EFFECT OF MODULATORS ON 5-FLUOROURACIL METABOLITE PATTERNS IN MURINE COLON-CARCINOMA DETERMINED BY IN-VITRO F-19 NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY

被引:0
作者
KAMM, YJL
RIETJENS, IMCM
VERVOORT, J
HEERSCHAP, A
ROSENBUSCH, G
HOFS, HP
WAGENER, DJT
机构
[1] UNIV NIJMEGEN HOSP,DEPT RADIODIAGNOST,6500 HB NIJMEGEN,NETHERLANDS
[2] AGR UNIV WAGENINGEN,DEPT BIOCHEM,WAGENINGEN,NETHERLANDS
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
High-resolution F-19 nuclear magnetic resonance spectroscopy at 7 T was used to study the effect of modulators on the metabolism of 5 fluorouracil (5-FUra, 115 mg/kg i.p.) in C38 murine colon tumors grown in CS7BL/6 mice. Distinct 5-FUra metabolite patterns were found in perchloric acid extracts of these tumors after treatment. The F-19 nuclear magnetic resonance spectra exhibited resonances representing 5-FUra, the catabolites alpha-fluoro-beta-ureidopropionic acid and alpha-fluoro-beta-alanine, as well as four distinct fluoronucleotide anabolites. Using this model system the effect of several modulators on 5-FUra tumor metabolite patterns was investigated: methotrexate (300 mg/kg); alpha-interferon (10(5) IU/animal); N-(phosphonacetyl)-L-aspartate (100 and 250 mg/kg); and leucovorin (300 and 750 mg/kg), A significant increase in the anabolite:catabolite ratio was observed for the groups treated with 5-FUra in combination with the modulators methotrexate (n = 8), alpha-interferon (n = 7), and high-dose leucovorin (n = 14), but not for low-dose leucovorin (n = 7). Cotreatment with high-dose N-(phosphonacetyl)-L-aspartate (n = 8) resulted in a significant decrease in the anabolite: catabolite ratio compared to treatment with 5-FUra alone (n = 16). Possible correlations of metabolite profiles with therapy response are discussed.
引用
收藏
页码:4321 / 4326
页数:6
相关论文
共 47 条
[31]  
Peters G J, 1987, In Vivo, V1, P113
[32]   PROLONGED RETENTION OF HIGH-CONCENTRATIONS OF 5-FLUOROURACIL IN HUMAN AND MURINE TUMORS AS COMPARED WITH PLASMA [J].
PETERS, GJ ;
LANKELMA, J ;
KOK, RM ;
NOORDHUIS, P ;
VANGROENINGEN, CJ ;
VANDERWILT, CL ;
MEYER, S ;
PINEDO, HM .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1993, 31 (04) :269-276
[33]   CLINICAL RELEVANCE OF BIOCHEMICAL MODULATION OF 5-FLUOROURACIL [J].
PETERS, GJ ;
VANGROENINGEN, CJ .
ANNALS OF ONCOLOGY, 1991, 2 (07) :469-480
[34]  
PIEDBOIS P, 1992, J CLIN ONCOL, V10, P896
[35]   FLUOROURACIL - BIOCHEMISTRY AND PHARMACOLOGY [J].
PINEDO, HM ;
PETERS, GFJ .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (10) :1653-1664
[36]   HUMAN TUMOR FLUOROURACIL TRAPPING - CLINICAL CORRELATIONS OF INVIVO F-19 NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY PHARMACOKINETICS [J].
PRESANT, CA ;
WOLF, W ;
ALBRIGHT, MJ ;
SERVIS, KL ;
RING, R ;
ATKINSON, D ;
ONG, RL ;
WISEMAN, C ;
KING, M ;
BLAYNEY, D ;
KENNEDY, P ;
ELTAHTAWY, A ;
SINGH, M ;
SHANI, J .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (11) :1868-1873
[37]   INVIVO F-19 NMR-SPECTROSCOPY OF THE ANTIMETABOLITE 5-FLUOROURACIL AND ITS ANALOGS - AN ASSESSMENT OF DRUG-METABOLISM [J].
PRIOR, MJW ;
MAXWELL, RJ ;
GRIFFITHS, JR .
BIOCHEMICAL PHARMACOLOGY, 1990, 39 (05) :857-863
[38]  
Rustum Y M, 1987, NCI Monogr, P165
[39]   STIMULATION OF 5-FLUOROURACIL METABOLIC-ACTIVATION BY INTERFERON-ALPHA IN HUMAN COLON-CARCINOMA CELLS [J].
SCHWARTZ, EL ;
HOFFMAN, M ;
OCONNOR, CJ ;
WADLER, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 182 (03) :1232-1239
[40]   MULTINUCLEAR MR INVESTIGATION OF THE METABOLIC RESPONSE OF THE MURINE RIF-1 TUMOR TO 5-FLUOROURACIL CHEMOTHERAPY [J].
SIJENS, PE ;
BALDWIN, NJ ;
NG, TC .
MAGNETIC RESONANCE IN MEDICINE, 1991, 19 (02) :373-385