SCC-4 Cells
545,10 CAD$*
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).
Renseignements généraux
| Description | SCC-4 is a human tongue squamous cell carcinoma (SCC) cell line widely used in cancer research to explore mechanisms of oral cancer progression, apoptosis, and response to chemotherapeutic agents. Oral squamous cell carcinoma is a common malignancy in the oral cavity and is often linked to lifestyle factors such as tobacco use and alcohol consumption. SCC-4 cells are characterized by their aggressive nature and are used to model tumor behavior and treatment resistance in vitro. Studies using SCC-4 have shown that several compounds, such as rhein, emodin, and berberine, induce apoptosis through both intrinsic (mitochondria-dependent) and extrinsic (death receptor-mediated) pathways. Rhein induces S-phase cell cycle arrest and apoptosis through endoplasmic reticulum stress, ROS generation, and mitochondrial dysfunction, triggering the activation of caspase-8, -9, and -3. Similarly, emodin was shown to cause G2/M-phase arrest and induce apoptosis by disrupting mitochondrial membrane potential and promoting cytochrome c release. Berberine also induces apoptosis in SCC-4 cells by enhancing ROS production, increasing intracellular Ca2+, and decreasing mitochondrial membrane potential, thereby activating caspase-9 and caspase-3 pathways. These findings demonstrate that SCC-4 is an effective model for studying the molecular mechanisms of apoptosis in response to potential anticancer agents, providing insight into therapeutic strategies targeting oral squamous cell carcinoma. |
|---|---|
| Organisme | Human |
| Tissu | Tongue |
| Maladie | Squamous cell carcinoma |
| Synonymes | SCC 4, SCC4 |
Caractéristiques
| Âge | 55 years |
|---|---|
| Genre | Male |
| Origine ethnique | Caucasian |
| Morphologie | Epithelial-like |
| Propriétés de croissance | Adherent |
Données réglementaires
| Référence | SCC-4 (Cytion catalog number 305384) |
|---|---|
| Niveau de biosécurité | 1 |
| NCBI_Numéro d'identification fiscale | 9606 |
| Cellosaurus - Numéro d'enregistrement | CVCL_1684 |
Données biomoléculaires
| Profil mutationnel | Mutation: TP53, p.Pro151Ser (c.451C>T) |
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Manipulation
| Milieu de culture | DMEM:Ham's F12 (1:1), w: 3.1 g/L Glucose, w: 2.5 mM L-Glutamine, w: 15 mM HEPES, w: 0.5 mM Sodium pyruvate, w: 1.2 g/L NaHCO3 (Cytion article number 820400a) |
|---|---|
| Suppléments | Supplement the medium with 10% FBS and 400 ng/mL hydrocortisone |
| Réactif de dissociation | Accutase |
| Repiquage | 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. |
| Milieu de congélation | 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. |
| Décongélation et culture des cellules |
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| Atmosphère d'incubation | 37°C, 5% CO2, humidified atmosphere. |
| Conditions d'expédition | 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. |
| Conditions d'entreposage | 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. |
Contrôle de la qualité et analyse moléculaire
| Stérilité | 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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Certificat d'analyse (CoA)
| Numéro de lot | Type de certificat | Date | Numéro de catalogue |
|---|---|---|---|
| 305384-021024 | Certificat d'analyse | 05. Dec. 2025 | 305384 |
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