Role of carbonate in the cytotoxicity of carboplatin

被引:25
作者
Di Pasqua, Anthony J.
Goodisman, Jerry
Kerwood, Deborah J.
Toms, Bonnie B.
Dubowy, Ronald L.
Dabrowiak, James C.
机构
[1] Syracuse Univ, Dept Chem, Syracuse, NY 13244 USA
[2] Upstate Med Univ SUNY, Dept Pediat, Syracuse, NY 13210 USA
关键词
D O I
10.1021/tx700058f
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Carboplatin, [Pt(NH3)(2)(CBDCA-O,O')], 1, where CBDCA is cyclobutane-1,1-dicarboxylate, is used against ovarian, lung, and other types of cancer. We recently showed (Di Pasqua et al. (2006) Chem. Res. Toxicol. 19, 139-149) that carboplatin reacts with carbonate under conditions that simulate therapy to produce carbonato carboplatin, cis-[Pt(NH3)(2)(O-CBDCA)(CO3)](2-), 2. We use C-13 and H-1 NMR and UV-visible absorption spectroscopy to show that solutions containing carboplatin that have been aged in carbonate buffer under various conditions contain 1, 2, and other compounds. We then show that aging carboplatin in carbonate produces compounds that are more toxic to human neuroblastoma (SK-N-SH), proximal renal tubule (HK-2) and Namalwa-luc Burkitt's lymphoma (BL) cells than carboplatin alone. Moreover, increasing the aging time increases the cytotoxicity of the platinum solutions as measured by the increase in cell death. Although HK-2 cells experience a large loss in survival upon exposure to carbonato forms of the drug, they have the highest values of IC50 of the three cell lines studied, so that HK-2 cells remain the most resistant to the toxic effects of the carbonato forms in the culture medium. This is consistent with the well-known low renal toxicity observed for carboplatin in therapy. The uptake rates for normal Jurkat cells (NJ) and cisplatin-resistant Jurkat cells (RJ), measured by inductively coupled plasma mass spectrometry (ICP-MS), are 16.6 +/- 4.2 and 12.3 +/- 4.8 amol of Pt h(-1) cell(-1), respectively, when exposed to carboplatin alone. However, when these cells are exposed to carboplatin that has been aged in carbonate media, normal Jurkat cells strongly bind/take up Pt at a rate of 14.5 +/- 4.1 amol of Pt h(-1) cell(-1), while resistant cells strongly bind/take up 5.1 +/- 3.3 amol of Pt h(-1) cell(-1). Collectively, these studies show that carboplatin carbonato species may play a major role in the cytotoxicity and uptake of carboplatin by cells.
引用
收藏
页码:896 / 904
页数:9
相关论文
共 62 条
[51]   THE CHEMISTRY OF METAL CARBONATO AND CARBON-DIOXIDE COMPLEXES [J].
PALMER, DA ;
VANELDIK, R .
CHEMICAL REVIEWS, 1983, 83 (06) :651-731
[52]   The development of platinum compounds and their possible combination [J].
Pasetto, Lara Maria ;
D'Andrea, Mario Rosario ;
Brandes, Alba Ariela ;
Rossi, Elena ;
Monfardini, Silvio .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2006, 60 (01) :59-75
[53]   Impaired hydrolysis of cisplatin derivatives to aquated species prevents energy-dependent uptake in GLC4 cells resistant to cisplatin [J].
Pereira-Maia, E ;
Garnier-Suillerot, A .
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2003, 8 (06) :626-634
[54]   H-1-NMR STUDIES OF HUMAN URINE - URINARY ELIMINATION OF THE ANTICANCER DRUG CARBOPLATIN [J].
RANFORD, JD ;
SADLER, PJ ;
BALMANNO, K ;
NEWELL, DR .
MAGNETIC RESONANCE IN CHEMISTRY, 1991, 29 :S125-S129
[55]   PLATINUM COMPOUNDS - A NEW CLASS OF POTENT ANTITUMOUR AGENTS [J].
ROSENBERG, B ;
VANCAMP, L ;
TROSKO, JE ;
MANSOUR, VH .
NATURE, 1969, 222 (5191) :385-+
[56]   Investigations on the decomposition of carboplatin in infusion solutions II. effect of 1,1-cyclobutanedicarboxylic acid admixture [J].
Schnurr, B ;
Heinrich, H ;
Gust, R .
MICROCHIMICA ACTA, 2002, 140 (1-2) :141-148
[57]   Characterization of methotrexate transport and its drug interactions with human organic anion transporters [J].
Takeda, M ;
Khamdang, S ;
Narikawa, S ;
Kimura, H ;
Hosoyamada, M ;
Cha, SH ;
Sekine, T ;
Endou, H .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 302 (02) :666-671
[58]   CLINICAL PHARMACOKINETICS OF CARBOPLATIN [J].
VANDERVIJGH, WJF .
CLINICAL PHARMACOKINETICS, 1991, 21 (04) :242-261
[59]   Cellular processing of platinum anticancer drugs [J].
Wang, D ;
Lippard, SJ .
NATURE REVIEWS DRUG DISCOVERY, 2005, 4 (04) :307-320
[60]  
WERNER A, 1903, BER, V36, P2380