8305C

Cat.No.: CSC-C0290

Species: Homo sapiens (Human)

Source: Thyroid Gland

Morphology: adherent, large spindle-shaped cells growing as monolayer

Culture Properties: monolayer

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Cat.No.
CSC-C0290
Description
Established from the primary tumor of a 67-year-old woman with primary thyroid carcinoma (undifferentiated carcinoma, composed of spindle, polygonal and giant cells)
Species
Homo sapiens (Human)
Source
Thyroid Gland
Recommended Medium
80-90% RPMI-1640 + 10-20% h.i. FBS
Culture Properties
monolayer
Morphology
adherent, large spindle-shaped cells growing as monolayer
Karyotype
Human flat-moded hypertriploid karyotype with 22% polyploidy - 74(67-76)<3n>XXX, -2, +9, -10, -12, -13, +14, +15, +15, +18, -19, +20, +4mar, 1-20 dm in most cells, der(6)t(6;7)(q22;q36q11.23), add(15)(p11)x2, del(17)(p12)x2 - subclonal rearrangements, e.g
Disease
Thyroid Gland Anaplastic Carcinoma
Quality Control
Mycoplasma: negative in DAPI, microbiological culture, RNA hybridization assays
Immunology: cytokeratin +, cytokeratin-7 +, cytokeratin-8 +, cytokeratin-17 -, cytokeratin-18 +, cytokeratin-19 -, desmin -, endothel -, EpCAM -, GFAP +, neurofilament -, thyr
Storage and Shipping
Frozen with 70% medium, 20% FBS, 10% DMSO at about 1 x 10^6 cells/ampoule; ship in dry ice; store in liquid nitrogen
Synonyms
8305c; 8305-C; 8305C_1
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.

8305C is a human cell line that was developed from an anaplastic thyroid carcinoma (ATC) tumor. ATC is a rare, undifferentiated, and highly aggressive form of thyroid cancer with poor differentiation and resistance to most forms of treatment. This cell line was originally derived from a thyroid tumor sample that was taken from a 67-year-old woman with ATC. 8305C cells show epithelial-like morphology with significant pleomorphism, a common feature of malignancy, and are adherent cells that grow in standard cell culture media.

8305C cells lose common thyroid features, such as iodine uptake, with dedifferentiation but retain a high proliferative and invasive potential, similar to ATC in the clinic. This cell line is used to study the molecular basis of tumor progression, metastasis, and drug and radiation resistance, including to targeted agents such as tyrosine kinase inhibitors (TKIs). It has also been used to define the signaling pathways (e.g., PI3K/AKT, MAPK) involved in the pathogenesis of ATC and its aggressive clinical course.

8305C's rapid growth rate and genetic stability have made it a widely used cell line for drug screening assays, apoptosis studies, and molecular profiling, which have led to the development of novel anticancer therapies. The 8305C cell line has also been used in radiation biology studies due to its relative radioresistance, which can provide insights into strategies to increase the efficacy of this treatment modality. Overall, 8305C continues to be an important tool in the study of thyroid cancer and has contributed to many translational and clinical advances in this deadly disease.

TF Containment of the Malignant Tumor Phenotype of 8305C Cells

Anaplastic thyroid cancer (ATC) is a rare but extremely aggressive type of thyroid cancer derived from follicular cells of the thyroid gland. Theaflavin (TF) has anti-cancer effects; however, no study has examined whether TF inhibits the malignant progression of ATC. Therefore, Cai's team explored the effects of TF on ATC and to provide a preliminary exploration of its mechanism.

As Figure 1 shows, TF dose-dependently inhibited 8305C growth: viability fell from 100% to 12.01% after 48 h, IC50 = 21.79 µg/mL; 11 µg/mL (½ IC50) was used hereafter (Fig. 1A). CCK-8 assay was used to detect the cell viability and cell proliferation ability of the control and TF cells at 24, 48, 72, 96, and 120 h (Fig. 1B). The effects of TF on 8305C cell migration and invasion were examined by transwell assay. In the transwell chamber, the number of cells migrating to the bottom side of the membrane in the TF-treated group was significantly inhibited compared to that of the control group (Fig. 1C and D). The invasion experiment results also showed that TF inhibited the invasive behavior of the 8305C cells (Fig. 1E and F). Flow cytometry was used to detect the level of cell apoptosis (Fig.1G and H). Compared with the control group, the level of cell apoptosis in the TF group was significantly increased after 48 h.

TF containment of the malignant tumor phenotype of 8305C cells.

Fig. 1. TF containment of the malignant tumor phenotype of 8305C cells (Cai S J, Zhang L Y, et al., 2025).

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