Activity of TER286 against human tumor colony-forming units

被引:17
作者
Izbicka, E [1 ]
Lawrence, R [1 ]
Cerna, C [1 ]
VonHoff, DD [1 ]
Sanderson, PE [1 ]
机构
[1] TERRAPIN TECHNOL INC,S SAN FRANCISCO,CA 94080
关键词
cancer; cytotoxicity; glutathione S-transferase; soft agar cloning; TER286;
D O I
10.1097/00001813-199704000-00006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glutathione S-transferase (GST) isozymes have been shown to be elevated in many human cancer types as compared to normal tissues. TER286, one in a class of glutathione-based GST-activated cytotoxins, was tested in a soft agar cloning assay to determine its in vitro activity against primary human tumor colony-forming units, Breast and lung specimens from patients who had received prior therapy and those who were previously untreated were exposed to TER286 at concentrations of 1, 10 and 50 mu M using both Ih and continuous exposures, Overall in vitro responses (50% or less survival compared to untreated controls) were observed in 0% (0/14), 14% (2/14) and 29% (4/14), respectively, in specimens exposed to TER286 for 1 h, and in 5% (2/41), 10% (4/41) and 61% (25/41), respectively, in specimens exposed to TER286 continuously. TER286 has cytotoxic activity against both breast and lung cancer colony-forming units, and demonstrates a concentration-response effect. At 50 mu M, there is a significant difference between 1 h and continuous exposures in head-to-head comparisons. These data suggest that TER286 can be activated in human tumor colony-forming units and should be pursued as a treatment candidate for patients whose tumors are resistant to drug treatment based on up-regulation of GST.
引用
收藏
页码:345 / 348
页数:4
相关论文
共 17 条
[1]  
COLVIN M, 1981, CANCER TREAT REP, V65, P89
[2]  
FOULKE RS, 1990, CANCER RES, V50, P6264
[3]   PRIMARY BIOASSAY OF HUMAN MYELOMA STEM-CELLS [J].
HAMBURGER, A ;
SALMON, SE .
JOURNAL OF CLINICAL INVESTIGATION, 1977, 60 (04) :846-854
[4]  
HAMBURGER AW, 1977, SCIENCE, V197, P471
[5]  
KAUVAR LM, 1996, GLUTATHIONE S TRANSF, P187
[6]   VARIABILITY OF GLUTATHIONE-S-TRANSFERASE ISOENZYME PATTERNS IN MATCHED NORMAL AND CANCER HUMAN BREAST-TISSUE [J].
KELLEY, MK ;
ENGQVISTGOLDSTEIN, A ;
MONTALI, JA ;
WHEATLEY, JB ;
SCHMIDT, DE ;
KAUVAR, LM .
BIOCHEMICAL JOURNAL, 1994, 304 :843-848
[7]   GLUTATHIONE-S-TRANSFERASE ACTIVATES NOVEL ALKYLATING-AGENTS [J].
LYTTLE, MH ;
SATYAM, A ;
HOCKER, MD ;
BAUER, KE ;
CALDWELL, CG ;
HUI, HC ;
MORGAN, AS ;
MERGIA, A ;
KAUVAR, LM .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (10) :1501-1507
[8]  
Montali J. A., 1995, Cellular Pharmacology, V2, P241
[9]  
Nishimura T, 1996, CLIN CANCER RES, V2, P1859
[10]   EXAMINATION OF BRONCHOALVEOLAR WASH FLUID FOR RAS, MYC AND FOS ONCOPROTEINS AND GLUTATHIONE-S-TRANSFERASE ISOENZYMES - AN ATTEMPT TO IMPROVE THE ACCURACY OF LUNG-CANCER DIAGNOSIS [J].
PINKHAM, JM ;
STRANGE, RC ;
PANTIN, C .
CLINICA CHIMICA ACTA, 1994, 227 (1-2) :211-215