Cell-based apoptosis assays in oncology drug discovery

被引:9
作者
Drewe, John [2 ]
Cai, Sui Xiong [1 ]
机构
[1] IMPACT Therapeut, High & New Technol Zone, Nanjing 210061, Jiangsu, Peoples R China
[2] Biomedicure, San Diego, CA 92009 USA
关键词
apoptosis inducers; cell-based assay; chemical genetics; druggable target; proteomics; THROUGHPUT SCREENING ASSAY; CHEMICAL GENETICS APPROACH; PROTEIN-KINASE PDK1; SMALL MOLECULES; TARGET IDENTIFICATION; CASPASE-3; SUBSTRATE; CANCER-THERAPY; KEY MEDIATORS; GAMBOGIC ACID; MISSING LINK;
D O I
10.1517/17460441.2010.486829
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Importance of the field: Screening compounds with a cell-based phenotypic approach complements target-based discovery programs because of the opportunity to investigate targets in the context of the cellular milieu and to discover novel targets. Areas covered in this review: Utilizing a cell-based apoptotic phenotype screen for discovery and optimization of apoptosis inducers and affirming activity as potential anticancer agents in vivo with xenograft models. Subsequently, chemical genetic tools are utilized to identify and validate previously unrecognized cancer targets. Case studies showing the various multidisciplinary approaches utilized for several years are reviewed. What the reader will gain: The interactive nature of the drug and target discovery processes, and insights that come from integration of cellular biology, medicinal chemistry and animal research. Take home message: Phenotype proapoptotic screen followed by chemical genetics is useful for anticancer drug research, for the discovery of potential drugs and identification of druggable targets.
引用
收藏
页码:583 / 596
页数:14
相关论文
共 82 条
[1]
Allosteric inhibitors of Bcr-abl-dependent cell proliferation [J].
Adrián, FJ ;
Ding, Q ;
Sim, TB ;
Velentza, A ;
Sloan, C ;
Liu, Y ;
Zhang, GB ;
Hur, W ;
Ding, S ;
Manley, P ;
Mestan, J ;
Fabbro, D ;
Gray, NS .
NATURE CHEMICAL BIOLOGY, 2006, 2 (02) :95-102
[2]
PURIFICATION OF TETRODOTOXIN-BINDING COMPONENT ASSOCIATED WITH VOLTAGE-SENSITIVE SODIUM CHANNEL FROM ELECTROPHORUS-ELECTRICUS ELECTROPLAX MEMBRANES [J].
AGNEW, WS ;
LEVINSON, SR ;
BRABSON, JS ;
RAFTERY, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (06) :2606-2610
[3]
An W. Frank, 2009, V486, P1, DOI 10.1007/978-1-60327-545-3_1
[4]
History, evolution, and trends in compound management for high throughput screening [J].
Archer, JR .
ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2004, 2 (06) :675-681
[5]
Identification and characterization of pleckstrin-homology-domain-dependent and isoenzyme-specific Akt inhibitors [J].
Barnett, SF ;
Defeo-Jones, D ;
Fu, S ;
Hancock, PJ ;
Haskell, KM ;
Jones, RE ;
Kahana, JA ;
Kral, AM ;
Leander, K ;
Lee, LL ;
Malinowski, J ;
McAvoy, EM ;
Nahas, DD ;
Robinson, RG ;
Huber, HE .
BIOCHEMICAL JOURNAL, 2005, 385 :399-408
[6]
Bartoli S, 2007, CURR OPIN DRUG DISC, V10, P422
[7]
An operational definition of epigenetics [J].
Berger, Shelley L. ;
Kouzarides, Tony ;
Shiekhattar, Ramin ;
Shilatifard, Ali .
GENES & DEVELOPMENT, 2009, 23 (07) :781-783
[8]
Chemogenomics: An emerging strategy for rapid target and drug discovery [J].
Bredel, M ;
Jacoby, E .
NATURE REVIEWS GENETICS, 2004, 5 (04) :262-275
[9]
Lessons learnt from assembling screening libraries for drug discovery for neglected diseases [J].
Brenk, Ruth ;
Schipani, Alessandro ;
James, Daniel ;
Krasowski, Agata ;
Gilbert, Ian Hugh ;
Frearson, Julie ;
Wyatt, Paul Graham .
CHEMMEDCHEM, 2008, 3 (03) :435-444
[10]
Target identification in chemical genetics: The (often) missing link [J].
Burdine, L ;
Kodadek, T .
CHEMISTRY & BIOLOGY, 2004, 11 (05) :593-597