We would like to acknowledge the veterinary staff at the University of Illinois - Chicago&#39;s Biological Resources Laboratory.

The following protocol follows all requirements and guidelines mandated by the University of Illinois - Chicago. It was reviewed and approved by the local Institutional Animal Care and Use Committee prior to execution.
1. VX2 Hind Limb Tumor Development
<ol>
	<li>Procure the VX2 tumor cell line from the National Cancer Institute Division of Cancer Treatment Diagnosis and Treatment Tumor/Cell Line Repository. 
	Note: At this time, the order catalog can be found at the following link: https://dtp.cancer.gov/repositories/.</li>
	<li>To prepare the cell suspension for injection, place the frozen VX2 sample and methylcellulose medium in lukewarm water until they have thawed.
	<ol>
		<li>Aspirate 0.5&#8210;1 mL of the thawed cell suspension and an equal volume of thawed methylcellulose medium into a 5-mL syringe. 
		Note: It may help to use a 21 or 22 G needle to aspirate the cell suspension and a larger gauge needle to aspirate the methylcellulose medium. Place the syringes on ice.</li>
	</ol>
	</li>
	<li>Prepare the hind limb tumor donor rabbit for inoculation of cell suspension, starting with sedation using 1 mg/kg acepromazine and 0.02 mg/kg buprenorphine given intramuscularly. Shave the inoculation site (hind limb) with clippers and clean the shaved are with an alcohol- or iodine-based agent. 
	Note: Meloxicam can be given at a dose of 0.2 mg/kg subcutaneously for analgesia. Rabbit fur is difficult to shave. It is recommended that the researcher perform multiple passes, first focusing on clearing a bulk of the fur and then pressing the clippers against the skin and going against the grain.</li>
	<li>Attach a 16 G needle to the 5-mL syringe containing the cell suspension and inject 1 mL of the suspension into the belly of the hind limb muscle of the donor rabbit, roughly 1 cm deep. Be sure to guard the sciatic nerve running within a palpable groove along the femur. 
	Note: Fresh VX2 successfully inoculates 88% of subjects while frozen and thawed VX2 is only successful 33% of the time19. 
	CAUTION: The VX2 tumor will grow quickly. Side effects that may be noted as the tumor progresses are: increased respiratory rate, lethargy, decreased alertness, and/or behavioral changes (e.g., unusual aggressiveness). Consequently, recommendations are to monitor the animals closely and to plan for tumor harvest within two weeks after inoculation.</li>
</ol>
2. VX2 Hind Limb Tumor Growth and Harvesting
Note: Assuming successful inoculation, there should be a palpable (3&#8210;4 cm) tumor nodule at the injection site within 2 weeks. Usually, this nodule will be palpable around 1 week; however, it is better to let the tumor grow to allow for sufficient tissue collection. Typically, this nodule will be firm, indurated, and elevated above the level of the muscle. If
<ol>
	<li>Palpate the inoculated area at 2 weeks from inoculation. If no tumor growth is detected at 2 weeks, perform step 1 again. See Figure 1. 
	Note: The presence of tumor can also be assessed via ultrasound. While there have been no studies to assess the difference in tumor growth metrics when propagated from frozen stock as compared to fresh stock, it has been our experience that the frozen stock tumor grows slightly slower and will be detectable after its fresh stock counter-part. Regardless, either method should yield a harvestable tumor by 2 weeks.</li>
	<li>Prepare the hind limb tumor donor for tumor harvest. Anesthetize the rabbit with 45 mg/kg ketamine and 5 mg/kg xylazine. Euthanize with an intravenous (IV) dose of sodium pentobarbital exceeding 390 mg/kg.</li>
	<li>Once the rabbit has been euthanized, begin harvesting the tumor by removing the cutaneous and subcutaneous tissue overlying the tumor nodule using a scalpel with whichever size blade the researcher sees fit. See Figure 2.</li>
	<li>Once the tumor nodule has been identified within the hind limb muscle, remove the tumor en bloc using wide curvilinear margins. For this, cut the tendinous attachment points at the proximal and distal ends of the of the muscle and then trace the scalpel blade along the underlying bone. Bisect the explanted specimen exposing the tumor capsule and necrotic core. See Figure 3. 
	Note: The VX2 tumor has a highly necrotic core. Be sure to use proper eye protection and other personal protective equipment when harvesting the tumor, since any damage to the tumor capsule can result in high pressure ejection of necrotic debris.</li>
	<li>Gently scrape the necrotic core with a blunt object (e.g. forceps, hemostats) to clean the tumor. This should allow for better visualization of the tumor capsule and the transition point between capsule and surrounding muscle. See Figure 4.</li>
	<li>From this sample, harvest several pieces of tumor approximately 1&#8210;2 mm3 and immediately store them in a cup containing room temperature sterile saline. 
	Note: These tumor samples will be used for subsequent intrahepatic implantation.</li>
	<li>Place the remaining tumor in a sterile Petri dish and bathe it with Dulbecco&#39;s Modified Eagle&#39;s Medium (DMEM). If this specimen is kept cold on ice, it can be preserved for handling up to 2&#8210;3 h later.</li>
</ol>
3. Liver Tumor Implantation via Laparotomy
<ol>
	<li>Prepare the recipient rabbit for laparotomy. Anesthetize the recipient rabbit using 45 mg/kg ketamine and 5 mg/kg xylazine for induction followed by intubation and maintenance with 1%--3% isoflurane as needed. When the rabbit is anesthetized, shave the surgical site using hair clippers. Clean the incision area&#160;using triplicate wash with betadine scrub, 70% ethanol solution, and betadine solution, and drape the abdomen in a sterile surgical fashion.&#160;</li>
	<li>Using a #15-blade, initiate the laparotomy by making a small downward vertical midline incision through the rabbit&#8217;s skin starting from the xiphoid process. This should be easily palpated and tends to be roughly the size of an American penny. See Figure 5.</li>
	<li>Reflect the skin and identify the linea alba. This should be a reflective white band of tissue traveling inferiorly in the midline. Use blunt dissection to traverse the linea alba and expose the peritoneum. See Figure 6. 
	Note: The peritoneum is easily identified since it will be directly overlying the bowel, which can be seen moving with respiration. 
	CAUTION: The peritoneum tends to be adherent to the underlying bowel due to surface tension. Using blunt trauma to dissect the linea alba helps to dissipate the risk of perforating the underlying bowel.</li>
	<li>Once the peritoneum is exposed, carefully dissect through it to enter the peritoneal cavity. The liver can now be identified. To better navigate the abdominal space, extend the midline incision 1&#8210;2 cm inferiorly through the skin, muscle, and peritoneum. 
	Note: Extending the midline incision can be easily and safely done by carefully inserting a curved hemostat into the peritoneal space with the curved tip facing superficially towards the peritoneum. Then open the hemostat slightly and use a blade to cute the tissue between the two arms of the hemostat.</li>
	<li>Identify the left lobe of the liver in order to select a site for tumor implantation. The left lobe is infero-lateral to the medial lobe which sits in the midline.</li>
	<li>Before attempting to draw the liver out of the peritoneal space, place a dry piece of gauze at the inferior aspect of the incision. 
	Note: The gauze will provide an adherent surface to lay the liver on to prevent it from retracting back into the abdomen.</li>
	<li>Using either atraumatic forceps or a piece of wet gauze over the fingers, carefully draw the left lobe of the liver out of the abdomen through the incision and lay it down on the dry gauze placed earlier. See Figure 7. 
	CAUTION: The liver capsule is sensitive and can easily rupture. It is critical to be gentle when handling this organ to prevent capsular bleed, liver bruising, and/or eventual hemoperitoneum. 
	Note: Usually, the liver will declare itself visually upon entering the peritoneal space; however, if the rabbit&#8217;s stomach is distended, the liver can be pushed cranially out of sight. If this is the case, gently lift the abdominal wall using a blunt probe. In this scenario, the liver tends to adhere to the ventral aspect of the diaphragm due to surface tension so carefully separate the liver using a blunt probe and it should detach. Then use atraumatic forceps to draw the liver out.</li>
	<li>At this point, prepare the tumor tissue for implantation and place a piece of wet gauze over the liver to protect it.</li>
	<li>Select a 1&#8210;2 mm3 piece of tumor tissue that was generated during step 2.6 for implantation into the liver. See Figure 8.</li>
	<li>Using a #11-blade, puncture the liver tissue at a 45&#176; angle making a 0.5 cm deep pocket, taking care not to penetrate the dorsal aspect of the liver capsule. Leave the blade in place after making the puncture. See Figure 9.</li>
	<li>Gently lift the blade in a ventral direction to create a small pocket in the liver bed. Take the tumor piece using forceps, place the tumor piece in this pocket and then remove the blade. 
	Note: The blade can be removed prior to inserting the tumor piece, however, the liver will bleed and this can obscure the puncture site making it difficult to identify. 
	CAUTION: Be sure to minimize contact of the tumor with any other structures to prevent unintentional tumor seeding. This can also be avoided by setting aside any tools used to assist with implantation afterwards.</li>
	<li>At this point, place a piece of hemostatic agent, such as gel foam, over the tumor pocket to promote hemostasis and to prevent ejection of the tumor piece.</li>
	<li>Return the liver to the abdomen, once hemostasis is confirmed.</li>
	<li>Close the abdominal wall with 3-0 polydioxanone suture on a taper needle using a simple continuous stitch and close the skin with 4-0 polyglactin 910 sutures on a cutting needle using continuous subcuticular stitch. 
	CAUTION: When closing the abdominal wall, take care not to damage the omentum or other bowel structures in a suture throw. 
	Note: While this tumor will take at least 2 weeks to be definitively radiographically identifiable, it reaches a size of 1.5&#8210;2 cm diameter at 3 weeks of growth. Be careful not to allow the hepatic tumor to grow past 3.5&#8210;4 weeks since the tumor will form an exophytic mass and aggressively spread locally.</li>
</ol>
4. VX2 Tumor Suspension Preparation
<ol>
	<li>Place a 40 &#181;m strainer into the mouth of a 50-mL conical propylene tube. Using the tumor from step 2.7, use a #15-blade to scrape the tumor surface to collect viable tumor and place these scrapings into the strainer.</li>
	<li>Wash the viable tumor scrapings through a strainer using DMEM and then centrifuge the propylene tube at 1600 rpm for 8 min.</li>
	<li>After the centrifuge is complete, remove the supernatant and discard it. Then add methylcellulose to the remaining cell block at a 1:1 volumetric ratio.</li>
	<li>Inject this suspension into a hind limb donor rabbit following steps 1.3&#8210;1.4. Place the remaining suspension into 1 mL aliquots in cryogenic tubes and freeze them in liquid nitrogen for later use.</li>
</ol>
5. Angiographic Utilization of the VX2 Liver Tumor
<ol>
	<li>Prepare the rabbit as described in step 3.1.</li>
	<li>Palpate the femoral groove in the groin. When the groove has been identified, make a 2&#8210;3 cm linear incision along the groove. See Figure 10.</li>
	<li>Using blunt dissection, locate and isolate the femoral bundle containing the femoral vein, artery, and nerve. See Figure 11.</li>
	<li>Again, use blunt dissection to separate the femoral artery from the rest of the structures in the bundle and isolate the artery atop a scalpel handle. See Figure 12.</li>
	<li>With a 3-French introducer kit, utilize the Seldinger technique to gain access with a needle. Insert a guidewire and remove the needle to advance the 3-French sheath into the vessel. See Figure 13. 
	CAUTION: Avoid using excessive force in advancing the 3-French sheath, as this can result in transection of the femoral artery.</li>
	<li>Under fluoroscopic guidance and using a catheter, guidewire, and iohexol contrast agent, select for the celiac trunk &#8212; typically located at the T12 level &#8212; and then advance the catheter into the left hepatic artery via the common hepatic and proper hepatic.</li>
	<li>At this point, administer the agent of choice through the catheter. Once the agent is administered, remove the catheter.</li>
	<li>Using 3-0 silk suture, ligate the femoral artery proximally and distally to the insertion point of the sheath. Be sure to tighten the knot proximal to the sheath as it is withdrawn to prevent bleeding.</li>
	<li>Close the groin incision with 4-0 polyglactin 910 sutures on a cutting needle using a subcuticular stitch.</li>
	<li>Maintain standard post-operative care and monitor animal recovery. Perform euthanasia and necropsy as needed using standard techniques.</li>
</ol>

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The work depicted in this report was supported by a research grant from Guerbet LLC.

The first critical step in the VX2 tumor methodology is successful propagation of a tumor in the hind limb of a donor rabbit. Refer to the first paragraph in the &#34;Representative Results&#34; section for more information regarding this step.
The next critical step is ensuring that the viable tumor capsule is properly identified. Not only will this be necessary for tumor suspension preparation, but it is also important for selecting and generating tumor pieces for hepatic implantation. The d...

The rabbit VX2 tumor model has played a role in experimental oncology since its development in 19351,2. This tumor is a virus-induced anaplastic squamous cell carcinoma characterized by hypervascularity, rapid growth, and easy propagation in skeletal muscle3,4. While the rabbit VX2 tumor model has been used to investigate a multitude of cancers5,6,7,8; the focus of this paper is liver cancer9.
The purpose of the method described is to present a model for primary liver cancer, or hepatocellular carcinoma (HCC), that can be used by Interventional Radiologists for translational research. It can be used for pharmacokinetic studies, therapeutic investigations, and ablative method testing10,11,12,13,14,15.
The method detailed herein yields multiple advantages over other models within the same sphere such as rodent models like rats, mice, and woodchucks, or larger models like primates16. One of the primary benefits is the rapid and reliable tumor growth which allows researchers to establish an active tumor line within a month of first hind limb propagation17. Additionally, this tumor has straightforward sonographic visibility and a hypervascular periphery which allows for both transarterial locoregional treatments and ablative therapies. Finally, and most importantly, the size of the rabbit vasculature permits feasible and technically easy utilization of vascular instrumentation18.

<table><tbody><tr><td>MethoCult (Methycellulose)</td><td>Stemcell Technologies</td><td>M3134</td><td></td></tr><tr><td>VX2 Cell Line</td><td>NCI</td><td>VX-2</td><td></td></tr><tr><td>5 mL Syringe</td><td>BD</td><td>309646</td><td></td></tr><tr><td>16 G Needle</td><td>BD</td><td>305197</td><td></td></tr><tr><td>22 G Needle</td><td>BD</td><td>305155</td><td></td></tr><tr><td>Hair Clippers</td><td>Wahl</td><td>41870-0438</td><td></td></tr><tr><td>Foam Insulated Box</td><td>Mr. Box Online</td><td>10 x 10 x 4</td><td></td></tr><tr><td>Acepromazine</td><td>Henry Schein</td><td>003845</td><td></td></tr><tr><td>Buprenorphine</td><td>Par</td><td>42023-179-05</td><td></td></tr><tr><td>Meloxicam</td><td>Henry Schein</td><td>049755</td><td></td></tr><tr><td>Alcohol Pads</td><td>Covidien</td><td>5033</td><td></td></tr><tr><td>Ketamine</td><td>Henry Schein</td><td>056344</td><td></td></tr><tr><td>Xylazine</td><td>Akorn</td><td>59399-110-20</td><td></td></tr><tr><td>Pentobarbital (Fatal-Plus)</td><td>Vortech</td><td>9373</td><td></td></tr><tr><td>Sterile Petri Dish</td><td>Thermo Fisher</td><td>172931</td><td></td></tr><tr><td>DMEM</td><td>Gibco</td><td>11965092</td><td></td></tr><tr><td>Saline</td><td>Baxter</td><td>2F7124</td><td></td></tr><tr><td>15-Blade</td><td>Steris</td><td>02-050-015</td><td></td></tr><tr><td>Scalpel Handle x 2</td><td>Steris</td><td>22-2381</td><td></td></tr><tr><td>Curved Hemostat</td><td>WPI</td><td>501288</td><td></td></tr><tr><td>Atraumatic Forceps</td><td>Sklar</td><td>52-5077</td><td></td></tr><tr><td>Gauze</td><td>Medline</td><td>NON21430LF</td><td></td></tr><tr><td>11-Blade</td><td>Steris</td><td>02-050-011</td><td></td></tr><tr><td>Surgicel</td><td>Ethicon</td><td>1951</td><td></td></tr><tr><td>3-0 PDS / Taper</td><td>Ethicon</td><td>Z305H</td><td></td></tr><tr><td>4 - 0 Vicryl / Cutting</td><td>Ethicon</td><td>J392H</td><td></td></tr><tr><td>40 &amp;mu;m strainer</td><td>BD</td><td>352340</td><td></td></tr><tr><td>50 mL conical tube</td><td>Thermo Fisher</td><td>339652</td><td></td></tr><tr><td>plastic pipette</td><td>Thomas Scientific</td><td>HS206371B</td><td></td></tr><tr><td>Centrifuge</td><td>Sorvall</td><td>75004240</td><td></td></tr><tr><td>1.40 mL Tubes (Internal Thread)</td><td>Micronic</td><td>MP32131-Z20</td><td></td></tr><tr><td>3-F VSI Micro-HV Introducer Kit</td><td>Vascular Solutions</td><td>Custom Order (P15180391)</td><td></td></tr><tr><td>.018 45&amp;deg; angle glidewire</td><td>Terumo</td><td>RG*GA1818SA</td><td></td></tr><tr><td>Direxion bern-shape microcatheter</td><td>Boston Scientific</td><td>M001195230</td><td></td></tr><tr><td>Omnipaque</td><td>GE</td><td>Y510</td><td></td></tr></tbody></table>

development and angiographic use of the rabbit vx2 model for liver cancer

The rabbit VX2 tumor is an animal model commonly utilized for translational research regarding hepatocellular carcinoma (HCC) in the field of Interventional Radiology. This model employs an anaplastic squamous cell carcinoma that is easily and reliably propagated in the skeletal muscle of donor rabbits for eventual harvest and allograft implantation into the liver of na&#239;ve recipients. This tumor graft rapidly grows within the liver of recipient rabbits into an angiographically identifiable tumor characterized by a necrotic core surrounded by a viable hypervascular capsule. The physical size of the rabbit anatomy is sufficient to facilitate vascular instrumentation allowing for the application and testing of various interventional techniques. Despite these benefits, there exists a paucity of technical resources to act as a concrete reference for researchers working with the model. Herein, we present a comprehensive visual outline for the technical aspects of development, growth, propagation, and angiographic utilization of the rabbit VX2 tumor model for use by novice and experienced researchers alike.

When looking at Figure 1, it is clear that the quadricep of the rabbit is enlarged. Additionally, multiple small discrete nodules, typically correlating with tumor growth through the fascia, are visible. Upon palpation, the injected limb should appear than the non-injected limb. If a researcher requires more definitive assurance of tumor presence, ultrasound imaging can be used to identify the tumor embedded in the muscle. If a tumor is not detected, the hind...

Watch this Scientific Journal Video about Development and Angiographic Use of the Rabbit VX2 Model for Liver Cancer at JoVE.com

Development and Angiographic Use of the Rabbit VX2 Model for Liver Cancer

The goal of this article is to provide a primer for the development and use of the VX2 carcinoma rabbit model for liver cancer.

The rabbit VX2 tumor is an animal model commonly utilized for translational research regarding hepatocellular carcinoma (HCC) in the field of ...

development-angiographic-use-rabbit-vx2-model-for-liver

Universidad de Cartagena UDEC

Research

JoVE Journal

Cancer Research

11.3K Views.  University of Illinois. The goal of this article is to provide a primer for the development and use of the VX2 carcinoma rabbit model for liver cancer.

Video: Development and Angiographic Use of the Rabbit VX2 Model for Liver Cancer

Advanced Animal Model of Colorectal Metastasis in Liver: Imaging Techniques and Properties of Metastatic Clones

Patients with a limited number of hepatic metastases and slow rates of progression can be successfully treated with local treatment approaches1,2. However, little is known about the heterogeneity of liver metastases, and animal models capable of evaluating the development of individual metastatic colonies are needed. Here, we present an advanced model of hepatic metastases that provides the ability to quantitatively visualize the development of individual tumor clones in the liver and estimate their growth kinetics and colonization efficiency. We generated a panel of monoclonal derivatives of HCT116 human colorectal cancer cells stably labeled with luciferase and tdTomato and possessing different growth properties. With a splenic injection followed by a splenectomy, the majority of these clones are able to generate hepatic metastases, but with different frequencies of colonization and varying growth rates. Using the In Vivo&#160;Imaging System (IVIS), it is possible to visualize and quantify metastasis development with in vivo luminescent and ex vivo fluorescent imaging. In addition, Diffuse Luminescent Imaging Tomography (DLIT) provides a 3D distribution of liver metastases in vivo. Ex vivo fluorescent imaging of harvested livers provides quantitative measurements of individual hepatic metastatic colonies, allowing for the evaluation of the frequency of liver colonization and the growth kinetics of metastases. Since the model is similar to clinically observed liver metastases, it can serve as a modality for detecting genes associated with liver metastasis and for testing potential ablative or adjuvant treatments for liver metastatic disease.

The ability of metastatic clones to colonize distant sites depends on their proliferation capacity and/or their ability to survive in the host microenvironment without significant proliferation. Here, we present an animal model that allows quantitative visualization of both types of liver colonization by metastatic clones.

Patients with a limited number of hepatic metastases and slow rates of progression can be successfully treated with local treatment approaches1,2. ...

Microsurgical Venous Pouch Arterial-Bifurcation Aneurysms in the Rabbit Model: Technical Aspects

For ruptured human cerebral aneurysms endovascular embolization has become an equivalent alternative to aneurysm clipping.1 However, large clinical trials have shown disappointing long-term results with unacceptable high rates of aneurysm recanalization and delayed aneurysm rupture.2 To overcome these problems, animal experimental studies are crucial for the development of better endovascular devices.3-5
Several animal models in rats, rabbits, canines and swine are available.6-8 Comparisons of the different animal models showed the superiority of the rabbit model with regard to hemodynamics and comparability of the coagulation system and cost-effectiveness.9-11 
The venous pouch arterial bifurcation model in rabbits is formed by a venous pouch sutured into an artificially created true bifurcation of both common carotid arteries (CCA). The main advantage of this model are true bifurcational hemodynamics.12 The major drawbacks are the sofar high microsurgical technical demands and high morbidity and mortality rates of up to 50%.13 These limitations have resulted in less frequent use of this aneurysm model in the recent years. These shortcomings could be overcome with improved surgical procedures and modified peri- and postoperative analgetic management and anticoagulation.14-16 Our techniques reported in this paper demonstrate this optimized technique for microsurgical creation of arterial bifurcation aneurysms.

An optimized technique for the microsurgical creation of arterial bifurcation aneurysms mimicking bifurcation human cerebral aneurysms is described. A venous pouch is sutured into an artificially created true bifurcation of both common carotid arteries. Facilitated microsurgical techniques and aggressive postoperative anticoagulation and analgesia lead to minimized morbidity rates and high aneurysm patency rates.

For ruptured human cerebral aneurysms endovascular embolization has become an equivalent alternative to aneurysm clipping.1 However, large clinical trials ...

Medicine

An Orthotopic Endometrial Cancer Model with Retroperitoneal Lymphadenopathy Made From In Vivo Propagated and Cultured VX2 Cells

Endometrial cancer is the most common gynecologic malignancy in North America and the incidence is rising worldwide. Treatment consists of surgery with or without adjuvant therapy depending on lymph node involvement as determined by lymphadenectomy. Lymphadenectomy is a morbid procedure, which has not been shown to have a therapeutic benefit in many patients, and thus a new method to diagnose lymph node metastases is required. To test novel imaging agents, a reliable model of endometrial cancer with retroperitoneal lymph node metastases is needed. The VX2 endometrial cancer model has been described frequently in the literature; however, significant variation exists with respect to the method of model establishment. Furthermore, no studies have reported on the use of cultured VX2 cells to create this model as only cells propagated in vivo have been previously used. Herein, we present a standardized surgical method and post-operative monitoring method for the establishment of the VX2 endometrial cancer model and report on the first use of cultured VX2 cells to create this model.

This protocol presents a standardized method to grow VX2 cells in culture and to create an orthotopic VX2 model of endometrial cancer with retroperitoneal lymph node metastases in rabbits. Orthotopic endometrial cancer models are important for the pre-clinical study of novel imaging modalities for the diagnosis of lymph node metastases.

Endometrial cancer is the most common gynecologic malignancy in North America and the incidence is rising worldwide. Treatment consists of surgery with or ...

Portal Vein Injection of Colorectal Cancer Organoids to Study the Liver Metastasis Stroma

Hepatic metastasis of colorectal cancer (CRC) is a leading cause of cancer-related death. Cancer-associated fibroblasts (CAFs), a major component of the tumor microenvironment, play a crucial role in metastatic CRC progression and predict poor patient prognosis. However, there is a lack of satisfactory mouse models to study the crosstalk between metastatic cancer cells and CAFs. Here, we present a method to investigate how liver metastasis progression is regulated by the metastatic niche and possibly could be restrained by stroma-directed therapy. Portal vein injection of CRC organoids generated a desmoplastic reaction, which faithfully recapitulated the fibroblast-rich histology of human CRC liver metastases. This model was tissue-specific with a higher tumor burden in the liver when compared to an intra-splenic injection model, simplifying mouse survival analyses. By injecting luciferase-expressing tumor organoids, tumor growth kinetics could be monitored by in vivo imaging. Moreover, this preclinical model provides a useful platform to assess the efficacy of therapeutics targeting the tumor mesenchyme. We describe methods to examine whether adeno-associated virus-mediated delivery of a tumor-inhibiting stromal gene to hepatocytes could remodel the tumor microenvironment and improve mouse survival. This approach enables the development and assessment of novel therapeutic strategies to inhibit hepatic metastasis of CRC.

Portal vein injection of colorectal cancer (CRC) organoids generates stroma-rich liver metastasis. This mouse model of CRC hepatic metastasis represents a useful tool to study tumor-stroma interactions and develop novel stroma-directed therapeutics such as adeno-associated virus-mediated gene therapies.

Hepatic metastasis of colorectal cancer (CRC) is a leading cause of cancer-related death. Cancer-associated fibroblasts (CAFs), a major component of the ...

Transarterial Administration of Oncolytic Viruses for Locoregional Therapy of Orthotopic HCC in Rats

Hepatocellular carcinoma (HCC) is a disease with limited treatment options and poor prognosis. In recent years, oncolytic virotherapies have proven themselves to be potentially powerful tools to fight malignancy. Due to the unique dual blood supply in the liver, it is possible to apply therapies locally to orthotopic liver tumors, which are predominantly fed by arterial blood flow. We have previously demonstrated that hepatic arterial delivery of oncolytic viruses results in safe and efficient transduction efficiency of multifocal HCC lesions, resulting in significant prolongation of survival in immune competent rats. This procedure closely mimics the application of transarterial embolization in patients, which is the standard palliative care provided to many HCC patients. The ability to administer tumor therapies through the hepatic artery in rats allows for a highly sophisticated preclinical model for evaluating novel viral vectors under development. Here we describe the detailed protocol for microdissection of the hepatic artery for infusion of oncolytic virus vectors to treat orthotopic HCC.

Oncolytic virotherapies are under development as novel therapeutics for the treatment of hepatocellular carcinoma (HCC). Here we describe a method for locoregional therapy of HCC via hepatic arterial administration of oncolytic virus.

Hepatocellular carcinoma (HCC) is a disease with limited treatment options and poor prognosis.  In recent years, oncolytic virotherapies have proven ...

Rat Model of the Associating Liver Partition and Portal Vein Ligation for Staged Hepatectomy (ALPPS) Procedure

Recent clinical data support an aggressive surgical approach to both primary and metastatic liver tumors. For some indications, like colorectal liver metastases, the amount of liver tissue left behind after liver resection has become the main limiting factor of resectability of large or multiple liver tumors. A minimal amount of functional tissue is required to avoid the severe complication of post-hepatectomy liver failure, which has high morbidity and mortality. Inducing liver growth of the prospective remnant prior to resection has become more established in liver surgery, either in the form of portal vein embolization by interventional radiologists or in the form of portal vein ligation several weeks prior to resection. Recently, it was shown that liver regeneration is more extensive and rapid, when the parenchymal transection is added to portal vein ligation in a first stage and then, after only one week of waiting, resection performed in a second stage (Associating Liver Partition and Portal vein ligation for Staged hepatectomy = ALPPS). ALPPS has rapidly become popular across the world, but has been criticized for its high perioperative mortality. The mechanism of accelerated and extensive growth induced by this procedure has not been well understood. Animal models have been developed to explore both the physiological and molecular mechanisms of accelerated liver regeneration in ALPPS. This protocol presents a rat model that allows mechanistic exploration of accelerated regeneration.

Rat Model of the Associating Liver Partition and Portal Vein Ligation for Staged Hepatectomy ALPPS Procedure

Inducing rapid liver hypertrophy using Associating Liver Partition and Portal vein ligation for a Staged hepatectomy (ALPPS) has been proposed for resection of borderline resectable liver tumors. This model may elucidate mechanisms involved in rapid hypertrophy and allows testing of drugs that promote or block the acceleration of regeneration.

Recent clinical data support an aggressive surgical approach to both primary and metastatic liver tumors. For some indications, like colorectal liver ...

Liver Transplantation in Mouse and Analyzing Allograft Patency

Successful Orthotopic Liver Transplantation in Mice Utilizing Microcomputed Tomography Angiography

Microcomputed tomography (microCT) angiography is an invaluable resource to researchers. New advances in this technology have allowed for high-quality images to be obtained of micro-vasculature and are high-fidelity tools in the field of organ transplantation. In this model of orthotopic liver transplantation (OLT) in mice, microCT affords the opportunity to evaluate allograft anastomosis in real time and has the added benefit of not having to sacrifice study animals. The choice of contrast, as well as image acquisition settings, create a high-definition image, which gives researchers invaluable information. This allows for evaluation of the technical aspects of the procedure as well as potentially evaluating different therapeutics over an extended duration of time. In this protocol, we detail an OLT model in mice in a stepwise fashion and finally describe a microCT protocol that can give high-quality images, which aid researchers in in-depth analysis of solid organ transplantation. We provide a step-by-step guide for liver transplantation in a mouse, as well as briefly discuss a protocol for evaluating the patency of the graft through microCT angiography.

Author Spotlight: Enhancing Transplantation Research Through MicroCT Angiography in Murine Models 

In this protocol, we discuss the implementation of a model of successful orthotopic liver transplantation (OLT) in mice. Additionally, adjuvants to further analyze allograft patency after successful OLT in a mouse are discussed as well, specifically utilizing microcomputed tomography (microCT) scans.

Microcomputed tomography (microCT) angiography is an invaluable resource to researchers. New advances in this technology have allowed for high-quality ...

Modeling Metastatic Endometrial Cancer  Model: A Technique to Generate Endometrial Cancer with Lymph Node Metastasis in Rabbit Models

Source: Lauren Philp et al. <a href="https://jove.unicartagenaproxy.elogim.com/t/59340">An Orthotopic Endometrial Cancer Model with Retroperitoneal Lymphadenopathy Made From In Vivo Propagated and Cultured VX2 Cells.</a> J. Vis. Exp. (2019)
This video demonstrates the generation of a rabbit model of endometrial cancer by injecting a highly metastatic VX2 cell suspension into the sutured uterine horns of the rabbit. This leads to generation of primary endometrial cancer with retroperitoneal lymph node metastases.

Modelowanie przerzutowego modelu raka endometrium: technika generowania raka endometrium z przerzutami do węzłów chłonnych w modelach królików

Source: Lauren Philp et al. An Orthotopic Endometrial Cancer Model with Retroperitoneal Lymphadenopathy Made From In Vivo Propagated and Cultured VX2 ...

JoVE Encyclopedia of Experiments

Gynecologic Cancer

Animal model studies

Generating Rabbit Liver Carcinoma Model: A Surgical Procedure to Implant Tumor Tissue in Left Lobe of Liver for Induction of Hepatocellular Carcinoma

Source: Khabbaz, R. C. et al. <a href="https://jove.unicartagenaproxy.elogim.com/v/58600">Development and Angiographic Use of the Rabbit VX2 Model for Liver Cancer.</a> J. Vis. Exp. (2019)
In this video, we demonstrate the surgical implantation of tumor tissue into a rabbit liver to induce hepatocellular carcinoma. The procedure helps establish a reliable animal model to study tumor behavior and development of locoregional treatments targeting cancers of the liver.

Generowanie modelu raka wątroby królika: zabieg chirurgiczny polegający na wszczepieniu tkanki nowotworowej w lewym płacie wątroby w celu indukcji raka wątrobowokomórkowego

Source: Khabbaz, R. C. et al. Development and Angiographic Use of the Rabbit VX2 Model for Liver Cancer. J. Vis. Exp. (2019)
In this video, we demonstrate ...

Biology

Large Animal Models

Leporine

Hepatic Angiography: A Procedure to Visualize Liver Tumor Vessels in a Rabbit Model

Source: Khabbaz, R. C., et al. <a href="https://jove.unicartagenaproxy.elogim.com/v/58600">Development and Angiographic Use of the Rabbit VX2 Model for Liver Cancer.</a> J. Vis. Exp. (2019).
In this video, we demonstrate a step-by-step procedure to perform hepatic angiography using a fluoroscope that enables the real-time visualization of blood vessels associated with a liver tumor in a rabbit model.