SUP-B15 Cells
General information
| Description | SUP-B15 is a human B-cell precursor acute lymphoblastic leukemia (BCP-ALL) cell line derived from the bone marrow of a child with Philadelphia chromosome-positive (Ph+) ALL. It is characterized by the presence of the BCR-ABL1 fusion gene, resulting from the t(9;22)(q34;q11) chromosomal translocation, which is a hallmark of Ph+ ALL. This translocation leads to the production of the constitutively active BCR-ABL1 tyrosine kinase, driving leukemogenesis by promoting uncontrolled proliferation and inhibiting apoptosis. As a result, SUP-B15 has been widely utilized in leukemia research, particularly for studying the molecular mechanisms underlying Ph+ ALL and for testing tyrosine kinase inhibitors (TKIs) such as imatinib and dasatinib. Studies have shown that SUP-B15 cells exhibit overexpression of the MDM2 gene, which negatively regulates the tumor suppressor protein p53. This overexpression occurs despite the presence of wild-type p53, suggesting that MDM2-mediated inactivation of p53 contributes to leukemic cell survival. The deregulation of p53 signaling in SUP-B15 and other BCP-ALL cell lines highlights potential therapeutic vulnerabilities, particularly for MDM2 inhibitors that aim to restore p53 function and induce apoptosis in leukemic cells. Comprehensive genomic and transcriptomic profiling of SUP-B15 has provided additional insights into its molecular landscape. Whole-exome and RNA sequencing studies have identified mutations and gene expression patterns associated with leukemia progression and drug resistance. In pharmacogenomic analyses, SUP-B15 has been included in large-scale drug sensitivity screening efforts, such as those conducted in the Cancer Cell Line Encyclopedia (CCLE). These studies have helped define its responsiveness to various targeted therapies, including TKIs and other small-molecule inhibitors. Given its well-characterized genetic background and clinical relevance, SUP-B15 remains a crucial model for preclinical leukemia research and drug development. |
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| Organism | Human |
| Tissue | Bone marrow |
| Disease | Acute lymphoblastic leukemia ALL |
| Applications | 3D cell culture, Immune system disorder research, Immunology |
| Synonyms | Sup-B15, SUPB-15, SUPB15, SupB15, SupB15W, SupB15WT |
Characteristics
| Age | 8 years |
|---|---|
| Gender | Male |
| Ethnicity | Caucasian |
| Morphology | Lymphoblast |
| Cell type | B lymphoblast |
| Growth properties | Suspension |
Regulatory Data
| Citation | SUP-B15 (Cytion catalog number 305385) |
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| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_0103 |
Biomolecular Data
| Protein expression | Immunoglobulin (cytoplasmic) |
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| Antigen expression | CD1a -; CD2 -; CD3 -; CD4 -; CD5 -; CD8 -; CD10 +; CD13 +; CD38 +; CD71 +; HLA DR + |
| Mutational profile | Gene Fusion: ABL1 + HGNC, HGNC:1014, BCR, Name(s)=BCR-ABL1, BCR-ABL, Note=BCR exon 1 fused to ABL1 exon 2 (e1a2 transcript) |
| Karyotype | 46, XY; the following markers are present: t(9;22)(q34;q11), t(4;14) (p11;q24), der(4)t(1;4) (p11;q33), t(9;22) (q34;q11), der(10)t(3;10) (q25;q26), add(16); Philadelphia chromosome is present. |
Handling
| Culture Medium | IMDM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 25 mM HEPES, w: 1.0 mM Sodium pyruvate, w: 3.024 g/L NaHCO3 (Cytion article number 820800a) |
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| Supplements | Supplement the medium with 20% FBS and 0.05 mM 2-mercaptoethanol |
| Doubling time | 18 hours |
| Seeding density | 2 to 4 X 105 cells/mL |
| 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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Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 305385-080626 | Certificate of Analysis | 23. Jul. 2026 | 305385 |