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Contemporary Oncology/Współczesna Onkologia
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vol. 16
 
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Original paper

New fluphenazine analogues as inhibitors of P-glycoprotein in human lymphocyte cultures

Agata Jaszczyszyn, Kazimierz Gąsiorowski, Piotr Świątek, Wiesław Malinka, Katarzyna Cieślik-Boczula, Joanna Petrus, Bogusława Czarnik-Matusewicz

Wspolczesna Onkol 2012; 16 (4): 332–337
Online publish date: 2012/09/29
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Introduction

Development of multidrug resistance (MDR) in cancer and in genotoxically damaged cells is the main reason for failure of cytostatic therapy [1]. MDR is defined as gradual lowering of sensitivity of neoplastic and/or genotoxically damaged cells to various cytostatic drugs, which develops in the course of a chemotherapy [2]. The mechanisms of MDR occurrence comprise the increase of cell-membrane transport, which leads to lower accumulation of cytostatic drugs inside cancer cells, the diminution of intracellular target enzyme affinity, the increase of metabolism and detoxification systems of cytostatic drugs, stimulation of the DNA repair systems and inhibition of apoptosis [1, 2].

The well-known mechanism responsible for MDR appearance is the increased expression of P-glycoprotein (Pgp) in neoplastic cells which leads to elevation of the energy-dependent transport of many drug molecules, including cytostatics, from the inner part of the cell membrane to the extracellular environment [2–4]. A decrease of cytostatic drug accumulation in a cytoplasm and occurrence of cell resistance to cytostatics appear as a result of Pgp overexpression [4, 5]. That is why the application to cancer chemotherapy of natural or synthetic compounds, able to inhibit the Pgp transport function, has been recognized as an effective strategy for restoration of sensitivity of neoplastic cells to cytostatic drugs [1, 6]. These compounds, administered together with cytostatic drugs, markedly elevate intracellular accumulation and thereby raise their cytotoxic/cytostatic effects. Such compounds are called MDR modulators, and are recommended as adjuvant agents in neoplastic disease treatment [7, 8].

Phenothiazine derivatives belong to the group of MDR modulators; they are recognized as Pgp inhibitors. Fluphenazine (FPh), a drug from the phenothiazine family, for years has been used in psychopharmacotherapy [6, 8, 9]. Our previous research proved that in culture of genotoxically damaged cells FPh also significantly inhibited the transport function of Pgp [10]. It could be considered as a good adjuvant drug in cancer chemotherapy. However, its application in oncological therapy is limited by numerous undesirable effects on the central nervous system, even induction of drug-induced parkinsonism [11]. Therefore we have undertaken chemical syntheses to obtain new FPh derivatives exhibiting comparably strong chemopreventive activity as the parent FPh but possessing lower ability to pass through the blood-brain barrier.

The newly synthesized FPh analogues are characterized by lower lipophilicity value (logP) or a higher molecular weight (MW). Therefore it can be assumed that they should poorly penetrate into the central nervous system and will cause extrapyramidal symptoms to a lesser extent [12].

Aim of the study

The aim of this study was to estimate the effect of 17 newly synthesized FPh analogues on the inhibition of Pgp transport function in genotoxically damaged human lymphocyte cultures. It was our intention to identify analogues that are more effective than FPh in Pgp inhibition while also promising lower penetration through the blood-brain barrier to the central nervous system.

Material and methods

Chemicals



Phytohaemagglutinin, Minimum Essential Medium Eagle (MEM) and fetal calf serum were purchased from GIBCO (Gaithesburg, MD, USA). FPh-2HCl was obtained from Jelfa (Jelenia Góra, Poland), Rod-123 and all other reagents were obtained from SIGMA-ALDRICH (St. Louis, MO, USA). Lymphoflot and benzo[]pyrene (B[]P) were purchased from Bio-Rad Medical Diagnostics (Dreieich, Germany) and Fluka (Buchs, Switzerland), respectively.



Synthesis and properties of new FPh analogues



New chemical FPh analogues were synthesized in the Department of Drug Chemistry (Wrocław Medical University). The chemical structures of FPh and its analogues are given in Table 1.

Estimations of physical properties of FPh and its analogues – lipophilicity expressed as the logP was calculated with the ChemPlus program from Hypercube, Inc., IBM PC version. The main physicochemical properties (MW, logP) of FPh and its analogues are provided in Table 2.

Detailed information concerning synthesis of new FPh analogues investigated in this work and their physicochemical and spectral properties are available exclusively on request (e-mail: wieslaw.malinka@am.wroc.pl).



Lymphocyte separation from peripheral blood



The research was approved by the Wrocław Medical University Ethics Committee. Heparinized venous blood (20 ml) was obtained by venipuncture from 5 volunteers, healthy, non-smoking males, aged 20–26 years. Human lymphocytes were separated by the method of gradient centrifugation with Histopaque-1077 (Lymphoflot) [13]. The obtained mononuclear buffy coats were rinsed three times in MEM and monocytes were removed by the cell adhesion procedure. Lymphocytes were counted and viability of the cells was checked under a microscope after staining of the cell suspension with 0.4% trypan blue solution. The viability of isolated lymphocytes exceeded 90% of cells.



Lymphocyte cultures



Lymphocytes were seeded into 96-well plates at a density of 4  104 cells/well. Cells were grown in MEM containing 10% fetal calf serum and phytohaemagglutinin (2% v/v) at 37°C in a humidified CO2 incubator. Cells were stimulated to increase the Pgp expression and to introduce genotoxic damage by incubation with benzo[]pyrene (B[]P) (7.5 M, 48 h). Lymphocyte cultures kept in the presence of B[]P without the tested compounds were used as controls. After pre treatment with B[]P for 48 h, cells were incubated with 10 M FPh or its new analogues in culture medium at 37°C in 5% CO2 for 2 h.



Rhodamine 123 accumulation assay



The rhodamine 123 (Rod-123) accumulation test was used to estimate the effect of FPh and its chemical analogues on inhibition of the Pgp transport function activity [14]. Rod-123 is a substrate for Pgp, which substitutes many cytostatics transported by protein in the in vitro tests [14].

After incubation with tested compounds, lymphocytes were cultured with 5 M Rod-123 in culture medium, in the dark, at 37°C in 5% CO2 for 60 min. The fluorescence of intracellular Rod-123 accumulation was measured at 488–530 nm using Victor2 reader.



Statistical evaluation



Statistical analyses were performed using the program STATISTICA 9.1 PL. All experiments were repeated 5 times (n = 5). Values were expressed as mean, standard deviation (SD), minimal value, maximal value and median. t-test was applied to determine significant differences between the lymphocyte cultures.

Results

The effect of FPh and its 17 analogues on Pgp transport function in the tested lymphocyte cultures was estimated by measurement of fluorescence intensity of Rod-123 accumulated inside the cells, and was expressed as fluorescence arbitrary units (FAU). The results obtained in lymphocyte cultures with the tested compounds (E) were compared with the results in the control cultures (Eo) and defined as the E/Eo ratio; they are presented in histograms in Fig. 1.

The descriptive statistics and the statistical significance of the data shown in Fig. 1 are collected in Table 3.

Figure 1 and Table 3 show that among the 17 examined FPh analogues, 10 of them significantly (p < 0.05; p < 0.01) increased the accumulation of Rod-123 (inhibited the transport function of Pgp) in lymphocyte cultures which were genotoxically damaged (with B[]P), in comparison with the control cultures. The greatest increase of Rod-123 accumulation, by 21–36% (on average by 25%), was observed with analogues 1a, 1b, 1d, 3f, 3h and 3i. Depending on their inhibition of Pgp transport function, the examined FPh analogues can be ranged as follows: 3i > 3f > 1b > 3h > 1a = 1d.

In the above series of experiments, the parent drug, FPh [10 μM], did not significantly influence (p > 0.05) the Rod-123 accumulation in the genotoxically damaged lymphocyte cultures.

Discussion

It is assumed that an effective chemosensitizing compound should inhibit the transport function of Pgp [15]. FPh belongs to the group of potential modulators of Pgp activity [16]. Our previous results showed that the FPh chemosensitizing effect was inversely proportional to its concentration in human lymphocytes cultures, genotoxically damaged by the model promutagen B[]P [10]. We found that FPh in low concentration [0.125 μM; 0.25 μM] inhibited Pgp activity more strongly than in a concentration of 10 M or higher [10]. Moreover, it was observed that the effect depended on the cell cycle in the period of incubation with FPh [10 μM] being statistically significant or insignificant [10, 17].

It can be surmised that FPh in a concentration over 10 M revealed an additional mechanism of impact on Pgp activity – together with direct interactions with the protein and/or its phosphorylation pathways, it also induced reorganization of the lipid environment of the cell membrane in the vicinity of Pgp. In the higher concentration of FPh [> 10 μM] we observed a cytotoxic effect of the drug, which could also be explained by the interaction of the drug with membrane lipids. Therefore the FPh chemosensitizing activity and that of its 17 newly synthesized analogues in human lymphocytes cultures was tested in a concentration of 10 M and incubation time of 2 hours. In these incubation conditions toxic effects of the tested compounds on lymphocytes were not observed. The spectrofluorometric test of fluorochrome Rod-123 retention enables one not only to examine the transport function of Pgp, but also to assess the real chemosensitizing effect [18].

Human lymphocytes are recommended in the literature for in vitro tests of Pgp activity, because they express Pgp, which is functionally similar to the transport protein in neoplastic cells with MDR phenotype [19]. Pre incubation of lymphocytes with B[]P led to genotoxic damage and increased expression of Pgp in lymphocytes. Concentration [7.5 μM] and the pre incubation time of B[]P with model cells [48 h] were previously experimentally assessed as well-tolerated by lymphocytes and inducing the expected effects.

The unwanted extrapyramidal side effects of FPh are the consequence of its accumulation in brain tissue and the interaction with dopaminergic receptors. To decrease the affinity of new analogues to dopaminergic receptors in the brain’s nigrostriatal system, a hydroxylic group (-OH) was introduced to a propyl bond {-(CH2)3}, which connects nitrogen (N), from the main phenothiazine tricyclic system, with an amine group in the side chain (Table 1) [20].

Only the 2c analogue did not have the -OH group in that place, but it had a butyl bond {-(CH2)4} instead of a propyl bond (Table 1) as the only one out of all the examined FPh analogues.

According to the literature data, the butyl bond in the compounds’ structure from the phenothiazine group determines their ability to reverse MDR [21]. The results of our research did not confirm these results − the 2c analogue did not exhibit greater chemosensitizing activity in comparison to FPh and to its analogues (Fig. 1; Table 3).

Out of the 17 new FPh analogues (10 M), the strongest inhibitory effect on Pgp transport function in human genotoxically damaged lymphocyte cultures was established in the cases of compounds 1a, 1b, 1d, 3f, 3h and 3i. The greatest increase in Rod-123 accumulation in lymphocyte cultures was observed in the presence of analogues which contain a tertiary amine in the side chain: a piperazine amine (compounds 3i and 3f) or aliphatic amine (1b compound). The 1d analogue also had a tertiary aliphatic amine in its side chain, but in comparison to the most active 1b analogue it had fewer -OH groups in the side chain. Chemosensitizing activity, similar to 1a and 1d analogues, had bisphenothiazine – 3 h analogue.

The obtained results showed that the chemosensitizing effect of the new FPh analogues depends on their chemical structure − the presence of piperazine tertiary amine and the next amine groups, or the presence of aliphatic tertiary amine in the environment of at least three -OH groups seemed to be advantageous for blocking Pgp transport function and overcoming MDR. These observations determine further directions of chemical FPh compound modifications and the synthesis of its next analogues.

In conclusion, the search for new FPh analogues, effective Pgp modulators, is promising and should be continued. At the moment, the compounds 1a, 1b, 1d, 3f, 3h and 3i have been identified as good candidates for adjuvant agents in cancer chemotherapy.



This work was supported by the Polish Ministry of Sciences and Higher Education (Grant No. NN204 150338), Wrocław Medical University (Grant No. 1945) and in part by the research fellowship within “Development programme of Wroclaw Medical University” funded by the European Social Fund, Human Capital, National Cohesion Strategy (contract no. UDA-POKL.04.01.01-00-010/08-01) and ST-413.

This paper was presented at the 3rd Congress of Contemporary Oncology, Poznań, Poland, April 14-16, 2011.

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Address for correspondence



Agata Jaszczyszyn




Department of Basic Medical Sciences

Wrocław Medical University

Kochanowskiego 14

51-601 Wrocław

tel. + 48 71 348 43 10

e-mail: ludwig5@op.pl



Submitted: 7.12.2011

Accepted: 7.05.2012
Copyright: © 2012 Termedia Sp. z o. o. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
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