High-volume cellular screening for anticancer agents with combinatorial chemical libraries: A new methodology

被引:43
作者
Salmon, SE [1 ]
LiuStevens, RH [1 ]
Zhao, Y [1 ]
Lebl, M [1 ]
Krchnak, V [1 ]
Wertman, K [1 ]
Sepetov, N [1 ]
Lam, KS [1 ]
机构
[1] SELECTIDE CORP,TUCSON,AZ 85737
关键词
combinatorial chemical libraries; anticancer drugs; tumor cell line screening;
D O I
10.1007/BF01718701
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A single-step cancer cell cytotoxic assay system for anticancer drug discovery has been developed which facilitates rapid screening of large combinatorial chemical libraries synthesized using the 'one-bead-one-compound' (OBOC) methodology. Each OBOC library bead incorporates two orthogonally cleavable linkers that release the bead-bound compound at a different pH. The assay utilizes high concentrations of tumor cells mixed directly with OBOC beads and plated in soft agarose containing tissue culture medium. One of the orthogonal linkers is cleaved at neutral pH in tissue culture releasing an aliquot of compound to diffuse at a relatively high local concentration into the soft agarose immediately surrounding the bead. Active compounds are identified visually from a clear ring of tumor cell lysis which forms within 48 h around just the rare bead releasing a cytotoxic compound. The bead releasing a cytotoxin is then plucked from the agar and the remaining compound still linked to the bead can be released for structural analysis, followed by compound resynthesis and confirmatory testing. This assay system has been successfully applied to identification of lead cytotoxic compounds from model peptidic and non-peptidic combinatorial chemical libraries. Use of this methodology may facilitate anticancer drug discovery.
引用
收藏
页码:57 / 63
页数:7
相关论文
共 17 条
[1]  
[Anonymous], CANC CLIN TRIALS
[2]   SOME PRACTICAL CONSIDERATIONS AND APPLICATIONS OF THE NATIONAL-CANCER-INSTITUTE IN-VITRO ANTICANCER DRUG DISCOVERY SCREEN [J].
BOYD, MR ;
PAULI, KD .
DRUG DEVELOPMENT RESEARCH, 1995, 34 (02) :91-109
[3]   GENERAL-METHOD FOR RAPID SYNTHESIS OF MULTICOMPONENT PEPTIDE MIXTURES [J].
FURKA, A ;
SEBESTYEN, F ;
ASGEDOM, M ;
DIBO, G .
INTERNATIONAL JOURNAL OF PEPTIDE AND PROTEIN RESEARCH, 1991, 37 (06) :487-493
[4]   GENERATION AND USE OF SYNTHETIC PEPTIDE COMBINATORIAL LIBRARIES FOR BASIC RESEARCH AND DRUG DISCOVERY [J].
HOUGHTEN, RA ;
PINILLA, C ;
BLONDELLE, SE ;
APPEL, JR ;
DOOLEY, CT ;
CUERVO, JH .
NATURE, 1991, 354 (6348) :84-86
[5]   CREATION AND FUNCTIONAL SCREENING OF A MULTIUSE PEPTIDE LIBRARY [J].
JAYAWICKREME, CK ;
GRAMINSKI, GF ;
QUILLAN, JM ;
LERNER, MR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (05) :1614-1618
[6]   SYMMETRICAL STRUCTURE ALLOWING THE SELECTIVE MULTIPLE RELEASE OF A DEFINED QUANTITY OF PEPTIDE FROM A SINGLE BEAD OF POLYMERIC SUPPORT [J].
KOCIS, P ;
KRCHNAK, V ;
LEBL, M .
TETRAHEDRON LETTERS, 1993, 34 (45) :7251-7252
[7]  
Lam Kit S., 1994, Methods (Orlando), V6, P372, DOI 10.1006/meth.1994.1037
[8]   A NEW TYPE OF SYNTHETIC PEPTIDE LIBRARY FOR IDENTIFYING LIGAND-BINDING ACTIVITY [J].
LAM, KS ;
SALMON, SE ;
HERSH, EM ;
HRUBY, VJ ;
KAZMIERSKI, WM ;
KNAPP, RJ .
NATURE, 1991, 354 (6348) :82-84
[9]  
LAM KS, 1996, PEPTIDE NONPEPTIDE L, P173
[10]  
LAM KS, 1996, Patent No. 5510240