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.
Customer Q&As
In what ways does the Human EGFR Stable Cell Line - CT26 provide a relevant model for evaluating the oncogenic potential of EGFR mutations?
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.
How could the Human EGFR Stable Cell Line - CT26 be employed to screen for and characterize the efficacy of novel EGFR-targeting agents?
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.
What methodological approaches would be most effective in confirming the stable transfection and expression of human EGFR in the CT26 cell line?
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.
Can the Human EGFR Stable Cell Line - CT26 be utilized to understand the differential cellular responses to EGFR tyrosine kinase inhibitors versus monoclonal antibodies targeting EGFR?
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.
What are the advantages of using the Human EGFR Stable Cell Line - CT26 for studying the interactions between EGFR and other cell surface receptors in the tumor microenvironment?
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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Customer Reviews
Comparative Treatment Analysis
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.
Drug Screening Platform
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.
Therapeutic Target Validation
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.
United Kingdom
03/19/2021
Stable EGFR Expression
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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