U266B1

Cat.No.: CSC-C9138W

Species: Homo sapiens (Human)

Source: Blood; Peripheral Blood

Morphology: round to polygonal

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Cat.No.
CSC-C9138W
Description
Established from the peripheral blood of a 53-year-old man with IgE-secreting myeloma (refractory, terminal) in 1968; cells were described to produce IgE lambda; possible fusion partner for hybridoma production; cells express mRNA for BCL2 gene
Species
Homo sapiens (Human)
Source
Blood; Peripheral Blood
Recommended Medium
Morphology
round to polygonal
Disease
Plasma Cell Myeloma
Storage and Shipping
frozen with 70% medium, 20% FBS, 10% DMSO
Synonyms
U266-B1; U266 B1; U-266; U 266; U266; U266S; U266BL; U266 Bl; 266 Bl
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.

U266B1, also referred to as U-266, is an established human multiple myeloma cell line. It was originally derived from the peripheral blood of a 53-year-old male patient with IgE-producing myeloma. As their name suggests, U266B1 cells are lymphoblast-like in morphology. They proliferate almost exclusively in suspension with minimal attachment to substrata. These cells secrete the cytokine interleukin-6 (IL-6) and immunoglobulin E (IgE) with λ light chains. These cells express classic plasma cell-associated antigens, including CD38, CD44, CD56, syndecan-1 (CD138) and BCMA, while they do not express classical B-cell antigens, such as CD19 and CD20.

Functionally, U266B1 cells exhibit autocrine signaling through IL-6, as these cells grow without exogenous IL-6. The doubling time of these cells has been reported to be approximately 55-144 hours depending on culture conditions. These cells are tumorigenic in vivo, as they engraft and proliferate in immunocompromised mice in either the bone marrow compartment (when given systemically) or as subcutaneous xenografts. The U266B1 cell line is used in multiple myeloma research to model malignant plasma cell biology, IL-6-mediated growth and survival, mechanisms of drug resistance and tumor-microenvironment interactions. U266B1 has also been used as a fusion partner to produce human monoclonal antibodies using hybridoma technology.

Doxorubicin Synergized Bortezomib-Induced Cell Death in U266B1 Cells

Bortezomib is a standard treatment for multiple myeloma (MM) but faces resistance due to aggresome formation, which sequesters misfolded proteins. Here, Yu et al. screened anticancer compounds in U266B1 MM cells to enhance bortezomib efficacy.

They screened various anticancer agents for their potential to enhance bortezomib-induced cell death in the MM cell line U266B1. This included gemcitabine, regorafenib, lenalidomide, pomalidomide, dexamethasone, doxorubicin, EPZ01566, and alisertib. Bortezomib at 6.25 nM caused ~30-40% cell death. Test compounds, each inducing 10-20% cell death, were used alone or with bortezomib. Cell viability was assessed 24 h later using the trypan blue exclusion assay. Results showed that only doxorubicin produced synergistic cell death with bortezomib, evidenced by a significantly higher observed cell death rate (E) compared to the sum of the cell death rates from bortezomib and doxorubicin (T) (Fig. 1). Other compounds either produced an additive effect (E ≈ T) or failed to achieve an additive effect (E < T).

Doxorubicin synergized with bortezomib to induce cell death in U266B1 cells.

Fig. 1. Doxorubicin synergized with bortezomib to induce cell death in U266B1 cells (Yu CT R., Liao YT A, et al., 2024).

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