Transfected Stable Cell Lines
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Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : CSC-RO0451
Host Cell : CT26 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RO0451 |
| Description | This cell line is derived from CT26 and is engineered to stably overexpress Human EGFR. |
| Target Gene | EGFR |
| Gene Species | Homo sapiens (Human) |
| Host Cell | CT26 |
| Host Cell Species | Mus musculus (Mouse) |
| Applications | Drug screening and biological assays |
| Size | >1x10^6 frozen cells/vial, 1 mL |
| Stability | Stable in culture over a minimum of 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 |
| Gene Name | EGFR epidermal growth factor receptor [ Homo sapiens ] |
| Gene Symbol | EGFR |
| Synonyms | ERBB; HER1; mENA; ERBB1; PIG61 |
| Gene Description | epidermal growth factor receptor (erythroblastic leukemia viral (v-erb-b) oncogene homolog, avian) |
| GeneID | 1956 |
| Uni ProtID | P00533 |
| mRNA Refseq | NM_005228.3 |
| Protein Refseq | NP_005219.2 |
| Chromosome Location | 7p12 |
| Function | ATP binding; MAP kinase kinase kinase activity; actin filament binding; double-stranded DNA binding; enzyme binding; epidermal growth factor-activated receptor activity; epidermal growth factor-activated receptor activity; identical protein binding; contributes_to nitric-oxide synthase regulator activity; protein binding; protein heterodimerization activity; protein phosphatase binding; protein tyrosine kinase activity; protein tyrosine kinase activity; protein tyrosine kinase activity; receptor signaling protein tyrosine kinase activity; transmembrane receptor protein tyrosine kinase activity; transmembrane signaling receptor activity; |
| Pathway | Adaptive Immune System, organism-specific biosystem; Adherens junction, organism-specific biosystem; Adherens junction, conserved biosystem; Alpha6-Beta4 Integrin Signaling Pathway, organism-specific biosystem; Androgen Receptor Signaling Pathway, organism-specific biosystem; Arf6 signaling events, organism-specific biosystem; Axon guidance, organism-specific biosystem; |
| MIM | 131550 |
The EGFR (epidermal growth factor receptor) gene encodes a transmembrane receptor tyrosine kinase that is involved in cell growth, proliferation, and survival. EGFR is expressed in various tissues and is frequently dysregulated in several types of cancer, including non-small cell lung cancer (NSCLC), colorectal cancer, and head and neck cancer. Mutations and amplifications of the EGFR gene are associated with increased receptor activity and poor prognosis in cancer patients.
The CT26 cell line is a murine colon carcinoma cell line that has been used to study cancer biology and as a model for cancer therapy. When CT26 cells are engineered to stably express the human EGFR gene, they provide a valuable system for studying the effects of EGFR activation and the development of EGFR-targeted therapies. This stable cell line is particularly useful for investigating the mechanisms of resistance to EGFR inhibitors and for identifying novel therapeutic strategies to overcome such resistance in EGFR-driven cancers.
Photodynamic therapy (PDT) is a promising treatment modality that induces cell death and immune activation in tumors by generating reactive oxygen species. However, its effectiveness can be limited by the cytoprotective response of tumor cells, including increased expression of glucose-regulated protein 78 (GRP78). To overcome this challenge, the researchers explored combining PDT with EGF-SubA, a cytotoxin that targets GRP78, to enhance PDT's immunostimulatory effects. In their study, they used the CT26 mouse colon cancer cell line, which was stably transfected to express human EGFR. This enabled the researchers to evaluate the impact of EGFR overexpression on the efficacy of PDT combined with EGF-SubA. The researchers demonstrated that EGFR-expressing CT26 cells were more sensitive to EGF-SubA, which cleaves GRP78 and enhances the cytotoxicity of PDT in vitro. This study supports the potential of combining PDT with GRP78-targeting strategies in cancer treatment.
Figure 1. The researchers infected CT26 cells with retroviruses carrying human EGFR to generate CT26-EGFR cells and confirmed high EGFR expression by flow cytometry. (Gabrysiak M, et al., 2016)
Creative Biogene's Human EGFR Stable Cell Line - CT26 is an ideal model for investigating EGFR-targeted therapies. The cell line offers a robust system to study the effects of EGFR overexpression on cancer cell response to various treatments, including PDT and targeted cytotoxins like EGF-SubA.
(1)Cancer Research: The Human EGFR Stable Cell Line in CT26 provides a valuable model for studying the epidermal growth factor receptor's role in cancer biology, particularly in colorectal cancer. Researchers can use this cell line to explore EGFR signaling pathways, investigate mechanisms of tumorigenesis, and identify potential biomarkers for diagnosis and prognosis. This insight is crucial for developing targeted cancer therapies.
(2)Therapeutic Antibody Screening: This cell line is instrumental in screening and evaluating the efficacy of anti-EGFR antibodies and other targeted therapeutics. By assessing the ability of these compounds to inhibit EGFR signaling in a colorectal cancer context, scientists can prioritize candidates for further development and clinical trials, aiming to improve treatment options for patients with EGFR-positive tumors.
(3)Resistance Mechanism Studies: Understanding the mechanisms by which cancer cells develop resistance to EGFR inhibitors is essential for improving therapeutic outcomes. The Human EGFR Stable Cell Line in CT26 enables researchers to model resistance development under controlled laboratory conditions, facilitating the identification of resistance pathways and the exploration of strategies to overcome or prevent resistance in colorectal cancer treatment.
A: This cell line enables the study of mutant EGFR in the context of the CT26 colon carcinoma background, allowing researchers to investigate the contribution of specific EGFR mutations to cellular proliferation, transformation, and tumorigenicity in vitro and in vivo.
A: The cell line can be used in drug screening assays to identify compounds that inhibit EGFR signaling. The efficacy of these agents can then be characterized by measuring downstream signaling pathways, cell proliferation, and apoptosis.
A: Confirming stable transfection and expression would involve PCR analysis for the presence of the human EGFR gene, and Western blot or flow cytometry for the expression of the EGFR protein. Additionally, functional assays could be performed to confirm receptor activity.
A: Yes, this cell line can be treated with both tyrosine kinase inhibitors and monoclonal antibodies to compare their effects on cell signaling, proliferation, and death, providing insights into the mechanisms of action and potential resistance.
A: The advantage lies in the ability to study EGFR in a complex cellular environment that closely mimics the tumor microenvironment. This cell line can be co-cultured with other cell types or in 3D cultures to assess EGFR's interaction with other receptors and its role in processes like angiogenesis, metastasis, and immune modulation.
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It allows for the comparison of the effects of EGFR tyrosine kinase inhibitors versus monoclonal antibodies targeting EGFR, providing insights into the mechanisms of action and potential resistance.
The cell line can be used in drug screening assays to identify compounds that inhibit EGFR signaling, a critical step in the development of targeted cancer therapies.
It enables the study of mutant EGFR in the context of the CT26 colon carcinoma background, allowing us to investigate the contribution of specific EGFR mutations to cellular processes.
This cell line stably overexpresses the human EGFR, providing a reliable model for studying the effects of EGFR activation and targeted therapies.
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