MURINE MONOCLONAL-ANTIBODY RECOGNIZING A 90-KDA CELL-SURFACE DETERMINANT SELECTIVELY LOST BY MULTI-DRUG-RESISTANT VARIANTS OF CEM CELLS

被引:27
作者
CIANFRIGLIA, M
CENCIARELLI, C
TOMBESI, M
BARCA, S
MARIANI, M
MORRONE, S
SANTONI, A
SAMOGGIA, P
ALESSIO, M
MALAVASI, F
机构
[1] SORIN BIOMED SPA,ONCOL BIOCHIM,SALUGGIA,ITALY
[2] UNIV ROME LA SAPIENZA,FAC MED,IST PATOL GEN,CATTEDRA 3,I-00185 ROME,ITALY
[3] IST SUPER SANITA,EMATOL LAB,I-00161 ROME,ITALY
[4] UNIV TURIN,DIPARTIMENTO GENET BIOL & CHIM MED,BIOL CELLULARE LAB,I-10124 TURIN,ITALY
关键词
D O I
10.1002/ijc.2910450118
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We describe a murine IgG, monoclonal antibody (MAb56), specific for a cell‐surface protein structure (MC56 determinant) expressed by the human CEM cell line. A large band of approximately 90 kDa was identified as the main specific component of the MC56 determinant. Such a 90‐kDa protein is significantly associated with the drug‐sensitive phenotype, its expression being progressively reduced quantitatively in multi‐drug‐resistant (MDR) variants of CEM cells, according to the extent of drug resistance. In addition, the MC56 determinant is expressed de novo in drug‐sensitive revertant cell lines derived from MDR cells and unreactive with the MAb56. The MAb56 shows a high affinity towards the immunizing drug‐sensitive CEM cell line (Ka =1.86 × 109 L/mole) while not binding to MDR cell variants. The expression of the MC56 molecule on a variety of human cells and tissues makes such a cellular determinant a candidate as a marker for studying the MDR phenomenon both in vivo and in vitro. Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company
引用
收藏
页码:95 / 103
页数:9
相关论文
共 45 条
[2]  
BAKER RM, 1978, METHODS MEMBRANE BIO, V9, P337
[3]  
BECK WT, 1979, CANCER RES, V39, P2070
[4]   CHROMOSOMAL LOCATION OF HUMAN P-GLYCOPROTEIN GENE-SEQUENCES [J].
BELL, DR ;
TRENT, JM ;
WILLARD, HF ;
RIORDAN, JR ;
LING, V .
CANCER GENETICS AND CYTOGENETICS, 1987, 25 (01) :141-148
[5]   IDENTIFICATION OF A NEW EPITOPE OF THE 4F2/44D7 MOLECULAR-COMPLEX PRESENT ON SARCOLEMMA AND ISOLATED CARDIAC FIBERS [J].
BELLONE, G ;
ALLOATTI, G ;
LEVI, R ;
GEUNA, M ;
TETTA, C ;
PERUZZI, L ;
LETARTE, M ;
MALAVASI, F .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1989, 19 (01) :1-8
[6]  
BIEDLER JL, 1981, MOL ACTIONS TARGETS, P453
[7]   MECHANISM OF CELLULAR DRUG RESISTANCE [J].
BOSMANN, HB .
NATURE, 1971, 233 (5321) :566-&
[8]   SOME FURTHER INFORMATION ABOUT ABNORMAL MEMBRANE GLYCOPROTEIN ASSOCIATED WITH MALIGNANCY [J].
BRAMWELL, ME ;
HARRIS, H .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1978, 203 (1150) :93-99
[9]   ABNORMAL MEMBRANE GLYCOPROTEIN ASSOCIATED WITH MALIGNANCY IN A WIDE-RANGE OF DIFFERENT TUMORS [J].
BRAMWELL, ME ;
HARRIS, H .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1978, 201 (1142) :87-106
[10]   INTERNAL DUPLICATION AND HOMOLOGY WITH BACTERIAL TRANSPORT PROTEINS IN THE MDR1 (P-GLYCOPROTEIN) GENE FROM MULTIDRUG-RESISTANT HUMAN-CELLS [J].
CHEN, CJ ;
CHIN, JE ;
UEDA, K ;
CLARK, DP ;
PASTAN, I ;
GOTTESMAN, MM ;
RONINSON, IB .
CELL, 1986, 47 (03) :381-389