SK-UT-1 Cells
USD$395.00*
Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 106 cells for adherent lines or 5 × 106 cells for suspension lines (refer to the batch CoA for details).
General information
| Description | The SK-UT-1 cell line is derived from human uterine leiomyosarcoma (ULMS), a highly aggressive form of cancer originating in the smooth muscle of the uterus. This cell line is a key model for studying tumorigenesis, metastasis, and drug resistance in ULMS. SK-UT-1 cells exhibit features of sarcomas, including rapid proliferation, poor differentiation, and resistance to conventional therapies. In particular, they are used to investigate cancer stem-like cells (CSCs), which play a significant role in cancer recurrence and resistance to chemotherapy. Research has identified a subpopulation of CD133+ CSCs within SK-UT-1 cells, which demonstrate enhanced self-renewal, colony formation, and resistance to apoptosis. Studies using SK-UT-1 have focused on characterizing the CD133+ CSCs, revealing their ability to form tumorspheres, a feature indicative of stem cell-like behavior. This subpopulation shows increased tumorigenic potential in vivo, where even a small number of cells (104) are sufficient to initiate tumor formation in xenograft models. The CD133+ cells exhibit resistance to chemotherapeutic agents such as doxorubicin, which further supports their role in therapy resistance. Additionally, elevated levels of CSC-related markers, including CD44, ALDH1, and BMI1, were found in CD133+ cells compared to their CD133− counterparts, confirming their role as cancer stem cells. SK-UT-1 cells have become a vital tool in understanding ULMS progression and in developing potential therapeutic strategies. Targeting the CD133+ cancer stem-like cell population within these tumors may offer a promising approach to improve outcomes in patients with ULMS by addressing the root causes of metastasis and chemoresistance. |
|---|---|
| Organism | Human |
| Tissue | Uterine |
| Disease | Mixed mesodermal tumor, consistent with leiomyosarcoma (grade III) |
| Synonyms | SK UT 1, SKUT-1, SKUT1, Skut1 |
Characteristics
| Age | 75 years |
|---|---|
| Gender | Female |
| Ethnicity | Caucasian |
| Morphology | Epithelial-like |
| Growth properties | Adherent |
Regulatory Data
| Citation | SK-UT-1 (Cytion catalog number 300455) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_0533 |
Biomolecular Data
| Isoenzymes | Me-2, 1-2, PGM3, 1, PGM1, 1, ES-D, 1, AK-1, 1, GLO-1, 1-2, G6PD, B. |
|---|---|
| Tumorigenic | Yes, in nude mice. Forms spindle cell sarcoma |
| Karyotype | (P8) hypodiploid to hyperdiploid. Phenotype Frequency Product: 0.0590 |
Handling
| Culture Medium | EMEM (MEM Eagle), w: 2 mM L-Glutamine, w: 2.2 g/L NaHCO3, w: EBSS (Cytion article number 820100a) |
|---|---|
| Supplements | Supplement the medium with 10% FBS and 1% NEAA |
| Dissociation Reagent | Accutase |
| Subculturing | Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium. |
| Seeding density | 1 x 104 cells/cm2 |
| Fluid renewal | 2 times per week |
| Freeze medium | As a cryopreservation medium, we use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress. |
| Thawing and Culturing Cells |
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| Incubation Atmosphere | 37°C, 5% CO2, humidified atmosphere. |
| Shipping Conditions | Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage. |
| Storage Conditions | For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen. |
Quality Control & Molecular Analysis
| Sterility | Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods. To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections. |
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Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 300455-290825 | Certificate of Analysis | 05. Dec. 2025 | 300455 |
| 300455-413 | Certificate of Analysis | 23. May. 2025 | 300455 |