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Research Article | Open Access
Andrew D. Ludwig, Kevin P. Labadie, Y. David Seo, Donald K. Hamlin, Holly M. Nguyen, Vimukta M. Mahadev, Raymond S. Yeung, D. S. Wilbur, James O. Park, "Yttrium-90-Labeled Anti-Glypican 3 Radioimmunotherapy Halts Tumor Growth in an Orthotopic Xenograft Model of Hepatocellular Carcinoma", Journal of Oncology, vol. 2019, Article ID 4564707, 7 pages, 2019. https://doi.org/10.1155/2019/4564707
Yttrium-90-Labeled Anti-Glypican 3 Radioimmunotherapy Halts Tumor Growth in an Orthotopic Xenograft Model of Hepatocellular Carcinoma
Hepatocellular carcinoma (HCC) is the second most lethal malignancy globally and is increasing in incidence in the United States. Unfortunately, there are few effective systemic treatment options, particularly for disseminated disease. Glypican-3 (GPC3) is a proteoglycan cell surface receptor overexpressed in most HCCs and provides a unique target for molecular therapies. We have previously demonstrated that PET imaging using a 89Zr-conjugated monoclonal anti-GPC3 antibody (αGPC3) can bind to minute tumors and allow imaging with high sensitivity and specificity in an orthotopic xenograft mouse model of HCC and that serum alpha-fetoprotein (AFP) levels are highly correlated with tumor size in this model. In the present study, we conjugated 90Y, a high-energy beta-particle-emitting radionuclide, to our αGPC3 antibody to develop a novel antibody-directed radiotherapeutic approach for HCC. Luciferase-expressing HepG2 human hepatoblastoma cells were orthotopically implanted in the livers of athymic nude mice, and tumor establishment was verified at 6 weeks after implantation by bioluminescent imaging and serum AFP concentration. Tumor burden by bioluminescence and serum AFP concentration was highly correlated in our model. Yttrium-90 was conjugated to αGPC3 using the chelating agent 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) and injected via the tail vein into the experimental mice at a dose of 200 μCi/mouse or 300 μCi/mouse. Control mice received DOTA-αGPC3 without radionuclide. At 30 days after a single dose of the radioimmunotherapy agent, mean serum AFP levels in control animals increased dramatically, while animals treated with 200 μCi only experienced a minor increase, indicating cessation of tumor growth, and animals treated with 300 μCi experienced a reduction in serum AFP concentration, indicating tumor shrinkage. Mean tumor-bearing liver weight in control animals was also significantly greater than that in animals that received either dose of 90Y-αGPC3. These results were achieved without significant toxicity as measured by body condition scoring and body weight. The results of this preclinical pilot demonstrate that GPC3 can be used as a target for radioimmunotherapy in an orthotopic mouse model of HCC and may be a target of clinical significance, particularly for disseminated HCC.
Hepatocellular carcinoma (HCC) is recognized as the fifth most common cancer and second leading cause of cancer-related deaths worldwide, resulting in over 750,000 deaths annually . Though there has been progress in surgical and nonsurgical treatment for HCC, the prognosis remains poor, particularly for late-stage disease. Sorafenib, a multikinase inhibitor and the best form of chemotherapy for advanced disease, has been shown to prolong median survival and time to progression by only 3 months . Because of this dismal prognosis, novel targets and therapies are desperately needed.
Glypican-3 (GPC3) is a heparan sulfate proteoglycan found on the cell surface of human embryonic stem cells. It is anchored by glycosylphosphatidylinositol and regulates growth and morphogenesis through insulin-like growth factor and hedgehog signaling pathways [3, 4]. Its importance in regulating cell growth is underscored by a loss-of-function mutation in GPC3 that causes Simpson–Golabi–Behmel syndrome, a condition of skeletal and organ overgrowth . Expression of GPC3 in the fetal liver is observed from 18 to 30 weeks of gestation, but no GPC3 expression is seen in normal adult liver cells [3, 6, 7]. Conversely, high expression of GPC3 is seen in HCC, is correlated with AFP expression, and can be used to differentiate HCCs from benign liver lesions [8–10]. In addition, the level of expression of GPC3 in HCC patients is correlated with poorer prognosis and risk of recurrence after primary resection or liver transplant [11–15].
Because of this differential expression and cell surface location, GPC3 is a promising tumor marker for diagnostic and therapeutic purposes in HCC. We have previously demonstrated the utility of antibody-directed 89Zr radioisotopes as PET contrast agents to identify GPC3-expressing orthotopic liver tumors in vivo [16, 17]. In the current report, we describe the development of a novel antibody-directed therapeutic radioisotope in the form of a 90Y-αGPC3 conjugate and study its effect on in vivo HCC tumor growth in our orthotopic mouse model.
2. Materials and Methods
2.1. Cell Lines and Tissue Culture
Luciferase-expressing GPC3-positive HepG2-Red-FLuc HCC cells were purchased from PerkinElmer (Bioware, cat. no. BW134280). Cell lines were maintained in a monolayer at 37°C in Dulbecco’s modified Eagle’s medium (DMEM; Gibco) supplemented with 10% fetal bovine serum (FBS; Gibco) in a humidified atmosphere of 95%/5% air/CO2.
2.2. Anti-GPC3 IgG1 Generation (as Previously Described )
RBF/DnJ mice were immunized with recombinant carrier-free human GPC3 protein in Freund’s adjuvant solution. After several boost injections, antiserum ELISAs confirmed the presence of the αGPC3 IgG. Additional boost injections were delivered to ensure IgM/IgG switch, which was verified on ELISA with IgG titrated to 1 : 10,000. After final prefusion boost injections, mice were euthanized, their spleens were harvested, 1 × 108 splenocytes were fused on a ratio of 1 : 1 with FOX-NY myeloma cells, and the resultant hybridomas were resuspended in adenine/aminopterin/thymidine FBS solution. Clones producing high titers of GPC3 IgG1 were selected using capture ELISA with goat antimouse IgG1 for isotyping.
2.3. Production of 90Y-αGPC3 Antibody
To demetallate the αGPC3 antibody, it was dialyzed against metal-free HEPES (50 mM HEPES (N-(2-hydroxyethyl)piperazine-N′-ethanesulfonic acid), 150 mM NaCl, and 1 mM EDTA adjusted to 8.5 pH and passed over a Chelex 100 (Biorad) column to remove metals) with a minimum of 6 buffer changes over 3 days at 4°C using Chelex 100 resin at each buffer change to scavenge metals. The metal-free αGPC3 was added to a DOTA-Bn-NCS (Macrocyclics) solution (10 mg/mL in DMSO), and the reaction was allowed to run overnight at room temperature with gentle mixing. The reaction mixture was then dialyzed against a metal-free citrate buffer (50 mM sodium citrate and 150 mM NaCl with pH 5.5) over 3 days at 4°C followed by dialysis against 150 mM saline for another 3 days. Each buffer change contained Chelex resin to scavenge metals. Demetallated ammonium acetate (500 mM, pH 5.3) and 90Y were combined followed by αGPC3-DOTA, prepared as above, and incubated at 45°C for 1 hr before cooling to room temperature. The reaction was quenched with diethylenetriamine pentaacetic acid (DTPA). The labeled antibody was then separated from unreacted 90Y via a PD-10 column (GE Healthcare) and eluted in PBS prior to analysis by thin layer chromatography (TLC) to verify radiochemical purity. Acid-washed vials and pipette tips were used for all steps.
2.4. Flow Cytometry
In vitro binding of the DOTA-αGPC3 conjugate was evaluated by flow cytometry. HepG2-Red-FLuc cells were grown as above until 70% confluent and then detached with 0.25% trypsin, counted, washed, and resuspended in cold phosphate-buffered saline (PBS) at a concentration of 1 × 106 cells/mL. One microgram of unconjugated or DOTA-αGPC3 primary antibody was added to the cell suspension and incubated for 45 minutes on ice. Primary antibody control samples received 1 μg of isotype-matched IgG1 control antibody (BD Biosciences, cat. no. 555746). Unstained samples did not receive primary antibody. The cells were then washed in cold PBS, and 1 μg of FITC-labeled goat-α-mouse IgG1 secondary antibody (Southern Biotech, cat. no. 1070-02) was added to the cell suspension and incubated on ice for 30 minutes in the dark. Unstained samples did not receive secondary antibody. The cells were washed in cold PBS, fixed with 1% paraformaldehyde for 15 minutes, and then washed and resuspended in cold PBS. Fixed cells were analyzed with a BD FACSCanto flow cytometer (Becton Dickinson Biosciences, Franklin Lakes, NJ) using the FACSDiva software. A minimum of 10,000 cells were analyzed for each sample in triplicate. Data analysis was performed on the FlowJo software, version 8.8.6 (Tree Star, Ashland, OR).
2.5. Animal Models
All animal studies were performed in accordance with the University of Washington Office of Animal Welfare guidelines for the humane use of animals, and all procedures were reviewed and approved by the Institutional Animal Care and Use Committee. To generate the orthotopic xenograft model, 8-week-old female athymic Nu/J mice (The Jackson Laboratory) were anesthetized using 1.5% inhaled isoflurane, and the left lobe of the liver was exposed through an upper midline laparotomy. HepG2-Red-FLuc cells (2 × 106) in 50 μL of Dulbecco’s modified Eagle’s medium containing 50% Matrigel (BD Biosciences) were injected into the subcapsular space of the left lobe.
2.6. Bioluminescent Imaging
Six weeks after orthotopic HepG2 cell injection, a 75 mg/kg intraperitoneal injection of VivoGlo luciferin (Promega) was administered and imaging was performed using an IVIS Lumina II system (PerkinElmer) to verify tumor establishment and monitor the growth of intrahepatic tumors. Tumor size was calculated based on the average photon emission (photons/sec) in a 2D region of interest (ROI) covering the entire animal. The ROI was corrected for background bioluminescence, and the size of the ROI (32 cm2) was identical for every animal imaged. Calculations were performed using the Living Image software (version 4.2; Caliper Life Sciences).
2.7. Measurement of Mouse Serum AFP
At the specified times, whole blood was obtained from animals using submandibular bleeding  and collected in EDTA-coated Eppendorf tubes. Serum was extracted from the fresh whole blood and then frozen and allowed to decay 10 half-lives (∼27 days) in accordance with the University of Washington Environmental Health and Safety policy. The serum concentration of AFP was determined on the UniCel Dxl 800 Access Immunoassay System (Beckman Coulter) using an Access AFP alpha-fetoprotein pack (Quest Diagnostics).
2.8. In Vivo Radioimmunotherapy
Animals bearing established tumors as determined by IVIS imaging and serum AFP concentration using the above methods were randomly assigned to three experimental groups. All animals received the antibody conjugate via tail vein injections. Control animals were injected with 70 μg DOTA-conjugated αGPC3 antibody without radioisotope. Treated animals received 70 μg 90Y-αGPC3 at the specified dosages of radionuclide. At 14 days after antibody injection, serum AFP was measured based on the above protocol. At 30 days after antibody injection, the animals were euthanized, blood was extracted via cardiac puncture, and livers were harvested, wet-weighed, and then placed in 10% (w/v) neutral-buffered formalin.
2.9. Statistical Analysis
All numeric data are expressed as mean ± SEM unless otherwise indicated. Excel (version 12.0.6; Microsoft) was used for statistical analysis. For continuous variables, an unpaired, 2-tailed Student’s t-test was used. For multigroup comparisons, a one-way analysis of variance (ANOVA) was used. In all cases, a value ≤0.05 was considered statistically significant.
3.1. Flow Cytometry
Flow cytometry confirmed binding of both unconjugated and DOTA-conjugated αGPC3 to the luciferase-expressing HepG2-Red-FLuc cell line (Figure 1). The normalized geometric mean fluorescence of both unconjugated (1619.7 ± 23.2 a.u.) and DOTA-conjugated αGPC3 (1076 ± 30.0 a.u.) is significantly greater than that of unstained (95.2 ± 1.4 a.u.) and IgG1 isotype-matched primary antibody control (125.7 ± 10.5 a.u.) samples ( vs. isotype control). Though DOTA conjugation did appear to marginally affect αGPC3 antibody binding in vitro, mean fluorescence of conjugated samples remained >8-fold higher than that of control samples.
3.2. Orthotopic Tumor Establishment
Serum AFP concentration was measured in tumor-bearing mice at six weeks after HepG2-Red-FLuc orthotopic implantation. Tumor establishment was verified by IVIS imaging at the time of serum sampling. Serum AFP levels in study animals ranged from 474.3 ng/mL to 421,600 ng/mL. Tumor bioluminescence ranged from 48.6 photons/sec to 50,340 photons/sec. Tumor bioluminescence as demonstrated by IVIS imaging correlates with serum AFP concentration with a correlation coefficient R2 of 0.92 (Figure 2). This finding indicates that serum AFP concentration can be used to monitor tumor growth and response to treatment.
To track tumor growth and response to radioimmunotherapy treatment, serum AFP concentration was monitored at 0, 14, and 30 days after administration of either low-dose (200 μCi, n = 9) or high-dose (300 μCi, n = 9) 90Y conjugated to 70 μg of DOTA-αGPC3 via tail vein injection. Control animals (n = 7) received DOTA-αGPC3 without radionuclide. At the time of antibody injection, mean serum AFP concentration for control (75,258 ± 38,683 ng/mL), low-dose (66,434 ± 35,895 ng/ml), and high-dose (75,568 ± 45,467 ng/mL) groups was not statistically significantly different (), indicating equivalent overall tumor burden between groups at the initiation of the therapy (Figure 3).
At 14 days after antibody injection, mean serum AFP concentration of control animals increased by 578% (to 510,284 ± 300,473 ng/ml), whereas animals that received low-dose radioimmunotherapy treatment experienced a 127% increase (to 150,800 ± 76,392 ng/mL) and animals that received high-dose treatment only experienced a 37% increase (to 103,344 ± 79,120 ng/mL). Though this trend was strong, the mean change in serum AFP concentration at 14 days between control and low-dose or high-dose treatment groups did not reach statistical significance ( and , respectively). The mean serum AFP concentration of animals treated with low-dose and high-dose 90Y-αGPC3 was not statistically different from each other at 14 days () and was not statistically different from pretreatment levels ( and , respectively).
By 30 days after radioimmunotherapy administration, mean serum AFP concentration of control animals had increased by 953% (to 792,566 ± 441,503 ng/mL) from pretreatment levels, while animals that received low-dose radioimmunotherapy treatment experienced a modest 17% increase over 30 days (to 77,820 ± 37,895 ng/mL) and animals that received high-dose treatment saw a decrease in mean serum AFP concentration by 35% (to 49,342 ± 36,800 ng/mL).
Notably, both low-dose and high-dose treatment groups experienced a decrease in mean serum AFP concentration from 14 days to 30 days by 48% and 52%, respectively. The mean change in AFP concentration over the 30-day study period was significantly different between control and low-dose groups, between control and high-dose groups, and between low- and high-dose groups (). However, the mean serum AFP concentrations of low-dose and high-dose treatment groups did not differ statistically from each other at 30 days after antibody injection ().
At 30 days after radioimmunotherapy treatment, study animals were euthanized and livers were removed en bloc to gauge tumor growth. The mean weight of control animal livers (2.36 ± 0.55 g) was significantly greater than that of animals that received either low-dose (1.33 ± 0.07 g) or high-dose (1.28 ± 0.08 g) 90Y-αGPC3 treatment (; Figure 4). The mean weight of livers from animals receiving low-dose or high-dose 90Y-αGPC3 treatment did not differ statistically (). During the course of the study, no animals were noted to have a significant change in body weight or body condition scoring, nor were any animal euthanized prior to the end date of the study.
HCC is a common and deadly form of cancer for which few treatment options exist for late-stage or disseminated disease. In this preclinical study, we report the ability of a novel radioimmunotherapy agent, combining the radionuclide 90Y with an HCC-specific antibody targeting the cell surface proteoglycan GPC3, to halt tumor growth in an orthotopic xenograft model.
To create a radioimmunotherapy agent, we conjugated a high-energy beta-emitting radionuclide, 90Y, to a tumor-specific antibody using the chelating agent 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA). We demonstrated that conjugating this agent to αGPC3 maintained binding of the antibody in vitro by flow cytometry. We have previously shown that conjugating 89Zr to αGPC3 with deferoxamine preserves antibody binding and specificity in vitro and in vivo . Conjugation of 90Y to monoclonal antibodies with DOTA is clinically relevant and has been used in clinical trials for the treatment of pancreatic cancer , B-cell lymphoma , and leukemia . Similarly, 90Y itself is used clinically in the treatment of HCC. Radioembolization with 90Y has been used in the treatment of HCC since the 1960s , and 90Y microspheres have been shown to significantly prolong time to progression in HCC when compared to chemoembolization . These efforts have demonstrated that 90Y treatment is well tolerated in advanced-stage HCC .
In our orthotopic mouse model, we used serum AFP concentration as a corollary of tumor size, allowing a simple blood draw to track the response to treatment while animals were under radionuclide treatment. Serum AFP concentration prior to treatment was highly correlated with tumor size as established by bioluminescent imaging of the luciferase-expressing orthotopic tumors. Because of the intra-abdominal location of these tumors, external measurement of tumor volume is not possible. Others have demonstrated that serum AFP concentration is correlated with tumor size by bioluminescent and magnetic resonance imaging in a HepG2 orthotopic xenograft model . Similarly, this method of correlating bioluminescence with tumor serum markers to track treatment response in orthotopic xenografts undergoing immunotherapy has been utilized successfully in several other tumor models . In the clinical setting, high serum AFP concentration (>400 ng/mL) is considered diagnostic for HCC in the appropriate patient (e.g., cirrhotic or high-risk for HCC) and can be used to monitor the treatment effect and recurrence in patients whose tumors expressed AFP at diagnosis . Serum AFP concentration decreasing in response to therapy in HCC was first described in the late 1970s  and continues to be clinically relevant as a predictor of outcome across the spectrum of HCC therapies. A similar phenomenon is present in our orthotopic model of HCC undergoing radioimmunotherapy.
We have previously demonstrated that 89Zr-αGPC3 can be used as a novel imaging agent in this orthotopic xenograft HCC model. Using the same antibody and similar conjugation techniques, we extend the utility of this antibody to a therapeutic platform using 90Y. Naturally, this presents the opportunity to combine tumor-specific diagnostic and therapeutic modalities using the same antibody and introduces the possibility of targeting small tumors and disseminated disease. Studies of this theranostics platform in our orthotopic xenograft model are in process. It is possible that the presence of 90Y alone could account for some of the treatment effects seen in our model. However, our study utilized a single dose of radioimmunotherapy, and it is unlikely that such a dose administered systemically without tumor-specific activity could result in the sustained arrest of tumor growth over 30 days seen here. Nevertheless, we anticipate using nontargeting antibody controls in future preclinical experiments.
In addition, the direct cytotoxic effect of αGPC3 monoclonal antibodies is widely recognized. Since its characterization as a diagnostic and prognostic marker in HCC, GPC3 has been studied as a therapeutic target. A cytotoxic humanized αGPC3 monoclonal antibody, GC33, is capable of inhibiting orthotopic xenograft tumor growth , and clinical trials have been underway in HCC patients since 2013 . Though our antibody was not designed with the intention of inducing a cytotoxic effect, control animals received DOTA-conjugated αGPC3 to account for the possible direct effect of the antibody itself. Progression of tumor growth in control animals during our study suggests that such an effect, if present, is not significant with our αGPC3 antibody.
The tumor-targeting effect of the αGPC3 antibody localizes the treatment effect of 90Y to the tumor, prolonging the exposure of tumor cells to β-particle emission and limiting systemic effects. In the present study, all animals were noted to tolerate radioimmunotherapy without significant morbidity or mortality. Efforts to better quantify potential off-target effects of this novel radioimmunotherapy agent deserve further study and are currently underway.
In this study, we report the ability of a novel 90Y-αGPC3 conjugate radioimmunotherapy to successfully halt the growth of luciferase-expressing HepG2 tumors in an orthoptic xenograft model of hepatocellular carcinoma. We used serum AFP as a marker of tumor size, validated by bioluminescent imaging. In our model, serum AFP levels in animals treated with a single dose of 200 μCi remained at pretreatment levels while in control animals serum AFP increased by over 900% by 30 days after treatment. In animals treated with 300 μCi of our conjugate, serum AFP levels decreased below pretreatment levels, indicating a reduction in tumor size.
The data used to support the findings of this study, including values behind means and standard deviations and images of in vivo bioluminescence, are available from the corresponding author upon request.
This work was presented at the 58th Annual Meeting of the Society for Surgery of the Alimentary Tract (SSAT 2017).
Conflicts of Interest
The authors declare that there are no conflicts of interest regarding the publication of this paper.
The authors would like to acknowledge the University of Washington Shared IVIS Core, which was supported by the NIH Shared Instrumentation Grant (1S10OD010652-01). This work was funded through United States Department of Energy Grant (DE-SC0012445 MOD03), Chugai Pharmaceuticals Grant (UW OSP #A103633 AM02), and University of Washington ITHS Pilot Grant.
- L. A. Torre, F. Bray, R. L. Siegel, J. Ferlay, J. Lortet-tieulent, and A. Jemal, “Global cancer statistics, 2012,” CA: A Cancer Journal for Clinicians, vol. 65, no. 2, pp. 87–108, 2015.
- J. Bruix and J. M. Llovet, “Major achievements in hepatocellular carcinoma,” Lancet, vol. 373, no. 9664, pp. 614–616, 2009.
- B. V. Iglesias, G. Centeno, H. Pascuccelli et al., “Expression pattern of glypican-3 (GPC3) during human embryonic and fetal development,” Histology and Histopathology, vol. 23, pp. 1333–1340, 2008.
- M. I. Capurro, P. Xu, W. Shi, F. Li, A. Jia, and J. Filmus, “Glypican-3 inhibits hedgehog signaling during development by competing with patched for hedgehog binding,” Developmental Cell, vol. 14, no. 5, pp. 700–711, 2008.
- G. Pilia, R. M. Hughes-Benzie, A. MacKenzie et al., “Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome,” Nature Genetics, vol. 12, no. 3, pp. 241–247, 1996.
- M. I. Capurro, Y.-Y. Xiang, C. Lobe, and J. Filmus, “Glypican-3 promotes the growth of hepatocellular carcinoma by stimulating canonical Wnt signaling,” Cancer Research, vol. 65, no. 14, pp. 6245–6254, 2005.
- N. Yamauchi, A. Watanabe, M. Hishinuma et al., “The glypican 3 oncofetal protein is a promising diagnostic marker for hepatocellular carcinoma,” Modern Pathology, vol. 18, no. 12, pp. 1591–1598, 2005.
- H. C. Hsu, W. Cheng, and P. L. Lai, “Cloning and expression of a developmentally regulated transcript MXR7 in hepatocellular carcinoma: biological significance and temporospatial distribution,” Cancer Research, vol. 57, pp. 5179–5184, 1997.
- H. Jia, Q. Ye, L. Qin et al., “Human cancer biology gene expression profiling reveals potential biomarkers of human hepatocellular,” Carcinoma, vol. 13, no. 4, pp. 1133–1140, 2007.
- X. Jia, J. Liu, Y. Gao, Y. Huang, and Z. Du, “Diagnosis accuracy of serum glypican-3 in patients with hepatocellular carcinoma: a systematic review with meta-analysis,” Archives of Medical Research, vol. 45, no. 7, pp. 580–588, 2014.
- Y. Haruyama and H. Kataoka, “Glypican-3 is a prognostic factor and an immunotherapeutic target in hepatocellular carcinoma,” World Journal of Gastroenterology, vol. 22, no. 1, pp. 275–283, 2016.
- K. Ofuji, K. Saito, T. Yoshikawa, and T. Nakatsura, “Critical analysis of the potential of targeting GPC3 in hepatocellular carcinoma,” Journal of Hepatocellular Carcinoma, vol. 1, pp. 35–42, 2014.
- Y. Wu, H. Liu, and H. Ding, “GPC-3 in hepatocellular carcinoma: current perspectives,” Journal of Hepatocellular Carcinoma, vol. 3, pp. 63–67, 2016.
- L. Wang, L. Pan, M. Yao, Y. Cai, Z. Dong, and D. Yao, “Expression of oncofetal antigen glypican-3 associates significantly with poor prognosis in HBV-related hepatocellular carcinoma,” Oncotarget, vol. 7, no. 27, pp. 42150–42158, 2016.
- A. O. Kaseb, M. Hassan, S. Lacin et al., “Evaluating clinical and prognostic implications of glypican-3 in hepatocellular carcinoma,” Oncotarget, vol. 7, no. 43, pp. 69916–69926, 2016.
- J. G. Sham, F. M. Kievit, J. R. Grierson et al., “Glypican-3-Targeted 89Zr PET imaging of hepatocellular carcinoma,” Journal of Nuclear Medicine, vol. 55, no. 5, pp. 799–804, 2014.
- J. G. Sham, F. M. Kievit, J. R. Grierson et al., “Glypican-3-Targeting F(ab′)2 for 89Zr PET of hepatocellular carcinoma,” Journal of Nuclear Medicine, vol. 55, no. 12, pp. 2032–2037, 2014.
- W. T. Golde, P. Gollobin, and L. L. Rodriguez, “A rapid, simple, and humane method for submandibular bleeding of mice using a lancet,” Lab Animal, vol. 34, no. 9, pp. 39–43, 2005.
- A. J. Ocean, K. L. Pennington, M. J. Guarino et al., “Fractionated radioimmunotherapy with 90Y-clivatuzumab tetraxetan and low-dose gemcitabine is active in advanced pancreatic cancer: a phase 1 trial,” Cancer, vol. 118, no. 22, pp. 5497–5506, 2012.
- F. Kraeber-Bodere, A. Pallardy, H. Maisonneuve et al., “Consolidation anti-CD22 fractionated radioimmunotherapy with 90Y-epratuzumab tetraxetan following R-CHOP in elderly patients with diffuse large B-cell lymphoma: a prospective, single group, phase 2 trial,” The Lancet Haematology, vol. 4, no. 1, pp. e35–e45, 2017.
- P. Chevallier, T. Eugene, N. Robillard et al., “90Y-labelled anti-CD22 epratuzumab tetraxetan in adults with refractory or relapsed CD22-positive B-cell acute lymphoblastic leukaemia: a phase 1 dose-escalation study,” The Lancet Haematology, vol. 2, no. 3, pp. e108–e117, 2015.
- I. M. Ariel, “Treatment of inoperable primary pancreatic and liver cancer by the intra-arterial administration of radioactive isotopes (Y90 radiating microspheres),” Annals of Surgery, vol. 162, no. 2, pp. 267–278, 1965.
- R. Salem, A. C. Gordon, S. Mouli et al., “Y90 radioembolization significantly prolongs time to progression compared with chemoembolization in patients with hepatocellular carcinoma,” Gastroenterology, vol. 151, no. 6, pp. 1155–1163.e2, 2016.
- A. Saini, A. Wallace, S. Alzubaidi et al., “History and evolution of Yttrium-90 radioembolization for hepatocellular carcinoma,” Journal of Clinical Medicine, vol. 8, no. 1, p. 55, 2019.
- S. E. Woodfield, Y. Shi, R. H. Patel et al., “A novel cell line based orthotopic xenograft mouse model that recapitulates human hepatoblastoma,” Scientific Reports, vol. 7, no. 1, Article ID 17751, 2017.
- T. Poeschinger, A. Renner, T. Weber, and W. Scheuer, “Bioluminescence imaging correlates with tumor serum marker, organ weights, histology, and human DNA levels during treatment of orthotopic tumor xenografts with antibodies,” Molecular Imaging and Biology, vol. 15, no. 1, pp. 28–39, 2013.
- E. S. Bialecki and A. M. Di Bisceglie, “Diagnosis of hepatocellular carcinoma,” HPB, vol. 7, no. 1, pp. 26–34, 2005.
- P. J. Johnson, R. Williams, H. Thomas, S. Sherlock, and I. M. Murray-Lyon, “Induction of remission in hepatocellular carcinoma with doxorubicin,” The Lancet, vol. 311, no. 8072, pp. 1006–1009, 1978.
- T. Ishiguro, M. Sugimoto, Y. Kinoshita et al., “Anti-glypican 3 antibody as a potential antitumor agent for human liver cancer,” Cancer Research, vol. 68, pp. 9832–9838, 2008.
- A. X. Zhu, P. J. Gold, A. B. El-Khoueiry et al., “First-in-man phase I study of GC33, a novel recombinant humanized antibody against glypican-3, in patients with advanced hepatocellular carcinoma,” Clinical Cancer Research, vol. 19, no. 4, pp. 920–928, 2013.
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