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Developing and characterization of single chain variable fragment (scFv) antibody against frizzled 7 (Fzd7) receptor.
- Source :
-
Bioengineered [Bioengineered] 2017 Sep 03; Vol. 8 (5), pp. 501-510. Date of Electronic Publication: 2016 Nov 16. - Publication Year :
- 2017
-
Abstract
- ABSTACT Wnt/β-catenin signaling pathway through Frizzled receptors has been shown to play a key role in both normal development and tumorigenesis. Overexpression of Wnt pathway genes, such as Fzd7 in several malignancies is well-documented. Therefore, targeting of Fzd7 and its ligand inhibits cancer cells proliferation metastasis. In the present study we isolated single chain variable fragments (scFvs) against Fzd7 receptor using phage display method. Semi-synthetic human naive antibody libraries (Tomlinson I + J) was employed in panning procedure to isolate specific scFv against specific peptide from extracellular domain of Fzd7 receptor. The reactivity and growth inhibition effects of the selected antibodies was evaluated using enzyme-linked immunosorbent assay (ELISA), MTT and annexin V assays, respectively. Seven scFvs reactive to Fzd7 were selected following 4 rounds of panning. The results showed that the selected scFvs inhibits cell growth through apoptosis cell death in a triple negative breast cancer cells, MDA-MB-231. Given that Fzd7 and Wnt pathway plays a critical role in tumor progression, selected blocking scFvs represent significant potential for immunotherapy of breast cancer cells.
- Subjects :
- Apoptosis drug effects
Apoptosis immunology
Cell Line, Tumor
Cell Surface Display Techniques
Drug Screening Assays, Antitumor methods
Enzyme-Linked Immunosorbent Assay methods
Humans
Immunoassay methods
Treatment Outcome
Triple Negative Breast Neoplasms pathology
Frizzled Receptors administration & dosage
Frizzled Receptors immunology
Single-Chain Antibodies administration & dosage
Single-Chain Antibodies immunology
Triple Negative Breast Neoplasms drug therapy
Triple Negative Breast Neoplasms immunology
Subjects
Details
- Language :
- English
- ISSN :
- 2165-5987
- Volume :
- 8
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Bioengineered
- Publication Type :
- Academic Journal
- Accession number :
- 27849134
- Full Text :
- https://doi.org/10.1080/21655979.2016.1255383