CHARACTERIZATION BY SOMATIC-CELL GENETICS OF A MONOCLONAL-ANTIBODY TO THE MDR1 GENE-PRODUCT (P-GLYCOPROTEIN) - DETERMINATION OF P-GLYCOPROTEIN EXPRESSION IN MULTI-DRUG-RESISTANT KB AND CEM CELL VARIANTS

被引:52
作者
CENCIARELLI, C
CURRIER, SJ
WILLINGHAM, MC
THIEBAUT, F
GERMANN, UA
RUTHERFORD, AV
GOTTESMAN, MM
BARCA, S
TOMBESI, M
MORRONE, S
SANTONI, A
MARIANI, M
RAMONI, C
DUPUIS, ML
CIANFRIGLIA, M
机构
[1] IST SUPER SANITA, IMMUNOL LAB, VIALE REGINA ELENA 299, I-00161 ROME, ITALY
[2] NCI, MOLEC BIOL LAB, BETHESDA, MD 20892 USA
[3] UNIV ROME LA SAPIENZA, FAC MED, CATTEDRA 3A, IST PATOL GEN, I-00185 ROME, ITALY
[4] SORIN BIOMED SPA, ONCOL BIOCHIM LAB, SALUGGIA, ITALY
关键词
D O I
10.1002/ijc.2910470411
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We isolated an IgG(2a) murine monoclonal antibody (MAb) termed MAb57, specifically reactive with multi-drug-resistant (MDR) human cells. Its specificity toward the MDRI gene product (P-glycoprotein) has been demonstrated by the concordant segregation of the MAb57 epitope with the MDRI gene in interspecific mouse x human cell hybrids, and the reactivity of several different MDRI gene-expressing cells with MAb57, particularly insect cells acutely infected with a baculovirus encoding the MDRI gene. MAb57 can be used to detect, by flow cytometry, variations in the relative drug-resistance levels of several MDR KB and CEM cell variants. This immunological probe has also proven useful in selectively destroying MDR target cells in an antibody-dependent cell-mediated (ADCC) assay system as well as in detecting P-glycoprotein expression in normal and malignant tissues and cells.
引用
收藏
页码:533 / 543
页数:11
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