Loading…

Immunoscreening of urinary bladder cancer cDNA library and identification of potential tumor antigen

Objective To identify potential tumor antigen by immunoscreening the urinary bladder cancer cDNA library with monoclonal antibodies. Methods Monoclonal antibodies were prepared. A cDNA expression library was constructed from bladder cancer cell line BLZ211. Immunogenic proteins were identified by im...

Full description

Saved in:
Bibliographic Details
Published in:World journal of urology 2009-02, Vol.27 (1), p.107-112
Main Authors: Chen, Ling, Chen, Wei, Zhao, Le, Yu, Hai-Zhen, Li, Xu
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Objective To identify potential tumor antigen by immunoscreening the urinary bladder cancer cDNA library with monoclonal antibodies. Methods Monoclonal antibodies were prepared. A cDNA expression library was constructed from bladder cancer cell line BLZ211. Immunogenic proteins were identified by immunoscreening the cDNA library with ten monoclonal antibodies. Results The cDNA library of BLZ211 cells was established using λZAP as vector. The titer of unamplified cDNA library was 1.39×10 6  pfu/ml with a recombinant rate of 97.72%, and titer of amplified one was 8.4×10 9  pfu/ml. After immunoscreening, ten positive clones representing ten different antigens were identified, which include two proteins with unknown function; coactosin-like 1, eukaryotic translation elongation factor, HNRPA1, histidine triad nucleotide binding protein, KRT7, LCN2, TSTA3, zinc finger protein, C11orf48 and HSPC148. Conclusion The cDNA library was of high quality and can be used in further study. By immunoscreening the bladder cancer cDNA library with ten monoclonal antibodies, we identified ten immunogenic proteins that otherwise would not have been identified as potential diagnostic marker and vaccinogens of bladder cancer using the gene discovery effort.
ISSN:0724-4983
1433-8726
DOI:10.1007/s00345-008-0326-4