SK-MEL-3

Cat.No.: CSC-C0099

Species: Homo sapiens (Human)

Source: Lymph Node Metastasis

Morphology: adherent epithelial cells growing as monolayer

Culture Properties: monolayer

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Cat.No.
CSC-C0099
Description
Established from the lymph node metastasis of a malignant melanoma from a 42-year-old Caucasian woman
Species
Homo sapiens (Human)
Source
Lymph Node Metastasis
Recommended Medium
Culture Properties
monolayer
Morphology
adherent epithelial cells growing as monolayer
Karyotype
Human near-tetraploid karyotype with 3% polyploidy - 92(80-93)<4n>XX, -X, -X, -6, +7, +7, +7, -10, -10, -16, -16, +20, +20, +20, +20, +22, dup(7)(p15p22)x2, der(9)t(7;9)(p11;p21)dup(7)(p15p22)x2 - sideline with add(2)(p23) marker - resembles published kar
Disease
Cutaneous Melanoma
Quality Control
Mycoplasma: negative in DAPI, microbiological culture, RNA hybridization assays
Immunology: cytokeratin -, desmin -, endothel -, EpCAM -, GFAP -, HMB-45 +, neurofilament -, vimentin +
Viruses: ELISA: reverse transcriptase negative; PCR: EBV -, HBV -, HCV
Storage and Shipping
Frozen with 70% medium, 20% FBS, 10% DMSO at about 2 x 10^6 cells/ampoule; ship in dry ice; store in liquid nitrogen
Synonyms
SK-Mel-3; Sk-mel-3; SK-MEL3; SK-Mel3; SKMEL3
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

SK-MEL-3 is a human malignant melanoma cell line, derived from a lymph node metastasis of a patient with cutaneous melanoma. It is one of the related lines in the famous SK-MEL cell series. The cells are in the late stage of melanoma and still have a lot of phenotypic and molecular traits similar to metastatic disease.

At the molecular and immunophenotypic level, SK-MEL-3 cells express the melanoma-associated antigens MART-1 (Melan-A), gp100 (PMEL), and tyrosinase and have been used widely in immunologic studies of melanoma. At the genetic level, this cell line also shares a number of alterations with melanoma in general, such as aberrant MAPK pathway activation, leading to increased proliferation and survival of these cells. Functionally, SK-MEL-3 cells show malignant phenotypes, such as high proliferative capacity and invasive growth. Expression of the tumor-associated antigens MART-1, gp100, and tyrosinase in these cells has made this cell line particularly useful in studies of tumor immunogenicity, tumor antigen presentation, and immune-mediated killing of tumor cells. The SK-MEL-3 cell line is commonly used to study immune checkpoint signaling, cancer vaccines, and adoptive cell therapies as well as for preclinical testing of targeted and immunotherapeutic drugs.

Anticancer Activity of CuO/TiO2-chitosan-farnesol NCs

This investigation synthesizing copper oxide (CuO)-titanium oxide (TiO2)-chitosan-farnesol nanocomposites with potential antibacterial, antifungal, and anticancer properties against Melanoma cells (melanoma cells [SK-MEL-3]).

SK-MEL-3 cells were first treated with CuO/TiO2-chitosan-farnesol nanocomposites using MTT assays to determine cytotoxic effect. The IC50 was determined to be 10 and 12.5 µg/mL. IC50 values were used in all subsequent experiments to evaluate the anticancer efficacy (Fig. 1a and b). SK-MEL-3 cells were then treated with CuO/TiO2-chitosan-farnesol nanocomposites at 12.5 and 15 µg/mL for 24 h. Cells were then fixed, stained, and visualized with a fluorescence microscope. Treated cells had significantly higher AO/ETBR staining than control cells (p < 0.05) indicating greater cell damage (Fig. 2a and b). SK-MEL-3 cells were treated with CuO/TiO2-chitosan-farnesol nanocomposites (12.5 and 15 µg/mL) in the dark for 24 hours. ROS production was significantly higher in treated cells between 6 and 12 hours (p < 0.05), while control cells produced little to no ROS. ROS analysis was done three times, with the average data shown in a bar graph (Fig. 3a and b).

shows CuO/TiO2-chitosan-farnesol nanocomposites on the viability of SK-MEL-3 and L929 cells through MTT assay.

Fig. 1. shows CuO/TiO2-chitosan-farnesol nanocomposites on the viability of SK-MEL-3 and L929 cells through MTT assay (Indumathi T, Suriyaprakash J, et al., 2023).

CuO/TiO2-chitosan-farnesol nanocomposites on the apoptosis in the melanoma cells (SK-MEL-3) cells.

Fig. 2. CuO/TiO2-chitosan-farnesol nanocomposites on the apoptosis in the melanoma cells (SK-MEL-3) cells (Indumathi T, Suriyaprakash J, et al., 2023).

CuO/TiO2-chitosan-farnesol nanocomposites on the intracellular reactive oxygen species generation in the melanoma cells (SK-MEL-3) cells.

Fig. 3. CuO/TiO2-chitosan-farnesol nanocomposites on the intracellular reactive oxygen species generation in the melanoma cells (SK-MEL-3) cells (Indumathi T, Suriyaprakash J, et al., 2023).

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