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SK-UT-1
Tissue
Uterine
Disease
Mixed mesodermal tumor, consistent with leiomyosarcoma (grade III)
Synonyms
SK UT 1, SKUT-1, SKUT1, Skut1

Documents

SK-UT-1

Cell line · Product number 300455

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 uter...

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01General 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.

Tissue
Uterine
Disease
Mixed mesodermal tumor, consistent with leiomyosarcoma (grade III)
Synonyms
  • SK UT 1
  • SKUT-1
  • SKUT1
  • Skut1

02Classification

Organism
Human
Sex
Female
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
Epithelial-like
Tumourigenic
Yes, in nude mice. Forms spindle cell sarcoma
Karyotype
(P8) hypodiploid to hyperdiploid. Phenotype Frequency Product: 0.0590

04Identifiers

Citation
SK-UT-1 (Cytion catalog number 300455)
NCBI TaxID
9606
Cellosaurus
CVCL_0533

05Expression and susceptibility

Isoenzymes
Me-2, 1-2, PGM3, 1, PGM1, 1, ES-D, 1, AK-1, 1, GLO-1, 1-2, G6PD, B.

06Handling and culture

Culture medium
EMEM (MEM Eagle), w: 2 mM L-Glutamine, w: 2.2 g/L NaHCO3, w: EBSS (Cytion article number 820100a)
Incubation atmosphere

37°C, 5% CO2, humidified atmosphere.

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
Thawing and culturing
  1. Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.

  2. Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required.

  3. For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains.

  4. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.

  5. Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently.

  6. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.

  7. Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks; for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth.

  8. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.

07Quality control and cryopreservation

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.

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.
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.

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.

08Donor

Donor age
75 years
Ethnicity
Caucasian