Phage display in molecular imaging and diagnosis of cancer.
Phage display in molecular imaging and diagnosis of cancer.
复制标题
DOI:
10.1021/cr900317f
复制
发表时间:
2010-05-12
期刊:
影响因子:
62.1
通讯作者:
Deutscher, Susan L.
中科院分区:
文献类型:
--
作者:
Deutscher, Susan L.
New peptide-based probes to facilitate the molecular imaging of disease are rapidly evolving due to implementation of combinatorial chemistry and bacteriophage (phage) display. Phage display is a powerful technique that allows vast sequence space screening, providing a means to improve peptide affinity and generate unique peptides that bind any given target. Since its inception in 1985, many thousands of peptides have been isolated and investigated using phage display. Such peptides are being explored in vaccine development, enzyme inhibition, inflammation, plant pathology, cardiovascular disease, cancer, etc. The purpose of this review is to analyze and describe those peptides obtained from phage display that have been used successfully in the past five years in both radio and optical in vivo tumor imaging. New tumor targeting agents are required to advance cancer diagnosis and treatment, and phage display selected peptides may be an attractive means to obtain such agents. Unfortunately, the vast majority of the hundreds of peptides selected against tumor antigens have not been shown to function as cancer molecular imaging agents in vivo. Recently, progress has been made in translation of the peptides from in vitro to in vivo applications. Not only have the peptides displayed on phage been employed in vivo as tumor imaging agents, but the phage themselves have been used in imaging with a number of labeling platforms. The integration of phage as not only vehicles for peptide discovery but also as a nanomaterial has wide-ranging applications. Phage display technology is emerging as a powerful, economical, rapid, and efficacious approach to develop new agents for the molecular imaging and diagnosis of cancer.
登录
查看更多内容
DOI:
10.1073/pnas.152463399
发表时间:
2002-10-01
影响因子:
11.1
作者:
Åkerman, ME;Chan, WCW;Ruoslahti, E
通讯作者:
Ruoslahti, E
DOI:
10.1073/pnas.241655998
发表时间:
2002-02-05
影响因子:
11.1
作者:
Arap, W;Haedicke, W;Ruoslahti, E
通讯作者:
Ruoslahti, E
影响因子:
3.5
作者:
Böckmann, M;Drosten, M;Pützer, BM
通讯作者:
Pützer, BM
影响因子:
3.7
作者:
Chang DK;Lin CT;Wu CH;Wu HC
通讯作者:
Wu HC
影响因子:
82.9
作者:
Arap, W;Kolonin, MG;Pasqualini, R
通讯作者:
Pasqualini, R