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Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope
Published on: March 24, 2017
The RAV12 monoclonal antibody recognizes the N-linked glycotope RAAG12: expression in human normal and tumor tissues
Suzanne K Coberly1, Francine Z Chen, Mark P Armanini
1Department of Pathology, MacroGenics West, Inc, South San Francisco, California 94080, USA.
Archives of Pathology & Laboratory Medicine
|September 3, 2009
Summary
RAAG12 antigen is highly expressed on gastrointestinal cancers, making them targets for RAV12 therapy. Its differential localization in normal tissues may affect treatment accessibility.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- RAAG12 is a primate-restricted N-linked carbohydrate antigen found on membrane proteins.
- The RAV12 monoclonal antibody recognizes RAAG12 and has shown potential in targeting gastrointestinal adenocarcinomas.
Purpose of the Study:
- To profile RAAG12 expression in normal and cancerous tissues.
- To identify potential clinical applications and safety considerations for RAV12 therapy.
Main Methods:
- Immunohistochemistry was performed on 36 normal human tissues.
- A wide array of tumor tissues were analyzed to determine RAAG12 expression patterns.
Main Results:
- Over 90% of colon, gastric, and pancreatic adenocarcinomas expressed RAAG12 uniformly.
- Other cancers like esophageal, ovarian, liver, breast, and prostate carcinomas also showed RAAG12 expression, though less frequently.
- RAAG12 was detected on mucosal and glandular epithelium, with distinct subcellular localization in tumors compared to normal tissues.
Conclusions:
- High RAAG12 expression on gastrointestinal tumors supports their suitability as targets for RAV12 therapy.
- Differential subcellular localization of RAAG12 in normal epithelia may influence RAV12 accessibility and potential side effects.
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