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Analyzing Tumor and Tissue Distribution of Target Antigen Specific Therapeutic Antibody
Published on: May 16, 2020
Targeted therapy of solid tumors by monoclonal antibody specific to epidermal growth factor receptor
Behzad Baradaran1, Jafar Majidi1, Safar Farajnia1
1Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Abstract:
Tumor growth and progression depends largely on the activity of cell membrane receptors like epidermal growth factor receptor (EGFR) that plays a pivotal role in the progression and invasion of different solid tumors. As one of the most promising approaches for targeting and therapy, monoclonal antibodies (mAbs) have widely been used in the treatment of various malignancies. However, the clinical effects of mAbs appear to be dependent upon its specificity and potency. In the current investigation, a series of mAbs were produced against human EGFR using hybridoma technology. Balb/c mice were immunized against EGFR-positive A431 cancer cells and the most immune mouse was selected for fusion and generation of anti-EGFR mAbs. Isotyping of the generated mAbs was performed by ELISA method. Of various monoclones produced, IgG1 subclass (mAb BF4) displayed specific binding to the EGFR-expressing A431 cells. Flow cytometry and immunofluorescence staining revalidated its specific reactivity with EGFR and MTT assay revealed significant growth inhibition of A431 cells treated with mAb BF4 mainly through induction of apoptosis. Based on these findings, we propose the produced anti-EGFR mAb BF4 to be exploited for diagnostic and possibly treatment of various malignancies with overexpression of EGFR.
Insights
Researchers developed a new monoclonal antibody (mAb BF4) targeting epidermal growth factor receptor (EGFR). This antibody effectively inhibits the growth of EGFR-expressing cancer cells, showing promise for cancer diagnostics and therapy.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Epidermal growth factor receptor (EGFR) is crucial for solid tumor growth and invasion.
- Monoclonal antibodies (mAbs) are effective cancer therapies, but their efficacy relies on specificity and potency.
Purpose of the Study:
- To generate and characterize novel anti-EGFR monoclonal antibodies for potential cancer diagnostics and treatment.
- To evaluate the specificity and efficacy of a newly developed mAb against EGFR-expressing cancer cells.
Main Methods:
- Hybridoma technology was employed to produce monoclonal antibodies against human EGFR.
- Immunization of Balb/c mice with EGFR-positive A431 cancer cells.
- Characterization of antibody specificity using ELISA, flow cytometry, and immunofluorescence staining.
- Assessment of anti-cancer activity via MTT assay to determine growth inhibition and apoptosis induction.
Main Results:
- A specific IgG1 monoclonal antibody, designated mAb BF4, was successfully generated.
- mAb BF4 demonstrated specific binding to EGFR-expressing A431 cells.
- Treatment with mAb BF4 significantly inhibited A431 cell growth, primarily by inducing apoptosis.
Conclusions:
- The novel anti-EGFR mAb BF4 exhibits specific reactivity and potent anti-proliferative effects on EGFR-overexpressing cancer cells.
- mAb BF4 holds potential for development as a diagnostic tool and therapeutic agent for various malignancies.
- Further investigation into the therapeutic applications of mAb BF4 in EGFR-driven cancers is warranted.
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