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Luciferase Reporter Cell Line - U251MG

For research use only. Not intended for any clinical use.

Cat. No. :   CSC-RR00719

Host Cell :   U251MG Size :   >1x106 frozen cells/vial

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Cell Line Information

Cell Culture Information

Safety and Packaging

Gene Information

Cat. No. CSC-RR00719
Description U251MG-Luc reporter cell line is engineered to stably express Luciferase reporter gene in U251MG cell line.
Target Gene Luciferase
Host Cell U251MG
Host Cell Species Homo sapiens (Human)
Applications

1. Gene expression studies

2. Protein localization

3. Drug screening and toxicology

4. Live cell imaging

Size >1x106 frozen cells/vial
Stability Validated for at least 10 passages
Quality Control Negative for bacteria, yeast, fungi and mycoplasma.
Storage Liquid nitrogen
Shipping Dry ice
Revival Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into a 25 cm2 flask containing pre-warmed media.
Mycoplasma Negative
Format One frozen vial containing millions of cells
Storage Liquid nitrogen
Safety Considerations The following safety precautions should be observed.
1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum.
2. No eating, drinking or smoking while handling the stable line.
3. Wash hands after handling the stable line and before leaving the lab.
4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells.
5. All waste should be considered hazardous.
6. Dispose of all liquid waste after each experiment and treat with bleach.
Ship Dry ice
Target Gene Luciferase
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Background

Case Study

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Customer Reviews

U251MG cells are a human glioblastoma multiforme (GBM)-derived cell line widely used as an in vitro model for studying aggressive brain tumor biology and glioma progression. These cells are characterized by high proliferative capacity, invasive behavior, and genetic alterations commonly associated with high-grade gliomas, including dysregulation of pathways involved in cell survival, migration, angiogenesis, and resistance to therapy. U251MG cells exhibit mesenchymal-like features and are frequently used to model the highly heterogeneous and treatment-resistant nature of glioblastoma. The Luciferase Reporter Cell Line – U251MG is generated through stable integration of a luciferase reporter construct driven by pathway-responsive elements or specific transcription factor–binding promoters into the parental U251MG background, enabling real-time, quantitative monitoring of transcriptional and signaling activities while maintaining the intrinsic biological characteristics of the original glioma cell line.

The Luciferase Reporter Cell Line – U251MG is widely applied in neuro-oncology research, drug screening, and signaling pathway analysis in glioblastoma. It is particularly useful for studying key oncogenic and tumor microenvironment–related pathways, including NF-κB, STAT3, PI3K/AKT/mTOR, MAPK/ERK, and hypoxia-inducible factor (HIF) signaling, all of which contribute to tumor growth, immune evasion, and therapeutic resistance. The luciferase reporter system provides a sensitive and quantitative readout for evaluating pathway modulation in response to pharmacological compounds, biologics, or genetic interventions. This model is commonly used in high-throughput screening of anti-glioma agents, as well as in mechanistic studies of tumor invasion, stemness, and resistance to radiotherapy or chemotherapy. Its robustness, reproducibility, and strong signal sensitivity make it a valuable tool for both fundamental research and preclinical development of targeted therapies for glioblastoma.

Here, researchers explored the use of convection-enhanced delivery (CED) technology to treat orthotopic U251-Luc glioblastoma (GBM) tumors in NRG mice with 23 ± 3 nm gold nanoparticles labeled with the β-particle-emitting radionuclide 177Lu (177Lu-AuNPs). Compared to unlabeled AuNPs or saline-treated cells, 177Lu-AuNPs reduced the clonogenic survival of U251-Luc cells to 0.005 ± 0.002 and increased DNA double-strand breaks (DSBs) by 14.3-fold. Within U251-Luc tumors in NRG mice, 177Lu-AuNPs were retained for up to 21 days with minimal redistribution to the brain or other organs. The radiation dose within the tumor was relatively high. In addition to tumors, the dose was reduced 93-fold in the normal right cerebral hemisphere, while the dose was reduced 2000-3000-fold in the contralateral left cerebral hemisphere or cerebellum. The dose to peripheral organs was less than 0.1 Gy.

Bioluminescence imaging (BLI) showed that tumor growth in mice treated with 177Lu-AuNPs almost completely stopped, while tumors in control mice grew rapidly. Magnetic resonance imaging (MRI) and histological staining at 28 days post-treatment showed no obvious tumors in mice treated with 177Lu-AuNPs, while control mice developed large glioblastoma (GBM) tumors. All control mice reached the humanitarian endpoint at 39 days (saline group) or 45 days (unlabeled AuNPs group) post-treatment and were euthanized, while 5 out of 8 mice treated with 177Lu-AuNPs survived to 150 days. No normal tissue toxicity was observed in mice treated with 177Lu-AuNPs. These results demonstrate that the CED dose of 177Lu-AuNPs is highly effective in treating U251-Luc human glioblastoma in the brains of NRG mice and is non-toxic to normal tissues.

Figure 1. Representative BLI images in NRG mice with U251-Luc human GBM tumors at 21 d after CED ofFigure 1. Representative BLI images in NRG mice with U251-Luc human GBM tumors at 21 d after CED of (A) normal saline, (B) unlabeled AuNPs , or (C) 1.1 ± 0.2 MBq of 177Lu-AuNPs. (D) TGI vs time measured by BLI. (Georgiou C J, et al., 2022)

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Customer Reviews
Efficient Tool

The U251MG luciferase reporter line has been a cornerstone of our glioblastoma research program. The cells maintained their characteristic morphology and growth kinetics while providing a bright, stable luciferase signal. We used these cells for both in vitro proliferation assays and in vivo orthotopic glioma models, and the bioluminescence enabled precise tumor burden quantification.

Italy

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