GIST-T1 Cells
CAD$966.00*
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).
General information
| Description | The GIST-T1 cell line is a well-established human gastrointestinal stromal tumor (GIST) model derived from a metastatic pleural lesion secondary to a primary gastric GIST in an adult Japanese woman. Immunohistochemical analyses confirmed strong positivity for c-KIT (CD117) and CD34, two hallmark markers of GIST, while the line was negative for desmin, S-100, and α-smooth muscle actin, confirming its non-muscle and non-neural origin. Cytogenetic studies revealed a hypodiploid karyotype with complex chromosomal abnormalities, including a ring chromosome and several unbalanced translocations. Comparative genomic hybridization (CGH) and FISH analyses showed high-level amplifications at 3q26.1-27, 5p12-15.1, and 7q21.3-36-regions often associated with oncogene amplification in GIST. GIST-T1 harbors a clinically relevant 57-nucleotide in-frame deletion in exon 11 of the *KIT* gene (V570-Y578), one of the most common mutations in GIST patients and a critical target of tyrosine kinase inhibitors such as imatinib. This has made GIST-T1 an essential model for studying KIT-driven oncogenesis and therapeutic response. In long-term culture, GIST-T1 cells show stable proliferation and retain sensitivity to imatinib unless specifically selected for resistance. Derivative resistant sublines of GIST-T1 have been generated for research purposes and exhibit secondary KIT mutations (e.g., D820V or D820Y), enabling the study of resistance mechanisms and adaptive transcriptional changes. These resistant models show alterations in genes related to detoxification, cell cycle regulation, and apoptosis evasion. GIST-T1 has also contributed to the discovery of novel oncogenic drivers in GIST, including fusion genes such as EXOC2-AK7, identified in imatinib-resistant sublines. Functional studies demonstrated that these fusion genes enhance proliferative and migratory capacities of GIST cells and sensitize them to imatinib, pointing toward new therapeutic avenues. The presence of GIST-associated super-enhancers and transcription factor networks (e.g., HAND1 in metastatic progression) further reinforces the model’s utility in deciphering the epigenetic and transcriptional architecture of GIST. Altogether, GIST-T1 provides a robust, genetically and phenotypically validated system for studying the biology, drug response, and resistance mechanisms of gastrointestinal stromal tumors. |
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| Organism | Human |
| Tissue | Metastatic |
| Disease | Gastrointestinal stromal tumor |
| Metastatic site | Pleural effusion |
| Synonyms | GIST-T-1, GISTT1, T1 |
Characteristics
| Age | 47 years |
|---|---|
| Gender | Female |
| Ethnicity | Japanese |
| Cell type | Interstitial cell of Cajal |
| Growth properties | Adherent |
Regulatory Data
| Citation | GIST-T1 (Cytion catalog number 305777) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_4976 |
Biomolecular Data
| Mutational profile | Mutation: KIT, Simple, p.Val560_Tyr578del (c.1679_1735del), Heterozygous |
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Handling
| Culture Medium | RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a) |
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| Supplements | Supplement the medium with 10% FBS |
| Dissociation Reagent | Accutase |
| Doubling time | 48 hours |
| Seeding density | 1 to 4 x 104 cells/cm2 |
| Fluid renewal | 2 to 3 times per week |
| 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. |
| 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. |
Quality Control & Molecular Analysis
| 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. |
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| Metastatic site: | Pleural effusion |
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Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 305777-090326 | Certificate of Analysis | 08. Apr. 2026 | 305777 |