UM-SCC-112 Cells
General information
| Description | UM-SCC-112 is a human head and neck squamous cell carcinoma (HNSCC) cell line established at the University of Michigan Head and Neck Oncology laboratory as part of the UM-SCC panel. The UM-SCC series represents one of the most extensively characterized and widely distributed HNSCC cell line collections in the world, derived from patients with oral cavity, laryngeal, hypopharyngeal, and oropharyngeal squamous cell carcinomas treated at the University of Michigan Medical Center. UM-SCC-112 grows as an adherent monolayer with epithelial-like morphology and is used as part of a multi-line panel for comprehensive preclinical characterization of HNSCC biology. UM-SCC-112 is applicable in studies of HNSCC biology, drug sensitivity and resistance, radiation response, EGFR and other signalling pathway analyses, and comparative molecular characterization within the UM-SCC panel. The line is suitable for pharmacological assays, invasion and migration studies, and xenograft models in immunocompromised hosts. Site-specific and donor-specific details for UM-SCC-112 should be verified from the University of Michigan SPORE Tissue Core for the most current annotations. |
|---|---|
| Organism | Human |
| Tissue | Head and neck, oral cavity |
| Disease | Head and neck squamous cell carcinoma (HNSCC) |
| Applications | HNSCC research; drug sensitivity and resistance; radiation response; EGFR signalling; UM-SCC panel studies; invasion and migration assays; xenograft models |
Characteristics
| Age | Age unspecified |
|---|---|
| Gender | Sex unspecified |
| Ethnicity | Ethnicity unspecified |
| Morphology | Epithelial-like |
| Cell type | Epithelial cells |
| Growth properties | Adherent |
Regulatory Data
| Citation | UM-SCC-112 (Cytion catalog number 305720) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
Biomolecular Data
Handling
| Culture Medium | DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a) |
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| Supplements | Supplement the medium with 10% FBS and 1% non-essential amino acids (NEAA) |
| Dissociation Reagent | Accutase |
| Doubling time | approx. 24 to 48 hours |
| Subculturing | Remove medium, wash with PBS without calcium and magnesium, cover with Accutase, incubate 8–10 min at RT, resuspend in medium, centrifuge 300×g 3 min, discard supernatant, reseed in fresh medium. |
| Split ratio | 1 to 5 |
| Seeding density | 1 to 3 × 10⁴ cells/cm² |
| Fluid renewal | Every 2 to 3 days |
| Freeze medium | As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability. |
| 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. |