Bicinchoninic acid protein assay in the determination of adriamycin cytotoxicity modulated by the MDR glycoprotein

被引:17
作者
Hall, AM
Croy, V
Chan, T
Ruff, D
Kuczek, T
Chang, CJ
机构
[1] PURDUE UNIV,DEPT MED CHEM & PHARMACOGNOSY,W LAFAYETTE,IN 47907
[2] PURDUE UNIV,DEPT VET PHYSIOL & PHARMACOL,W LAFAYETTE,IN 47907
[3] PURDUE UNIV,DEPT STAT,W LAFAYETTE,IN 47907
来源
JOURNAL OF NATURAL PRODUCTS | 1996年 / 59卷 / 01期
关键词
D O I
10.1021/np960024c
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The development of simultaneous resistance to structurally unrelated drugs in cancer cells is a major obstacle to effective cancer chemotherapy. This multidrug-resistance (MDR) phenomenon is largely attributed to overexpression of a 170 kD glycoprotein, which serves as a transmembrane efflux pump in extruding a variety of natural anticancer drugs such as vinblastine, doxorubicin, and taxol from cancer cells. It is desirable, therefore, to discover compounds that can block the efflux mechanism and thus reverse drug resistance. The bicinchoninic acid protein assay has been adapted for use in a microtiter plate, into an easy, indirect method for screening MDR efflux blockers in plant-extracts. This spectrophotometric assay is used to determine the enhancement of adriamycin cytotoxicity against resistant cancer cells by plant extracts or pure compounds indirectly. We have shown that-the optical density measured (amount of cellular protein present) correlates with the number of viable cells and that fluorescence of Adriamycin associated with the cell correlates with the concentrations of Adriamycin added to the media. In addition, the relative efficacy of MDR reversal by various alkaloids has been determined.
引用
收藏
页码:35 / 40
页数:6
相关论文
共 23 条
[1]   ISOLATION AND GENETIC-CHARACTERIZATION OF HUMAN KB-CELL LINES RESISTANT TO MULTIPLE-DRUGS [J].
AKIYAMA, SI ;
FOJO, A ;
HANOVER, JA ;
PASTAN, I ;
GOTTESMAN, MM .
SOMATIC CELL AND MOLECULAR GENETICS, 1985, 11 (02) :117-126
[2]   EFFECTS OF INDOLE ALKALOIDS ON MULTIDRUG RESISTANCE AND LABELING OF P-GLYCOPROTEIN BY A PHOTOAFFINITY ANALOG OF VINBLASTINE [J].
BECK, WT ;
CIRTAIN, MC ;
GLOVER, CJ ;
FELSTED, RL ;
SAFA, AR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 153 (03) :959-966
[3]  
CANOGAUCI DF, 1991, MOL CELLULAR BIOL MU, P340
[4]   SIMILAR BIOCHEMICAL-CHANGES ASSOCIATED WITH MULTIDRUG RESISTANCE IN HUMAN-BREAST CANCER-CELLS AND CARCINOGEN-INDUCED RESISTANCE TO XENOBIOTICS IN RATS [J].
COWAN, KH ;
BATIST, G ;
TULPULE, A ;
SINHA, BK ;
MYERS, CE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (24) :9328-9332
[5]   ACTIVE OUTWARD TRANSPORT OF DAUNOMYCIN IN RESISTANT EHRLICH ASCITES TUMOR-CELLS [J].
DANO, K .
BIOCHIMICA ET BIOPHYSICA ACTA, 1973, 323 (03) :466-483
[6]   EXPRESSION OF A MULTIDRUG-RESISTANCE GENE IN HUMAN-TUMORS AND TISSUES [J].
FOJO, AT ;
UEDA, K ;
SLAMON, DJ ;
POPLACK, DG ;
GOTTESMAN, MM ;
PASTAN, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (01) :265-269
[7]  
GNANPATHI R, 1983, CANCER RES, V43, P3696
[8]  
GOTTESMAN MM, 1993, ANN REV BIOCH, V62, P387
[9]   UPTAKE AND RETENTION OF ADRIAMYCIN AND DAUNORUBICIN BY SENSITIVE AND ANTHRACYCLINE-RESISTANT SUBLINES OF P388-LEUKEMIA [J].
INABA, M ;
JOHNSON, RK .
BIOCHEMICAL PHARMACOLOGY, 1978, 27 (17) :2123-2130
[10]  
KELLEN JA, 1994, REVERSAL MULTIDRUG R, pCH5