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Int. J. Mol. Sci. 2010, 11(12), 4826-4842; doi:10.3390/ijms11124826
Published: 26 November 2010
Abstract: The drugs based on platinum metals represent one of the oldest, but also one of the most effective groups of chemotherapeutic agents. Thanks to many clinical studies it is known that resistance of tumor cells to drugs is a frequent cause of chemotherapy failure. With regard to platinum based drugs, multidrug resistance can also be connected with increased expression of low-molecular weight protein metallothionein (MT). This study aimed at investigating the interactions of MT with cisplatin or carboplatin, using the adsorptive transfer technique coupled with differential pulse voltammetry Brdicka reaction (AdTS DPV Brdicka reaction), and a comparison of in vitro results with results obtained in vivo. The results obtained from the in vitro study show a strong affinity between platinum based drugs and MT. Further, we analyzed extracts of neuroblastoma cell lines treated with cisplatin or carboplatin. It is clear that neuroblastoma UKF-NB-4 cisplatin-resistant and cisplatin-sensitive cell lines unlikely respond to the presence of the platinum-based cytostatics cisplatin and carboplatin. Finally, we determined the level of MT in samples from rabbits treated with carboplatin and patients with retinoblastoma treated with the same drug.
From a contemporary point of view, the process of the origin of malignant tumors is complex and multifactorial, comprising changes in expression of individual genes, physical factors and exposure to different chemical and biological impulses. Research and development in the field of tumor diagnostics and prevention, as well as methods of modern therapeutic approaches, belong to the priorities of all European Union countries. Individual tumor treatment strategies result from a number of treatment protocols combining an economic point of view and maximum benefit for the patient. One of the most important parts of the therapy is an efficacious chemotherapy application connected with the individualization of the therapy [1–10].
1.1. Cisplatin Based Chemotherapeutics
Drugs based on platinum metals represent one of the oldest, but also one of the most effective groups of chemotherapeutic agents [11–21]. Platinum-complex based chemotherapeutics are presently used in the therapy of a broad-spectrum of malignancies. The biological activity of the first-time-used platinum-based cytostatic agent, cisplatin, was discovered in 1965 by Rosenberg during research of the electric current influence on bacteria growth . Since then, hundreds of platinum complexes have been synthesized and verified as anticancer chemotherapeutics, such as cisplatin, carboplatin, oxaliplatin, lobaplatin and ormaplatin, belonging to the best known. Though cisplatin has been successfully used in the therapy of malignant tumors for more than 25 years, its biochemical mechanism of action is still not clear. The cytotoxic effect of cisplatin consists in DNA adducts formation, especially to guanine and adenine, which causes DNA strands crossing and thereby inhibition of DNA synthesis and consequently mitosis. The therapeutic effect of platinum-based therapeutics is permanently irreplaceable and brings considerable benefits to patients [23–30].
1.2. Tumor Therapy Resistance
Thanks to many clinical research studies, it is known that resistance of tumor cells to drugs is a common cause of chemotherapy failure. This resistance develops via various mechanisms and the whole process is multifactorial at the cell level. Treatment of complications caused by multidrug resistance (MDR) is particularly difficult. One of the causes of tumor cell resistance is lowered therapeutic concentration of the cytostatic agent(s) in the target site. Membrane proteins such as Pgp, MRP and LRP participate in decreasing the cytostatics level in tumor cells. The complexity of MDR origination is also supported by changes in expression of genes participating in apoptosis or tumor suppressor genes. Cytostatics detoxification can be another factor leading to MDR, in which an increased activity of enzymes involved in oxidation or conjugation of xenobiotics with endogenic agents are most frequently found. In addition to these mechanisms, MDR can be also connected with the increased expression of low-molecular weight protein metallothionein (MT) [12,17–20,23,24,26,27,30–36].
1.3. Metallothionein Significance
Metallothionein (MT) belongs to the group of intracellular, cysteine-rich proteins (Cys content up to 30% of the molecule) with a molecular weight of 6–10 kDa. The MT molecule consists of two binding domains composed of two cysteine clusters. The N-terminal part of the protein (β-domain) has three binding sites for divalent ions and the C-terminal protein part (α-domain) is able to bind four divalent metal ions. One MT molecule is able to bind 12 univalent and/or seven divalent metal ions. However, it is known that single MT molecules differ in their metal ions content and, thus, heavy metal binding sites in the MT molecule are not saturated under physiological conditions [37,38]. This is important for MT biological function (heavy metals homeostasis and detoxification, immunomodulation and regulation functions) [35,36,39,40]. One of the most important MT feature is its ability to interact with metal-containing therapeutics, such as platinum-based cytostatics. This ability can result in a decrease of the free cytostatic agent therapeutic level and thereby increase the resistance of tumor cells against cytostatic agent therapeutic concentrations. A review in Current Protein and Peptide Science aimed at clarifying the relationship between MT and tumor diseases was recently published . Figure 1 shows a simplified scheme of interaction between MT and platinum-based cytostatics. Platinum-based therapeutic agents are probably able to bind to metal transcription inhibitor (MTI) that consequently releases the metal transcription factor-1 (MTF-1). Herewith, the MT biosynthesis is initiated and biosynthesized MT can interact with platinum-based cytostatic agent molecules. Thanks to inactivation of executive free therapeutic molecules by MT, the cytostatic agent therapeutic concentrations decreases and this leads to the growth of new cell subpopulations resistant to tumor therapy. The mechanisms of this process are still not clear [11,30,31,35,41–53]. This present study is aimed at studying interactions of metallothionein and cisplatin or carboplatin using the adsorptive transfer technique coupled with differential pulse voltammetry Brdicka reaction (AdTS DPV Brdicka reaction). We also aim to compare in vitro results with results obtained in vivo. Particularly, attention is paid to analysis of in vitro experiments, neuroblastoma cell line extracts, blood from rabbits treated with carboplatin, and patients with retinoblastoma treated with the same drug.
2. Results and Discussion
2.1. Significance of Thiol Compounds in Resistance Origination
It is known that thiol compounds play a very important role in the processes linked to the formation of tumor cell resistance to platinum-based cytostatics [35,54,55]. Recently, we suggested a unique electrochemical technique enabling direct MT detection in blood serum. This method is based on removal of interfering proteins by heat treatment and consequent adsorption of metallothionein to the surface of the working electrode [56,57].
2.2. Study of Platinum-Based Therapeutics Interactions with Metallothionein Modified Electrode
In the first in vitro experiment, we targeted the monitoring of cisplatin and carboplatin interactions with MT. We utilized an adsorptive transfer technique differential pulse voltammetry coupled Brdicka reaction (AdTS DPV Brdicka reaction) for this purpose. This technique has been successfully used for MT determination in numerous samples [57–60] and excellent correlation between immunochemical techniques was found [55,61]. The scheme of the experimental arrangement for the interaction studies is shown in Figure 2. A hanging mercury drop electrode (HMDE) was immersed in a 5 μL drop of MT for 120 s (point 1 and 2), after unbound molecules were released (3), the modified HMDE was immersed into a drop with a cytostatic agent (4). Then the electrode was carefully rinsed with water and analyzed (6) with computer treatment of the data obtained (7). Modification of the electrode and other experimental conditions were optimized in our previously published paper .
MT (0.4 μg/mL) modified HMDE was utilized for studying its interactions with cisplatin and carboplatin. For both compounds we obtained characteristic voltammograms (Figure 3). It clearly follows from the obtained results that the catalytic signal Cat2 diminished with increasing interaction time. After 20 min, the Cat2 signal decreased by more than 60% for both cytostatics. With increasing interaction times, no decrease of the signal was observed. For both drugs similar results were obtained, but the decrease of the signal was more rapid for cisplatin; where after 15 min interaction no further decrease of the signal was observed. For carboplatin, the decrease of the signal was slower and the lowering of the signal was complete after 20 min interaction. Similar results were obtained for interactions between cisplatin or carboplatin drugs, but a more distinct Cat2 signal decrease was observed after 10 min interaction for carboplatin and after 5 min for cisplatin (Figure 4).
The observed differences in the Cat2 signal decrease indicate that the studied compounds have different affinities for MT, probably due to their chemical structures. Differences between active substances and pharmaceutical drugs are probably caused by the presence of adjuvants in pharmaceutical drugs that significantly change their physicochemical properties (ionic strength, pH). Some of these parameters were investigated in our previous experiments , the obtained knowledge is possible to utilize for MT detection via hydrogen evolution. We can assume which platinum-based therapeutics (cisplatin, carboplatin) were captured by MT anchored onto HMDE surface and we were able to observe only changes directly connected with MT - drug interactions. In addition, El-Hourch et al. published the utilization of cisplatin for hydrogen evolution from supporting electrolyte . However, platinum ions were not in the supporting electrolyte, thus they could not influence the catalytic reaction. The arrangement of the experiment also unambiguously points at the fact that carboplatin and cisplatin were strongly bound to the MT structure.
2.3. Changes in Cell Cultures
As it was demonstrated in our previous experiment in vitro, MT very rapidly and effectively binds platinum-based cytostatics (cisplatin and carboplatin). However, experiments carried out in vitro do not show the behavior of the analyzed compounds in an organism. Therefore, experiments in vivo were carried out to elucidate the significance of MT for resistance origination after the treatment by platinum-based therapeutics.
2.4. Automated Detection of Metallothionein
For routine analysis of larger sets of samples, an automated electroanalytical method for MT determination was found . Reproducibility of determination varied within the range of 96 to 99% (n = 30). Dependence of studied MT signal height was linear in the concentration interval 0.1–5 μM. In our preliminary experiment, we demonstrated that the MT level increases in the presence of platinum-based cytostatics according to the applied concentration. Differences between cisplatin-resistant and cisplatin-sensitive tumor cell lines were also determined [48,55].
We were further interested in studying the time-dependence of these changes in greater detail. We compared the effect of cisplatin and carboplatin in concentrations of 0.01, 0.1 and 1 μM on resistant and sensitive tumor cell lines derived from neuroblastoma - UKF-NB-4. Cell lines were cultivated for 0.5, 1, 2, 4, 6, 12, 24 and 48 h in the presence of platinum-based cytostatic drugs such as cisplatin and carboplatin. At the end of the experiment, cells were homogenized and consequently MT level was determined in cell lysates using the procedure shown in .
Sensitive cell lines demonstrated a significant growth depression in the presence of cytostatic agents. MT level was significantly increased in all sensitive tumor cell lines by about 50–90% in comparison with the control cell line. As it is well evident from Figure 5, the MT level increased in resistant tumor cell lines compared to sensitive cells. In the resistant tumor cell lines, the increase of MT level was dependent on the cytostatic agent used and its concentration. With carboplatin, changes in MT level were observable from the beginning of the experiment, whereas under the two highest carboplatin concentrations the MT level was significantly increased in resistant tumor cells compared to sensitive ones. In the case of the cisplatin-resistant tumor cell line, the MT level increase was firstly observable after six hours of treatment. This increase was consequently followed by a moderate decrease in comparison with the resistant tumor cell line, whose maximum MT level was well evident already in the first hours of the experiment. Then, MT level relatively rapidly decreased to that of the values of sensitive tumor cell lines. Fluctuation in MT after cisplatin as well as carboplatin exposition with a similar development in the presence of all applied concentrations can be interpreted by initiatory free MT saturation by cytostatic agent and its resulting elimination from cells, which results in a decrease of MT level in cells. Resistant tumor cell lines, in contrast to the sensitive ones, responded to the cytostatic agent presence by significantly enhancing MT expression, which was well evident as a rapid increase of the MT level. Determined differences in MT levels during platinum-based cytostatics treatment are in good agreement with our knowledge about cytostatics detoxification via thiol compounds that increase the ability of these tumor cell lines to survive in the presence of platinum-based therapeutics. From the obtained results, it clearly follows that neuroblastoma UKF-NB-4 cisplatin-resistant and cisplatin-sensitive cell lines unlikely respond to the presence of platinum-based cytostatics cisplatin and carboplatin.
2.5. Changes of MT Level in Rabbits after Intravitreal Carboplatin Administration
Retinoblastoma is one of the most frequent intraocular malignant tumors and it is the malignancy with the highest incidence in children. Retinoblastoma genesis is connected with gene mutation of both alleles of the retinoblastoma gene RB1 localized on chromosome 13q1.4. Its therapy is still very difficult, thus, new therapeutic possibilities as well as new ways of cytostatics application are intensively searched. One of these applications is direct injection of cytostatics—in this case especially carboplatin—into the eye. For this purpose, carboplatin was applied to experimental animals and consequently MT level was determined using automated electrochemical detection. Figure 6 shows the changes in MT levels according to the length of the carboplatin treatment. At the beginning, the MT level was about 3.5 μM in healthy rabbits. After carboplatin application, a significant increase in the MT level was determined in all experimental animals up to 5 μM. An enhanced MT level was detected for the following seven days in all experimental animals. A slight decrease in MT level was observed 14 days after carboplatin application. From the obtained results, it clearly follows that MT level was induced by carboplatin application directly into the eyes and can be probably connected with the resistance origination.
2.6. MT Changes in Retinoblastoma Patients
Retinoblastoma is a very rare malignant disease in the Czech Republic. Its treatment is centralized into a specialized workplace: FN Motol, Prague. Samples of retinoblastoma patients (n = 2) treated long-term with carboplatin were analyzed. Figure 7 shows the changes in MT level during long-term therapy in relation to the time-dependent changes after cytostatic agent application. MT levels were monitored 4 or 24 hours after application of the drug and the same procedure was repeated after a few days during the next treatment with carboplatin. In short-time monitoring of MT concentrations, a higher increase was observed with each dose of carboplatin; nevertheless, long periods had a stabilization effect on MT levels in the plasma after carboplatin application.
Immediately after carboplatin application, no MT level increase was detected; only in the first minutes after application a moderate MT level decrease was determined. This is probably connected with the interaction with carboplatin and free MT. Three days after the first application of carboplatin, a moderate MT level decrease (about 9%) was observed in comparison with the first application. Application after 27 days since the first application led to a significant MT level enhancement (165%) compared to the first day. Maximal MT levels were determined between the 30th and 60th day after initial carboplatin application. After the 60th day after the first carboplatin application, MT levels slowly decreased. Figure 7 shows characteristic voltammetric records of individual samples with well distinguishable signals.
3. Experimental Section
3.1. Chemicals and pH Measurements
Rabbit liver MT (MW 7143), containing 5.9% Cd and 0.5% Zn, was purchased from Sigma Aldrich (St. Louis, MO, USA). Tris(2-carboxyethyl)phosphine (TCEP) was produced by Molecular Probes (Evgen, Oregon, WI, USA). Other chemicals used were purchased from Sigma Aldrich. The stock standard solutions of MT at 10 μg/mL with 1 mM TCEP were prepared with ACS water (Sigma-Aldrich, St. Louis, MO, USA) and stored in the dark at −20 °C. Working standard solutions were prepared daily by dilution of the stock solutions. The pH was measured using pH meter WTW inoLab (Weilheim, Germany). The pH-electrode (SenTix-H, pH 0–14/3M KCl) was regularly calibrated by a set of WTW buffers (Weilheim, Germany).
3.2. Tumor Cell Lines
The following cell lines obtained from the Department of Paediatric Haematology and Oncology, Charles University, Prague, Czech Republic were used: UKF-NB4—cisplatin or carboplatin sensitive (prepared from recurrence of neuroblastoma into bone marrow, with MYCN amplification, del 1p34.2ter, del 13iso 17q) and UKF-NB4—cisplatin or carboplatin resistant (the line derived from the previous line—UKF-NB4 with in vitro induced resistance to cisplatin or carboplatin). The cell lines were prepared by cultivation with increasing concentration of cisplatin or carboplatin. The cells were cultivated in IMDM medium with 10% fetal calf serum at 37 °C, the chemoresistant cell lines were cultivated in medium with cisplatin or carboplatin added.
3.3. Human Blood Serum
The samples of blood were obtained using vein tapping to the closed tapping units without another reagent during medical treatment of two patients with malignancies at Teaching Hospital Motol, Czech Republic. All patients subscribed to informed consent with utilization of their blood samples for the research.
3.4. Preparation of the Samples for Electroanalytical Determination of Metallothionein
3.4.1. Human Blood Serum
Human blood serum samples were prepared by heat treatment and solvent precipitation. Briefly, samples were kept at 99 °C in a thermomixer (Eppendorf 5430, USA) for 15 min with occasional stirring, and then cooled to 4 °C. The denatured homogenates were centrifuged at 4 °C, 15,000 × g for 30 min (Eppendorf 5402, USA). Heat treatment effectively denatures and removes high molecular weight proteins from samples . Determination of MT in the human blood serum samples was performed by differential pulse voltammetry Brdicka reaction. Analyzed sample volume was 5 μL.
3.4.2. Tumor Cell Lines
The harvested cells were transferred to a test tube and deep frozen in liquid nitrogen to disrupt the cells. The frozen cells were mixed with extraction buffer (100 mM potassium phosphate, pH 8.7) to a final volume of 1 mL and homogenized using hand-operated homogenizer ULTRA-TURRAX T8 (IKA, Germany) placed in an ice bath for 3 min at 25,000 rpm. The homogenate was centrifuged at 10,000 × g for 15 min and at 4 °C (Eppendorf 5402, USA) . The supernatant were processed in the same way as the human blood serum samples mentioned in Section 3.4.1. The processed samples were measured by adsorptive transfer stripping technique coupled with chronopotentiometric stripping analysis.
3.4.3. Intravitreal Administration of Carboplatin in Rabbits
Administration of carboplatin was performed according to data which indicate that periocular or intravitreal (transcorneal) carboplatin injections rather than systematically administrated carboplatin can effectively treat children with intraocular retinoblastoma. Six adult New Zealand White Rabbits (Anlab, Czech Republic) with an average weight of 2.45 kg (SD ± 0.38) were handled according to the statement Nr.207/2004 s.11 of the Ministry of Agriculture of the Czech Republic for the use of animals in experiments. In vivo experiments were further approved by the ethical committee for animal welfare of Charles University, 2nd Faculty of Medicine. The animals were kept at 22–25 °C room temperature, at 55–65% relative air humidity, and on a 12 h light/dark cycle, and were provided with tap water and rabbit chow TM MaK 1 (Bergman, Kocanda, Czech Republic) ad libitum. The rabbits were anesthetized intramuscularly with a mixture of 30–50 mg/kg of ketamine hydrochloride (Narketan 10, Vétoquinol, France) and 5 mg/kg of xylazine hydrochlorid (Rometar 2%., Spofa, Czech Republic) throughout the experiment. Topical oxybuprocaine eye drops (0.4%, Benoxi, Unimed Pharma, Slovakia) were used to anesthetize the ocular surface before intravitreal puncture.
Carboplatin (Carboplatin, TEVA, Netherlands) solution was prepared immediately before injection by dissolving carboplatin in sterile water with mannitol to the final used concentrations. A single transcorneal intravitreal injection of carboplatin (0.05 mg in total volume of 0.1 mL) was applied with a 25-gauge needle into the right eye; the left eye of all animals served as uninjected controls. Blood samples were taken at 0, 6, 24 and 48 h, 7 and 14 days after injection. Blood samples were drawn from the peripheral auricular vein and collected in tubes with ammonium heparinate. The blood was centrifuged at 3,000 rpm for 10 minutes to separate blood plasma.
3.5. Electrochemical Measurements
3.5.1. Electroanalytical Determination of Metallothionein
An adsorptive transfer stripping technique (AdTS) coupled with DPV Brdicka reaction was employed for the determination of metallothionein in the cell lines extracts. The electrochemical measurements were performed using an AUTOLAB analyzer (EcoChemie, The Netherlands) connected to VA-Stand 663 (Metrohm, Switzerland), using a standard electrochemical cell with a classical three-electrode connection. The three-electrode system consisted of a hanging mercury drop electrode as the working electrode, an Ag/AgCl/3 M KCl reference electrode and a glassy carbon auxiliary electrode. For smoothing and baseline correction, the software GPES 4.9 supplied by EcoChemie was employed. The Brdicka supporting electrolyte (1 mM Co(NH3)6Cl3 in 1 M ammonia buffer (NH3(aq) + NH4Cl, pH = 9.6) was used; no surface-active agent was added. AdTS DPV Brdicka reaction parameters were as follows: initial potential of −0.6 V, end potential −1.6 V, modulation time 0.057 s, time interval 0.2 s, step potential of 1.05 mV, modulation amplitude of 250 mV, Eads = 0 V. Temperature of the supporting electrolyte was 4 °C.
3.5.2. Automated Electroanalytical Determination of Metallothionein
Differential pulse voltammetric Brdicka’s reaction measurements were performed with 747 VA Stand instrument connected to 746 VA Trace Analyzer and 695 Autosampler (Metrohm, Switzerland), using a standard cell with three electrodes and a cooled sample holder (4 °C). A hanging mercury drop electrode (HMDE) with a drop area of 0.4 mm2 was the working electrode. An Ag/AgCl/3M KCl electrode was the reference and glassy carbon electrode was the auxiliary electrode. The software GPES 4.9 supplied by EcoChemie was employed for smoothing and baseline correction of the raw data. The analyzed samples were deoxygenated prior to measurements by purging with argon (99.999%), saturated with water for 120 s. The Brdicka’s supporting electrolyte containing 1 mM Co(NH3)6Cl3 and 1 M ammonia buffer (NH3(aq) + NH4Cl, pH = 9.6) was used and after each measurement the supporting electrolyte was exchanged. The parameters of the measurement were as follows: initial potential of −0.7 V, end potential of −1.75 V, modulation time 0.057 s, time interval 0.2 s, step potential 2 mV, modulation amplitude −250 mV, Eads = 0 V. All experiments were carried out at 4 °C employing thermostat Julabo F12 (Labortechnik GmbH, Germany). One hundred-times diluted sample with 0.1 M phosphate buffer pH 7.0 (20 μL) was used.
3.6. Descriptive Statistics
Data were processed using MICROSOFT EXCEL® (USA) and STATISTICA.CZ Version 8.0 (Czech Republic). Results are expressed as mean ± standard deviation (S.D.) unless otherwise noted (EXCEL®). Statistical significance of the differences between MT levels and rat weight were determined using STATISTICA.CZ. Differences with p < 0.05 were considered significant and were determined using one way ANOVA test (particularly Scheffe test), which was applied for means comparison.
Adsorptive transfer technique differential pulse voltammetry coupled with Brdicka reaction presents a unique possibility for studying interactions between proteins and cytostatics. Catalytic signals are very sensitive and enable the study of interactions at the nanomolar level. In addition, our in vivo experiments verify the hypothesis that MT levels significantly increase after platinum-based therapeutic application. In the case of platinum-resistant tumor cell lines, the MT level significantly increases. Thus, MT can act as one of the factors of tumor therapy resistance. For understanding these mechanisms, experiments on experimental animals were carried out and in addition MT levels were monitored in patients with a rare malignant disease—retinoblastoma—after platinum-based cytostatics treatment.
This work was supported by grants: GA AV IAA401990701, IGA MZ Czech Republic NR/9532-3/2007, IGA MZ 10200-3, INCHEMBIOL MSM0021622412 and LPR 2011.
- Bosetti, C; Bertuccio, P; Levi, F; Lucchini, F; Negri, E; La Vecchia, C. Cancer mortality in the European Union, 1970–2003, with a joinpoint analysis. Ann. Oncol 2008, 19, 631–640. [Google Scholar]
- Levi, F; Ferlay, J; Galeone, C; Lucchini, F; Negri, E; Boyle, P; La Vecchia, C. The changing pattern of kidney cancer incidence and mortality in Europe. BJU Int 2008, 101, 949–958. [Google Scholar]
- Ferlay, J; Randi, G; Bosetti, C; Levi, F; Negri, E; Boyle, P; La Vecchia, C. Declining mortality from bladder cancer in Europe. BJU Int 2008, 101, 11–19. [Google Scholar]
- Zatonski, WA; Manczuk, M; Powles, J; Negri, E. Convergence of male and female lung cancer mortality at younger ages in the European Union and Russia. Eur. J. Public Health 2007, 17, 450–454. [Google Scholar]
- Black, RJ; Bray, F; Ferlay, J; Parkin, DM. Cancer incidence and mortality in the European Union: Cancer registry data and estimates of national incidence for 1990. Eur. J. Cancer 1997, 33, 1075–1107. [Google Scholar]
- Boyle, P; Ferlay, J. Cancer incidence and mortality in Europe, 2004. Ann. Oncol 2005, 16, 481–488. [Google Scholar]
- Levi, F; Lucchini, F; Negri, E; Boyle, P; La Vecchia, C. Cancer mortality in Europe, 1995–1999, and an overview of trends since 1960. Int. J. Cancer 2004, 110, 155–169. [Google Scholar]
- Levi, F; Lavecchia, C; Lucchini, F; Negri, E. Cancer Mortality in Europe, 1990–92. Eur. J. Cancer Prev 1995, 4, 389–417. [Google Scholar]
- Levi, F; Lucchini, F; Negri, E; La Vecchia, C. Trends in mortality from major cancers in the European Union, including acceding countries, in 2004. Cancer 2004, 101, 2843–2850. [Google Scholar]
- Levi, F; La Vecchia, C; Negri, E; Lucchini, F. Childhood cancer mortality in Europe, 1955–1995. Eur. J. Cancer 2001, 37, 785–809. [Google Scholar]
- Okazaki, Y; Namikawa, K; Minami, T. Studies of metals and metallothionein in tissue. Yakugaku Zasshi-J. Pharm. Soc. Jpn 2000, 120, 282–289. [Google Scholar]
- Sakai, W; Swisher, EM; Karlan, BY; Agarwal, MK; Higgins, J; Friedman, C; Villegas, E; Jacquemont, C; Farrugia, DJ; Couch, FJ; Urban, N; Taniguchi, T. Secondary mutations as a mechanism of cisplatin resistance in BRCA2-mutated cancers. Nature 2008, 451, 1116–1119. [Google Scholar]
- Cavaletti, G. Peripheral neurotoxicity of platinum-based chemotherapy. Nat. Rev. Cancer 2008, 8, 1. [Google Scholar]
- Damsma, GE; Alt, A; Brueckner, F; Carell, T; Cramer, P. Mechanism of transcriptional stalling at cisplatin-damaged DNA. Nat. Struct. Mol. Biol 2007, 14, 1127–1133. [Google Scholar]
- Loehrer, PJ; Einhorn, LH. Drugs 5 years later - cisplatin. Ann. Intern. Med 1984, 100, 704–713. [Google Scholar]
- Sancar, A. DNA excision repair. Annu. Rev. Biochem 1996, 65, 43–81. [Google Scholar]
- Borst, P; Evers, R; Kool, M; Wijnholds, J. A family of drug transporters: The multidrug resistance-associated proteins. J. Natl. Cancer Inst 2000, 92, 1295–1302. [Google Scholar]
- Borst, P; Evers, R; Kool, M; Wijnholds, J. The multidrug resistance protein family. Biochim. Biophys. Acta-Biomembr 1999, 1461, 347–357. [Google Scholar]
- Siddik, ZH. Cisplatin: Mode of cytotoxic action and molecular basis of resistance. Oncogene 2003, 22, 7265–7279. [Google Scholar]
- Gately, DP; Howell, SB. Cellular Accumulation of the Anticancer Agent Cisplatin - a Review. Br. J. Cancer 1993, 67, 1171–1176. [Google Scholar]
- Prestayko, AW; Daoust, JC; Issell, BF; Crooke, ST. Cisplatin (Cis-Diamminedichloroplatinum-Ii). Cancer Treat. Rev 1979, 6, 17–39. [Google Scholar]
- Rosenberg, B; van Camp, L; Krigas, T. Inhibition of cell division in Escherichia coli by electrolysis products from a platinum electrode. Nature 1965, 205, 698–699. [Google Scholar]
- Fink, D; Aebi, S; Howell, SB. The role of DNA mismatch repair in drug resistance. Clin. Cancer Res 1998, 4, 1–6. [Google Scholar]
- Raymond, E; Chaney, SG; Taamma, A; Cvitkovic, E. Oxaliplatin: A review of preclinical and clinical studies. Ann. Oncol 1998, 9, 1053–1071. [Google Scholar]
- Wang, D; Lippard, SJ. Cellular processing of platinum anticancer drugs. Nat. Rev. Drug Discov 2005, 4, 307–320. [Google Scholar]
- Kartalou, M; Essigmann, JM. Mechanisms of resistance to cisplatin. Mutat. Res.-Fundam. Mol. Mech. Mutagen 2001, 478, 23–43. [Google Scholar]
- Weiss, RB; Christian, MC. New cisplatin analogs in development - a review. Drugs 1993, 46, 360–377. [Google Scholar]
- Go, RS; Adjei, AA. Review of the comparative pharmacology and clinical activity of cisplatin and carboplatin. J. Clin. Oncol 1999, 17, 409–422. [Google Scholar]
- Cohen, SM; Lippard, SJ. Cisplatin: From DNA damage to cancer chemotherapy. In Progress in Nucleic Acid Research and Molecular Biology; Academic Press Inc: San Diego, CA, USA, 2001; Volume 67, pp. 93–130. [Google Scholar]
- Krizkova, S; Adam, V; Petrlova, J; Zitka, O; Stejskal, K; Zehnalek, J; Sures, B; Trnkova, L; Beklova, M; Kizek, R. A suggestion of electrochemical biosensor for study of platinum(II)-DNA interactions. Electroanalysis 2007, 19, 331–338. [Google Scholar]
- Sato, M; Suzuki, S. Endoplasmic reticulum stress and metallothionein. Yakugaku Zasshi-J. Pharm. Soc. Jpn 2007, 127, 703–708. [Google Scholar]
- Kerbel, RS. Molecular origins of cancer: Tumor angiogenesis. N. Engl. J. Med 2008, 358, 2039–2049. [Google Scholar]
- Adam, V; Fabrik, I; Eckschlager, T; Stiborova, M; Trnkova, L; Kizek, R. Vertebrate metallothioneins as target molecules for analytical techniques. TRAC-Trends Anal. Chem 2010, 29, 409–418. [Google Scholar]
- Adam, V; Petrlova, J; Wang, J; Eckschlager, T; Trnkova, L; Kizek, R. Zeptomole electrochemical detection of metallothioneins. PLoS ONE 2010, 5, e11441. [Google Scholar]
- Eckschlager, T; Adam, V; Hrabeta, J; Figova, K; Kizek, R. Metallothioneins and cancer. Curr. Protein Pept. Sci 2009, 10, 360–375. [Google Scholar]
- Krizkova, S; Fabrik, I; Adam, V; Hrabeta, J; Eckschlager, T; Kizek, R. Metallothionein – a promising tool for cancer diagnostics. Bratisl. Med. J.-Bratisl. Lek. Listy 2009, 110, 93–97. [Google Scholar]
- Bell, SG; Vallee, BL. The metallothionein/thionein system: An oxidoreductive metabolic zinc link. ChemBioChem 2009, 10, 55–62. [Google Scholar]
- Haase, H; Maret, W. Partial oxidation and oxidative polymerization of metallothionein. Electrophoresis 2008, 29, 4169–4176. [Google Scholar]
- Li, Y; Maret, W. Human metallothionein metallomics. J. Anal. At. Spectrom 2007, 23, 1055–1062. [Google Scholar]
- Pedersen, MO; Larsen, A; Stoltenberg, M; Penkowa, M. The role of metallothionein in oncogenesis and cancer prognosis. Prog. Histochem. Cytochem 2009, 44, 29–64. [Google Scholar]
- Miura, N; Koizumi, S. Heavy metal responses of the human metallothionein isoform genes. Yakugaku Zasshi-J. Pharm. Soc. Jpn 2007, 127, 665–673. [Google Scholar]
- Otsuka, F; Ohno, S; Suzuki, K; Takahashi, K; Ohsawa, M; Koizumi, S. Mechanism of metallothionein gene activation mediated by heavy-metal dependent transcription factor MTF-1. Yakugaku Zasshi-J. Pharm. Soc. Jpn 2007, 127, 675–684. [Google Scholar]
- Itoh, N; Kimura, T. Cytokine-induced metallothionein expression and modulation of cytokine expression by metallothionein. Yakugaku Zasshi-J. Pharm. Soc. Jpn 2007, 127, 685–694. [Google Scholar]
- Min, KS. The physiological significance of metallothionein in oxidative stress. Yakugaku Zasshi-J. Pharm. Soc. Jpn 2007, 127, 695–702. [Google Scholar]
- Satoh, M. Analysis of toxicity using metallothionein knockout mice. Yakugaku Zasshi-J. Pharm. Soc. Jpn 2007, 127, 709–717. [Google Scholar]
- Ohashi, T; Satoh, T; Kuwata, M; Fujimura, T; Taketani, S. Visualization and evaluation of the promoter activities of genes for stress-inducible proteins in response to environmental pollutants. Yakugaku Zasshi-J. Pharm. Soc. Jpn 2007, 127, 757–764. [Google Scholar]
- Kaji, T. Cell biology of heavy metal toxicity in vascular tissue. Yakugaku Zasshi-J. Pharm. Soc. Jpn 2004, 124, 113–120. [Google Scholar]
- Fabrik, I; Krizkova, S; Huska, D; Adam, V; Hubalek, J; Trnkova, L; Eckschlager, T; Kukacka, J; Prusa, R; Kizek, R. Employment of electrochemical techniques for metallothionein determination in tumor cell lines and patients with a tumor disease. Electroanalysis 2008, 20, 1521–1532. [Google Scholar]
- Adam, V; Baloun, J; Fabrik, I; Trnkova, L; Kizek, R. An electrochemical detection of metallothioneins at the zeptomole level in nanolitre volumes. Sensors 2008, 8, 2293–2305. [Google Scholar]
- Adam, V; Hanustiak, P; Krizkova, S; Beklova, M; Zehnalek, J; Trnkova, L; Horna, A; Sures, B; Kizek, R. Palladium biosensor. Electroanalysis 2007, 19, 1909–1914. [Google Scholar]
- Adam, V; Krizkova, S; Zitka, O; Trnkova, L; Petrlova, J; Beklova, M; Kizek, R. Determination of apo-metallothionein using adsorptive transfer stripping technique in connection with differential pulse voltammetry. Electroanalysis 2007, 19, 339–347. [Google Scholar]
- Petrlova, J; Potesil, D; Mikelova, R; Blastik, O; Adam, V; Trnkova, L; Jelen, F; Prusa, R; Kukacka, J; Kizek, R. Attomole voltammetric determination of metallothionein. Electrochim. Acta 2006, 51, 5112–5119. [Google Scholar]
- Adam, V; Petrlova, J; Potesil, D; Zehnalek, J; Sures, B; Trnkova, L; Jelen, F; Kizek, R. Study of metallothionein modified electrode surface behavior in the presence of heavy metal ions-biosensor. Electroanalysis 2005, 17, 1649–1657. [Google Scholar]
- Hou, XF; Fan, QX; Wang, LX; Lu, SX. Role of metallothionein1h in cisplatin resistance of non-small cell lung cancer cells. Chin. J. Cancer Res 2009, 21, 247–254. [Google Scholar]
- Krizkova, S; Adam, V; Eckschlager, T; Kizek, R. Using of chicken antibodies for metallothionein detection in human blood serum and cadmium-treated tumor cell lines after dot- and electroblotting. Electrophoresis 2009, 30, 3726–3735. [Google Scholar]
- Erk, M; Ivankovic, D; Raspor, B; Pavicic, J. Evaluation of different purification procedures for the electrochemical quantification of mussel metallothioneins. Talanta 2002, 57, 1211–1218. [Google Scholar]
- Adam, V; Beklova, M; Pikula, J; Hubalek, J; Trnkova, L; Kizek, R. Shapes of differential pulse voltammograms and level of metallothionein at different animal species. Sensors 2007, 7, 2419–2429. [Google Scholar]
- Adam, V; Blastik, O; Krizkova, S; Lubal, P; Kukacka, J; Prusa, R; Kizek, R. Application of the Brdicka reaction in determination of metallothionein in patients with tumours. Chem. Listy 2008, 102, 51–58. [Google Scholar]
- Diopan, V; Shestivska, V; Adam, V; Macek, T; Mackova, M; Havel, L; Kizek, R. Determination of content of metallothionein and low molecular mass stress peptides in transgenic tobacco plants. Plant Cell Tissue Organ Cult 2008, 94, 291–298. [Google Scholar]
- Fabrik, I; Ruferova, Z; Hilscherova, K; Adam, V; Trnkova, L; Kizek, R. A determination of metallothionein in larvae of freshwater midges (Chironomus riparius) using Brdicka reaction. Sensors 2008, 8, 4081–4094. [Google Scholar]
- Krizkova, S; Blahova, P; Nakielna, J; Fabrik, I; Adam, V; Eckschlager, T; Beklova, M; Svobodova, Z; Horak, V; Kizek, R. Comparison of metallothionein detection by using brdicka reaction and enzyme-linked immunosorbent assay employing chicken yolk antibodies. Electroanalysis 2009, 21, 2575–2583. [Google Scholar]
- Huska, D; Fabrik, I; Baloun, J; Adam, V; Masarik, M; Hubalek, J; Vasku, A; Trnkova, L; Horna, A; Zeman, L; Kizek, R. Study of interactions between metallothionein and cisplatin by using differential pulse voltammetry brdicka’s reaction and quartz crystal microbalance. Sensors 2009, 9, 1355–1369. [Google Scholar]
- El Hourch, M; Dudoit, A; Amiard, JC. An optimization procedure for determination of metallothionein by square wave cathodic stripping voltammetry: Application to marine worms. Anal. Bioanal. Chem 2004, 378, 776–781. [Google Scholar]
- Supalkova, V; Petrek, J; Baloun, J; Adam, V; Bartusek, K; Trnkova, L; Beklova, M; Diopan, V; Havel, L; Kizek, R. Multi-instrumental investigation of affecting of early somatic embryos of Spruce by cadmium(II) and lead(II) ions. Sensors 2007, 7, 743–759. [Google Scholar]
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