained from Invitrogen. All other cell culture reagents were obtained from Mediatech.


A recombinant measles virus expressing the NIS gene was engineered at our institution and previously described [14]. The MV-NIS preparation used in all experiments in this study was produced by the Mayo Viral Vector Core [33] and contains 3.5 × 107 Vero cell tissue culture infective dose (TCID50)/mL.

Bicistronic lentiviral vector construction and production of NIS-expressing BxPC-3 cell line (polymerase chain reaction [PCR]) was used to construct a self-inactivating bicistronic lentiviral vector with human NIS (hNIS) and an internal ribosome entry site (IRES)-linked emerald green fluorescence protein (Em) under the control of a spleen focus-forming virus (SFFV) promoter. Primers used were forward: 5’-AAGGATCCACCATGGAGGCCGTGGAGACCGG-3’ and reverse: 5’-TTCTCGAGTCAGAGGTTTGTCTCCTG-3’. A previously constructed vector [32] was used as hNIS template DNA for the PCR reaction. The PCR product was cloned into pHR-SIN-B/X-IRES-Em to create plasmid pHR-SIN-hNIS-IRES-Em. Production of self-inactivating lentivirus was achieved using a 3 plasmid contransfection of 293T cells. Plasmids pMDG (which encodes the vesicular stomatitis virus glycoprotein under the control of a cytomegalovirus (CMV) promoter) and pCMVΔ8.91 (HIV1 gag, pol, tat, and rev) were gifts from the laboratory of D. Trono [34]. A total of 105 BxPC-3 cells were infected with lentivirus at a multiplicity of infection of 10, expanded to 107 cells, and sorted on a FACS Vantage system (Becton-Dickenson) at the Mayo Flow Cytometry/Optical Morphology Core Facility. The population of viable and fluorescent cells was sorted for emerald green fluorescence protein intensity and the sub-population that exhibited the highest 10% intensity was recovered and expanded in culture. At passage 12, BxPC-3-hNIS-IRES-Em cells were used for iodide uptake assays or tumor engraftment in mice, and the remaining cells were frozen in small aliquots.

Western Blot

BxPC-3-hNIS-IRES-Em or BxPC-3 control cells were grown to 90% confluency in a T175 flask. Cells were harvested by scraping in phosphate-buffered saline (PBS), washed twice in PBS, suspended in 1 mL radioimmunoprecipitation assay (RIPA) buffer; incubated for 15 minutes at 4°C, vortexed, and centrifuged at 15,000g. Aliquots of RIPA lysate supernatant were mixed with an equal volume of 4X reducing sodium dodecyl sulfate-loading buffer, heated to 55°C for 15 minutes, and separated on NuPage 10% Bis-Tris gels with 3-morpholino-propane sulfonic acid running buffer. Gels were then transferred to nitrocellulose membranes and probed with a mouse monoclonal antibody against the C-terminal peptide of hNIS (provided by Morris JC, Mayo Clinic), followed by a goat-antimouse IgG-horseradish peroxidase conjugate, and developed with an enhanced electrogenerated chemiluminescence kit. The total protein in the RIPA lysates was determined by the microbromochloroacetic acid assay.

NIS-mediated Radioiodine Uptake in Vitro

Iodide uptake assays were performed as previously described [14] using 10 kBq 125I-Na.

Animal Experiments

Experiments were approved by and performed in accordance with our institutional animal care and use committee guidelines. Five- to 7-week-old female nude mice were used in all experiments (Harlan Sprague-Dawley). Mice were housed in a pathogen-free barrier facility with access to food and water ad libitum. Mice were maintained on a PicoLab 5053 mouse diet (LabDiet), which contains 0.97 ppm total iodine. One week prior to intraperitoneal administration of 123I for imaging and/or 131I for radiotherapy [35], 5.625 µM L-thyroxine was added to the drinking water, and mice were placed on a low-iodine diet (<0.05 ppm total iodine; Harlan Teklad). To establish xenografts, mice were inoculated subcutaneously in the right flank with 3 × 106 BxPC-3 or BxPC-3 hNIS-IRES-Em cells in 100-µl of PBS. Tumors were measured in two dimensions with calipers, and volume was calculated from an ellipsoid formula. Mice were observed daily and euthanized on day 90 for survival studies or immediately if they met euthanization criteria (≥15% loss of body weight, inability to access food and water, tumor ulceration, or tumor burden exceeding 2 cm3).

Small Animal Imaging

A high-resolution micro-SPECT/CT system (X-SPECT, Gamma Medica Ideas) was used for planar and fusion micro-SPECT/CT imaging. A thorough description of the instrument can be found in the study by Carlson et al [36]. This system offers small animal functional and anatomical imaging with a micro-SPECT resolution of 3–4-mm (using a low-energy, high-resolution parallel-hole collimator with a 12.5-cm field of view) and a micro-CT resolution of approximately 155 µm. An 18.5 MBq dose of 123I was administered by intraperitoneal injection to all mice 1 hour before imaging. During imaging, animals were maintained under general anesthesia with isoflurane in O2 supplied from a veterinary vaporizer and delivered through mouse-specific nose cones. Image acquisition time was 5 minutes for planar and 13 minutes for micro-SPECT imaging (64 projections at 10 seconds per projection). Micro-CT image acquisition (155-µm slice thickness, 256 images) was performed in 1 minute at 0.25 mA and 80 kVp.

Image Analysis and Quantitation

Whole body activity (injected dose) in each mouse was determined by measuring activity in the syringe in a dose calibrator immediately prior to and after injection. Tumor activity was determined by region of interest (ROI) or volume of interest (VOI) analysis using PMOD Biomedical Image Quantification and Kinetic Modeling Software (PMOD Technologies) and previously described image analysis techniques [36]. Corresponding planar or VOI SPECT pixel counts were converted to activity using a constant derived from scanning 123I standards [36]. Counts were corrected for decay, and are reported as percentage of the initial intraperitoneal injected dose. Tumor micro-SPECT activities were corrected for partial volume effect losses by application of a recovery coefficient on the basis of a previous study performed with a series of spherical phantoms containing 123I [36].

Combination MV-NIS and 131I Radiotherapy In Vivo

A total of 29 mice with subcutaneous BxPC-3 human pancreatic xenografts were used for the first study. When tumors reached approximately 5 mm in diameter, they were directly injected with 3.5 × 106 TCID50/100 µL MV-NIS (n = 24 mice) or 100 µL Opti-MEM (Invitrogen) (vehicle control, n = 5 mice) using a 28-gauge needle. All tumors were injected with a second dose of virus or Opti-Mem 48 hours later. Planar mouse images were obtained with our micro-SPECT/CT scanner (1 hour after intraperitoneal injection of 18.5 MBq 123I) on day 6 after first injection of virus. Mice were injected intraperitoneal with 37 MBq or 74 MBq of 131I (n = 8 mice per group) immediately after imaging and followed for tumor regression and survival for 90 days.

Serial Imaging after MV-NIS Infection

Serial imaging with 123I micro-SPECT/CT on days 2, 3, 4, 6, and 9 after intratumoral MV-NIS injection (3.5 × 106 TCID50/100 µL) was performed on eight mice with subcutaneous BxPC-3 tumors to further characterize peak intratumoral iodide localization and determine the optimal therapeutic time frame for 131I administration. Mice were euthanized when their tumors showed a decrease in intratumoral iodide localization to background levels. Tumors were immediately frozen in Tissue-Tek optimum cutting temperature compound (Sakura Finetek) for immunohistochemistry analysis of intratumoral MV-NIS infection. Serial 12 µm cryosections were obtained uniformly throughout the tumor and developed with a biotinylated monoclonal antibody against measles nucleoprotein as described by Carlson et al. [13].

131I Radiotherapy in Stable NIS-Expressing Tumors

To evaluate the effects of 131I radiotherapy alone on BxPC-3 tumors (and thus determine their sensitivity to 131I), stable NIS-expressing BxPC-3-hNIS-IRES-Em subcutaneous xenografts were established in 30 mice. This model simulates an “ideal” 131I radiotherapy survival study whereby every tumor cell in the xenograft expresses NIS. Mice were randomly divided into groups of six on the basis of tumor size (approximately 5 mm diameter); imaged with 123I micro-SPECT/CT (as described previously); and treated with 0, 3.7, 18.5, 37, or 74 MBq of 131I after imaging. All mice were followed for tumor regression and survival up to 90 days. Control groups included mice with BxPC-3-NIS flank tumors that received no 131I, and mice with BxPC-3 tumors that received 74 MBq 131I.

Calculation of Absorbed Radiation Dose to Tumor Xenografts

Tumor dose in Gy was calculated for both the MV-NIS infected BxPC-3 xenografts and stable NIS-expressing xenografts to estimate the potential efficacy of 131I radiotherapy for tumor cell killing in these tumor models. Dosimetric calculations for intratumoral 123I were performed using medical internal radiation dose software and assuming a tumor density of 1 g/mL, homogeneous radionuclide distribution, a spherical shape of the tumor, and tumor effective half-life of 131I of 4.5 hours [37].

Statistical Analysis

Survival curves were compared by the log-rank test using Prism version 4.03 (GraphPad Software) for Microsoft Windows to determine whether the treatment groups were significantly different from the control groups. Spearman’s correlation analyses between survival and percentage ID/g and between tumor volume and peak 131I localization were performed with GraphPad Prism 4.03. Differences are considered statistically significant if p<0.05.


Combination MV-NIS and 131I Radiotherapy In Vivo

Figure 1 shows representative micro-SPECT/CT images of a control mouse and an intratumoral MV-NIS infected mouse. Areas of endogenous NIS-mediated radioiodide uptake in the thyroid, stomach, salivary glands were observed in all mice. A strong bladder signal was observed in some mice and depended on whether the bladder was voided prior to imaging. In contrast to control tumors, significant iodide accumulation was seen in the MV-NIS infected xenografts. MV-NIS infected tumors exhibited varying degrees of intratumoral iodide uptake with a mean (± standard error [SE]) of 8.0 ±1.3 % ID/g. The minimum and maximum uptake observed in MV-NIS infected tumors were 1.7 and 24.8 % ID/g, respectively. Control tumors not injected with MV-NIS showed normal physiologic uptake only (due to tumor vasculature and blood pooling in areas of tumor necrosis) with a mean of 1.5 ± 0.3 % ID/g and a range of 1.0 – 2.1 % ID/g.

Fig. 1
Representative 123I micro-SPECT/CT images of BxPC-3 flank tumor-bearing nude mice

The effects of intratumoral MV-NIS and combination intratumoral MV-NIS plus intraperitoneal 131I on BxPC-3 tumor volume and mouse survival are shown in Figure 2. Two mice treated with MV-NIS only and one mouse treated with MV-NIS plus 74MBq 131I survived to the end of the study (90 days). A trend of increased efficacy with combination MV-NIS plus 131I therapy was observed in early tumor volume measurements (Fig. 2A); however, we did not observe a significant prolongation of survival in mice administered combination therapy versus MV-NIS alone (Fig. 2B). All treatment groups exhibited a significant (p < 0.05) prolongation of survival versus vehicle-injected tumors.

Fig. 2
Tumor volume measurements and survival analysis

A trend, but not a significant correlation, was observed between tumor percentage ID/g determined by 123I imaging and prolongation of survival (Fig. 3A) n = 8 mice injected intratumorally twice with MV-NIS and imaged 6 days after first injection). A significant negative correlation (p = 0.04, two-tailed) was observed between tumor volume and peak tumor uptake of 131I (Fig. 3B). The calculations are based on tumor perecentage ID/g and the administered intraperitoneal dose of either 37 or 74 MBq (n=14 mice). This suggests that the reduction in tumor volume is likely due to the combined effects of MV-NIS-induced oncolysis and the antitumor effect of the administered dose of 131I.

Fig. 3
Correlation for treatment with MV-NIS

Serial Imaging after MV-NIS Infection

Serial imaging with 123I micro-SPECT/CT on days 2, 3, 4, 6, and 9 after virus injection showed a considerable temporal variability in peak tumor iodide localization and tumor response following a single intratumoral MV-NIS injection (Fig. 4). Most mice exhibited peak tumor iodide localization on approximately day 6. Three of eight mice had early peak tumor iodide localization between days 2 and 4 after virus injection. By day 9, tumor signals had returned to near background levels for all mice. Interestingly, two of the three mice that displayed peak tumor iodide uptake around day 3 also exhibited complete, but markedly delayed, tumor regression. Whereas functional imaging with micro-SPECT showed an early burst of NIS expression and iodide uptake on day 3 after virus injection, it took more than 2 weeks for the tumors to show a significant reduction in volume as measured by micro-CT or external calipers. This likely represents a delayed clearance of viral-lysed cell debris.

Fig. 4
Serial imaging and immunohistochemistry

In addition to variability in temporal expression of NIS, immunohistochemistry revealed a dramatic heterogeneity in the spatial distribution of MV-NIS infected cells within the tumor. Figure 4C shows a representative immunohistochemical section from a BxPC-3 tumor excised day 6 after virus injection. Regions of nearly uniform infection often containing several thousand cells were consistently observed. Few if any individual infected cells were observed, suggesting that MV-NIS is highly fusogenic in this tumor model. Mouse fibroblasts in the tumor capsule and within the tumor stroma appear to be resistant to viral infection, as bands of uninfected fibroblasts often were observed surrounded by infected BxPC-3 cells. These tumors were quite heterogeneous, typically with one prominent encapsulated nodule and one or more small, newly developing, adjacent nodules.

Stable BxPC-3-hNIS-IRES-Em Experiments

Stable NIS-expressing BxPC-3 tumors cells were produced (BxPC-3-hNIS-IRES-Em) (Figs. 5A&B). In vitro, these cells concentrated iodide intracellularly 101 times that of extracellular iodide (Fig. 5 C). In vivo, BxPC-3-hNIS-IRES-Em tumors exhibited significant intratumoral iodide uptake (mean, 34.7 % ID/g) (Fig. 6). Compared to BxPC-3-hNIS-IRES-Em xenografts receiving no 131I and non-transduced BxPC-3 xenografts receiving 131I, a significant dose-dependent response to 131I radiotherapy (tumor volume reduction and increased mouse survival) was observed in the stable NIS-expressing tumors (Fig. 7). Dosimetry calculations based on a tumor effective half-life of 4.5 hours yielded a mean tumor dose of 10.8 Gy per mCi (0.29 Gy/MBq) of administered 131I. Tumor mass at the time of intraperitoneal 131I administration was 0.35 ± 0.16 g (mean ± SD).

Fig. 5
Construction and in vitro characterization of BxPC-3 hNIS-IRES-Em cells
Fig. 6
Mouse with stable NIS-expressing right flank tumor
Fig. 7Fig. 7
131I radiotherapy study in stable NIS-expressing tumors


In a previous study, we showed that intratumoral injection of MV-NIS in human pancreatic cancer xenografts led to decreased tumor volume and prolongation of mouse survival compared with mice with control tumor xenografts, but it rarely led to complete elimination of the tumors [13]. In this report, we evaluated the addition of NIS-mediated 131I radiotherapy to enhance the oncolytic potency of MV-NIS therapy for pancreatic cancer.

In our first in vivo experiment, we studied the effect of combination MV-NIS and 131I radiotherapy (radiovirotherapy) in pancreatic cancer xenografts that had been administered intratumoral MV-NIS. Intraperitoneal 131I was given on day 6 after the first injection of virus (the timing of 131I therapy was based on a previous serial imaging study performed in our laboratory) [13]. Although we did see a trend towards decreased tumor volume and increased mouse survival, the tumors were not completely eradicated and there was no significant benefit of 131I radiovirotherapy over MV-NIS virotherapy alone. Three possible explanations for this lack of synergy are inappropriate timing of 131I administration; lack of a bystander effect from 131I in certain tumor regions, particularly at the tumor periphery and in newly developing tumor nodules which were not infected; and the possibility that BxPC-3 cells are not sensitive to radiation at these dose levels. These three possible explanations were directly tested by performing a micro-SPECT/CT serial imaging study following intratumoral MV-NIS injection, documenting the intratumoral distribution of MV-NIS infection with immunohistochemistry, and by creating a stable NIS-expressing xenograft model whereby 100% of the BxPC-3 cells in the tumor would express NIS.

Effective MV-NIS oncolysis in this model results in a transient NIS-mediated intratumoral iodide uptake. Therefore, the timing of imaging NIS expression is critical. Given that we did find a significant correlation between percentage ID/g and tumor volume reduction and that tumors occasionally can be cured with MV-NIS alone, we anticipated that had we performed serial 123I imaging in these mice we could have better timed the 131I radiotherapy on the day of maximal NIS expression in each mouse. The conclusion led us to repeat our previous study and perform serial imaging in a second group of mice with pancreatic cancer xenografts after a single intratumoral MV-NIS injection. Serial imaging demonstrated maximum intratumoral iodide uptake on approximately day 3 (n = 3 mice) or day 6 (n = 5 mice) after virus injection. The mice that exhibited maximum intratumoral 123I uptake on day 3 had background levels of intratumoral iodide uptake on day 6 due to cell killing by the virus. Had these mice been given 131I therapy on day 6 (as we did in the radiovirotherapy study) it would have been past the peak of iodide accumulation in the tumors and the benefit of adding 131I to the therapeutic protocol would be considerably reduced. This shows the considerable temporal variation in NIS-mediated intratumoral iodide uptake and the importance of reporter gene imaging to accurately direct the timing of additional radiotherapy, decide if additional radiotherapy would even be appropriate, and help determine an individual’s specific response to therapy.

In this and other studies, we have examined more than 20 BxPC-3 tumors at various times after MV-NIS injection (day 2 – 14) by serial sectioning and immunohistochemistry with an anti-measles nucleoprotein antibody. The immunohistochemical analysis of MV-NIS infected tumors reveals patches of nearly uniform infection containing thousands of infected cells and giant syncytia (indicating that the virus is able to successfully infect human pancreatic cancer cells and that the infected cells are highly fusogenic). However, even after 6 days of infection, there appears to be little additional spread of infection to distant regions of the tumor beyond the initial zone of viral distribution from the injection. Also the propensity of mitotic activity at the periphery of these tumors appears to create a situation where the tumor grows away from the zones of central infection. While the path length of 131I β particles (mean of approximately 400 µm in H2O) may be sufficient to reach most of the non-infected cells in small tumors, geometrical dilution of radiation-induced DNA damage due to the inverse square law likely severely limits the therapeutic bystander effect in any areas of non-uniform 131I uptake within the tumor.

To evaluate the effects of 131I radiotherapy alone on BxPC-3 tumors (and thus determine their sensitivity to 131I), stable NIS-expressing BxPC-3 tumors cells were produced. These cells were then used to create tumor xenografts (with 100% of the viable tumors cells expressing NIS) to simulate an ideal 131I radiotherapy survival study. In this study, we did show a significant dose-dependent response to 131I in both tumor volume reduction and mouse survival compared to BxPC-3-hNIS-IRES-Em xenografts receiving no 131I and non-transduced BxPC-3 xenografts receiving 131I. Somewhat surprisingly, all mice with the stable NIS-expressing tumors administered ≥ 18.5 MBq 131I (estimated dose of 5.4 Gy to the tumor) exhibited rapid tumor regression. Two of the six mice administered 3.7 MBq also exhibited a delayed tumor regression. In the MV-NIS plus 131I synergy study, tumors treated with 37 MBq had a mean estimated tumor dose of 3.0 Gy whereas those administered 74 MBq 131I had a mean estimated tumor dose of 5.8 Gy. In contrast to the results in the stable NIS-expressing tumor study many of the MV-NIS + 131I tumors with an absorbed dose greater than 4 Gy did not exhibit tumor regression. The direct comparison of tumor response to 131I between stable NIS-expressing tumors and MV-NIS infected tumors with similar absorbed radiation doses provides further evidence for the necessity of a relatively uniform distribution of 131I for a therapeutic response at these absorbed doses.

In conclusion, NIS appears to a valuable quantitative reporter of MV-NIS infection; however, a benefit of combination therapy with MV-NIS and 131I was not observed. Further efforts aimed at optimizing both the initial distribution of virions in the tumors as well as enhancement of the propagation of virus are likely required to achieve a synergistic effect in this tumor model.


We thank our nuclear medicine technologist, Tracy Decklever, for technical expertise and imaging assistance. We thank Mark J. Federspiel for supplying MV-NIS and Yasuhiro Ikeda for supplying the lentiviral vectors. This work was supported by the National Cancer Institute (grant K08 CA103859-03A1 and grant P50 CA102701).


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