Implementation of an orthotopic model of renal cell carcinoma in immunocompetent mice affords the investigator a clinically-relevant system defined by the presence of a primary renal tumor and lung metastases in the same animal. This system can be used to preclinically test a variety of treatments in vivo.
Renal cell carcinoma (RCC) affects > 60,000 people in the United States annually, and ~ 30% of RCC patients have multiple metastases at the time of diagnosis. Metastatic RCC (mRCC) is incurable, with a median survival time of only 18 months. Immune-based interventions (e.g., interferon (IFN) and interleukin (IL)-2) induce durable responses in a fraction of mRCC patients, and multikinase inhibitors (e.g., sunitinib or sorafenib) or anti-VEGF receptor monoclonal antibodies (mAb) are largely palliative, as complete remissions are rare. Such shortcomings in current therapies for mRCC patients provide the rationale for the development of novel treatment protocols. A key component in the preclinical testing of new therapies for mRCC is a suitable animal model. Beneficial features that recapitulate the human condition include a primary renal tumor, renal tumor metastases, and an intact immune system to investigate any therapy-driven immune effector responses and the formation of tumor-induced immunosuppressive factors. This report describes an orthotopic mRCC mouse model that has all of these features. We describe an intrarenal implantation technique using the mouse renal adenocarcinoma cell line Renca, followed by the assessment of tumor growth in the kidney (primary site) and lungs (metastatic site).
Renal cell carcinoma (RCC) accounts for the majority of malignant kidney neoplasms and roughly 3% of all adult malignancies worldwide1,2. Due to lack of symptoms, misdiagnosis, and insufficient screening tools for RCC, almost 30% of patients will present with metastatic RCC (mRCC) at the time of diagnosis, with an additional 20-30% of patients progressing to a metastatic stage2. These cases result in ~13,500 deaths annually1,3. Though earlier detection and treatment of primary RCC has improved, the rate of RCC-related death continues to increase, suggesting that metastatic disease is largely responsible for mortality3. Therapy development for RCC has progressed over the last decade with the discovery and implementation of targeted therapies and immunotherapies. Unfortunately, progression-free survival and overall survival of advanced cases are still well under 2 years for the majority of patients4,5,6. These statistics warrant the need for further research into the identification and development of efficacious treatments for RCC. To adequately advance therapeutic interventions for mRCC, translationally-relevant pre-clinical models of the disease are first needed.
Development of a relevant and consistent model to recapitulate the human condition of advanced RCC should address several key questions: 1) Is the model anatomically relevant; 2) Does the tumor progress similarly to the human pathology; 3) Do metastases arise from the primary tumor; and 4) Can primary and metastatic tumor progression be monitored over time? Depending on the type of treatment being investigated, mouse RCC tumor cell lines, human RCC tumor cell lines, and human RCC patient-derived xenografts may be used in immunocompetent or immunodeficient mice. A host with an intact and functional immune system is required for those studies evaluating some aspect of immunotherapy, necessitating the use of the well-described Renca cell line derived from a spontaneous renal adenocarcinoma of Balb/c mice7. Most studies inject Renca cells subcutaneously (s.c.), which forms an easy-to-measure local tumor, or intravenously (i.v.) into Balb/c mice to produce experimental lung "metastases"8,9,10,11,12. Use of an s.c.-implanted Renca tumor to model human RCC has a number of limitations, including inaccurate innervation of vasculature13, differences in microenvironment14,15, and a lack of organ/tumor cellular communication13,16. Additionally, many s.c. tumors (especially Renca) do not metastasize to distal organs, inhibiting the study of an event that is a common clinical characteristic17. To study mRCC, Renca cells can be injected i.v. to establish tumor burden in the lungs-the primary location of metastases in RCC patients. The i.v. injection method of initiating metastatic tumors, however, does not allow the investigation of how, when, or why the cells have migrated from the primary organ (i.e., the kidney) to the distant site. A model with both primary and metastatic disease evident in the same animal is crucial to study the progression and treatment of advanced disease, especially considering that metastases are typically the cause of mortality in these patients.
Our lab has developed a murine model of mRCC that incorporates all of the features outlined above. To establish primary, orthotopic tumors, Renca cells are implanted directly into the kidney of the animal through the translucent peritoneum. A small incision in the left flank allows for visualization of the spleen (as a landmark) and the left kidney. Using a small-gauge needle, Renca tumor cells are injected directly into the kidney through the peritoneum for orthotopic implantation. Compared to other methods of implanting Renca cells below the kidney capsule18, this method of implantation allows for a higher throughput, as it is fairly non-invasive, does not require suturing, is of a low pain class, and is time-efficient when practiced.
This well-characterized model results in reproducible primary tumor burden (~ 99% take rate) in the injected kidney as well as metastatic tumor load in the lungs. The significant advantages of this model include its syngeneic nature, allowing for immunotherapy investigations; its spontaneous metastases, to study advanced disease; and its orthotopic implantation, to model the anatomical impact on disease progression and treatment. Therapies aimed at targeting RCC would greatly benefit from the utilization of this model during preclinical development.
The following protocol describes an experimental procedure for inducing and monitoring the growth of experimental orthotopic renal tumors and any potential spontaneous metastases. All of the following procedures are done in accordance with institutional policies and approved procedures regarding the humane use of experimental animals.
1. Maintenance of Cell Lines
2. Surgical Area Preparation
3. Animal Preparation
4. Bioluminescent Imaging
5. Organ Harvest
The successful implantation of Renca cells will result in tumor development in the kidney and metastasis to the lungs of the mice. After the excision of the tumor-bearing and the contralateral kidneys, wet tissue weights (g) were measured to demonstrate the tumor burden based on increased weight (Figure 1). Renca tumors can be identified by immunohistochemistry through cytokeratin 8 and 18 staining (Figure 2). For longitudinal studies, a luciferase-expressing Renca cell line was implanted. Bioluminescent imaging was performed using an in vivo imaging system (IVIS) to track tumor burden and response to therapy over time (Figure 3A). Metastasis to the lungs was confirmed by bioluminescent imaging (Figure 3B) and India ink lung inflation (Figure 3C).
Figure 1. Orthotopic implantation of Renca tumor cells forms a large renal mass. Renca-GL cells (2 x 105 in 0.1 mL) were injected intrarenally, and the weights of the excised tumor-bearing kidneys and tumor-free contralateral kidneys in grams (+SEM) were determined on day 24. n = 15 tumor-free and tumor-bearing kidneys. Please click here to view a larger version of this figure.
Figure 2. Immunofluorescent microscopic image of tumor-free contralateral and tumor-bearing kidneys. Renca-GL cells (2 x 105 in 0.1 mL) were injected intrarenally, and the tumor-bearing and tumor-free kidneys were harvested on day 12. The kidneys were snap-frozen and processed for immunofluorescence imaging to visualize the location of collagen, cytokeratin 8 and 18, and CD31. 10x images were taken and stitched together to view the entire tumor-bearing kidney. Scale bars = 1 mm. Please click here to view a larger version of this figure.
Figure 3. Orthotopic implantation of Renca tumor cells leads to spontaneous lung metastases. A. Renca-GL cells (2 x 105 in 0.1 mL) were injected intrarenally into Balb/c mice. Bioluminescent images were taken on the indicated days. B. On day 23, the lungs from tumor-free and tumor-bearing mice were excised and bioluminescent images were taken. C. Parallel sets of mice on day 23 had their lungs inflated with India ink to visualize lung tumor nodules. Scale bars = 1 cm. Please click here to view a larger version of this figure.
We present a protocol for an orthotopic RCC mouse model. Implantation of mouse renal adenocarcinoma tumor cells into the mouse kidney provides a clinically-relevant model of mRCC. This model results in a primary tumor within the kidney and distant metastasis in the lungs, both of which are hallmarks of advanced RCC. The description presented herein is specific for the Renca cell line in immunocompetent Balb/c mice. Using this orthotopic model, we have shown that the Renca tumors are responsive to immunotherapy, demonstrating the usefulness of this model for therapeutic testing17,24,25,26,27. The ability to use a syngeneic tumor cell line for implantation provides the advantage of studying tumor progression in an immunologically intact animal. The syngeneic, orthotopic, and clinically-relevant characteristics of this system provide a superior model that allows for the testing of therapies in a relevant pre-clinical model. This cannot be replicated when the tumors are implanted subcutaneously. It is important to mention that such a modeling system is not limited to evaluating anti-tumor immune responses or various immunotherapeutic approaches for treating RCC. It would be feasible to use human tumor cells implanted intrarenally into immunodeficient mice, depending on the type of experimentation being conducted. The availability of established RCC cell lines that can be cultured in vitro improves the reproducibility of this in vivo orthotopic model, as all animals can be implanted with an equal number of tumor cells at the same time. Furthermore, the tumor cells can be manipulated in vitro prior to intrarenal implantation offering the possibility to control how the cells grow and/or respond to environmental signals. One limitation with this (and most) implantable tumor models is that they circumvent the early events responsible for tumor formation, a benefit that is afforded by using a mouse model genetically engineered for the formation of autochthonous tumors.
One drawback of the orthotopic model is the general inability to visualize tumor growth, a feature that is easily monitored for an s.c. tumor by caliper measurement. Current technology using genetically-engineered tumor cells and bioluminescent imaging allows for longitudinal measurements of internal tumors. We have demonstrated the ability to determine primary renal tumor and metastatic burden at various time points based on bioluminescent imaging and/or organ extraction17,24,25. A strength of our model is the availability of the GFP and luciferase-expressing Renca cell line, but the model does not require this feature for success. We have characterized the orthotopic RCC model with both parental Renca and Renca-GL cells. Following implantation of Renca-GL cells, primary tumors can be readily measured by bioluminescent imaging. It can be difficult to monitor metastases in the whole animal, however, as the primary tumor can produce a signal that overwhelms the lower signals that might be emitted from the metastatic site. Excising and imaging the individual organs from the whole animal allows for the visualization and quantification of metastases in those organs. In the Renca orthotopic model, the primary kidney tumors give rise to spontaneous micro-metastases in the lungs of the animals as early as 7 days post-implant, as seen by luminescence in the excised lung tissue17.
While the use of a luciferase-expressing tumor cell line in this system provides the user with the ability to track tumor progression longitudinally in the same animal, it also provides the user with the ability to evaluate the precision of the implantation technique. The mouse kidney is a small anatomical structure, making it possible, especially when using a long needle, to inject the tumor cells through the kidney and directly into the peritoneum. Imaging the mouse within several days of injection determines the extent to which the implantation of the tumor cells is localized to the kidney. Another feature that can complicate the intrarenal injection is the presence of an abundance of visceral fat, which can accumulate as the animal ages. The kidney is easily visible through the peritoneum in a lean mouse, but the kidney can become obscured under lobes of visceral fat that can develop over time.
At the termination of a given experiment, a number of assessments can be used to determine the whole-body tumor burden. Bioluminescent imaging of the excised organs provides an objective measure of tumor burden. The wet weight of primary tumors normalized to the contralateral kidney as an internal control provides a bulk mass measurement. The metastatic burden in the lung can also be determined by inflating the lungs with India ink en bloc to allow for the visualization of white lung tumor nodules using a dissecting microscope. These readouts can establish total-body tumor burden, which can be used as a baseline for investigating the therapeutic efficacy at the pre-clinical stage of drug development. The expression of GFP by the Renca-GL cells also lends itself to flow cytometric analyses of the tumor-bearing tissues. However, caution must be exercised for any flow cytometric assessment of the tumor-bearing kidney, especially when investigating the composition and magnitude of any immunological response generated as a consequence of therapy. Kidneys are highly vascular organs, making it likely that evaluation of the immune response (either pro-tumor or anti-tumor) in the whole tumor-bearing kidneys will include both "tissue- and vasculature-localized" immune cells at the time of organ harvest. To distinguish tissue versus blood immune cells, we use a technique where fluorochrome-labeled anti-CD45.2 monoclonal antibody (mAb) is injected i.v. before euthanasia. The kidneys are then prepared for flow cytometry, which includes ex vivo staining with different fluorochrome-labeled anti-CD45.2 mAb28,29. Dual CD45.2 staining discriminates cells within the vasculature from the tissue at the time of harvest. This simple protocol enables the identification of major leukocyte lineages contained within the vasculature that might otherwise confuse the interpretation of adaptive and innate immune responses in tissues. This protocol also eliminates the need for perfusion, which may have unintended consequences28,29.
There is currently an increased appreciation for and use of immunotherapy to treat cancer. The development of future immunologically-based treatments for mRCC (and other cancers) starts in the laboratory using a clinically- and physiologically-relevant model. The orthotopic RCC model described herein contains a number of key features (e.g., primary renal tumor, distant metastases, tumor-induced immune suppression, and components for longitudinal monitoring of tumor growth) for testing the efficacy of a variety of therapeutic modalities. It is also tempting to speculate that this model could be adapted in the future to evaluate advances in other means of treating RCC, such as surgical and/or focal therapy protocols.
The authors have nothing to disclose.
This work was supported by grants from the National Cancer Institute (R15CA173657 to A.W. and R01CA109446 to T.S.G.), the Simmons Cancer Institute (to A.W.), and the University of Minnestoa Climb 4 Kidney Cancer Foundation (to T.S.G.). We thank Dr. Kristin Anderson for assistance with the immunofluorescence.
Artificial tears ophthalmic ointment | Akorn | NDC 17478-162-35 | |
Vetbond Tissue Adhesive | 3M | CBGBIW011019 | |
Betadine Solution (Povidone-iodine, 5%) | Purdue Products, L.P. | NDC 67618-155-32 | |
0.25% Marcaine (bupivavaine HCL injection) | Hospira | 0409-1587-50 | |
Heating pad | Sunbeam | ||
Syringes | BD | 309659 | |
Gauze | Venture | 908291 | |
Ketamine | Phoenix Pharmaceuticals | NDC 57319-609-02 | |
Xylazine | Akorn | NDC 59399-111 | |
Hank’s Balanced Salts | Sigma-Aldrich | H2387 | |
IVIS | Caliper | ||
D-Luciferin, Potassium Salt | GoldBio | LUCK-1G | |
India Ink | Chartpak Inc | 44201 | |
Scissors | |||
Forceps | |||
Sleeping Beauty (SB) transposon system | Neuromics | SBT0200 | |
Renca | ATCC | CRL-2947 |