A protocol to co-inject cancer cells and fibroblasts and monitor tumor growth over time is provided. This protocol can be used to understand the molecular basis for the role of fibroblasts as regulators of tumor growth.
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Method Article
A protocol to co-inject cancer cells and fibroblasts and monitor tumor growth over time is provided. This protocol can be used to understand the molecular basis for the role of fibroblasts as regulators of tumor growth.
Cancer-associated fibroblasts (CAFs) can play an important role in tumor growth by creating a tumor-promoting microenvironment. Models to study the role of CAFs in the tumor microenvironment can be helpful for understanding the functional importance of fibroblasts, fibroblasts from different tissues, and specific genetic factors in fibroblasts. Mouse models are essential for understanding the contributors to tumor growth and progression in an in vivo context. Here, a protocol in which cancer cells are mixed with fibroblasts and introduced into mice to develop tumors is provided. Tumor sizes over time and final tumor weights are determined and compared among groups. The protocol described can provide more insight into the functional role of CAFs in tumor growth and progression.
Within the tumor microenvironment, one of the most prominent cell type is the cancer-associated fibroblast (CAF)1. These carcinoma-associated fibroblasts can play a tumor-suppressive role2,3. For example, S100A-expressing fibroblasts secrete collagens that can encapsulate carcinogens and protect against carcinoma formation4. Further, depletion of α-smooth muscle actin (SMA)-positive myofibroblasts in pancreatic cancer causes immunosuppression and accelerates pancreatic cancer progression2. CAFs can also co-evolve with cancer cells and....
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All experiments described were approved by the Animal Care Committee at the University of California, Los Angeles.
NOTE: Select cancer cells and fibroblasts that match the host mice for mouse strain. Select cancer cells and fibroblasts that match the sex of the host mouse. Obtain mice from breeding colonies or purchase them from reputable vendors. Introduce tumors into mice that are ~8-10 weeks of age. Mice with fur will be in the telogen or resting phase of the hair follicle cycle. Plan for a ratio of 0.5 to 3 fibroblasts to cancer cell.
1. Determine the appropriate number of mice to be used for experimentation
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A2058 human melanoma cells and primary human dermal fibroblasts were cultured under sterile conditions. Cells were collected and washed three times with PBS. Immunodeficient mice (NU/J - Foxn1 nude strain) were injected subcutaneously on one flank with 0.25 million A2058 melanoma cells alone. On the other flank, mice were injected with a mixture of 0.25 million A2058 melanoma cells and 0.75 million fibroblasts. Cells were injected into 12 immune-deficient mice. Injections into left and ri.......
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In the experiment in Figure 1, co-introducing human dermal fibroblasts with human A2058 melanoma cells resulted in larger tumors than when the melanoma cells were introduced without co-injected fibroblasts. This difference could be easily detected based on tumor volume and tumor weight. The results are consistent with multiple reports that cancer-associated fibroblasts can promote tumor growth5,6,7
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The authors have nothing to disclose.
The authors would like to acknowledge all of the members of the Coller laboratory for helpful input. H.A.C. was the Milton E. Cassel scholar of the Rita Allen Foundation. We acknowledge NIH/NCI 1 R01 CA221296-01A1, NIH 1 R01 AR070245-01A1, Melanoma Research Alliance Team Science Award, Cancer Research Institute Clinical Laboratory Integration Program Award, the Iris Cantor Women's Health Center/UCLA CTSI NIH Grant UL1TR000124, University of California Cancer Research Coordinating Committee, David Geffen School of Medicine Metabolism Theme Award, the Clinical Translational Science Institute and Jonsson Comprehensive Cancer Center, Innovation Awards from the Broad S....
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| Name | Company | Catalog Number | Comments |
|---|---|---|---|
| 26G Needles | Fisher Scientific | 14-826-10 | |
| Alcohol swabs | Fisher Scientific | 326895 | |
| Animal clipper miniARCO with surgical blade #40 | WAHL Professional | 8787-450A | |
| Athymic nude mice (NU/J) | The Jackson labs | 002019 | These mice are immunocompromised and can be used for experiments in which human cells are introduced. Immunocompetent mice can also be used if mouse cancer cells and fibroblasts will be introduced. |
| Cancer cells | ATCC | ATCC® CRL-11147™ | This is the catalog number for a primary human melanoma cell line. Other cancer cell types can also be used. |
| Cell Culture Multi Flasks | Fisher Scientific | 14-826-95 | |
| Centrifuge for conical tubes capable of reaching 180 x g | Fisher Scientific | 14-432-22 | |
| Countess Cell Counting Chamber | Fisher Scientific | C10228 | |
| Dulbecco's Modified Eagle Medium | Fisher Scientific | 11965-118 | |
| Fetal bovine serum | Fisher Scientific | MT35010CV | |
| Fibroblasts | ATCC | PCS-201-012 | We isolate fibroblasts from skin in our lab. This is a catalog number for an adult primary human dermal fibroblast cell line. MEFs and fibroblasts derived from other sites can also be used. |
| Isoflurane | Henry Schein Animal Health | NDC 11695-6776-2 | |
| PBS USP grade for injection into mice | Fisher Scientific | 50-751-7476 | |
| Sterile 10 ml serological pipet | Celltreat | 667210B | |
| Sterile 5 ml serological pipet | Celltreat | 229005B | |
| Sterile 50 ml centrifuge tubes | Genesee Scientific | 28-108 | |
| Sterile Syringe Filters pore size 0.2 microns | Fisher Scientific | 09-740-61A | |
| Sterile tissue culture-grade Trypsin-EDTA | Fisher Scientific | 15400054 | |
| Sterile tissue-culture grade PBS | Fisher Scientific | 50-751-7476 | |
| Sterle 25 ml serological pipet | Celltreat | 667225B | |
| TC treated 100 x 20 mm dishes | Genesee Scientific | 25-202 | |
| TC treated 150 x 20 mm dishes | Genesee Scientific | 25-203 | |
| TC treated 60 x 15 mm dishes | Genesee Scientific | 25-260 | |
| Trypan blue | Fisher Scientific | C10228 |
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