SCC-9

Cat.No.: CSC-C9248W

Species: Homo sapiens (Human)

Source: Oral Cavity; Tongue

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  • Background
  • Scientific Data
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Cat.No.
CSC-C9248W
Description
Growth of SCC-9 is enhanced by using a feeder layer of Mitomycin C-treated STO cells
Species
Homo sapiens (Human)
Source
Oral Cavity; Tongue
Recommended Medium
90% EMEM+10% FBS
Disease
Tongue Squamous Cell Carcinoma
Storage and Shipping
liquid nitrogen vapor phase
Synonyms
SCC 9; SCC9
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.

The SCC-9 cell line is a human squamous cell carcinoma cell line originally isolated from tongue carcinoma. SCC-9 cells are commonly used as an in vitro model for oral squamous cell carcinoma (OSCC). These cells are derived from malignant epithelial cells of the oral cavity and have been utilized in numerous studies concerning tumor biology, tumor invasion, and response to treatment in head and neck cancers.

Cultured SCC-9 cells adhere to the growth surface, showing a polygonal, epithelial-like appearance and forming compact colonies characterized by strong cell-cell junctions. Similar to other epithelial-derived and squamous cell carcinoma cells, SCC-9 cells express epithelial markers such as cytokeratins (CK13, CK14), E-cadherin, involucrin, and p63. Expression of epidermal growth factor receptor (EGFR) may also be present but is known to be variable. Dysregulation of EGFR has been shown to play a role in head and neck cancers.

Because of this, SCC-9 cells have been used to study many aspects of oral cancer including proliferation, differentiation, migration, invasion, and epithelial-mesenchymal transition (EMT). These cells are frequently used to study head and neck cancer related signaling pathways such as EGFR, PI3K/AKT, MAPK, and NF-κB and have been used to study mechanisms of tumor metastasis and chemoresistance/radiosensitivity. SCC-9 cells are also utilized for anticancer drug screening assays, radiosensitivity assays, and biomarker identification to aid in the development of targeted therapeutics for oral cancer and head and neck cancers.

Effects of Curcumin on the Viability of SCC-9 Cells

In this study, Udompatankorn et al. investigated the proliferation and apoptosis of SCC-9 oral squamous cell carcinoma (OSCC) cells induced by curcumin and Lactobacillus rhamnosus GG cell-free supernatant (LGG CFS) both alone and in combination.

Curcumin decreased the viability of SCC-9 cells in a dose- and time-dependent manner. Curcumin concentrations ranging from 5 to 20 µg/ml did not markedly decrease the viability of SCC-9 cells after 24 and 48 h. However, treatment with 40 or 80 µg/ml curcumin decreased cell viability after 24 and 48 h (p < 0.05) (Fig. 1). Cell viabilities after treatment with 0, 5, 10, 20, 40, and 80 µg/ml curcumin for 24 h were 97.1%, 94.4%, 91.8%, 66.4%, 27.6%, and 28.2%, respectively, and similar results were obtained after 48 h. Therefore, we selected concentrations of 5 µg/ml (~5% inhibition, referred to as curcumin-L) and 40 µg/ml (>50% inhibition, referred to as curcumin-H) for additional studies with an incubation time of 24 h.

Effects of curcumin on the viability of SCC-9 cells.

Fig. 1. Effects of curcumin on the viability of SCC-9 cells (Udompatankorn C, Ratthawongjirkal P,et al., 2024).

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