A protein kinase Cβ inhibitor attenuates multidrug resistance of neuroblastoma cells

Neuroblastoma is a childhood tumor originating from the peripheral sympathetic nervous system. It is characterized of two different patterns of disease progress. One, frequently occurring in very young children and without amplification of the MYCN gene, is often associated with good prognosis and sometimes even with spontaneous regression. The other group of tumors, however, often involving slightly older children and with MYCN amplification is associated with poor prognosis [1]. A common feature of highly malignant neuroblastoma is the acquisition of multidrug resistance [2].

Protein kinase C (PKC) constitutes a family of closely related protein serine/threonine kinase which are sub-grouped into classical (PKCα, βI, βII, and γ), novel (PKCδ, ε, η, and θ), and atypical (PKCι and ζ) isoforms. The basis for this classification is different domain structure and activator requirements of the isoforms [3]. The members of the PKC family are involved in the regulation of numerous cell processes including proliferation, apoptosis, and differentiation. It is likely that each isoform has a specific role in a given cell.

We have shown that neuroblastoma cells express PKCα, βI, and βII of the classical isoforms and PKCδ and ε of the novel isoforms [4, 5]. Of these isoforms PKCε is a positive regulator of neurite outgrowth during differentiation of these cells [6, 7] whereas PKCβI seems to have a positive role for neuroblastoma cell proliferation [5]. The latter study also indicated that inhibition of PKCβ could potentiate the growth suppressive effect of microtubule-interacting anticancer drugs.

The aim of this study was to investigate whether inhibition of PKCβ isoforms could be utilized to potentiate the effects of chemotherapeutic drugs on neuroblastoma cells. For that purpose three cell lines, one without MYCN amplification (SH-SY5Y), and two MYCN-amplified (IMR-32 and SK-N-BE(2)), were screened for the combinatorial effects of the PKCβ inhibitor and several chemotherapeutic drugs. One of these cell lines, SK-N-BE(2), has been shown to exhibit resistance to a broad range of anti-cancer compounds.

We found that the specific PKCβ inhibitor LY379196 suppressed the growth of all three neuroblastoma cell lines studied and that it potentiated the growth-suppressive effect of all investigated chemotherapeutics, except carboplatin, on the drug-resistant SK-N-BE(2) cell line. Furthermore, LY379196 potentiated the accumulation of [³H]vincristine in the SK-N-BE(2) cells suggesting that an effect on the elimination of the chemotherapeutic drugs is the mechanism whereby LY379196 influences the effect on cell growth.

In a previous study we found that inhibition of PKCβ with LY379196 suppresses the proliferation and growth of SK-N-BE(2) cells [5]. In order to examine whether this is a cell line-specific effect, or if it is more general in terms of neuroblastoma cells, three neuroblastoma cell lines – IMR-32, SH-SY5Y, and SK-N-BE(2) – were cultured in the presence of increasing concentrations of LY379196 (Figure 1). This showed that all cell lines were sensitive to LY379196. At a concentration of 300 nM, LY379196 suppressed the number of viable cells with 16–24% for the three cell lines, which indicates that a PKCβ isoform has a positive effect on neuroblastoma cell growth.

To elucidate a putative synergistic effect of the PKCβ inhibitor and different anticancer drugs used for neuroblastoma therapy the three cell lines were cultured in the presence of increasing concentrations of doxorubicin, etoposide, paclitaxel, vincristine, or carboplatin together with different concentrations of LY379196 (Figure 2, Table 1). The cell lines displayed different sensitivity to the anticancer drugs. IMR-32 was consistently the most sensitive to all drugs investigated. SH-SY5Y and IMR-32 were equally sensitive to the topoisomerase inhibitors doxorubicin and etoposide whereas SH-SY5Y cells were three- to four-fold less sensitive to the microtubule interacting agents paclitaxel and vincristine and to the DNA intercalator carboplatin. SK-N-BE(2) was the most resistant cell line being more than fifty-fold more resistant to doxorubicin, etoposide and carboplatin than the other cell lines. SK-N-BE(2) cells also displayed a substantially higher resistance to vincristine and paclitaxel.

When LY379196 was included in the medium there was a clear difference in effect depending on the cell line studied. For IMR-32, the least drug-resistant cell line, no effect of LY379196 on the potency of the chemotherapeutic drugs was observed. With 500 nM there was a suppression of the number of viable cells but this reflects the inherent growth-suppressive effect of LY379196 (Figure 1) and was not due to an enhancement of the potency of anticancer agents on IMR-32 cells.

For SH-SY5Y cells, concomitant exposure to 500 nM LY379196 led to approximately a doubling of the potency of doxorubicin, paclitaxel, and vincristine. The ED₅₀ values were decreased from 9.3, 8.3 and 1.41 nM, respectively, in the absence of LY379196 to 5.0, 4.3 and 0.57 nM (column A in Table 1), respectively, in the presence of 500 nM LY379196. These values reflect the potency of the chemotherapeutic drugs, since the growth-suppressing effect of LY379196 has been compensated for in the calculation. If the combined effect of 500 nM LY379196 and the chemotherapeutic drugs is studied, the drug concentration necessary to suppress the number of viable cells to 50% of the amount obtained in the absence of both chemotherapeutic agent and LY379196 is further reduced to 2.0 nM, 27 nM and 0.33 nM (column B in Table 1) for doxorubicin, paclitaxel and vincristine, respectively. This correlates to some degrees to the spectrum of drug resistance of SH-SY5Y cells compared to IMR-32 cells since SH-SY5Y cells are more resistant to both paclitaxel and vincristine. However, no effect was observed on the potency of carboplatin, despite the fact that SH-SY5Y cells are less sensitive to this compound.

The effect of LY379196 was most pronounced on SK-N-BE(2) cells, the cell line with the lowest sensitivity to the anticancer drugs. When 500 nM LY379196 was included in the medium, there was an eight-fold decrease in the ED₅₀ value of vincristine (from 42 to 5.2 nM), approximately a three-fold decrease of the values for doxorubicin (from 920 to 270 nM) and paclitaxel (from 117 to 40 nM), and also an enhancement of the etoposide effect (column A in Table 1). These changes reflect an effect of LY379196 on the potency of the chemotherapeutic compounds since the inherent growth-inhibitory effect of LY379196 was compensated for in the calculations. As for SH-SY5Y cells, there was no effect of LY379196 on the cytotoxic/growth suppressive effect of carboplatin (Figure 2, Table 1).

If the potentiating effect on the chemotherapeutic drugs is mediated via an inhibition of PKCβ isoforms, other inhibitors of PKC would be expected to yield a similar effect. Therefore the effect of two PKC inhibitors, GF109203X which inhibits all PKC isoforms and Gö6976 which only inhibits classical isoforms, on the growth-inhibiting effects of vincristine on SK-N-BE(2) cells was investigated (Figure 3, Table 2). This experiment demonstrated that both these inhibitors increase the sensitivity of SK-N-BE(2) cells to vincristine. When the growth-suppressing effects of the inhibitors were compensated for, we found that the ED₅₀ of vincristine was roughly halved in the presence of 500 nM of either inhibitor (column A in Table 2). Gö6976 by itself also caused a substantial decrease of the amount viable cells.

The largest effect of LY379196 was observed for chemotherapeutic agents of the natural compound group and no effect was seen together with carboplatin. Resistance towards natural products has mostly been associated with a multidrug resistance phenotype, which has been suggested to be due to an increased expression of proteins, which pump out the compounds from the cells. To investigate whether inhibition of PKCβ influences this mechanism of resistance, the accumulation of [³H]vincristine was analyzed in the presence of increasing concentrations of PKC inhibitors (Figure 4). All inhibitors used (LY379196, GF109203X, and Gö6976) caused an enhancement of the accumulation of [³H]vincristine. The specific PKCβ inhibitor, LY379196, was the most potent compound and the concentrations which augmented the vincristine accumulation reflected the concentrations that sensitized the SK-N-BE(2) cells to vincristine.

We have previously seen that inhibition of a PKCβ isoform, conceivably PKCβI, suppresses the proliferation of the SK-N-BE(2) neuroblastoma cell line [5]. The data in this study indicate that the proliferation supporting effect of a PKCβ isoform may be general for neuroblastoma cells since the growth of the two other cell lines tested also were sensitive to the PKCβ inhibitor. When 300 nM LY379196 was included in the medium there were fewer cells after four days in culture of all cell lines suggesting that the effect may be general for neuroblastoma cells.

The data in this study also demonstrate that the PKCβ inhibitor augments the effect of natural product chemotherapeutic agents on multidrug-resistant neuroblastoma cells. In contrast to the effect on proliferation, which influenced all cell lines, the augmentation of the anticancer drugs was related to the grade of drug resistance of the cell line. It is therefore conceivable that LY379196 interferes with mechanisms that confer drug resistance to neuroblastoma cells, although it can not be excluded that other factors than the degree of drug resistance explain the difference in sensitivity to LY379196 in the presence of chemotherapeutic drugs.

The acquisition of multidrug resistance upon treatment with anti-cancer drugs is a common phenomenon for neuroblastomas [2]. This is a major reason for the high frequency of fatal outcome of the disease. Drug resistance of cancer cells has been suggested to be caused by increased expression of proteins of the ATP-binding cassette transporter family such as the MDR1 protein product P-glycoprotein and MRP. High expression of MDR1 in neuroblastomas was shown to be related to previous chemotherapeutic treatment [8], to drug resistance [9] and to bad prognosis in a subset of cases [10]. However, it was also shown to correlate inversely to MYCN amplification [11] and to good prognosis [12]. High expression of MRP has been reported to be prognostic for pour outcome [13] although other studies have not found this connection [14, 15]. The expression of MRP is positively influenced by MYCN [16], which is frequently amplified in neuroblastomas with pour outcome. Thus, the specific role of the MDR1 and MRP genes in the acquisition of drug-resistance of neuroblastomas has not yet been settled.

Another study has instead indicated a role for mutation and inactivation of the TP53 tumor suppressor gene in drug resistant neuroblastomas [17, 18]. Furthermore a recent report has shown that chromosome reassortments can lead to drug resistance in cells that lack the MDR1 and MRP1 genes that are thought to confer multidrug resistance [19].

The data in this study demonstrate a correlation between the potentiation of cytotoxic/growth suppressing effects of natural compound anti-cancer drugs and an enhancement of [³H]vincristine accumulation by PKC inhibitors in neuroblastoma cells. This suggests that the drug resistance of the SK-N-BE(2) cells is at least partially mediated by increased elimination of natural products by efflux pumps such as products of the MDR1 and MRP genes. This is supported by studies which have shown that agents that interfere with these pumps sensitizes drug resistant neuroblastoma cells to chemotherapeutic agents of the natural compound class [20, 21]. Furthermore, LY379196 did not augment the effect of carboplatin, which is not a substrate for pumps of the P-glycoprotein family.

PKC activity was initially thought to support the activity of P-glycoprotein since it was shown to be a PKC substrate [22–24] and PKC inhibitors were reported to suppress the activity of the protein [22, 24, 25]. However, later studies demonstrated that phosphorylation of P-glycoprotein did not influence its function [26, 27]. It has also been shown that GF109203X directly influences the activity of P-glycoprotein by competing with other substrates [28] and a similar mechanism of action has also been suggested for the effect of GF109203X on MRP [29] and for the reversal of drug resistance by the PKC inhibitor Ro 32-2241 [30]. The effect of LY379196 may therefore be due to a competition with the anticancer drugs for P-glycoprotein or other members of this family.

However, there are other reports demonstrating attenuating effects of PKC inhibitors on drug resistance that do not involve P-glycoprotein. Safingol and a myristoylated PKC pseudosubstrate peptide have been shown to inhibit PKC and potentiate drug accumulation independently of effects on P-glycoprotein [31–33]. The data in this study indicate that a PKCβ isoform could be a relevant isoform to inhibit in order to attenuate PKC-supported drug resistance. It is notable that the inhibitor with highest specificity for PKCβ also had the most profound effect on the cytotoxicity of vincristine. The smaller effect of the other inhibitors could for instance be due to inhibition of pro-apoptotic PKC isoforms such as PKCδ, which has been shown to be important for apoptosis in several cell types [34–38]. It should be noted that Gö6976 alone causes a substantial decrease of viable neuroblastoma cells, which may imply toxic effects attendant to the lack of isoform specificity. This could mask a potentiating effect on the cytotoxicity of vincristine and also preclude the use of Gö6976 at effective concentrations.

this study raises the potential to use PKCβ isoforms as targets to both partially suppress proliferation and to attenuate the multidrug resistance of neuroblastoma cells.