Skin cancers include carcinomas of all layers of the skin with the most common being basal cell (BCC) and squamous cell carcinomas (SCC). Melanoma and non-melanoma skin cancers (Merkel cell carcinoma, Kaposi sarcoma, cutaneous lymphoma and other sarcomas) are much less common. Of all the skin cancer types, melanoma is a serious form of skin cancer that begins in melanocytes, the melanin-producing neural crest-derived cells located in the bottom layer (the stratum basale) of the skin’s epidermis. While malignant BCC and SCC are rarely metastatic, the less common malignant melanoma, on the other hand, is highly aggressive and spreads rapidly to other parts of the body. Melanomas present in many different shapes, sizes and colors with a comprehensive set of warning signs.
Melanoma is curable, when detected and treated early, with a 98 percent estimated five-year survival rate for U.S. patients. Once melanoma becomes invasive into the skin or other parts of the body, it is more difficult to treat and can be fatal. The American Cancer Society’s estimates for melanoma in the United States for 2019 are about 192,310 new melanomas diagnosed of which 96,480 cases will be invasive, and about 7,230 people are expected to die of melanoma. The rates of melanoma have been rising rapidly over the past few decades and melanoma is one of the most common cancers in young adults (especially young women). Light skin color is a major risk factor for melanoma which is 20 times more common in whites than in African Americans, although no race is immune. The risk for each person can be affected by several factors including exposure to sun, UV light, moles, previous cancers, genetic and familial factors.
Treatment options depend on the stage of the disease, location of the tumor and overall health of the patient, and include surgical removal of the melanoma, immunotherapy, targeted therapy, chemotherapy and radiation. Frequently used single agent therapies target mutations in the B-RAF gene, the C-KIT gene and other abnormal genes. In addition, chemotherapy agents such as dacarbazine, temozolomide, nab-paclitaxel, cisplatin and carboplatin can all be utilized. Clinical trials with immunotherapy agents like IL-2, ipilimumab (CTLA-4 inhibitor), and pembrolizumab and nivolumab (PD-1 inhibitors) are underway and actively recruiting patients. These immunomodulatory drugs are also being tested in the combination setting as well as in neo-adjuvant approaches. Additionally, melanoma vaccines, BCG vaccines for stage III melanomas, and oncolytic viruses (T-VEC) are being tested. New treatment options are focused on improving quality of life and increasing survival rates for patients with advanced melanoma.
The murine B16 melanoma model is the most commonly used metastatic melanoma model for preclinical studies. We have established the syngeneic B16-F10 model to evaluate responses to immuno-oncology agents and support development of novel therapeutics. The B16-F10 cell line was generated as the 10th serial passage subclone of the B16 parent tumor line in C57BL/6 mice. In vitro, these cells grow as an adherent population taking on an epithelial morphology. In vivo, intradermal implant of B16-F10 cells in C57BL/6 mice results in aggressively growing tumors. Our growth studies show efficient growth kinetics following a range of inocula with a doubling time of approximately 2-3 days (Fig. 1). Control animals stay on study for 20-25 days before they reach euthanasia criteria of excessive tumor burden. This results in a model which can facilitate up to a two-week dosing window for test agents to elicit their anti-tumor activity. While the model itself does not result in reduction of body weight, tumor scabbing, and ulcerations are common clinical symptoms associated with subcutaneous and intradermal B16-F10 tumor growth.