Figure 3A was taken from our previous publication12 and was generated in Dr. Jann Sarkaria&#39;s lab at the Mayo Clinic.

The following are a series of step-by-step protocols used for both establishing PDX models by subcutaneous flank implantation and for setting up preclinical studies that enable testing of treatments, which can aid in assessing biological changes and various steps of the metastatic cascade. All the studies and models used 3-8 weeks old female NOG mice. All the tissue samples were collected under informed consent in accordance with a protocol approved by the Institutional Review Board (IRB). All animal experiments were performed in accordance with an Institutional Animal Care and Use Committee (IACUC) approved protocol.
1. Establishment and propagation of PDX models by flank implantation
<ol>
	<li>Establishment of PDX models
	<ol>
		<li>Following surgical resection of the tumor from the patient in the operating room, store the fresh tumor tissues in a suitable solution (such as DMEM) and immediately place it on ice. Use an excess of storage solution (&#62;10 mL) to ensure that the tissue is fully submerged.</li>
		<li>Transfer tissue to tissue culture dish and rinse with 5 mL DPBS. 
		NOTE: This step should be conducted in a biosafety cabinet using aseptic techniques. Precautions should be taken by wearing appropriate personal protective equipment (PPE) to protect against possible human infectious agents.</li>
		<li>Remove necrotic regions from the tumor. 
		NOTE: This can be recognized as a white mushy region toward the center of the tissue.</li>
		<li>Cut the remaining tissue into approximately 2 x 2 x 2 mm pieces.</li>
		<li>Transfer the tissues into a microcentrifuge tube containing the growth factor reduced basement membrane matrix and store them on ice. Ensure that sufficient basement membrane matrix (&#62;200 &#181;L) is used to fully submerge each tissue piece.</li>
		<li>Cryopreserve the remaining tissues that will not be implanted according to protocol described in the step 1.3.</li>
		<li>Anesthetize the animal in an induction chamber with 2-5% isoflurane and oxygen. Once anesthetized, transfer the animal to a nose cone to maintain anesthesia at&#160;1.5-2.5% isoflurane with a continuous oxygen supply. Confirm the anesthesia depth via&#160;lack of pedal reflex. Apply the veterinary ophthalmic ointment to prevent eye dryness&#160;during surgery. Provide thermal support for the animal throughout the procedure until the animal recovers.&#160;</li>
		<li>Identify the implantation site on the mouse. 
		NOTE: This should be on the right or left flank of the mouse, generally landmarked laterally on the side of the abdominal region, caudal to the ribcage.</li>
		<li>To prepare the surgical area, shave the fur and disinfect with three alternating scrubs of povidone iodine and 70% ethanol.</li>
		<li>Using forceps, lift the skin of the mouse and make a 0.5-1 cm incision on the skin.</li>
		<li>Insert a pair of surgical scissors slowly under the skin at the incision site to create a pocket (0.5-1 cm deep) in the subcutaneous space.</li>
		<li>Carefully place one tumor piece in the pocket and push it push it to the bottom of the pocket to prevent the tumor from slipping out.</li>
		<li>Close the incision using 4-0 nylon surgical sutures. 
		NOTE: Other wound closure methods such as non-absorbable or absorbable sutures and wound clips can also be used.</li>
		<li>Transfer the mouse back to the cage and monitor the animal&#39;s recovery from anesthesia, until it is ambulatory. 
		NOTE: Analgesics are not required but can be administered if pain is observed in the mice.</li>
		<li>Monitor the tumor growth weekly. One tumor is expected per mouse. 
		NOTE: The tumor&#39;s volume at transplantation will seem to initially decrease but this is not a cause for concern. A tumor is considered to have taken once it becomes palpable and enters a logarithmic growth phase. This first passage represents the F0 generation.</li>
		<li>Once the tumors start growing, measure the tumors three times per week. Measure the length and width of the tumors with a caliper. To calculate the volume of the tumor, use the formula: length x width x width / 2.</li>
		<li>Euthanize the mice implanted with PDX tumors when the tumors are greater than 15 mm in diameter using the longest side of the tumor. Perform the euthanasia by CO2 inhalation in a CO2 induction chamber, followed by cervical dislocation as a secondary method.</li>
		<li>Resect the tumor from the flank of the animal by making an incision. Dissect the excised tumor gently with blunt scissors and forceps. To do this, first cut off the skin on top of the tumor, then cut the tumor away from the muscle layer below it.</li>
		<li>Transfer the tumor tissue to &#62;10 mL of a suitable storage solution (such as DMEM). Immediately place it on ice. This tumor can be cryopreserved or passaged to another set of mice. Consider this passage as F1. 
		NOTE: Passaging again would render the tumor passage F2 and so on.</li>
	</ol>
	</li>
	<li>Propagation of PDX models
	<ol>
		<li>Begin with the resected tumor kept in storage solution from step 1.1.19.</li>
		<li>Transfer the tissue to a tissue culture dish and rinse with 5 mL DPBS.</li>
		<li>Remove the necrotic regions from the tumor.</li>
		<li>Cut the tissue into approximately 2 x 2 x 2 mm pieces.</li>
		<li>Transfer the tissues into a microcentrifuge tube containing growth factor reduced basement membrane matrix (&#62;200 &#181;L) and store on ice.</li>
		<li>Cryopreserve the remaining tissue that is not used for propagation according to the protocol described in step 1.3.</li>
		<li>Anesthetize the animal in an induction chamber with 2-5% isoflurane and&#160;oxygen. Once anesthetized,&#160;transfer the animal to a nose cone to maintain anesthesia at&#160;1.5-2.5% isoflurane with a continuous oxygen supply. Confirm the anesthesia depth via&#160;lack of pedal reflex.&#160;Apply the veterinary ophthalmic ointment to prevent eye dryness&#160;during surgery. Provide thermal support for the animal throughout the procedure until the animal recovers.</li>
		<li>Identify the implantation site on the mouse. 
		NOTE: This should be on the right or left flank of the mouse, generally in the abdominal region, caudal to the ribcage.</li>
		<li>To prepare the surgical area, shave the fur and disinfect with three alternating scrubs of povidone iodine and 70% ethanol.</li>
		<li>Make a 0.5-1 cm incision on one flank of the mouse.</li>
		<li>Insert a pair of surgical scissors slowly under the skin at the incision to create a pocket (0.5-1 cm deep) in the subcutaneous space.</li>
		<li>Carefully place one tumor piece in the pocket and push it to the bottom of the pocket to prevent the tumor from slipping out.</li>
		<li>Close the incision using 4-0 nylon surgical sutures or other wound closure methods.</li>
		<li>Transfer the mouse back to the cage and monitor its recovery from anesthesia, until it is ambulatory. 
		NOTE: Analgesics are not required but can be administered if pain is observed in the mice.</li>
		<li>During latency (non-growth phase), monitor the tumor growth weekly. One tumor is expected per mouse. 
		NOTE: The tumor&#39;s volume at transplantation will seem to initially decrease but this is not a cause for concern. A tumor is considered to be taken once it becomes palpable and starts to continually grow.</li>
		<li>Once the tumors start growing, measure the tumors three times per week. Measure the length and width of the tumors with a caliper. Calculate the volume of the tumor using the formula: length x width x width / 2.</li>
		<li>Euthanize the mice implanted with PDX tumors when the tumors are greater than 15 mm in diameter using the longest side of the tumor. Perform euthanasia by CO2 inhalation in a CO2 induction chamber, followed by cervical dislocation as a secondary method.</li>
		<li>Resect the tumor from the flank of the animal by making an incision and dissecting the tumor out gently with blunt scissors and forceps.</li>
		<li>Transfer the tumor tissue to &#62;10 mL of a suitable storage solution (such as DMEM) and then immediately place on ice.</li>
	</ol>
	</li>
	<li>Cryopreservation of PDX tumors
	<ol>
		<li>Euthanize the mice implanted with PDX tumors when the tumors are greater than 15 mm in diameter using the longest side of the tumor. Perform euthanasia by CO2 inhalation in a CO2 induction chamber, followed by cervical dislocation as a secondary method.</li>
		<li>Resect the tumor from the flank of the animal by making an incision and dissecting the tumor out gently with blunt scissors and forceps.</li>
		<li>Transfer the tumor tissue to &#62;10 mL of a suitable storage solution (such as DMEM) and then immediately place on ice.</li>
		<li>Transfer the tissue to a tissue culture dish and rinse with 5 mL DPBS.</li>
		<li>Remove necrotic regions from the tumor.</li>
		<li>Cut the tissue into approximately 2 x 2 x 2 mm pieces.</li>
		<li>Transfer the tissue into cryotubes containing 20% DMEM, 70% FBS, and 10% DMSO.</li>
		<li>Transfer the cryotubes to a cryopreservation container and place in a -80 &#176;C freezer.</li>
		<li>When the cryotubes are chilled to -80 &#176;C, transfer them to liquid nitrogen storage.</li>
	</ol>
	</li>
</ol>
2. Inoculation routes for preclinical studies
<ol>
	<li>Subcutaneous flank implantation. 
	NOTE: Subcutaneous flank implantation can be used for ease and can be helpful for studying all steps of the metastatic cascade.
	<ol>
		<li>Use growing PDX tumors or cryopreserved PDX tumors for initial flank implantation.</li>
		<li>For growing PDX tumors, euthanize the mice using an IACUC-approved method when the tumors are greater than 15 mm in length; resect the tumor and transfer the tumor tissue to a suitable storage solution (such as DMEM) and immediately place on ice.</li>
		<li>For cryopreserved PDX tumors, thaw the cryopreserved PDX tissue quickly by immersing in 37 &#176;C water bath.</li>
		<li>Follow the steps 1.2.2-1.2.19.</li>
	</ol>
	</li>
	<li>Orthotopic implantation by intracranial injection into the brain. 
	NOTE: This model can be used for testing efficacy of drugs to cross the BBB and to study tumor colonization. This section primarily references the use of the tumor dissociation kit (see Table of Materials). Different tissue types require different dissociation protocols. It is recommended that the user test and optimize the protocol to maximize the dissociation efficiency.
	<ol>
		<li>Euthanize the mice implanted with PDX tumors using an &#160;IACUC-approved method when the tumors are greater than 15 mm in length.</li>
		<li>Under sterile conditions in a biosafety cabinet, surgically resect the PDX tumors and store in DMEM on ice.</li>
		<li>Prepare the dissociation solution in the appropriate tube by adding the enzyme mix into DMEM as indicated by the manufacturer&#39;s protocol.</li>
		<li>Wash the tumor in 5 mL DPBS in a tissue culture dish.</li>
		<li>Remove the necrotic regions from the tumor.</li>
		<li>Cut the tumor into small pieces of 2-4 mm in length.</li>
		<li>Transfer the tumor pieces into the tube containing the enzyme mix.</li>
		<li>Attach the tube to the tissue dissociator and run the program suitable for the tissue type. Consult the manufacturer&#39;s protocol for the appropriate program to run, and the dissociation time required.</li>
		<li>After completion of the program, strain the cells through a 70 &#181;m cell strainer.</li>
		<li>Wash the cell strainer with 20 mL of DMEM.</li>
		<li>Centrifuge the dissociated cells at 300 x g for 7 min.</li>
		<li>Aspirate the supernatant and resuspend the cells in DPBS.</li>
		<li>Count the cells and dilute to the required concentration.</li>
		<li>Set up the stereotaxic frame according to the manufacturer&#39;s instructions and prepare a heating pad for the mice. Sanitize all areas with 70% ethanol.</li>
		<li>Anesthetize the animal in an induction chamber with 2-5% isoflurane and&#160;oxygen. Once anesthetized,&#160;transfer the animal to a nose cone to maintain anesthesia at&#160;1.5-2.5% isoflurane with a continuous oxygen supply. Confirm the anesthesia depth via&#160;lack of pedal reflex.&#160;Apply the veterinary ophthalmic ointment to prevent eye dryness&#160;during surgery. Provide thermal support for the animal throughout the procedure until the animal recovers.</li>
		<li>Prepare the surgical area by shaving the fur on the mouse&#39;s head to expose the scalp.</li>
		<li>Provide the mouse with the appropriate analgesic, such as one dose of 1 mg/kg Buprenorphine sustained release (SR) administered by subcutaneous injection.</li>
		<li>Transfer the mouse to the stereotaxic frame. Ensure that the mouse is biting on the bite-block. Use the ear bars to firmly secure the head of the mouse. 
		NOTE: The mouse is properly secured if the head does not move when pushed gently with forceps.</li>
		<li>Disinfect the shaved area with three alternating scrubs of povidone-iodine and 70% ethanol.</li>
		<li>Make a 5-7 mm longitudinal incision on the scalp to expose the skull and retract the scalp.</li>
		<li>Scrape off the periosteum with a blunt surgical instrument such as forceps.</li>
		<li>Locate the bregma on the skull.</li>
		<li>Position the needle of the stereotactic frame on top of the bregma and reset the coordinates to 0 or note the coordinate on the arm.</li>
		<li>Move the arm 1 mm posterior (caudally)&#160;and 1 mm lateral, right of the midline.</li>
		<li>Mark this location with a permanent marker. If the arm contains a slot for the syringe, attach a marker to the syringe slot to mark the location.</li>
		<li>Drill a small burr hole in the skull at this location. Do not apply too much pressure to prevent drilling into the brain.</li>
		<li>Load a 5 &#181;L, 26 G Hamilton syringe with 5-10 x 104 cells, in a volume of 1-2 &#181;L, and attach to the stereotaxic arm.</li>
		<li>Slowly insert the Hamilton syringe needle 2 mm into brain.</li>
		<li>Begin injecting cells at the desired rate, usually 0.2-0.5 &#181;L/min.</li>
		<li>After the injection is complete, slowly retract the needle from the brain.</li>
		<li>Fill the burr hole with bone wax.</li>
		<li>Close the incision with surgical sutures or surgical glue.</li>
		<li>Transfer the mouse back to the cage and monitor its recovery from anesthesia.</li>
		<li>Monitor the condition of the animals regularly and euthanize them when the humane endpoint criteria are reached in the approved protocol. 
		NOTE: Successful tumor growth in the brain results in deteriorating condition of the animal, which often manifests with head tilt, rough hair coat, hunched body, squinted eyes, reduced activity, and low body condition score (BCS &#60; 2).</li>
		<li>Perform a necropsy on the euthanized animals, followed by histological analysis to confirm the presence of tumors in the brain. Record the length of time it takes from implantation to euthanasia.</li>
	</ol>
	</li>
	<li>Implantation of PDX models by intracardiac injection 
	NOTE: This model can be used to study organ tropism once tumor cells are in circulation. This section also uses the Tumor Dissociation Kit and requires optimization by tissue type.
	<ol>
		<li>Follow the steps 2.2.1-2.2.13.</li>
		<li>Anesthetize the animal in an induction chamber with 2-5% isoflurane and&#160;oxygen. Once anesthetized,&#160;transfer the animal to a nose cone to maintain anesthesia at&#160;1.5-2.5% isoflurane with a continuous oxygen supply. Confirm the anesthesia depth via&#160;lack of pedal reflex.&#160;Apply the veterinary ophthalmic ointment to prevent eye dryness&#160;during surgery. Provide thermal support for the animal throughout the procedure until the animal recovers.</li>
		<li>Then, position the mouse in a supine position.</li>
		<li>To prepare the surgical area on the chest, shave the fur and disinfect it with three alternating scrubs of povidone-iodine and 70% ethanol.</li>
		<li>Draw 0.5-10 x 105 cells into a syringe on a 28 G needle, up to a volume of 100 &#181;L. 
		NOTE: The number of cells required varies depending on the aggressiveness of the model and the optimal number of cells should be empirically determined for each model.</li>
		<li>Locate the injection site (slightly left of the mouse&#39;s sternum and halfway between the sternal notch and xyphoid process).</li>
		<li>Insert the needle vertically into the mouse at the injection site.</li>
		<li>Observe the successful entry into the left ventricle through a backflow of blood entering the syringe. Slowly dispense the cells into the left ventricle without moving the needle.</li>
		<li>Slowly pull the needle out vertically from the mouse.</li>
		<li>Apply a piece of sterile gauze over the injection site and apply pressure for around 1 min until the bleeding stops, while still allowing chest movement for respiration.</li>
		<li>Remove the mouse from anesthesia and allow it to recover on a heated pad. 
		NOTE: Successful tumor growth results in deteriorating condition of the animal, which often manifests with ruffled hair coat, hunched body, squinted eyes, reduced activity, and low body condition score (BCS &#60; 2).</li>
		<li>Monitor the condition of the animals regularly and euthanize them when the humane endpoint criteria are reached in the approved protocol.</li>
		<li>Perform a necropsy to identify metastases on the euthanized animals, followed by histological analysis to confirm the presence of tumors in the target organ. Record the length of time it takes from intracardiac injection to euthanasia.</li>
	</ol>
	</li>
</ol>

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The authors have no disclosures.

In the current manuscript, methods for PDX establishment and propagation have been detailed. Three different inoculation methods that can be used for setting up preclinical studies when evaluating CNS metastasis have also been demonstrated. The method of choice should depend on the goals of the experiment. In some cases, it would be beneficial to use more than one inoculation route. For example, subcutaneous flank implantation provides a simple approach to study the effectiveness of a drug on tumor growth and assess the drug on its target and it also provides a visual for tumor size that is easily monitored and measured. However, once target feasibility and anti-tumor growth properties are established, one could set up an orthotopic study to assess the efficacy of the biologic to cross the BBB and study its effect within the brain tumor microenvironment. Also, survival is better assessed in orthotopic and intracardiac injection studies.
Intracranial injection of brain metastasis PDX models is often the preclinical model of choice due to the presence of the brain microenvironment and BBB. However, studies have shown that brain metastases have the ability to modify the BBB, which affects the permeability of molecules to the tumor16. These changes in the BBB would not be reflected by intracranially implanted tumors, and because of this preclinical drug studies may not fully reflect the response of patient tumors. Even with this caveat, intracranial injection remains the best method to test the permeability and efficacy of drugs to cross the BBB in preclinical models. Another challenge with intracranial models is that they are difficult for monitoring tumor growth and require the use of imaging techniques. Viral transduction of PDXs with fluorescent or bioluminescent markers has been traditionally used but can be challenging to perform. However, several imaging techniques are being developed for use in mice that do not require introduction of markers, which could improve the ease of monitoring these orthotopic brain tumors for preclinical studies. These include imaging technologies such as magnetic resonance imaging (MRI) and positron emission tomography (PET) imaging and micro computed tomography (micro-CT). Finally, intracranial injection may not accurately reflect the microenvironment of CNS metastases outside the brain, such as in leptomeningeal metastasis. In this case, injection into the cisterna magna could be performed to more accurately represent leptomeningeal metastases17.
Characterization of both the phenotypic and molecular features of the PDX model is important for selecting the best models for preclinical studies. Tumor latency can range from 7-140 days and take rates can also be highly variable12. The optimal number of animals to implant and timing to starting treatment would have to be based on the characteristics of each PDX model and needs to be empirically determined. Furthermore, the molecular profile of PDX tumors is also important for the selection of the most representative PDX models for preclinical studies. The closer the model molecularly represents the donor tissue the more predictive of clinical response it is likely to be. Also, it is critical to ensure that the targets selected from human data are present in the PDXs being chosen for studies and are sustained through a few generations, as shown clonal succession is associated with a different genomic profile of the incumbent dominant clone. In light of this, the phenotypic and molecular profiles of the CNS metastasis PDX tumors have been extensively characterized over multiple generations12.
Despite the many advantages of using CNS metastasis PDX models, there are several limitations related to their use. First, an alternate tumor microenvironment and especially lack of an immune system are well-documented limitations of PDX models18. The xenograft of a human tumor into mice results in the replacement of human stroma with mouse stroma with each subsequent passage and the human stroma is generally completely replaced after several passages19. However, the differences in the tumor microenvironment do not result in large differences in the molecular profile of flank-implanted PDX tumors compared to the original patient tumor12, suggesting that flank models still represent good experimental models to study CNS metastasis. Second, the use of immunocompromised animals results in a lack of immune cell infiltration in the tumor and a general immune response by the host, limiting a fundamental way in which the host attempts to combat cancer growth12. While humanized mice engrafted with human immune cells are available for studying the interactions of specific immune cells with the tumor, there are still many questions and controversies about the approaches, methods, and interpretation of those results20.
While the majority of PDXs have been shown to be genetically stable, we and others have shown that in rare cases, even in the absence of treatments or other external selective pressures, there could be changes in the clones of the tumors, such as minor clone takeover12,14,15. This could result in dramatic changes in the molecular profile, which would ultimately render the tumor not reflecting the dominant clones in the patient tumor12. While PDXs displaying clonal succession can have use in preclinical studies, many genes intended for targeting (e.g., Her2) could be lost with clonal succession. Therefore, frequent screening of PDX models to determine whether they still maintain the molecular profile of the desired clone is encouraged.
In summary, PDX models represent an excellent model system for the study of not only CNS metastasis but also other tumor types. Developing these models have shown that they largely reflect the phenotypic, molecular profile and heterogeneity of human CNS metastasis8,9,10,12. They serve as effective models for studying both CNS metastasis biology and also serve well as physiologically relevant preclinical models, replacing overused cell line models historically used for in vivo studies of CNS metastasis. Undoubtedly, differences between the PDX and donor patient tumor exists12,18. Knowing what these differences are is important for proper planning and execution of preclinical studies. Lastly, by choosing between several inoculation routes, PDX models are versatile in their use allowing the study of multiple aspects of the disease. PDXs models will no doubt play an important role in advancing our understanding of CNS metastasis and the development of novel therapies.

The incidence of metastasis to the central nervous system (CNS) has increased over recent years1,2,3. Traditional therapies for CNS metastasis, such as tumor resection, whole brain radiotherapy, and stereotactic radiosurgery, have been largely palliative and rarely curative, and can lead to debilitating side effects, such as cognitive deterioration1. Recently, many new targeted and immunological therapies are being developed for the treatment of CNS metastasis that show promise in being more effective treatments, while having fewer side effects4.
Translating preclinical results into meaningful clinical endpoints often requires effective and predictive modeling strategies. Historically, cell line xenograft models were the standard for preclinical research in CNS metastasis research. However, these cell line models do not reflect the true tumor behavior of the host tumor or represent the histological or molecular heterogeneity of the disease. Furthermore, cell line models are able to adapt to in vitro growth conditions and, therefore, lose the original properties of the host tumor. Patient derived xenografts (PDXs), which engraft a patient&#39;s tumor into an immunodeficient or humanized mouse, are increasingly used in translational cancer research. Researchers have shown that PDX models can usually faithfully recapitulate tumor growth, histological characteristics, maintain tumor heterogeneity, metastatic potential, and molecular genetic features. In addition, PDX models are prognostic whereby the PDX tumor latency period correlates with patient overall survival and they have also been shown to accurately predict therapeutic response in patient trials5,6.
There has been an emergence of CNS metastasis PDXs. Mostly, these have been developed representing tumors originating from a single origin, such as non-small cell lung cancer (NSCLC)7, breast cancer8,9, and melanoma10,11. More recently, a large and diverse collection of PDX models have been developed and characterized, representing eight different histological subtypes12. It has been demonstrated that PDX models for CNS metastasis closely resemble their original patient tumor, both histologically and molecularly and have also demonstrated histological unique differences and similarities10,12. Furthermore, while most CNS metastasis PDX models maintain the clonal heterogeneity of human tumors, some displayed evidence of clonal succession12, making them also ideal for studying resistance to therapies by monitoring clonal changes after treatment.
The protocols described here outline methods of PDX establishment and various routes of inoculation used in preclinical studies of CNS metastasis (Figure 1). These implantation methods vary in their ability to mimic growth and metastasis. Here, the protocol highlights the applications for each route of implantation and demonstrates how they could be used for the study of CNS metastasis.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>25G needle</td>
			<td>VWR</td>
			<td>BD305122</td>
			<td></td>
		</tr>
		<tr>
			<td>70 &#181;m Cell strainer</td>
			<td>VWR</td>
			<td>21008-952</td>
			<td></td>
		</tr>
		<tr>
			<td>70% ethanol wipes</td>
			<td>VWR</td>
			<td>470106-486</td>
			<td></td>
		</tr>
		<tr>
			<td>Bone wax</td>
			<td>MedVet</td>
			<td>W31G-RL</td>
			<td></td>
		</tr>
		<tr>
			<td>CIEA NOG mouse</td>
			<td>Taconic</td>
			<td>NOG-F</td>
			<td></td>
		</tr>
		<tr>
			<td>DMEM</td>
			<td>ThermoFisher</td>
			<td>11965092</td>
			<td></td>
		</tr>
		<tr>
			<td>Ethiqa XR (buprenorphine SR)</td>
			<td>MWI</td>
			<td>072117</td>
			<td></td>
		</tr>
		<tr>
			<td>FBS</td>
			<td>ThermoFisher</td>
			<td>16000044</td>
			<td></td>
		</tr>
		<tr>
			<td>gentleMACS C Tube</td>
			<td>Miltenyi</td>
			<td>130-093-237</td>
			<td></td>
		</tr>
		<tr>
			<td>gentleMACS Octo Dissociator</td>
			<td>Miltenyi</td>
			<td>130-095-937</td>
			<td></td>
		</tr>
		<tr>
			<td>Hamilton syringe</td>
			<td>Sigma</td>
			<td>20919</td>
			<td></td>
		</tr>
		<tr>
			<td>Matrigel growth factor reduced (GFR)</td>
			<td>Corning</td>
			<td>354230</td>
			<td></td>
		</tr>
		<tr>
			<td>Ophthalmic ointment</td>
			<td>MedVet</td>
			<td>PH-PURALUBE-VET</td>
			<td></td>
		</tr>
		<tr>
			<td>PBS/DPBS</td>
			<td>ThermoFisher</td>
			<td>14040133</td>
			<td></td>
		</tr>
		<tr>
			<td>Povidone iodine swabs</td>
			<td>VWR</td>
			<td>15648-906</td>
			<td></td>
		</tr>
		<tr>
			<td>Stereotaxic frame</td>
			<td>Stoelting</td>
			<td>51730</td>
			<td></td>
		</tr>
		<tr>
			<td>Surgical drill</td>
			<td>Stoelting</td>
			<td>58610</td>
			<td></td>
		</tr>
		<tr>
			<td>Surgical glue</td>
			<td>MedVet</td>
			<td>VG3</td>
			<td></td>
		</tr>
		<tr>
			<td>Surgical sutures</td>
			<td>MedVet</td>
			<td>MMV-661-V</td>
			<td></td>
		</tr>
		<tr>
			<td>Syringe</td>
			<td>VWR</td>
			<td>53548-001</td>
			<td></td>
		</tr>
		<tr>
			<td>Tumor dissociation kit</td>
			<td>Miltenyi</td>
			<td>130-095-929</td>
			<td></td>
		</tr>
	</tbody>
</table>

the establishment and utilization of patient derived xenograft models of central nervous system metastasis

The development of novel therapies for central nervous system (CNS) metastasis has been hindered by the lack of preclinical models that accurately represent the disease. Patient derived xenograft (PDX) models of CNS metastasis have been shown to better represent the phenotypic and molecular characteristics of the human disease, as well as better reflect the heterogeneity and clonal dynamics of human patient tumors compared to historic cell line models. There are multiple sites that can be used to implant patient-derived tissue when setting up preclinical trials, each with their own advantages and disadvantages, and each suited for studying different aspects of the metastatic cascade. Here, the protocol describes how to establish PDX models and present three different approaches for utilizing CNS metastasis PDX models in pre-clinical studies, discussing each of their applications and limitations. These include flank implantation, orthotopic injection in the brain, and intracardiac injection. Subcutaneous flank implantation is the easiest to monitor and, therefore, most convenient for pre-clinical studies. In addition, metastases to brain and other tissues from flank implantation were observed, indicating that the tumor has undergone multiple steps of metastasis, including intravasation, extravasation, and colonization. Orthotopic injection in the brain is the best option for recapitulating the brain tumor microenvironment and is useful for determining the efficacy of biologics to cross the blood-brain barrier (BBB) but bypasses most steps of the metastatic cascade. Intracardiac injection facilitates metastasis to the brain and is also useful for studying organ tropism. While this method forgoes earlier steps of the metastatic cascade, these cells will still have to survive circulation, extravasate, and colonize. The utility of a PDX model, is therefore, impacted by the route of tumor inoculation and the choice of which one to utilize should be dictated by the scientific question and overall goals of the experiment.

Flank-propagated PDX tumors are the easiest to implant, monitor, and resect, and is generally recommended for initial establishment and propagation of PDX tumors (Figure 1). When establishing or propagating PDX tumors, it is prudent to implant tumors in multiple animals, as the tumor take rate may vary and not every piece of tumor will always take in mice. Methods have been developed for the establishment and propagation of CNS metastasis PDXs directly in the brain13. However, these methods are still more challenging with lower take rates and the tumors are significantly more difficult to propagate and monitor than flank implantation.
If patient tumors are not readily available, CNS metastasis PDX tumors can also be obtained from a variety of sources, including repositories of academic labs or commercial companies. After acquiring the tumors, the first priority would be to propagate and cryopreserve as much material as possible, ensuring a great number of low passage tumors are preserved. This ensures that sufficient material is available for an indefinite number of subsequent studies with the PDX models. Much like immortalized cell lines, PDX tumors should be cryopreserved and used at low passage numbers, as genetic drifting results in changes to the phenotype and genotype of the PDXs over time12,14,15. Regardless of the source of PDX tumors, it is important to perform frequent screening of PDX and mouse colonies for both human and mouse pathogens, such as HIV and hepatitis for humans and Corynebacterium bovis for mice. This will limit the spreading of unwanted pathogens from the PDX to both the individual handling them and other mice in the study and vivarium.
The implantation methods described here can be used to study tumor biology, evaluate multiple aspects of the metastatic cascade, and for preclinical studies. The main advantage of flank implantation is the ease of tumor monitoring over time, as tumors are visible, and its growth can be easily measured using a caliper. This method can be a good place to start for establishing feasibility of a drug target. Intracranial implantation is preferred if the presence of the brain microenvironment is important and could alter the growth or molecular profile of the tumor. In addition, intracranial implantation places the tumor behind the blood brain barrier (BBB), making it essential for preclinical studies examining the efficacy of drugs required to traverse the BBB. However, it is difficult to monitor the growth of PDX tumors and requires radiological imaging or bioluminescent imaging if the cells are labeled. Knowing when to start the drug treatment preclinically would require either imaging data to monitor growth or knowledge of average survival of mice bearing a particular PDX tumor. Furthermore, intracranial implantation bypasses all the essential steps of the metastatic cascade, making it only suitable for studying drug efficacy and tumor microenvironment within the brain. Despite the differences in the tumor microenvironment, the morphology of PDX tumors is similar regardless of the site of implantation as can be seen in this PDX tumor (CM04) derived from a brain metastasis that originated from a small cell lung cancer primary tumor (Figure 2). The small cell lung cancer morphology of tumor cells with small nuclei and scant cytoplasm can be observed in the flank tumor, intracranial tumor, and abdominal metastasis resulting from intracardiac injection. Furthermore, spontaneous metastasis from tumors implanted in the flank have been previously observed12, suggesting that the metastatic processes such as intravasation, extravasation, and colonization can be recapitulated and studied in flank tumors which would otherwise not be possible with orthotopic tumors in the brain. In general, it is observed that flank implantation is a suitable method for studying CNS metastasis biology and conducting preclinical studies.
Intracardiac injection is most often used to study organ tropism and metastatic potential of tumors. Injected tumor cells would have to undergo several steps of the metastatic cascade, including surviving circulation, extravasation, and colonization of the metastatic site. Much like orthotopic injection into the brain, it may be difficult to track the progress of tumor metastasis without radiological imaging or cell labeling. However, as with orthotopic implantation, successful inoculation results in deterioration of the condition of the animals over time as the tumor spreads. Figure 3A demonstrates metastasis to the brain after intracardiac injection in CNS metastasis PDX model, M2, which originated from a melanoma. Intracardiac injection of PDX tumor (CM04) resulted in metastasis to the abdominal cavity and liver (Figure 3B). Other organs assessed, such as the lung, kidney, and ovaries had no visible metastases.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/62264/62264fig01.jpg" /> 
Figure 1: Flow chart showing the general workflow of establishing, propagating, and using PDX for preclinical studies. For each inoculation method, steps of the metastatic cascade involved are listed below each method. <a href="https://www.jove.com/files/ftp_upload/62264/62264fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/62264/62264fig02.jpg" /> 
Figure 2: Histology of PDX tumors following different inoculation methods. Hematoxylin and eosin (H&#38;E) staining of a CNS metastasis PDX tumor that originated from small cell lung cancer (CM04) implanted into immunocompromised mice by the three methods have similar tumor pathohistological and morphological features of small cell lung cancers, with small nuclei and scant cytoplasm. The intracardiac injection panel shows an abdominal metastasis. Nests of small-sized cells and high nuclear to cytoplasmic ratio is evident in all the three images. Images were taken on a slide scanner and magnified to 10x. <a href="https://www.jove.com/files/ftp_upload/62264/62264fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/62264/62264fig03.jpg" /> 
Figure 3: Metastases observed after intracardiac injection. H&#38;E staining of tissues with visible metastasis during assessment by necropsy after intracardiac injection of (A) M2 and (B) CM04. Images were taken (A) on a slide scanner and magnified to 1x (left) or 20x (right) or (B) on a regular microscope at 10x magnification. This figure has been modified from our previous publication12.&#160;<a href="https://www.jove.com/files/ftp_upload/62264/62264fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about The Establishment and Utilization of Patient Derived Xenograft Models of Central Nervous System Metastasis at JoVE.com

The Establishment and Utilization of Patient Derived Xenograft Models of Central Nervous System Metastasis

Central nervous system metastasis PDX models represent the phenotypic and molecular characteristics of human metastasis, making them excellent models for preclinical studies. Described here is how to establish PDX models and the inoculation routes that are best used for preclinical studies.

The development of novel therapies for central nervous system (CNS) metastasis has been hindered by the lack of preclinical models that accurately ...

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2.2K Views.  University of Southern California. Central nervous system metastasis PDX models represent the phenotypic and molecular characteristics of human metastasis, making them excellent models for preclinical studies. Described here is how to establish PDX models and the inoculation routes that are best used for preclinical studies.

Video: The Establishment and Utilization of Patient Derived Xenograft Models of Central Nervous System Metastasis

Development and Maintenance of a Preclinical Patient Derived Tumor Xenograft Model for the Investigation of Novel Anti-Cancer Therapies

Patient derived tumor xenograft (PDTX) models provide a necessary platform in facilitating anti-cancer drug development prior to human trials. Human tumor pieces are injected subcutaneously into athymic nude mice (immunocompromised, T cell deficient) to create a bank of tumors and subsequently are passaged into different generations of mice in order to maintain these tumors from patients. Importantly, cellular heterogeneity of the original tumor is closely emulated in this model, which provides a more clinically relevant model for evaluation of drug efficacy studies (single agent and combination), biomarker analysis, resistant pathways and cancer stem cell biology. Some limitations of the PDTX model include the replacement of the human stroma with mouse stroma after the first generation in mice, inability to investigate treatment effects on metastasis due to the subcutaneous injections of the tumors, and the lack of evaluation of immunotherapies due to the use of immunocompromised mice. However, even with these limitations, the PDTX model provides a powerful preclinical platform in the drug discovery process.

Utilizing patient-derived tumors in a subcutaneous preclinical model is an excellent way to study the efficacy of novel therapies, predictive biomarker discovery, and drug resistant pathways. This model, in the drug development process, is essential in determining the fate of many novel anti-cancer therapies prior to clinical investigation.

Patient derived tumor xenograft (PDTX) models provide a necessary platform in facilitating anti-cancer drug development prior to human trials. Human tumor ...

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma

Soft tissue sarcomas (STS) represent a spectrum of heterogeneous malignancies with a difficult diagnosis, classification, and management. To date, more than 50 histological subtypes of these rare solid tumors have been identified. Thus, due to their extraordinary diversity and low incidence, our understanding of the biology of these tumors is still limited. Patient-derived cultures represent the ideal platform to study STS pathophysiology and pharmacology. We thus developed a human preclinical model of STS starting from tumor specimens harvested from patients undergoing surgical resection. Patient-derived STS cell cultures were obtained from the surgical specimens by collagenase digestion and isolated by filtration. Cells were counted, seeded, and left for 14 days in standard monolayer cultures and then processed by downstream analysis. Before performing molecular or pharmaceutical analyses, the establishment of STS primary cultures was confirmed through the evaluation of cytomorphologic features and, when available, immunohistochemical markers. This method represents a useful tool 1) to study the natural history of these poorly explored malignancies and 2) to test the effects of different drugs in an effort to learn more about their mechanisms of action.

The following protocol focuses on the establishment of a primary culture of patient-derived soft tissue sarcoma (STS). This model could help us to better understand the molecular background and pharmacological profile of these rare malignancies and could represent a starting point for further research aimed at improving STS management.

Soft tissue sarcomas (STS) represent a spectrum of heterogeneous malignancies with a difficult diagnosis, classification, and management. To date, more ...

Utilization of Ultrasound Guided Tissue-directed Cellular Implantation for the Establishment of Biologically Relevant Metastatic Tumor Xenografts

Preclinical testing of anticancer therapies relies on relevant xenograft models that mimic the innate tendencies of cancer. Advantages of standard subcutaneous flank models include procedural ease and the ability to monitor tumor progression and response without invasive imaging. Such models are often inconsistent in translational clinical trials and have limited biologically relevant characteristics with low proclivity to produce metastasis, as there is a lack of a native microenvironment. In comparison, orthotopic xenograft models at native tumor sites have been shown to mimic the tumor microenvironment and replicate important disease characteristics such as distant metastatic spread. These models often require tedious surgical procedures with prolonged anesthetic time and recovery periods. To address this, cancer researchers have recently utilized ultrasound-guided injection techniques to establish cancer xenograft models for preclinical experiments, which allows for rapid and reliable establishment of tissue-directed murine models. Ultrasound visualization also provides a noninvasive method for longitudinal assessment of tumor engraftment and growth. Here, we describe the method for ultrasound-guided injection of cancer cells, utilizing the adrenal gland for NB and renal sub capsule for ES. This minimally invasive approach overcomes tedious open surgery implantation of cancer cells in tissue-specific locations for growth and metastasis, and abates morbid recovery periods. We describe the utilization of both established cell lines and patient derived cell lines for orthotopic injection. Pre-made commercial kits are available for tumor dissociation and luciferase tagging of cells. Injection of cell suspension using image-guidance provides a minimally invasive and reproducible platform for the creation of preclinical models. This method is utilized to create reliable preclinical models for other cancers such as bladder, liver and pancreas exemplifying its untapped potential for numerous cancer models.

Here, we present a protocol to utilize ultrasound-guided injection of neuroblastoma (NB) and Ewing's sarcoma (ES) cells (established cell lines and patient-derived tumor cells) at biologically relevant sites to create reliable preclinical models for cancer research.

Preclinical testing of anticancer therapies relies on relevant xenograft models that mimic the innate tendencies of cancer. Advantages of standard ...

Patient-derived Orthotopic Xenograft Models for Human Urothelial Cell Carcinoma and Colorectal Cancer Tumor Growth and Spontaneous Metastasis

Cancer patients have poor prognoses when lymph node (LN) involvement is present in both high-grade urothelial cell carcinoma (HG-UCC) of the bladder and colorectal cancer (CRC). More than 50% of patients with muscle-invasive UCC, despite curative therapy for clinically-localized disease, will develop metastases and die within 5 years, and metastatic CRC is a leading cause of cancer-related deaths in the US. Xenograft models that consistently mimic UCC and CRC metastasis seen in patients are needed. This study aims to generate patient-derived orthotopic xenograft (PDOX) models of UCC and CRC for primary tumor growth and spontaneous metastases under the influence of LN stromal cells mimicking the progression of human metastatic diseases for drug screening. Fresh UCC and CRC tumors were obtained from consented patients undergoing resection for HG-UCC and colorectal adenocarcinoma, respectively. Co-inoculated with LN stromal cell (LNSC) analog HK cells, luciferase-tagged UCC cells were intra-vesically (IB) instilled into female non-obese diabetic/severe combined immunodeficiency (NOD/SCID) mice, and CRC cells were intra-rectally (IR) injected into male NOD/SCID mice. Tumor growth and metastasis were monitored weekly using bioluminescence imaging (BLI). Upon sacrifice, primary tumors and mouse organs were harvested, weighed, and formalin-fixed for Hematoxylin and Eosin and immunohistochemistry staining. In our unique PDOX models, xenograft tumors resemble patient pre-implantation tumors. In the presence of HK cells, both models have high tumor implantation rates measured by BLI and tumor weights, 83.3% for UCC and 96.9% for CRC, and high distant organ metastasis rates (33.3% detected liver or lung metastasis for UCC and 53.1% for CRC). In addition, both models have zero mortality from the procedure. We have established unique, reproducible PDOX models for human HG-UCC and CRC, which allow for tumor formation, growth, and metastasis studies. With these models, testing of novel therapeutic drugs can be performed efficiently and in a clinically-mimetic manner.

This protocol describes the generation of patient-derived orthotopic xenograft models by intra-vesically instilling high-grade urothelial cell carcinoma cells or intra-rectally injecting colorectal cancer cells into non-obese diabetic/severe combined immunodeficiency (NOD/SCID) mice for primary tumor growth and spontaneous metastases under the influence of lymph node stromal cells, which mimics the progression of human metastatic diseases.

Cancer patients have poor prognoses when lymph node (LN) involvement is present in both high-grade urothelial cell carcinoma (HG-UCC) of the bladder and ...

Patient-derived Heterogeneous Xenograft Model of Pancreatic Cancer Using Zebrafish Larvae as Hosts for Comparative Drug Assessment

Patient-derived tumor xenograft (PDX) and cell-derived tumor xenograft (CDX) are important techniques for preclinical assessment, medication guidance and basic cancer researches. Generations of PDX models in traditional host mice are time-consuming and only working for a small proportion of samples. Recently, zebrafish PDX (zPDX) has emerged as a unique host system, with the characteristics of small-scale and high efficiency. Here, we describe an optimized methodology for generating a dual fluorescence-labeled tumor xenograft model for comparative chemotherapy assessment in zPDX models. Tumor cells and fibroblasts were enriched from freshly-harvested or frozen pancreatic cancer tissue at different culture conditions. Both cell groups were labeled by lentivirus expressing green or red fluorescent proteins, as well as an anti-apoptosis gene BCL2L1. The transfected cells were pre-mixed and co-injected into the 2 dpf larval zebrafish that were then bred in modified E3 medium at 32 &#176;C. The xenograft models were treated by chemotherapy drugs and/or BCL2L1 inhibitor, and the viabilities of both tumor cells and fibroblasts were investigated simultaneously. In summary, this protocol allows researchers to quickly generate a large amount of zPDX models with a heterogeneous tumor microenvironment and provides a longer observation window and a more precise quantitation in assessing the efficiency of drug candidates.

This protocol describes optimization procedures in a virus-based dual fluorescence-labeled tumor xenograft model using larval zebrafish as hosts. This heterogeneous xenograft model mimics the tissue composition of pancreatic cancer microenvironment in vivo and serves as a more precise tool for assessing drug responses in personalized zPDX (zebrafish patient-derived xenograft) models.

Patient-derived tumor xenograft (PDX) and cell-derived tumor xenograft (CDX) are important techniques for preclinical assessment, medication guidance and ...

A Melanoma Patient-Derived Xenograft Model

Accumulating evidence suggests that molecular and biological properties differ in melanoma cells grown in traditional two-dimensional tissue culture vessels versus in vivo in human patients. This is due to the bottleneck selection of clonal populations of melanoma cells that can robustly grow in vitro in the absence of physiological conditions. Further, responses to therapy in two-dimensional tissue cultures overall do not faithfully reflect responses to therapy in melanoma patients, with the majority of clinical trials failing to show the efficacy of therapeutic combinations shown to be effective in vitro. Although xenografting of melanoma cells into mice provides the physiological in vivo context absent from two-dimensional tissue culture assays, the melanoma cells used for engraftment have already undergone bottleneck selection for cells that could grow under two-dimensional conditions when the cell line was established. The irreversible alterations that occur as a consequence of the bottleneck include changes in growth and invasion properties, as well as the loss of specific subpopulations. Therefore, models that better recapitulate the human condition in vivo may better predict therapeutic strategies that effectively increase the overall survival of patients with metastatic melanoma. The patient-derived xenograft (PDX) technique involves the direct implantation of tumor cells from the human patient to a mouse recipient. In this manner, tumor cells are consistently grown under physiological stresses in vivo and never undergo the two-dimensional bottleneck, which preserves the molecular and biological properties present when the tumor was in the human patient. Notable, PDX models derived from organ sites of metastases (i.e., brain) display similar metastatic capacity, while PDX models derived from therapy naive patients and patients with acquired resistance to therapy (i.e., BRAF/MEK inhibitor therapy) display similar sensitivity to therapy.

Patient-derived xenograft (PDX) models more robustly recapitulate melanoma molecular and biological features and are more predictive of therapy response compared to traditional plastic tissue culture-based assays. Here we describe our standard operating protocol for the establishment of new PDX models and the characterization/experimentation of existing PDX models.

Accumulating evidence suggests that molecular and biological properties differ in melanoma cells grown in traditional two-dimensional tissue culture ...

Establishment of Gastric Cancer Patient-derived Xenograft Models and Primary Cell Lines

The use of preclinical models to advance our understanding of tumor biology and investigate the efficacy of therapeutic agents is key to cancer research. Although there are many established gastric cancer cell lines and many conventional transgenic mouse models for preclinical research, the disadvantages of these in vitro and in vivo models limit their applications. Because the characteristics of these models have changed in culture, they no longer model tumor heterogeneity, and their responses have not been able to predict responses in humans. Thus, alternative models that better represent tumor heterogeneity are being developed. Patient-derived xenograft (PDX) models preserve the histologic appearance of cancer cells, retain intratumoral heterogeneity, and better reflect the relevant human components of the tumor microenvironment. However, it usually takes 4-8 months to develop a PDX model, which is longer than the expected survival of many gastric patients. For this reason, establishing primary cancer cell lines may be an effective complementary method for drug response studies. The current protocol describes methods to establish PDX models and primary cancer cell lines from surgical gastric cancer samples. These methods provide a useful tool for drug development and cancer biology research.

The current protocol describes methods to establish patient-derived xenograft (PDX) models and primary cancer cell lines from surgical gastric cancer samples. The methods provide a useful tool for drug development and cancer biology research.

The use of preclinical models to advance our understanding of tumor biology and investigate the efficacy of therapeutic agents is key to cancer research. ...

Isolation and Characterization of Patient-derived Pancreatic Ductal Adenocarcinoma Organoid Models

Pancreatic ductal adenocarcinoma (PDAC) is amongst the most lethal malignancies. Recently, next-generation organoid culture methods enabling the 3-dimensional (3D) modeling of this disease have been described. Patient-derived organoid (PDO) models can be isolated from both surgical specimens as well as small biopsies and form rapidly in culture. Importantly, organoid models preserve the pathogenic genetic alterations detected in the patient&#39;s tumor and are predictive of the patient&#39;s treatment response, thus enabling translational studies. Here, we provide comprehensive protocols for adapting tissue culture workflow to study 3D, matrix embedded, organoid models. We detail methods and considerations for isolating and propagating primary PDAC organoids. Furthermore, we describe how bespoke organoid media is prepared and quality controlled in the laboratory. Finally, we describe assays for downstream characterization of the organoid models such as isolation of nucleic acids (DNA and RNA), and drug testing. Importantly we provide critical considerations for implementing organoid methodology in a research laboratory.

Patient-derived organoid cultures of pancreatic ductal adenocarcinoma are a rapidly established 3-dimensional model that represent epithelial tumor cell compartments with high fidelity, enabling translational research into this lethal malignancy. Here, we provide detailed methods to establish and propagate organoids as well as to perform relevant biological assays using these models.

Pancreatic ductal adenocarcinoma (PDAC) is amongst the most lethal malignancies. Recently, next-generation organoid culture methods enabling the ...

Establishment and Analysis of Three-Dimensional (3D) Organoids Derived from Patient Prostate Cancer Bone Metastasis Specimens and their Xenografts

Three-dimensional (3D) culture of organoids from tumor specimens of human patients and patient-derived xenograft (PDX) models of prostate cancer, referred to as patient-derived organoids (PDO), are an invaluable resource for studying the mechanism of tumorigenesis and metastasis of prostate cancer. Their main advantage is that they maintain the distinctive genomic and functional heterogeneity of the original tissue compared to conventional cell lines that do not. Furthermore, 3D cultures of PDO can be used to predict the effects of drug treatment on individual patients and are a step towards personalized medicine. Despite these advantages, few groups routinely use this method in part because of the extensive optimization of PDO culture conditions that may be required for different patient samples. We previously demonstrated that our prostate cancer bone metastasis PDX model, PCSD1, recapitulated the resistance of the donor patient&rsquo;s bone metastasis to anti-androgen therapy. We used PCSD1 3D organoids to characterize further the mechanisms of anti-androgen resistance. Following an overview of currently published studies of PDX and PDO models, we describe a step-by-step protocol for 3D culture of PDO using domed or floating basement membrane (e.g., Matrigel) spheres in optimized culture conditions. In vivo stitch imaging and cell processing for histology are also described. This protocol can be further optimized for other applications including western blot, co-culture, etc. and can be used to explore characteristics of 3D cultured PDO pertaining to drug resistance, tumorigenesis, metastasis and therapeutics.

Establishment and Analysis of Three-Dimensional 3D Organoids Derived from Patient Prostate Cancer Bone Metastasis Specimens and their Xenografts

Three-dimensional cultures of patient BMPC specimens and xenografts of bone metastatic prostate cancer maintain the functional heterogeneity of their original tumors resulting in cysts, spheroids and complex, tumor-like organoids. This manuscript provides an optimization strategy and protocol for 3D culture of heterogeneous patient derived samples and their analysis using IFC.

Three-dimensional (3D) culture of organoids from tumor specimens of human patients and patient-derived xenograft (PDX) models of prostate cancer, referred ...

Establishment and Culture of Patient-Derived Breast Organoids

Breast cancer is a complex disease that has been classified into several different histological and molecular subtypes. Patient-derived breast tumor organoids developed in our laboratory consist of a mix of multiple tumor-derived cell populations, and thus represent a better approximation of tumor cell diversity and milieu than the established 2D cancer cell lines. Organoids serve as an ideal in vitro model, allowing for cell-extracellular matrix interactions, known to play an important role in cell-cell interactions and cancer progression. Patient-derived organoids also have advantages over mouse models as they are of human origin. Furthermore, they have been shown to recapitulate the genomic, transcriptomic as well as metabolic heterogeneity of patient tumors; thus, they are capable of representing tumor complexity as well as patient diversity. As a result, they are poised to provide more accurate insights into target discovery and validation and drug sensitivity assays. In this protocol, we provide a detailed demonstration of how patient-derived breast organoids are established from resected breast tumors (cancer organoids) or reductive mammoplasty-derived breast tissue (normal organoids). This is followed by a comprehensive account of 3D organoid culture, expansion, passaging, freezing, as well as thawing of patient-derived breast organoid cultures.

A detailed protocol is provided here for establishing human breast organoids from patient-derived breast tumor resections or normal breast tissue. The protocol provides comprehensive step-by-step instructions for culturing, freezing, and thawing human patient-derived breast organoids.

Breast cancer is a complex disease that has been classified into several different histological and molecular subtypes. Patient-derived breast tumor ...